ClinVar for Gene (Select 84869) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3304126	NM_001166108.2(PALLD):c.2560C>T (p.His854Tyr)	CBR4, PALLD (H455Y +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3304125	NM_001166108.2(PALLD):c.2777T>A (p.Phe926Tyr)	CBR4, PALLD (F219Y +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3304122	NM_001166108.2(PALLD):c.2335G>A (p.Asp779Asn)	CBR4, PALLD (D380N +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3304118	NM_001166108.2(PALLD):c.3105C>T (p.Asn1035=)	CBR4, PALLD	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3304117	NM_001166108.2(PALLD):c.2572T>A (p.Ser858Thr)	CBR4, PALLD (S858T +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3304114	NM_001166108.2(PALLD):c.2798C>G (p.Ala933Gly)	CBR4, PALLD (A933G +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3304111	NM_001166108.2(PALLD):c.3074A>T (p.Lys1025Ile)	CBR4, PALLD (K1008I +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3304108	NM_001166108.2(PALLD):c.3362C>A (p.Ser1121Tyr)	CBR4, PALLD (S1104Y +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3304104	NM_001166108.2(PALLD):c.2497C>A (p.Gln833Lys)	CBR4, PALLD (Q126K +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3304097	NM_001166108.2(PALLD):c.2291A>C (p.Glu764Ala)	CBR4, PALLD (E40A +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3304092	NM_001166108.2(PALLD):c.2345A>G (p.Gln782Arg)	CBR4, PALLD (Q383R +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3304087	NM_001166108.2(PALLD):c.3219A>T (p.Arg1073=)	CBR4, PALLD	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3304085	NM_001166108.2(PALLD):c.2117A>G (p.Glu706Gly)	CBR4, PALLD (E219G +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3304084	NM_001166108.2(PALLD):c.2557C>T (p.Leu853Phe)	CBR4, PALLD (L146F +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3304083	NM_001166108.2(PALLD):c.2597A>G (p.Tyr866Cys)	CBR4, PALLD (Y467C +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3304082	NM_001166108.2(PALLD):c.2157T>G (p.Thr719=)	CBR4, PALLD	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3304073	NM_001166108.2(PALLD):c.2705C>A (p.Pro902His)	CBR4, PALLD (P178H +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3304070	NM_001166108.2(PALLD):c.3196T>A (p.Ser1066Thr)	CBR4, PALLD (S1049T +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3304063	NM_001166108.2(PALLD):c.3175T>C (p.Phe1059Leu)	CBR4, PALLD (F1042L +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3304062	NM_001166108.2(PALLD):c.2623G>T (p.Gly875Cys)	CBR4, PALLD (G476C +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3304059	NM_001166108.2(PALLD):c.2183A>G (p.Glu728Gly)	CBR4, PALLD (E21G +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3304057	NM_001166108.2(PALLD):c.2191G>A (p.Ala731Thr)	CBR4, PALLD (A24T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3304056	NM_001166108.2(PALLD):c.2132G>T (p.Arg711Leu)	CBR4, PALLD (R329L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3304055	NM_001166108.2(PALLD):c.3229C>G (p.His1077Asp)	CBR4, PALLD (H1060D +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3304052	NM_001166108.2(PALLD):c.2662G>A (p.Val888Ile)	CBR4, PALLD (V164I +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3304051	NM_001166108.2(PALLD):c.2719C>T (p.Pro907Ser)	CBR4, PALLD (P403S +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3304046	NM_001166108.2(PALLD):c.2783C>T (p.Pro928Leu)	CBR4, PALLD (P529L +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3304041	NM_001166108.2(PALLD):c.2686C>G (p.Arg896Gly)	CBR4, PALLD (R879G +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3304038	NM_001166108.2(PALLD):c.3300T>G (p.Thr1100=)	CBR4, PALLD	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3304036	NM_001166108.2(PALLD):c.2617C>A (p.Pro873Thr)	CBR4, PALLD (P149T +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3304021	NM_001166108.2(PALLD):c.3285T>C (p.Asp1095=)	CBR4, PALLD	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3304020	NM_001166108.2(PALLD):c.3248A>C (p.Tyr1083Ser)	CBR4, PALLD (Y359S +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3263656	NM_032783.5(CBR4):c.197C>T (p.Thr66Ile)	CBR4 (T66I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3263655	NM_032783.5(CBR4):c.360G>T (p.Arg120Ser)	CBR4 (R120S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226807	NM_001166108.2(PALLD):c.3326T>C (p.Ile1109Thr)	CBR4, PALLD (I1092T +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226806	NM_001166108.2(PALLD):c.3309C>T (p.Ala1103=)	CBR4, PALLD	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3226804	NM_001166108.2(PALLD):c.3287C>G (p.Ala1096Gly)	CBR4, PALLD (A1079G +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226802	NM_001166108.2(PALLD):c.3254G>T (p.Cys1085Phe)	CBR4, PALLD (C1068F +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226801	NM_001166108.2(PALLD):c.3253T>C (p.Cys1085Arg)	CBR4, PALLD (C1068R +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226798	NM_001166108.2(PALLD):c.3165A>T (p.Pro1055=)	CBR4, PALLD	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3226794	NM_001166108.2(PALLD):c.3020C>G (p.Ala1007Gly)	CBR4, PALLD (A1007G +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226793	NM_001166108.2(PALLD):c.2950C>T (p.His984Tyr)	CBR4, PALLD (H260Y +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226791	NM_001166108.2(PALLD):c.2929C>T (p.Leu977=)	CBR4, PALLD	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3226790	NM_001166108.2(PALLD):c.2915G>A (p.Ser972Asn)	CBR4, PALLD (S248N +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226789	NM_001166108.2(PALLD):c.2902G>T (p.Val968Leu)	CBR4, PALLD (V244L +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226788	NM_001166108.2(PALLD):c.2896A>C (p.Lys966Gln)	CBR4, PALLD (K242Q +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226787	NM_001166108.2(PALLD):c.2888T>C (p.Leu963Pro)	CBR4, PALLD (L239P +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226786	NM_001166108.2(PALLD):c.2887C>T (p.Leu963=)	CBR4, PALLD	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3226784	NM_001166108.2(PALLD):c.2813C>T (p.Thr938Ile)	CBR4, PALLD (T214I +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226783	NM_001166108.2(PALLD):c.2709T>C (p.His903=)	CBR4, PALLD	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3226782	NM_001166108.2(PALLD):c.2683C>A (p.Pro895Thr)	CBR4, PALLD (P171T +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226781	NM_001166108.2(PALLD):c.2675G>T (p.Gly892Val)	CBR4, PALLD (G168V +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226780	NM_001166108.2(PALLD):c.2672G>C (p.Arg891Thr)	CBR4, PALLD (R167T +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226778	NM_001166108.2(PALLD):c.2621A>C (p.Gln874Pro)	CBR4, PALLD (Q150P +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226777	NM_001166108.2(PALLD):c.2595T>G (p.Asn865Lys)	CBR4, PALLD (N141K +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226776	NM_001166108.2(PALLD):c.2526C>T (p.Thr842=)	CBR4, PALLD	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3226775	NM_001166108.2(PALLD):c.2508A>G (p.Pro836=)	CBR4, PALLD	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3226772	NM_001166108.2(PALLD):c.2391G>A (p.Glu797=)	CBR4, PALLD	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3226771	NM_001166108.2(PALLD):c.2369A>G (p.Asn790Ser)	CBR4, PALLD (N286S +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226769	NM_001166108.2(PALLD):c.2315C>G (p.Ser772Cys)	CBR4, PALLD (S268C +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226768	NM_001166108.2(PALLD):c.2261T>C (p.Val754Ala)	CBR4, PALLD (V250A +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3226767	NM_001166108.2(PALLD):c.2159T>C (p.Val720Ala)	CBR4, PALLD (V13A +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3208125	NM_001166108.2(PALLD):c.*93G>C	CBR4, PALLD (R636P +3 more)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3208119	NM_001166108.2(PALLD):c.2627G>T (p.Arg876Leu)	CBR4, PALLD (R169L +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3208118	NM_001166108.2(PALLD):c.2548A>G (p.Thr850Ala)	CBR4, PALLD (T143A +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3138043	NM_032783.5(CBR4):c.550G>C (p.Asp184His)	CBR4 (D184H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3138042	NM_032783.5(CBR4):c.530C>T (p.Ala177Val)	CBR4 (A177V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3138041	NM_032783.5(CBR4):c.359G>A (p.Arg120Lys)	CBR4 (R120K)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3138040	NM_032783.5(CBR4):c.355A>G (p.Met119Val)	CBR4 (M119V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3138039	NM_032783.5(CBR4):c.136C>G (p.Leu46Val)	CBR4 (L46V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3062804	GRCh37/hg19 4q27-35.2(chr4:123399154-190957473)x3	FAT1, FAT4 +197 more	Copy number gain	not specified	GPathogenic
Select item 3062803	GRCh37/hg19 4q32.1-35.2(chr4:161589441-190957473)x1	AADAT, ACSL1 +85 more	Copy number loss	not specified	GPathogenic
Select item 3062767	GRCh37/hg19 4q24-35.2(chr4:101203509-190957473)x3	AADAT, ABCE1 +286 more	Copy number gain	not specified	GPathogenic
Select item 3058626	NM_001166108.2(PALLD):c.2242G>C (p.Gly748Arg)	CBR4, PALLD (G41R +1 more)	Single nucleotide variant (missense variant +1 more)	PALLD-related disorder	GUncertain significance
Select item 3024634	GRCh37/hg19 4q32.3-35.2(chr4:169060637-191154276)x1	AADAT, ACSL1 +68 more	Copy number loss	not provided	GPathogenic
Select item 3024631	GRCh37/hg19 4p12-q35.2(chr4:45455621-191003541)x3	CAMK2D, GIMD1 +537 more	Copy number gain	not provided	GPathogenic
Select item 3013308	NM_001166108.2(PALLD):c.2818C>A (p.Gln940Lys)	CBR4, PALLD (Q923K +5 more)	Single nucleotide variant (missense variant)	Pancreatic adenocarcinoma	GUncertain significance
Select item 3003877	NM_001166108.2(PALLD):c.*136G>C	CBR4, PALLD	Single nucleotide variant (3 prime UTR variant +1 more)	Pancreatic adenocarcinoma	GLikely benign
Select item 2999840	NM_001166108.2(PALLD):c.3225-16_3225-15del	CBR4, PALLD	Deletion (intron variant)	Pancreatic adenocarcinoma	GLikely benign
Select item 2998346	NM_001166108.2(PALLD):c.*182T>A	CBR4, PALLD (L666M +3 more)	Single nucleotide variant (3 prime UTR variant +1 more)	Pancreatic adenocarcinoma	GUncertain significance
Select item 2991700	NM_001166108.2(PALLD):c.2260G>A (p.Val754Ile)	CBR4, PALLD (V47I +5 more)	Single nucleotide variant (missense variant)	Pancreatic adenocarcinoma	GUncertain significance
Select item 2980037	NM_001166108.2(PALLD):c.2747A>G (p.Asp916Gly)	CBR4, PALLD (D209G +5 more)	Single nucleotide variant (missense variant)	Pancreatic adenocarcinoma	GUncertain significance
Select item 2979902	NM_001166108.2(PALLD):c.2998A>G (p.Thr1000Ala)	CBR4, PALLD (T496A +5 more)	Single nucleotide variant (missense variant)	Pancreatic adenocarcinoma	GUncertain significance
Select item 2960067	NM_001166108.2(PALLD):c.2254T>C (p.Tyr752His)	CBR4, PALLD (Y752H +5 more)	Single nucleotide variant (missense variant)	Pancreatic adenocarcinoma	GUncertain significance
Select item 2919923	NM_001166108.2(PALLD):c.3059-13C>T	CBR4, PALLD	Single nucleotide variant (intron variant)	Pancreatic adenocarcinoma	GLikely benign
Select item 2919879	NM_001166108.2(PALLD):c.2949G>A (p.Val983=)	CBR4, PALLD	Single nucleotide variant (synonymous variant)	Pancreatic adenocarcinoma	GLikely benign
Select item 2919576	NM_001166108.2(PALLD):c.3017G>A (p.Arg1006Gln)	CBR4, PALLD (R1006Q +5 more)	Single nucleotide variant (missense variant)	Pancreatic adenocarcinoma	GUncertain significance
Select item 2918513	NM_001166108.2(PALLD):c.2473-18C>T	CBR4, PALLD	Single nucleotide variant (intron variant)	Pancreatic adenocarcinoma	GLikely benign
Select item 2912553	NM_001166108.2(PALLD):c.2101-11dup	CBR4, PALLD	Duplication (intron variant)	Pancreatic adenocarcinoma	GLikely benign
Select item 2891260	NM_001166108.2(PALLD):c.3059-6T>C	CBR4, PALLD	Single nucleotide variant (intron variant)	Pancreatic adenocarcinoma	GLikely benign
Select item 2886138	NM_001166108.2(PALLD):c.2853C>T (p.Val951=)	CBR4, PALLD	Single nucleotide variant (synonymous variant)	not specified +1 more	GLikely benign
Select item 2885263	NM_001166108.2(PALLD):c.2472+8G>A	CBR4, PALLD	Single nucleotide variant (intron variant)	Pancreatic adenocarcinoma	GLikely benign
Select item 2855028	NM_001166108.2(PALLD):c.2491G>A (p.Gly831Arg)	CBR4, PALLD (G124R +5 more)	Single nucleotide variant (missense variant)	Pancreatic adenocarcinoma	GUncertain significance
Select item 2854729	NM_001166108.2(PALLD):c.*136G>T	CBR4, PALLD	Single nucleotide variant (synonymous variant +1 more)	Pancreatic adenocarcinoma	GLikely benign
Select item 2828962	NM_001166108.2(PALLD):c.3225-18C>G	CBR4, PALLD	Single nucleotide variant (intron variant)	Pancreatic adenocarcinoma	GLikely benign
Select item 2827343	NM_001166108.2(PALLD):c.*73A>T	CBR4, PALLD (K409N +3 more)	Single nucleotide variant (3 prime UTR variant +1 more)	Pancreatic adenocarcinoma	GUncertain significance
Select item 2811452	NM_001166108.2(PALLD):c.2988C>A (p.Ala996=)	CBR4, PALLD	Single nucleotide variant (synonymous variant)	Pancreatic adenocarcinoma	GLikely benign
Select item 2807372	NM_001166108.2(PALLD):c.2428C>T (p.Pro810Ser)	CBR4, PALLD (P793S +5 more)	Single nucleotide variant (missense variant)	Pancreatic adenocarcinoma	GUncertain significance
Select item 2806716	NM_001166108.2(PALLD):c.2708A>G (p.His903Arg)	CBR4, PALLD (H179R +5 more)	Single nucleotide variant (missense variant)	Pancreatic adenocarcinoma	GUncertain significance
Select item 2802897	NM_001166108.2(PALLD):c.2815G>A (p.Val939Ile)	CBR4, PALLD (V939I +5 more)	Single nucleotide variant (missense variant)	Pancreatic adenocarcinoma	GUncertain significance

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