PRC1[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 154848	GRCh38/hg38 15q22.2-26.3(chr15:59828460-101920998)x3	LOC130057927, LOC130057928 +1764 more	Copy number gain	See cases	GPathogenic
Select item 154952	GRCh38/hg38 15q23-26.3(chr15:72154949-101920998)x3	LOC116268473, LOC116268474 +1244 more	Copy number gain	See cases	GPathogenic
Select item 147691	GRCh38/hg38 15q25.2-26.3(chr15:82859676-101810992)x3	LOC130057943, LOC130057944 +664 more	Copy number gain	See cases	GPathogenic
Select item 146595	GRCh38/hg38 15q25.2-26.3(chr15:83711377-101843270)x3	LOC130057907, LOC130057908 +630 more	Copy number gain	See cases	GPathogenic
Select item 58580	GRCh38/hg38 15q25.2-26.3(chr15:84169153-101904929)x3	ABHD2, ACAN +611 more	Copy number gain	See cases	GPathogenic
Select item 153554	GRCh38/hg38 15q25.3-26.3(chr15:85397539-101888909)x3	ABHD2, ACAN +552 more	Copy number gain	See cases	GPathogenic
Select item 148189	GRCh38/hg38 15q25.3-26.3(chr15:85826665-101920998)x4	MIR11181, MIR1179 +517 more	Copy number gain	See cases	GPathogenic
Select item 146259	GRCh38/hg38 15q25.3-26.3(chr15:87904735-101843270)x3	LOC130057997, LOC130057998 +500 more	Copy number gain	See cases	GPathogenic
Select item 154660	GRCh38/hg38 15q26.1-26.3(chr15:88676575-98364743)x3	LOC130057929, LOC130057930 +311 more	Copy number gain	See cases	GPathogenic
Select item 58582	GRCh38/hg38 15q26.1-26.3(chr15:89679237-101978958)x3	ADAMTS17, ALDH1A3 +422 more	Copy number gain	See cases	GPathogenic
Select item 157651	NM_003981.4(PRC1):c.*919G>T	PRC1	Single nucleotide variant (3 prime UTR variant)	Familial cancer of breast	GUncertain significance
Select item 157646	NM_003981.4(PRC1):c.*769A>G	PRC1	Single nucleotide variant (3 prime UTR variant)	Familial cancer of breast	GUncertain significance
Select item 157650	NM_003981.4(PRC1):c.*733G>A	PRC1, PRC1-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	Familial cancer of breast	GUncertain significance
Select item 157645	NM_003981.4(PRC1):c.*627T>C	PRC1, PRC1-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	Familial cancer of breast	GUncertain significance
Select item 157649	NM_003981.4(PRC1):c.*441C>A	PRC1, PRC1-AS1	Single nucleotide variant (3 prime UTR variant)	Familial cancer of breast	GUncertain significance
Select item 157648	NM_003981.4(PRC1):c.*342A>G	PRC1, PRC1-AS1	Single nucleotide variant (3 prime UTR variant)	Familial cancer of breast	GUncertain significance
Select item 2491346	NM_003981.4(PRC1):c.1802C>T (p.Ser601Leu)	PRC1, PRC1-AS1 (S587L +1 more)	Single nucleotide variant (synonymous variant +1 more)	not specified	GUncertain significance
Select item 157644	NM_003981.4(PRC1):c.1792-828T>C	PRC1, PRC1-AS1	Single nucleotide variant (intron variant)	Familial cancer of breast	GUncertain significance
Select item 2622271	NM_003981.4(PRC1):c.1755T>G (p.Asp585Glu)	PRC1, PRC1-AS1 (D585E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2362018	NM_003981.4(PRC1):c.1739C>T (p.Ser580Phe)	PRC1, PRC1-AS1 (S580F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2311592	NM_003981.4(PRC1):c.1703G>A (p.Arg568His)	PRC1, PRC1-AS1 (R568H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2376487	NM_003981.4(PRC1):c.1672G>T (p.Gly558Cys)	PRC1, PRC1-AS1 (A517S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2599345	NM_003981.4(PRC1):c.1657G>A (p.Gly553Ser)	PRC1, PRC1-AS1 (G553S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218294	NM_003981.4(PRC1):c.1635C>G (p.Asn545Lys)	PRC1, PRC1-AS1 (N504K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218293	NM_003981.4(PRC1):c.1619G>A (p.Gly540Asp)	PRC1, PRC1-AS1 (G540D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3309722	NM_003981.4(PRC1):c.1612C>T (p.Arg538Cys)	PRC1, PRC1-AS1 (R497C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218292	NM_003981.4(PRC1):c.1559C>T (p.Pro520Leu)	PRC1, PRC1-AS1 (P479L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218291	NM_003981.4(PRC1):c.1553T>G (p.Leu518Arg)	PRC1, PRC1-AS1 (L477R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2565419	NM_003981.4(PRC1):c.1550G>A (p.Arg517Gln)	PRC1, PRC1-AS1 (R517Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2567606	NM_003981.4(PRC1):c.1543G>A (p.Val515Met)	PRC1, PRC1-AS1 (V474M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 157643	NM_003981.4(PRC1):c.1532A>G (p.Tyr511Cys)	PRC1, PRC1-AS1 (Y470C +1 more)	Single nucleotide variant (missense variant)	Familial cancer of breast	GUncertain significance
Select item 2366876	NM_003981.4(PRC1):c.1507C>T (p.Arg503Trp)	PRC1, PRC1-AS1 (R462W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218290	NM_003981.4(PRC1):c.1496A>G (p.Asn499Ser)	PRC1, PRC1-AS1 (N458S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 157642	NM_003981.4(PRC1):c.1462-1016G>A	PRC1, PRC1-AS1	Single nucleotide variant (intron variant)	Breast carcinoma	Gassociation
Select item 3309720	NM_003981.4(PRC1):c.1457G>T (p.Arg486Leu)	PRC1, PRC1-AS1 (R445L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2473088	NM_003981.4(PRC1):c.1423C>G (p.Arg475Gly)	PRC1, PRC1-AS1 (R434G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2219724	NM_003981.4(PRC1):c.1406G>A (p.Arg469Gln)	PRC1, PRC1-AS1 (R469Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 157641	NM_003981.4(PRC1):c.1351-3C>T	PRC1, PRC1-AS1	Single nucleotide variant (intron variant)	Familial cancer of breast	GUncertain significance
Select item 157647	NM_003981.3(PRC1):c.1351-124_1351-123insoAC068831.17:g.63209_63266	PRC1, PRC1-AS1	Insertion	Familial cancer of breast	GUncertain significance
Select item 157640	NM_003981.4(PRC1):c.1350+35C>G	PRC1-AS1, PRC1	Single nucleotide variant (intron variant)	Familial cancer of breast	GUncertain significance
Select item 2617635	NM_003981.4(PRC1):c.1331A>G (p.Glu444Gly)	PRC1, PRC1-AS1 (E444G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218289	NM_003981.4(PRC1):c.1318C>G (p.Arg440Gly)	PRC1, PRC1-AS1 (R399G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218288	NM_003981.4(PRC1):c.1266G>A (p.Met422Ile)	PRC1, PRC1-AS1 (M381I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3309719	NM_003981.4(PRC1):c.1235T>C (p.Leu412Ser)	PRC1, PRC1-AS1 (L371S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2464523	NM_003981.4(PRC1):c.1034A>G (p.Tyr345Cys)	PRC1, PRC1-AS1 (Y304C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2359130	NM_003981.4(PRC1):c.1018C>T (p.Arg340Trp)	PRC1, PRC1-AS1 (R340W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 710276	NM_003981.4(PRC1):c.971-4G>A	PRC1, PRC1-AS1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 157639	NM_003981.4(PRC1):c.971-375A>G	PRC1, PRC1-AS1	Single nucleotide variant (intron variant)	Familial cancer of breast	GUncertain significance
Select item 157638	NM_003981.4(PRC1):c.971-441G>A	PRC1, PRC1-AS1	Single nucleotide variant (intron variant)	Familial cancer of breast	GUncertain significance
Select item 157637	NM_003981.4(PRC1):c.971-442C>T	PRC1, PRC1-AS1	Single nucleotide variant (intron variant)	Breast carcinoma	Gassociation
Select item 157636	NM_003981.4(PRC1):c.971-466T>C	PRC1, PRC1-AS1	Single nucleotide variant (intron variant)	Familial cancer of breast	GUncertain significance
Select item 157635	NM_003981.4(PRC1):c.970+436G>A	PRC1, PRC1-AS1	Single nucleotide variant (intron variant)	Familial cancer of breast	GUncertain significance
Select item 2593095	NM_003981.4(PRC1):c.935A>G (p.Gln312Arg)	PRC1, PRC1-AS1 (Q271R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218298	NM_003981.4(PRC1):c.896T>C (p.Val299Ala)	PRC1, PRC1-AS1 (V299A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2411963	NM_003981.4(PRC1):c.893G>A (p.Arg298Gln)	PRC1, PRC1-AS1 (R257Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3218297	NM_003981.4(PRC1):c.875A>C (p.Lys292Thr)	PRC1, PRC1-AS1 (K292T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2595210	NM_003981.4(PRC1):c.863A>G (p.Gln288Arg)	PRC1, PRC1-AS1 (Q247R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2487226	NM_003981.4(PRC1):c.742G>A (p.Asp248Asn)	PRC1, PRC1-AS1 (D207N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2211139	NM_003981.4(PRC1):c.719G>A (p.Arg240His)	PRC1, PRC1-AS1 (R240H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3309723	NM_003981.4(PRC1):c.712G>A (p.Gly238Arg)	PRC1, PRC1-AS1 (G197R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2354421	NM_003981.4(PRC1):c.680T>C (p.Met227Thr)	PRC1, PRC1-AS1 (M186T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2233983	NM_003981.4(PRC1):c.667C>T (p.Arg223Trp)	PRC1, PRC1-AS1 (R182W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2208889	NM_003981.4(PRC1):c.644T>C (p.Ile215Thr)	PRC1, PRC1-AS1 (I215T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2252320	NM_003981.4(PRC1):c.613G>A (p.Glu205Lys)	PRC1, PRC1-AS1 (E205K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2309569	NM_003981.4(PRC1):c.440T>C (p.Val147Ala)	PRC1, PRC1-AS1 (V106A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2511961	NM_003981.4(PRC1):c.332G>A (p.Arg111Gln)	PRC1, PRC1-AS1 (R70Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 157632	NM_003981.4(PRC1):c.282G>A (p.Thr94=)	PRC1-AS1, PRC1	Single nucleotide variant (non-coding transcript variant +1 more)	Familial cancer of breast	GUncertain significance
Select item 157634	NM_003981.4(PRC1):c.268-107G>A	PRC1, PRC1-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	Familial cancer of breast	GUncertain significance
Select item 157633	NM_003981.4(PRC1):c.268-203A>G	PRC1, PRC1-AS1	Single nucleotide variant (intron variant)	Familial cancer of breast	GUncertain significance
Select item 2544012	NM_003981.4(PRC1):c.233C>T (p.Thr78Ile)	LOC126862223, PRC1 +1 more (T78I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 157630	NM_003981.4(PRC1):c.145-81A>T	LOC126862223, PRC1 +1 more	Single nucleotide variant (intron variant)	Familial cancer of breast	GUncertain significance
Select item 3218287	NM_003981.4(PRC1):c.113A>G (p.Gln38Arg)	PRC1, PRC1-AS1 (Q38R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 157631	NM_003981.4(PRC1):c.12-2765T>C	PRC1, PRC1-AS1	Single nucleotide variant (intron variant)	Familial cancer of breast	GUncertain significance
Select item 3063360	GRCh37/hg19 15q26.1(chr15:91488314-91521367)x1	PRC1, RCCD1 +1 more	Copy number loss	not specified	GUncertain significance
Select item 2580298	GRCh37/hg19 15q24.1-26.3(chr15:75165490-102520892)x3	ABHD17C, ABHD2 +174 more	Copy number gain	See cases	GPathogenic
Select item 2498631	GRCh37/hg19 15q25.2-26.3(chr15:84228005-102264590)x3	ABHD2, ACAN +86 more	Copy number gain	not provided	GPathogenic
Select item 2498630	GRCh37/hg19 15q22.33-26.1(chr15:67358491-91644328)x3	AAGAB, ABHD17C +209 more	Copy number gain	not provided	GPathogenic
Select item 2422891	NC_000015.9:g.(?_89379429)_(91565479_?)dup	ABHD2, ACAN +37 more	Duplication	D-2-hydroxyglutaric aciduria 2	GUncertain significance
Select item 1809424	GRCh37/hg19 15q24.3-26.3(chr15:77512817-102035027)x3	ABHD17C, ABHD2 +139 more	Copy number gain	not provided	GPathogenic
Select item 1340806	GRCh37/hg19 15q26.1(chr15:89520451-93926491)x1	ABHD2, ANPEP +41 more	Copy number loss	not provided	GPathogenic
Select item 1328111	GRCh37/hg19 15q25.3-26.2(chr15:88465861-94411846)x1	ABHD2, ACAN +50 more	Copy number loss	not provided	GPathogenic
Select item 1027033	NC_000015.9:g.(?_91290623)_(91512067_?)dup	BLM, FES +6 more	Duplication	Bloom syndrome	GUncertain significance
Select item 983158	GRCh37/hg19 15q25.3-26.3(chr15:86962053-102531392)x1	ABHD2, ACAN +77 more	Copy number loss	See cases	GPathogenic
Select item 833278	NC_000015.10:g.(?_90782812)_(90968837_?)dup	BLM, FES +6 more	Duplication	Bloom syndrome	GUncertain significance
Select item 815743	GRCh37/hg19 15q25.3-26.3(chr15:87189245-102429112)x1	ABHD2, ACAN +76 more	Copy number loss	not provided	GPathogenic
Select item 688677	GRCh37/hg19 15q26.1(chr15:91276782-91550953)x1	BLM, FES +7 more	Copy number loss	not provided	GUncertain significance
Select item 687287	GRCh37/hg19 15q26.1(chr15:91229877-93677014)x1	BLM, C15orf32 +14 more	Copy number loss	not provided	GPathogenic
Select item 686177	GRCh37/hg19 15q26.1-26.3(chr15:90288175-102429112)x3	ADAMTS17, ALDH1A3 +54 more	Copy number gain	not provided	GPathogenic
Select item 625751	GRCh37/hg19 15q25.2-26.1(chr15:83883823-92165844)	ABHD2, ACAN +58 more	Copy number loss	not provided	GPathogenic
Select item 564229	GRCh37/hg19 15q26.1-26.3(chr15:89743929-102429112)x3	ABHD2, ADAMTS17 +66 more	Copy number gain	not provided	GPathogenic
Select item 564221	GRCh37/hg19 15q24.3-26.3(chr15:77479244-102429112)x3	ABHD17C, ABHD2 +143 more	Copy number gain	not provided	GPathogenic
Select item 564214	GRCh37/hg19 15q23-26.3(chr15:71329220-102270758)x3	ABHD17C, ABHD2 +215 more	Copy number gain	not provided	GPathogenic
Select item 560049	Single allele	PDIA3, PEAK1 +521 more	Duplication	not provided	GPathogenic
Select item 443650	GRCh37/hg19 15q25.3-26.3(chr15:86899001-98734014)x3	ABHD2, ACAN +55 more	Copy number gain	See cases	GLikely pathogenic
Select item 443269	GRCh37/hg19 15q24.2-26.3(chr15:76061144-102429112)x3	ABHD17C, ABHD2 +153 more	Copy number gain	See cases	GPathogenic
Select item 442893	GRCh37/hg19 15q11.2-26.3(chr15:22770422-102429112)x3	AAGAB, ABHD17C +559 more	Copy number gain	See cases	GPathogenic
Select item 442892	GRCh37/hg19 15q11.2-26.3(chr15:22770422-102429112)	NOX5, NPAP1 +559 more	Copy number gain	See cases	GPathogenic
Select item 395560	GRCh37/hg19 15q25.3-26.3(chr15:86148286-102511616)x3	ABHD2, ACAN +79 more	Copy number gain	See cases	GPathogenic
Select item 395145	GRCh37/hg19 15q11.2-26.3(chr15:20733395-102511616)x4	CHRFAM7A, CHRM5 +566 more	Copy number gain	See cases	GPathogenic
Select item 395056	GRCh37/hg19 15q26.1-26.3(chr15:90346994-102354798)	ADAMTS17, ALDH1A3 +51 more	Copy number loss	See cases	GPathogenic

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