HNRNPD[gene] - ClinVar

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Items: 70

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58029	GRCh38/hg38 4q12-22.3(chr4:51831622-97505618)x3	LOC129389216, LOC129389217 +757 more	Copy number gain	See cases	GPathogenic
Select item 1684642	NC_000004.12:g.67833055_82716065del	LOC129992745, LOC129992746 +330 more	Deletion	See cases	GPathogenic
Select item 155391	GRCh38/hg38 4q13.2-22.3(chr4:68686088-95294456)x3	LOC129992695, LOC129992696 +533 more	Copy number gain	See cases	GPathogenic
Select item 149262	GRCh38/hg38 4q13.3-21.3(chr4:72262258-86002147)x3	ABRAXAS1, ADAMTS3 +331 more	Copy number gain	See cases	GPathogenic
Select item 57143	GRCh38/hg38 4q21.1-21.23(chr4:75453111-84094295)x1	LOC129992714, LOC129992715 +236 more	Copy number loss	See cases	GPathogenic
Select item 2579270	GRCh38/hg38 4q21.21-23(chr4:79123548-99457773)x1	ABCG2, ABRAXAS1 +338 more	Copy number loss	Chromosome 4q21 deletion syndrome	GPathogenic
Select item 59455	GRCh38/hg38 4q21.21-22.1(chr4:79575748-92412449)x1	ABCG2, ABRAXAS1 +251 more	Copy number loss	See cases	GPathogenic
Select item 146518	GRCh38/hg38 4q21.21-21.22(chr4:79742612-83153725)x1	ANTXR2, BMP3 +83 more	Copy number loss	See cases	GUncertain significance
Select item 147709	GRCh38/hg38 4q21.21-21.23(chr4:79786514-85832807)x1	BMP3, CDS1 +137 more	Copy number loss	See cases	GPathogenic
Select item 151718	GRCh38/hg38 4q21.21-21.3(chr4:80043949-86948317)x1	ABRAXAS1, AFF1 +146 more	Copy number loss	See cases	GPathogenic
Select item 148194	GRCh38/hg38 4q21.21-24(chr4:80427023-100855441)x1	ABCG2, ABRAXAS1 +335 more	Copy number loss	See cases	GPathogenic
Select item 145649	GRCh38/hg38 4q21.21-22.3(chr4:80879777-94809447)x1	ABCG2, ABRAXAS1 +244 more	Copy number loss	See cases	GPathogenic
Select item 148797	GRCh38/hg38 4q21.21-21.23(chr4:80908016-84329610)x1	ABRAXAS1, BMP3 +90 more	Copy number loss	See cases	GLikely pathogenic
Select item 59456	GRCh38/hg38 4q21.21-21.23(chr4:81061483-83332595)x1	COPS4, COQ2 +68 more	Copy number loss	See cases	GPathogenic
Select item 155254	GRCh38/hg38 4q21.22-21.23(chr4:81675848-83970410)x1	ABRAXAS1, COPS4 +74 more	Copy number loss	See cases	GLikely pathogenic
Select item 59457	GRCh38/hg38 4q21.22-21.23(chr4:81733333-83448842)x1	COPS4, COQ2 +60 more	Copy number loss	See cases	GPathogenic
Select item 59458	GRCh38/hg38 4q21.22-21.23(chr4:81802008-83437114)x1	COPS4, COQ2 +60 more	Copy number loss	See cases	GPathogenic
Select item 1264087	NM_031370.3(HNRNPD):c.*30+71C>T	HNRNPD	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1233935	NM_031370.3(HNRNPD):c.*30+18dup	HNRNPD	Duplication (intron variant)	not provided	GBenign
Select item 3284562	NM_031370.3(HNRNPD):c.1008G>C (p.Gln336His)	HNRNPD (Q268H +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3106397	NM_031370.3(HNRNPD):c.943T>G (p.Tyr315Asp)	HNRNPD (Y315D +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2554834	NM_031370.3(HNRNPD):c.928C>G (p.Gln310Glu)	HNRNPD (Q310E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2340172	NM_031370.3(HNRNPD):c.890A>G (p.Tyr297Cys)	HNRNPD (Y297C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2537370	NM_031370.3(HNRNPD):c.848G>C (p.Gly283Ala)	HNRNPD (G283A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3051593	NM_031370.3(HNRNPD):c.786A>G (p.Gln262=)	HNRNPD	Single nucleotide variant (synonymous variant)	HNRNPD-related disorder	GLikely benign
Select item 2406306	NM_031370.3(HNRNPD):c.703C>T (p.Pro235Ser)	HNRNPD (P216S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3284563	NM_031370.3(HNRNPD):c.691A>G (p.Lys231Glu)	HNRNPD (K231E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2329473	NM_031370.3(HNRNPD):c.659A>G (p.Asn220Ser)	HNRNPD (N201S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 624014	NM_031370.3(HNRNPD):c.635_638dup (p.Pro214fs)	HNRNPD (P214fs +1 more)	Duplication (frameshift variant)	not provided	GUncertain significance
Select item 1224234	NM_031370.3(HNRNPD):c.622-181A>G	HNRNPD	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1275527	NM_031370.3(HNRNPD):c.622-318A>T	HNRNPD	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1234705	NM_031370.3(HNRNPD):c.621+90A>G	HNRNPD	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1277518	NM_031370.3(HNRNPD):c.621+81G>A	HNRNPD	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1273209	NM_031370.3(HNRNPD):c.234-296T>A	HNRNPD	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2378074	NM_031370.3(HNRNPD):c.187T>G (p.Ser63Ala)	HNRNPD, LOC129992757 (S63A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2556313	NM_031370.3(HNRNPD):c.182C>T (p.Ala61Val)	HNRNPD, LOC129992757 (A61V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3284561	NM_031370.3(HNRNPD):c.166A>T (p.Thr56Ser)	HNRNPD, LOC129992757 (T56S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3106395	NM_031370.3(HNRNPD):c.146G>A (p.Gly49Asp)	HNRNPD, LOC129992757 (G49D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3026803	NM_031370.3(HNRNPD):c.104_105del (p.Gln35fs)	HNRNPD, LOC129992757 (Q35fs)	Deletion (frameshift variant)	not provided	GPathogenic
Select item 3044881	NM_031370.3(HNRNPD):c.54G>A (p.Ala18=)	HNRNPD	Single nucleotide variant (synonymous variant)	HNRNPD-related disorder	GLikely benign
Select item 2604388	NM_031370.3(HNRNPD):c.41C>T (p.Ala14Val)	HNRNPD (A14V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2208162	NM_031370.3(HNRNPD):c.26A>T (p.Asp9Val)	HNRNPD (D9V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3047673	NM_031370.3(HNRNPD):c.18C>A (p.Phe6Leu)	HNRNPD (F6L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1180954	NC_000004.12:g.82374077dup	HNRNPD, LOC129992758	Duplication	not provided	GBenign
Select item 3062764	GRCh37/hg19 4q21.21-22.3(chr4:81558759-95965995)x1	ABCG2, ABRAXAS1 +59 more	Copy number loss	not specified	GPathogenic
Select item 3024631	GRCh37/hg19 4p12-q35.2(chr4:45455621-191003541)x3	HPGDS, SCRG1 +537 more	Copy number gain	not provided	GPathogenic
Select item 1808776	GRCh37/hg19 4q21.22(chr4:82769768-83287770)x1	HNRNPD	Copy number loss	not provided	GUncertain significance
Select item 1527103	GRCh37/hg19 4q21.21-22.1(chr4:81054789-90667421)	ABCG2, ABRAXAS1 +53 more	Copy number loss	not specified	GPathogenic
Select item 1527100	GRCh37/hg19 4q21.21-22.2(chr4:79780152-94873225)	ABCG2, ABRAXAS1 +63 more	Copy number loss	not specified	GPathogenic
Select item 1527097	GRCh37/hg19 4q13.3-22.1(chr4:75737340-91131156)	ABCG2, ABRAXAS1 +91 more	Copy number gain	not specified	GPathogenic
Select item 1341211	GRCh37/hg19 4q21.21-22.1(chr4:80467886-93362064)x1	ABCG2, ABRAXAS1 +58 more	Copy number loss	not provided	GPathogenic
Select item 1340288	GRCh37/hg19 4q12-31.21(chr4:52866944-143582507)x3	AASDH, ABCG2 +359 more	Copy number gain	not provided	GPathogenic
Select item 983172	GRCh37/hg19 4q13.3-21.3(chr4:71412409-87920784)x1	ABRAXAS1, ADAMTS3 +97 more	Copy number loss	See cases	GPathogenic
Select item 830313	Single allele	CDS1, COPS4 +16 more	Deletion	Chromosome 4q21 deletion syndrome	GPathogenic
Select item 814577	GRCh37/hg19 4q21.22(chr4:83026373-83367140)x1	HNRNPDL, ENOPH1 +1 more	Copy number loss	not provided	GLikely pathogenic
Select item 814576	GRCh37/hg19 4q21.22-21.23(chr4:82593140-85651685)x1	ENOPH1, MRPS18C +17 more	Copy number loss	not provided	GPathogenic
Select item 814566	GRCh37/hg19 4q13.3-21.23(chr4:72680879-86426232)x1	CXCL3, LIN54 +82 more	Copy number loss	not provided	GPathogenic
Select item 687488	GRCh37/hg19 4q21.21-21.22(chr4:80199183-84074906)x1	ANTXR2, BMP3 +18 more	Copy number loss	not provided	GPathogenic
Select item 686225	GRCh37/hg19 4q21.1-21.23(chr4:78769297-84968832)x1	ABRAXAS1, ANTXR2 +29 more	Copy number loss	not provided	GPathogenic
Select item 638111	GRCh37/hg19 4q21.21-22.1(chr4:80482400-92572499)x1	GPRIN3, HELQ +57 more	Copy number loss	See cases	GPathogenic
Select item 625784	GRCh37/hg19 4q21.21-22.1(chr4:82043901-88334228)	ABRAXAS1, AFF1 +28 more	Copy number loss	not provided	GPathogenic
Select item 562937	GRCh37/hg19 4q21.21-22.3(chr4:81314915-96636651)x1	ABCG2, ABRAXAS1 +60 more	Copy number loss	not provided	GPathogenic
Select item 443596	GRCh37/hg19 4q21.22(chr4:83003904-83575588)x1	ENOPH1, HNRNPD +3 more	Copy number loss	See cases	GUncertain significance
Select item 443518	GRCh37/hg19 4q21.22(chr4:83264510-83454808)x1	ENOPH1, HNRNPD +2 more	Copy number loss	See cases	GUncertain significance
Select item 442797	GRCh37/hg19 4q21.21-21.23(chr4:82359656-84155605)x1	COPS4, ENOPH1 +9 more	Copy number loss	See cases	GLikely pathogenic
Select item 442695	GRCh37/hg19 4q21.22(chr4:82790850-83567592)x1	ENOPH1, HNRNPD +3 more	Copy number loss	See cases	GUncertain significance
Select item 441728	GRCh37/hg19 4p16.3-q35.2(chr4:68346-190957473)	AADAT, AASDH +745 more	Copy number gain	See cases	GPathogenic
Select item 441727	GRCh37/hg19 4p16.3-q35.2(chr4:68346-190957473)x3	MRPL1, MSANTD1 +745 more	Copy number gain	See cases	GPathogenic
Select item 394976	GRCh37/hg19 4q21.21-22.1(chr4:82283358-90341831)x1	ABCG2, ABRAXAS1 +47 more	Copy number loss	See cases	GPathogenic
Select item 394609	GRCh37/hg19 4p16.3-q35.2(chr4:12440-190904441)x3	H2AZ1, HADH +744 more	Copy number gain	See cases	GPathogenic

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Items: 70