SULT1B1[gene] - ClinVar

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Items: 42

	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 1098574	GRCh38/hg38 4q12-21.1(chr4:51891814-76009719)x1	ENAM, LOC116158492 +360 more	Copy number loss	Piebaldism	GPathogenic
Select item 59451	GRCh38/hg38 4q13.1-13.3(chr4:65454562-72313693)x1	LOC129992665, LOC129992666 +103 more	Copy number loss	See cases	GPathogenic
Select item 57091	GRCh38/hg38 4q13.2-13.3(chr4:66842408-70831557)x1	AMBN, AMTN +76 more	Copy number loss	See cases	GPathogenic
Select item 154298	GRCh38/hg38 4q13.2-13.3(chr4:67744481-70267689)x1	CSN1S1, CSN2 +43 more	Copy number loss	See cases	GUncertain significance
Select item 148549	GRCh38/hg38 4q13.2-13.3(chr4:67799665-74240920)x1	ADAMTS3, AFM +121 more	Copy number loss	See cases	GLikely pathogenic
Select item 1684642	NC_000004.12:g.67833055_82716065del	LINC01088, LINC01094 +330 more	Deletion	See cases	GPathogenic
Select item 155391	GRCh38/hg38 4q13.2-22.3(chr4:68686088-95294456)x3	LOC129992716, LOC129992717 +533 more	Copy number gain	See cases	GPathogenic
Select item 152287	GRCh38/hg38 4q13.2-13.3(chr4:68796335-69850009)x3	LOC105377267, LOC111589210 +22 more	Copy number gain	See cases	GUncertain significance
Select item 155054	GRCh38/hg38 4q13.2-13.3(chr4:68799852-69853815)x3	LOC105377267, LOC111589210 +22 more	Copy number gain	See cases	GUncertain significance
Select item 160854	GRCh38/hg38 4q13.2-13.3(chr4:68852530-69850009)x3	LOC105377267, LOC111589210 +21 more	Copy number gain	See cases	GUncertain significance
Select item 147584	GRCh38/hg38 4q13.2-13.3(chr4:68902161-70620273)x3	AMBN, AMTN +38 more	Copy number gain	See cases	GPathogenic
Select item 2654791	NM_014465.4(SULT1B1):c.782C>T (p.Thr261Met)	SULT1B1 (T261M)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2344336	NM_014465.4(SULT1B1):c.665A>G (p.Asp222Gly)	SULT1B1 (D222G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2256193	NM_014465.4(SULT1B1):c.628A>G (p.Arg210Gly)	SULT1B1 (R210G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2549372	NM_014465.4(SULT1B1):c.569T>A (p.Leu190His)	SULT1B1 (L190H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 775983	NM_014465.4(SULT1B1):c.433T>G (p.Leu145Val)	SULT1B1 (L145V)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2619149	NM_014465.4(SULT1B1):c.392G>C (p.Arg131Pro)	SULT1B1 (R131P)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2573327	NM_014465.4(SULT1B1):c.376-6044T>C	SULT1B1	Single nucleotide variant (intron variant)	Levothyroxine response	Gother
Select item 787615	NM_014465.4(SULT1B1):c.192T>C (p.Asp64=)	SULT1B1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2494740	NM_014465.4(SULT1B1):c.10C>T (p.Pro4Ser)	SULT1B1 (P4S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 60167	GRCh38/hg38 4q13.3(chr4:69758599-70193037)x1	CSN1S1, CSN2 +10 more	Copy number loss	See cases	GUncertain significance
Select item 3062785	GRCh37/hg19 4q13.3(chr4:70563498-71253752)x1	CABS1, CSN1S1 +12 more	Copy number loss	not specified	GUncertain significance
Select item 3024631	GRCh37/hg19 4p12-q35.2(chr4:45455621-191003541)x3	TMA16, CXCL1 +537 more	Copy number gain	not provided	GPathogenic
Select item 2685970	GRCh37/hg19 4q13.1-13.3(chr4:63684557-71480358)x3	AMBN, AMTN +38 more	Copy number gain	not provided	GPathogenic
Select item 2685114	GRCh37/hg19 4q13.2-13.3(chr4:69146217-75500577)x1	ADAMTS3, AFM +58 more	Copy number loss	not provided	GPathogenic
Select item 2685109	GRCh37/hg19 4q12-13.3(chr4:57584845-72430996)x1	ADGRL3, AMBN +52 more	Copy number loss	not provided	GPathogenic
Select item 1809429	GRCh37/hg19 4q13.2-13.3(chr4:70479061-70985189)x1	CSN1S1, CSN2 +7 more	Copy number loss	not provided	GUncertain significance
Select item 1808523	GRCh37/hg19 4q13.2-13.3(chr4:69661413-70724847)x3	UGT2A1, UGT2A2 +8 more	Copy number gain	not provided	GUncertain significance
Select item 1808451	GRCh37/hg19 4q13.2-13.3(chr4:70478978-70985189)x1	CSN1S1, CSN2 +7 more	Copy number loss	not provided	GUncertain significance
Select item 1527090	GRCh37/hg19 4q13.1-13.3(chr4:61867555-74711517)	ADAMTS3, ADGRL3 +58 more	Copy number loss	not specified	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 814564	GRCh37/hg19 4q13.3(chr4:70618421-71083238)x1	CSN1S1, PRR27 +7 more	Copy number loss	not provided	GUncertain significance
Select item 814563	GRCh37/hg19 4q13.2-21.21(chr4:68950363-79738598)x1	ADAMTS3, AFM +92 more	Copy number loss	not provided	GPathogenic
Select item 685236	GRCh37/hg19 4q13.2-21.22(chr4:68242784-82991431)x3	CCNG2, CCNI +109 more	Copy number gain	not provided	GPathogenic
Select item 562928	GRCh37/hg19 4q13.3(chr4:70594519-70885440)x3	CSN1S1, STATH +3 more	Copy number gain	not provided	GUncertain significance
Select item 562927	GRCh37/hg19 4q13.2-13.3(chr4:70012338-71167321)x3	CSN1S1, SULT1E1 +14 more	Copy number gain	not provided	GUncertain significance
Select item 562920	GRCh37/hg19 4q13.1-13.3(chr4:64705501-73469716)x3	ADAMTS3, AMBN +49 more	Copy number gain	not provided	GPathogenic
Select item 443262	GRCh37/hg19 4q13.1-21.1(chr4:66017575-76772947)x1	ADAMTS3, AFM +75 more	Copy number loss	See cases	GPathogenic
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	SCRG1, SDAD1 +745 more	Copy number gain	See cases	GPathogenic
Select item 394609	GRCh37/hg19 4p16.3-q35.2(chr4:12440-190904441)x3	CCKAR, CWH43 +744 more	Copy number gain	See cases	GPathogenic

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Items: 42