Variant #0000854486 (NC_000016.9:g.30998266G>A, NM_014712.1:c.*2922G>A (SETD1A))

Chromosome 16
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.30998266G>A
DNA change (hg38) -
Published as HSD3B7(NM_025193.3):c.637G>A (p.G213R)
ISCN -
DB-ID HSD3B7_000025
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00012 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:47:41 +02:00 (CEST)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HSD3B7 NM_001142777.1 ?/. - c.531+241G>A r.(=) p.(=)
SETD1A NM_014712.1 ?/. - c.*2922G>A r.(=) p.(=)
HSD3B7 NM_025193.3 ?/. - c.637G>A r.(?) p.(Gly213Arg)
STX1B NM_052874.3 ?/. - c.*5876C>T r.(=) p.(=)


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