Variant #0000281426 (NC_000016.9:g.30999462T>C, NM_014712.1:c.*4118T>C (SETD1A))

Chromosome 16
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.30999462T>C
DNA change (hg38) g.30988141T>C
Published as HSD3B7(NM_025193.4):c.1068T>C (p.R356=)
ISCN -
DB-ID HSD3B7_000005
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) 0.58646 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
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.*314T>C r.(=) p.(=)
SETD1A NM_014712.1 -/. - c.*4118T>C r.(=) p.(=)
HSD3B7 NM_025193.3 -/. - c.1068T>C r.(?) p.(Arg356=)
STX1B NM_052874.3 -/. - c.*4680A>G r.(=) p.(=)


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