Variant #0000892940 (NC_000016.9:g.31004511G>C, NM_014712.1:c.*9167G>C (SETD1A))

Chromosome 16
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.31004511G>C
DNA change (hg38) -
Published as STX1B(NM_052874.5):c.726C>G (p.Y242*)
ISCN -
DB-ID HSD3B7_000026
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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2022-11-01 13:41:49 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +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.*5363G>C r.(=) p.(=)
SETD1A NM_014712.1 +/. - c.*9167G>C r.(=) p.(=)
HSD3B7 NM_025193.3 +/. - c.*5007G>C r.(=) p.(=)
STX1B NM_052874.3 +/. - c.726C>G r.(?) p.(Tyr242*)


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