Variant #0000324743 (NC_000016.9:g.31004732A>G, NM_014712.1:c.*9388A>G (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.31004732A>G
DNA change (hg38) g.30993411A>G
Published as STX1B(NM_052874.3):c.611T>C (p.(Leu204Pro))
ISCN -
DB-ID STX1B_000001
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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.*5584A>G r.(=) p.(=)
SETD1A NM_014712.1 ?/. - c.*9388A>G r.(=) p.(=)
HSD3B7 NM_025193.3 ?/. - c.*5228A>G r.(=) p.(=)
STX1B NM_052874.3 ?/. - c.611T>C r.(?) p.(Leu204Pro)


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