Variant #0000807360 (NC_000016.9:g.31004164A>G, NM_014712.1:c.*8820A>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.31004164A>G
DNA change (hg38) -
Published as STX1B(NM_052874.3):c.845T>C (p.(Ile282Thr)), STX1B(NM_052874.5):c.845T>C (p.I282T)
ISCN -
DB-ID HSD3B7_000023 See all 3 reported entries
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HSD3B7 NM_001142777.1 ?/. - c.*5016A>G r.(=) p.(=)
SETD1A NM_014712.1 ?/. - c.*8820A>G r.(=) p.(=)
HSD3B7 NM_025193.3 ?/. - c.*4660A>G r.(=) p.(=)
STX1B NM_052874.3 ?/. - c.845T>C r.(?) p.(Ile282Thr)


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