Variant #0000282383 (NC_000005.9:g.56177872_56177874del, NM_005921.1:c.2845_2847del (MAP3K1))

Chromosome 5
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.56177872_56177874del
DNA change (hg38) g.56882045_56882047del
Published as MAP3K1(NM_005921.1):c.2822_2824del (p.(Thr944del)), MAP3K1(NM_005921.1):c.2845_2847delACA (p.T949del), MAP3K1(NM_005921.2):c.2845_2847delACA (p.T9...)
ISCN -
DB-ID MAP3K1_000015
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MAP3K1 NM_005921.1 -/. - c.2845_2847del r.(?) p.(Thr949del)


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