Variant #0000525844 (NC_000005.9:g.56161787G>A, NM_005921.1:c.1284G>A (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.56161787G>A
DNA change (hg38) g.56865960G>A
Published as MAP3K1(NM_005921.1):c.1284G>A (p.T428=), MAP3K1(NM_005921.2):c.1284G>A (p.T428=)
ISCN -
DB-ID MAP3K1_000041 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) 0.84277 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +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.1284G>A r.(?) p.(Thr428=)


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