Variant #0000720463 (NC_000005.9:g.56111858C>T, NM_005921.1:c.458C>T (MAP3K1))

Chromosome 5
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.56111858C>T
DNA change (hg38) -
Published as MAP3K1(NM_005921.1):c.458C>T (p.P153L), MAP3K1(NM_005921.2):c.458C>T (p.(Pro153Leu))
ISCN -
DB-ID MAP3K1_000024 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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +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.458C>T r.(?) p.(Pro153Leu)


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