Variant #0000253214 (NC_000005.9:g.56178217A>C, NM_005921.1:c.3190A>C (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.56178217A>C
DNA change (hg38) g.56882390A>C
Published as MAP3K1(NM_005921.1):c.3190A>C (p.R1064=), MAP3K1(NM_005921.2):c.3190A>C (p.R1064=)
ISCN -
DB-ID MAP3K1_000017 See all 2 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) 0.75869 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 2018-01-15 20:58:59 +01:00 (CET)
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.3190A>C r.(?) p.(Arg1064=)


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