Variant #0001048129 (NC_000015.9:g.66727453A>G, NM_002755.3:c.169A>G (MAP2K1))

Chromosome 15
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.66727453A>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID MAP2K1_000042
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs397516790
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-09-19 12:16:01 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MAP2K1 NM_002755.3 +/. - c.169A>G r.(?) p.(Lys57Glu)


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