Variant #0001001599 (NC_000015.9:g.66779598A>G, NM_002755.3:c.928A>G (MAP2K1))

Chromosome 15
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.66779598A>G
DNA change (hg38) -
Published as MAP2K1(NM_002755.3):c.928A>G (p.(Ile310Val))
ISCN -
DB-ID MAP2K1_000038
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MAP2K1 NM_002755.3 ?/. - c.928A>G r.(?) p.(Ile310Val)
SNAPC5 NM_006049.2 ?/. - c.*3479T>C r.(=) p.(=)


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