Variant #0000892214 (NC_000015.9:g.66777429_66777431del, NM_002755.3:c.795_797del (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.66777429_66777431del
DNA change (hg38) -
Published as MAP2K1(NM_002755.4):c.795_797delTCC (p.P266del)
ISCN -
DB-ID MAP2K1_000036
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2022-11-01 13:41:49 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MAP2K1 NM_002755.3 ?/. - c.795_797del r.(?) p.(Pro266del)
SNAPC5 NM_006049.2 ?/. - c.*5651_*5653del r.(=) p.(=)


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