Variant #0000995097 (NC_000005.9:g.56111414_56111416dup, NM_005921.1:c.14_16dup (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.56111414_56111416dup
DNA change (hg38) -
Published as MAP3K1(NM_005921.1):c.14_16dupCGG (p.(Ala5dup)), MAP3K1(NM_005921.2):c.14_16dupCGG (p.A5dup)
ISCN -
DB-ID MAP3K1_000033 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_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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MAP3K1 NM_005921.1 -?/. - c.14_16dup r.(?) p.(Ala5dup)


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