Variant #0000966477 (NC_000011.9:g.64573799del, NM_001370259.2:c.954del (MEN1))

Chromosome 11
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.64573799del
DNA change (hg38) -
Published as MEN1(NM_130799.2):c.954delC (p.Y319Tfs*49)
ISCN -
DB-ID MAP4K2_000016
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2024-02-26 20:06:56 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MEN1 NM_001370259.2 +/. - c.954del r.(?) p.(Tyr319Thrfs*49)
MAP4K2 NM_004579.3 +/. - c.-3178del r.(?) p.(=)


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