Variant #0001014856 (NC_000011.9:g.64572600C>T, NM_001370259.2:c.1256G>A (MEN1))

Chromosome 11
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.64572600C>T
DNA change (hg38) -
Published as MEN1(NM_130799.3):c.1256G>A (p.G419D)
ISCN -
DB-ID MAP4K2_000020
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 2024-10-29 21:08:56 +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.1256G>A r.(?) p.(Gly419Asp)
MAP4K2 NM_004579.3 ?/. - c.-1979G>A r.(?) p.(=)


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