Variant #0001053921 (NC_000011.9:g.64572098G>C, NM_001370259.2:c.1541C>G (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.64572098G>C
DNA change (hg38) -
Published as MEN1(NM_001370259.2):c.1541C>G (p.(Pro514Arg))
ISCN -
DB-ID MAP4K2_000023
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) 0 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +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.1541C>G r.(?) p.(Pro514Arg)
MAP4K2 NM_004579.3 ?/. - c.-1477C>G r.(?) p.(=)


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