Variant #0001026041 (NC_000011.9:g.64571974_64571977del, NM_001370259.2:c.1665_1668del (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.64571974_64571977del
DNA change (hg38) -
Published as MEN1(NM_130799.3):c.1665_1668delTGAG (p.S555Rfs*3)
ISCN -
DB-ID MAP4K2_000021
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 2025-02-07 18:57:27 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MEN1 NM_001370259.2 +/. - c.1665_1668del r.(?) p.(Ser555Argfs*3)
MAP4K2 NM_004579.3 +/. - c.-1353_-1350del r.(?) p.(=)


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