Variant #0000282475 (NC_000011.9:g.64572009G>A, NM_004579.3:c.-1388C>T (MAP4K2))

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.64572009G>A
DNA change (hg38) g.64804537G>A
Published as MEN1(NM_130799.3):c.1630C>T (p.P544S), MEN1(NM_130803.2):c.1645C>T (p.P549S)
ISCN -
DB-ID MEN1_000007 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) 0 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-11-27 17:27:23 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MAP4K2 NM_004579.3 ?/. - c.-1388C>T r.(?) p.(=)


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