Variant #0000282473 (NC_000011.9:g.64572560C>T, NM_004579.3:c.-1939G>A (MAP4K2))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.64572560C>T
DNA change (hg38) g.64805088C>T
Published as MEN1(NM_000244.3):c.1311G>A (p.L437=), MEN1(NM_130799.2):c.1296G>A (p.L432=), MEN1(NM_130803.2):c.1311G>A (p.L437=), MEN1(NM_130803.3):c.1311G>A ...)
ISCN -
DB-ID MEN1_000014 See all 5 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) 0.00113 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 2025-02-07 18:57:27 +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.-1939G>A r.(?) p.(=)


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