Variant #0000282474 (NC_000011.9:g.64572018T>C, NM_004579.3:c.-1397A>G (MAP4K2))

Chromosome 11
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.64572018T>C
DNA change (hg38) g.64804546T>C
Published as MEN1(NM_130799.2):c.1621A>G (p.T541A), MEN1(NM_130803.3):c.1636A>G (p.T546A)
ISCN -
DB-ID MEN1_000008 See all 2 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) 0.93905 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.-1397A>G r.(?) p.(=)


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