Variant #0000283664 (NC_000011.9:g.64574710_64574711del, NM_004579.3:c.-4085_-4084del (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.64574710_64574711del
DNA change (hg38) g.64807238_64807239del
Published as MEN1(NM_000244.3):c.799-15_799-14delTC, MEN1(NM_130803.3):c.799-15_799-14delTC
ISCN -
DB-ID MEN1_000036 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) Retrieve
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
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.-4085_-4084del r.(?) p.(=)


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