Variant #0000892008 (NC_000015.9:g.37187370T>G, NM_170677.3:c.1129A>C (MEIS2))

Chromosome 15
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.37187370T>G
DNA change (hg38) -
Published as MEIS2(NM_001220482.1):c.1108A>C (p.(Met370Leu)), MEIS2(NM_170674.5):c.1108A>C (p.M370L)
ISCN -
DB-ID MEIS2_000028 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) 4.0E-5 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 2022-11-01 13:41:49 +01:00 (CET)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MEIS2 NM_170677.3 -?/. - c.1129A>C r.(?) p.(Met377Leu)


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