Variant #0000292099 (NC_000005.9:g.174156168T>C, NM_002449.4:c.386T>C (MSX2))

Chromosome 5
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.174156168T>C
DNA change (hg38) g.174729165T>C
Published as MSX2(NM_002449.4):c.386T>C (p.M129T), MSX2(NM_002449.5):c.386T>C (p.M129T)
ISCN -
DB-ID MSX2_000001 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) 0.88545 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MSX2 NM_002449.4 -/. - c.386T>C r.(?) p.(Met129Thr)


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