Variant #0000922765 (NC_000002.11:g.176983892T>A, NM_002148.3:c.956T>A (HOXD10))

Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.176983892T>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID HOXD10_000003
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs104893634
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2023-04-13 21:20:01 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HOXD10 NM_002148.3 +/. - c.956T>A r.(?) p.(Met319Lys)


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