Variant #0001013415 (NC_000002.11:g.176982167C>G, NM_002148.3:c.606C>G (HOXD10))

Chromosome 2
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.176982167C>G
DNA change (hg38) -
Published as HOXD10(NM_002148.4):c.606C>G (p.N202K)
ISCN -
DB-ID HOXD8_000013
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) 0.00035 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2024-10-29 20:49:11 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HOXD8 NM_001199746.1 -/. - c.-12928C>G r.(?) p.(=)
HOXD10 NM_002148.3 -/. - c.606C>G r.(?) p.(Asn202Lys)
HOXD9 NM_014213.3 -/. - c.-5330C>G r.(?) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.