Variant #0000991847 (NC_000002.11:g.176983799A>G, NM_002148.3:c.863A>G (HOXD10))

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.176983799A>G
DNA change (hg38) -
Published as HOXD10(NM_002148.3):c.863A>G (p.(Asn288Ser))
ISCN -
DB-ID HOXD8_000012
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 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:07:21 +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     
HOXD8 NM_001199746.1 ?/. - c.-11296A>G r.(?) p.(=)
HOXD10 NM_002148.3 ?/. - c.863A>G r.(?) p.(Asn288Ser)
HOXD9 NM_014213.3 ?/. - c.-3698A>G r.(?) p.(=)


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