Variant #0000980374 (NC_000012.11:g.54333196C>A, NM_017410.2:c.506C>A (HOXC13))

Chromosome 12
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.54333196C>A
DNA change (hg38) -
Published as HOXC13(NM_017410.3):c.506C>A (p.(Ala169Asp))
ISCN -
DB-ID HOXC13_000007
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HOXC13 NM_017410.2 ?/. - c.506C>A r.(?) p.(Ala169Asp)
HOXC-AS5 NR_047507.1 ?/. - n.173+59G>T r.(?) -


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