Variant #0000614304 (NC_000012.11:g.54338917_54338919dup, NM_017410.2:c.870_872dup (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.54338917_54338919dup
DNA change (hg38) g.53945133_53945135dup
Published as HOXC13(NM_017410.3):c.870_872dupCCG (p.R292dup)
ISCN -
DB-ID HOXC13_000005
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-12-04 15:24:38 +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     
HOXC13 NM_017410.2 ?/. - c.870_872dup r.(?) p.(Arg292dup)


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