Variant #0000614303 (NC_000012.11:g.54332735_54332737dup, NM_017410.2:c.45_47dup (HOXC13))

Chromosome 12
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.54332735_54332737dup
DNA change (hg38) g.53938951_53938953dup
Published as HOXC13(NM_017410.2):c.43_44insTTA (p.(Leu15_Met16insIle))
ISCN -
DB-ID HOXC13_000004
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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +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.45_47dup r.(?) p.(Leu15_Met16insIle)
HOXC-AS5 NR_047507.1 -?/. - n.173+519_173+521dup r.(?) -


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