Variant #0000654290 (NC_000002.11:g.176958235A>G, NM_000523.3:c.617A>G (HOXD13))

Chromosome 2
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.176958235A>G
DNA change (hg38) g.176093507A>G
Published as HOXD13(NM_000523.3):c.617A>G (p.(Tyr206Cys)), HOXD13(NM_000523.4):c.617A>G (p.Y206C)
ISCN -
DB-ID HOXD13_000017 See all 2 reported entries
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) 0.00118 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 2020-03-23 16:13:27 +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     
HOXD13 NM_000523.3 -?/. - c.617A>G r.(?) p.(Tyr206Cys)


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