Variant #0000930804 (NC_000017.10:g.46804358G>A, NM_006361.5:c.649C>T (HOXB13))

Chromosome 17
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.46804358G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID HOXB13_000045
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) 0.00014 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2023-07-07 10:10:56 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HOXB13 NM_006361.5 ?/. - c.649C>T r.(?) p.(Arg217Cys)
PRAC NM_032391.2 ?/. - c.-4604C>T r.(?) p.(=)


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