Variant #0000854976 (NC_000017.10:g.46804155del, NM_006361.5:c.853del (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.46804155del
DNA change (hg38) -
Published as HOXB13(NM_006361.5):c.853delT (p.*285Kfs*97)
ISCN -
DB-ID HOXB13_000043
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:47:41 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HOXB13 NM_006361.5 ?/. - c.853del r.(?) p.(*285Lysext*96)
PRAC NM_032391.2 ?/. - c.-4400del r.(?) p.(=)


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