Variant #0000562108 (NC_000017.10:g.46608194_46608202dup, NM_002144.3:c.74_82dup (HOXB1))

Chromosome 17
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.46608194_46608202dup
DNA change (hg38) g.48530832_48530840dup
Published as HOXB1(NM_002144.4):c.74_82dupACAGCGCCC (p.H25_A27dup)
ISCN -
DB-ID HOXB1_000007
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 2019-07-18 18:22:55 +02:00 (CEST)
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     
HOXB1 NM_002144.3 -/. - c.74_82dup r.(?) p.(His25_Ala27dup)


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