Variant #0000281225 (NC_000002.11:g.26477127_26477129dup, NM_000183.2:c.5_7dup (HADHB))

Chromosome 2
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.26477127_26477129dup
DNA change (hg38) g.26254259_26254261dup
Published as HADHB(NM_000183.3):c.5_7dupCTA (p.T2dup), HADHB(NM_000183.3):c.8delTinsCTAT (p.T2dup)
ISCN -
DB-ID HADHB_000004 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) 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 2018-01-15 20:58:59 +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     
HADHB NM_000183.2 -/. - c.5_7dup r.(?) p.(Thr2dup)


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