Variant #0000539205 (NC_000010.10:g.115405712_115405713dup, NM_004132.3:c.*57584_*57585dup (HABP2))

Chromosome 10
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.115405712_115405713dup
DNA change (hg38) g.113645953_113645954dup
Published as NRAP(NM_001261463.1):c.994-5_994-4dupTT
ISCN -
DB-ID HABP2_000013
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HABP2 NM_004132.3 -/. - c.*57584_*57585dup r.(=) p.(=)
NRAP NM_198060.3 -/. - c.994-5_994-4dup r.spl? p.?


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