Variant #0000913224 (NC_000010.10:g.115380496dup, NM_004132.3:c.*32368dup (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.115380496dup
DNA change (hg38) -
Published as NRAP(NM_001261463.2):c.2770-17dupT
ISCN -
DB-ID HABP2_000023
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 2023-01-11 15:44:22 +01:00 (CET)
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.*32368dup r.(?) p.(=)
NRAP NM_198060.3 -/. - c.2770-17dup r.(=) p.(=)


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