Variant #0000537513 (NC_000009.11:g.139905695G>A, NM_207511.1:c.-17735G>A (C9orf139))

Chromosome 9
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.139905695G>A
DNA change (hg38) g.137011243G>A
Published as ABCA2(NM_001606.5):c.5866C>T (p.H1956Y)
ISCN -
DB-ID ABCA2_000008
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C9orf139 NM_207511.1 ?/. - c.-17735G>A r.(?) p.(=)
ABCA2 NM_212533.2 ?/. - c.5956C>T r.(?) p.(His1986Tyr)


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