Variant #0000978583 (NC_000009.11:g.139912047G>A, NM_207511.1:c.-11383G>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.139912047G>A
DNA change (hg38) -
Published as ABCA2(NM_001606.5):c.2309C>T (p.(Ala770Val))
ISCN -
DB-ID C9orf139_000017
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) 9.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C9orf139 NM_207511.1 ?/. - c.-11383G>A r.(?) p.(=)
ABCA2 NM_212533.2 ?/. - c.2399C>T r.(?) p.(Ala800Val)


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