Variant #0000978581 (NC_000009.11:g.139908448C>T, NM_207511.1:c.-14982C>T (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.139908448C>T
DNA change (hg38) -
Published as ABCA2(NM_001606.5):c.4283G>A (p.(Arg1428His))
ISCN -
DB-ID C9orf139_000015
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) 0.00014 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.-14982C>T r.(?) p.(=)
ABCA2 NM_212533.2 ?/. - c.4373G>A r.(?) p.(Arg1458His)


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