Variant #0000852196 (NC_000009.11:g.139917424C>G, NM_207511.1:c.-6006C>G (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.139917424C>G
DNA change (hg38) -
Published as ABCA2(NM_212533.2):c.334G>C (p.E112Q)
ISCN -
DB-ID C9orf139_000011
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 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FUT7 NM_004479.3 ?/. - c.*7738G>C r.(=) p.(=)
C9orf139 NM_207511.1 ?/. - c.-6006C>G r.(?) p.(=)
ABCA2 NM_212533.2 ?/. - c.334G>C r.(?) p.(Glu112Gln)


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