Variant #0000268031 (NC_000009.11:g.27548388C>T, NM_001256054.1:c.1292G>A (C9orf72))

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.27548388C>T
DNA change (hg38) g.27548390C>T
Published as C9orf72(NM_001256054.3):c.1292G>A (p.R431Q)
ISCN -
DB-ID C9orf72_000014
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) 5.0E-5 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-11-27 17:27:23 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
C9orf72 NM_001256054.1 ?/. - c.1292G>A - r.(?) p.(Arg431Gln)
C9orf72 NM_018325.3 ?/. - c.1292G>A - r.(?) p.(Arg431Gln)


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