Variant #0000861621 (NC_000009.11:g.27561593A>G, NM_001256054.1:c.655T>C (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.27561593A>G
DNA change (hg38) -
Published as C9orf72(NM_001256054.1):c.655T>C (p.F219L)
ISCN -
DB-ID C9orf72_000050
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 15:51:19 +02:00 (CEST)
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.655T>C - r.(?) p.(Phe219Leu)
C9orf72 NM_018325.3 ?/. - c.655T>C - r.(?) p.(Phe219Leu)


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