Variant #0000861347 (NC_000009.11:g.108382329G>A, NM_001079802.1:c.1159G>A (FKTN))

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.108382329G>A
DNA change (hg38) -
Published as FKTN(NM_001079802.1):c.1159G>A (p.(Gly387Arg), p.G387R), FKTN(NM_001079802.2):c.1159G>A (p.G387R), FKTN(NM_006731.2):c.1159G>A (p.G387R)
ISCN -
DB-ID FKTN_000088 See all 8 reported entries
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) 0.00044 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 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FKTN NM_001079802.1 ?/. - c.1159G>A r.(?) p.(Gly387Arg)


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