Variant #0000336525 (NC_000009.11:g.108358967A>G, FKTN(NM_001079802.1):c.165+29A>G)

Individual ID 00151538
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.108358967A>G
DNA change (hg38) g.105596686A>G
Published as -
ISCN -
DB-ID FKTN_000063
Variant remarks -
Reference from website {DBsub-Emory}
ClinVar ID -
dbSNP ID -
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00028 View details
Owner Madhuri Hegde
Database submission license No license selected
Created by Madhuri Hegde
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FKTN NM_001079802.1 ?/. 4i c.165+29A>G r.(?) p.(=)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000152393 DNA SEQ - - FKTN 1 Madhuri Hegde