Genomic variant #0000108739

Individual ID 00000001
Chromosome 1
Allele Unknown
Affects function (reported) Not classified
Affects function (concluded) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.1999314C>T
Reference dbSNP
DB-ID CFAP74_000005
Frequency -
Average frequency (large NGS studies) Variant not found in online data sets
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CFAP74 NM_001304360.1 ./. - c.-20+4387G>A - -



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA arraySNP - 905346 Admin