Genomic variant #0000237416

Individual ID 00000001
Chromosome 5
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.138286989G>A
Reference -
DB-ID SIL1_000003
dbSNP ID rs35080367
Frequency 0.005814
Allele Count 3
Allele Number 516
Combined Depth 6595
Homozygous -
Heterozygote -
Average frequency (large NGS studies) 0.00401 View details
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SIL1 NM_022464.4 ./. - c.900C>T r.(=) p.(=)



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA SEQ-NG-I - 825713 Admin