Genomic variant #0000383908

Individual ID 00000001
Chromosome 9
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.130242109C>T
Reference -
DB-ID LRSAM1_000034
dbSNP ID rs1539568
Frequency 0.424
Allele Count 219
Allele Number 516
Combined Depth 3778
Homozygous -
Heterozygote -
Average frequency (large NGS studies) 0.44623 View details
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LRSAM1 NM_138361.5 ./. - c.904-9C>T r.(=) p.(=)



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA SEQ-NG-I - 825713 Admin