Genomic variant #0000383919

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.130251689G>A
Reference -
DB-ID LRSAM1_000045
dbSNP ID rs55828933
Frequency 0.033
Allele Count 17
Allele Number 516
Combined Depth 9805
Homozygous -
Heterozygote -
Average frequency (large NGS studies) 0.0416 View details
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LRSAM1 NM_138361.5 ./. - c.1348-34G>A r.(=) p.(=)



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA SEQ-NG-I - 825713 Admin