Genomic variant #0000383909

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.130242166A>G
Reference -
DB-ID LRSAM1_000035
dbSNP ID rs1539567
Frequency 0.758
Allele Count 391
Allele Number 516
Combined Depth 9386
Homozygous -
Heterozygote -
Average frequency (large NGS studies) 0.74181 View details
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LRSAM1 NM_138361.5 ./. - c.952A>G r.(?) p.(Asn318Asp)



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA SEQ-NG-I - 825713 Admin