Genomic variant #0000383943

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.130263454C>T
Reference -
DB-ID LRSAM1_000069
dbSNP ID rs7019372
Frequency 0.014
Allele Count 7
Allele Number 516
Combined Depth 3204
Homozygous -
Heterozygote -
Average frequency (large NGS studies) 0.0223 View details
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LRSAM1 NM_138361.5 ./. - c.2046+32C>T r.(=) p.(=)



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA SEQ-NG-I - 825713 Admin