Genomic variant #0000611151

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.130218372G>T
Reference dbSNP
DB-ID LRSAM1_000003
dbSNP ID rs10987655
Frequency 0.16554
Average frequency (large NGS studies) Variant not found in online data sets
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Position     

RNA change     

Protein     
LRSAM1 NM_138361.5 ./. - c.174+473G>T - r.(=) p.(=)



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA arrayCNV - 904756 Admin