Genomic variant #0000500226

Individual ID 00000001
Chromosome 12
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.57897959C>T
Reference -
DB-ID MARS_000029
dbSNP ID rs188212968
Frequency 0.005814
Allele Count 3
Allele Number 516
Combined Depth 4403
Homozygous -
Heterozygote -
Average frequency (large NGS studies) 0.00461 View details
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MARS NM_004990.3 ./. - c.1294-49C>T r.(=) p.(=)



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA SEQ-NG-I - 825713 Admin