Genomic variant #0000000037

Individual ID 00000001
Chromosome 1
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.777232C>T
Reference -
DB-ID chr1_000011
dbSNP ID rs112618790
Frequency 0.053
Allele Count 27
Allele Number 514
Combined Depth 2128
Homozygous 1
Heterozygote 25
Average frequency (large NGS studies) Variant not found in online data sets
Owner Admin




Variant on transcripts

Stop! No variants on transcripts found!



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA SEQ-NG-I - 825713 Admin