Genomic variant #0000561587

Individual ID 00000003
Chromosome 11
Allele Unknown
Affects function (reported) Not classified
Affects function (concluded) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.77872220G>A
Reference dbSNP
DB-ID AAMDC_000003
Frequency 0.127
Allele Count 27
Allele Number 212
Depth 3531
Average frequency (large NGS studies) Variant not found in online data sets
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     
AAMDC NM_024684.2 ./.
AAMDC XM_005273938.3 ./.
AAMDC XM_011544968.1 ./.
AAMDC XM_011544969.1 ./.



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000003 DNA SEQ-NG-I - 624137 Admin