Genomic variant #0000561586

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.77872089C>G
Reference dbSNP
DB-ID AAMDC_000002
Frequency 0.004762
Allele Count 1
Allele Number 210
Depth 636
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