Genomic variant #0000685092

Individual ID 00000001
Chromosome 18
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.12337322C>T
Reference -
DB-ID AFG3L2_000021
dbSNP ID rs117096851
Frequency 0.017
Allele Count 9
Allele Number 516
Combined Depth 3256
Homozygous -
Heterozygote -
Average frequency (large NGS studies) 0.01207 View details
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AFG3L2 NM_006796.2 ./. - c.2175+18G>A r.(=) p.(=)



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA SEQ-NG-I - 825713 Admin