Genomic variant #0000151948

Individual ID 00000001
Chromosome 3
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.48916665A>G
Reference -
DB-ID SLC25A20_000010
dbSNP ID -
Frequency 0.004149
Allele Count 2
Allele Number 482
Combined Depth 844
Homozygous 1
Heterozygote 0
Average frequency (large NGS studies) Variant not found in online data sets
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC25A20 NM_000387.5 ./. - c.417+126T>C r.(=) p.(=)



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA SEQ-NG-I - 825713 Admin