Genomic variant #0000472827

Individual ID 00000001
Chromosome 11
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.119025443C>G
Reference -
DB-ID ABCG4_000017
dbSNP ID rs11822683
Frequency 0.012
Allele Count 6
Allele Number 516
Combined Depth 5493
Homozygous -
Heterozygote -
Average frequency (large NGS studies) 0.02671 View details
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ABCG4 NM_022169.4 ./. - c.541-37C>G r.(=) p.(=)



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA SEQ-NG-I - 825713 Admin