Genomic variant #0000472845

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.119030921C>T
Reference -
DB-ID ABCG4_000024
dbSNP ID rs200475405
Frequency 0.001938
Allele Count 1
Allele Number 516
Combined Depth 9196
Homozygous -
Heterozygote -
Average frequency (large NGS studies) 0.00046 View details
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ABCG4 NM_022169.4 ./. - c.1438-16C>T r.(=) p.(=)



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA SEQ-NG-I - 825713 Admin