Genomic variant #0000450314

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.58892377del
Reference -
DB-ID FAM111B_000008
dbSNP ID rs768272759
Frequency 0.001938
Allele Count 1
Allele Number 516
Combined Depth 7049
Homozygous -
Heterozygote -
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     
FAM111B NM_198947.3 ./. - c.807del r.(?) p.(Ala273Hisfs*26)



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA SEQ-NG-I - 825713 Admin