Genomic variant #0000903067

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.58893761C>G
Reference dbSNP
DB-ID FAM111B_000003
dbSNP ID rs17153376
Frequency 0.09628
Average frequency (large NGS studies) 0.00124 View details
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Position     

RNA change     

Protein     
FAM111B NM_198947.3 ./. - c.2191C>G - r.(?) p.(Pro731Ala)



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA arrayCNV - 904756 Admin