Genomic variant #0000556174

Individual ID 00000001
Chromosome 14
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.92403527G>A
Reference -
DB-ID FBLN5_000033
dbSNP ID rs141200859
Frequency 0.001938
Allele Count 1
Allele Number 516
Combined Depth 9277
Homozygous -
Heterozygote -
Average frequency (large NGS studies) 0.00015 View details
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FBLN5 NM_006329.3 ./. - c.143C>T r.(?) p.(Thr48Ile)



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA SEQ-NG-I - 825713 Admin