Genomic variant #0000043262

Individual ID 00000001
Chromosome 1
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.115829363C>T
Reference -
DB-ID NGF_000006
dbSNP ID rs6325
Frequency 0.023
Allele Count 12
Allele Number 516
Combined Depth 10437
Homozygous -
Heterozygote -
Average frequency (large NGS studies) 0.04083 View details
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NGF NM_002506.2 ./. - c.54G>A r.(=) p.(=)



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA SEQ-NG-I - 825713 Admin