Genomic variant #0000043261

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.115829313G>A
Reference -
DB-ID NGF_000005
dbSNP ID rs6330
Frequency 0.372
Allele Count 192
Allele Number 516
Combined Depth 16102
Homozygous -
Heterozygote -
Average frequency (large NGS studies) 0.36914 View details
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NGF NM_002506.2 ./. - c.104C>T r.(?) p.(Ala35Val)



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA SEQ-NG-I - 825713 Admin