Genomic variant #0000612279

Individual ID 00000001
Chromosome 1
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.156825993A>G
Reference -
DB-ID NTRK1_000002
dbSNP ID rs7516736
Frequency 0.6176
Homozygous 126
Heterozygote 167
Average frequency (large NGS studies) Retrieve
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NTRK1 NM_001007792.1 ./. - c.9+10155A>G - -



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA arrayCNV - 904861 Admin