Genomic variant #0000877623

Individual ID 00000001
Chromosome 4
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.154139306C>T
Reference dbSNP
DB-ID TRIM2_000008
dbSNP ID rs7660732
Frequency 0.34291
Average frequency (large NGS studies) Variant not found in online data sets
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Position     

RNA change     

Protein     
TRIM2 NM_001130067.1 ./. - c.-48-52184C>T - - -



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA arrayCNV - 904756 Admin