Genomic variant #0000041392

Individual ID 00000001
Chromosome 4
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.153323162C>T
Reference -
DB-ID TRIM2_000001
dbSNP ID rs17029874
Frequency 0.2706
Homozygous 37
Heterozygote 109
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)     

RNA change     

Protein     
TRIM2 NM_001130067.1 ./. - c.1870+346C>T - -



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA arrayCNV - 904861 Admin