Genomic variant #0000078014

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.153318733C>T
Reference -
DB-ID TRIM2_000029
dbSNP ID rs2405969
Frequency 0.0265
Homozygous 2
Heterozygote 14
Average frequency (large NGS studies) Retrieve
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRIM2 NM_001130067.1 ./. - c.1701+2734C>T - -



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA arrayCNV - 904861 Admin