Genomic variant #0000132042

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.153183269A>G
Reference -
DB-ID TRIM2_000032
dbSNP ID rs5019720
Frequency 0.2618
Homozygous 27
Heterozygote 124
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.-49+29999A>G - -



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA arrayCNV - 904861 Admin