Genomic variant #0000374744

Individual ID 00000001
Chromosome 22
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.30942482C>T
Reference -
DB-ID MORC2_000007
dbSNP ID rs737927
Frequency 0.6853
Homozygous 169
Heterozygote 127
Average frequency (large NGS studies) Retrieve
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MORC2 NM_014941.2 ./. - c.241-211G>A - -



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA arrayCNV - 904861 Admin