Genomic variant #0000795539

Individual ID 00000001
Chromosome 22
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.31334218G>T
Reference -
DB-ID MORC2_000012
dbSNP ID rs8137040
Frequency 0.014
Allele Count 7
Allele Number 516
Combined Depth 7176
Homozygous -
Heterozygote -
Average frequency (large NGS studies) 0.01146 View details
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MORC2 NM_014941.1 ./. - c.888-26C>A r.(=) p.(=)



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA SEQ-NG-I - 825713 Admin