Genomic variant #0000795553

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.31337950T>C
Reference -
DB-ID MORC2_000040
dbSNP ID rs76273991
Frequency 0.003876
Allele Count 2
Allele Number 516
Combined Depth 9202
Homozygous -
Heterozygote -
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     
MORC2 NM_014941.1 ./. - c.440A>G r.(?) p.(Asn147Ser)



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA SEQ-NG-I - 825713 Admin