Genomic variant #0000169626

Individual ID 00000001
Chromosome 3
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.131188528T>G
Reference -
DB-ID MRPL3_000013
dbSNP ID rs2291382
Frequency 0.132
Allele Count 68
Allele Number 516
Combined Depth 4887
Homozygous -
Heterozygote -
Average frequency (large NGS studies) 0.12835 View details
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MRPL3 NM_007208.3 ./. - c.816+12A>C r.(=) p.(=)



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA SEQ-NG-I - 825713 Admin