Genomic variant #0000169636

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.131220371T>G
Reference -
DB-ID MRPL3_000023
dbSNP ID rs77947063
Frequency 0.004762
Allele Count 2
Allele Number 420
Combined Depth 542
Homozygous -
Heterozygote -
Average frequency (large NGS studies) 0.03314 View details
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MRPL3 NM_007208.3 ./. - c.277+4A>C r.spl? p.?



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA SEQ-NG-I - 825713 Admin