Genomic variant #0000132969

Individual ID 00000001
Chromosome 3
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.131471102A>G
Reference -
DB-ID MRPL3_000002
dbSNP ID rs16836775
Frequency 0.9838
Homozygous 330
Heterozygote 7
Average frequency (large NGS studies) Retrieve
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MRPL3 NM_007208.3 ./. - c.738+69T>C - -



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA arrayCNV - 904861 Admin