Variant #0000655444 (NC_000006.11:g.107031255A>G, RTN4IP1(NM_032730.4):c.1031T>C)

Chromosome 6
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.107031255A>G
DNA change (hg38) g.106583380A>G
Published as RTN4IP1(NM_032730.5):c.1031T>C (p.M344T)
ISCN -
DB-ID QRSL1_000007
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (large NGS studies) 2.0E-5 View details
Owner VKGL-NL_Rotterdam
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
QRSL1 NM_018292.4 -?/. - c.-46302A>G r.(?) p.(=)
RTN4IP1 NM_032730.4 -?/. - c.1031T>C r.(?) p.(Met344Thr)