Variant #0000570000 (NC_000020.10:g.5283256C>G, PROKR2(NM_144773.2):c.585G>C)

Chromosome 20
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.5283256C>G
DNA change (hg38) g.5302610C>G
Published as PROKR2(NM_144773.3):c.585G>C (p.T195=)
ISCN -
DB-ID PROKR2_000004 See all 3 reported entries
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) 0.74688 View details
Owner VKGL-NL_AMC
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PROKR2 NM_144773.2 -/. - c.585G>C r.(?) p.(Thr195=)