Full data view for gene PROKR2

Information The variants shown are described using the NM_144773.2 transcript reference sequence.

3 entries on 1 page. Showing entries 1 - 3.
Legend   How to query  

Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Allele     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
-/. - c.585G>C r.(?) p.(Thr195=) Unknown - benign g.5283256C>G g.5302610C>G PROKR2(NM_144773.3):c.585G>C (p.T195=) - PROKR2_000004 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - - - - - - - - - - - - - - - - - - -
-/. - c.585G>C r.(?) p.(Thr195=) Unknown - benign g.5283256C>G g.5302610C>G PROKR2(NM_144773.3):c.585G>C (p.T195=) - PROKR2_000004 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - - - - - - - - - - - - - - - - - - -
-/. - c.585G>C r.(?) p.(Thr195=) Unknown - benign g.5283256C>G g.5302610C>G PROKR2(NM_144773.3):c.585G>C (p.T195=) - PROKR2_000004 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
Legend   How to query