Unique variants in gene PRRC2A

Information The variants shown are described using the NM_080686.2 transcript reference sequence.

3 entries on 1 page. Showing entries 1 - 3.
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Effect     

Reported     

Exon     

AscendingDNA change (cDNA)     

ClassClinical     

RNA change     

Protein     

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     

Owner     
-?/. 1 - c.2961C>G likely benign r.(?) p.(=) g.31599411C>G - PRRC2A(NM_004638.3):c.2961C>G (p.T987=) - PRRC2A_000002 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL
-/. 1 - c.3536_3538del benign r.(?) p.(Pro1179del) g.31599986_31599988del - PRRC2A(NM_004638.4):c.3536_3538delCTC (p.P1179del) - PRRC2A_000003 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL
?/. 1 - c.*4266C>T VUS r.(=) p.(=) g.31609629C>T - BAG6(NM_004639.3):c.2339G>A (p.R780Q) - BAG6_000001 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL
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