All transcript variants in gene PRRC2A

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

6 entries on 1 page. Showing entries 1 - 6.
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Effect     

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     
-?/. - c.2811C>G likely benign - - g.31599261C>G - PRRC2A:NM_004638.3:c.2811C>G, NM_080686.2:c.2811C>G - PRRC2A_000001 VKGL data sharing initiative Nederland; correct HGVS to be checked - - - CLASSIFICATION record - - - 0 - VKGL-NL_Leiden
-?/. - c.2961C>G likely benign r.(=) p.(=) g.31599411C>G - PRRC2A:c.2961C>G (T987=) - PRRC2A_000002 VKGL data sharing initiative Nederland; correct HGVS to be checked - - - CLASSIFICATION record - - - 0 - VKGL-NL_Rotterdam
-?/. - c.3532_3534del likely benign - - g.31599982_31599984del - PRRC2A:NM_004638.3:c.3532_3534del, NM_080686.2:c.3532_3534del - PRRC2A_000003 VKGL data sharing initiative Nederland; correct HGVS to be checked - - - CLASSIFICATION record - - - 0 - VKGL-NL_Leiden
-?/. - c.3563C>T likely benign - - g.31600013C>T - PRRC2A:NM_004638.3:c.3563C>T, NM_080686.2:c.3563C>T - PRRC2A_000004 VKGL data sharing initiative Nederland; correct HGVS to be checked - - - CLASSIFICATION record - - - 0 - VKGL-NL_Leiden
-?/. - c.6223C>T likely benign - - g.31604894C>T - BAG6:NM_001098534.1:c.*2014G>A, NM_001199697.1:c.*2014G>A, … - PRRC2A_000005 VKGL data sharing initiative Nederland; correct HGVS to be checked - - - CLASSIFICATION record - - - 0 - VKGL-NL_Leiden
-?/. - c.6248T>C likely benign - - g.31605016T>C - BAG6:NM_001098534.1:c.*1892A>G, NM_001199697.1:c.*1892A>G, … - PRRC2A_000006 VKGL data sharing initiative Nederland; correct HGVS to be checked - - - CLASSIFICATION record - - - 0 - VKGL-NL_Leiden
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