Unique variants in gene PGR

Information The variants shown are described using the NM_000926.4 transcript reference sequence.

2 entries on 1 page. Showing entries 1 - 2.
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Effect     

Reported     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

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     

Owner     
-/. 1 - c.1179C>T r.(?) p.(Gly393=) - benign g.100998623G>A g.101127892G>A PGR(NM_000926.4):c.1179C>T (p.G393=) - PGR_000002 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Groningen
?/. 1 - c.1301C>G r.(?) p.(Pro434Arg) - VUS g.100998501G>C g.101127770G>C PGR(NM_000926.4):c.1301C>G (p.P434R) - PGR_000001 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Rotterdam
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