PRR29 proline rich 29

Information
Symbol
PRR29
Type
protein-coding
Description
proline rich 29
Entrez Gene ID
92340
Genome
hg19
Position
chr17:62,075,711-62,079,876
Genome
hg38
Position
chr17:63,998,351-64,002,516
HGNC
HGNC:25673 HGNC
Ensembl
ENSG00000224383 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 8
Uncertain significance 0 60
Ranking
ClinVar
0
0
0
68
0
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Variant name Gene AA change CDS Japanese
frequency		 TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence		 Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
SYNONYM C17orf72
HGNC HGNC:25673 HGNC
Ensembl ENSG00000224383 Ensembl
AllianceGenome HGNC:25673
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000580752.1 hg38 chr17 63,998,355 64,002,049 3,695
ENST00000577953.5 hg38 chr17 63,998,351 64,001,969 3,619
ENST00000582540.5 hg38 chr17 63,998,351 64,002,220 3,870
ENST00000425164.7 hg38 chr17 63,998,351 64,002,516 4,166
ENST00000412177.6 hg38 chr17 63,998,351 64,004,305 5,955
ENST00000579184.5 hg38 chr17 63,998,351 64,002,250 3,900
ENST00000577953.5 hg19 chr17 62,075,711 62,079,329 3,619
ENST00000582540.5 hg19 chr17 62,075,711 62,079,580 3,870
ENST00000579184.5 hg19 chr17 62,075,711 62,079,610 3,900
ENST00000425164.7 hg19 chr17 62,075,711 62,079,876 4,166
ENST00000412177.6 hg19 chr17 62,075,711 62,081,665 5,955
ENST00000580752.1 hg19 chr17 62,075,715 62,079,409 3,695
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