RGD:8628725 Rat Genome Database

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Variant: RGD:8628725 -  Homo sapiens

RGD ID: 8628725
ClinVar ID: CV83869
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PRRG3  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 X 150,868,575
GRCh38 X 151,700,103
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_024082.3:c.115G>T
NG_016589.1:g.9846G>T
NC_000023.11:g.151700103G>T
NC_000023.10:g.150868575G>T
More... 		stop-gain|nonsense|non-coding transcript variant not provided Malignant melanoma, somatic

Variant Details
Variant Transcripts
Gene Symbol:PRRG3
Accession:NM_024082
Location:EXON
Amino Acid Prediction: E to * (nonsynonymous)
Amino Acid Position: 39
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MAVFLEAKDAHSVLKRFPRANEFLEELRQGTIERECME*ICSYEEVKEVFENKEKTMEFWKGYPNAVYSVRDPSQSSDAM
YVVVPLLGVALLIVIALFIIWRCQLQKATRHHPSYAQNRYLASRAGHTLPRVMVYRGTVHSQGEPSGHREAANSPQVVLG
PSRGGRTTVRLESTLYLPELSLSRLSSTTPPPSYEEVTAPQESSSEEASVSYSDPPPKYEEIVAANPGADK*

Gene Symbol:PRRG3
Accession:NM_001372165
Location:EXON
Amino Acid Prediction: E to * (nonsynonymous)
Amino Acid Position: 3
Amino Acid Sequence
(Calculated using NCBI transcript definition)
ME*ICSYEEVKEVFENKEKTMEFWKGYPNAVYSVRDPSQSSDAMYVVVPLLGVALLIVIALFIIWRCQLQKATRHHPSYA
QNRYLASRAGHTLPRVMVYRGTVHSQGEPSGHREAANSPQVVLGPSRGGRTTVRLESTLYLPELSLSRLSSTTPPPSYEE
VTAPQESSSEEASVSYSDPPPKYEEIVAANPGADK*

Gene Symbol:PRRG3
Accession:NM_001372163
Location:EXON
Amino Acid Prediction: E to * (nonsynonymous)
Amino Acid Position: 39
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MAVFLEAKDAHSVLKRFPRANEFLEELRQGTIERECME*ICSYEEVKEVFENKEKTMEFWKGYPNAVYSVRDPSQSSDAM
YVVVPLLGVALLIVIALFIIWRCQLQKATRHHPSYAQNRYLASRAGHTLPRVMVYRGTVHSQGEPSGHREAANSPQVVLG
PSRGGRTTVRLESTLYLPELSLSRLSSTTPPPSYEEVTAPQESSSEEASVSYSDPPPKYEEIVAANPGADK*

Gene Symbol:PRRG3
Accession:NR_033262
Location:EXON;NON-CODING

Variant Samples