RGD:15201802 Rat Genome Database

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Variant: RGD:15201802 -  Homo sapiens

RGD ID: 15201802
RS ID: rs2231456
ClinVar ID: CV752653
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CD59  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 11 33,743,938
GRCh38 11 33,722,392
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001127225.2:c.54C>T
NM_001127226.2:c.54C>T
NM_001127227.2:c.54C>T
NM_203329.3:c.54C>T
More...
07/05/2018 synonymous variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:CD59
Accession:NM_001127225
Location:EXON
Amino Acid Prediction: V to V (synonymous)
Amino Acid Position: 18
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MGIQGGSVLFGLLLVLAVFCHSGHSLQCYNCPNPTADCKTAVNCSSDFDACLITKAGLQVYNKCWKFEHCNFNDVTTRLR
ENELTYYCCKKDLCNFNEQLENGGTSLSEKTVLLLVTPFLAAAWSLHP*

Gene Symbol:CD59
Accession:NM_001127223
Location:EXON
Amino Acid Prediction: V to V (synonymous)
Amino Acid Position: 18
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MGIQGGSVLFGLLLVLAVFCHSGHSLQCYNCPNPTADCKTAVNCSSDFDACLITKAGLQVYNKCWKFEHCNFNDVTTRLR
ENELTYYCCKKDLCNFNEQLENGGTSLSEKTVLLLVTPFLAAAWSLHP*

Gene Symbol:CD59
Accession:NM_203331
Location:EXON
Amino Acid Prediction: V to V (synonymous)
Amino Acid Position: 18
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MGIQGGSVLFGLLLVLAVFCHSGHSLQCYNCPNPTADCKTAVNCSSDFDACLITKAGLQVYNKCWKFEHCNFNDVTTRLR
ENELTYYCCKKDLCNFNEQLENGGTSLSEKTVLLLVTPFLAAAWSLHP*

Gene Symbol:CD59
Accession:NM_203329
Location:EXON
Amino Acid Prediction: V to V (synonymous)
Amino Acid Position: 18
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MGIQGGSVLFGLLLVLAVFCHSGHSLQCYNCPNPTADCKTAVNCSSDFDACLITKAGLQVYNKCWKFEHCNFNDVTTRLR
ENELTYYCCKKDLCNFNEQLENGGTSLSEKTVLLLVTPFLAAAWSLHP*

Gene Symbol:CD59
Accession:NM_000611
Location:EXON
Amino Acid Prediction: V to V (synonymous)
Amino Acid Position: 18
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MGIQGGSVLFGLLLVLAVFCHSGHSLQCYNCPNPTADCKTAVNCSSDFDACLITKAGLQVYNKCWKFEHCNFNDVTTRLR
ENELTYYCCKKDLCNFNEQLENGGTSLSEKTVLLLVTPFLAAAWSLHP*

Gene Symbol:CD59
Accession:NM_001127226
Location:EXON
Amino Acid Prediction: V to V (synonymous)
Amino Acid Position: 18
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MGIQGGSVLFGLLLVLAVFCHSGHSLQCYNCPNPTADCKTAVNCSSDFDACLITKAGLQVYNKCWKFEHCNFNDVTTRLR
ENELTYYCCKKDLCNFNEQLENGGTSLSEKTVLLLVTPFLAAAWSLHP*

Gene Symbol:CD59
Accession:NM_203330
Location:EXON
Amino Acid Prediction: V to V (synonymous)
Amino Acid Position: 18
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MGIQGGSVLFGLLLVLAVFCHSGHSLQCYNCPNPTADCKTAVNCSSDFDACLITKAGLQVYNKCWKFEHCNFNDVTTRLR
ENELTYYCCKKDLCNFNEQLENGGTSLSEKTVLLLVTPFLAAAWSLHP*

Gene Symbol:CD59
Accession:NM_001127227
Location:EXON
Amino Acid Prediction: V to V (synonymous)
Amino Acid Position: 18
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MGIQGGSVLFGLLLVLAVFCHSGHSLQCYNCPNPTADCKTAVNCSSDFDACLITKAGLQVYNKCWKFEHCNFNDVTTRLR
ENELTYYCCKKDLCNFNEQLENGGTSLSEKTVLLLVTPFLAAAWSLHP*

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000913248 CLINVAR
dbSNP (RS) rs2231456 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CD59 CLINVAR
OMIM 107271 CLINVAR