RGD:15199349 Rat Genome Database

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Variant: RGD:15199349 -  Homo sapiens

RGD ID: 15199349
RS ID: rs1015783138
ClinVar ID: CV755433
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: WFDC1  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 16 84,346,590
GRCh38 16 84,312,984
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001282466.2:c.168C>A
NM_001282467.2:c.168C>A
NM_021197.4:c.168C>A
NC_000016.10:g.84312984C>A
More... 		03/01/2018 synonymous variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:WFDC1
Accession:NM_021197
Location:EXON
Amino Acid Prediction: G to G (synonymous)
Amino Acid Position: 56
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MPLTGVGPGSCRRQIIRALCLLLLLLHAGSAKNIWKRALPARLAEKSRAEEAGAPGGPRQPRADRCPPPPRTLPPGACQA
ARCQADSECPRHRRCCYNGCAYACLEAVPPPPVLDWLVQPKPRWLGGNGWLLDGPEEVLQAEACSTTEDGAEPLLCPSGY
ECHILSPGDVAEGIPNRGQCVKQRRQADGRILRHKLYKEYPEGDSKNVAEPGRGQQKHFQ*

Gene Symbol:WFDC1
Accession:NM_001282466
Location:EXON
Amino Acid Prediction: G to G (synonymous)
Amino Acid Position: 56
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MPLTGVGPGSCRRQIIRALCLLLLLLHAGSAKNIWKRALPARLAEKSRAEEAGAPGGPRQPRADRCPPPPRTLPPGACQA
ARCQADSECPRHRRCCYNGCAYACLEAVPPPPVLDWLVQPKPRWLGGNGWLLDGPEEVLQAEACSTTEDGAEPLLCPSGY
ECHILSPGDVAEGIPNRGQCVKQRRQADGRILRHKLYKEYPEGDSKNVAEPGRGQQKHFQ*

Gene Symbol:WFDC1
Accession:NM_001282467
Location:EXON
Amino Acid Prediction: G to G (synonymous)
Amino Acid Position: 56
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MPLTGVGPGSCRRQIIRALCLLLLLLHAGSAKNIWKRALPARLAEKSRAEEAGAPGGPRQPRADRCPPPPRTLPPGACQA
ARCQADSECPRHRRCCYNGCAYACLEAVPPPPVLDWLVQPKPRWLGGNGWLLDGPEEVLQEACSTTEDGAEPLLCPSGYE
CHILSPGDVAEGIPNRGQCVKQRRQADGRILRHKLYKEYPEGDSKNVAEPGRGQQKHFQ*

Gene Symbol:WFDC1
Accession:XM_047434411
Location:EXON
Amino Acid Prediction: G to G (synonymous)
Amino Acid Position: 56
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MPLTGVGPGSCRRQIIRALCLLLLLLHAGSAKNIWKRALPARLAEKSRAEEAGAPGGPRQPRADRCPPPPRTLPPGACQA
ARCQADSECPRHRRCCYNGCAYACLEAVPPPPAEACSTTEDGAEPLLCPSGYECHILSPGDVAEGIPNRGQCVKQRRQAD
GRILRHKLYKEYPEGDSKNVAEPGRGQQKHFQ*
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000912521 CLINVAR
dbSNP (RS) rs1015783138 CLINVAR
MedGen CN517202 CLINVAR
NCBI Gene WFDC1 CLINVAR
OMIM 605322 CLINVAR