RGD:8626760 Rat Genome Database

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Variant: RGD:8626760 -  Homo sapiens

RGD ID: 8626760
ClinVar ID: CV81904
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: DPCD  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 10 103,369,154
GRCh38 10 101,609,397
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000010.9:g.103359144G>A
NM_015448.1:c.538G>A
NC_000010.11:g.101609397G>A
NC_000010.10:g.103369154G>A
More... 		missense|missense variant not provided Malignant melanoma, somatic

Variant Details
Variant Transcripts
Gene Symbol:DPCD
Accession:NM_001329744
Location:3UTRS;EXON

Gene Symbol:DPCD
Accession:NM_001329742
Location:EXON
Amino Acid Prediction: E to K (nonsynonymous)
Amino Acid Position: 191
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MAVTGWLESLRTAQKTALLQDGRRKVHYLFPDGKEMAEEYDEKTSELLVRKWRVKSALGAMGQWQLEVGDPAPLGAGNLG
PELIKESNANEQSSSWICLLQPIFMRKDTKMSFQWRIRNLPYPKDVYSVSVDQKERCIIVRTTNKKYYKKFSIPDLDRHQ
LPLDDALLSFAHANCTLIISYQKPKEVVVAKSELQKELKKVKTAHSNDGDCKTQ*

Gene Symbol:DPCD
Accession:NM_001329743
Location:EXON
Amino Acid Prediction: E to K (nonsynonymous)
Amino Acid Position: 168
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MAVTGWLESLRTAQKTALLQDGRRKVHYLFPDGKEMAEEYDEKTSELLVRKWRVKSALGAMGQWQLEVGDPAPLGAGNLG
PELIKESNANPIFMRKDTKMSFQWRIRNLPYPKDVYSVSVDQKERCIIVRTTNKKHQLPLDDALLSFAHANCTLIISYQK
PKEVVVAKSELQKELKKVKTAHSNDGDCKTQ*

Gene Symbol:DPCD
Accession:NM_001329745
Location:EXON
Amino Acid Prediction: E to K (nonsynonymous)
Amino Acid Position: 91
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MSIVSLWTRRSAASLSEQPTRSGLVGGFSGPLWPCGVQVCMAPPLRYYKKFSIPDLDRHQLPLDDALLSFAHANCTLIIS
YQKPKEVVVAKSELQKELKKVKTAHSNDGDCKTQ*

Gene Symbol:DPCD
Accession:NM_015448
Location:EXON
Amino Acid Prediction: E to K (nonsynonymous)
Amino Acid Position: 180
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MAVTGWLESLRTAQKTALLQDGRRKVHYLFPDGKEMAEEYDEKTSELLVRKWRVKSALGAMGQWQLEVGDPAPLGAGNLG
PELIKESNANPIFMRKDTKMSFQWRIRNLPYPKDVYSVSVDQKERCIIVRTTNKKYYKKFSIPDLDRHQLPLDDALLSFA
HANCTLIISYQKPKEVVVAKSELQKELKKVKTAHSNDGDCKTQ*

Gene Symbol:DPCD
Accession:NM_001329746
Location:INTRON

Variant Samples