RGD:15141356 Rat Genome Database

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Variant: RGD:15141356 -  Homo sapiens

RGD ID: 15141356
RS ID: rs145586650
ClinVar ID: CV707857
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CDCA7  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 2 174,231,085
GRCh38 2 173,366,357
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_031942.5:c.1110C>T
NM_145810.3:c.873C>T
NG_047202.1:g.17341C>T
NC_000002.12:g.173366357C>T
More... 		06/01/2018 synonymous variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:CDCA7
Accession:NM_031942
Location:EXON
Amino Acid Prediction: G to G (synonymous)
Amino Acid Position: 370
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MDARRVPQKDLRVKKNLKKFRYVKLISMETSSSSDDSCDSFASDNFANTKPKFRSDISEELANVFYEDSDNESFCGFSES
EVQDVLDHCGFLQKPRPDVTNELAGIFHADSDDESFCGFSESEIQDGMRLQSVREGCRTRSQCRHSGPLRVAMKFPARST
RGATNKKAESRQPSENSVTDSNSDSEDESGMNFLEKRALNIKQNKAMLAKLMSELESFPGSFRGRHPLPGSDSQSRRPRR
RTFPGVASRRNPERRARPLTRSRSRILGSLDALPMEEEEEEDKYMLVRKRKTVDGYMNEDDLPRSRRSRSSVTLPHIIRP
VEEITEEELENVCSNSREKIYNRSLGSTCHQCRQKTIDTKTNCRNPDCWGVRGQFCGPCLRNRYGEEVRDALLDPNWHCP
PCRGICNCSFCRQRDGRCATGVLVYLAKYHGFGNVHAYLKSLKQEFEMQA*

Gene Symbol:CDCA7
Accession:NM_145810
Location:EXON
Amino Acid Prediction: G to G (synonymous)
Amino Acid Position: 291
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MDARRVPQKDLRVKKNLKKFRYVKLISMETSSSSDDSCDSFASDNFANTRLQSVREGCRTRSQCRHSGPLRVAMKFPARS
TRGATNKKAESRQPSENSVTDSNSDSEDESGMNFLEKRALNIKQNKAMLAKLMSELESFPGSFRGRHPLPGSDSQSRRPR
RRTFPGVASRRNPERRARPLTRSRSRILGSLDALPMEEEEEEDKYMLVRKRKTVDGYMNEDDLPRSRRSRSSVTLPHIIR
PVEEITEEELENVCSNSREKIYNRSLGSTCHQCRQKTIDTKTNCRNPDCWGVRGQFCGPCLRNRYGEEVRDALLDPNWHC
PPCRGICNCSFCRQRDGRCATGVLVYLAKYHGFGNVHAYLKSLKQEFEMQA*

Gene Symbol:CDCA7
Accession:XM_047445957
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000966293 CLINVAR
dbSNP (RS) rs145586650 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CDCA7 CLINVAR
OMIM 609937 CLINVAR