rs145975858 Rat Genome Database

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Variant: rs145975858 -  Homo sapiens

RGD ID: 150532406
RS ID: rs145975858
ClinVar ID: CV1307951
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CCDC78  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 16 776,638
GRCh38 16 726,638
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001378033.1:c.-226+151C>G
LRG_705:g.4836C>G
NG_032932.1:g.4836C>G
NC_000016.10:g.726638G>C
More... 		08/30/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:CCDC78
Accession:NM_001378033
Location:5UTRS;INTRON

Gene Symbol:CCDC78
Accession:XM_047433606
Location:5UTRS;INTRON

Gene Symbol:CCDC78
Accession:XM_047433605
Location:5UTRS;INTRON

Gene Symbol:CCDC78
Accession:XM_047433604
Location:5UTRS;INTRON

Gene Symbol:CCDC78
Accession:XM_047433603
Location:5UTRS;INTRON

Gene Symbol:CCDC78
Accession:NM_001031737
Location:INTRON

Gene Symbol:CCDC78
Accession:XM_006720838
Location:INTRON

Gene Symbol:CCDC78
Accession:XM_006720843
Location:INTRON

Gene Symbol:CCDC78
Accession:XM_011522363
Location:INTRON

Gene Symbol:CCDC78
Accession:XM_011522361
Location:INTRON

Gene Symbol:CCDC78
Accession:XM_011522369
Location:INTRON

Gene Symbol:CCDC78
Accession:XM_011522368
Location:INTRON

Gene Symbol:CCDC78
Accession:XM_011522367
Location:INTRON

Gene Symbol:CCDC78
Accession:XM_011522365
Location:INTRON

Gene Symbol:CCDC78
Accession:XM_011522360
Location:INTRON

Gene Symbol:CCDC78
Accession:XM_011522359
Location:INTRON

Gene Symbol:CCDC78
Accession:XM_011522357
Location:INTRON

Gene Symbol:CCDC78
Accession:XM_011522358
Location:INTRON

Gene Symbol:CCDC78
Accession:XM_011522356
Location:INTRON

Gene Symbol:CCDC78
Accession:XM_011522370
Location:INTRON

Gene Symbol:CCDC78
Accession:XM_011522366
Location:INTRON

Gene Symbol:CCDC78
Accession:XM_011522364
Location:INTRON

Gene Symbol:CCDC78
Accession:XM_011522362
Location:INTRON

Gene Symbol:CCDC78
Accession:XM_017022929
Location:INTRON

Gene Symbol:CCDC78
Accession:NM_001378031
Location:INTRON

Gene Symbol:CCDC78
Accession:NM_001378030
Location:INTRON

Gene Symbol:CCDC78
Accession:XM_047433602
Location:INTRON

Gene Symbol:CCDC78
Accession:XM_047433607
Location:INTRON

Gene Symbol:CCDC78
Accession:NR_165384
Location:INTRON;NON-CODING

Gene Symbol:CCDC78
Accession:NR_165383
Location:INTRON;NON-CODING

Gene Symbol:CCDC78
Accession:NR_165386
Location:INTRON;NON-CODING

Gene Symbol:CCDC78
Accession:NR_165385
Location:INTRON;NON-CODING

Gene Symbol:CCDC78
Accession:NR_165382
Location:INTRON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:25741868  


Additional Information

Database Acc Id Source(s)
ClinVar RCV001757673 CLINVAR
dbSNP (RS) rs145975858 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CCDC78 CLINVAR
OMIM 614666 CLINVAR