RGD:11664105 Rat Genome Database

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Variant: RGD:11664105 -  Homo sapiens

RGD ID: 11664105
RS ID: rs886048839
ClinVar ID: CV322691
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MYBPC1  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 12 102,079,617
GRCh38 12 101,685,839
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_031912.1:g.95909T>C
NC_000012.12:g.101685839T>C
NC_000012.11:g.102079617T>C
NM_002465.4:c.*277T>C
More... 		06/14/2016 3 prime utr variant uncertain significance
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:MYBPC1
Accession:NM_001404678
Location:3UTRS;EXON

Gene Symbol:MYBPC1
Accession:NM_001404681
Location:3UTRS;EXON

Gene Symbol:MYBPC1
Accession:NM_001254720
Location:3UTRS;EXON

Gene Symbol:MYBPC1
Accession:XM_006719409
Location:3UTRS;EXON

Gene Symbol:MYBPC1
Accession:XM_017019320
Location:3UTRS;EXON

Gene Symbol:MYBPC1
Accession:XM_017019319
Location:3UTRS;EXON

Gene Symbol:MYBPC1
Accession:XM_017019317
Location:3UTRS;EXON

Gene Symbol:
Accession:
Location:3UTRS;EXON

Gene Symbol:MYBPC1
Accession:NM_206819
Location:3UTRS;EXON

Gene Symbol:MYBPC1
Accession:XM_006719407
Location:3UTRS;EXON

Gene Symbol:MYBPC1
Accession:NM_001254719
Location:3UTRS;EXON

Gene Symbol:MYBPC1
Accession:XM_006719406
Location:3UTRS;EXON

Gene Symbol:MYBPC1
Accession:XM_006719410
Location:3UTRS;EXON

Gene Symbol:MYBPC1
Accession:XM_047428875
Location:3UTRS;EXON

Gene Symbol:MYBPC1
Accession:NM_001404680
Location:3UTRS;EXON

Gene Symbol:MYBPC1
Accession:XM_006719411
Location:3UTRS;EXON

Gene Symbol:MYBPC1
Accession:NM_001404679
Location:3UTRS;EXON

Gene Symbol:MYBPC1
Accession:NM_002465
Location:3UTRS;EXON

Gene Symbol:MYBPC1
Accession:NM_001404675
Location:3UTRS;EXON

Gene Symbol:
Accession:
Location:3UTRS;EXON

Gene Symbol:MYBPC1
Accession:XM_017019318
Location:3UTRS;EXON

Gene Symbol:MYBPC1
Accession:NM_206820
Location:3UTRS;EXON

Gene Symbol:MYBPC1
Accession:NM_206821
Location:3UTRS;EXON

Gene Symbol:MYBPC1
Accession:XM_005268876
Location:3UTRS;EXON

Gene Symbol:MYBPC1
Accession:NM_001404676
Location:3UTRS;EXON

Gene Symbol:MYBPC1
Accession:NM_001254723
Location:3UTRS;EXON

Gene Symbol:
Accession:
Location:3UTRS;EXON

Gene Symbol:MYBPC1
Accession:NM_001254718
Location:3UTRS;EXON

Gene Symbol:MYBPC1
Accession:NM_001254721
Location:3UTRS;EXON

Gene Symbol:MYBPC1
Accession:NM_001254722
Location:3UTRS;EXON

Gene Symbol:MYBPC1
Accession:XM_006719405
Location:3UTRS;EXON

Gene Symbol:MYBPC1
Accession:NM_001404677
Location:3UTRS;EXON

Gene Symbol:MYBPC1
Accession:XM_017019315
Location:3UTRS;EXON

Gene Symbol:MYBPC1
Accession:XM_017019316
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000402459 CLINVAR
dbSNP (RS) rs886048839 CLINVAR
MedGen C3280526 CLINVAR
NCBI Gene MYBPC1 CLINVAR
OMIM 160794 CLINVAR
  614335 CLINVAR