rs142282008 Rat Genome Database

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Variant: rs142282008 -  Homo sapiens

RGD ID: 15190840
RS ID: rs142282008
ClinVar ID: CV738574
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MGP  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 12 15,038,693
GRCh38 12 14,885,759
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_000900.5:c.33C>T
NM_001190839.3:c.33C>T
NG_023331.2:g.5161C>T
NC_000012.12:g.14885759G>A
More... 		07/03/2023 synonymous variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:MGP
Accession:NM_001190839
Location:EXON
Amino Acid Prediction: A to A (synonymous)
Amino Acid Position: 11
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MKSLILLAILAALAVVTLCYGEWQKEENFGFDIVSVLSLNWHRAQESHESMESYELNPFINRRNANTFISPQQRWRAKVQ
ERIRERSKPVHELNREACDDYRLCERYAMVYGYNAAYNRYFRKRRGTK*

Gene Symbol:MGP
Accession:NM_000900
Location:EXON
Amino Acid Prediction: A to A (synonymous)
Amino Acid Position: 11
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MKSLILLAILAALAVVTLCYESHESMESYELNPFINRRNANTFISPQQRWRAKVQERIRERSKPVHELNREACDDYRLCE
RYAMVYGYNAAYNRYFRKRRGTK*
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000910069 CLINVAR
dbSNP (RS) rs142282008 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene MGP CLINVAR
OMIM 154870 CLINVAR