rs374434209 Rat Genome Database

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Variant: rs374434209 -  Homo sapiens

RGD ID: 151748694
RS ID: rs374434209
ClinVar ID: CV1442432
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MGP  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 12 15,035,203
GRCh38 12 14,882,269
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.182G>A
NM_001190839.3:c.257G>A
NG_023331.2:g.8651G>A
NC_000012.12:g.14882269C>T
More... 		12/09/2021 missense variant uncertain significance none provided

Variant Details
Variant Transcripts
Gene Symbol:MGP
Accession:NM_000900
Location:EXON
Amino Acid Prediction: R to H (nonsynonymous)
Amino Acid Position: 61
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MKSLILLAILAALAVVTLCYESHESMESYELNPFINRRNANTFISPQQRWRAKVQERIREHSKPVHELNREACDDYRLCE
RYAMVYGYNAAYNRYFRKRRGTK*

Gene Symbol:MGP
Accession:NM_001190839
Location:EXON
Amino Acid Prediction: R to H (nonsynonymous)
Amino Acid Position: 86
Amino Acid Sequence
(Calculated using NCBI transcript definition)
MKSLILLAILAALAVVTLCYGEWQKEENFGFDIVSVLSLNWHRAQESHESMESYELNPFINRRNANTFISPQQRWRAKVQ
ERIREHSKPVHELNREACDDYRLCERYAMVYGYNAAYNRYFRKRRGTK*
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002043042 CLINVAR
dbSNP (RS) rs374434209 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene MGP CLINVAR
OMIM 154870 CLINVAR