Product Details

SNP ID: rs200369661
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.19:49583634 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CCACTGGGACCTGGAGCTGCTCACA[C/T]CAGGGAACCTGGAACGGGAGTGTCT
Phenotype: MIM: 616759 MIM: 616633 MIM: 604429
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: NOSIP PubMed Links

Gene Details

Gene: NOSIP
Gene Name: nitric oxide synthase interacting protein

There are no transcripts associated with this gene.

Gene: PRR12
Gene Name: proline rich 12

There are no transcripts associated with this gene.

Gene: PRRG2
Gene Name: proline rich and Gla domain 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000951.2	510	Missense Mutation	CCA,TCA	P60S	NP_000942.1
NM_001316335.1	510	Missense Mutation	CCA,TCA	P37S	NP_001303264.1
XM_006723286.2	510	Missense Mutation	CCA,TCA	P60S	XP_006723349.1
XM_011527124.1	510	Missense Mutation	CCA,TCA	P37S	XP_011525426.1

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