Product Details

SNP ID

rs146341754

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.14:70046157 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGGTGACGGAGAAGGCCAGTGTGCC[A/G]GCCGACACGTGGAACTCCTGTCCCT

Phenotype

MIM: 607991

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

SLC8A3 PubMed Links

Gene Details

Gene

SLC8A3

Gene Name

solute carrier family 8 member A3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001130417.2	1025	Silent Mutation	GCC,GCT	A229A	NP_001123889.1
NM_033262.4	1025	Silent Mutation	GCC,GCT	A856A	NP_150287.1
NM_058240.3	1025	Silent Mutation	GCC,GCT	A855A	NP_489479.1
NM_182932.2	1025	Silent Mutation	GCC,GCT	A852A	NP_891977.1
NM_182936.2	1025	Silent Mutation	GCC,GCT	A215A	NP_891981.1
NM_183002.2	1025	Silent Mutation	GCC,GCT	A858A	NP_892114.1
XM_006720240.3	1025	Silent Mutation	GCC,GCT	A235A	XP_006720303.1
XM_017021606.1	1025	Silent Mutation	GCC,GCT	A858A	XP_016877095.1
XM_017021607.1	1025	Silent Mutation	GCC,GCT	A857A	XP_016877096.1
XM_017021608.1	1025	Silent Mutation	GCC,GCT	A852A	XP_016877097.1
XM_017021609.1	1025	Silent Mutation	GCC,GCT	A851A	XP_016877098.1
XM_017021610.1	1025	Intron			XP_016877099.1
XM_017021611.1	1025	Silent Mutation	GCC,GCT	A242A	XP_016877100.1

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