Product Details

SNP ID

rs1937132

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.6:25756789 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CATTGCATTCATTGATTCAATAAAT[A/G]TTTACTGAATCAATGAATGAACTTG

Phenotype

MIM: 182308 MIM: 604216

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

SLC17A1 PubMed Links

Gene Details

Gene

SLC17A1

Gene Name

solute carrier family 17 member 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005074.3		Intron			NP_005065.2
XM_011514818.2		Intron			XP_011513120.2
XM_011514819.2		Intron			XP_011513121.2
XM_011514820.2		Intron			XP_011513122.2
XM_011514821.2		Intron			XP_011513123.1
XM_017011199.1		Intron			XP_016866688.1
XM_017011200.1		Intron			XP_016866689.1
XM_017011201.1		Intron			XP_016866690.1
XM_017011202.1		Intron			XP_016866691.1

Gene

SLC17A4

Gene Name

solute carrier family 17 member 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001286121.1		Intron			NP_001273050.1
NM_005495.2		Intron			NP_005486.1
XM_011514211.1		Intron			XP_011512513.1
XM_011514213.2		Intron			XP_011512515.1
XM_011514214.2		Intron			XP_011512516.1
XM_011514215.2		Intron			XP_011512517.1
XM_011514217.2		Intron			XP_011512519.1
XM_011514218.2		Intron			XP_011512520.1
XM_011514219.2		Intron			XP_011512521.1
XM_017010150.1		Intron			XP_016865639.1
XM_017010151.1		Intron			XP_016865640.1

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