Product Details

SNP ID

rs324149

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.6:44229258 on Build GRCh38

Set Membership

Validated

Context Sequence [VIC/FAM]

ACACCCATAAGAGGACACATGCAAA[C/T]GGACACAAACACAGACGCCCTGTGC

Phenotype

MIM: 602193

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

SLC29A1 PubMed Links

Additional Information

For this assay, SNP(s) [rs148126154,rs7750723] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene

SLC29A1

Gene Name

solute carrier family 29 member 1 (Augustine blood group)

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001078175.2		Intron			NP_001071643.1
NM_001078177.1		Intron			NP_001071645.1
NM_001304462.1		Intron			NP_001291391.1
NM_001304463.1		Intron			NP_001291392.1
NM_001304465.1		Intron			NP_001291394.1
NM_001304466.1		Intron			NP_001291395.1
XM_005248876.4		Intron			XP_005248933.1
XM_005248878.3		Intron			XP_005248935.1
XM_005248879.3		Intron			XP_005248936.1
XM_005248880.3		Intron			XP_005248937.1
XM_005248881.3		Intron			XP_005248938.1
XM_005248882.3		Intron			XP_005248939.1
XM_011514341.2		Intron			XP_011512643.1

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