Product Details

SNP ID

rs6901782

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.6:42991162 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TGCTTCTTTCCTACCTCTGTGTACT[C/T]GTGCAGTTGGTTCATAGTAAATGCT

Phenotype

MIM: 143170 MIM: 601646

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

MEA1 PubMed Links

Additional Information

For this assay, SNP(s) [rs199508198] 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

MEA1

Gene Name

male-enhanced antigen 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001318942.1		Intron			NP_001305871.1
NM_001318943.1		Intron			NP_001305872.1
NM_014623.3		Intron			NP_055438.1
XM_005249121.3		Intron			XP_005249178.1
XM_017010868.1		Intron			XP_016866357.1

Gene

PPP2R5D

Gene Name

protein phosphatase 2 regulatory subunit B'delta

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001270476.1		Intron			NP_001257405.1
NM_006245.3		Intron			NP_006236.1
NM_180976.2		Intron			NP_851307.1
NM_180977.2		Intron			NP_851308.1

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