Product Details

SNP ID

rs115073289

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.9:127742048 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGCGCTGCCTGTGGTTGGGCCGGGA[A/G]AGGCGGAGGGCGGAGCCAACGTGAG

Phenotype

MIM: 604722 MIM: 608052

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

SH2D3C PubMed Links

Additional Information

For this assay, SNP(s) [rs3217145] 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

SH2D3C

Gene Name

SH2 domain containing 3C

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001142531.1		Intron			NP_001136003.1
NM_001142532.1		Intron			NP_001136004.1
NM_001142533.1		Intron			NP_001136005.1
NM_001142534.1		Intron			NP_001136006.1
NM_001252334.1		Intron			NP_001239263.1
NM_005489.3		Intron			NP_005480.2
NM_170600.2		Intron			NP_733745.1
XM_005251639.1		Intron			XP_005251696.1
XM_011518114.1		Intron			XP_011516416.1
XM_011518115.1		Intron			XP_011516417.1
XM_011518117.2		Intron			XP_011516419.1
XM_017014174.1		Intron			XP_016869663.1

Gene

TOR2A

Gene Name

torsin family 2 member A

There are no transcripts associated with this gene.

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