Product Details

SNP ID

rs1453562

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:98999387 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TGATTCCATTTACATGACAACCTGG[A/G]AAAGGCAAAACTAGAGAGGCAGGAA

Phenotype

MIM: 607166

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

TSGA10 PubMed Links

Gene Details

Gene

TSGA10

Gene Name

testis specific 10

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_025244.2		Intron			NP_079520.1
NM_182911.3		Intron			NP_878915.2
XM_005264023.1		Intron			XP_005264080.1
XM_005264024.2		Intron			XP_005264081.1
XM_005264025.1		Intron			XP_005264082.1
XM_005264026.1		Intron			XP_005264083.1
XM_005264027.1		Intron			XP_005264084.1
XM_005264029.1		Intron			XP_005264086.1
XM_006712781.2		Intron			XP_006712844.1
XM_011511934.1		Intron			XP_011510236.1
XM_011511935.2		Intron			XP_011510237.1
XM_011511937.1		Intron			XP_011510239.1
XM_011511939.1		Intron			XP_011510241.1
XM_011511940.2		Intron			XP_011510242.1
XM_011511941.1		Intron			XP_011510243.1
XM_011511942.1		Intron			XP_011510244.1
XM_011511943.2		Intron			XP_011510245.1
XM_017005035.1		Intron			XP_016860524.1
XM_017005036.1		Intron			XP_016860525.1
XM_017005037.1		Intron			XP_016860526.1
XM_017005038.1		Intron			XP_016860527.1
XM_017005039.1		Intron			XP_016860528.1
XM_017005040.1		Intron			XP_016860529.1
XM_017005041.1		Intron			XP_016860530.1
XM_017005042.1		Intron			XP_016860531.1
XM_017005043.1		Intron			XP_016860532.1
XM_017005044.1		Intron			XP_016860533.1
XM_017005045.1		Intron			XP_016860534.1
XM_017005046.1		Intron			XP_016860535.1
XM_017005047.1		Intron			XP_016860536.1
XM_017005048.1		Intron			XP_016860537.1

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