Product Details

SNP ID

rs1453561

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:98997461 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CCAGATTACAGACAGCTGCCACAGA[C/T]AATAAAATAAAATCGCAATTAAGTT

Phenotype

MIM: 607166

Polymorphism

C/T, 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	3215	UTR 3			NP_079520.1
NM_182911.3	3215	UTR 3			NP_878915.2
XM_005264023.1	3215	UTR 3			XP_005264080.1
XM_005264024.2	3215	UTR 3			XP_005264081.1
XM_005264025.1	3215	UTR 3			XP_005264082.1
XM_005264026.1	3215	UTR 3			XP_005264083.1
XM_005264027.1	3215	UTR 3			XP_005264084.1
XM_005264029.1	3215	UTR 3			XP_005264086.1
XM_006712781.2	3215	UTR 3			XP_006712844.1
XM_011511934.1	3215	UTR 3			XP_011510236.1
XM_011511935.2	3215	UTR 3			XP_011510237.1
XM_011511937.1	3215	UTR 3			XP_011510239.1
XM_011511939.1	3215	UTR 3			XP_011510241.1
XM_011511940.2	3215	UTR 3			XP_011510242.1
XM_011511941.1	3215	UTR 3			XP_011510243.1
XM_011511942.1	3215	UTR 3			XP_011510244.1
XM_011511943.2	3215	UTR 3			XP_011510245.1
XM_017005035.1	3215	UTR 3			XP_016860524.1
XM_017005036.1	3215	Intron			XP_016860525.1
XM_017005037.1	3215	Intron			XP_016860526.1
XM_017005038.1	3215	Intron			XP_016860527.1
XM_017005039.1	3215	UTR 3			XP_016860528.1
XM_017005040.1	3215	UTR 3			XP_016860529.1
XM_017005041.1	3215	UTR 3			XP_016860530.1
XM_017005042.1	3215	UTR 3			XP_016860531.1
XM_017005043.1	3215	UTR 3			XP_016860532.1
XM_017005044.1	3215	UTR 3			XP_016860533.1
XM_017005045.1	3215	UTR 3			XP_016860534.1
XM_017005046.1	3215	UTR 3			XP_016860535.1
XM_017005047.1	3215	UTR 3			XP_016860536.1
XM_017005048.1	3215	UTR 3			XP_016860537.1

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