Product Details

SNP ID

rs148816283

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:99018285 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGACATTTTGTATTTGGCTTCATTG[G/T]AGAACTCATATGATAAGCATTACTT

Phenotype

MIM: 607166

Polymorphism

G/T, Transversion 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	2369	Missense Mutation			NP_079520.1
NM_182911.3	2369	Missense Mutation			NP_878915.2
XM_005264023.1	2369	Missense Mutation			XP_005264080.1
XM_005264024.2	2369	Missense Mutation			XP_005264081.1
XM_005264025.1	2369	Missense Mutation			XP_005264082.1
XM_005264026.1	2369	Missense Mutation			XP_005264083.1
XM_005264027.1	2369	Missense Mutation			XP_005264084.1
XM_005264029.1	2369	Missense Mutation			XP_005264086.1
XM_006712781.2	2369	Missense Mutation			XP_006712844.1
XM_011511934.1	2369	Missense Mutation			XP_011510236.1
XM_011511935.2	2369	Missense Mutation			XP_011510237.1
XM_011511937.1	2369	Missense Mutation			XP_011510239.1
XM_011511939.1	2369	Missense Mutation			XP_011510241.1
XM_011511940.2	2369	Missense Mutation			XP_011510242.1
XM_011511941.1	2369	Missense Mutation			XP_011510243.1
XM_011511942.1	2369	Missense Mutation			XP_011510244.1
XM_011511943.2	2369	Missense Mutation			XP_011510245.1
XM_017005035.1	2369	Missense Mutation			XP_016860524.1
XM_017005036.1	2369	Intron			XP_016860525.1
XM_017005037.1	2369	Intron			XP_016860526.1
XM_017005038.1	2369	Intron			XP_016860527.1
XM_017005039.1	2369	Missense Mutation			XP_016860528.1
XM_017005040.1	2369	Missense Mutation			XP_016860529.1
XM_017005041.1	2369	Missense Mutation			XP_016860530.1
XM_017005042.1	2369	Missense Mutation			XP_016860531.1
XM_017005043.1	2369	Missense Mutation			XP_016860532.1
XM_017005044.1	2369	Missense Mutation			XP_016860533.1
XM_017005045.1	2369	Missense Mutation			XP_016860534.1
XM_017005046.1	2369	Missense Mutation			XP_016860535.1
XM_017005047.1	2369	Missense Mutation			XP_016860536.1
XM_017005048.1	2369	Missense Mutation			XP_016860537.1

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