Product Details

SNP ID

rs149213112

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:99018305 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CATTGTAGAACTCATATGATAAGCA[C/T]TACTTGAATAATTTTGGCGGCGAAG

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	2349	Missense Mutation	AAT,AGT	N656S	NP_079520.1
NM_182911.3	2349	Missense Mutation	AAT,AGT	N656S	NP_878915.2
XM_005264023.1	2349	Missense Mutation	AAT,AGT	N656S	XP_005264080.1
XM_005264024.2	2349	Missense Mutation	AAT,AGT	N656S	XP_005264081.1
XM_005264025.1	2349	Missense Mutation	AAT,AGT	N656S	XP_005264082.1
XM_005264026.1	2349	Missense Mutation	AAT,AGT	N656S	XP_005264083.1
XM_005264027.1	2349	Missense Mutation	AAT,AGT	N656S	XP_005264084.1
XM_005264029.1	2349	Missense Mutation	AAT,AGT	N656S	XP_005264086.1
XM_006712781.2	2349	Missense Mutation	AAT,AGT	N656S	XP_006712844.1
XM_011511934.1	2349	Missense Mutation	AAT,AGT	N856S	XP_011510236.1
XM_011511935.2	2349	Missense Mutation	AAT,AGT	N784S	XP_011510237.1
XM_011511937.1	2349	Missense Mutation	AAT,AGT	N656S	XP_011510239.1
XM_011511939.1	2349	Missense Mutation	AAT,AGT	N656S	XP_011510241.1
XM_011511940.2	2349	Missense Mutation	AAT,AGT	N656S	XP_011510242.1
XM_011511941.1	2349	Missense Mutation	AAT,AGT	N656S	XP_011510243.1
XM_011511942.1	2349	Missense Mutation	AAT,AGT	N656S	XP_011510244.1
XM_011511943.2	2349	Missense Mutation	AAT,AGT	N656S	XP_011510245.1
XM_017005035.1	2349	Missense Mutation	AAT,AGT	N851S	XP_016860524.1
XM_017005036.1	2349	Intron			XP_016860525.1
XM_017005037.1	2349	Intron			XP_016860526.1
XM_017005038.1	2349	Intron			XP_016860527.1
XM_017005039.1	2349	Missense Mutation	AAT,AGT	N656S	XP_016860528.1
XM_017005040.1	2349	Missense Mutation	AAT,AGT	N656S	XP_016860529.1
XM_017005041.1	2349	Missense Mutation	AAT,AGT	N656S	XP_016860530.1
XM_017005042.1	2349	Missense Mutation	AAT,AGT	N656S	XP_016860531.1
XM_017005043.1	2349	Missense Mutation	AAT,AGT	N656S	XP_016860532.1
XM_017005044.1	2349	Missense Mutation	AAT,AGT	N656S	XP_016860533.1
XM_017005045.1	2349	Missense Mutation	AAT,AGT	N656S	XP_016860534.1
XM_017005046.1	2349	Missense Mutation	AAT,AGT	N656S	XP_016860535.1
XM_017005047.1	2349	Missense Mutation	AAT,AGT	N656S	XP_016860536.1
XM_017005048.1	2349	Missense Mutation	AAT,AGT	N656S	XP_016860537.1

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