Product Details

SNP ID

rs73965254

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:99018296 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATTTGGCTTCATTGTAGAACTCATA[C/T]GATAAGCATTACTTGAATAATTTTG

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	2358	Missense Mutation	CAT,CGT	H659R	NP_079520.1
NM_182911.3	2358	Missense Mutation	CAT,CGT	H659R	NP_878915.2
XM_005264023.1	2358	Missense Mutation	CAT,CGT	H659R	XP_005264080.1
XM_005264024.2	2358	Missense Mutation	CAT,CGT	H659R	XP_005264081.1
XM_005264025.1	2358	Missense Mutation	CAT,CGT	H659R	XP_005264082.1
XM_005264026.1	2358	Missense Mutation	CAT,CGT	H659R	XP_005264083.1
XM_005264027.1	2358	Missense Mutation	CAT,CGT	H659R	XP_005264084.1
XM_005264029.1	2358	Missense Mutation	CAT,CGT	H659R	XP_005264086.1
XM_006712781.2	2358	Missense Mutation	CAT,CGT	H659R	XP_006712844.1
XM_011511934.1	2358	Missense Mutation	CAT,CGT	H859R	XP_011510236.1
XM_011511935.2	2358	Missense Mutation	CAT,CGT	H787R	XP_011510237.1
XM_011511937.1	2358	Missense Mutation	CAT,CGT	H659R	XP_011510239.1
XM_011511939.1	2358	Missense Mutation	CAT,CGT	H659R	XP_011510241.1
XM_011511940.2	2358	Missense Mutation	CAT,CGT	H659R	XP_011510242.1
XM_011511941.1	2358	Missense Mutation	CAT,CGT	H659R	XP_011510243.1
XM_011511942.1	2358	Missense Mutation	CAT,CGT	H659R	XP_011510244.1
XM_011511943.2	2358	Missense Mutation	CAT,CGT	H659R	XP_011510245.1
XM_017005035.1	2358	Missense Mutation	CAT,CGT	H854R	XP_016860524.1
XM_017005036.1	2358	Intron			XP_016860525.1
XM_017005037.1	2358	Intron			XP_016860526.1
XM_017005038.1	2358	Intron			XP_016860527.1
XM_017005039.1	2358	Missense Mutation	CAT,CGT	H659R	XP_016860528.1
XM_017005040.1	2358	Missense Mutation	CAT,CGT	H659R	XP_016860529.1
XM_017005041.1	2358	Missense Mutation	CAT,CGT	H659R	XP_016860530.1
XM_017005042.1	2358	Missense Mutation	CAT,CGT	H659R	XP_016860531.1
XM_017005043.1	2358	Missense Mutation	CAT,CGT	H659R	XP_016860532.1
XM_017005044.1	2358	Missense Mutation	CAT,CGT	H659R	XP_016860533.1
XM_017005045.1	2358	Missense Mutation	CAT,CGT	H659R	XP_016860534.1
XM_017005046.1	2358	Missense Mutation	CAT,CGT	H659R	XP_016860535.1
XM_017005047.1	2358	Missense Mutation	CAT,CGT	H659R	XP_016860536.1
XM_017005048.1	2358	Missense Mutation	CAT,CGT	H659R	XP_016860537.1

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