Product Details

SNP ID

rs112384084

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:195867623 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGGCTCCTCGGGGCTCTGGGCCTCA[C/T]GCAGGAAGCGCTGGTAGCGCTCCAG

Phenotype

MIM: 606994

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

LOC101929697 PubMed Links

Gene Details

Gene

LOC101929697

Gene Name

uncharacterized LOC101929697

There are no transcripts associated with this gene.

Gene

TNK2

Gene Name

tyrosine kinase non receptor 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001010938.1	3173	Missense Mutation	CAT,CGT	H955R	NP_001010938.1
NM_001308046.1	3173	Missense Mutation	CAT,CGT	H909R	NP_001294975.1
NM_005781.4	3173	Missense Mutation	CAT,CGT	H877R	NP_005772.3
XM_005269268.3	3173	Missense Mutation	CAT,CGT	H955R	XP_005269325.1
XM_005269270.3	3173	Missense Mutation	CAT,CGT	H892R	XP_005269327.1
XM_005269274.3	3173	Missense Mutation	CAT,CGT	H653R	XP_005269331.1
XM_005269275.3	3173	Missense Mutation	CAT,CGT	H578R	XP_005269332.1
XM_011512317.2	3173	Missense Mutation	CAT,CGT	H1056R	XP_011510619.1
XM_011512318.2	3173	Missense Mutation	CAT,CGT	H924R	XP_011510620.2
XM_011512320.1	3173	Missense Mutation	CAT,CGT	H892R	XP_011510622.1
XM_011512321.2	3173	Missense Mutation	CAT,CGT	H816R	XP_011510623.1
XM_017005508.1	3173	Missense Mutation	CAT,CGT	H909R	XP_016860997.1
XM_017005509.1	3173	Missense Mutation	CAT,CGT	H909R	XP_016860998.1
XM_017005510.1	3173	Missense Mutation	CAT,CGT	H924R	XP_016860999.1

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