Product Details

SNP ID

rs138330429

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:195867632 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGGGCTCTGGGCCTCACGCAGGAAG[C/T]GCTGGTAGCGCTCCAGGTAGGATGG

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	3164	Missense Mutation	CAC,CGC	H952R	NP_001010938.1
NM_001308046.1	3164	Missense Mutation	CAC,CGC	H906R	NP_001294975.1
NM_005781.4	3164	Missense Mutation	CAC,CGC	H874R	NP_005772.3
XM_005269268.3	3164	Missense Mutation	CAC,CGC	H952R	XP_005269325.1
XM_005269270.3	3164	Missense Mutation	CAC,CGC	H889R	XP_005269327.1
XM_005269274.3	3164	Missense Mutation	CAC,CGC	H650R	XP_005269331.1
XM_005269275.3	3164	Missense Mutation	CAC,CGC	H575R	XP_005269332.1
XM_011512317.2	3164	Missense Mutation	CAC,CGC	H1053R	XP_011510619.1
XM_011512318.2	3164	Missense Mutation	CAC,CGC	H921R	XP_011510620.2
XM_011512320.1	3164	Missense Mutation	CAC,CGC	H889R	XP_011510622.1
XM_011512321.2	3164	Missense Mutation	CAC,CGC	H813R	XP_011510623.1
XM_017005508.1	3164	Missense Mutation	CAC,CGC	H906R	XP_016860997.1
XM_017005509.1	3164	Missense Mutation	CAC,CGC	H906R	XP_016860998.1
XM_017005510.1	3164	Missense Mutation	CAC,CGC	H921R	XP_016860999.1

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