Product Details

SNP ID

rs111695615

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:195867470 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGGTGGTGGCCGGGCCCCTGGGTTG[C/T]TGTTGTTGGTGGAGAAGTTGGCCTT

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	3326	Missense Mutation	AAC,AGC	N1006S	NP_001010938.1
NM_001308046.1	3326	Missense Mutation	AAC,AGC	N960S	NP_001294975.1
NM_005781.4	3326	Missense Mutation	AAC,AGC	N928S	NP_005772.3
XM_005269268.3	3326	Missense Mutation	AAC,AGC	N1006S	XP_005269325.1
XM_005269270.3	3326	Missense Mutation	AAC,AGC	N943S	XP_005269327.1
XM_005269274.3	3326	Missense Mutation	AAC,AGC	N704S	XP_005269331.1
XM_005269275.3	3326	Missense Mutation	AAC,AGC	N629S	XP_005269332.1
XM_011512317.2	3326	Missense Mutation	AAC,AGC	N1107S	XP_011510619.1
XM_011512318.2	3326	Missense Mutation	AAC,AGC	N975S	XP_011510620.2
XM_011512320.1	3326	Missense Mutation	AAC,AGC	N943S	XP_011510622.1
XM_011512321.2	3326	Missense Mutation	AAC,AGC	N867S	XP_011510623.1
XM_017005508.1	3326	Missense Mutation	AAC,AGC	N960S	XP_016860997.1
XM_017005509.1	3326	Missense Mutation	AAC,AGC	N960S	XP_016860998.1
XM_017005510.1	3326	Missense Mutation	AAC,AGC	N975S	XP_016860999.1

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