Product Details

SNP ID

rs143348369

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:195867197 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CAGATACTGGGCAGCCCTCTGCACG[C/T]TCCAGCCGTGGCACTGCAGGGCCGC

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	3497	Intron			NP_001010938.1
NM_001308046.1	3497	Intron			NP_001294975.1
NM_005781.4	3497	Missense Mutation	AAC,AGC	N985S	NP_005772.3
XM_005269268.3	3497	Missense Mutation	AAC,AGC	N1065S	XP_005269325.1
XM_005269270.3	3497	Missense Mutation	AAC,AGC	N1002S	XP_005269327.1
XM_005269274.3	3497	Missense Mutation	AAC,AGC	N763S	XP_005269331.1
XM_005269275.3	3497	Missense Mutation	AAC,AGC	N688S	XP_005269332.1
XM_011512317.2	3497	Missense Mutation	AAC,AGC	N1166S	XP_011510619.1
XM_011512318.2	3497	Missense Mutation	AAC,AGC	N1032S	XP_011510620.2
XM_011512320.1	3497	Missense Mutation	AAC,AGC	N1002S	XP_011510622.1
XM_011512321.2	3497	Missense Mutation	AAC,AGC	N926S	XP_011510623.1
XM_017005508.1	3497	Missense Mutation	AAC,AGC	N1019S	XP_016860997.1
XM_017005509.1	3497	Missense Mutation	AAC,AGC	N1017S	XP_016860998.1
XM_017005510.1	3497	Intron			XP_016860999.1

View Full Product Details