Product Details

SNP ID
rs28416852
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.15:62397607 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATACTGTGTGACTCTCTGAATCCTG[A/T]TGGGAGATCCAGAATCTCAACCCAC
Phenotype
MIM: 607349
Polymorphism
A/T, Transversion substitution
Allele Nomenclature
Literature Links
TLN2 PubMed Links

Gene Details

Gene
TLN2
Gene Name
talin 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_015059.2 Intron NP_055874.2
XM_005254708.4 Intron XP_005254765.1
XM_005254710.4 Intron XP_005254767.1
XM_005254711.4 Intron XP_005254768.1
XM_005254712.4 Intron XP_005254769.1
XM_005254713.4 Intron XP_005254770.1
XM_005254714.3 Intron XP_005254771.1
XM_005254715.2 Intron XP_005254772.1
XM_006720717.3 Intron XP_006720780.1
XM_017022665.1 Intron XP_016878154.1
XM_017022666.1 Intron XP_016878155.1
XM_017022667.1 Intron XP_016878156.1
XM_017022668.1 Intron XP_016878157.1
XM_017022669.1 Intron XP_016878158.1

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