Product Details

SNP ID

rs2899682

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.15:62643751 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TCCAGAGGTCAAAGGCATCAGGAGG[C/T]GTGGAATTGAGCCTGCACCTCAGAC

Phenotype

MIM: 607349

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

MGC15885 PubMed Links

Gene Details

Gene

MGC15885

Gene Name

uncharacterized protein MGC15885

There are no transcripts associated with this gene.

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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