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See other LOC105370854 GT Assays ›
SNP ID:
rs937418
Gene
LOC105370854 TLN2
Gene Name
Set Membership:
> HapMap > Validated
Chromosome Location:
Chr.15: 62838918 - 62838918 on Build GRCh38
Polymorphism:
A/T, Transversion substitution
Context Sequence [VIC/FAM]:

TTGTCCGTGCAGCCCAGAAGGCAGC[A/T]TTTGGCAAAGCTGATGACGACGATG

Assay ID C___9654106_1_
Size
Availability Made To Order
Catalog # 4351379
Price
Your Price
Online offer:
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Assay Details



Species:

 Human

dbSNP Submissions:

 NA

Phenotype:

 MIM: 607349

Literature Links:

 LOC105370854 PubMed Links

Allele Nomenclature:

Minor Allele Frequency:
1000Genome Applied Biosystems® HapMap
Global
A (0.42)
(0.58)
Caucasian
A (0.24)
(0.76)
CEPH (CEU)
A (0.17)
(0.83)
EAS
A (0.29)
(0.71)
African American
T (0.44)
(0.56)
YRI (Yoruba)
T (0.35)
(0.65)
SAS
A (0.42)
(0.58)
Japanese
A (0.40)
(0.60)
JPT (Japanese)
A (0.25)
(0.75)
AFR
T (0.30)
(0.70)
Chinese
A (0.28)
(0.72)
CHB (Han Chinese)
A (0.38)
(0.62)
EUR
A (0.23)
(0.77)
AMR
A (0.37)
(0.63)
LOC105370854 - uncharacterized LOC105370854
There are no transcripts associated with this gene.
TLN2 - talin 2
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
NM_015059.2 7753 Silent Mutation GCA,GCT A,A 2479 NP_055874.2
XM_005254708.4 7753 Silent Mutation GCA,GCT A,A 2494 XP_005254765.1
XM_005254710.4 7753 Silent Mutation GCA,GCT A,A 2494 XP_005254767.1
XM_005254711.4 7753 Silent Mutation GCA,GCT A,A 2494 XP_005254768.1
XM_005254712.4 7753 Silent Mutation GCA,GCT A,A 2494 XP_005254769.1
XM_005254713.4 7753 Silent Mutation GCA,GCT A,A 2494 XP_005254770.1
XM_005254714.3 7753 Silent Mutation GCA,GCT A,A 2494 XP_005254771.1
XM_005254715.2 7753 Silent Mutation GCA,GCT A,A 2494 XP_005254772.1
XM_006720717.3 7753 Silent Mutation GCA,GCT A,A 2494 XP_006720780.1
XM_017022665.1 7753 Silent Mutation GCA,GCT A,A 2494 XP_016878154.1
XM_017022666.1 7753 Silent Mutation GCA,GCT A,A 2494 XP_016878155.1
XM_017022667.1 7753 Silent Mutation GCA,GCT A,A 2494 XP_016878156.1
XM_017022668.1 7753 Silent Mutation GCA,GCT A,A 2479 XP_016878157.1
XM_017022669.1 7753 Silent Mutation GCA,GCT A,A 2449 XP_016878158.1

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