Product Details

SNP ID

rs3781958

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:1923707 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GAGCTTGTCAATCAACCTTCCATCT[C/T]CCTCATCATTAGTCACTAACAATCA

Phenotype

MIM: 600692

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

TNNT3 PubMed Links

Gene Details

Gene

TNNT3

Gene Name

troponin T3, fast skeletal type

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001042780.2		Intron			NP_001036245.1
NM_001042781.2		Intron			NP_001036246.1
NM_001042782.2		Intron			NP_001036247.1
NM_001297646.1		Intron			NP_001284575.1
NM_006757.3		Intron			NP_006748.1
XM_006718288.3		Intron			XP_006718351.1
XM_006718290.3		Intron			XP_006718353.1
XM_006718293.2		Intron			XP_006718356.1
XM_006718294.3		Intron			XP_006718357.1
XM_006718296.3		Intron			XP_006718359.1
XM_006718299.2		Intron			XP_006718362.1
XM_006718300.3		Intron			XP_006718363.1
XM_006718302.3		Intron			XP_006718365.1
XM_011520343.2		Intron			XP_011518645.1
XM_017018205.1		Intron			XP_016873694.1
XM_017018206.1		Intron			XP_016873695.1
XM_017018207.1		Intron			XP_016873696.1
XM_017018208.1		Intron			XP_016873697.1
XM_017018209.1		Intron			XP_016873698.1
XM_017018210.1		Intron			XP_016873699.1
XM_017018211.1		Intron			XP_016873700.1
XM_017018212.1		Intron			XP_016873701.1
XM_017018213.1		Intron			XP_016873702.1
XM_017018214.1		Intron			XP_016873703.1
XM_017018215.1		Intron			XP_016873704.1
XM_017018216.1		Intron			XP_016873705.1
XM_017018217.1		Intron			XP_016873706.1
XM_017018218.1		Intron			XP_016873707.1
XM_017018219.1		Intron			XP_016873708.1

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