Product Details

SNP ID
rs141774400
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:55137134 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGTTCCTCCCCCATGTAGTCAATGT[C/T]CAGAGGCTTCTTACGCTCGGAGAGG
Phenotype
MIM: 191041
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
TNNT1 PubMed Links

Gene Details

Gene
TNNT1
Gene Name
troponin T1, slow skeletal type
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001126132.2 847 Missense Mutation AAC,GAC N194D NP_001119604.1
NM_001126133.2 847 Missense Mutation AAC,GAC N183D NP_001119605.1
NM_001291774.1 847 Missense Mutation AAC,GAC N183D NP_001278703.1
NM_003283.5 847 Missense Mutation AAC,GAC N194D NP_003274.3
XM_011527246.2 847 Missense Mutation AAC,GAC N190D XP_011525548.1
XM_017027186.1 847 Missense Mutation AAC,GAC N194D XP_016882675.1
XM_017027187.1 847 Missense Mutation AAC,GAC N190D XP_016882676.1

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