Product Details
- SNP ID
-
rs199476301
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.15:63042874 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- AGATGCAGATGCTGAAGCTCGACAA[G/T]GAGAACGCCTTGGATCGAGCTGAGC
- Phenotype
-
MIM: 191010
- Polymorphism
- G/T, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
TPM1
PubMed Links
Gene Details
- Gene
- TPM1
- Gene Name
- tropomyosin 1 (alpha)
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_000366.5 |
679 |
Silent Mutation |
AAG,AAT |
K15N |
NP_000357.3 |
NM_001018004.1 |
679 |
Silent Mutation |
AAG,AAT |
K15N |
NP_001018004.1 |
NM_001018005.1 |
679 |
Silent Mutation |
AAG,AAT |
K15N |
NP_001018005.1 |
NM_001018006.1 |
679 |
Silent Mutation |
AAG,AAT |
K15N |
NP_001018006.1 |
NM_001018007.1 |
679 |
Silent Mutation |
AAG,AAT |
K15N |
NP_001018007.1 |
NM_001018008.1 |
679 |
Intron |
|
|
NP_001018008.1 |
NM_001018020.1 |
679 |
Silent Mutation |
AAG,AAT |
K15N |
NP_001018020.1 |
NM_001301244.1 |
679 |
Silent Mutation |
AAG,AAT |
K15N |
NP_001288173.1 |
NM_001301289.1 |
679 |
Intron |
|
|
NP_001288218.1 |
XM_005254637.1 |
679 |
Silent Mutation |
AAG,AAT |
K15N |
XP_005254694.1 |
XM_005254638.3 |
679 |
Silent Mutation |
AAG,AAT |
K99N |
XP_005254695.2 |
XM_005254639.3 |
679 |
Silent Mutation |
AAG,AAT |
K99N |
XP_005254696.2 |
XM_005254645.2 |
679 |
Silent Mutation |
AAG,AAT |
K99N |
XP_005254702.2 |
XM_005254646.2 |
679 |
Intron |
|
|
XP_005254703.1 |
XM_005254647.3 |
679 |
Intron |
|
|
XP_005254704.1 |
XM_005254650.3 |
679 |
Intron |
|
|
XP_005254707.1 |
XM_005254651.1 |
679 |
Intron |
|
|
XP_005254708.1 |
XM_005254652.1 |
679 |
Intron |
|
|
XP_005254709.1 |
XM_005254653.2 |
679 |
Intron |
|
|
XP_005254710.1 |
XM_006720667.3 |
679 |
Silent Mutation |
AAG,AAT |
K99N |
XP_006720730.2 |
XM_017022534.1 |
679 |
Silent Mutation |
AAG,AAT |
K99N |
XP_016878023.1 |
XM_017022535.1 |
679 |
Silent Mutation |
AAG,AAT |
K15N |
XP_016878024.1 |
XM_017022536.1 |
679 |
Silent Mutation |
AAG,AAT |
K99N |
XP_016878025.1 |
XM_017022537.1 |
679 |
Silent Mutation |
AAG,AAT |
K15N |
XP_016878026.1 |
XM_017022538.1 |
679 |
Silent Mutation |
AAG,AAT |
K99N |
XP_016878027.1 |
XM_017022539.1 |
679 |
Silent Mutation |
AAG,AAT |
K99N |
XP_016878028.1 |
XM_017022540.1 |
679 |
Intron |
|
|
XP_016878029.1 |
XM_017022541.1 |
679 |
Intron |
|
|
XP_016878030.1 |
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