Product Details
- SNP ID
-
rs202079010
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.17:17847700 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TTCCGGCCAGAAGGGTTTGAGGCTG[G/T]GGCAGGAGCCTCCATGGGGGGCGAG
- Phenotype
-
MIM: 615519
- Polymorphism
- G/T, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
TOM1L2
PubMed Links
Gene Details
- Gene
- TOM1L2
- Gene Name
- target of myb1 like 2 membrane trafficking protein
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001033551.2 |
1345 |
Missense Mutation |
ACA,CCA |
T437P |
NP_001028723.1 |
NM_001082968.1 |
1345 |
Missense Mutation |
ACA,CCA |
T487P |
NP_001076437.1 |
NM_001288786.1 |
1345 |
Missense Mutation |
ACA,CCA |
T463P |
NP_001275715.1 |
NM_001288787.1 |
1345 |
Missense Mutation |
ACA,CCA |
T442P |
NP_001275716.1 |
NM_001288788.1 |
1345 |
Missense Mutation |
ACA,CCA |
T369P |
NP_001275717.1 |
NM_001288789.1 |
1345 |
Missense Mutation |
ACA,CCA |
T368P |
NP_001275718.1 |
XM_005256461.2 |
1345 |
Missense Mutation |
ACA,CCA |
T516P |
XP_005256518.1 |
XM_005256462.1 |
1345 |
Missense Mutation |
ACA,CCA |
T471P |
XP_005256519.1 |
XM_005256463.2 |
1345 |
Missense Mutation |
ACA,CCA |
T467P |
XP_005256520.1 |
XM_005256466.1 |
1345 |
Missense Mutation |
ACA,CCA |
T418P |
XP_005256523.1 |
XM_011523662.1 |
1345 |
Missense Mutation |
ACA,CCA |
T466P |
XP_011521964.1 |
XM_017024201.1 |
1345 |
Missense Mutation |
ACA,CCA |
T422P |
XP_016879690.1 |
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