Product Details
- SNP ID
-
rs201301483
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.11:62602607 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CGTCCTTGCCGCCCAGCGAGACGAG[A/G]TGCGAGTCGTCGTGCGTGAATCGGA
- Phenotype
-
MIM: 603947
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
EML3
PubMed Links
Gene Details
- Gene
- EML3
- Gene Name
- echinoderm microtubule associated protein like 3
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001300793.1 |
3242 |
Missense Mutation |
CCT,TCT |
P818S |
NP_001287722.1 |
NM_001300794.1 |
3242 |
Missense Mutation |
CCT,TCT |
P817S |
NP_001287723.1 |
NM_153265.2 |
3242 |
Silent Mutation |
CAC,CAT |
H853H |
NP_694997.2 |
XM_005273878.3 |
3242 |
Silent Mutation |
CAC,CAT |
H854H |
XP_005273935.1 |
XM_006718489.3 |
3242 |
Missense Mutation |
CCT,TCT |
P868S |
XP_006718552.1 |
XM_006718490.3 |
3242 |
Silent Mutation |
CAC,CAT |
H904H |
XP_006718553.1 |
XM_006718491.3 |
3242 |
Silent Mutation |
CAC,CAT |
H903H |
XP_006718554.1 |
XM_011544896.2 |
3242 |
Missense Mutation |
CCT,TCT |
P867S |
XP_011543198.1 |
XM_011544897.2 |
3242 |
Missense Mutation |
CCT,TCT |
P816S |
XP_011543199.1 |
XM_017017480.1 |
3242 |
Missense Mutation |
CCT,TCT |
P701S |
XP_016872969.1 |
XM_017017481.1 |
3242 |
Missense Mutation |
CCT,TCT |
P701S |
XP_016872970.1 |
XM_017017482.1 |
3242 |
Silent Mutation |
CAC,CAT |
H737H |
XP_016872971.1 |
XM_017017483.1 |
3242 |
Missense Mutation |
CCT,TCT |
P600S |
XP_016872972.1 |
- Gene
- MTA2
- Gene Name
- metastasis associated 1 family member 2
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