Product Details
- SNP ID
-
rs73721713
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.6:17764220 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TGGAGCCCATCGGAGACAGTCTTGC[C/T]GCCTGTTTTATTTGGTAGACTCCTC
- Phenotype
-
MIM: 605433
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
KIF13A
PubMed Links
Gene Details
- Gene
- KIF13A
- Gene Name
- kinesin family member 13A
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001105566.2 |
5463 |
Missense Mutation |
AGC,GGC |
S1735G |
NP_001099036.1 |
NM_001105567.2 |
5463 |
Missense Mutation |
AGC,GGC |
S1722G |
NP_001099037.1 |
NM_001105568.2 |
5463 |
Missense Mutation |
AGC,GGC |
S1722G |
NP_001099038.1 |
NM_001243423.1 |
5463 |
Intron |
|
|
NP_001230352.1 |
NM_022113.5 |
5463 |
Missense Mutation |
AGC,GGC |
S1770G |
NP_071396.4 |
XM_011514806.2 |
5463 |
Intron |
|
|
XP_011513108.1 |
XM_017011188.1 |
5463 |
Missense Mutation |
AGC,GGC |
S1770G |
XP_016866677.1 |
XM_017011189.1 |
5463 |
Missense Mutation |
AGC,GGC |
S1757G |
XP_016866678.1 |
XM_017011190.1 |
5463 |
Missense Mutation |
AGC,GGC |
S1749G |
XP_016866679.1 |
XM_017011191.1 |
5463 |
Missense Mutation |
AGC,GGC |
S1736G |
XP_016866680.1 |
XM_017011192.1 |
5463 |
Missense Mutation |
AGC,GGC |
S1735G |
XP_016866681.1 |
XM_017011193.1 |
5463 |
Missense Mutation |
AGC,GGC |
S1659G |
XP_016866682.1 |
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