Product Details
- SNP ID
-
rs201668470
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.17:74326362 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- ACCTGCTGCAATCATGAAGGACAGC[A/G]GGGACTCCAAGGACCAGCAACTCAT
- Phenotype
-
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
KIF19
PubMed Links
Gene Details
- Gene
- KIF19
- Gene Name
- kinesin family member 19
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_153209.3 |
151 |
Missense Mutation |
AGG,GGG |
R5G |
NP_694941.2 |
XM_005257029.1 |
151 |
Missense Mutation |
AGG,GGG |
R5G |
XP_005257086.1 |
XM_005257030.1 |
151 |
Missense Mutation |
AGG,GGG |
R5G |
XP_005257087.1 |
XM_017024150.1 |
151 |
Missense Mutation |
AGG,GGG |
R5G |
XP_016879639.1 |
XM_017024151.1 |
151 |
Missense Mutation |
AGG,GGG |
R5G |
XP_016879640.1 |
XM_017024152.1 |
151 |
Missense Mutation |
AGG,GGG |
R5G |
XP_016879641.1 |
XM_017024153.1 |
151 |
Missense Mutation |
AGG,GGG |
R5G |
XP_016879642.1 |
XM_017024154.1 |
151 |
Missense Mutation |
AGG,GGG |
R5G |
XP_016879643.1 |
XM_017024155.1 |
151 |
Missense Mutation |
AGG,GGG |
R5G |
XP_016879644.1 |
XM_017024156.1 |
151 |
Missense Mutation |
AGG,GGG |
R5G |
XP_016879645.1 |
XM_017024157.1 |
151 |
Missense Mutation |
AGG,GGG |
R5G |
XP_016879646.1 |
XM_017024158.1 |
151 |
Missense Mutation |
AGG,GGG |
R5G |
XP_016879647.1 |
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