Product Details
- SNP ID
-
rs199566972
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.12:39294481 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CTGTGTCAGAGATCTGACCATCTTG[A/C]AAATTGCGAGCCTTCCAAATTCTCA
- Phenotype
-
MIM: 608283
- Polymorphism
- A/C, Transversion Substitution
- Allele Nomenclature
-
- Literature Links
-
KIF21A
PubMed Links
Gene Details
- Gene
- KIF21A
- Gene Name
- kinesin family member 21A
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001173463.1 |
5322 |
Missense Mutation |
TTG,TTT |
L1619F |
NP_001166934.1 |
NM_001173464.1 |
5322 |
Missense Mutation |
TTG,TTT |
L1656F |
NP_001166935.1 |
NM_001173465.1 |
5322 |
Missense Mutation |
TTG,TTT |
L1603F |
NP_001166936.1 |
NM_017641.3 |
5322 |
Missense Mutation |
TTG,TTT |
L1643F |
NP_060111.2 |
XM_005269007.2 |
5322 |
Missense Mutation |
TTG,TTT |
L1657F |
XP_005269064.1 |
XM_005269008.2 |
5322 |
Missense Mutation |
TTG,TTT |
L1652F |
XP_005269065.1 |
XM_005269009.2 |
5322 |
Missense Mutation |
TTG,TTT |
L1650F |
XP_005269066.1 |
XM_005269010.2 |
5322 |
Missense Mutation |
TTG,TTT |
L1644F |
XP_005269067.1 |
XM_005269011.2 |
5322 |
Missense Mutation |
TTG,TTT |
L1639F |
XP_005269068.1 |
XM_005269012.2 |
5322 |
Missense Mutation |
TTG,TTT |
L1614F |
XP_005269069.1 |
XM_005269013.2 |
5322 |
Missense Mutation |
TTG,TTT |
L1609F |
XP_005269070.1 |
XM_005269014.2 |
5322 |
Missense Mutation |
TTG,TTT |
L1596F |
XP_005269071.1 |
XM_006719493.2 |
5322 |
Missense Mutation |
TTG,TTT |
L1637F |
XP_006719556.1 |
XM_006719494.2 |
5322 |
Missense Mutation |
TTG,TTT |
L1613F |
XP_006719557.1 |
XM_011538556.2 |
5322 |
Missense Mutation |
TTG,TTT |
L1634F |
XP_011536858.1 |
XM_017019607.1 |
5322 |
Missense Mutation |
TTG,TTT |
L1639F |
XP_016875096.1 |
XM_017019608.1 |
5322 |
Missense Mutation |
TTG,TTT |
L1626F |
XP_016875097.1 |
XM_017019609.1 |
5322 |
Missense Mutation |
TTG,TTT |
L1589F |
XP_016875098.1 |
XM_017019610.1 |
5322 |
Missense Mutation |
TTG,TTT |
L1589F |
XP_016875099.1 |
XM_017019611.1 |
5322 |
Missense Mutation |
TTG,TTT |
L1583F |
XP_016875100.1 |
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