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

View Full Product Details