Product Details

SNP ID

rs2271477

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:39301643 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ACTGGGTGGTCTGGCACCACTCCCA[A/G]GGCACAGACCCAATCCTTATGTGCA

Phenotype

MIM: 608283

Polymorphism

A/G, Transition 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	5122	Silent Mutation	CTG,TTG	L1553L	NP_001166934.1
NM_001173464.1	5122	Silent Mutation	CTG,TTG	L1590L	NP_001166935.1
NM_001173465.1	5122	Silent Mutation	CTG,TTG	L1537L	NP_001166936.1
NM_017641.3	5122	Silent Mutation	CTG,TTG	L1577L	NP_060111.2
XM_005269007.2	5122	Silent Mutation	CTG,TTG	L1591L	XP_005269064.1
XM_005269008.2	5122	Silent Mutation	CTG,TTG	L1586L	XP_005269065.1
XM_005269009.2	5122	Silent Mutation	CTG,TTG	L1584L	XP_005269066.1
XM_005269010.2	5122	Silent Mutation	CTG,TTG	L1578L	XP_005269067.1
XM_005269011.2	5122	Silent Mutation	CTG,TTG	L1573L	XP_005269068.1
XM_005269012.2	5122	Silent Mutation	CTG,TTG	L1548L	XP_005269069.1
XM_005269013.2	5122	Silent Mutation	CTG,TTG	L1543L	XP_005269070.1
XM_005269014.2	5122	Silent Mutation	CTG,TTG	L1530L	XP_005269071.1
XM_006719493.2	5122	Silent Mutation	CTG,TTG	L1571L	XP_006719556.1
XM_006719494.2	5122	Silent Mutation	CTG,TTG	L1547L	XP_006719557.1
XM_011538556.2	5122	Silent Mutation	CTG,TTG	L1568L	XP_011536858.1
XM_017019607.1	5122	Silent Mutation	CTG,TTG	L1573L	XP_016875096.1
XM_017019608.1	5122	Silent Mutation	CTG,TTG	L1560L	XP_016875097.1
XM_017019609.1	5122	Silent Mutation	CTG,TTG	L1523L	XP_016875098.1
XM_017019610.1	5122	Silent Mutation	CTG,TTG	L1523L	XP_016875099.1
XM_017019611.1	5122	Silent Mutation	CTG,TTG	L1517L	XP_016875100.1

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