Product Details

SNP ID

rs143551813

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.15:43534983 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGCATGGCTGGCTGACCTCCTCGGA[A/G]TTCTCCAGACATAGCTGGCAAACTT

Phenotype

MIM: 600178 MIM: 610979

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

MAP1A PubMed Links

Gene Details

Gene

MAP1A

Gene Name

microtubule associated protein 1A

There are no transcripts associated with this gene.

Gene

PPIP5K1

Gene Name

diphosphoinositol pentakisphosphate kinase 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001130858.2	4185	Silent Mutation	AAC,AAT	N1331N	NP_001124330.1
NM_001130859.2	4185	Silent Mutation	AAC,AAT	N1306N	NP_001124331.1
NM_001190214.1	4185	Silent Mutation	AAC,AAT	N1304N	NP_001177143.1
NM_014659.5	4185	Silent Mutation	AAC,AAT	N1306N	NP_055474.3
XM_005254803.1	4185	Silent Mutation	AAC,AAT	N1327N	XP_005254860.1
XM_005254804.1	4185	Silent Mutation	AAC,AAT	N1306N	XP_005254861.1
XM_006720786.2	4185	Silent Mutation	AAC,AAT	N1264N	XP_006720849.1
XM_011522249.1	4185	Silent Mutation	AAC,AAT	N1377N	XP_011520551.1
XM_011522250.1	4185	Silent Mutation	AAC,AAT	N1377N	XP_011520552.1
XM_011522252.1	4185	Silent Mutation	AAC,AAT	N1377N	XP_011520554.1
XM_011522254.1	4185	Silent Mutation	AAC,AAT	N1377N	XP_011520556.1
XM_011522258.1	4185	Silent Mutation	AAC,AAT	N1122N	XP_011520560.1
XM_011522259.1	4185	Silent Mutation	AAC,AAT	N1319N	XP_011520561.1
XM_017022735.1	4185	Silent Mutation	AAC,AAT	N1377N	XP_016878224.1
XM_017022736.1	4185	Silent Mutation	AAC,AAT	N1377N	XP_016878225.1
XM_017022737.1	4185	Silent Mutation	AAC,AAT	N1377N	XP_016878226.1
XM_017022738.1	4185	Silent Mutation	AAC,AAT	N1369N	XP_016878227.1
XM_017022739.1	4185	Silent Mutation	AAC,AAT	N1356N	XP_016878228.1
XM_017022740.1	4185	Silent Mutation	AAC,AAT	N1327N	XP_016878229.1
XM_017022741.1	4185	Silent Mutation	AAC,AAT	N1327N	XP_016878230.1
XM_017022742.1	4185	Silent Mutation	AAC,AAT	N1327N	XP_016878231.1
XM_017022743.1	4185	Silent Mutation	AAC,AAT	N1327N	XP_016878232.1
XM_017022744.1	4185	Silent Mutation	AAC,AAT	N1327N	XP_016878233.1
XM_017022745.1	4185	Silent Mutation	AAC,AAT	N1319N	XP_016878234.1
XM_017022746.1	4185	Silent Mutation	AAC,AAT	N1319N	XP_016878235.1
XM_017022747.1	4185	Silent Mutation	AAC,AAT	N1314N	XP_016878236.1
XM_017022748.1	4185	Silent Mutation	AAC,AAT	N1306N	XP_016878237.1
XM_017022749.1	4185	Silent Mutation	AAC,AAT	N1306N	XP_016878238.1
XM_017022750.1	4185	Silent Mutation	AAC,AAT	N1306N	XP_016878239.1
XM_017022751.1	4185	Silent Mutation	AAC,AAT	N1306N	XP_016878240.1
XM_017022752.1	4185	Silent Mutation	AAC,AAT	N1298N	XP_016878241.1
XM_017022753.1	4185	Silent Mutation	AAC,AAT	N1298N	XP_016878242.1
XM_017022754.1	4185	Silent Mutation	AAC,AAT	N1264N	XP_016878243.1
XM_017022755.1	4185	Silent Mutation	AAC,AAT	N1264N	XP_016878244.1
XM_017022756.1	4185	Silent Mutation	AAC,AAT	N1264N	XP_016878245.1
XM_017022757.1	4185	Silent Mutation	AAC,AAT	N1264N	XP_016878246.1
XM_017022758.1	4185	Silent Mutation	AAC,AAT	N1051N	XP_016878247.1
XM_017022759.1	4185	Intron			XP_016878248.1
XM_017022760.1	4185	Silent Mutation	AAC,AAT	N663N	XP_016878249.1

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