Product Details

SNP ID
rs145799391
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:17724160 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCCTGCACCACCGTGGAGACAACCT[A/G]GAGACCCTGGTCCTCCTGAACCCAT
Phenotype
MIM: 607573
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
MAP1S PubMed Links

Gene Details

Gene
MAP1S
Gene Name
microtubule associated protein 1S
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001308363.1 647 Silent Mutation CTA,CTG L59L NP_001295292.1
NM_018174.5 647 Silent Mutation CTA,CTG L85L NP_060644.4
XM_017026930.1 647 Silent Mutation CTA,CTG L85L XP_016882419.1
XM_017026931.1 647 Silent Mutation CTA,CTG L59L XP_016882420.1

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