Product Details

SNP ID
rs140695822
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:17724142 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCCCCACAGGCCAGCGGAGCCTGCA[C/T]CACCGTGGAGACAACCTGGAGACCC
Phenotype
MIM: 607573
Polymorphism
C/T, 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_001308363.1 629 Silent Mutation CAC,CAT H53H NP_001295292.1
NM_018174.5 629 Silent Mutation CAC,CAT H79H NP_060644.4
XM_017026930.1 629 Silent Mutation CAC,CAT H79H XP_016882419.1
XM_017026931.1 629 Silent Mutation CAC,CAT H53H XP_016882420.1

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