Product Details

SNP ID
rs190962863
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:50508550 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCCGCCCAAGTTGATCGGTGGATGC[A/G]CGCCCCCGCGCGGGGCACCGGTTGC
Phenotype
MIM: 609835
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
MYCBPAP PubMed Links

Gene Details

Gene
MYCBPAP
Gene Name
MYCBP associated protein
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_032133.4 10 Missense Mutation CAC,CGC H2R NP_115509.4
XM_005257725.3 10 Missense Mutation CAC,CGC H2R XP_005257782.1
XM_005257726.2 10 Missense Mutation CAC,CGC H2R XP_005257783.1
XM_011525342.1 10 Missense Mutation CAC,CGC H2R XP_011523644.1
XM_011525343.1 10 Missense Mutation CAC,CGC H2R XP_011523645.1
XM_017025205.1 10 Missense Mutation CAC,CGC H2R XP_016880694.1

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