Product Details

SNP ID
rs199579160
Assay Type
Functionally tested
NCBI dbSNP Submissions
12
Location
Chr.1:31790832 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CAGGGCTTGGTGGGGACAGGAGTCC[C/T]TGTGGAAGTGCTGGCCACGGCCAAA
Phenotype
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
SPOCD1 PubMed Links

Gene Details

Gene
SPOCD1
Gene Name
SPOC domain containing 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001281987.1 3296 Missense Mutation AAG,AGG K1128R NP_001268916.1
NM_001281988.1 3296 Missense Mutation AAG,AGG K621R NP_001268917.1
NM_144569.5 3296 Missense Mutation AAG,AGG K1141R NP_653170.3
XM_011542413.2 3296 Missense Mutation AAG,AGG K621R XP_011540715.1
XM_011542414.2 3296 Missense Mutation AAG,AGG K621R XP_011540716.1
XM_017002779.1 3296 Missense Mutation AAG,AGG K1127R XP_016858268.1
XM_017002780.1 3296 Missense Mutation AAG,AGG K1114R XP_016858269.1
XM_017002781.1 3296 Missense Mutation AAG,AGG K1086R XP_016858270.1
XM_017002782.1 3296 Missense Mutation AAG,AGG K871R XP_016858271.1

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