Product Details

SNP ID
rs73026965
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.3:9411728 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGCTGCCTTTATTTTGGAAGTGGTT[A/G]TTGTTACGAGTATTTGATCAGTTCT
Phenotype
MIM: 615743
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
SETD5 PubMed Links

Gene Details

Gene
SETD5
Gene Name
SET domain containing 5
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001080517.2 Intron NP_001073986.1
NM_001292043.1 Intron NP_001278972.1
XM_005265301.1 Intron XP_005265358.1
XM_005265303.1 Intron XP_005265360.1
XM_011533920.1 Intron XP_011532222.1
XM_011533921.1 Intron XP_011532223.1
XM_011533922.1 Intron XP_011532224.1
XM_011533927.1 Intron XP_011532229.1
XM_011533928.1 Intron XP_011532230.1
XM_011533930.1 Intron XP_011532232.1
XM_011533932.1 Intron XP_011532234.1
XM_011533933.1 Intron XP_011532235.1
XM_017006767.1 Intron XP_016862256.1
XM_017006768.1 Intron XP_016862257.1
XM_017006769.1 Intron XP_016862258.1
XM_017006770.1 Intron XP_016862259.1
XM_017006771.1 Intron XP_016862260.1
XM_017006772.1 Intron XP_016862261.1
XM_017006773.1 Intron XP_016862262.1
XM_017006774.1 Intron XP_016862263.1
XM_017006775.1 Intron XP_016862264.1
XM_017006776.1 Intron XP_016862265.1
XM_017006777.1 Intron XP_016862266.1
XM_017006778.1 Intron XP_016862267.1
XM_017006779.1 Intron XP_016862268.1
XM_017006780.1 Intron XP_016862269.1
XM_017006781.1 Intron XP_016862270.1
XM_017006782.1 Intron XP_016862271.1
XM_017006783.1 Intron XP_016862272.1
XM_017006784.1 Intron XP_016862273.1
XM_017006785.1 Intron XP_016862274.1
XM_017006786.1 Intron XP_016862275.1

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