Product Details

SNP ID
rs190262523
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:110180602 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCATCAAAGCCGTCTCTAGCAGTGG[C/T]AGTGGACTCGGCTCCGGAGGTGGCA
Phenotype
MIM: 605585 MIM: 605035
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
CDC40 PubMed Links

Gene Details

Gene
CDC40
Gene Name
cell division cycle 40
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_015891.2 182 Missense Mutation GCA,GTA A53V NP_056975.1
Gene
WASF1
Gene Name
WAS protein family member 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001024934.1 182 Intron NP_001020105.1
NM_001024935.1 182 Intron NP_001020106.1
NM_001024936.1 182 Intron NP_001020107.1
NM_003931.2 182 Intron NP_003922.1
XM_005267203.3 182 Intron XP_005267260.1
XM_005267205.2 182 Intron XP_005267262.1
XM_005267206.2 182 Intron XP_005267263.1
XM_005267207.2 182 Intron XP_005267264.1
XM_011536233.1 182 Intron XP_011534535.1
XM_011536234.1 182 Intron XP_011534536.1
XM_011536235.1 182 Intron XP_011534537.1
XM_017011437.1 182 Intron XP_016866926.1
XM_017011438.1 182 Intron XP_016866927.1
XM_017011439.1 182 Intron XP_016866928.1
XM_017011440.1 182 Intron XP_016866929.1
XM_017011441.1 182 Intron XP_016866930.1
XM_017011442.1 182 Intron XP_016866931.1
XM_017011443.1 182 Intron XP_016866932.1
XM_017011444.1 182 Intron XP_016866933.1

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