Product Details

SNP ID
rs3128285
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:139586451 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCACAGTGCTGGTGTGTTCCAATTC[A/C]GTTTCCTCAGTACTTATAAAAGCTC
Phenotype
MIM: 311030
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
MCF2 PubMed Links

Gene Details

Gene
MCF2
Gene Name
MCF.2 cell line derived transforming sequence
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001099855.1 3007 Silent Mutation ACG,ACT T913T NP_001093325.1
NM_001171876.1 3007 Silent Mutation ACG,ACT T929T NP_001165347.1
NM_001171877.1 3007 Intron NP_001165348.1
NM_001171878.1 3007 Intron NP_001165349.1
NM_001171879.1 3007 Silent Mutation ACG,ACT T869T NP_001165350.1
NM_005369.4 3007 Silent Mutation ACG,ACT T853T NP_005360.3
XM_005262413.4 3007 Silent Mutation ACG,ACT T972T XP_005262470.1
XM_011531339.2 3007 Silent Mutation ACG,ACT T929T XP_011529641.1
XM_017029529.1 3007 Silent Mutation ACG,ACT T972T XP_016885018.1
XM_017029530.1 3007 Intron XP_016885019.1
XM_017029531.1 3007 Silent Mutation ACG,ACT T929T XP_016885020.1
XM_017029532.1 3007 Silent Mutation ACG,ACT T869T XP_016885021.1

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