Product Details

SNP ID
rs143274733
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:139585623 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTAGGCATTTCTCCAAAGAAGTCTA[C/T]GCTGTTGATCCTAGAGTTGTTTAGG
Phenotype
MIM: 311030
Polymorphism
C/T, Transition 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 Intron NP_001093325.1
NM_001171876.1 Intron NP_001165347.1
NM_001171877.1 Intron NP_001165348.1
NM_001171878.1 Intron NP_001165349.1
NM_001171879.1 Intron NP_001165350.1
NM_005369.4 Intron NP_005360.3
XM_005262413.4 Intron XP_005262470.1
XM_011531339.2 Intron XP_011529641.1
XM_017029529.1 Intron XP_016885018.1
XM_017029530.1 Intron XP_016885019.1
XM_017029531.1 Intron XP_016885020.1
XM_017029532.1 Intron XP_016885021.1

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