Product Details

SNP ID
rs201181200
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:139586437 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTCACAGACCTCCACCACAGTGCTG[A/G]TGTGTTCCAATTCAGTTTCCTCAGT
Phenotype
MIM: 311030
Polymorphism
A/G, 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 3021 Missense Mutation ACC,ATC T918I NP_001093325.1
NM_001171876.1 3021 Missense Mutation ACC,ATC T934I NP_001165347.1
NM_001171877.1 3021 Intron NP_001165348.1
NM_001171878.1 3021 Intron NP_001165349.1
NM_001171879.1 3021 Missense Mutation ACC,ATC T874I NP_001165350.1
NM_005369.4 3021 Missense Mutation ACC,ATC T858I NP_005360.3
XM_005262413.4 3021 Missense Mutation ACC,ATC T977I XP_005262470.1
XM_011531339.2 3021 Missense Mutation ACC,ATC T934I XP_011529641.1
XM_017029529.1 3021 Missense Mutation ACC,ATC T977I XP_016885018.1
XM_017029530.1 3021 Intron XP_016885019.1
XM_017029531.1 3021 Missense Mutation ACC,ATC T934I XP_016885020.1
XM_017029532.1 3021 Missense Mutation ACC,ATC T874I XP_016885021.1

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