Product Details

SNP ID
rs141940257
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.13:112902349 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCATCAGGCTTGTTCAAGACACACC[A/G]GAGGCGACGGCCATGGCCACAGGTA
Phenotype
MIM: 609499
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
MCF2L PubMed Links

Gene Details

Gene
MCF2L
Gene Name
MCF.2 cell line derived transforming sequence like
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001112732.2 205 Intron NP_001106203.2
NM_001320815.1 205 Intron NP_001307744.1
NM_001320816.1 205 Intron NP_001307745.1
NM_001320817.1 205 Intron NP_001307746.1
NM_024979.4 205 Intron NP_079255.4
XM_011537482.1 205 Silent Mutation CCA,CCG P49P XP_011535784.1
XM_011537483.2 205 Silent Mutation CCA,CCG P49P XP_011535785.1
XM_011537484.1 205 Intron XP_011535786.1
XM_011537485.1 205 Intron XP_011535787.1
XM_011537486.2 205 Intron XP_011535788.2
XM_011537487.1 205 Intron XP_011535789.1
XM_011537488.1 205 Intron XP_011535790.1
XM_011537490.1 205 Intron XP_011535792.1
XM_011537491.1 205 Intron XP_011535793.1
XM_017020493.1 205 Intron XP_016875982.1
XM_017020494.1 205 Intron XP_016875983.1
XM_017020495.1 205 Intron XP_016875984.1
XM_017020496.1 205 Intron XP_016875985.1
XM_017020497.1 205 Intron XP_016875986.1
XM_017020498.1 205 Intron XP_016875987.1
XM_017020499.1 205 Intron XP_016875988.1

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