Product Details

SNP ID
rs78490320
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.13:112902287 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCCACAACGGCCCAATGAGGCCAAA[A/C]AGGAGGAAACGGATCACCAAATTGA
Phenotype
MIM: 609499
Polymorphism
A/C, Transversion 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_001112732.2 143 Intron NP_001106203.2
NM_001320815.1 143 Intron NP_001307744.1
NM_001320816.1 143 Intron NP_001307745.1
NM_001320817.1 143 Intron NP_001307746.1
NM_024979.4 143 Intron NP_079255.4
XM_011537482.1 143 Missense Mutation AAG,CAG K29Q XP_011535784.1
XM_011537483.2 143 Missense Mutation AAG,CAG K29Q XP_011535785.1
XM_011537484.1 143 Intron XP_011535786.1
XM_011537485.1 143 Intron XP_011535787.1
XM_011537486.2 143 Intron XP_011535788.2
XM_011537487.1 143 Intron XP_011535789.1
XM_011537488.1 143 Intron XP_011535790.1
XM_011537490.1 143 Intron XP_011535792.1
XM_011537491.1 143 Intron XP_011535793.1
XM_017020493.1 143 Intron XP_016875982.1
XM_017020494.1 143 Intron XP_016875983.1
XM_017020495.1 143 Intron XP_016875984.1
XM_017020496.1 143 Intron XP_016875985.1
XM_017020497.1 143 Intron XP_016875986.1
XM_017020498.1 143 Intron XP_016875987.1
XM_017020499.1 143 Intron XP_016875988.1

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