Product Details

SNP ID
rs9549605
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.13:112901909 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGTCTGAATGTCGAGGGGAAAACCT[C/T]GGTTGTTGTTGTTTTTCTTTTCTTC
Phenotype
MIM: 609499
Polymorphism
C/T, 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 Intron NP_001106203.2
NM_001320815.1 Intron NP_001307744.1
NM_001320816.1 Intron NP_001307745.1
NM_001320817.1 Intron NP_001307746.1
NM_024979.4 Intron NP_079255.4
XM_011537482.1 Intron XP_011535784.1
XM_011537483.2 Intron XP_011535785.1
XM_011537484.1 Intron XP_011535786.1
XM_011537485.1 Intron XP_011535787.1
XM_011537486.2 Intron XP_011535788.2
XM_011537487.1 Intron XP_011535789.1
XM_011537488.1 Intron XP_011535790.1
XM_011537490.1 Intron XP_011535792.1
XM_011537491.1 Intron XP_011535793.1
XM_017020493.1 Intron XP_016875982.1
XM_017020494.1 Intron XP_016875983.1
XM_017020495.1 Intron XP_016875984.1
XM_017020496.1 Intron XP_016875985.1
XM_017020497.1 Intron XP_016875986.1
XM_017020498.1 Intron XP_016875987.1
XM_017020499.1 Intron XP_016875988.1

View Full Product Details