Product Details

SNP ID
rs141206026
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.20:57498637 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTCTGGCTGTGGTTTCTCTGCAGGC[A/G]ACAGGAAACATCTCTCCTGGGAACT
Phenotype
MIM: 607022
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
CTCFL PubMed Links

Gene Details

Gene
CTCFL
Gene Name
CCCTC-binding factor like
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001269040.1 2391 Silent Mutation GTC,GTT V635V NP_001255969.1
NM_001269041.1 2391 Silent Mutation GTC,GTT V635V NP_001255970.1
NM_001269042.1 2391 Silent Mutation GTC,GTT V634V NP_001255971.1
NM_001269043.1 2391 Silent Mutation GTC,GTT V635V NP_001255972.1
NM_001269044.1 2391 Intron NP_001255973.1
NM_001269045.1 2391 Intron NP_001255974.1
NM_001269046.1 2391 Silent Mutation GTC,GTT V585V NP_001255975.1
NM_001269047.1 2391 Intron NP_001255976.1
NM_001269048.1 2391 Intron NP_001255977.1
NM_001269049.1 2391 Intron NP_001255978.1
NM_001269050.1 2391 Intron NP_001255979.1
NM_001269051.1 2391 Intron NP_001255980.1
NM_001269052.1 2391 Intron NP_001255981.1
NM_001269054.1 2391 Intron NP_001255983.1
NM_001269055.1 2391 Intron NP_001255984.1
NM_080618.3 2391 Silent Mutation GTC,GTT V635V NP_542185.2

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