Product Details

SNP ID
rs1366024
Assay Type
Validated
NCBI dbSNP Submissions
NA
Location
Chr.12:45919855 on Build GRCh38
Set Membership
HapMap Validated
Context Sequence [VIC/FAM]
AAAACTTTAGAACTTGTTTGCAAAA[A/G]CTAAATGGTATAAAACACATTTTAA
Phenotype
MIM: 603668
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
SCAF11 PubMed Links

Gene Details

Gene
SCAF11
Gene Name
SR-related CTD associated factor 11
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_004719.2 8391 UTR 3 NP_004710.2
XM_005269230.2 8391 UTR 3 XP_005269287.2
XM_011538984.2 8391 UTR 3 XP_011537286.1
XM_011538985.1 8391 UTR 3 XP_011537287.1
XM_017020217.1 8391 UTR 3 XP_016875706.1
XM_017020218.1 8391 Intron XP_016875707.1
XM_017020219.1 8391 UTR 3 XP_016875708.1
XM_017020220.1 8391 UTR 3 XP_016875709.1
XM_017020221.1 8391 UTR 3 XP_016875710.1
XM_017020222.1 8391 UTR 3 XP_016875711.1
XM_017020223.1 8391 UTR 3 XP_016875712.1

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