Product Details

SNP ID
rs114785923
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:3595797 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCTGCCTCCTACCTGGATGCCTTGC[A/G]CTAGGAACTGGCGGTCTTTTTAGAG
Phenotype
MIM: 612502
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
COLEC11 PubMed Links

Gene Details

Gene
COLEC11
Gene Name
collectin subfamily member 11
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001255982.1 Intron NP_001242911.1
NM_001255983.1 Intron NP_001242912.1
NM_001255984.1 Intron NP_001242913.1
NM_001255985.1 Intron NP_001242914.1
NM_001255986.1 Intron NP_001242915.1
NM_001255987.1 Intron NP_001242916.1
NM_001255988.1 Intron NP_001242917.1
NM_001255989.1 Intron NP_001242918.1
NM_024027.4 Intron NP_076932.1
NM_199235.2 Intron NP_954705.1
XM_005263853.4 Intron XP_005263910.1
XM_006711897.3 Intron XP_006711960.1

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