Product Details

SNP ID
rs199779082
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.2:3604321 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TATTCCTTCCTCTGTGTAGGAGTTG[A/G]TGTCCTGCCTGCGCTCAGGATGAGG
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_001255982.1 344 UTR 5 NP_001242911.1
NM_001255983.1 344 UTR 5 NP_001242912.1
NM_001255984.1 344 UTR 5 NP_001242913.1
NM_001255985.1 344 Missense Mutation GAT,GGT D8G NP_001242914.1
NM_001255986.1 344 Intron NP_001242915.1
NM_001255987.1 344 Intron NP_001242916.1
NM_001255988.1 344 Intron NP_001242917.1
NM_001255989.1 344 Intron NP_001242918.1
NM_024027.4 344 UTR 5 NP_076932.1
NM_199235.2 344 UTR 5 NP_954705.1
XM_005263853.4 344 Missense Mutation GAT,GGT D8G XP_005263910.1
XM_006711897.3 344 Missense Mutation GAT,GGT D8G XP_006711960.1

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