Product Details

SNP ID
rs139947767
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.20:51391263 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGGCGAGCTCCTTAAGTGAGAGTCC[A/G]CTTAGTGCCCATACATTGATCCGCG
Phenotype
MIM: 600490
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
NFATC2 PubMed Links

Gene Details

Gene
NFATC2
Gene Name
nuclear factor of activated T-cells 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001136021.2 2432 UTR 3 NP_001129493.1
NM_001258292.1 2432 UTR 3 NP_001245221.1
NM_001258294.1 2432 UTR 3 NP_001245223.1
NM_001258295.1 2432 UTR 3 NP_001245224.1
NM_001258296.1 2432 UTR 3 NP_001245225.1
NM_001258297.1 2432 UTR 3 NP_001245226.1
NM_012340.4 2432 UTR 3 NP_036472.2
NM_173091.3 2432 UTR 3 NP_775114.1
XM_011528824.2 2432 Intron XP_011527126.1
XM_011528825.2 2432 Intron XP_011527127.1
XM_011528826.2 2432 Intron XP_011527128.1
XM_017027850.1 2432 Intron XP_016883339.1
XM_017027851.1 2432 UTR 3 XP_016883340.1

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