Product Details

SNP ID
rs202140125
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.20:59300823 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCCTGATCTAGGTTCATGGAGCCGG[C/G]GCTGTGGCTCCTTTTCGGGCTCACA
Phenotype
MIM: 131242
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
EDN3 PubMed Links

Gene Details

Gene
EDN3
Gene Name
endothelin 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001302455.1 408 Missense Mutation GCG,GGG A4G NP_001289384.1
NM_001302456.1 408 Missense Mutation GCG,GGG A4G NP_001289385.1
NM_207032.2 408 Missense Mutation GCG,GGG A4G NP_996915.1
NM_207033.2 408 Missense Mutation GCG,GGG A4G NP_996916.1
NM_207034.2 408 Missense Mutation GCG,GGG A4G NP_996917.1
XM_005260312.4 408 Missense Mutation GCG,GGG A4G XP_005260369.1
XM_005260313.4 408 Missense Mutation GCG,GGG A4G XP_005260370.1
XM_006723734.3 408 Missense Mutation GCG,GGG A4G XP_006723797.1
XM_011528655.2 408 Missense Mutation GCG,GGG A4G XP_011526957.1

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