Product Details

SNP ID
rs77113016
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:30653465 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCAGGTGGGCGACCGAGGGGTCACA[T/C]AGCGGCCGTCTGCTTGATGCTGTGG
Phenotype
MIM: 602034
Polymorphism
T/C, Transition substitution
Allele Nomenclature
Literature Links
CRHR2 PubMed Links

Gene Details

Gene
CRHR2
Gene Name
corticotropin releasing hormone receptor 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001202475.1 2420 Missense Mutation ATG,GTG M438V NP_001189404.1
NM_001202481.1 2420 Missense Mutation ATG,GTG M397V NP_001189410.1
NM_001202482.1 2420 Missense Mutation ATG,GTG M410V NP_001189411.1
NM_001202483.1 2420 UTR 3 NP_001189412.1
NM_001883.4 2420 Missense Mutation ATG,GTG M411V NP_001874.2
XM_011515127.2 2420 Missense Mutation TAT,TGT Y481C XP_011513429.1
XM_011515128.2 2420 Intron XP_011513430.1
XM_011515129.2 2420 Intron XP_011513431.1
XM_017011751.1 2420 Missense Mutation TAT,TGT Y480C XP_016867240.1
XM_017011752.1 2420 Missense Mutation ATG,GTG M397V XP_016867241.1

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