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GCAGGTGGGCGACCGAGGGGTCACA[T/C]AGCGGCCGTCTGCTTGATGCTGTGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602034 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CRHR2 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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CRHR2 - corticotropin releasing hormone receptor 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001202475.1 | 2420 | Missense Mutation | ATG,GTG | M,V 438 | NP_001189404.1 | |
NM_001202481.1 | 2420 | Missense Mutation | ATG,GTG | M,V 397 | NP_001189410.1 | |
NM_001202482.1 | 2420 | Missense Mutation | ATG,GTG | M,V 410 | NP_001189411.1 | |
NM_001202483.1 | 2420 | UTR 3 | NP_001189412.1 | |||
NM_001883.4 | 2420 | Missense Mutation | ATG,GTG | M,V 411 | NP_001874.2 | |
XM_011515127.2 | 2420 | Missense Mutation | TAT,TGT | Y,C 481 | 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 | Y,C 480 | XP_016867240.1 | |
XM_017011752.1 | 2420 | Missense Mutation | ATG,GTG | M,V 397 | XP_016867241.1 |