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TGCAAGCCTGCACAAAAATAAAAGA[A/G]ATAAGAAAAACAGTAAAGTAAATAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 615650 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
RGS22 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
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
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
|
RGS22 - regulator of G-protein signaling 22 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001286692.1 | Intron | NP_001273621.1 | ||||
NM_001286693.1 | Intron | NP_001273622.1 | ||||
NM_015668.4 | Intron | NP_056483.3 | ||||
XM_005250856.2 | Intron | XP_005250913.1 | ||||
XM_005250857.2 | Intron | XP_005250914.1 | ||||
XM_005250858.2 | Intron | XP_005250915.1 | ||||
XM_005250860.2 | Intron | XP_005250917.1 | ||||
XM_006716540.2 | Intron | XP_006716603.1 | ||||
XM_011516957.1 | Intron | XP_011515259.1 | ||||
XM_011516958.1 | Intron | XP_011515260.1 | ||||
XM_011516959.2 | Intron | XP_011515261.1 | ||||
XM_017013309.1 | Intron | XP_016868798.1 | ||||
XM_017013310.1 | Intron | XP_016868799.1 | ||||
XM_017013311.1 | Intron | XP_016868800.1 |