Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ATAGTTGAAGAGCTAGCCTTAAAAT[C/T]TGTGAGAGGTTGCAAGCCTGCACAA
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 - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
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 | 4115 | Missense Mutation | AAT,GAT | N,D 1231 | NP_001273621.1 | |
NM_001286693.1 | 4115 | Missense Mutation | AAT,GAT | N,D 1062 | NP_001273622.1 | |
NM_015668.4 | 4115 | Missense Mutation | AAT,GAT | N,D 1243 | NP_056483.3 | |
XM_005250856.2 | 4115 | Missense Mutation | AAT,GAT | N,D 1190 | XP_005250913.1 | |
XM_005250857.2 | 4115 | Missense Mutation | AAT,GAT | N,D 1190 | XP_005250914.1 | |
XM_005250858.2 | 4115 | Missense Mutation | AAT,GAT | N,D 1189 | XP_005250915.1 | |
XM_005250860.2 | 4115 | Intron | XP_005250917.1 | |||
XM_006716540.2 | 4115 | Missense Mutation | AAT,GAT | N,D 1147 | XP_006716603.1 | |
XM_011516957.1 | 4115 | Missense Mutation | AAT,GAT | N,D 1147 | XP_011515259.1 | |
XM_011516958.1 | 4115 | Missense Mutation | AAT,GAT | N,D 1147 | XP_011515260.1 | |
XM_011516959.2 | 4115 | Intron | XP_011515261.1 | |||
XM_017013309.1 | 4115 | Missense Mutation | AAT,GAT | N,D 1137 | XP_016868798.1 | |
XM_017013310.1 | 4115 | Missense Mutation | AAT,GAT | N,D 1136 | XP_016868799.1 | |
XM_017013311.1 | 4115 | Missense Mutation | AAT,GAT | N,D 788 | XP_016868800.1 |