Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TCCATGAGGCTGTGTACTTTTCCTT[G/T]GGCTTGGTCAAAGCAAGTCAGGGAT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
2 submissions
|
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Phenotype: |
MIM: 607189 | ||||||||||||||||||||
Literature Links: |
RGS8 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 |
RGS8 - regulator of G-protein signaling 8 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001102450.2 | 601 | Missense Mutation | AAA,CAA | K,Q 147 | NP_001095920.1 | |
NM_033345.3 | 601 | Missense Mutation | AAA,CAA | K,Q 165 | NP_203131.1 | |
XM_005245555.3 | 601 | Missense Mutation | AAA,CAA | K,Q 147 | XP_005245612.1 | |
XM_011510089.2 | 601 | Missense Mutation | AAA,CAA | K,Q 165 | XP_011508391.1 | |
XM_011510090.2 | 601 | Missense Mutation | AAA,CAA | K,Q 147 | XP_011508392.1 | |
XM_011510091.2 | 601 | Missense Mutation | AAA,CAA | K,Q 145 | XP_011508393.1 | |
XM_017002631.1 | 601 | Missense Mutation | AAA,CAA | K,Q 165 | XP_016858120.1 | |
XM_017002632.1 | 601 | Missense Mutation | AAA,CAA | K,Q 165 | XP_016858121.1 | |
XM_017002633.1 | 601 | Missense Mutation | AAA,CAA | K,Q 165 | XP_016858122.1 | |
XM_017002634.1 | 601 | Missense Mutation | AAA,CAA | K,Q 165 | XP_016858123.1 | |
XM_017002635.1 | 601 | Missense Mutation | AAA,CAA | K,Q 147 | XP_016858124.1 | |
XM_017002636.1 | 601 | Missense Mutation | AAA,CAA | K,Q 147 | XP_016858125.1 | |
XM_017002637.1 | 601 | Missense Mutation | AAA,CAA | K,Q 147 | XP_016858126.1 |