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TCCTGCCTGCTCTGGTCTGTCTGTC[C/T]CCCTCAAAGCTCACATGTTGAAAGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
10 submissions
|
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Phenotype: |
MIM: 602517 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
RGS7 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
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
|
RGS7 - regulator of G-protein signaling 7 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001282773.1 | Intron | NP_001269702.1 | ||||
NM_001282775.1 | Intron | NP_001269704.1 | ||||
NM_001282778.1 | Intron | NP_001269707.1 | ||||
NM_002924.5 | Intron | NP_002915.3 | ||||
XM_005273218.3 | Intron | XP_005273275.1 | ||||
XM_006711800.3 | Intron | XP_006711863.1 | ||||
XM_011544246.2 | Intron | XP_011542548.1 | ||||
XM_011544247.2 | Intron | XP_011542549.1 | ||||
XM_017002001.1 | Intron | XP_016857490.1 | ||||
XM_017002002.1 | Intron | XP_016857491.1 | ||||
XM_017002003.1 | Intron | XP_016857492.1 | ||||
XM_017002004.1 | Intron | XP_016857493.1 | ||||
XM_017002005.1 | Intron | XP_016857494.1 | ||||
XM_017002006.1 | Intron | XP_016857495.1 | ||||
XM_017002007.1 | Intron | XP_016857496.1 | ||||
XM_017002008.1 | Intron | XP_016857497.1 | ||||
XM_017002009.1 | Intron | XP_016857498.1 | ||||
XM_017002010.1 | Intron | XP_016857499.1 | ||||
XM_017002011.1 | Intron | XP_016857500.1 | ||||
XM_017002012.1 | Intron | XP_016857501.1 | ||||
XM_017002013.1 | Intron | XP_016857502.1 |