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CTGTGCTTAAGAAAACATTTGAAGC[A/G]ATGGGAATATGGGAACAAAGACATG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
24 submissions
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Phenotype: |
MIM: 611012 | ||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
RGSL1 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 | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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RGSL1 - regulator of G-protein signaling like 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001137669.1 | Intron | NP_001131141.1 | ||||
XM_005245137.1 | Intron | XP_005245194.1 | ||||
XM_011509494.2 | Intron | XP_011507796.1 | ||||
XM_011509496.1 | Intron | XP_011507798.1 | ||||
XM_011509500.1 | Intron | XP_011507802.1 | ||||
XM_011509503.1 | Intron | XP_011507805.1 | ||||
XM_011509504.2 | Intron | XP_011507806.1 | ||||
XM_017001188.1 | Intron | XP_016856677.1 | ||||
XM_017001189.1 | Intron | XP_016856678.1 | ||||
XM_017001190.1 | Intron | XP_016856679.1 | ||||
XM_017001191.1 | Intron | XP_016856680.1 | ||||
XM_017001192.1 | Intron | XP_016856681.1 | ||||
XM_017001193.1 | Intron | XP_016856682.1 | ||||
XM_017001194.1 | Intron | XP_016856683.1 | ||||
XM_017001195.1 | Intron | XP_016856684.1 | ||||
XM_017001196.1 | Intron | XP_016856685.1 | ||||
XM_017001197.1 | Intron | XP_016856686.1 |
Set Membership: |
HapMap |