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TCAGCAGCTGAATAGTGAATCTCAC[A/C]GAGCTGAGTGACTTTTTTTGTTTGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
14 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 | |||
---|---|---|---|---|---|
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 | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
|
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 |