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TGTCATCTGTGAGAGAAAACTTGAG[A/C]AAGAGAAGAGACAGGCGTGGCCTAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607993 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SUGP2 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 | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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SUGP2 - SURP and G-patch domain containing 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001017392.4 | Intron | NP_001017392.2 | ||||
NM_001321697.1 | Intron | NP_001308626.1 | ||||
NM_001321698.1 | Intron | NP_001308627.1 | ||||
NM_001321699.1 | Intron | NP_001308628.1 | ||||
NM_014884.4 | Intron | NP_055699.2 | ||||
XM_017026137.1 | Intron | XP_016881626.1 |