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TCCTGTCTTTTCTCAGGCAATCGCC[A/G]TGGTACCCAGGGCTGGCCTTGTTTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 610423 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
PACS2 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
|
PACS2 - phosphofurin acidic cluster sorting protein 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001100913.2 | Intron | NP_001094383.2 | ||||
NM_001243127.2 | Intron | NP_001230056.1 | ||||
NM_015197.3 | Intron | NP_056012.2 | ||||
XM_006720090.1 | Intron | XP_006720153.1 | ||||
XM_006720091.1 | Intron | XP_006720154.1 | ||||
XM_006720092.2 | Intron | XP_006720155.1 | ||||
XM_017021105.1 | Intron | XP_016876594.1 | ||||
XM_017021106.1 | Intron | XP_016876595.1 | ||||
XM_017021107.1 | Intron | XP_016876596.1 | ||||
XM_017021108.1 | Intron | XP_016876597.1 | ||||
XM_017021109.1 | Intron | XP_016876598.1 | ||||
XM_017021110.1 | Intron | XP_016876599.1 | ||||
XM_017021111.1 | Intron | XP_016876600.1 | ||||
XM_017021112.1 | Intron | XP_016876601.1 |