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TTCTTTTGGAATCAGAAGGGAGCCT[C/T]GGGTAGTTTCTTGCTTGCCCTTTAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 603142 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
PPFIBP2 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
|
PPFIBP2 - PPFIA binding protein 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001256568.1 | Intron | NP_001243497.1 | ||||
NM_001256569.1 | Intron | NP_001243498.1 | ||||
NM_003621.3 | Intron | NP_003612.2 | ||||
XM_005253177.2 | Intron | XP_005253234.1 | ||||
XM_006718349.2 | Intron | XP_006718412.1 | ||||
XM_006718350.2 | Intron | XP_006718413.1 | ||||
XM_006718351.2 | Intron | XP_006718414.1 | ||||
XM_006718352.2 | Intron | XP_006718415.1 | ||||
XM_006718353.2 | Intron | XP_006718416.1 | ||||
XM_011520413.2 | Intron | XP_011518715.1 | ||||
XM_011520414.2 | Intron | XP_011518716.1 | ||||
XM_011520415.2 | Intron | XP_011518717.1 | ||||
XM_011520416.2 | Intron | XP_011518718.1 | ||||
XM_011520417.2 | Intron | XP_011518719.1 | ||||
XM_011520418.2 | Intron | XP_011518720.1 | ||||
XM_011520419.2 | Intron | XP_011518721.1 | ||||
XM_011520420.2 | Intron | XP_011518722.1 | ||||
XM_017018443.1 | Intron | XP_016873932.1 | ||||
XM_017018444.1 | Intron | XP_016873933.1 | ||||
XM_017018445.1 | Intron | XP_016873934.1 | ||||
XM_017018446.1 | Intron | XP_016873935.1 | ||||
XM_017018447.1 | Intron | XP_016873936.1 |