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TTAGAAATAGCAGAAGTAAAAGTGC[A/G]GCTGTTGTTAGTTTAGAATCTCATC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616785 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
PHTF2 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
|
PHTF2 - putative homeodomain transcription factor 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001127357.1 | Intron | NP_001120829.1 | ||||
NM_001127358.1 | Intron | NP_001120830.1 | ||||
NM_001127359.1 | Intron | NP_001120831.1 | ||||
NM_001127360.1 | Intron | NP_001120832.1 | ||||
NM_020432.4 | Intron | NP_065165.3 | ||||
XM_005250508.4 | Intron | XP_005250565.1 | ||||
XM_005250509.4 | Intron | XP_005250566.1 | ||||
XM_006716063.3 | Intron | XP_006716126.1 | ||||
XM_011516422.2 | Intron | XP_011514724.1 | ||||
XM_011516423.2 | Intron | XP_011514725.1 | ||||
XM_011516424.2 | Intron | XP_011514726.1 | ||||
XM_017012458.1 | Intron | XP_016867947.1 | ||||
XM_017012459.1 | Intron | XP_016867948.1 |