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AAAAACGTTGCTCTTCCAACTAAAC[A/G]TTTTCCTTGGGTACCTAATGCCTAA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601060 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ENPP2 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
|
ENPP2 - ectonucleotide pyrophosphatase/phosphodiesterase 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001040092.2 | Intron | NP_001035181.1 | ||||
NM_001130863.2 | Intron | NP_001124335.1 | ||||
NM_006209.4 | Intron | NP_006200.3 | ||||
XM_006716584.1 | Intron | XP_006716647.1 | ||||
XM_006716585.1 | Intron | XP_006716648.1 | ||||
XM_006716587.1 | Intron | XP_006716650.1 | ||||
XM_017013571.1 | Intron | XP_016869060.1 | ||||
XM_017013572.1 | Intron | XP_016869061.1 | ||||
XM_017013573.1 | Intron | XP_016869062.1 | ||||
XM_017013574.1 | Intron | XP_016869063.1 | ||||
XM_017013575.1 | Intron | XP_016869064.1 |