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CCAGAGTGTAGACCTTTTTATTTTA[C/T]TTTTAAAAGCAATTCTGTGCTCACA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610306 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
NPNT PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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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
|
NPNT - nephronectin | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001033047.2 | Intron | NP_001028219.1 | ||||
NM_001184690.1 | Intron | NP_001171619.1 | ||||
NM_001184691.1 | Intron | NP_001171620.1 | ||||
NM_001184692.1 | Intron | NP_001171621.1 | ||||
NM_001184693.1 | Intron | NP_001171622.1 | ||||
XM_005262888.4 | Intron | XP_005262945.1 | ||||
XM_005262890.1 | Intron | XP_005262947.1 | ||||
XM_011531820.2 | Intron | XP_011530122.1 | ||||
XM_011531822.2 | Intron | XP_011530124.1 | ||||
XM_011531823.2 | Intron | XP_011530125.1 | ||||
XM_011531824.2 | Intron | XP_011530126.1 | ||||
XM_011531825.2 | Intron | XP_011530127.1 | ||||
XM_017007984.1 | Intron | XP_016863473.1 |