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CAACTGTGAGTATGAGATATGGCTT[G/T]AAGATCCTACCTGCCCCCTTCTTAT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 605954 | ||||||||||||||||||||
Literature Links: |
FETUB PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
FETUB - fetuin B | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001308077.1 | Intron | NP_001295006.1 | ||||
NM_001308079.1 | Intron | NP_001295008.1 | ||||
NM_014375.2 | Intron | NP_055190.2 | ||||
XM_005247351.3 | Intron | XP_005247408.1 | ||||
XM_011512681.2 | Intron | XP_011510983.1 | ||||
XM_011512682.2 | Intron | XP_011510984.1 | ||||
XM_011512683.2 | Intron | XP_011510985.1 |