Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GTTTTTGGATTTTCACTGAGAACGA[A/C]CTTCCCTTAATCGTCTTCTAGATCC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608777 | ||||||||||||||||||||
Literature Links: |
POSTN 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 |
POSTN - periostin | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001135934.1 | 2451 | Missense Mutation | GGT,GTT | G,V 776 | NP_001129406.1 | |
NM_001135935.1 | 2451 | Missense Mutation | GGT,GTT | G,V 778 | NP_001129407.1 | |
NM_001135936.1 | 2451 | Missense Mutation | GGT,GTT | G,V 748 | NP_001129408.1 | |
NM_001286665.1 | 2451 | Missense Mutation | GGT,GTT | G,V 806 | NP_001273594.1 | |
NM_001286666.1 | 2451 | Missense Mutation | GGT,GTT | G,V 746 | NP_001273595.1 | |
NM_001286667.1 | 2451 | Missense Mutation | GGT,GTT | G,V 718 | NP_001273596.1 | |
NM_006475.2 | 2451 | Missense Mutation | GGT,GTT | G,V 833 | NP_006466.2 | |
XM_005266231.2 | 2451 | Missense Mutation | GGT,GTT | G,V 805 | XP_005266288.1 | |
XM_005266232.2 | 2451 | Missense Mutation | GGT,GTT | G,V 803 | XP_005266289.1 | |
XM_017020355.1 | 2451 | Intron | XP_016875844.1 | |||
XM_017020356.1 | 2451 | Intron | XP_016875845.1 |