Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GTAATCATCATCAGGAAGGTCCTAT[C/T]GAAGGAGACAGTGAAGTAAGAGGGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 615677 | ||||||||||||||||||||
Literature Links: |
SERPINA9 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 |
SERPINA9 - serpin family A member 9 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001042518.1 | 1299 | Missense Mutation | AAT,GAT | N,D 308 | NP_001035983.1 | |
NM_001284275.1 | 1299 | Missense Mutation | AAT,GAT | N,D 372 | NP_001271204.1 | |
NM_001284276.1 | 1299 | Missense Mutation | AAT,GAT | N,D 259 | NP_001271205.1 | |
NM_175739.3 | 1299 | Missense Mutation | AAT,GAT | N,D 408 | NP_783866.2 | |
XM_011536714.2 | 1299 | Missense Mutation | AAT,GAT | N,D 390 | XP_011535016.1 | |
XM_011536715.2 | 1299 | Missense Mutation | AAT,GAT | N,D 390 | XP_011535017.1 | |
XM_011536716.2 | 1299 | Missense Mutation | AAT,GAT | N,D 310 | XP_011535018.1 | |
XM_011536717.1 | 1299 | Missense Mutation | AAT,GAT | N,D 310 | XP_011535019.1 |