Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGGGGAGACTTGGTATTTTGTTCAA[C/T]CATTAAGAAGACAAAGGGTTTGTTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 107400 | ||||||||||||||||||||
Literature Links: |
SERPINA1 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 |
SERPINA1 - serpin family A member 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000295.4 | 1728 | Missense Mutation | ATT,GTT | I,V 399 | NP_000286.3 | |
NM_001002235.2 | 1728 | Missense Mutation | ATT,GTT | I,V 399 | NP_001002235.1 | |
NM_001002236.2 | 1728 | Missense Mutation | ATT,GTT | I,V 399 | NP_001002236.1 | |
NM_001127700.1 | 1728 | Missense Mutation | ATT,GTT | I,V 399 | NP_001121172.1 | |
NM_001127701.1 | 1728 | Missense Mutation | ATT,GTT | I,V 399 | NP_001121173.1 | |
NM_001127702.1 | 1728 | Missense Mutation | ATT,GTT | I,V 399 | NP_001121174.1 | |
NM_001127703.1 | 1728 | Missense Mutation | ATT,GTT | I,V 399 | NP_001121175.1 | |
NM_001127704.1 | 1728 | Missense Mutation | ATT,GTT | I,V 399 | NP_001121176.1 | |
NM_001127705.1 | 1728 | Missense Mutation | ATT,GTT | I,V 399 | NP_001121177.1 | |
NM_001127706.1 | 1728 | Missense Mutation | ATT,GTT | I,V 399 | NP_001121178.1 | |
NM_001127707.1 | 1728 | Missense Mutation | ATT,GTT | I,V 399 | NP_001121179.1 | |
XM_017021370.1 | 1728 | Missense Mutation | ATT,GTT | I,V 399 | XP_016876859.1 |