Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
1 submissions
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Phenotype: |
MIM: 603061 | ||||||||||||||||||||
Literature Links: |
ENSA 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 |
ENSA - endosulfine alpha | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_004436.2 | 411 | Intron | NP_004427.1 | |||
NM_207042.1 | 411 | Intron | NP_996925.1 | |||
NM_207043.1 | 411 | Intron | NP_996926.1 | |||
NM_207044.1 | 411 | Intron | NP_996927.1 | |||
NM_207045.1 | 411 | Intron | NP_996928.1 | |||
NM_207046.1 | 411 | Intron | NP_996929.1 | |||
NM_207047.1 | 411 | Intron | NP_996930.1 | |||
NM_207168.1 | 411 | Missense Mutation | CTG,GTG | L,V 87 | NP_997051.1 |