Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TAAATGGAGAGAAGAACAAATGGAA[C/T]GCTTGGAAGCCCTTGGTAAGGAATC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 118960 | ||||||||||||||||||||
Literature Links: |
CLTA 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 |
CLTA - clathrin light chain A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001076677.2 | 559 | Missense Mutation | CGC,TGC | R,C 120 | NP_001070145.1 | |
NM_001184760.1 | 559 | Missense Mutation | CGC,TGC | R,C 120 | NP_001171689.1 | |
NM_001184761.1 | 559 | Missense Mutation | CGC,TGC | R,C 120 | NP_001171690.1 | |
NM_001184762.1 | 559 | Intron | NP_001171691.1 | |||
NM_001311203.1 | 559 | Intron | NP_001298132.1 | |||
NM_001311204.1 | 559 | Intron | NP_001298133.1 | |||
NM_001311205.1 | 559 | Intron | NP_001298134.1 | |||
NM_001311206.1 | 559 | Missense Mutation | CGC,TGC | R,C 3 | NP_001298135.1 | |
NM_001833.3 | 559 | Missense Mutation | CGC,TGC | R,C 120 | NP_001824.1 | |
NM_007096.3 | 559 | Missense Mutation | CGC,TGC | R,C 120 | NP_009027.1 | |
XM_017014257.1 | 559 | Intron | XP_016869746.1 | |||
XM_017014258.1 | 559 | Intron | XP_016869747.1 |