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GTTTAGGGCCTGTATATCATTGGGA[C/T]CAAGAACTCGAGCCATTGGAAATGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
HSPA4L PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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HSPA4L - heat shock protein family A (Hsp70) member 4 like | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001317381.1 | 459 | Missense Mutation | CCA,TCA | P,S 74 | NP_001304310.1 | |
NM_001317382.1 | 459 | Missense Mutation | CCA,TCA | P,S 17 | NP_001304311.1 | |
NM_001317383.1 | 459 | Missense Mutation | CCA,TCA | P,S 43 | NP_001304312.1 | |
NM_014278.3 | 459 | Missense Mutation | CCA,TCA | P,S 43 | NP_055093.2 | |
XM_011531745.2 | 459 | Missense Mutation | CCA,TCA | P,S 43 | XP_011530047.1 |