Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TCCTGGCACACAGGGCAGGCAAGGG[G/C]CTCTTCTCTCCGCTTCTGAGAATGT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
ZNF488 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 |
ZNF488 - zinc finger protein 488 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_153034.2 | 1157 | Missense Mutation | CCC,GCC | P,A 316 | NP_694579.1 | |
XM_006717617.3 | 1157 | Missense Mutation | CCC,GCC | P,A 316 | XP_006717680.1 | |
XM_011539244.2 | 1157 | Missense Mutation | CCC,GCC | P,A 316 | XP_011537546.1 | |
XM_017015642.1 | 1157 | Missense Mutation | CCC,GCC | P,A 316 | XP_016871131.1 | |
XM_017015643.1 | 1157 | Missense Mutation | CCC,GCC | P,A 316 | XP_016871132.1 |