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GGAGCCTTTGCCTCTGGAAACAGCA[C/G]GAGAGTCACCGAGCTTCAAGCTGGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604191 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ZNF263 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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ZNF263 - zinc finger protein 263 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_005741.4 | 890 | Missense Mutation | CGA,GGA | R,G 151 | NP_005732.2 | |
XM_006720831.1 | 890 | Missense Mutation | CGA,GGA | R,G 151 | XP_006720894.1 | |
XM_006720832.1 | 890 | Missense Mutation | CGA,GGA | R,G 151 | XP_006720895.1 | |
XM_006720833.1 | 890 | Intron | XP_006720896.1 | |||
XM_006720834.3 | 890 | Intron | XP_006720897.1 | |||
XM_011522344.1 | 890 | Missense Mutation | CGA,GGA | R,G 151 | XP_011520646.1 | |
XM_017022850.1 | 890 | Intron | XP_016878339.1 |