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TTCTCCAGTGTGAGTCCTTTCATGC[A/G]TCTTAAAAGAACAAGAAAATCTGAA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
5 submissions
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Phenotype: |
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Literature Links: |
C1orf229 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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C1orf229 - chromosome 1 open reading frame 229 | ||||||
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There are no transcripts associated with this gene. |
ZNF669 - zinc finger protein 669 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001142572.1 | 850 | Missense Mutation | ACG,ATG | T,M 237 | NP_001136044.1 | |
NM_024804.2 | 850 | Missense Mutation | ACG,ATG | T,M 323 | NP_079080.2 | |
XM_005273270.2 | 850 | Missense Mutation | ACG,ATG | T,M 200 | XP_005273327.1 | |
XM_005273271.2 | 850 | Missense Mutation | ACG,ATG | T,M 200 | XP_005273328.1 |