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TCGCGGCGGCGTTGGTGTTATGCTC[C/T]GGGCCATTCCTGAGCTCGGGTAAGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 614030 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SPDYC 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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SPDYC - speedy/RINGO cell cycle regulator family member C | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001008778.1 | 7 | Missense Mutation | CGG,TGG | R,W 3 | NP_001008778.1 | |
XM_017017705.1 | 7 | Intron | XP_016873194.1 | |||
XM_017017706.1 | 7 | Intron | XP_016873195.1 | |||
XM_017017707.1 | 7 | Intron | XP_016873196.1 | |||
XM_017017708.1 | 7 | Intron | XP_016873197.1 | |||
XM_017017709.1 | 7 | Intron | XP_016873198.1 | |||
XM_017017710.1 | 7 | Intron | XP_016873199.1 |