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CTCGGCGGCGGATCTTCGATGCTGT[C/T]GGCTTCACCTTCCCCAATCGTCTCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
8 submissions
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Phenotype: |
MIM: 613535 MIM: 608458 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
KIAA0319L 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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KIAA0319L - KIAA0319 like | ||||||
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There are no transcripts associated with this gene. |
NCDN - neurochondrin | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001014839.1 | 299 | Silent Mutation | GTC,GTT | V,V 80 | NP_001014839.1 | |
NM_001014841.1 | 299 | Silent Mutation | GTC,GTT | V,V 63 | NP_001014841.1 | |
NM_014284.2 | 299 | Silent Mutation | GTC,GTT | V,V 80 | NP_055099.1 |