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AGATGGTCCTGGGAGGGAAGGTGGA[C/T]GTAGGAACCTGTTGGTGGACGCAGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
5 submissions
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Phenotype: |
MIM: 610393 MIM: 608741 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
GON4L 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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GON4L - gon-4 like | ||||||
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There are no transcripts associated with this gene. |
SYT11 - synaptotagmin 11 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_152280.4 | 579 | Missense Mutation | CGT,TGT | R,C 91 | NP_689493.3 | |
XM_005245014.2 | 579 | Missense Mutation | CGT,TGT | R,C 91 | XP_005245071.1 | |
XM_017000759.1 | 579 | Missense Mutation | CGT,TGT | R,C 91 | XP_016856248.1 |