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GCTGGTGGTGTGTGTCTCGGTGACC[G/T]TCTTTGTCTGGTCATGCTGCCACCA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
4 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 |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
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 | 408 | Missense Mutation | GTC,TTC | V,F 34 | NP_689493.3 | |
XM_005245014.2 | 408 | Missense Mutation | GTC,TTC | V,F 34 | XP_005245071.1 | |
XM_017000759.1 | 408 | Missense Mutation | GTC,TTC | V,F 34 | XP_016856248.1 |