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GGTTCAGGCGTGGACCGCAGTGCCA[C/T]TGTGGACGTGCTGACCAACCGGAGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
14 submissions
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Phenotype: |
MIM: 603319 MIM: 606920 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ANXA9 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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ANXA9 - annexin A9 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_003568.2 | 380 | Missense Mutation | ACT,ATT | T,I 64 | NP_003559.2 | |
XM_011510058.2 | 380 | Missense Mutation | ACT,ATT | T,I 64 | XP_011508360.1 |
CERS2 - ceramide synthase 2 | ||||||
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There are no transcripts associated with this gene. |