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GGTGCACGCGCTCGAGGCGGTGCAG[A/G]GGCGTGAAGAGGTCGTGGGGCAGCG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 615324 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ASPDH 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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ASPDH - aspartate dehydrogenase domain containing | ||||||
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There are no transcripts associated with this gene. |
JOSD2 - Josephin domain containing 2 | ||||||
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There are no transcripts associated with this gene. |
LRRC4B - leucine rich repeat containing 4B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001080457.1 | 1213 | Silent Mutation | CCC,CCT | P,P 299 | NP_001073926.1 | |
XM_005259429.4 | 1213 | Silent Mutation | CCC,CCT | P,P 299 | XP_005259486.1 | |
XM_006723506.3 | 1213 | Silent Mutation | CCC,CCT | P,P 299 | XP_006723569.1 | |
XM_011527520.2 | 1213 | Silent Mutation | CCC,CCT | P,P 299 | XP_011525822.1 |