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CCCAGGCTGATGCTGTGCTGCTCCA[G/C]CAGGGCCCCAAGATCTTGCTGGGCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602640 MIM: 605964 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ARL2-SNX15 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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ARL2-SNX15 - ARL2-SNX15 readthrough (NMD candidate) | ||||||
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There are no transcripts associated with this gene. |
NAALADL1 - N-acetylated alpha-linked acidic dipeptidase-like 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_005468.2 | 2011 | Missense Mutation | CTG,GTG | L,V 611 | NP_005459.2 | |
XM_011544706.2 | 2011 | Missense Mutation | CTG,GTG | L,V 608 | XP_011543008.1 | |
XM_011544707.2 | 2011 | Missense Mutation | CTG,GTG | L,V 563 | XP_011543009.1 | |
XM_011544708.2 | 2011 | Missense Mutation | CTG,GTG | L,V 558 | XP_011543010.1 | |
XM_011544709.2 | 2011 | Intron | XP_011543011.1 | |||
XM_011544710.2 | 2011 | UTR 3 | XP_011543012.1 | |||
XM_011544711.2 | 2011 | Intron | XP_011543013.1 | |||
XM_011544712.2 | 2011 | Intron | XP_011543014.1 |
SAC3D1 - SAC3 domain containing 1 | ||||||
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There are no transcripts associated with this gene. |
SNX15 - sorting nexin 15 | ||||||
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There are no transcripts associated with this gene. |