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CTTCACGACGTCCGGCTCAATAGAC[C/T]CCATTAGGTCACACTCATTTGCAAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606281 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
RAB38 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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RAB38 - RAB38, member RAS oncogene family | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_022337.2 | 640 | Missense Mutation | GAG,GGG | E,G 186 | NP_071732.1 | |
XM_017017455.1 | 640 | Intron | XP_016872944.1 | |||
XM_017017456.1 | 640 | Intron | XP_016872945.1 |