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GGAATGTTAAGTGGCTTCAGGAGTC[A/G]TGTGGACAGCACGATTACCTAACAA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612404 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
RASL11B 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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RASL11B - RAS like family 11 member B | ||||||
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There are no transcripts associated with this gene. |
SCFD2 - sec1 family domain containing 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_152540.3 | 2115 | Silent Mutation | NP_689753.2 | |||
XM_011534375.2 | 2115 | Intron | XP_011532677.1 | |||
XM_011534376.2 | 2115 | Intron | XP_011532678.1 | |||
XM_011534378.2 | 2115 | Intron | XP_011532680.1 | |||
XM_017007786.1 | 2115 | Intron | XP_016863275.1 | |||
XM_017007787.1 | 2115 | Intron | XP_016863276.1 |