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TTGTTATGGGATTAAAAAAGATGAA[A/G]GGGTAAGGTCTTGAAAGACACGAGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608686 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
LOC101928002 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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LOC101928002 - uncharacterized LOC101928002 | ||||||
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There are no transcripts associated with this gene. |
RAB3IP - RAB3A interacting protein | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001024647.3 | 478 | Intron | NP_001019818.1 | |||
NM_001278402.1 | 478 | Intron | NP_001265331.1 | |||
NM_022456.4 | 478 | Intron | NP_071901.2 | |||
NM_175623.3 | 478 | Silent Mutation | AAA,AAG | K,K 7 | NP_783322.1 | |
NM_175624.3 | 478 | Intron | NP_783323.1 | |||
NM_175625.3 | 478 | Silent Mutation | AAA,AAG | K,K 7 | NP_783324.1 | |
XM_006719226.3 | 478 | Intron | XP_006719289.3 | |||
XM_006719227.3 | 478 | Intron | XP_006719290.3 | |||
XM_017018773.1 | 478 | Intron | XP_016874262.1 | |||
XM_017018774.1 | 478 | Intron | XP_016874263.1 | |||
XM_017018775.1 | 478 | Intron | XP_016874264.1 | |||
XM_017018776.1 | 478 | Intron | XP_016874265.1 | |||
XM_017018777.1 | 478 | UTR 5 | XP_016874266.1 |