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CATCAGAAGGGGCTTGGGCTTGGCT[C/T]TGATTGCTTCCACCTCCTGTTGCCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611462 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
MFSD6L 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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MFSD6L - major facilitator superfamily domain containing 6 like | ||||||
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There are no transcripts associated with this gene. |
PIK3R6 - phosphoinositide-3-kinase regulatory subunit 6 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001010855.3 | 2029 | Missense Mutation | AAA,AGA | K,R 736 | NP_001010855.1 | |
NM_001290211.1 | 2029 | Missense Mutation | AAA,AGA | K,R 600 | NP_001277140.1 | |
XM_011523677.2 | 2029 | Silent Mutation | CAA,CAG | Q,Q 696 | XP_011521979.1 | |
XM_011523678.2 | 2029 | Silent Mutation | CAA,CAG | Q,Q 692 | XP_011521980.1 | |
XM_011523680.2 | 2029 | Silent Mutation | CAA,CAG | Q,Q 656 | XP_011521982.1 | |
XM_011523681.2 | 2029 | Silent Mutation | CAA,CAG | Q,Q 617 | XP_011521983.1 | |
XM_011523683.2 | 2029 | Silent Mutation | CAA,CAG | Q,Q 617 | XP_011521985.1 | |
XM_011523686.2 | 2029 | Silent Mutation | CAA,CAG | Q,Q 408 | XP_011521988.1 | |
XM_017024228.1 | 2029 | Silent Mutation | CAA,CAG | Q,Q 697 | XP_016879717.1 | |
XM_017024229.1 | 2029 | Missense Mutation | AAA,AGA | K,R 736 | XP_016879718.1 | |
XM_017024230.1 | 2029 | Missense Mutation | AAA,AGA | K,R 695 | XP_016879719.1 | |
XM_017024231.1 | 2029 | Silent Mutation | CAA,CAG | Q,Q 617 | XP_016879720.1 |