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GGAGCCAAGAAGAAAGGTTTGCTCC[A/C]GGGTGGAACAGGGATTATCCTCCTC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 606886 | ||||||||||||||||||||
Literature Links: |
RBM6 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
RBM6 - RNA binding motif protein 6 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001167582.1 | 595 | Intron | NP_001161054.1 | |||
NM_005777.2 | 595 | Silent Mutation | CCA,CCC | P,P 24 | NP_005768.1 | |
XM_005264784.1 | 595 | UTR 5 | XP_005264841.1 | |||
XM_005264785.1 | 595 | Intron | XP_005264842.1 | |||
XM_005264786.1 | 595 | Intron | XP_005264843.1 | |||
XM_005264787.2 | 595 | Intron | XP_005264844.1 | |||
XM_006712916.1 | 595 | UTR 5 | XP_006712979.1 | |||
XM_017005496.1 | 595 | Intron | XP_016860985.1 | |||
XM_017005497.1 | 595 | Intron | XP_016860986.1 | |||
XM_017005498.1 | 595 | Intron | XP_016860987.1 | |||
XM_017005499.1 | 595 | UTR 5 | XP_016860988.1 | |||
XM_017005500.1 | 595 | UTR 5 | XP_016860989.1 | |||
XM_017005501.1 | 595 | UTR 5 | XP_016860990.1 | |||
XM_017005502.1 | 595 | Intron | XP_016860991.1 |