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TGCTGTCTATGCTGGCTCAGTGGCT[A/G]TCGCCATTTTTATTAATGATACACT
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601558 | |||||||||||||||||||||||||||||||||||||||||
Literature Links: |
RBPMS 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)
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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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RBPMS - RNA binding protein with multiple splicing | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001008710.2 | Intron | NP_001008710.1 | ||||
NM_001008711.2 | Intron | NP_001008711.1 | ||||
NM_001008712.2 | Intron | NP_001008712.1 | ||||
NM_006867.3 | Intron | NP_006858.1 | ||||
XM_017012980.1 | Intron | XP_016868469.1 | ||||
XM_017012981.1 | Intron | XP_016868470.1 | ||||
XM_017012982.1 | Intron | XP_016868471.1 | ||||
XM_017012983.1 | Intron | XP_016868472.1 | ||||
XM_017012984.1 | Intron | XP_016868473.1 | ||||
XM_017012985.1 | Intron | XP_016868474.1 | ||||
XM_017012986.1 | Intron | XP_016868475.1 | ||||
XM_017012987.1 | Intron | XP_016868476.1 | ||||
XM_017012988.1 | Intron | XP_016868477.1 | ||||
XM_017012989.1 | Intron | XP_016868478.1 | ||||
XM_017012990.1 | Intron | XP_016868479.1 | ||||
XM_017012991.1 | Intron | XP_016868480.1 | ||||
XM_017012992.1 | Intron | XP_016868481.1 |
Set Membership: |
HapMap |