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TGTCCTTGGGGGTCTGAGACTTCTC[A/C]GTAGGCTTGCCAATCAAGTTCTCAA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608522 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
RSF1 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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RSF1 - remodeling and spacing factor 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_016578.3 | 4058 | Silent Mutation | ACG,ACT | T,T 1388 | NP_057662.3 | |
XM_005274051.2 | 4058 | Silent Mutation | ACG,ACT | T,T 1385 | XP_005274108.1 | |
XM_017017923.1 | 4058 | Silent Mutation | ACG,ACT | T,T 1347 | XP_016873412.1 |