Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CTAGGTGATTCTGGAGCGGCGGGCG[C/T]GGCGGCTCTGAGCTCCGCCTCGTCA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602895 MIM: 608066 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SAFB 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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SAFB - scaffold attachment factor B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001201338.1 | 218 | Missense Mutation | GCG,GTG | A,V 16 | NP_001188267.1 | |
NM_001201339.1 | 218 | Missense Mutation | GCG,GTG | A,V 16 | NP_001188268.1 | |
NM_001201340.1 | 218 | Missense Mutation | GCG,GTG | A,V 16 | NP_001188269.1 | |
NM_001320571.1 | 218 | UTR 5 | NP_001307500.1 | |||
NM_001320572.1 | 218 | Missense Mutation | GCG,GTG | A,V 16 | NP_001307501.1 | |
NM_002967.3 | 218 | Missense Mutation | GCG,GTG | A,V 16 | NP_002958.2 | |
XM_017027114.1 | 218 | UTR 5 | XP_016882603.1 | |||
XM_017027115.1 | 218 | UTR 5 | XP_016882604.1 | |||
XM_017027116.1 | 218 | UTR 5 | XP_016882605.1 | |||
XM_017027117.1 | 218 | UTR 5 | XP_016882606.1 | |||
XM_017027118.1 | 218 | UTR 5 | XP_016882607.1 |
SAFB2 - scaffold attachment factor B2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_014649.2 | 218 | Intron | NP_055464.1 | |||
XM_011528449.2 | 218 | Intron | XP_011526751.1 | |||
XM_011528450.2 | 218 | Intron | XP_011526752.1 | |||
XM_017027520.1 | 218 | Intron | XP_016883009.1 | |||
XM_017027521.1 | 218 | Intron | XP_016883010.1 | |||
XM_017027522.1 | 218 | Intron | XP_016883011.1 |