Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GTACCTTGCCACCTGGCGTGCTCCC[A/G]GCTAGCCGCGCCTGCGTCCATGGCA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608066 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SAFB2 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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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 | 2179 | Missense Mutation | CGG,TGG | R,W 873 | NP_055464.1 | |
XM_011528449.2 | 2179 | Missense Mutation | CGG,TGG | R,W 873 | XP_011526751.1 | |
XM_011528450.2 | 2179 | Missense Mutation | CGG,TGG | R,W 419 | XP_011526752.1 | |
XM_017027520.1 | 2179 | Missense Mutation | CGG,TGG | R,W 419 | XP_016883009.1 | |
XM_017027521.1 | 2179 | Missense Mutation | CGG,TGG | R,W 419 | XP_016883010.1 | |
XM_017027522.1 | 2179 | Missense Mutation | CGG,TGG | R,W 419 | XP_016883011.1 |