Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607939 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
SUMF1 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)
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EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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SUMF1 - sulfatase modifying factor 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001164674.1 | 1297 | Intron | NP_001158146.1 | |||
NM_001164675.1 | 1297 | Intron | NP_001158147.1 | |||
NM_182760.3 | 1297 | Intron | NP_877437.2 | |||
XM_011533624.2 | 1297 | Missense Mutation | TTG,TTT | L,F 423 | XP_011531926.1 | |
XM_011533625.2 | 1297 | Intron | XP_011531927.1 | |||
XM_011533626.2 | 1297 | Intron | XP_011531928.1 | |||
XM_017006252.1 | 1297 | Missense Mutation | TTG,TTT | L,F 403 | XP_016861741.1 | |
XM_017006253.1 | 1297 | Missense Mutation | TTG,TTT | L,F 398 | XP_016861742.1 | |
XM_017006254.1 | 1297 | Intron | XP_016861743.1 | |||
XM_017006255.1 | 1297 | Intron | XP_016861744.1 |