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GGTGGGCCTCTGTGCATCATGTGCG[A/G]TGGCATGGGACGGGGCGGCATCAAA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616023 MIM: 147450 | ||||||||||||||||||||
Literature Links: |
SCAF4 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
SCAF4 - SR-related CTD associated factor 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001145444.1 | 3028 | Missense Mutation | CCG,TCG | P,S 868 | NP_001138916.1 | |
NM_001145445.1 | 3028 | Missense Mutation | CCG,TCG | P,S 861 | NP_001138917.1 | |
NM_020706.2 | 3028 | Missense Mutation | CCG,TCG | P,S 883 | NP_065757.1 | |
XM_005261017.2 | 3028 | Missense Mutation | CCG,TCG | P,S 824 | XP_005261074.1 | |
XM_006724035.2 | 3028 | Missense Mutation | CCG,TCG | P,S 879 | XP_006724098.1 | |
XM_006724036.2 | 3028 | Missense Mutation | CCG,TCG | P,S 857 | XP_006724099.1 | |
XM_017028415.1 | 3028 | Missense Mutation | CCG,TCG | P,S 882 | XP_016883904.1 | |
XM_017028416.1 | 3028 | Missense Mutation | CCG,TCG | P,S 860 | XP_016883905.1 | |
XM_017028417.1 | 3028 | Missense Mutation | CCG,TCG | P,S 802 | XP_016883906.1 |
SOD1 - superoxide dismutase 1, soluble | ||||||
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There are no transcripts associated with this gene. |