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GCCCTCTGCTGCTGGGAGCTGACTG[A/G]AGGCTCCATCCTCAGCAGCCCTCTC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 186355 | ||||||||||||||||||||
Literature Links: |
SDC1 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 |
SDC1 - syndecan 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001006946.1 | 981 | Missense Mutation | TCC,TTC | S,F 197 | NP_001006947.1 | |
NM_002997.4 | 981 | Missense Mutation | TCC,TTC | S,F 197 | NP_002988.3 | |
XM_005262620.4 | 981 | Missense Mutation | TCC,TTC | S,F 221 | XP_005262677.1 | |
XM_005262621.3 | 981 | Missense Mutation | TCC,TTC | S,F 192 | XP_005262678.3 | |
XM_005262622.2 | 981 | Missense Mutation | TCC,TTC | S,F 179 | XP_005262679.1 |