Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TGCTTGTCAGGCTTCTGGTATGTGA[C/T]GCTCGCCTGCTTGGGTTCCTCCAGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
17 submissions
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 186357 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SDC3 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
|||||
AMR
|
SDC3 - syndecan 3 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_014654.3 | 1332 | Missense Mutation | ATC,GTC | I,V 429 | NP_055469.3 | |
XM_011542463.1 | 1332 | Missense Mutation | ATC,GTC | I,V 418 | XP_011540765.1 | |
XM_011542464.2 | 1332 | Missense Mutation | ATC,GTC | I,V 417 | XP_011540766.1 | |
XM_011542466.1 | 1332 | Missense Mutation | ATC,GTC | I,V 387 | XP_011540768.1 |