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TTGAGTTCTTTAAAATCTTCGTTCA[A/C]AACAAGAGATTTTCATCTATGTCCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606041 | ||||||||||||||||||||
Literature Links: |
SPARCL1 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 |
SPARCL1 - SPARC like 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001128310.2 | 2222 | Missense Mutation | TTG,TTT | L,F 664 | NP_001121782.1 | |
NM_001291976.1 | 2222 | Missense Mutation | TTG,TTT | L,F 539 | NP_001278905.1 | |
NM_001291977.1 | 2222 | Missense Mutation | TTG,TTT | L,F 539 | NP_001278906.1 | |
NM_004684.5 | 2222 | Missense Mutation | TTG,TTT | L,F 664 | NP_004675.3 |