Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGTGGGACCACGGGGCAGGGCTCAC[A/G]TCCATCTGCCTTTCGAAAGAAGGCC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611782 | ||||||||||||||||||||
Literature Links: |
DSCAML1 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 |
DSCAML1 - DS cell adhesion molecule like 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_020693.3 | 4208 | Missense Mutation | CGT,TGT | R,C 1977 | NP_065744.2 | |
XM_011542917.1 | 4208 | Missense Mutation | CGT,TGT | R,C 1929 | XP_011541219.1 | |
XM_011542918.1 | 4208 | Missense Mutation | CGT,TGT | R,C 1841 | XP_011541220.1 | |
XM_011542919.2 | 4208 | Missense Mutation | CGT,TGT | R,C 1490 | XP_011541221.1 | |
XM_011542920.2 | 4208 | Missense Mutation | CGT,TGT | R,C 1407 | XP_011541222.1 | |
XM_011542921.2 | 4208 | Missense Mutation | CGT,TGT | R,C 1208 | XP_011541223.1 | |
XM_011542924.2 | 4208 | Missense Mutation | CGT,TGT | R,C 1134 | XP_011541226.1 | |
XM_011542925.2 | 4208 | Missense Mutation | CGT,TGT | R,C 1128 | XP_011541227.1 |