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TCCGTGTCCCCTGAGCCGGGGTATG[C/T]TGGGGGGCTCTGGTCGTCCACGGGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
18 submissions
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Phenotype: |
MIM: 615827 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SUSD4 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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SUSD4 - sushi domain containing 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001037175.2 | 1456 | Intron | NP_001032252.1 | |||
NM_017982.3 | 1456 | Missense Mutation | ACA,GCA | T,A 413 | NP_060452.3 | |
XM_005273169.1 | 1456 | Missense Mutation | ACA,GCA | T,A 415 | XP_005273226.1 | |
XM_005273172.1 | 1456 | Missense Mutation | ACA,GCA | T,A 253 | XP_005273229.1 | |
XM_006711408.1 | 1456 | Missense Mutation | ACA,GCA | T,A 415 | XP_006711471.1 | |
XM_011509685.1 | 1456 | Missense Mutation | ACA,GCA | T,A 415 | XP_011507987.1 | |
XM_011509687.1 | 1456 | Missense Mutation | ACA,GCA | T,A 255 | XP_011507989.1 | |
XM_017001583.1 | 1456 | Missense Mutation | ACA,GCA | T,A 487 | XP_016857072.1 | |
XM_017001584.1 | 1456 | Missense Mutation | ACA,GCA | T,A 485 | XP_016857073.1 | |
XM_017001585.1 | 1456 | Missense Mutation | ACA,GCA | T,A 472 | XP_016857074.1 | |
XM_017001586.1 | 1456 | Missense Mutation | ACA,GCA | T,A 472 | XP_016857075.1 | |
XM_017001587.1 | 1456 | Missense Mutation | ACA,GCA | T,A 413 | XP_016857076.1 | |
XM_017001588.1 | 1456 | Missense Mutation | ACA,GCA | T,A 413 | XP_016857077.1 | |
XM_017001589.1 | 1456 | Intron | XP_016857078.1 |