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CCCTGGCCCACAGAGGCCATGTACC[C/T]GGGGCCTAAGGCACTCAAGCCGCCA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
10 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 |
---|---|---|
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 |
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 | 1396 | Intron | NP_001032252.1 | |||
NM_017982.3 | 1396 | Missense Mutation | AGG,GGG | R,G 393 | NP_060452.3 | |
XM_005273169.1 | 1396 | Missense Mutation | AGG,GGG | R,G 395 | XP_005273226.1 | |
XM_005273172.1 | 1396 | Missense Mutation | AGG,GGG | R,G 233 | XP_005273229.1 | |
XM_006711408.1 | 1396 | Missense Mutation | AGG,GGG | R,G 395 | XP_006711471.1 | |
XM_011509685.1 | 1396 | Missense Mutation | AGG,GGG | R,G 395 | XP_011507987.1 | |
XM_011509687.1 | 1396 | Missense Mutation | AGG,GGG | R,G 235 | XP_011507989.1 | |
XM_017001583.1 | 1396 | Missense Mutation | AGG,GGG | R,G 467 | XP_016857072.1 | |
XM_017001584.1 | 1396 | Missense Mutation | AGG,GGG | R,G 465 | XP_016857073.1 | |
XM_017001585.1 | 1396 | Missense Mutation | AGG,GGG | R,G 452 | XP_016857074.1 | |
XM_017001586.1 | 1396 | Missense Mutation | AGG,GGG | R,G 452 | XP_016857075.1 | |
XM_017001587.1 | 1396 | Missense Mutation | AGG,GGG | R,G 393 | XP_016857076.1 | |
XM_017001588.1 | 1396 | Missense Mutation | AGG,GGG | R,G 393 | XP_016857077.1 | |
XM_017001589.1 | 1396 | Intron | XP_016857078.1 |