Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CAGGGCTTGGTGGGGACAGGAGTCC[C/T]TGTGGAAGTGCTGGCCACGGCCAAA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
12 submissions
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Phenotype: |
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Literature Links: |
SPOCD1 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 |
SPOCD1 - SPOC domain containing 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001281987.1 | 3296 | Missense Mutation | AAG,AGG | K,R 1128 | NP_001268916.1 | |
NM_001281988.1 | 3296 | Missense Mutation | AAG,AGG | K,R 621 | NP_001268917.1 | |
NM_144569.5 | 3296 | Missense Mutation | AAG,AGG | K,R 1141 | NP_653170.3 | |
XM_011542413.2 | 3296 | Missense Mutation | AAG,AGG | K,R 621 | XP_011540715.1 | |
XM_011542414.2 | 3296 | Missense Mutation | AAG,AGG | K,R 621 | XP_011540716.1 | |
XM_017002779.1 | 3296 | Missense Mutation | AAG,AGG | K,R 1127 | XP_016858268.1 | |
XM_017002780.1 | 3296 | Missense Mutation | AAG,AGG | K,R 1114 | XP_016858269.1 | |
XM_017002781.1 | 3296 | Missense Mutation | AAG,AGG | K,R 1086 | XP_016858270.1 | |
XM_017002782.1 | 3296 | Missense Mutation | AAG,AGG | K,R 871 | XP_016858271.1 |