Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GCACTCACCTGGGCCCCCCAAAGGG[C/T]GCAGCCTGGTGGGCAGGGGCTGGAA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
13 submissions
|
||||||||||||||||||||
Phenotype: |
|||||||||||||||||||||
Literature Links: |
SPOCD1 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
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 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001281987.1 | 2858 | Missense Mutation | CAC,CGC | H,R 982 | NP_001268916.1 | |
NM_001281988.1 | 2858 | Missense Mutation | CAC,CGC | H,R 475 | NP_001268917.1 | |
NM_144569.5 | 2858 | Missense Mutation | CAC,CGC | H,R 982 | NP_653170.3 | |
XM_011542413.2 | 2858 | Missense Mutation | CAC,CGC | H,R 475 | XP_011540715.1 | |
XM_011542414.2 | 2858 | Missense Mutation | CAC,CGC | H,R 475 | XP_011540716.1 | |
XM_017002779.1 | 2858 | Missense Mutation | CAC,CGC | H,R 981 | XP_016858268.1 | |
XM_017002780.1 | 2858 | Missense Mutation | CAC,CGC | H,R 968 | XP_016858269.1 | |
XM_017002781.1 | 2858 | Missense Mutation | CAC,CGC | H,R 940 | XP_016858270.1 | |
XM_017002782.1 | 2858 | Missense Mutation | CAC,CGC | H,R 725 | XP_016858271.1 |