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Search Thermo Fisher Scientific
CCTCCTTCTGAAACAGAGGCTGTGG[C/G]CTCCTCTACTGTTAAACGTCTGTGC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609978 MIM: 613301 | ||||||||||||||||||||
Literature Links: |
CADPS2 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 |
CADPS2 - calcium dependent secretion activator 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001009571.3 | 3971 | Missense Mutation | CCC,GCC | P,A 1231 | NP_001009571.2 | |
NM_001167940.1 | 3971 | Missense Mutation | CCC,GCC | P,A 1276 | NP_001161412.1 | |
NM_017954.10 | 3971 | Missense Mutation | CCC,GCC | P,A 1272 | NP_060424.9 | |
XM_005250695.4 | 3971 | Missense Mutation | CCC,GCC | P,A 1284 | XP_005250752.1 | |
XM_005250696.4 | 3971 | Missense Mutation | CCC,GCC | P,A 1281 | XP_005250753.1 | |
XM_005250697.4 | 3971 | Missense Mutation | CCC,GCC | P,A 1281 | XP_005250754.1 | |
XM_005250698.4 | 3971 | Missense Mutation | CCC,GCC | P,A 1279 | XP_005250755.1 | |
XM_005250699.4 | 3971 | Missense Mutation | CCC,GCC | P,A 1277 | XP_005250756.1 | |
XM_005250700.4 | 3971 | Missense Mutation | CCC,GCC | P,A 1276 | XP_005250757.1 | |
XM_005250701.4 | 3971 | Missense Mutation | CCC,GCC | P,A 1274 | XP_005250758.1 | |
XM_005250702.4 | 3971 | Missense Mutation | CCC,GCC | P,A 1269 | XP_005250759.1 | |
XM_005250703.4 | 3971 | Missense Mutation | CCC,GCC | P,A 1244 | XP_005250760.1 | |
XM_005250704.4 | 3971 | Missense Mutation | CCC,GCC | P,A 1241 | XP_005250761.1 | |
XM_005250705.4 | 3971 | Missense Mutation | CCC,GCC | P,A 1236 | XP_005250762.1 | |
XM_005250706.4 | 3971 | Missense Mutation | CCC,GCC | P,A 1236 | XP_005250763.1 | |
XM_005250707.4 | 3971 | Missense Mutation | CCC,GCC | P,A 1234 | XP_005250764.1 | |
XM_005250708.3 | 3971 | Missense Mutation | CCC,GCC | P,A 1226 | XP_005250765.1 | |
XM_011516695.2 | 3971 | Missense Mutation | CCC,GCC | P,A 1239 | XP_011514997.1 | |
XM_011516696.2 | 3971 | Missense Mutation | CCC,GCC | P,A 1232 | XP_011514998.1 | |
XM_011516697.2 | 3971 | Missense Mutation | CCC,GCC | P,A 1229 | XP_011514999.1 | |
XM_017012794.1 | 3971 | Missense Mutation | CCC,GCC | P,A 1271 | XP_016868283.1 | |
XM_017012795.1 | 3971 | Missense Mutation | CCC,GCC | P,A 1233 | XP_016868284.1 | |
XM_017012796.1 | 3971 | Missense Mutation | CCC,GCC | P,A 1123 | XP_016868285.1 | |
XM_017012797.1 | 3971 | Missense Mutation | CCC,GCC | P,A 1118 | XP_016868286.1 | |
XM_017012798.1 | 3971 | Missense Mutation | CCC,GCC | P,A 1116 | XP_016868287.1 | |
XM_017012799.1 | 3971 | Missense Mutation | CCC,GCC | P,A 1078 | XP_016868288.1 | |
XM_017012800.1 | 3971 | Missense Mutation | CCC,GCC | P,A 913 | XP_016868289.1 |
FEZF1 - FEZ family zinc finger 1 | ||||||
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There are no transcripts associated with this gene. |