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- SNP ID:
- rs371145987
- Gene
-
CCSER1 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.4: 90723954 - 90723954 on Build GRCh38
- Polymorphism:
- C/T, Transition substitution
- Context Sequence [VIC/FAM]:
CCAGCAAGCAGTACCACGTCACTTC[C/T]TGTTAGTCCTCTTACTGAAGAGCCA
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
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Literature Links: |
CCSER1 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 |
| CCSER1 - coiled-coil serine rich protein 1 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001145065.1 | 2548 | Missense Mutation | CCT,CTT | P,L 658 | NP_001138537.1 | |
| NM_207491.2 | 2548 | Missense Mutation | CCT,CTT | P,L 658 | NP_997374.1 | |
| XM_011531936.1 | 2548 | Missense Mutation | CCT,CTT | P,L 690 | XP_011530238.1 | |
| XM_011531937.2 | 2548 | Missense Mutation | CCT,CTT | P,L 690 | XP_011530239.1 | |
| XM_011531938.2 | 2548 | Missense Mutation | CCT,CTT | P,L 690 | XP_011530240.1 | |
| XM_011531939.2 | 2548 | Missense Mutation | CCT,CTT | P,L 690 | XP_011530241.1 | |
| XM_011531941.2 | 2548 | Missense Mutation | CCT,CTT | P,L 690 | XP_011530243.1 | |
| XM_011531942.2 | 2548 | Missense Mutation | CCT,CTT | P,L 690 | XP_011530244.1 | |
| XM_011531943.2 | 2548 | Missense Mutation | CCT,CTT | P,L 690 | XP_011530245.1 | |
| XM_011531945.1 | 2548 | Missense Mutation | CCT,CTT | P,L 690 | XP_011530247.1 | |
| XM_011531946.2 | 2548 | Missense Mutation | CCT,CTT | P,L 690 | XP_011530248.1 | |
| XM_011531947.2 | 2548 | Missense Mutation | CCT,CTT | P,L 690 | XP_011530249.1 | |
| XM_011531948.1 | 2548 | Missense Mutation | CCT,CTT | P,L 690 | XP_011530250.1 | |
| XM_011531949.2 | 2548 | Missense Mutation | CCT,CTT | P,L 690 | XP_011530251.1 | |
| XM_011531950.2 | 2548 | Missense Mutation | CCT,CTT | P,L 690 | XP_011530252.1 | |
| XM_011531951.2 | 2548 | Missense Mutation | CCT,CTT | P,L 690 | XP_011530253.1 | |
| XM_011531955.2 | 2548 | Missense Mutation | CCT,CTT | P,L 690 | XP_011530257.1 | |
| XM_011531956.2 | 2548 | Missense Mutation | CCT,CTT | P,L 690 | XP_011530258.1 | |
| XM_011531957.2 | 2548 | Missense Mutation | CCT,CTT | P,L 690 | XP_011530259.1 | |
| XM_011531958.2 | 2548 | Missense Mutation | CCT,CTT | P,L 690 | XP_011530260.1 | |
| XM_017008194.1 | 2548 | Missense Mutation | CCT,CTT | P,L 690 | XP_016863683.1 | |
| XM_017008195.1 | 2548 | Missense Mutation | CCT,CTT | P,L 690 | XP_016863684.1 | |
| XM_017008196.1 | 2548 | Missense Mutation | CCT,CTT | P,L 690 | XP_016863685.1 | |
| XM_017008197.1 | 2548 | Missense Mutation | CCT,CTT | P,L 658 | XP_016863686.1 | |
| XM_017008198.1 | 2548 | Missense Mutation | CCT,CTT | P,L 690 | XP_016863687.1 | |
| XM_017008199.1 | 2548 | Missense Mutation | CCT,CTT | P,L 658 | XP_016863688.1 | |
| XM_017008200.1 | 2548 | Intron | XP_016863689.1 | |||
| XM_017008201.1 | 2548 | Intron | XP_016863690.1 | |||
| XM_017008202.1 | 2548 | Intron | XP_016863691.1 | |||
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