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AATACAGTTTGTAAGTGGAGGTTAG[A/G]AGTAGCTGAGCAATCTGGTAGAGAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616906 MIM: 602003 | ||||||||||||||||||||
Literature Links: |
CASC1 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 |
CASC1 - cancer susceptibility candidate 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001082972.2 | 2328 | UTR 3 | NP_001076441.1 | |||
NM_001082973.2 | 2328 | Missense Mutation | TCC,TTC | S,F 716 | NP_001076442.1 | |
NM_001204101.2 | 2328 | Missense Mutation | TCC,TTC | S,F 657 | NP_001191030.1 | |
NM_001204102.2 | 2328 | Missense Mutation | TCC,TTC | S,F 676 | NP_001191031.1 | |
NM_001319977.1 | 2328 | UTR 3 | NP_001306906.1 | |||
NM_001319978.1 | 2328 | Missense Mutation | TCC,TTC | S,F 676 | NP_001306907.1 | |
NM_018272.4 | 2328 | Missense Mutation | TCC,TTC | S,F 722 | NP_060742.3 | |
XM_005253406.1 | 2328 | Missense Mutation | TCC,TTC | S,F 780 | XP_005253463.1 | |
XM_005253408.1 | 2328 | Missense Mutation | TCC,TTC | S,F 604 | XP_005253465.1 | |
XM_005253409.1 | 2328 | Missense Mutation | TCC,TTC | S,F 604 | XP_005253466.1 | |
XM_006719101.1 | 2328 | Missense Mutation | TCC,TTC | S,F 674 | XP_006719164.1 | |
XM_011520723.1 | 2328 | Missense Mutation | TCC,TTC | S,F 780 | XP_011519025.1 | |
XM_011520726.1 | 2328 | Intron | XP_011519028.1 | |||
XM_011520727.1 | 2328 | Intron | XP_011519029.1 | |||
XM_017019560.1 | 2328 | Missense Mutation | TCC,TTC | S,F 774 | XP_016875049.1 | |
XM_017019561.1 | 2328 | Missense Mutation | TCC,TTC | S,F 676 | XP_016875050.1 | |
XM_017019562.1 | 2328 | UTR 3 | XP_016875051.1 | |||
XM_017019563.1 | 2328 | Missense Mutation | TCC,TTC | S,F 616 | XP_016875052.1 | |
XM_017019564.1 | 2328 | Missense Mutation | TCC,TTC | S,F 610 | XP_016875053.1 | |
XM_017019565.1 | 2328 | UTR 3 | XP_016875054.1 | |||
XM_017019566.1 | 2328 | Missense Mutation | TCC,TTC | S,F 570 | XP_016875055.1 | |
XM_017019567.1 | 2328 | Missense Mutation | TCC,TTC | S,F 551 | XP_016875056.1 | |
XM_017019568.1 | 2328 | UTR 3 | XP_016875057.1 |
LRMP - lymphoid restricted membrane protein | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001204126.1 | 2328 | Intron | NP_001191055.1 | |||
NM_001204127.1 | 2328 | Intron | NP_001191056.1 | |||
NM_006152.3 | 2328 | Intron | NP_006143.2 | |||
XM_005253370.3 | 2328 | Intron | XP_005253427.1 | |||
XM_005253372.2 | 2328 | Intron | XP_005253429.1 | |||
XM_005253374.3 | 2328 | Intron | XP_005253431.1 | |||
XM_006719076.2 | 2328 | Intron | XP_006719139.1 | |||
XM_011520667.1 | 2328 | Intron | XP_011518969.1 | |||
XM_011520668.2 | 2328 | Intron | XP_011518970.1 | |||
XM_011520669.2 | 2328 | Intron | XP_011518971.1 | |||
XM_011520670.1 | 2328 | Intron | XP_011518972.1 | |||
XM_017019300.1 | 2328 | Intron | XP_016874789.1 | |||
XM_017019301.1 | 2328 | Intron | XP_016874790.1 | |||
XM_017019302.1 | 2328 | Intron | XP_016874791.1 |