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CCCTCTGGCTCTCTATTGCATTCAT[A/T]GTACTGTTTGCAGCTTTGATGAGCT
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 | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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LRMP - lymphoid restricted membrane protein | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001204126.1 | 2357 | Silent Mutation | ATA,ATT | I,I 448 | NP_001191055.1 | |
NM_001204127.1 | 2357 | Silent Mutation | ATA,ATT | I,I 448 | NP_001191056.1 | |
NM_006152.3 | 2357 | Silent Mutation | ATA,ATT | I,I 448 | NP_006143.2 | |
XM_005253370.3 | 2357 | Silent Mutation | ATA,ATT | I,I 448 | XP_005253427.1 | |
XM_005253372.2 | 2357 | Silent Mutation | ATA,ATT | I,I 448 | XP_005253429.1 | |
XM_005253374.3 | 2357 | Silent Mutation | ATA,ATT | I,I 448 | XP_005253431.1 | |
XM_006719076.2 | 2357 | Silent Mutation | ATA,ATT | I,I 448 | XP_006719139.1 | |
XM_011520667.1 | 2357 | Silent Mutation | ATA,ATT | I,I 448 | XP_011518969.1 | |
XM_011520668.2 | 2357 | Silent Mutation | ATA,ATT | I,I 395 | XP_011518970.1 | |
XM_011520669.2 | 2357 | Silent Mutation | ATA,ATT | I,I 395 | XP_011518971.1 | |
XM_011520670.1 | 2357 | Silent Mutation | ATA,ATT | I,I 208 | XP_011518972.1 | |
XM_017019300.1 | 2357 | Silent Mutation | ATA,ATT | I,I 448 | XP_016874789.1 | |
XM_017019301.1 | 2357 | Silent Mutation | ATA,ATT | I,I 448 | XP_016874790.1 | |
XM_017019302.1 | 2357 | Silent Mutation | ATA,ATT | I,I 448 | XP_016874791.1 |