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Search Thermo Fisher Scientific
GAGTGAAAATACAATTTATTTTTCG[C/G]ATTCCTCTGGAGGATTAAAAAGTTT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
CMC2 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 |
CMC2 - C-X9-C motif containing 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_020188.3 | 512 | Missense Mutation | TCC,TGC | S,C 77 | NP_064573.1 | |
XM_017023461.1 | 512 | Missense Mutation | TCC,TGC | S,C 203 | XP_016878950.1 | |
XM_017023462.1 | 512 | UTR 3 | XP_016878951.1 | |||
XM_017023463.1 | 512 | Intron | XP_016878952.1 | |||
XM_017023464.1 | 512 | Missense Mutation | TCC,TGC | S,C 160 | XP_016878953.1 | |
XM_017023465.1 | 512 | UTR 3 | XP_016878954.1 | |||
XM_017023466.1 | 512 | UTR 3 | XP_016878955.1 | |||
XM_017023467.1 | 512 | Missense Mutation | TCC,TGC | S,C 77 | XP_016878956.1 | |
XM_017023468.1 | 512 | Missense Mutation | TCC,TGC | S,C 77 | XP_016878957.1 | |
XM_017023469.1 | 512 | Missense Mutation | TCC,TGC | S,C 77 | XP_016878958.1 | |
XM_017023470.1 | 512 | Missense Mutation | TCC,TGC | S,C 77 | XP_016878959.1 |