Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TCTTGGTCACTTTGTCTGGACTGGC[C/T]GTGACCTTCAGCTCCAGGGTCTGGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613127 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CHRDL2 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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CHRDL2 - chordin like 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001278473.2 | 1454 | Silent Mutation | ACA,ACG | T,T 420 | NP_001265402.1 | |
NM_001304390.1 | 1454 | Missense Mutation | AGC,GGC | S,G 419 | NP_001291319.1 | |
NM_001304391.1 | 1454 | Missense Mutation | AGC,GGC | S,G 354 | NP_001291320.1 | |
NM_001304415.1 | 1454 | Silent Mutation | ACA,ACG | T,T 335 | NP_001291344.1 | |
NM_001304416.1 | 1454 | Silent Mutation | ACA,ACG | T,T 304 | NP_001291345.1 | |
NM_001304417.1 | 1454 | Missense Mutation | AGC,GGC | S,G 374 | NP_001291346.1 | |
NM_015424.5 | 1454 | Missense Mutation | AGC,GGC | S,G 439 | NP_056239.3 |