Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CTGTTAGGTCTTTGTTATGTCTTGG[A/T]CACTTTGTCTGGACTGGCCGTGACC
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 |
---|---|---|
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 |
CHRDL2 - chordin like 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001278473.2 | 1473 | Missense Mutation | ACC,TCC | T,S 427 | NP_001265402.1 | |
NM_001304390.1 | 1473 | Missense Mutation | GAC,GTC | D,V 425 | NP_001291319.1 | |
NM_001304391.1 | 1473 | Missense Mutation | GAC,GTC | D,V 360 | NP_001291320.1 | |
NM_001304415.1 | 1473 | Missense Mutation | ACC,TCC | T,S 342 | NP_001291344.1 | |
NM_001304416.1 | 1473 | Missense Mutation | ACC,TCC | T,S 311 | NP_001291345.1 | |
NM_001304417.1 | 1473 | Missense Mutation | GAC,GTC | D,V 380 | NP_001291346.1 | |
NM_015424.5 | 1473 | Missense Mutation | GAC,GTC | D,V 445 | NP_056239.3 |