Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TCTACCTGAGGTGGTCTCTCAGTCT[C/T]CAGTGCTATTTTTCTGGTTGTCTCC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 300350 | ||||||||||||||||||||
Literature Links: |
CHRDL1 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 |
CHRDL1 - chordin like 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001143981.1 | 1256 | Missense Mutation | AAG,GAG | K,E 369 | NP_001137453.1 | |
NM_001143982.1 | 1256 | Missense Mutation | AAG,GAG | K,E 368 | NP_001137454.1 | |
NM_001143983.2 | 1256 | Missense Mutation | AAG,GAG | K,E 289 | NP_001137455.2 | |
NM_145234.3 | 1256 | Missense Mutation | AAG,GAG | K,E 367 | NP_660277.2 | |
XM_005262221.1 | 1256 | Missense Mutation | AAG,GAG | K,E 369 | XP_005262278.1 | |
XM_005262222.3 | 1256 | Missense Mutation | AAG,GAG | K,E 368 | XP_005262279.1 | |
XM_005262223.1 | 1256 | Missense Mutation | AAG,GAG | K,E 364 | XP_005262280.1 | |
XM_005262224.1 | 1256 | Missense Mutation | AAG,GAG | K,E 363 | XP_005262281.1 | |
XM_017029959.1 | 1256 | Missense Mutation | AAG,GAG | K,E 364 | XP_016885448.1 |