Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TCTACTGATATCCTGTAAGAACTGG[A/G]CCTTATCCCTCGCTTCCATGGGACT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
IQCD 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 |
IQCD - IQ motif containing D | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_138451.2 | 817 | Missense Mutation | GCC,GTC | A,V 209 | NP_612460.1 | |
XM_005253832.4 | 817 | Missense Mutation | GCC,GTC | A,V 209 | XP_005253889.1 | |
XM_005253833.4 | 817 | Missense Mutation | GCC,GTC | A,V 209 | XP_005253890.1 | |
XM_005253834.4 | 817 | Intron | XP_005253891.1 | |||
XM_011537862.2 | 817 | Missense Mutation | GCC,GTC | A,V 209 | XP_011536164.1 | |
XM_011537863.2 | 817 | Missense Mutation | GCC,GTC | A,V 209 | XP_011536165.1 | |
XM_011537864.1 | 817 | Missense Mutation | GCC,GTC | A,V 209 | XP_011536166.1 | |
XM_011537865.2 | 817 | Intron | XP_011536167.1 | |||
XM_011537866.2 | 817 | Intron | XP_011536168.1 | |||
XM_017018771.1 | 817 | Intron | XP_016874260.1 |