Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AAGCTGAGCAGTGACGAGAACAGCA[A/T]TCCAGACCTCTCTGGAGACGAGAAT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605984 | ||||||||||||||||||||
Literature Links: |
EED 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 |
EED - embryonic ectoderm development | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001308007.1 | 775 | Missense Mutation | AAT,ATT | N,I 30 | NP_001294936.1 | |
NM_003797.4 | 775 | Missense Mutation | AAT,ATT | N,I 30 | NP_003788.2 | |
XM_005274373.2 | 775 | Missense Mutation | AAT,ATT | N,I 30 | XP_005274430.1 | |
XM_011545330.1 | 775 | Missense Mutation | AAT,ATT | N,I 30 | XP_011543632.1 | |
XM_011545331.1 | 775 | Missense Mutation | AAT,ATT | N,I 30 | XP_011543633.1 | |
XM_017018512.1 | 775 | Missense Mutation | AAT,ATT | N,I 30 | XP_016874001.1 | |
XM_017018513.1 | 775 | Missense Mutation | AAT,ATT | N,I 30 | XP_016874002.1 |