Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TACTCTCGCAGGAAATGGGAATTCT[A/G]CTTGTGTGGGTAAGTACTCCAATGA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 131530 | ||||||||||||||||||||
Literature Links: |
EGF 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 |
EGF - epidermal growth factor | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001178130.2 | 571 | Missense Mutation | ACT,GCT | T,A 40 | NP_001171601.1 | |
NM_001178131.2 | 571 | Missense Mutation | ACT,GCT | T,A 40 | NP_001171602.1 | |
NM_001963.5 | 571 | Missense Mutation | ACT,GCT | T,A 40 | NP_001954.2 | |
XM_005262796.2 | 571 | Missense Mutation | ACT,GCT | T,A 40 | XP_005262853.1 | |
XM_011531707.1 | 571 | UTR 5 | XP_011530009.1 | |||
XM_017007845.1 | 571 | Missense Mutation | ACT,GCT | T,A 40 | XP_016863334.1 | |
XM_017007846.1 | 571 | Missense Mutation | ACT,GCT | T,A 40 | XP_016863335.1 | |
XM_017007847.1 | 571 | Missense Mutation | ACT,GCT | T,A 40 | XP_016863336.1 | |
XM_017007848.1 | 571 | Missense Mutation | ACT,GCT | T,A 40 | XP_016863337.1 | |
XM_017007849.1 | 571 | Missense Mutation | ACT,GCT | T,A 40 | XP_016863338.1 | |
XM_017007850.1 | 571 | Missense Mutation | ACT,GCT | T,A 40 | XP_016863339.1 | |
XM_017007851.1 | 571 | Missense Mutation | ACT,GCT | T,A 40 | XP_016863340.1 | |
XM_017007852.1 | 571 | Missense Mutation | ACT,GCT | T,A 40 | XP_016863341.1 | |
XM_017007853.1 | 571 | Missense Mutation | ACT,GCT | T,A 40 | XP_016863342.1 | |
XM_017007854.1 | 571 | Missense Mutation | ACT,GCT | T,A 40 | XP_016863343.1 | |
XM_017007855.1 | 571 | Missense Mutation | ACT,GCT | T,A 40 | XP_016863344.1 |