Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
FER1L5 PubMed Links | |||||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | ||||||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | ||||||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | ||||||
SAS
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Chinese - Not Available | CHB (Han Chinese)
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AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | ||||||
EUR
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AMR
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FER1L5 - fer-1 like family member 5 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001293083.1 | 1179 | Missense Mutation | ACT,ATT | T,I 354 | NP_001280012.1 | |
XM_011512110.2 | 1179 | Missense Mutation | ACT,ATT | T,I 354 | XP_011510412.1 | |
XM_011512111.2 | 1179 | Missense Mutation | ACT,ATT | T,I 354 | XP_011510413.1 | |
XM_011512113.2 | 1179 | Missense Mutation | ACT,ATT | T,I 354 | XP_011510415.1 | |
XM_011512114.2 | 1179 | Missense Mutation | ACT,ATT | T,I 354 | XP_011510416.1 | |
XM_011512115.2 | 1179 | Missense Mutation | ACT,ATT | T,I 354 | XP_011510417.1 | |
XM_011512116.2 | 1179 | Missense Mutation | ACT,ATT | T,I 354 | XP_011510418.1 | |
XM_011512117.2 | 1179 | Missense Mutation | ACT,ATT | T,I 354 | XP_011510419.1 | |
XM_011512118.2 | 1179 | Missense Mutation | ACT,ATT | T,I 314 | XP_011510420.1 | |
XM_011512119.2 | 1179 | Missense Mutation | ACT,ATT | T,I 354 | XP_011510421.1 | |
XM_011512120.2 | 1179 | Missense Mutation | ACT,ATT | T,I 284 | XP_011510422.1 | |
XM_011512122.2 | 1179 | Missense Mutation | ACT,ATT | T,I 354 | XP_011510424.1 | |
XM_011512124.2 | 1179 | Intron | XP_011510426.1 | |||
XM_011512125.2 | 1179 | Missense Mutation | ACT,ATT | T,I 354 | XP_011510427.1 | |
XM_011512126.2 | 1179 | Missense Mutation | ACT,ATT | T,I 354 | XP_011510428.1 | |
XM_011512127.2 | 1179 | Missense Mutation | ACT,ATT | T,I 354 | XP_011510429.1 | |
XM_011512128.2 | 1179 | Missense Mutation | ACT,ATT | T,I 354 | XP_011510430.1 | |
XM_017005222.1 | 1179 | Missense Mutation | ACT,ATT | T,I 354 | XP_016860711.1 | |
XM_017005223.1 | 1179 | Intron | XP_016860712.1 | |||
XM_017005224.1 | 1179 | Intron | XP_016860713.1 |
Set Membership: |
HapMap |