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TGGACAGTTGGATGGTTGCGGAAGT[C/T]TATAGTTTTGAGCCAACATCTGGAT
Species: |
Human | ||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606573 | ||||||||||||||||||||||||||
Literature Links: |
FRK PubMed Links | ||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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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 | JPT (Japanese)
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AFR - Not Available | Japanese - Not Available | CHB (Han Chinese)
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EUR - Not Available | |||||
AMR - Not Available |
FRK - fyn related Src family tyrosine kinase | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_002031.2 | 1989 | Missense Mutation | AAA,AGA | K,R 451 | NP_002022.1 | |
XM_005266880.4 | 1989 | Missense Mutation | AAA,AGA | K,R 451 | XP_005266937.1 | |
XM_005266881.2 | 1989 | Missense Mutation | AAA,AGA | K,R 451 | XP_005266938.1 | |
XM_005266882.4 | 1989 | Missense Mutation | AAA,AGA | K,R 451 | XP_005266939.1 | |
XM_011535653.2 | 1989 | Missense Mutation | AAA,AGA | K,R 451 | XP_011533955.1 | |
XM_011535654.2 | 1989 | Missense Mutation | AAA,AGA | K,R 451 | XP_011533956.1 | |
XM_011535655.2 | 1989 | Missense Mutation | AAA,AGA | K,R 451 | XP_011533957.1 | |
XM_011535656.2 | 1989 | Missense Mutation | AAA,AGA | K,R 338 | XP_011533958.1 | |
XM_017010645.1 | 1989 | Missense Mutation | AAA,AGA | K,R 451 | XP_016866134.1 |