Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TGTCATCATCTGCCAGGTCATCTTG[A/G]CAAAAGTCGGAGCATTTCTCAGTCA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600362 MIM: 600966 | ||||||||||||||||||||
Literature Links: |
FLII 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 |
FLII - FLII, actin remodeling protein | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001256264.1 | 3570 | Silent Mutation | TGC,TGT | C,C 1175 | NP_001243193.1 | |
NM_001256265.1 | 3570 | Silent Mutation | TGC,TGT | C,C 1131 | NP_001243194.1 | |
NM_002018.3 | 3570 | Silent Mutation | TGC,TGT | C,C 1186 | NP_002009.1 | |
XM_005256555.3 | 3570 | Silent Mutation | TGC,TGT | C,C 1186 | XP_005256612.1 | |
XM_005256556.3 | 3570 | Silent Mutation | TGC,TGT | C,C 1185 | XP_005256613.1 | |
XM_005256558.2 | 3570 | Silent Mutation | TGC,TGT | C,C 1185 | XP_005256615.1 |
LLGL1 - LLGL1, scribble cell polarity complex component | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_004140.3 | 3570 | Intron | NP_004131.3 | |||
XM_011523849.2 | 3570 | Intron | XP_011522151.1 | |||
XM_011523850.2 | 3570 | Intron | XP_011522152.1 | |||
XM_011523851.2 | 3570 | Intron | XP_011522153.1 | |||
XM_011523852.2 | 3570 | Intron | XP_011522154.1 | |||
XM_011523853.2 | 3570 | Intron | XP_011522155.1 | |||
XM_011523854.2 | 3570 | Intron | XP_011522156.1 | |||
XM_011523855.2 | 3570 | Intron | XP_011522157.1 | |||
XM_011523856.1 | 3570 | Intron | XP_011522158.1 |