Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GCAGCCCGAGCCGCCCCCCGAGCCC[A/G]CCTTCTCCGAGGCGCAGAAGTGGAT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
LIMCH1 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 |
LIMCH1 - LIM and calponin homology domains 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001112717.2 | 123 | Missense Mutation | ACC,GCC | T,A 23 | NP_001106188.1 | |
NM_001112718.2 | 123 | Missense Mutation | ACC,GCC | T,A 23 | NP_001106189.1 | |
NM_001112719.2 | 123 | Intron | NP_001106190.1 | |||
NM_001112720.2 | 123 | Intron | NP_001106191.1 | |||
NM_001289122.1 | 123 | Missense Mutation | ACC,GCC | T,A 23 | NP_001276051.1 | |
NM_001289124.1 | 123 | Intron | NP_001276053.1 | |||
NM_014988.3 | 123 | Missense Mutation | ACC,GCC | T,A 23 | NP_055803.2 | |
XM_005248057.1 | 123 | Missense Mutation | ACC,GCC | T,A 23 | XP_005248114.1 | |
XM_005248058.1 | 123 | Missense Mutation | ACC,GCC | T,A 23 | XP_005248115.1 | |
XM_005248060.1 | 123 | Missense Mutation | ACC,GCC | T,A 23 | XP_005248117.1 | |
XM_005248061.1 | 123 | Missense Mutation | ACC,GCC | T,A 23 | XP_005248118.1 | |
XM_005248067.2 | 123 | Intron | XP_005248124.1 | |||
XM_005248072.1 | 123 | Missense Mutation | ACC,GCC | T,A 23 | XP_005248129.1 | |
XM_005248074.1 | 123 | Missense Mutation | ACC,GCC | T,A 23 | XP_005248131.1 | |
XM_005248075.1 | 123 | Missense Mutation | ACC,GCC | T,A 23 | XP_005248132.1 | |
XM_006713996.1 | 123 | Missense Mutation | ACC,GCC | T,A 23 | XP_006714059.1 | |
XM_011513642.1 | 123 | Missense Mutation | ACC,GCC | T,A 23 | XP_011511944.1 | |
XM_011513643.1 | 123 | Missense Mutation | ACC,GCC | T,A 23 | XP_011511945.1 | |
XM_011513644.1 | 123 | Missense Mutation | ACC,GCC | T,A 23 | XP_011511946.1 | |
XM_011513645.1 | 123 | Missense Mutation | ACC,GCC | T,A 23 | XP_011511947.1 | |
XM_011513646.1 | 123 | Missense Mutation | ACC,GCC | T,A 23 | XP_011511948.1 | |
XM_011513648.1 | 123 | Missense Mutation | ACC,GCC | T,A 23 | XP_011511950.1 | |
XM_011513649.1 | 123 | Intron | XP_011511951.1 | |||
XM_011513651.2 | 123 | Intron | XP_011511953.1 | |||
XM_011513653.1 | 123 | Missense Mutation | ACC,GCC | T,A 23 | XP_011511955.1 | |
XM_011513654.1 | 123 | Missense Mutation | ACC,GCC | T,A 23 | XP_011511956.1 | |
XM_011513655.1 | 123 | Intron | XP_011511957.1 | |||
XM_011513656.1 | 123 | Intron | XP_011511958.1 | |||
XM_011513657.1 | 123 | Intron | XP_011511959.1 | |||
XM_011513658.2 | 123 | Intron | XP_011511960.1 | |||
XM_017007894.1 | 123 | Missense Mutation | ACC,GCC | T,A 23 | XP_016863383.1 | |
XM_017007895.1 | 123 | Missense Mutation | ACC,GCC | T,A 23 | XP_016863384.1 | |
XM_017007896.1 | 123 | Missense Mutation | ACC,GCC | T,A 23 | XP_016863385.1 | |
XM_017007897.1 | 123 | Missense Mutation | ACC,GCC | T,A 23 | XP_016863386.1 | |
XM_017007898.1 | 123 | Missense Mutation | ACC,GCC | T,A 23 | XP_016863387.1 | |
XM_017007899.1 | 123 | Missense Mutation | ACC,GCC | T,A 23 | XP_016863388.1 | |
XM_017007900.1 | 123 | Missense Mutation | ACC,GCC | T,A 23 | XP_016863389.1 | |
XM_017007901.1 | 123 | Missense Mutation | ACC,GCC | T,A 23 | XP_016863390.1 | |
XM_017007902.1 | 123 | Missense Mutation | ACC,GCC | T,A 23 | XP_016863391.1 | |
XM_017007903.1 | 123 | Intron | XP_016863392.1 | |||
XM_017007904.1 | 123 | Intron | XP_016863393.1 | |||
XM_017007905.1 | 123 | Intron | XP_016863394.1 |