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Search Thermo Fisher Scientific
ACAATTACCGAGCTCTGGTGGAATT[G/T]GTAAGAGGTCATTATTTTGAAGGTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
5 submissions
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Phenotype: |
MIM: 614453 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
LRRC40 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
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) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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LRRC40 - leucine rich repeat containing 40 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_017768.4 | 1547 | Missense Mutation | CAA,CCA | Q,P 556 | NP_060238.3 | |
XM_005271013.1 | 1547 | Missense Mutation | CAA,CCA | Q,P 338 | XP_005271070.1 | |
XM_011541763.1 | 1547 | Missense Mutation | CAA,CCA | Q,P 338 | XP_011540065.1 | |
XM_017001695.1 | 1547 | Missense Mutation | CAA,CCA | Q,P 315 | XP_016857184.1 | |
XM_017001696.1 | 1547 | Missense Mutation | CAA,CCA | Q,P 315 | XP_016857185.1 |
LRRC7 - leucine rich repeat containing 7 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_020794.2 | 1547 | Intron | NP_065845.1 | |||
XM_017001885.1 | 1547 | Intron | XP_016857374.1 | |||
XM_017001886.1 | 1547 | Intron | XP_016857375.1 | |||
XM_017001887.1 | 1547 | Intron | XP_016857376.1 | |||
XM_017001888.1 | 1547 | Intron | XP_016857377.1 | |||
XM_017001889.1 | 1547 | Intron | XP_016857378.1 | |||
XM_017001890.1 | 1547 | Intron | XP_016857379.1 | |||
XM_017001891.1 | 1547 | Intron | XP_016857380.1 | |||
XM_017001892.1 | 1547 | Intron | XP_016857381.1 | |||
XM_017001893.1 | 1547 | Intron | XP_016857382.1 | |||
XM_017001894.1 | 1547 | Intron | XP_016857383.1 | |||
XM_017001895.1 | 1547 | Intron | XP_016857384.1 |