Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TTCTGCCGGCGGACGCAGCAGCAGG[C/T]GGCCAGCGTGGTGAGGAGGATGGCA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 137207 | ||||||||||||||||||||
Literature Links: |
LRRC32 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 |
LRRC32 - leucine rich repeat containing 32 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001128922.1 | 2271 | Missense Mutation | ACC,GCC | T,A 647 | NP_001122394.1 | |
NM_005512.2 | 2271 | Missense Mutation | ACC,GCC | T,A 647 | NP_005503.1 | |
XM_005273902.3 | 2271 | Missense Mutation | ACC,GCC | T,A 647 | XP_005273959.1 | |
XM_005273903.4 | 2271 | Missense Mutation | ACC,GCC | T,A 625 | XP_005273960.2 | |
XM_011544935.2 | 2271 | Missense Mutation | ACC,GCC | T,A 647 | XP_011543237.1 | |
XM_017017527.1 | 2271 | Missense Mutation | ACC,GCC | T,A 647 | XP_016873016.1 |