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TATACACGTCCATCTACCACAAATG[C/G]CTCCACATCTGTATTGTCTGGTTTT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606042 | ||||||||||||||||||||
Literature Links: |
LRRC34 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 |
LRRC34 - leucine rich repeat containing 34 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001172779.1 | 1217 | Missense Mutation | CCA,GCA | P,A 417 | NP_001166250.1 | |
NM_001172780.1 | 1217 | Intron | NP_001166251.1 | |||
NM_153353.4 | 1217 | Missense Mutation | CCA,GCA | P,A 385 | NP_699184.2 | |
XM_006713508.3 | 1217 | Missense Mutation | CCA,GCA | P,A 399 | XP_006713571.1 | |
XM_011512442.2 | 1217 | Missense Mutation | CCA,GCA | P,A 416 | XP_011510744.1 | |
XM_017005746.1 | 1217 | Missense Mutation | CCA,GCA | P,A 355 | XP_016861235.1 |
MYNN - myoneurin | ||||||
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There are no transcripts associated with this gene. |