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AGTGTGACTTGGGCATGCCATAAGG[A/G]GGCTCATAGATGGAAACTAGGCAGT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
1 submissions
|
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Phenotype: |
MIM: 612889 | ||||||||||||||||||||
Literature Links: |
FLJ27354 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 |
FLJ27354 - uncharacterized LOC400761 | ||||||
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There are no transcripts associated with this gene. |
LRRC8C - leucine rich repeat containing 8 family member C | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_032270.4 | Intron | NP_115646.2 | ||||
XM_006710960.3 | Intron | XP_006711023.1 | ||||
XM_011542282.2 | Intron | XP_011540584.1 | ||||
XM_011542283.2 | Intron | XP_011540585.1 | ||||
XM_017002503.1 | Intron | XP_016857992.1 | ||||
XM_017002504.1 | Intron | XP_016857993.1 |