Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CTTGGCACAGGGCAAAGTGCATAGG[C/T]TGGTTTGAGAACCTCATTCTGCTAT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 613316 | ||||||||||||||||||||
Literature Links: |
LRRC18 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 |
LRRC18 - leucine rich repeat containing 18 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001006939.3 | Intron | NP_001006940.3 | ||||
XM_006717867.2 | Intron | XP_006717930.1 | ||||
XM_011539822.1 | Intron | XP_011538124.1 | ||||
XM_011539823.1 | Intron | XP_011538125.1 | ||||
XM_011539826.2 | Intron | XP_011538128.1 | ||||
XM_011539828.2 | Intron | XP_011538130.1 | ||||
XM_011539829.2 | Intron | XP_011538131.1 | ||||
XM_017016276.1 | Intron | XP_016871765.1 | ||||
XM_017016277.1 | Intron | XP_016871766.1 |
WDFY4 - WDFY family member 4 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_020945.1 | Intron | NP_065996.1 | ||||
XM_005270004.3 | Intron | XP_005270061.1 | ||||
XM_011539986.2 | Intron | XP_011538288.2 | ||||
XM_011539987.2 | Intron | XP_011538289.2 | ||||
XM_011539988.2 | Intron | XP_011538290.1 | ||||
XM_011539990.2 | Intron | XP_011538292.1 | ||||
XM_011539991.2 | Intron | XP_011538293.1 | ||||
XM_011539992.2 | Intron | XP_011538294.1 | ||||
XM_017016463.1 | Intron | XP_016871952.1 | ||||
XM_017016464.1 | Intron | XP_016871953.1 | ||||
XM_017016465.1 | Intron | XP_016871954.1 |