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ATAATTTCCTGTGGTTCCTACTGAC[C/T]AAGCTCACTGGCAGCCAGGAAGCCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 616557 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
LRRC37A3 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
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AMR
|
LRRC37A3 - leucine rich repeat containing 37 member A3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001303255.1 | Intron | NP_001290184.1 | ||||
NM_199340.3 | Intron | NP_955372.2 | ||||
XM_011524776.1 | Intron | XP_011523078.1 | ||||
XM_011524777.1 | Intron | XP_011523079.1 | ||||
XM_011524778.2 | Intron | XP_011523080.2 | ||||
XM_017024593.1 | Intron | XP_016880082.1 | ||||
XM_017024594.1 | Intron | XP_016880083.1 | ||||
XM_017024595.1 | Intron | XP_016880084.1 | ||||
XM_017024596.1 | Intron | XP_016880085.1 | ||||
XM_017024597.1 | Intron | XP_016880086.1 | ||||
XM_017024598.1 | Intron | XP_016880087.1 | ||||
XM_017024599.1 | Intron | XP_016880088.1 | ||||
XM_017024600.1 | Intron | XP_016880089.1 | ||||
XM_017024601.1 | Intron | XP_016880090.1 | ||||
XM_017024602.1 | Intron | XP_016880091.1 | ||||
XM_017024603.1 | Intron | XP_016880092.1 | ||||
XM_017024604.1 | Intron | XP_016880093.1 | ||||
XM_017024605.1 | Intron | XP_016880094.1 | ||||
XM_017024606.1 | Intron | XP_016880095.1 | ||||
XM_017024607.1 | Intron | XP_016880096.1 | ||||
XM_017024608.1 | Intron | XP_016880097.1 |