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ACTTGTTGTCCGGGACGTACATTTT[C/T]GCGGTCCTGCTAGCATGCGTGGTGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 300246 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
PCDH11X 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
|
PCDH11X - protocadherin 11 X-linked | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001168360.1 | Intron | NP_001161832.1 | ||||
NM_001168361.1 | Intron | NP_001161833.1 | ||||
NM_001168362.1 | Intron | NP_001161834.1 | ||||
NM_001168363.1 | Intron | NP_001161835.1 | ||||
NM_032968.4 | Intron | NP_116750.1 | ||||
NM_032969.4 | Intron | NP_116751.1 | ||||
XM_011530910.1 | Intron | XP_011529212.1 | ||||
XM_011530911.2 | Intron | XP_011529213.1 | ||||
XM_011530912.2 | Intron | XP_011529214.1 | ||||
XM_011530913.2 | Intron | XP_011529215.1 | ||||
XM_011530914.2 | Intron | XP_011529216.1 | ||||
XM_011530915.2 | Intron | XP_011529217.1 | ||||
XM_011530916.2 | Intron | XP_011529218.1 | ||||
XM_017029416.1 | Intron | XP_016884905.1 | ||||
XM_017029417.1 | Intron | XP_016884906.1 | ||||
XM_017029418.1 | Intron | XP_016884907.1 | ||||
XM_017029419.1 | Intron | XP_016884908.1 | ||||
XM_017029420.1 | Intron | XP_016884909.1 | ||||
XM_017029421.1 | Intron | XP_016884910.1 | ||||
XM_017029422.1 | Intron | XP_016884911.1 |