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TCTAGTTCAAGGCCATTTGTAGCTT[A/G]TTGTATAGCATTAGACAGGTTTTTA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 605622 MIM: 605675 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
PCDH12 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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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
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PCDH12 - protocadherin 12 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_016580.3 | Intron | NP_057664.1 |
RNF14 - ring finger protein 14 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001201365.1 | Intron | NP_001188294.1 | ||||
NM_004290.4 | Intron | NP_004281.1 | ||||
NM_183398.2 | Intron | NP_899645.1 | ||||
NM_183399.2 | Intron | NP_899646.1 | ||||
NM_183400.2 | Intron | NP_899647.1 | ||||
NM_183401.2 | Intron | NP_899648.1 | ||||
XM_005268536.2 | Intron | XP_005268593.1 | ||||
XM_005268537.2 | Intron | XP_005268594.1 | ||||
XM_005268539.2 | Intron | XP_005268596.1 | ||||
XM_005268540.3 | Intron | XP_005268597.1 | ||||
XM_005268541.3 | Intron | XP_005268598.1 | ||||
XM_005268542.2 | Intron | XP_005268599.1 | ||||
XM_005268543.4 | Intron | XP_005268600.1 | ||||
XM_011537714.2 | Intron | XP_011536016.1 | ||||
XM_017010070.1 | Intron | XP_016865559.1 | ||||
XM_017010071.1 | Intron | XP_016865560.1 | ||||
XM_017010072.1 | Intron | XP_016865561.1 | ||||
XM_017010073.1 | Intron | XP_016865562.1 | ||||
XM_017010074.1 | Intron | XP_016865563.1 | ||||
XM_017010075.1 | Intron | XP_016865564.1 | ||||
XM_017010076.1 | Intron | XP_016865565.1 | ||||
XM_017010077.1 | Intron | XP_016865566.1 |