Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GCCAAACTCACTGCACTCCCGGGTA[C/T]ATGTGCCTGTCATGGCGACATCAGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 603626 | ||||||||||||||||||||
Literature Links: |
PCDH1 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 |
PCDH1 - protocadherin 1 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001278613.1 | 5837 | Intron | NP_001265542.1 | |||
NM_001278615.1 | 5837 | Intron | NP_001265544.1 | |||
NM_002587.4 | 5837 | Intron | NP_002578.2 | |||
NM_032420.3 | 5837 | Missense Mutation | TAT,TGT | Y,C 1120 | NP_115796.2 | |
XM_005268452.2 | 5837 | Missense Mutation | TAT,TGT | Y,C 1164 | XP_005268509.1 | |
XM_005268454.4 | 5837 | UTR 3 | XP_005268511.1 | |||
XM_005268455.2 | 5837 | Missense Mutation | TAT,TGT | Y,C 741 | XP_005268512.1 | |
XM_017009517.1 | 5837 | Missense Mutation | TAT,TGT | Y,C 741 | XP_016865006.1 | |
XM_017009518.1 | 5837 | Intron | XP_016865007.1 |