Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AAACCTGAGGATCACATGGACCCAA[C/T]CATATCATCTGTGTGAAGAGACCAA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 300296 | ||||||||||||||||||||
Literature Links: |
LINC00629 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
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 |
LINC00629 - long intergenic non-protein coding RNA 629 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
PLAC1 - placenta specific 1 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001316887.1 | 911 | Missense Mutation | ATT,GTT | I,V 209 | NP_001303816.1 | |
NM_001316888.1 | 911 | Missense Mutation | ATT,GTT | I,V 209 | NP_001303817.1 | |
NM_001316889.1 | 911 | Missense Mutation | ATT,GTT | I,V 209 | NP_001303818.1 | |
NM_021796.3 | 911 | Missense Mutation | ATT,GTT | I,V 209 | NP_068568.1 | |
XM_011531257.2 | 911 | Missense Mutation | ATT,GTT | I,V 209 | XP_011529559.1 | |
XM_011531260.2 | 911 | Missense Mutation | ATT,GTT | I,V 209 | XP_011529562.1 | |
XM_017029236.1 | 911 | Missense Mutation | ATT,GTT | I,V 209 | XP_016884725.1 |