Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGTTCTCCTGTTTCTGGGTTACTGG[A/C]TAGGTTATATAGCAAGTAGGCAAGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 300195 MIM: 300965 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
AMMECR1 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||||||||||||||||||||
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
|
|||||
AMR
|
AMMECR1 - Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001025580.1 | Intron | NP_001020751.1 | ||||
NM_001171689.1 | Intron | NP_001165160.1 | ||||
NM_015365.2 | Intron | NP_056180.1 |
RGAG1 - retrotransposon gag domain containing 1 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_020769.2 | Intron | NP_065820.1 | ||||
XM_011530998.2 | Intron | XP_011529300.1 | ||||
XM_011530999.2 | Intron | XP_011529301.1 | ||||
XM_017029694.1 | Intron | XP_016885183.1 | ||||
XM_017029695.1 | Intron | XP_016885184.1 |