Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AAGTGTATCTTGCCTTCTCTGTAGC[A/G]AGAGCCAGCCTGCGGATATTGGATA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 615408 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ARMC4 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
|
ARMC4 - armadillo repeat containing 4 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001290020.1 | 2198 | Silent Mutation | CTC,CTT | L,L 1036 | NP_001276949.1 | |
NM_001290021.1 | 2198 | Missense Mutation | TCG,TTG | S,L 602 | NP_001276950.1 | |
NM_001312689.1 | 2198 | Silent Mutation | CTC,CTT | L,L 728 | NP_001299618.1 | |
NM_018076.4 | 2198 | Silent Mutation | CTC,CTT | L,L 1036 | NP_060546.2 | |
XM_011519527.1 | 2198 | Silent Mutation | CTC,CTT | L,L 1056 | XP_011517829.1 | |
XM_011519528.1 | 2198 | Silent Mutation | CTC,CTT | L,L 1056 | XP_011517830.1 | |
XM_011519533.2 | 2198 | Silent Mutation | CTC,CTT | L,L 748 | XP_011517835.1 | |
XM_011519534.2 | 2198 | Silent Mutation | CTC,CTT | L,L 748 | XP_011517836.1 | |
XM_011519535.2 | 2198 | Silent Mutation | CTC,CTT | L,L 694 | XP_011517837.1 | |
XM_011519537.2 | 2198 | Silent Mutation | CTC,CTT | L,L 581 | XP_011517839.1 | |
XM_017016368.1 | 2198 | Intron | XP_016871857.1 | |||
XM_017016369.1 | 2198 | Intron | XP_016871858.1 | |||
XM_017016370.1 | 2198 | Silent Mutation | CTC,CTT | L,L 986 | XP_016871859.1 | |
XM_017016371.1 | 2198 | Intron | XP_016871860.1 |