Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CCTGAGGTACTTACCACAGGGGTGG[A/G]CAGGCGAGTGAGAGCATGCATGCAC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 614777 MIM: 616750 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
MMS19 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
|
MMS19 - MMS19 homolog, cytosolic iron-sulfur assembly component | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001289403.1 | 3579 | Missense Mutation | CCC,TCC | P,S 942 | NP_001276332.1 | |
NM_001289404.1 | 3579 | Missense Mutation | CCC,TCC | P,S 826 | NP_001276333.1 | |
NM_001289405.1 | 3579 | Missense Mutation | CCC,TCC | P,S 985 | NP_001276334.1 | |
NM_022362.4 | 3579 | Missense Mutation | CCC,TCC | P,S 985 | NP_071757.4 | |
XM_005270035.2 | 3579 | Missense Mutation | CCC,TCC | P,S 827 | XP_005270092.1 | |
XM_005270041.1 | 3579 | Missense Mutation | CCC,TCC | P,S 784 | XP_005270098.1 | |
XM_006717944.3 | 3579 | Missense Mutation | CCC,TCC | P,S 984 | XP_006718007.2 | |
XM_006717945.2 | 3579 | Missense Mutation | CCC,TCC | P,S 621 | XP_006718008.1 | |
XM_011540062.1 | 3579 | Missense Mutation | CCC,TCC | P,S 784 | XP_011538364.1 | |
XM_011540063.2 | 3579 | Missense Mutation | CCC,TCC | P,S 570 | XP_011538365.1 | |
XM_017016515.1 | 3579 | Missense Mutation | CCC,TCC | P,S 1024 | XP_016872004.1 | |
XM_017016516.1 | 3579 | Missense Mutation | CCC,TCC | P,S 1023 | XP_016872005.1 | |
XM_017016517.1 | 3579 | Missense Mutation | CCC,TCC | P,S 981 | XP_016872006.1 | |
XM_017016518.1 | 3579 | Missense Mutation | CCC,TCC | P,S 941 | XP_016872007.1 | |
XM_017016519.1 | 3579 | Missense Mutation | CCC,TCC | P,S 926 | XP_016872008.1 | |
XM_017016520.1 | 3579 | Missense Mutation | CCC,TCC | P,S 887 | XP_016872009.1 | |
XM_017016521.1 | 3579 | Missense Mutation | CCC,TCC | P,S 886 | XP_016872010.1 | |
XM_017016522.1 | 3579 | Missense Mutation | CCC,TCC | P,S 827 | XP_016872011.1 | |
XM_017016523.1 | 3579 | Missense Mutation | CCC,TCC | P,S 827 | XP_016872012.1 | |
XM_017016524.1 | 3579 | Missense Mutation | CCC,TCC | P,S 826 | XP_016872013.1 | |
XM_017016525.1 | 3579 | Missense Mutation | CCC,TCC | P,S 621 | XP_016872014.1 | |
XM_017016526.1 | 3579 | Missense Mutation | CCC,TCC | P,S 621 | XP_016872015.1 | |
XM_017016527.1 | 3579 | Missense Mutation | CCC,TCC | P,S 621 | XP_016872016.1 | |
XM_017016528.1 | 3579 | Missense Mutation | CCC,TCC | P,S 621 | XP_016872017.1 | |
XM_017016529.1 | 3579 | Missense Mutation | CCC,TCC | P,S 621 | XP_016872018.1 | |
XM_017016530.1 | 3579 | Missense Mutation | CCC,TCC | P,S 621 | XP_016872019.1 | |
XM_017016531.1 | 3579 | Missense Mutation | CCC,TCC | P,S 621 | XP_016872020.1 | |
XM_017016532.1 | 3579 | Missense Mutation | CCC,TCC | P,S 621 | XP_016872021.1 | |
XM_017016533.1 | 3579 | Missense Mutation | CCC,TCC | P,S 620 | XP_016872022.1 | |
XM_017016534.1 | 3579 | Missense Mutation | CCC,TCC | P,S 569 | XP_016872023.1 | |
XM_017016535.1 | 3579 | Missense Mutation | CCC,TCC | P,S 569 | XP_016872024.1 |
ZDHHC16 - zinc finger DHHC-type containing 16 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |