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TAGGCCAGGACTGAGGGCTCAGCTG[C/T]CAGGGCTCCCCAACAGAAACCTGTA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 614777 MIM: 616750 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
MMS19 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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MMS19 - MMS19 homolog, cytosolic iron-sulfur assembly component | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001289403.1 | 3712 | Missense Mutation | GAC,GGC | D,G 986 | NP_001276332.1 | |
NM_001289404.1 | 3712 | Missense Mutation | GAC,GGC | D,G 870 | NP_001276333.1 | |
NM_001289405.1 | 3712 | Missense Mutation | GAC,GGC | D,G 1029 | NP_001276334.1 | |
NM_022362.4 | 3712 | Missense Mutation | GAC,GGC | D,G 1029 | NP_071757.4 | |
XM_005270035.2 | 3712 | Missense Mutation | GAC,GGC | D,G 871 | XP_005270092.1 | |
XM_005270041.1 | 3712 | Missense Mutation | GAC,GGC | D,G 828 | XP_005270098.1 | |
XM_006717944.3 | 3712 | Missense Mutation | GAC,GGC | D,G 1028 | XP_006718007.2 | |
XM_006717945.2 | 3712 | Missense Mutation | GAC,GGC | D,G 665 | XP_006718008.1 | |
XM_011540062.1 | 3712 | Missense Mutation | GAC,GGC | D,G 828 | XP_011538364.1 | |
XM_011540063.2 | 3712 | Missense Mutation | GAC,GGC | D,G 614 | XP_011538365.1 | |
XM_017016515.1 | 3712 | Missense Mutation | GAC,GGC | D,G 1068 | XP_016872004.1 | |
XM_017016516.1 | 3712 | Missense Mutation | GAC,GGC | D,G 1067 | XP_016872005.1 | |
XM_017016517.1 | 3712 | Missense Mutation | GAC,GGC | D,G 1025 | XP_016872006.1 | |
XM_017016518.1 | 3712 | Missense Mutation | GAC,GGC | D,G 985 | XP_016872007.1 | |
XM_017016519.1 | 3712 | Missense Mutation | GAC,GGC | D,G 970 | XP_016872008.1 | |
XM_017016520.1 | 3712 | Missense Mutation | GAC,GGC | D,G 931 | XP_016872009.1 | |
XM_017016521.1 | 3712 | Missense Mutation | GAC,GGC | D,G 930 | XP_016872010.1 | |
XM_017016522.1 | 3712 | Missense Mutation | GAC,GGC | D,G 871 | XP_016872011.1 | |
XM_017016523.1 | 3712 | Missense Mutation | GAC,GGC | D,G 871 | XP_016872012.1 | |
XM_017016524.1 | 3712 | Missense Mutation | GAC,GGC | D,G 870 | XP_016872013.1 | |
XM_017016525.1 | 3712 | Missense Mutation | GAC,GGC | D,G 665 | XP_016872014.1 | |
XM_017016526.1 | 3712 | Missense Mutation | GAC,GGC | D,G 665 | XP_016872015.1 | |
XM_017016527.1 | 3712 | Missense Mutation | GAC,GGC | D,G 665 | XP_016872016.1 | |
XM_017016528.1 | 3712 | Missense Mutation | GAC,GGC | D,G 665 | XP_016872017.1 | |
XM_017016529.1 | 3712 | Missense Mutation | GAC,GGC | D,G 665 | XP_016872018.1 | |
XM_017016530.1 | 3712 | Missense Mutation | GAC,GGC | D,G 665 | XP_016872019.1 | |
XM_017016531.1 | 3712 | Missense Mutation | GAC,GGC | D,G 665 | XP_016872020.1 | |
XM_017016532.1 | 3712 | Missense Mutation | GAC,GGC | D,G 665 | XP_016872021.1 | |
XM_017016533.1 | 3712 | Missense Mutation | GAC,GGC | D,G 664 | XP_016872022.1 | |
XM_017016534.1 | 3712 | Missense Mutation | GAC,GGC | D,G 613 | XP_016872023.1 | |
XM_017016535.1 | 3712 | Missense Mutation | GAC,GGC | D,G 613 | XP_016872024.1 |
ZDHHC16 - zinc finger DHHC-type containing 16 | ||||||
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There are no transcripts associated with this gene. |