Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ATATTGTATGGTGCTGCGTATGTCC[A/G]GAAAGTCTCAAATGGGAGTCTTTGT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
ZMAT1 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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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 |
ZMAT1 - zinc finger matrin-type 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001011657.3 | 1199 | Missense Mutation | CGG,TGG | R,W 278 | NP_001011657.2 | |
NM_001282400.1 | 1199 | Missense Mutation | CGG,TGG | R,W 107 | NP_001269329.1 | |
NM_001282401.1 | 1199 | Missense Mutation | CGG,TGG | R,W 107 | NP_001269330.1 | |
XM_005262212.4 | 1199 | Missense Mutation | CGG,TGG | R,W 358 | XP_005262269.2 | |
XM_005262213.4 | 1199 | Missense Mutation | CGG,TGG | R,W 357 | XP_005262270.2 | |
XM_005262214.3 | 1199 | Missense Mutation | CGG,TGG | R,W 335 | XP_005262271.2 | |
XM_005262216.4 | 1199 | Missense Mutation | CGG,TGG | R,W 238 | XP_005262273.2 | |
XM_006724711.3 | 1199 | Missense Mutation | CGG,TGG | R,W 107 | XP_006724774.1 | |
XM_017029903.1 | 1199 | Missense Mutation | CGG,TGG | R,W 237 | XP_016885392.1 | |
XM_017029904.1 | 1199 | Missense Mutation | CGG,TGG | R,W 107 | XP_016885393.1 |