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Search Thermo Fisher Scientific
ATTGTTTCAGGGATCAGTGATGTTC[A/G]GTGATGTGTCCATAGACTTCTCTCA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
ZNF383 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 |
ZNF383 - zinc finger protein 383 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_152604.1 | 1435 | Missense Mutation | AGT,GGT | S,G 9 | NP_689817.1 | |
XM_005258585.2 | 1435 | Missense Mutation | AGT,GGT | S,G 9 | XP_005258642.1 | |
XM_005258587.2 | 1435 | Missense Mutation | AGT,GGT | S,G 9 | XP_005258644.1 | |
XM_005258588.2 | 1435 | Missense Mutation | AGT,GGT | S,G 9 | XP_005258645.1 | |
XM_011526586.2 | 1435 | Missense Mutation | AGT,GGT | S,G 9 | XP_011524888.1 | |
XM_011526587.2 | 1435 | Missense Mutation | AGT,GGT | S,G 9 | XP_011524889.1 | |
XM_011526588.2 | 1435 | Missense Mutation | AGT,GGT | S,G 9 | XP_011524890.1 | |
XM_011526589.2 | 1435 | Missense Mutation | AGT,GGT | S,G 9 | XP_011524891.1 | |
XM_011526590.2 | 1435 | Missense Mutation | AGT,GGT | S,G 9 | XP_011524892.1 | |
XM_017026422.1 | 1435 | Missense Mutation | AGT,GGT | S,G 9 | XP_016881911.1 | |
XM_017026423.1 | 1435 | Missense Mutation | AGT,GGT | S,G 9 | XP_016881912.1 | |
XM_017026424.1 | 1435 | Intron | XP_016881913.1 |