Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TGGGAGTGACAGCGCTGAGGACACG[A/G]CTGCCGCCGCTGCGAGAGGTGAGGA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612344 | ||||||||||||||||||||
Literature Links: |
ZNF385B 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 |
ZNF385B - zinc finger protein 385B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001113397.1 | 1197 | Missense Mutation | GCC,GTC | A,V 350 | NP_001106868.1 | |
NM_001113398.1 | 1197 | Missense Mutation | GCC,GTC | A,V 324 | NP_001106869.1 | |
NM_001282725.1 | 1197 | Missense Mutation | GCC,GTC | A,V 324 | NP_001269654.1 | |
NM_152520.4 | 1197 | Missense Mutation | GCC,GTC | A,V 426 | NP_689733.3 | |
XM_011510713.2 | 1197 | Missense Mutation | GCC,GTC | A,V 481 | XP_011509015.1 | |
XM_011510714.2 | 1197 | Missense Mutation | GCC,GTC | A,V 468 | XP_011509016.1 | |
XM_011510715.2 | 1197 | Missense Mutation | GCC,GTC | A,V 454 | XP_011509017.1 | |
XM_011510716.2 | 1197 | Missense Mutation | GCC,GTC | A,V 384 | XP_011509018.1 | |
XM_011510717.2 | 1197 | Missense Mutation | GCC,GTC | A,V 384 | XP_011509019.1 | |
XM_011510719.2 | 1197 | Missense Mutation | GCC,GTC | A,V 364 | XP_011509021.1 | |
XM_011510720.2 | 1197 | Missense Mutation | GCC,GTC | A,V 364 | XP_011509022.1 | |
XM_011510721.2 | 1197 | Missense Mutation | GCC,GTC | A,V 351 | XP_011509023.1 | |
XM_011510723.2 | 1197 | Intron | XP_011509025.1 | |||
XM_017003435.1 | 1197 | Missense Mutation | GCC,GTC | A,V 441 | XP_016858924.1 | |
XM_017003436.1 | 1197 | Missense Mutation | GCC,GTC | A,V 364 | XP_016858925.1 | |
XM_017003437.1 | 1197 | Missense Mutation | GCC,GTC | A,V 358 | XP_016858926.1 | |
XM_017003438.1 | 1197 | Missense Mutation | GCC,GTC | A,V 324 | XP_016858927.1 | |
XM_017003439.1 | 1197 | Missense Mutation | GCC,GTC | A,V 324 | XP_016858928.1 | |
XM_017003440.1 | 1197 | Missense Mutation | GCC,GTC | A,V 312 | XP_016858929.1 | |
XM_017003441.1 | 1197 | Intron | XP_016858930.1 |