Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TGGCTTTGAAGGTTCTTTTGAAAAT[A/G]CTAATTTTACCTGCAAGGGAGAAAA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
ZNF385D 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 |
ZNF385D - zinc finger protein 385D | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_024697.2 | 1577 | Missense Mutation | GCA,GTA | A,V 322 | NP_078973.1 | |
XM_011534122.1 | 1577 | Intron | XP_011532424.1 | |||
XM_011534123.2 | 1577 | Intron | XP_011532425.1 | |||
XM_011534124.2 | 1577 | Intron | XP_011532426.1 | |||
XM_017007191.1 | 1577 | Missense Mutation | GCA,GTA | A,V 442 | XP_016862680.1 | |
XM_017007192.1 | 1577 | Missense Mutation | GCA,GTA | A,V 423 | XP_016862681.1 | |
XM_017007193.1 | 1577 | Missense Mutation | GCA,GTA | A,V 371 | XP_016862682.1 | |
XM_017007194.1 | 1577 | Missense Mutation | GCA,GTA | A,V 358 | XP_016862683.1 | |
XM_017007195.1 | 1577 | Missense Mutation | GCA,GTA | A,V 356 | XP_016862684.1 | |
XM_017007196.1 | 1577 | Missense Mutation | GCA,GTA | A,V 341 | XP_016862685.1 | |
XM_017007197.1 | 1577 | Missense Mutation | GCA,GTA | A,V 338 | XP_016862686.1 | |
XM_017007198.1 | 1577 | Missense Mutation | GCA,GTA | A,V 337 | XP_016862687.1 | |
XM_017007199.1 | 1577 | Missense Mutation | GCA,GTA | A,V 289 | XP_016862688.1 | |
XM_017007200.1 | 1577 | Missense Mutation | GCA,GTA | A,V 286 | XP_016862689.1 | |
XM_017007201.1 | 1577 | Missense Mutation | GCA,GTA | A,V 228 | XP_016862690.1 | |
XM_017007202.1 | 1577 | Missense Mutation | GCA,GTA | A,V 189 | XP_016862691.1 | |
XM_017007203.1 | 1577 | Intron | XP_016862692.1 |