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GGAGGGACACCCACCACTGGCTGAC[C/T]GTCTGGCGGCCCTCAAAGTCGGGTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607059 MIM: 604546 MIM: 611952 | ||||||||||||||||||||
Literature Links: |
SLC39A4 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 |
SLC39A4 - solute carrier family 39 member 4 | ||||||
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There are no transcripts associated with this gene. |
TONSL - tonsoku-like, DNA repair protein | ||||||
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There are no transcripts associated with this gene. |
VPS28 - VPS28, ESCRT-I subunit | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_016208.3 | 646 | Silent Mutation | ACA,ACG | T,T 179 | NP_057292.1 | |
NM_183057.2 | 646 | Silent Mutation | ACA,ACG | T,T 179 | NP_898880.1 | |
XM_005272323.3 | 646 | Silent Mutation | ACA,ACG | T,T 162 | XP_005272380.1 | |
XM_005272324.3 | 646 | Silent Mutation | ACA,ACG | T,T 162 | XP_005272381.1 | |
XM_005272325.3 | 646 | Silent Mutation | ACA,ACG | T,T 141 | XP_005272382.1 | |
XM_011517099.1 | 646 | Silent Mutation | ACA,ACG | T,T 141 | XP_011515401.1 | |
XM_011517100.1 | 646 | Silent Mutation | ACA,ACG | T,T 141 | XP_011515402.1 | |
XM_017013529.1 | 646 | Silent Mutation | ACA,ACG | T,T 141 | XP_016869018.1 |