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CTTTGAAGGGAGACGGGATCCTCAT[C/T]GTCGTCAACACAGTGGGTGCTGCGC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
2 submissions
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Phenotype: |
MIM: 605951 MIM: 191164 MIM: 613683 | ||||||||||||||||||||
Literature Links: |
DPM3 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 |
DPM3 - dolichyl-phosphate mannosyltransferase subunit 3 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
EFNA1 - ephrin A1 | ||||||
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There are no transcripts associated with this gene. |
SLC50A1 - solute carrier family 50 member 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001122837.1 | 213 | Intron | NP_001116309.1 | |||
NM_001122839.1 | 213 | Silent Mutation | ATC,ATT | I,I 70 | NP_001116311.1 | |
NM_001287586.1 | 213 | Silent Mutation | ATC,ATT | I,I 24 | NP_001274515.1 | |
NM_001287587.1 | 213 | Silent Mutation | ATC,ATT | I,I 63 | NP_001274516.1 | |
NM_001287588.1 | 213 | Intron | NP_001274517.1 | |||
NM_001287589.1 | 213 | Intron | NP_001274518.1 | |||
NM_001287590.1 | 213 | Intron | NP_001274519.1 | |||
NM_001287591.1 | 213 | Silent Mutation | ATC,ATT | I,I 38 | NP_001274520.1 | |
NM_001287592.1 | 213 | Intron | NP_001274521.1 | |||
NM_018845.3 | 213 | Silent Mutation | ATC,ATT | I,I 70 | NP_061333.2 | |
XM_005245339.4 | 213 | Silent Mutation | ATC,ATT | I,I 54 | XP_005245396.1 | |
XM_005245340.3 | 213 | Silent Mutation | ATC,ATT | I,I 53 | XP_005245397.1 | |
XM_005245341.4 | 213 | Silent Mutation | ATC,ATT | I,I 38 | XP_005245398.1 | |
XM_005245342.3 | 213 | Silent Mutation | ATC,ATT | I,I 38 | XP_005245399.1 | |
XM_006711453.2 | 213 | Silent Mutation | ATC,ATT | I,I 70 | XP_006711516.1 |