Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600523 | ||||||||||||||||||||
Literature Links: |
HIGD1C 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 |
HIGD1C - HIG1 hypoxia inducible domain family member 1C | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001109619.1 | Intron | NP_001103089.1 |
SLC11A2 - solute carrier family 11 member 2 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000617.2 | Intron | NP_000608.1 | ||||
NM_001174125.1 | Intron | NP_001167596.1 | ||||
NM_001174126.1 | Intron | NP_001167597.1 | ||||
NM_001174127.1 | Intron | NP_001167598.1 | ||||
NM_001174128.1 | Intron | NP_001167599.1 | ||||
NM_001174129.1 | Intron | NP_001167600.1 | ||||
NM_001174130.1 | Intron | NP_001167601.1 |