Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGGATTTGTTGTTGGAGCTGTGACT[C/T]TAGGTAACCCGCTTAATTTGTATCT
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 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001109619.1 | 1801 | Silent Mutation | CTA,TTA | L,L 76 | NP_001103089.1 | |
XM_011538649.2 | 1801 | Silent Mutation | CTA,TTA | L,L 76 | XP_011536951.1 | |
XM_017019783.1 | 1801 | Silent Mutation | CTA,TTA | L,L 124 | XP_016875272.1 | |
XM_017019784.1 | 1801 | Silent Mutation | CTA,TTA | L,L 124 | XP_016875273.1 | |
XM_017019785.1 | 1801 | Silent Mutation | CTA,TTA | L,L 84 | XP_016875274.1 |
SLC11A2 - solute carrier family 11 member 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000617.2 | 1801 | Intron | NP_000608.1 | |||
NM_001174125.1 | 1801 | Intron | NP_001167596.1 | |||
NM_001174126.1 | 1801 | Intron | NP_001167597.1 | |||
NM_001174127.1 | 1801 | Intron | NP_001167598.1 | |||
NM_001174128.1 | 1801 | Intron | NP_001167599.1 | |||
NM_001174129.1 | 1801 | Intron | NP_001167600.1 | |||
NM_001174130.1 | 1801 | Intron | NP_001167601.1 | |||
XM_005268911.3 | 1801 | Intron | XP_005268968.1 | |||
XM_005268912.4 | 1801 | Intron | XP_005268969.1 | |||
XM_011538404.2 | 1801 | Intron | XP_011536706.1 | |||
XM_011538405.2 | 1801 | Intron | XP_011536707.1 | |||
XM_017019355.1 | 1801 | Intron | XP_016874844.1 | |||
XM_017019356.1 | 1801 | Intron | XP_016874845.1 |