Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GTGGCATCTGGGGCCTCTTCTGAAA[A/G]GCAGTCATCAACTGGGTCCAGCAGG
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 142704 MIM: 603247 | |||||||||||||||||||||||||||||||||||||||||
Literature Links: |
HDC PubMed Links | |||||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | ||||||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | ||||||
EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | ||||||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | ||||||
EUR
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AMR
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HDC - histidine decarboxylase | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001306146.1 | 1868 | Missense Mutation | CTT,TTT | L,F 520 | NP_001293075.1 | |
NM_002112.3 | 1868 | Missense Mutation | CTT,TTT | L,F 553 | NP_002103.2 | |
XM_017022094.1 | 1868 | Missense Mutation | CTT,TTT | L,F 588 | XP_016877583.1 | |
XM_017022095.1 | 1868 | Missense Mutation | CTT,TTT | L,F 555 | XP_016877584.1 | |
XM_017022096.1 | 1868 | Missense Mutation | CTT,TTT | L,F 512 | XP_016877585.1 | |
XM_017022097.1 | 1868 | Missense Mutation | CTT,TTT | L,F 509 | XP_016877586.1 | |
XM_017022098.1 | 1868 | Missense Mutation | CTT,TTT | L,F 444 | XP_016877587.1 | |
XM_017022099.1 | 1868 | Intron | XP_016877588.1 |
SLC27A2 - solute carrier family 27 member 2 | ||||||
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There are no transcripts associated with this gene. |
Set Membership: |
HapMap |