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TCTTATTCCAGCTTGTGACATCTCA[A/G]TGAATTTCCCATTTCCACCTAACGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612386 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FECH 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) - Not Available | |||
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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FECH - ferrochelatase | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000140.3 | 6004 | UTR 3 | NP_000131.2 | |||
NM_001012515.2 | 6004 | UTR 3 | NP_001012533.1 | |||
XM_011525881.1 | 6004 | Intron | XP_011524183.1 | |||
XM_011525882.2 | 6004 | Intron | XP_011524184.1 | |||
XM_017025614.1 | 6004 | Intron | XP_016881103.1 |