Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ACATCTTTGCAGAGATGTGGAGAAG[A/C]CAGGAGGAAGTCCTTCCTAAAATAA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607030 MIM: 606951 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
GCA 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)
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EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Japanese
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JPT (Japanese)
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AFR
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Chinese
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CHB (Han Chinese)
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EUR
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AMR
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GCA - grancalcin | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
XM_005246446.2 | 362 | Intron | XP_005246503.1 | |||
XM_006712398.3 | 362 | Missense Mutation | AGA,AGC | R,S 4 | XP_006712461.1 | |
XM_006712400.3 | 362 | UTR 5 | XP_006712463.1 | |||
XM_006712401.3 | 362 | Missense Mutation | AGA,AGC | R,S 4 | XP_006712464.1 | |
XM_011510926.2 | 362 | Intron | XP_011509228.1 | |||
XM_011510927.2 | 362 | Intron | XP_011509229.1 | |||
XM_011510928.2 | 362 | Intron | XP_011509230.1 | |||
XM_017003764.1 | 362 | UTR 5 | XP_016859253.1 | |||
XM_017003765.1 | 362 | UTR 5 | XP_016859254.1 | |||
XM_017003766.1 | 362 | Intron | XP_016859255.1 | |||
XM_017003767.1 | 362 | Intron | XP_016859256.1 | |||
XM_017003768.1 | 362 | Intron | XP_016859257.1 | |||
XM_017003769.1 | 362 | Missense Mutation | AGA,AGC | R,S 4 | XP_016859258.1 |
IFIH1 - interferon induced with helicase C domain 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_022168.3 | 362 | Intron | NP_071451.2 |