Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TGCCAGAAGACTGCAACTAAAAAAC[A/G]GAAGACTTTTGATTCAAGCAGACAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 146660 | ||||||||||||||||||||
Literature Links: |
IL7 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 |
IL7 - interleukin 7 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000880.3 | 239 | Intron | NP_000871.1 | |||
NM_001199886.1 | 239 | Intron | NP_001186815.1 | |||
NM_001199887.1 | 239 | Intron | NP_001186816.1 | |||
NM_001199888.1 | 239 | Intron | NP_001186817.1 | |||
XM_011517522.2 | 239 | Intron | XP_011515824.1 | |||
XM_011517523.2 | 239 | Intron | XP_011515825.1 | |||
XM_017013397.1 | 239 | Intron | XP_016868886.1 |
ZC2HC1A - zinc finger C2HC-type containing 1A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_016010.2 | 239 | Missense Mutation | CAG,CGG | Q,R 46 | NP_057094.2 | |
XM_005251256.1 | 239 | Missense Mutation | CAG,CGG | Q,R 46 | XP_005251313.1 | |
XM_006716454.2 | 239 | Missense Mutation | CAG,CGG | Q,R 46 | XP_006716517.1 | |
XM_011517539.2 | 239 | Missense Mutation | CAG,CGG | Q,R 46 | XP_011515841.1 |