Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CAGCATCAGGATTTGAGAGTGGGTC[C/G]AGGTCAGCGAAGAGGCTGAACCAGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 147625 | ||||||||||||||||||||
Literature Links: |
ICA1 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 |
ICA1 - islet cell autoantigen 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001136020.2 | 1592 | Silent Mutation | CTC,CTG | L,L 462 | NP_001129492.1 | |
NM_001276478.1 | 1592 | Silent Mutation | CTC,CTG | L,L 461 | NP_001263407.1 | |
NM_004968.3 | 1592 | Silent Mutation | CTC,CTG | L,L 462 | NP_004959.2 | |
NM_022307.2 | 1592 | Silent Mutation | CTC,CTG | L,L 462 | NP_071682.1 | |
XM_005249735.3 | 1592 | Silent Mutation | CTC,CTG | L,L 461 | XP_005249792.1 | |
XM_011515345.1 | 1592 | Silent Mutation | CTC,CTG | L,L 491 | XP_011513647.1 | |
XM_011515346.1 | 1592 | Silent Mutation | CTC,CTG | L,L 491 | XP_011513648.1 | |
XM_011515347.2 | 1592 | Silent Mutation | CTC,CTG | L,L 491 | XP_011513649.1 | |
XM_011515348.1 | 1592 | Silent Mutation | CTC,CTG | L,L 491 | XP_011513650.1 | |
XM_011515349.1 | 1592 | Silent Mutation | CTC,CTG | L,L 491 | XP_011513651.1 | |
XM_011515350.1 | 1592 | Silent Mutation | CTC,CTG | L,L 490 | XP_011513652.1 | |
XM_011515351.1 | 1592 | Silent Mutation | CTC,CTG | L,L 490 | XP_011513653.1 | |
XM_011515352.1 | 1592 | Silent Mutation | CTC,CTG | L,L 490 | XP_011513654.1 | |
XM_011515353.2 | 1592 | Silent Mutation | CTC,CTG | L,L 490 | XP_011513655.1 | |
XM_011515354.1 | 1592 | Silent Mutation | CTC,CTG | L,L 417 | XP_011513656.1 | |
XM_011515355.2 | 1592 | Silent Mutation | CTC,CTG | L,L 282 | XP_011513657.1 | |
XM_011515356.2 | 1592 | Silent Mutation | CTC,CTG | L,L 282 | XP_011513658.1 | |
XM_011515357.2 | 1592 | Silent Mutation | CTC,CTG | L,L 265 | XP_011513659.1 | |
XM_017012116.1 | 1592 | Silent Mutation | CTC,CTG | L,L 490 | XP_016867605.1 | |
XM_017012117.1 | 1592 | Silent Mutation | CTC,CTG | L,L 462 | XP_016867606.1 | |
XM_017012118.1 | 1592 | Silent Mutation | CTC,CTG | L,L 462 | XP_016867607.1 | |
XM_017012119.1 | 1592 | Silent Mutation | CTC,CTG | L,L 461 | XP_016867608.1 | |
XM_017012120.1 | 1592 | Silent Mutation | CTC,CTG | L,L 461 | XP_016867609.1 | |
XM_017012121.1 | 1592 | Silent Mutation | CTC,CTG | L,L 461 | XP_016867610.1 | |
XM_017012122.1 | 1592 | Silent Mutation | CTC,CTG | L,L 388 | XP_016867611.1 | |
XM_017012123.1 | 1592 | Silent Mutation | CTC,CTG | L,L 388 | XP_016867612.1 | |
XM_017012124.1 | 1592 | Silent Mutation | CTC,CTG | L,L 388 | XP_016867613.1 | |
XM_017012125.1 | 1592 | Silent Mutation | CTC,CTG | L,L 388 | XP_016867614.1 |