Product Details
- SNP ID
-
rs143701895
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.7:8113989 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CAGCATCAGGATTTGAGAGTGGGTC[C/G]AGGTCAGCGAAGAGGCTGAACCAGG
- Phenotype
-
MIM: 147625
- Polymorphism
- C/G, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
ICA1
PubMed Links
Gene Details
- Gene
- ICA1
- Gene Name
- islet cell autoantigen 1
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001136020.2 |
1592 |
Silent Mutation |
CTC,CTG |
L462L |
NP_001129492.1 |
NM_001276478.1 |
1592 |
Silent Mutation |
CTC,CTG |
L461L |
NP_001263407.1 |
NM_004968.3 |
1592 |
Silent Mutation |
CTC,CTG |
L462L |
NP_004959.2 |
NM_022307.2 |
1592 |
Silent Mutation |
CTC,CTG |
L462L |
NP_071682.1 |
XM_005249735.3 |
1592 |
Silent Mutation |
CTC,CTG |
L461L |
XP_005249792.1 |
XM_011515345.1 |
1592 |
Silent Mutation |
CTC,CTG |
L491L |
XP_011513647.1 |
XM_011515346.1 |
1592 |
Silent Mutation |
CTC,CTG |
L491L |
XP_011513648.1 |
XM_011515347.2 |
1592 |
Silent Mutation |
CTC,CTG |
L491L |
XP_011513649.1 |
XM_011515348.1 |
1592 |
Silent Mutation |
CTC,CTG |
L491L |
XP_011513650.1 |
XM_011515349.1 |
1592 |
Silent Mutation |
CTC,CTG |
L491L |
XP_011513651.1 |
XM_011515350.1 |
1592 |
Silent Mutation |
CTC,CTG |
L490L |
XP_011513652.1 |
XM_011515351.1 |
1592 |
Silent Mutation |
CTC,CTG |
L490L |
XP_011513653.1 |
XM_011515352.1 |
1592 |
Silent Mutation |
CTC,CTG |
L490L |
XP_011513654.1 |
XM_011515353.2 |
1592 |
Silent Mutation |
CTC,CTG |
L490L |
XP_011513655.1 |
XM_011515354.1 |
1592 |
Silent Mutation |
CTC,CTG |
L417L |
XP_011513656.1 |
XM_011515355.2 |
1592 |
Silent Mutation |
CTC,CTG |
L282L |
XP_011513657.1 |
XM_011515356.2 |
1592 |
Silent Mutation |
CTC,CTG |
L282L |
XP_011513658.1 |
XM_011515357.2 |
1592 |
Silent Mutation |
CTC,CTG |
L265L |
XP_011513659.1 |
XM_017012116.1 |
1592 |
Silent Mutation |
CTC,CTG |
L490L |
XP_016867605.1 |
XM_017012117.1 |
1592 |
Silent Mutation |
CTC,CTG |
L462L |
XP_016867606.1 |
XM_017012118.1 |
1592 |
Silent Mutation |
CTC,CTG |
L462L |
XP_016867607.1 |
XM_017012119.1 |
1592 |
Silent Mutation |
CTC,CTG |
L461L |
XP_016867608.1 |
XM_017012120.1 |
1592 |
Silent Mutation |
CTC,CTG |
L461L |
XP_016867609.1 |
XM_017012121.1 |
1592 |
Silent Mutation |
CTC,CTG |
L461L |
XP_016867610.1 |
XM_017012122.1 |
1592 |
Silent Mutation |
CTC,CTG |
L388L |
XP_016867611.1 |
XM_017012123.1 |
1592 |
Silent Mutation |
CTC,CTG |
L388L |
XP_016867612.1 |
XM_017012124.1 |
1592 |
Silent Mutation |
CTC,CTG |
L388L |
XP_016867613.1 |
XM_017012125.1 |
1592 |
Silent Mutation |
CTC,CTG |
L388L |
XP_016867614.1 |
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