Product Details
- SNP ID
-
rs145926889
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.11:18728985 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GCTTTTCGTAGAGGCTCATGACGTG[A/G]TGCACAAACTGGTACTGCTCGCATG
- Phenotype
-
MIM: 176879
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
IGSF22
PubMed Links
Gene Details
- Gene
- IGSF22
- Gene Name
- immunoglobulin superfamily member 22
There are no transcripts associated with this gene.
- Gene
- PTPN5
- Gene Name
- protein tyrosine phosphatase, non-receptor type 5
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001039970.1 |
2816 |
Silent Mutation |
CAC,CAT |
H517H |
NP_001035059.1 |
NM_001278236.1 |
2816 |
Silent Mutation |
CAC,CAT |
H517H |
NP_001265165.1 |
NM_001278238.1 |
2816 |
Silent Mutation |
CAC,CAT |
H525H |
NP_001265167.1 |
NM_001278239.1 |
2816 |
Silent Mutation |
CAC,CAT |
H493H |
NP_001265168.1 |
NM_006906.1 |
2816 |
Silent Mutation |
CAC,CAT |
H549H |
NP_008837.1 |
NM_032781.3 |
2816 |
Silent Mutation |
CAC,CAT |
H549H |
NP_116170.3 |
XM_011520411.2 |
2816 |
UTR 3 |
|
|
XP_011518713.1 |
XM_017018434.1 |
2816 |
Missense Mutation |
CCA,TCA |
P496S |
XP_016873923.1 |
XM_017018435.1 |
2816 |
Missense Mutation |
CCA,TCA |
P496S |
XP_016873924.1 |
XM_017018436.1 |
2816 |
Missense Mutation |
CCA,TCA |
P472S |
XP_016873925.1 |
XM_017018437.1 |
2816 |
Missense Mutation |
CCA,TCA |
P464S |
XP_016873926.1 |
XM_017018438.1 |
2816 |
Missense Mutation |
CCA,TCA |
P457S |
XP_016873927.1 |
XM_017018439.1 |
2816 |
Missense Mutation |
CCA,TCA |
P440S |
XP_016873928.1 |
XM_017018440.1 |
2816 |
Silent Mutation |
CAC,CAT |
H511H |
XP_016873929.1 |
XM_017018441.1 |
2816 |
Intron |
|
|
XP_016873930.1 |
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