Product Details
- SNP ID
-
rs199803769
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.2:230328793 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GAGGTGTTTCACAAGTAGCAAATGA[G/T]ATGAACCATCTTCCTGCACACAGCC
- Phenotype
-
- Polymorphism
- G/T, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
SP140L
PubMed Links
Gene Details
- Gene
- SP140L
- Gene Name
- SP140 nuclear body protein like
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001308162.1 |
146 |
Intron |
|
|
NP_001295091.1 |
NM_001308163.1 |
146 |
Intron |
|
|
NP_001295092.1 |
NM_138402.4 |
146 |
Missense Mutation |
GAG,GAT |
E23D |
NP_612411.4 |
XM_006712855.2 |
146 |
Missense Mutation |
GAG,GAT |
E23D |
XP_006712918.1 |
XM_006712856.2 |
146 |
Missense Mutation |
GAG,GAT |
E23D |
XP_006712919.1 |
XM_006712858.3 |
146 |
Intron |
|
|
XP_006712921.1 |
XM_011512190.2 |
146 |
Missense Mutation |
GAG,GAT |
E23D |
XP_011510492.1 |
XM_011512191.1 |
146 |
Missense Mutation |
GAG,GAT |
E23D |
XP_011510493.1 |
XM_017005294.1 |
146 |
Missense Mutation |
GAG,GAT |
E23D |
XP_016860783.1 |
XM_017005295.1 |
146 |
Missense Mutation |
GAG,GAT |
E23D |
XP_016860784.1 |
XM_017005296.1 |
146 |
Missense Mutation |
GAG,GAT |
E23D |
XP_016860785.1 |
XM_017005297.1 |
146 |
Intron |
|
|
XP_016860786.1 |
XM_017005298.1 |
146 |
Missense Mutation |
GAG,GAT |
E23D |
XP_016860787.1 |
XM_017005299.1 |
146 |
Intron |
|
|
XP_016860788.1 |
XM_017005300.1 |
146 |
Missense Mutation |
GAG,GAT |
E23D |
XP_016860789.1 |
XM_017005301.1 |
146 |
Missense Mutation |
GAG,GAT |
E23D |
XP_016860790.1 |
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