Product Details
- SNP ID
-
rs138189929
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.X:130005292 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CAACTGGACCAGTTCTGACCGGATT[C/T]GCATGTGTGGCATCAACGAGGAGAG
- Phenotype
-
MIM: 300688
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
BCORL1
PubMed Links
Gene Details
- Gene
- BCORL1
- Gene Name
- BCL6 corepressor-like 1
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001184772.2 |
606 |
Missense Mutation |
CGC,TGC |
R21C |
NP_001171701.1 |
NM_021946.4 |
606 |
Missense Mutation |
CGC,TGC |
R21C |
NP_068765.3 |
XM_005262452.4 |
606 |
Missense Mutation |
CGC,TGC |
R21C |
XP_005262509.2 |
XM_005262453.4 |
606 |
Missense Mutation |
CGC,TGC |
R21C |
XP_005262510.2 |
XM_005262454.3 |
606 |
Missense Mutation |
CGC,TGC |
R21C |
XP_005262511.2 |
XM_005262455.4 |
606 |
Missense Mutation |
CGC,TGC |
R21C |
XP_005262512.2 |
XM_005262456.4 |
606 |
Missense Mutation |
CGC,TGC |
R21C |
XP_005262513.2 |
XM_006724776.3 |
606 |
Missense Mutation |
CGC,TGC |
R21C |
XP_006724839.1 |
XM_006724777.3 |
606 |
Missense Mutation |
CGC,TGC |
R21C |
XP_006724840.1 |
XM_006724779.2 |
606 |
UTR 5 |
|
|
XP_006724842.1 |
XM_017029721.1 |
606 |
Missense Mutation |
CGC,TGC |
R21C |
XP_016885210.1 |
XM_017029722.1 |
606 |
Missense Mutation |
CGC,TGC |
R21C |
XP_016885211.1 |
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