Product Details
- SNP ID
-
rs184825626
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.11:66686104 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- ACCCGTAGCCACGAGCTCATCTCTG[C/T]CTGTGGATGGAAAGACCCTCAATCA
- Phenotype
-
MIM: 604985
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
RBM4B
PubMed Links
Gene Details
- Gene
- RBM4B
- Gene Name
- RNA binding motif protein 4B
There are no transcripts associated with this gene.
- Gene
- SPTBN2
- Gene Name
- spectrin beta, non-erythrocytic 2
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_006946.2 |
7766 |
Missense Mutation |
ACA,GCA |
T2314A |
NP_008877.1 |
| XM_005274192.4 |
7766 |
Missense Mutation |
ACA,GCA |
T2314A |
XP_005274249.1 |
| XM_005274193.3 |
7766 |
Missense Mutation |
ACA,GCA |
T2314A |
XP_005274250.1 |
| XM_006718669.3 |
7766 |
Missense Mutation |
ACA,GCA |
T2321A |
XP_006718732.1 |
| XM_006718671.3 |
7766 |
Missense Mutation |
ACA,GCA |
T2314A |
XP_006718734.1 |
| XM_011545216.2 |
7766 |
Intron |
|
|
XP_011543518.1 |
| XM_011545217.2 |
7766 |
Intron |
|
|
XP_011543519.1 |
| XM_017018174.1 |
7766 |
Missense Mutation |
ACA,GCA |
T2314A |
XP_016873663.1 |
| XM_017018175.1 |
7766 |
Missense Mutation |
ACA,GCA |
T2314A |
XP_016873664.1 |
| XM_017018176.1 |
7766 |
Missense Mutation |
ACA,GCA |
T2314A |
XP_016873665.1 |
| XM_017018177.1 |
7766 |
Missense Mutation |
ACA,GCA |
T2314A |
XP_016873666.1 |
| XM_017018178.1 |
7766 |
Missense Mutation |
ACA,GCA |
T2314A |
XP_016873667.1 |
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