Product Details

SNP ID
rs200208681
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:47169399 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTGGGGAGAACCGCAGCCGAGACCA[C/T]GACTACCGGGACATGGACTACCGTT
Phenotype
MIM: 300080
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
RBM10 PubMed Links

Gene Details

Gene
RBM10
Gene Name
RNA binding motif protein 10
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001204466.1 264 Silent Mutation CAC,CAT H34H NP_001191395.1
NM_001204467.1 264 Silent Mutation CAC,CAT H34H NP_001191396.1
NM_001204468.1 264 Silent Mutation CAC,CAT H99H NP_001191397.1
NM_005676.4 264 Silent Mutation CAC,CAT H34H NP_005667.2
NM_152856.2 264 Silent Mutation CAC,CAT H34H NP_690595.1
XM_005272677.4 264 Silent Mutation CAC,CAT H99H XP_005272734.1
XM_005272678.4 264 Silent Mutation CAC,CAT H99H XP_005272735.1
XM_005272679.4 264 Silent Mutation CAC,CAT H99H XP_005272736.1
XM_006724563.1 264 UTR 5 XP_006724626.1
XM_011543989.2 264 Intron XP_011542291.1
XM_017029884.1 264 UTR 5 XP_016885373.1
XM_017029885.1 264 UTR 5 XP_016885374.1

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