Product Details
- SNP ID
-
rs278981
- Assay Type
- Validated
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.4:40425993 on Build GRCh38
- Set Membership
-
HapMap
Validated
- Context Sequence [VIC/FAM]
- ATGTAGCCTGCGTATCCTCCATACA[T/C]GGCGGCCGCGGCTGCCGCGTTCTTC
- Phenotype
-
- Polymorphism
- T/C, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
RBM47
PubMed Links
Gene Details
- Gene
- RBM47
- Gene Name
- RNA binding motif protein 47
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001098634.1 |
2524 |
Missense Mutation |
ATG,GTG |
M565V |
NP_001092104.1 |
NM_019027.3 |
2524 |
Missense Mutation |
ATG,GTG |
M496V |
NP_061900.2 |
XM_005248103.3 |
2524 |
Missense Mutation |
ATG,GTG |
M565V |
XP_005248160.1 |
XM_005248107.3 |
2524 |
Missense Mutation |
ATG,GTG |
M565V |
XP_005248164.1 |
XM_005248108.3 |
2524 |
Missense Mutation |
ATG,GTG |
M565V |
XP_005248165.1 |
XM_005248109.4 |
2524 |
Missense Mutation |
ATG,GTG |
M565V |
XP_005248166.1 |
XM_011513704.2 |
2524 |
Missense Mutation |
ATG,GTG |
M565V |
XP_011512006.1 |
XM_011513707.2 |
2524 |
Missense Mutation |
ATG,GTG |
M565V |
XP_011512009.1 |
XM_011513708.2 |
2524 |
Missense Mutation |
ATG,GTG |
M565V |
XP_011512010.1 |
XM_017008304.1 |
2524 |
Missense Mutation |
ATG,GTG |
M565V |
XP_016863793.1 |
XM_017008305.1 |
2524 |
Missense Mutation |
ATG,GTG |
M565V |
XP_016863794.1 |
XM_017008306.1 |
2524 |
Missense Mutation |
ATG,GTG |
M565V |
XP_016863795.1 |
XM_017008307.1 |
2524 |
Missense Mutation |
ATG,GTG |
M565V |
XP_016863796.1 |
XM_017008308.1 |
2524 |
Missense Mutation |
ATG,GTG |
M565V |
XP_016863797.1 |
XM_017008309.1 |
2524 |
Missense Mutation |
ATG,GTG |
M564V |
XP_016863798.1 |
XM_017008310.1 |
2524 |
Missense Mutation |
ATG,GTG |
M496V |
XP_016863799.1 |
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