Product Details
- SNP ID
-
rs148255294
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.14:22901824 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GACCCTGAGACTCACATGGTCTGGG[A/G]GGTAAAGAGGCTGGAGAGCTGGAAA
- Phenotype
-
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
RBM23
PubMed Links
Gene Details
- Gene
- RBM23
- Gene Name
- RNA binding motif protein 23
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001077351.1 |
1585 |
Missense Mutation |
CCC,TCC |
P436S |
NP_001070819.1 |
NM_001077352.1 |
1585 |
Missense Mutation |
CCC,TCC |
P402S |
NP_001070820.1 |
NM_001308044.1 |
1585 |
Missense Mutation |
CCC,TCC |
P266S |
NP_001294973.1 |
NM_018107.4 |
1585 |
Missense Mutation |
CCC,TCC |
P420S |
NP_060577.3 |
XM_011536890.2 |
1585 |
Missense Mutation |
CCC,TCC |
P480S |
XP_011535192.1 |
XM_011536892.2 |
1585 |
Missense Mutation |
CCC,TCC |
P464S |
XP_011535194.1 |
XM_011536893.2 |
1585 |
Missense Mutation |
CCC,TCC |
P464S |
XP_011535195.1 |
XM_011536894.2 |
1585 |
Missense Mutation |
CCC,TCC |
P462S |
XP_011535196.1 |
XM_011536895.2 |
1585 |
Missense Mutation |
CCC,TCC |
P446S |
XP_011535197.1 |
XM_011536896.2 |
1585 |
Missense Mutation |
CCC,TCC |
P446S |
XP_011535198.1 |
XM_011536897.2 |
1585 |
Missense Mutation |
CCC,TCC |
P438S |
XP_011535199.1 |
XM_011536900.1 |
1585 |
Missense Mutation |
CCC,TCC |
P418S |
XP_011535202.1 |
XM_011536902.1 |
1585 |
Missense Mutation |
CCC,TCC |
P266S |
XP_011535204.1 |
XM_011536903.1 |
1585 |
Missense Mutation |
CCC,TCC |
P266S |
XP_011535205.1 |
XM_011536904.1 |
1585 |
Missense Mutation |
CCC,TCC |
P266S |
XP_011535206.1 |
XM_011536905.1 |
1585 |
Missense Mutation |
CCC,TCC |
P266S |
XP_011535207.1 |
XM_011536906.1 |
1585 |
Missense Mutation |
CCC,TCC |
P266S |
XP_011535208.1 |
XM_017021398.1 |
1585 |
Missense Mutation |
CCC,TCC |
P496S |
XP_016876887.1 |
XM_017021399.1 |
1585 |
Missense Mutation |
CCC,TCC |
P478S |
XP_016876888.1 |
XM_017021400.1 |
1585 |
Missense Mutation |
CCC,TCC |
P470S |
XP_016876889.1 |
XM_017021401.1 |
1585 |
Missense Mutation |
CCC,TCC |
P468S |
XP_016876890.1 |
XM_017021402.1 |
1585 |
Missense Mutation |
CCC,TCC |
P468S |
XP_016876891.1 |
XM_017021403.1 |
1585 |
Missense Mutation |
CCC,TCC |
P452S |
XP_016876892.1 |
XM_017021404.1 |
1585 |
Missense Mutation |
CCC,TCC |
P452S |
XP_016876893.1 |
XM_017021405.1 |
1585 |
Missense Mutation |
CCC,TCC |
P450S |
XP_016876894.1 |
XM_017021406.1 |
1585 |
Missense Mutation |
CCC,TCC |
P454S |
XP_016876895.1 |
XM_017021407.1 |
1585 |
Missense Mutation |
CCC,TCC |
P436S |
XP_016876896.1 |
XM_017021408.1 |
1585 |
Missense Mutation |
CCC,TCC |
P434S |
XP_016876897.1 |
XM_017021409.1 |
1585 |
Missense Mutation |
CCC,TCC |
P436S |
XP_016876898.1 |
XM_017021410.1 |
1585 |
Missense Mutation |
CCC,TCC |
P402S |
XP_016876899.1 |
XM_017021411.1 |
1585 |
Missense Mutation |
CCC,TCC |
P420S |
XP_016876900.1 |
XM_017021412.1 |
1585 |
Intron |
|
|
XP_016876901.1 |
XM_017021413.1 |
1585 |
Intron |
|
|
XP_016876902.1 |
XM_017021414.1 |
1585 |
Missense Mutation |
CCC,TCC |
P298S |
XP_016876903.1 |
XM_017021415.1 |
1585 |
Missense Mutation |
CCC,TCC |
P298S |
XP_016876904.1 |
XM_017021416.1 |
1585 |
Missense Mutation |
CCC,TCC |
P298S |
XP_016876905.1 |
XM_017021417.1 |
1585 |
Missense Mutation |
CCC,TCC |
P298S |
XP_016876906.1 |
XM_017021418.1 |
1585 |
Missense Mutation |
CCC,TCC |
P298S |
XP_016876907.1 |
XM_017021419.1 |
1585 |
Missense Mutation |
CCC,TCC |
P298S |
XP_016876908.1 |
XM_017021420.1 |
1585 |
Missense Mutation |
CCC,TCC |
P266S |
XP_016876909.1 |
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