Product Details
- SNP ID
-
rs141100250
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.3:105659153 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TTTCCAATGCCGCCTCAGGCCCATG[A/G]GGTTTTCTGTGGTGAATTTCTGGTG
- Phenotype
-
MIM: 604491
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
CBLB
PubMed Links
Gene Details
- Gene
- CBLB
- Gene Name
- Cbl proto-oncogene B
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001321786.1 |
2652 |
Silent Mutation |
CCC,CCT |
P950P |
NP_001308715.1 |
NM_001321788.1 |
2652 |
Silent Mutation |
CCC,CCT |
P922P |
NP_001308717.1 |
NM_001321789.1 |
2652 |
Silent Mutation |
CCC,CCT |
P901P |
NP_001308718.1 |
NM_001321790.1 |
2652 |
Silent Mutation |
CCC,CCT |
P900P |
NP_001308719.1 |
NM_001321791.1 |
2652 |
Silent Mutation |
CCC,CCT |
P878P |
NP_001308720.1 |
NM_001321793.1 |
2652 |
Silent Mutation |
CCC,CCT |
P878P |
NP_001308722.1 |
NM_001321794.1 |
2652 |
Silent Mutation |
CCC,CCT |
P873P |
NP_001308723.1 |
NM_001321795.1 |
2652 |
Silent Mutation |
CCC,CCT |
P873P |
NP_001308724.1 |
NM_001321796.1 |
2652 |
Silent Mutation |
CCC,CCT |
P873P |
NP_001308725.1 |
NM_001321797.1 |
2652 |
Silent Mutation |
CCC,CCT |
P829P |
NP_001308726.1 |
NM_001321798.1 |
2652 |
Silent Mutation |
CCC,CCT |
P829P |
NP_001308727.1 |
NM_001321799.1 |
2652 |
Silent Mutation |
CCC,CCT |
P829P |
NP_001308728.1 |
NM_001321806.1 |
2652 |
Silent Mutation |
CCC,CCT |
P662P |
NP_001308735.1 |
NM_001321807.1 |
2652 |
Silent Mutation |
CCC,CCT |
P662P |
NP_001308736.1 |
NM_001321808.1 |
2652 |
Silent Mutation |
CCC,CCT |
P618P |
NP_001308737.1 |
NM_001321811.1 |
2652 |
Silent Mutation |
CCC,CCT |
P613P |
NP_001308740.1 |
NM_001321813.1 |
2652 |
Silent Mutation |
CCC,CCT |
P613P |
NP_001308742.1 |
NM_001321816.1 |
2652 |
Silent Mutation |
CCC,CCT |
P569P |
NP_001308745.1 |
NM_001321820.1 |
2652 |
Silent Mutation |
CCC,CCT |
P482P |
NP_001308749.1 |
NM_001321822.1 |
2652 |
Silent Mutation |
CCC,CCT |
P479P |
NP_001308751.1 |
NM_170662.4 |
2652 |
Silent Mutation |
CCC,CCT |
P922P |
NP_733762.2 |
XM_011513257.1 |
2652 |
Silent Mutation |
CCC,CCT |
P922P |
XP_011511559.1 |
XM_011513259.2 |
2652 |
Intron |
|
|
XP_011511561.2 |
XM_017007395.1 |
2652 |
Silent Mutation |
CCC,CCT |
P944P |
XP_016862884.1 |
XM_017007396.1 |
2652 |
Silent Mutation |
CCC,CCT |
P906P |
XP_016862885.1 |
XM_017007397.1 |
2652 |
Silent Mutation |
CCC,CCT |
P901P |
XP_016862886.1 |
XM_017007398.1 |
2652 |
Silent Mutation |
CCC,CCT |
P895P |
XP_016862887.1 |
XM_017007399.1 |
2652 |
Silent Mutation |
CCC,CCT |
P873P |
XP_016862888.1 |
XM_017007400.1 |
2652 |
Silent Mutation |
CCC,CCT |
P857P |
XP_016862889.1 |
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