Product Details
- SNP ID
-
rs191721728
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.2:20251627 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GTGGTCCTCCAATAGGTCCTAGGTC[C/T]GGGCTATTCTTCAAATAATACTTTT
- Phenotype
-
MIM: 607205
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
PUM2
PubMed Links
Gene Details
- Gene
- PUM2
- Gene Name
- pumilio RNA binding family member 2
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001282752.1 |
3008 |
Silent Mutation |
CCA,CCG |
P995P |
NP_001269681.1 |
NM_001282790.1 |
3008 |
Silent Mutation |
CCA,CCG |
P972P |
NP_001269719.1 |
NM_001282791.1 |
3008 |
Silent Mutation |
CCA,CCG |
P916P |
NP_001269720.1 |
NM_015317.2 |
3008 |
Silent Mutation |
CCA,CCG |
P1051P |
NP_056132.1 |
XM_005262607.1 |
3008 |
Silent Mutation |
CCA,CCG |
P1053P |
XP_005262664.1 |
XM_005262609.1 |
3008 |
Silent Mutation |
CCA,CCG |
P974P |
XP_005262666.1 |
XM_005262610.1 |
3008 |
Silent Mutation |
CCA,CCG |
P972P |
XP_005262667.1 |
XM_006711973.1 |
3008 |
Silent Mutation |
CCA,CCG |
P1053P |
XP_006712036.1 |
XM_006711974.2 |
3008 |
Silent Mutation |
CCA,CCG |
P1053P |
XP_006712037.1 |
XM_006711975.2 |
3008 |
Silent Mutation |
CCA,CCG |
P997P |
XP_006712038.1 |
XM_011532719.1 |
3008 |
Silent Mutation |
CCA,CCG |
P1053P |
XP_011531021.1 |
XM_011532720.2 |
3008 |
Silent Mutation |
CCA,CCG |
P1053P |
XP_011531022.1 |
XM_011532721.2 |
3008 |
Silent Mutation |
CCA,CCG |
P1053P |
XP_011531023.1 |
XM_011532723.1 |
3008 |
Silent Mutation |
CCA,CCG |
P827P |
XP_011531025.1 |
XM_011532724.2 |
3008 |
Intron |
|
|
XP_011531026.1 |
XM_011532725.2 |
3008 |
Intron |
|
|
XP_011531027.1 |
XM_017003701.1 |
3008 |
Silent Mutation |
CCA,CCG |
P1051P |
XP_016859190.1 |
XM_017003702.1 |
3008 |
Silent Mutation |
CCA,CCG |
P1051P |
XP_016859191.1 |
XM_017003703.1 |
3008 |
Silent Mutation |
CCA,CCG |
P997P |
XP_016859192.1 |
XM_017003704.1 |
3008 |
Silent Mutation |
CCA,CCG |
P997P |
XP_016859193.1 |
XM_017003705.1 |
3008 |
Silent Mutation |
CCA,CCG |
P997P |
XP_016859194.1 |
XM_017003706.1 |
3008 |
Silent Mutation |
CCA,CCG |
P997P |
XP_016859195.1 |
XM_017003707.1 |
3008 |
Silent Mutation |
CCA,CCG |
P974P |
XP_016859196.1 |
XM_017003708.1 |
3008 |
Silent Mutation |
CCA,CCG |
P974P |
XP_016859197.1 |
XM_017003709.1 |
3008 |
Silent Mutation |
CCA,CCG |
P972P |
XP_016859198.1 |
XM_017003710.1 |
3008 |
Silent Mutation |
CCA,CCG |
P972P |
XP_016859199.1 |
XM_017003711.1 |
3008 |
Silent Mutation |
CCA,CCG |
P972P |
XP_016859200.1 |
XM_017003712.1 |
3008 |
Silent Mutation |
CCA,CCG |
P972P |
XP_016859201.1 |
XM_017003713.1 |
3008 |
Silent Mutation |
CCA,CCG |
P916P |
XP_016859202.1 |
XM_017003714.1 |
3008 |
Silent Mutation |
CCA,CCG |
P825P |
XP_016859203.1 |
XM_017003715.1 |
3008 |
Silent Mutation |
CCA,CCG |
P746P |
XP_016859204.1 |
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