Product Details
- SNP ID
-
rs146054932
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.18:33852941 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CTGCAACAAGCTGTCTCACGGCATT[C/G]ATTTCAGTTGGACTCAGCTGGGGTC
- Phenotype
-
MIM: 603577
- Polymorphism
- C/G, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
NOL4
PubMed Links
Gene Details
- Gene
- NOL4
- Gene Name
- nucleolar protein 4
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001198546.1 |
1856 |
Silent Mutation |
ATC,ATG |
I542M |
NP_001185475.1 |
NM_001198547.1 |
1856 |
Silent Mutation |
ATC,ATG |
I532M |
NP_001185476.1 |
NM_001198548.1 |
1856 |
Silent Mutation |
ATC,ATG |
I504M |
NP_001185477.1 |
NM_001198549.1 |
1856 |
Silent Mutation |
ATC,ATG |
I321M |
NP_001185478.1 |
NM_001282527.1 |
1856 |
Silent Mutation |
ATC,ATG |
I387M |
NP_001269456.1 |
NM_003787.4 |
1856 |
Silent Mutation |
ATC,ATG |
I606M |
NP_003778.2 |
XM_006722563.2 |
1856 |
Silent Mutation |
ATC,ATG |
I606M |
XP_006722626.1 |
XM_006722564.2 |
1856 |
Silent Mutation |
ATC,ATG |
I468M |
XP_006722627.1 |
XM_006722565.1 |
1856 |
Silent Mutation |
ATC,ATG |
I451M |
XP_006722628.1 |
XM_011526237.1 |
1856 |
Missense Mutation |
ATC,ATG |
I606M |
XP_011524539.1 |
XM_011526238.1 |
1856 |
Silent Mutation |
ATC,ATG |
I492M |
XP_011524540.1 |
XM_011526239.2 |
1856 |
Silent Mutation |
ATC,ATG |
I451M |
XP_011524541.1 |
XM_017026052.1 |
1856 |
Silent Mutation |
ATC,ATG |
I486M |
XP_016881541.1 |
XM_017026053.1 |
1856 |
Silent Mutation |
ATC,ATG |
I451M |
XP_016881542.1 |
XM_017026054.1 |
1856 |
Silent Mutation |
ATC,ATG |
I451M |
XP_016881543.1 |
XM_017026055.1 |
1856 |
Silent Mutation |
ATC,ATG |
I387M |
XP_016881544.1 |
XM_017026056.1 |
1856 |
Silent Mutation |
ATC,ATG |
I387M |
XP_016881545.1 |
XM_017026057.1 |
1856 |
Silent Mutation |
ATC,ATG |
I355M |
XP_016881546.1 |
XM_017026058.1 |
1856 |
Silent Mutation |
ATC,ATG |
I451M |
XP_016881547.1 |
XM_017026059.1 |
1856 |
Silent Mutation |
ATC,ATG |
I321M |
XP_016881548.1 |
XM_017026060.1 |
1856 |
Silent Mutation |
ATC,ATG |
I291M |
XP_016881549.1 |
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