Product Details
- SNP ID
-
rs149763190
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.10:93676690 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CTTCAGATTTCTTTGAAGATGAATG[C/T]CCTGAAAAGGAAACATCATTGATTT
- Phenotype
-
MIM: 608866
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
FRA10AC1
PubMed Links
Gene Details
- Gene
- FRA10AC1
- Gene Name
- fragile site, folic acid type, rare, fra(10)(q23.3) or fra(10)(q24.2) candidate 1
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_145246.4 |
987 |
Silent Mutation |
GGA,GGG |
G263G |
NP_660289.2 |
| XM_005269515.4 |
987 |
Silent Mutation |
GGA,GGG |
G263G |
XP_005269572.1 |
| XM_005269516.4 |
987 |
Silent Mutation |
GGA,GGG |
G263G |
XP_005269573.1 |
| XM_011539259.2 |
987 |
Silent Mutation |
GGA,GGG |
G270G |
XP_011537561.1 |
| XM_011539260.2 |
987 |
Silent Mutation |
GGA,GGG |
G263G |
XP_011537562.1 |
| XM_017015656.1 |
987 |
Silent Mutation |
GGA,GGG |
G270G |
XP_016871145.1 |
| XM_017015657.1 |
987 |
Silent Mutation |
GGA,GGG |
G263G |
XP_016871146.1 |
| XM_017015658.1 |
987 |
Silent Mutation |
GGA,GGG |
G263G |
XP_016871147.1 |
| XM_017015659.1 |
987 |
Silent Mutation |
GGA,GGG |
G263G |
XP_016871148.1 |
| XM_017015660.1 |
987 |
Silent Mutation |
GGA,GGG |
G263G |
XP_016871149.1 |
| XM_017015661.1 |
987 |
Silent Mutation |
GGA,GGG |
G263G |
XP_016871150.1 |
| XM_017015662.1 |
987 |
Silent Mutation |
GGA,GGG |
G270G |
XP_016871151.1 |
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