Product Details
- SNP ID
-
rs1035442
- Assay Type
- Validated
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.19:8851305 on Build GRCh38
- Set Membership
-
HapMap
Validated
- Context Sequence [VIC/FAM]
- ACACCGCAGATCAGGCATGTGATGA[G/C]TCCCAGGAGTCCTGCCAAGCCGATG
- Phenotype
-
MIM: 607963
MIM: 606154
- Polymorphism
- G/C, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
MBD3L1
PubMed Links
Gene Details
- Gene
- MBD3L1
- Gene Name
- methyl-CpG binding domain protein 3 like 1
There are no transcripts associated with this gene.
- Gene
- MUC16
- Gene Name
- mucin 16, cell surface associated
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_024690.2 |
33467 |
Missense Mutation |
CTC,GTC |
L14466V |
NP_078966.2 |
XM_017027486.1 |
33467 |
Missense Mutation |
CTC,GTC |
L14216V |
XP_016882975.1 |
XM_017027487.1 |
33467 |
Missense Mutation |
CTC,GTC |
L14194V |
XP_016882976.1 |
XM_017027488.1 |
33467 |
Missense Mutation |
CTC,GTC |
L14187V |
XP_016882977.1 |
XM_017027489.1 |
33467 |
Missense Mutation |
CTC,GTC |
L14176V |
XP_016882978.1 |
XM_017027490.1 |
33467 |
Missense Mutation |
CTC,GTC |
L14061V |
XP_016882979.1 |
XM_017027491.1 |
33467 |
Missense Mutation |
CTC,GTC |
L14061V |
XP_016882980.1 |
XM_017027492.1 |
33467 |
Missense Mutation |
CTC,GTC |
L14060V |
XP_016882981.1 |
XM_017027493.1 |
33467 |
Missense Mutation |
CTC,GTC |
L14060V |
XP_016882982.1 |
XM_017027494.1 |
33467 |
Missense Mutation |
CTC,GTC |
L14060V |
XP_016882983.1 |
XM_017027495.1 |
33467 |
Missense Mutation |
CTC,GTC |
L14060V |
XP_016882984.1 |
XM_017027496.1 |
33467 |
Missense Mutation |
CTC,GTC |
L13593V |
XP_016882985.1 |
XM_017027497.1 |
33467 |
Missense Mutation |
CTC,GTC |
L13435V |
XP_016882986.1 |
XM_017027498.1 |
33467 |
Intron |
|
|
XP_016882987.1 |
XM_017027499.1 |
33467 |
Missense Mutation |
CTC,GTC |
L11145V |
XP_016882988.1 |
XM_017027500.1 |
33467 |
Missense Mutation |
CTC,GTC |
L11118V |
XP_016882989.1 |
XM_017027501.1 |
33467 |
Missense Mutation |
CTC,GTC |
L1774V |
XP_016882990.1 |
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