Product Details
- SNP ID
-
rs200511054
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.19:41848851 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CCCCGGAAGCCTCGCCCTTGTCCTG[G/T]ACTCCGGTGCCTCCTGGCCCTTGGG
- Phenotype
-
MIM: 614806
- Polymorphism
- G/T, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
DMRTC2
PubMed Links
Gene Details
- Gene
- DMRTC2
- Gene Name
- DMRT like family C2
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_001040283.2 |
609 |
Missense Mutation |
TGG,TGT |
W168C |
NP_001035373.1 |
| XM_011527214.1 |
609 |
Missense Mutation |
TGG,TGT |
W45C |
XP_011525516.1 |
| XM_011527215.1 |
609 |
Missense Mutation |
TGG,TGT |
W45C |
XP_011525517.1 |
| XM_011527216.2 |
609 |
Missense Mutation |
GAC,TAC |
D187Y |
XP_011525518.1 |
| XM_017027123.1 |
609 |
Missense Mutation |
TGG,TGT |
W173C |
XP_016882612.1 |
| XM_017027124.1 |
609 |
Missense Mutation |
TGG,TGT |
W171C |
XP_016882613.1 |
| XM_017027125.1 |
609 |
Missense Mutation |
TGG,TGT |
W168C |
XP_016882614.1 |
| XM_017027126.1 |
609 |
Missense Mutation |
TGG,TGT |
W168C |
XP_016882615.1 |
| XM_017027127.1 |
609 |
Missense Mutation |
TGG,TGT |
W168C |
XP_016882616.1 |
| XM_017027128.1 |
609 |
Missense Mutation |
TGG,TGT |
W168C |
XP_016882617.1 |
| XM_017027129.1 |
609 |
Missense Mutation |
TGG,TGT |
W173C |
XP_016882618.1 |
- Gene
- LYPD4
- Gene Name
- LY6/PLAUR domain containing 4
There are no transcripts associated with this gene.
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