Product Details
- SNP ID
-
rs190326991
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.19:47538304 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TTCAGGAGGCAGTCCACCAGGAACA[C/T]GGGTGACCGCAGGCGGCTCTGGTGG
- Phenotype
-
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
ZNF541
PubMed Links
Gene Details
- Gene
- ZNF541
- Gene Name
- zinc finger protein 541
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001277075.1 |
3229 |
Missense Mutation |
ATG,GTG |
M978V |
NP_001264004.1 |
XM_005259311.4 |
3229 |
Missense Mutation |
ATG,GTG |
M978V |
XP_005259368.1 |
XM_005259314.3 |
3229 |
Missense Mutation |
ATG,GTG |
M340V |
XP_005259371.1 |
XM_011527367.2 |
3229 |
Missense Mutation |
ATG,GTG |
M983V |
XP_011525669.1 |
XM_011527368.2 |
3229 |
Missense Mutation |
ATG,GTG |
M983V |
XP_011525670.1 |
XM_011527369.2 |
3229 |
Missense Mutation |
ATG,GTG |
M983V |
XP_011525671.1 |
XM_011527370.2 |
3229 |
Missense Mutation |
ATG,GTG |
M983V |
XP_011525672.1 |
XM_011527371.2 |
3229 |
Missense Mutation |
ATG,GTG |
M983V |
XP_011525673.1 |
XM_011527372.2 |
3229 |
Missense Mutation |
ATG,GTG |
M983V |
XP_011525674.1 |
XM_011527373.2 |
3229 |
Missense Mutation |
ATG,GTG |
M925V |
XP_011525675.1 |
XM_011527374.2 |
3229 |
Missense Mutation |
ATG,GTG |
M921V |
XP_011525676.1 |
XM_011527375.1 |
3229 |
Intron |
|
|
XP_011525677.1 |
XM_017027351.1 |
3229 |
Missense Mutation |
ATG,GTG |
M983V |
XP_016882840.1 |
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