Product Details
- SNP ID
-
rs78395865
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.17:63524301 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CCCAACACACCAAGCAGCGCCGTGT[C/T]CCGCCTAGCGCAGGCCCTGCTGGGG
- Phenotype
-
MIM: 608168
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
KCNH6
PubMed Links
Gene Details
- Gene
- KCNH6
- Gene Name
- potassium voltage-gated channel subfamily H member 6
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001278919.1 |
319 |
Missense Mutation |
TCC,TTC |
S80F |
NP_001265848.1 |
NM_001278920.1 |
319 |
Intron |
|
|
NP_001265849.1 |
NM_030779.3 |
319 |
Missense Mutation |
TCC,TTC |
S80F |
NP_110406.1 |
NM_173092.2 |
319 |
Missense Mutation |
TCC,TTC |
S80F |
NP_775115.1 |
XM_011525308.2 |
319 |
Missense Mutation |
TCC,TTC |
S80F |
XP_011523610.1 |
XM_011525309.2 |
319 |
Missense Mutation |
TCC,TTC |
S80F |
XP_011523611.1 |
XM_011525310.2 |
319 |
Missense Mutation |
TCC,TTC |
S80F |
XP_011523612.1 |
XM_011525311.1 |
319 |
Missense Mutation |
TCC,TTC |
S80F |
XP_011523613.1 |
XM_011525312.1 |
319 |
Missense Mutation |
TCC,TTC |
S80F |
XP_011523614.1 |
XM_011525313.1 |
319 |
Missense Mutation |
TCC,TTC |
S80F |
XP_011523615.1 |
XM_017025175.1 |
319 |
Missense Mutation |
TCC,TTC |
S80F |
XP_016880664.1 |
XM_017025176.1 |
319 |
Missense Mutation |
TCC,TTC |
S80F |
XP_016880665.1 |
XM_017025177.1 |
319 |
Missense Mutation |
TCC,TTC |
S80F |
XP_016880666.1 |
XM_017025178.1 |
319 |
Missense Mutation |
TCC,TTC |
S80F |
XP_016880667.1 |
XM_017025179.1 |
319 |
Missense Mutation |
TCC,TTC |
S80F |
XP_016880668.1 |
XM_017025180.1 |
319 |
Intron |
|
|
XP_016880669.1 |
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