dbSNP Short Genetic Variations
Welcome to the Reference SNP (rs) Report
All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.
Reference SNP (rs) Report
This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.
rs1469284538
Current Build 156
Released September 21, 2022
- Organism
- Homo sapiens
- Position
-
chr10:77637601 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
- Alleles
- G>A / G>C
- Variation Type
- SNV Single Nucleotide Variation
- Frequency
-
A=0.000004 (1/264690, TOPMED)A=0.000007 (1/139208, GnomAD)A=0.00009 (1/10680, ALFA)
- Clinical Significance
- Not Reported in ClinVar
- Gene : Consequence
- KCNMA1 : Synonymous Variant
- Publications
- 0 citations
- Genomic View
- See rs on genome
ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.
Release Version: 20231103111315
| Population | Group | Sample Size | Ref Allele | Alt Allele | Ref HMOZ | Alt HMOZ | HTRZ | HWEP |
|---|---|---|---|---|---|---|---|---|
| Total | Global | 10680 | G=0.99991 | A=0.00009 | 0.999813 | 0.0 | 0.000187 | 0 |
| European | Sub | 6962 | G=0.9999 | A=0.0001 | 0.999713 | 0.0 | 0.000287 | 0 |
| African | Sub | 2294 | G=1.0000 | A=0.0000 | 1.0 | 0.0 | 0.0 | N/A |
| African Others | Sub | 84 | G=1.00 | A=0.00 | 1.0 | 0.0 | 0.0 | N/A |
| African American | Sub | 2210 | G=1.0000 | A=0.0000 | 1.0 | 0.0 | 0.0 | N/A |
| Asian | Sub | 108 | G=1.000 | A=0.000 | 1.0 | 0.0 | 0.0 | N/A |
| East Asian | Sub | 84 | G=1.00 | A=0.00 | 1.0 | 0.0 | 0.0 | N/A |
| Other Asian | Sub | 24 | G=1.00 | A=0.00 | 1.0 | 0.0 | 0.0 | N/A |
| Latin American 1 | Sub | 146 | G=1.000 | A=0.000 | 1.0 | 0.0 | 0.0 | N/A |
| Latin American 2 | Sub | 610 | G=1.000 | A=0.000 | 1.0 | 0.0 | 0.0 | N/A |
| South Asian | Sub | 94 | G=1.00 | A=0.00 | 1.0 | 0.0 | 0.0 | N/A |
| Other | Sub | 466 | G=1.000 | A=0.000 | 1.0 | 0.0 | 0.0 | N/A |
Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").
Download| Study | Population | Group | Sample Size | Ref Allele | Alt Allele |
|---|---|---|---|---|---|
| TopMed | Global | Study-wide | 264690 | G=0.999996 | A=0.000004 |
| gnomAD - Genomes | Global | Study-wide | 139208 | G=0.999993 | A=0.000007 |
| gnomAD - Genomes | European | Sub | 75430 | G=0.99999 | A=0.00001 |
| gnomAD - Genomes | African | Sub | 41636 | G=1.00000 | A=0.00000 |
| gnomAD - Genomes | American | Sub | 13576 | G=1.00000 | A=0.00000 |
| gnomAD - Genomes | Ashkenazi Jewish | Sub | 3300 | G=1.0000 | A=0.0000 |
| gnomAD - Genomes | East Asian | Sub | 3116 | G=1.0000 | A=0.0000 |
| gnomAD - Genomes | Other | Sub | 2150 | G=1.0000 | A=0.0000 |
| Allele Frequency Aggregator | Total | Global | 10680 | G=0.99991 | A=0.00009 |
| Allele Frequency Aggregator | European | Sub | 6962 | G=0.9999 | A=0.0001 |
| Allele Frequency Aggregator | African | Sub | 2294 | G=1.0000 | A=0.0000 |
| Allele Frequency Aggregator | Latin American 2 | Sub | 610 | G=1.000 | A=0.000 |
| Allele Frequency Aggregator | Other | Sub | 466 | G=1.000 | A=0.000 |
| Allele Frequency Aggregator | Latin American 1 | Sub | 146 | G=1.000 | A=0.000 |
| Allele Frequency Aggregator | Asian | Sub | 108 | G=1.000 | A=0.000 |
| Allele Frequency Aggregator | South Asian | Sub | 94 | G=1.00 | A=0.00 |
Help
Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.
Genomic Placements
| Sequence name | Change |
|---|---|
| GRCh38.p14 chr 10 | NC_000010.11:g.77637601G>A |
| GRCh38.p14 chr 10 | NC_000010.11:g.77637601G>C |
| GRCh37.p13 chr 10 | NC_000010.10:g.79397359G>A |
| GRCh37.p13 chr 10 | NC_000010.10:g.79397359G>C |
| KCNMA1 RefSeqGene | NG_012270.1:g.5219C>T |
| KCNMA1 RefSeqGene | NG_012270.1:g.5219C>G |
Gene: KCNMA1, potassium calcium-activated channel subfamily M alpha 1
(minus strand)
| Molecule type | Change | Amino acid[Codon] | SO Term |
|---|---|---|---|
| KCNMA1 transcript variant 16 | NM_001322838.2:c. | N/A | Genic Upstream Transcript Variant |
| KCNMA1 transcript variant 3 | NM_001161352.2:c.42C>T | G [GGC] > G [GGT] | Coding Sequence Variant |
| Calcium-activated potassium channel subunit alpha-1 isoform c | NP_001154824.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant 3 | NM_001161352.2:c.42C>G | G [GGC] > G [GGG] | Coding Sequence Variant |
| Calcium-activated potassium channel subunit alpha-1 isoform c | NP_001154824.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant 4 | NM_001161353.2:c.42C>T | G [GGC] > G [GGT] | Coding Sequence Variant |
| Calcium-activated potassium channel subunit alpha-1 isoform d | NP_001154825.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant 4 | NM_001161353.2:c.42C>G | G [GGC] > G [GGG] | Coding Sequence Variant |
| Calcium-activated potassium channel subunit alpha-1 isoform d | NP_001154825.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant 14 | NM_001322836.2:c.42C>T | G [GGC] > G [GGT] | Coding Sequence Variant |
| Calcium-activated potassium channel subunit alpha-1 isoform k | NP_001309765.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant 14 | NM_001322836.2:c.42C>G | G [GGC] > G [GGG] | Coding Sequence Variant |
| Calcium-activated potassium channel subunit alpha-1 isoform k | NP_001309765.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant 17 | NM_001322839.2:c.42C>T | G [GGC] > G [GGT] | Coding Sequence Variant |
| Calcium-activated potassium channel subunit alpha-1 isoform short4 | NP_001309768.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant 17 | NM_001322839.2:c.42C>G | G [GGC] > G [GGG] | Coding Sequence Variant |
| Calcium-activated potassium channel subunit alpha-1 isoform short4 | NP_001309768.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant 6 | NM_001271519.2:c.42C>T | G [GGC] > G [GGT] | Coding Sequence Variant |
| Calcium-activated potassium channel subunit alpha-1 isoform f | NP_001258448.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant 6 | NM_001271519.2:c.42C>G | G [GGC] > G [GGG] | Coding Sequence Variant |
| Calcium-activated potassium channel subunit alpha-1 isoform f | NP_001258448.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant 12 | NM_001322832.2:c.42C>T | G [GGC] > G [GGT] | Coding Sequence Variant |
| Calcium-activated potassium channel subunit alpha-1 isoform i | NP_001309761.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant 12 | NM_001322832.2:c.42C>G | G [GGC] > G [GGG] | Coding Sequence Variant |
| Calcium-activated potassium channel subunit alpha-1 isoform i | NP_001309761.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant 15 | NM_001322837.2:c.42C>T | G [GGC] > G [GGT] | Coding Sequence Variant |
| Calcium-activated potassium channel subunit alpha-1 isoform l | NP_001309766.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant 15 | NM_001322837.2:c.42C>G | G [GGC] > G [GGG] | Coding Sequence Variant |
| Calcium-activated potassium channel subunit alpha-1 isoform l | NP_001309766.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant 9 | NM_001271522.2:c.42C>T | G [GGC] > G [GGT] | Coding Sequence Variant |
| Calcium-activated potassium channel subunit alpha-1 isoform short3 | NP_001258451.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant 9 | NM_001271522.2:c.42C>G | G [GGC] > G [GGG] | Coding Sequence Variant |
| Calcium-activated potassium channel subunit alpha-1 isoform short3 | NP_001258451.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant 13 | NM_001322835.2:c.42C>T | G [GGC] > G [GGT] | Coding Sequence Variant |
| Calcium-activated potassium channel subunit alpha-1 isoform j | NP_001309764.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant 13 | NM_001322835.2:c.42C>G | G [GGC] > G [GGG] | Coding Sequence Variant |
| Calcium-activated potassium channel subunit alpha-1 isoform j | NP_001309764.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant 1 | NM_001014797.3:c.42C>T | G [GGC] > G [GGT] | Coding Sequence Variant |
| Calcium-activated potassium channel subunit alpha-1 isoform a | NP_001014797.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant 1 | NM_001014797.3:c.42C>G | G [GGC] > G [GGG] | Coding Sequence Variant |
| Calcium-activated potassium channel subunit alpha-1 isoform a | NP_001014797.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant 8 | NM_001271521.2:c.42C>T | G [GGC] > G [GGT] | Coding Sequence Variant |
| Calcium-activated potassium channel subunit alpha-1 isoform short2 | NP_001258450.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant 8 | NM_001271521.2:c.42C>G | G [GGC] > G [GGG] | Coding Sequence Variant |
| Calcium-activated potassium channel subunit alpha-1 isoform short2 | NP_001258450.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant 2 | NM_002247.4:c.42C>T | G [GGC] > G [GGT] | Coding Sequence Variant |
| Calcium-activated potassium channel subunit alpha-1 isoform b | NP_002238.2:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant 2 | NM_002247.4:c.42C>G | G [GGC] > G [GGG] | Coding Sequence Variant |
| Calcium-activated potassium channel subunit alpha-1 isoform b | NP_002238.2:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant 5 | NM_001271518.2:c.42C>T | G [GGC] > G [GGT] | Coding Sequence Variant |
| Calcium-activated potassium channel subunit alpha-1 isoform e | NP_001258447.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant 5 | NM_001271518.2:c.42C>G | G [GGC] > G [GGG] | Coding Sequence Variant |
| Calcium-activated potassium channel subunit alpha-1 isoform e | NP_001258447.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant 7 | NM_001271520.2:c.42C>T | G [GGC] > G [GGT] | Coding Sequence Variant |
| Calcium-activated potassium channel subunit alpha-1 isoform short1 | NP_001258449.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant 7 | NM_001271520.2:c.42C>G | G [GGC] > G [GGG] | Coding Sequence Variant |
| Calcium-activated potassium channel subunit alpha-1 isoform short1 | NP_001258449.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant 11 | NM_001322830.2:c.42C>T | G [GGC] > G [GGT] | Coding Sequence Variant |
| Calcium-activated potassium channel subunit alpha-1 isoform h | NP_001309759.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant 11 | NM_001322830.2:c.42C>G | G [GGC] > G [GGG] | Coding Sequence Variant |
| Calcium-activated potassium channel subunit alpha-1 isoform h | NP_001309759.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant 10 | NM_001322829.2:c.42C>T | G [GGC] > G [GGT] | Coding Sequence Variant |
| Calcium-activated potassium channel subunit alpha-1 isoform g | NP_001309758.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant 10 | NM_001322829.2:c.42C>G | G [GGC] > G [GGG] | Coding Sequence Variant |
| Calcium-activated potassium channel subunit alpha-1 isoform g | NP_001309758.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X43 | XM_017016223.1:c. | N/A | Genic Upstream Transcript Variant |
| KCNMA1 transcript variant X29 | XM_024447986.2:c. | N/A | Genic Upstream Transcript Variant |
| KCNMA1 transcript variant X30 | XM_047425200.1:c. | N/A | Genic Upstream Transcript Variant |
| KCNMA1 transcript variant X1 | XM_017016207.3:c.42C>T | G [GGC] > G [GGT] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X1 | XP_016871696.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X1 | XM_017016207.3:c.42C>G | G [GGC] > G [GGG] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X1 | XP_016871696.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X2 | XM_017016208.3:c.42C>T | G [GGC] > G [GGT] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X2 | XP_016871697.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X2 | XM_017016208.3:c.42C>G | G [GGC] > G [GGG] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X2 | XP_016871697.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X3 | XM_017016209.3:c.42C>T | G [GGC] > G [GGT] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X3 | XP_016871698.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X3 | XM_017016209.3:c.42C>G | G [GGC] > G [GGG] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X3 | XP_016871698.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X4 | XM_011539773.3:c.42C>T | G [GGC] > G [GGT] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X4 | XP_011538075.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X4 | XM_011539773.3:c.42C>G | G [GGC] > G [GGG] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X4 | XP_011538075.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X5 | XM_017016210.3:c.42C>T | G [GGC] > G [GGT] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X5 | XP_016871699.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X5 | XM_017016210.3:c.42C>G | G [GGC] > G [GGG] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X5 | XP_016871699.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X6 | XM_011539774.3:c.42C>T | G [GGC] > G [GGT] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X6 | XP_011538076.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X6 | XM_011539774.3:c.42C>G | G [GGC] > G [GGG] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X6 | XP_011538076.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X7 | XM_011539775.3:c.42C>T | G [GGC] > G [GGT] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X7 | XP_011538077.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X7 | XM_011539775.3:c.42C>G | G [GGC] > G [GGG] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X7 | XP_011538077.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X8 | XM_011539777.3:c.42C>T | G [GGC] > G [GGT] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X8 | XP_011538079.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X8 | XM_011539777.3:c.42C>G | G [GGC] > G [GGG] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X8 | XP_011538079.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X9 | XM_011539778.3:c.42C>T | G [GGC] > G [GGT] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X9 | XP_011538080.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X9 | XM_011539778.3:c.42C>G | G [GGC] > G [GGG] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X9 | XP_011538080.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X10 | XM_017016211.3:c.42C>T | G [GGC] > G [GGT] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X10 | XP_016871700.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X10 | XM_017016211.3:c.42C>G | G [GGC] > G [GGG] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X10 | XP_016871700.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X11 | XM_047425195.1:c.42C>T | G [GGC] > G [GGT] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X11 | XP_047281151.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X11 | XM_047425195.1:c.42C>G | G [GGC] > G [GGG] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X11 | XP_047281151.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X12 | XM_047425196.1:c.42C>T | G [GGC] > G [GGT] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X12 | XP_047281152.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X12 | XM_047425196.1:c.42C>G | G [GGC] > G [GGG] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X12 | XP_047281152.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X13 | XM_017016213.3:c.42C>T | G [GGC] > G [GGT] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X13 | XP_016871702.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X13 | XM_017016213.3:c.42C>G | G [GGC] > G [GGG] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X13 | XP_016871702.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X14 | XM_017016214.3:c.42C>T | G [GGC] > G [GGT] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X14 | XP_016871703.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X14 | XM_017016214.3:c.42C>G | G [GGC] > G [GGG] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X14 | XP_016871703.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X15 | XM_011539780.3:c.42C>T | G [GGC] > G [GGT] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X15 | XP_011538082.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X15 | XM_011539780.3:c.42C>G | G [GGC] > G [GGG] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X15 | XP_011538082.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X16 | XM_005269778.3:c.42C>T | G [GGC] > G [GGT] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X16 | XP_005269835.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X16 | XM_005269778.3:c.42C>G | G [GGC] > G [GGG] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X16 | XP_005269835.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X17 | XM_005269781.3:c.42C>T | G [GGC] > G [GGT] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X17 | XP_005269838.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X17 | XM_005269781.3:c.42C>G | G [GGC] > G [GGG] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X17 | XP_005269838.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X18 | XM_024447984.2:c.42C>T | G [GGC] > G [GGT] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X18 | XP_024303752.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X18 | XM_024447984.2:c.42C>G | G [GGC] > G [GGG] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X18 | XP_024303752.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X19 | XM_047425197.1:c.42C>T | G [GGC] > G [GGT] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X19 | XP_047281153.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X19 | XM_047425197.1:c.42C>G | G [GGC] > G [GGG] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X19 | XP_047281153.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X20 | XM_011539781.4:c.42C>T | G [GGC] > G [GGT] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X20 | XP_011538083.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X20 | XM_011539781.4:c.42C>G | G [GGC] > G [GGG] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X20 | XP_011538083.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X21 | XM_011539782.3:c.42C>T | G [GGC] > G [GGT] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X21 | XP_011538084.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X21 | XM_011539782.3:c.42C>G | G [GGC] > G [GGG] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X21 | XP_011538084.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X22 | XM_017016217.2:c.42C>T | G [GGC] > G [GGT] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X22 | XP_016871706.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X22 | XM_017016217.2:c.42C>G | G [GGC] > G [GGG] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X22 | XP_016871706.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X23 | XM_011539783.3:c.42C>T | G [GGC] > G [GGT] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X23 | XP_011538085.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X23 | XM_011539783.3:c.42C>G | G [GGC] > G [GGG] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X23 | XP_011538085.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X24 | XM_005269789.3:c.42C>T | G [GGC] > G [GGT] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X24 | XP_005269846.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X24 | XM_005269789.3:c.42C>G | G [GGC] > G [GGG] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X24 | XP_005269846.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X25 | XM_005269792.3:c.42C>T | G [GGC] > G [GGT] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X25 | XP_005269849.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X25 | XM_005269792.3:c.42C>G | G [GGC] > G [GGG] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X25 | XP_005269849.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X26 | XM_047425199.1:c.42C>T | G [GGC] > G [GGT] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X26 | XP_047281155.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X26 | XM_047425199.1:c.42C>G | G [GGC] > G [GGG] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X26 | XP_047281155.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X27 | XM_006717826.3:c.42C>T | G [GGC] > G [GGT] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X27 | XP_006717889.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X27 | XM_006717826.3:c.42C>G | G [GGC] > G [GGG] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X27 | XP_006717889.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X28 | XM_024447985.2:c.42C>T | G [GGC] > G [GGT] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X28 | XP_024303753.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X28 | XM_024447985.2:c.42C>G | G [GGC] > G [GGG] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X28 | XP_024303753.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X29 | XM_005269796.3:c.42C>T | G [GGC] > G [GGT] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X29 | XP_005269853.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X29 | XM_005269796.3:c.42C>G | G [GGC] > G [GGG] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X29 | XP_005269853.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X31 | XM_017016219.3:c.42C>T | G [GGC] > G [GGT] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X31 | XP_016871708.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X31 | XM_017016219.3:c.42C>G | G [GGC] > G [GGG] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X31 | XP_016871708.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X32 | XM_011539784.3:c.42C>T | G [GGC] > G [GGT] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X32 | XP_011538086.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X32 | XM_011539784.3:c.42C>G | G [GGC] > G [GGG] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X32 | XP_011538086.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X33 | XM_047425201.1:c.42C>T | G [GGC] > G [GGT] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X33 | XP_047281157.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X33 | XM_047425201.1:c.42C>G | G [GGC] > G [GGG] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X33 | XP_047281157.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X35 | XM_005269776.5:c.42C>T | G [GGC] > G [GGT] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X34 | XP_005269833.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X35 | XM_005269776.5:c.42C>G | G [GGC] > G [GGG] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X34 | XP_005269833.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X36 | XM_024447987.2:c.42C>T | G [GGC] > G [GGT] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X35 | XP_024303755.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X36 | XM_024447987.2:c.42C>G | G [GGC] > G [GGG] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X35 | XP_024303755.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X37 | XM_005269787.5:c.42C>T | G [GGC] > G [GGT] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X36 | XP_005269844.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X37 | XM_005269787.5:c.42C>G | G [GGC] > G [GGG] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X36 | XP_005269844.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X38 | XM_011539785.3:c.42C>T | G [GGC] > G [GGT] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X37 | XP_011538087.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X38 | XM_011539785.3:c.42C>G | G [GGC] > G [GGG] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X37 | XP_011538087.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X39 | XM_024447988.2:c.42C>T | G [GGC] > G [GGT] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X38 | XP_024303756.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X39 | XM_024447988.2:c.42C>G | G [GGC] > G [GGG] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X38 | XP_024303756.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X40 | XM_024447989.2:c.42C>T | G [GGC] > G [GGT] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X39 | XP_024303757.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X40 | XM_024447989.2:c.42C>G | G [GGC] > G [GGG] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X39 | XP_024303757.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X41 | XM_024447990.2:c.42C>T | G [GGC] > G [GGT] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X40 | XP_024303758.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X41 | XM_024447990.2:c.42C>G | G [GGC] > G [GGG] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X40 | XP_024303758.1:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X42 | XM_017016222.3:c.42C>T | G [GGC] > G [GGT] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X41 | XP_016871711.2:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X42 | XM_017016222.3:c.42C>G | G [GGC] > G [GGG] | Coding Sequence Variant |
| calcium-activated potassium channel subunit alpha-1 isoform X41 | XP_016871711.2:p.Gly14= | G (Gly) > G (Gly) | Synonymous Variant |
| KCNMA1 transcript variant X34 | XR_007061964.1:n.208C>T | N/A | Non Coding Transcript Variant |
| KCNMA1 transcript variant X34 | XR_007061964.1:n.208C>G | N/A | Non Coding Transcript Variant |
Help
Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.
Not Reported in ClinVar
Help
Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".
| Placement | G= | A | C |
|---|---|---|---|
| GRCh38.p14 chr 10 | NC_000010.11:g.77637601= | NC_000010.11:g.77637601G>A | NC_000010.11:g.77637601G>C |
| GRCh37.p13 chr 10 | NC_000010.10:g.79397359= | NC_000010.10:g.79397359G>A | NC_000010.10:g.79397359G>C |
| KCNMA1 RefSeqGene | NG_012270.1:g.5219= | NG_012270.1:g.5219C>T | NG_012270.1:g.5219C>G |
| KCNMA1 transcript variant 2 | NM_002247.4:c.42= | NM_002247.4:c.42C>T | NM_002247.4:c.42C>G |
| KCNMA1 transcript variant 2 | NM_002247.3:c.42= | NM_002247.3:c.42C>T | NM_002247.3:c.42C>G |
| KCNMA1 transcript variant 1 | NM_001014797.3:c.42= | NM_001014797.3:c.42C>T | NM_001014797.3:c.42C>G |
| KCNMA1 transcript variant 1 | NM_001014797.2:c.42= | NM_001014797.2:c.42C>T | NM_001014797.2:c.42C>G |
| KCNMA1 transcript variant 11 | NM_001322830.2:c.42= | NM_001322830.2:c.42C>T | NM_001322830.2:c.42C>G |
| KCNMA1 transcript variant 11 | NM_001322830.1:c.42= | NM_001322830.1:c.42C>T | NM_001322830.1:c.42C>G |
| KCNMA1 transcript variant 13 | NM_001322835.2:c.42= | NM_001322835.2:c.42C>T | NM_001322835.2:c.42C>G |
| KCNMA1 transcript variant 13 | NM_001322835.1:c.42= | NM_001322835.1:c.42C>T | NM_001322835.1:c.42C>G |
| KCNMA1 transcript variant 10 | NM_001322829.2:c.42= | NM_001322829.2:c.42C>T | NM_001322829.2:c.42C>G |
| KCNMA1 transcript variant 10 | NM_001322829.1:c.42= | NM_001322829.1:c.42C>T | NM_001322829.1:c.42C>G |
| KCNMA1 transcript variant 12 | NM_001322832.2:c.42= | NM_001322832.2:c.42C>T | NM_001322832.2:c.42C>G |
| KCNMA1 transcript variant 12 | NM_001322832.1:c.42= | NM_001322832.1:c.42C>T | NM_001322832.1:c.42C>G |
| KCNMA1 transcript variant 5 | NM_001271518.2:c.42= | NM_001271518.2:c.42C>T | NM_001271518.2:c.42C>G |
| KCNMA1 transcript variant 5 | NM_001271518.1:c.42= | NM_001271518.1:c.42C>T | NM_001271518.1:c.42C>G |
| KCNMA1 transcript variant 3 | NM_001161352.2:c.42= | NM_001161352.2:c.42C>T | NM_001161352.2:c.42C>G |
| KCNMA1 transcript variant 3 | NM_001161352.1:c.42= | NM_001161352.1:c.42C>T | NM_001161352.1:c.42C>G |
| KCNMA1 transcript variant 4 | NM_001161353.2:c.42= | NM_001161353.2:c.42C>T | NM_001161353.2:c.42C>G |
| KCNMA1 transcript variant 4 | NM_001161353.1:c.42= | NM_001161353.1:c.42C>T | NM_001161353.1:c.42C>G |
| KCNMA1 transcript variant 15 | NM_001322837.2:c.42= | NM_001322837.2:c.42C>T | NM_001322837.2:c.42C>G |
| KCNMA1 transcript variant 15 | NM_001322837.1:c.42= | NM_001322837.1:c.42C>T | NM_001322837.1:c.42C>G |
| KCNMA1 transcript variant 6 | NM_001271519.2:c.42= | NM_001271519.2:c.42C>T | NM_001271519.2:c.42C>G |
| KCNMA1 transcript variant 6 | NM_001271519.1:c.42= | NM_001271519.1:c.42C>T | NM_001271519.1:c.42C>G |
| KCNMA1 transcript variant 14 | NM_001322836.2:c.42= | NM_001322836.2:c.42C>T | NM_001322836.2:c.42C>G |
| KCNMA1 transcript variant 14 | NM_001322836.1:c.42= | NM_001322836.1:c.42C>T | NM_001322836.1:c.42C>G |
| KCNMA1 transcript variant 9 | NM_001271522.2:c.42= | NM_001271522.2:c.42C>T | NM_001271522.2:c.42C>G |
| KCNMA1 transcript variant 9 | NM_001271522.1:c.42= | NM_001271522.1:c.42C>T | NM_001271522.1:c.42C>G |
| KCNMA1 transcript variant 7 | NM_001271520.2:c.42= | NM_001271520.2:c.42C>T | NM_001271520.2:c.42C>G |
| KCNMA1 transcript variant 7 | NM_001271520.1:c.42= | NM_001271520.1:c.42C>T | NM_001271520.1:c.42C>G |
| KCNMA1 transcript variant 17 | NM_001322839.2:c.42= | NM_001322839.2:c.42C>T | NM_001322839.2:c.42C>G |
| KCNMA1 transcript variant 17 | NM_001322839.1:c.42= | NM_001322839.1:c.42C>T | NM_001322839.1:c.42C>G |
| KCNMA1 transcript variant 8 | NM_001271521.2:c.42= | NM_001271521.2:c.42C>T | NM_001271521.2:c.42C>G |
| KCNMA1 transcript variant 8 | NM_001271521.1:c.42= | NM_001271521.1:c.42C>T | NM_001271521.1:c.42C>G |
| KCNMA1 transcript variant 18 | NM_001410940.1:c.42= | NM_001410940.1:c.42C>T | NM_001410940.1:c.42C>G |
| KCNMA1 transcript variant X35 | XM_005269776.5:c.42= | XM_005269776.5:c.42C>T | XM_005269776.5:c.42C>G |
| KCNMA1 transcript variant X35 | XM_005269776.4:c.42= | XM_005269776.4:c.42C>T | XM_005269776.4:c.42C>G |
| KCNMA1 transcript variant X34 | XM_005269776.3:c.42= | XM_005269776.3:c.42C>T | XM_005269776.3:c.42C>G |
| KCNMA1 transcript variant X21 | XM_005269776.2:c.42= | XM_005269776.2:c.42C>T | XM_005269776.2:c.42C>G |
| KCNMA1 transcript variant X4 | XM_005269776.1:c.42= | XM_005269776.1:c.42C>T | XM_005269776.1:c.42C>G |
| KCNMA1 transcript variant X37 | XM_005269787.5:c.42= | XM_005269787.5:c.42C>T | XM_005269787.5:c.42C>G |
| KCNMA1 transcript variant X37 | XM_005269787.4:c.42= | XM_005269787.4:c.42C>T | XM_005269787.4:c.42C>G |
| KCNMA1 transcript variant X35 | XM_005269787.3:c.42= | XM_005269787.3:c.42C>T | XM_005269787.3:c.42C>G |
| KCNMA1 transcript variant X22 | XM_005269787.2:c.42= | XM_005269787.2:c.42C>T | XM_005269787.2:c.42C>G |
| KCNMA1 transcript variant X15 | XM_005269787.1:c.42= | XM_005269787.1:c.42C>T | XM_005269787.1:c.42C>G |
| KCNMA1 transcript variant X20 | XM_011539781.4:c.42= | XM_011539781.4:c.42C>T | XM_011539781.4:c.42C>G |
| KCNMA1 transcript variant X20 | XM_011539781.3:c.42= | XM_011539781.3:c.42C>T | XM_011539781.3:c.42C>G |
| KCNMA1 transcript variant X20 | XM_011539781.2:c.42= | XM_011539781.2:c.42C>T | XM_011539781.2:c.42C>G |
| KCNMA1 transcript variant X11 | XM_011539781.1:c.42= | XM_011539781.1:c.42C>T | XM_011539781.1:c.42C>G |
| KCNMA1 transcript variant X1 | XM_017016207.3:c.42= | XM_017016207.3:c.42C>T | XM_017016207.3:c.42C>G |
| KCNMA1 transcript variant X1 | XM_017016207.2:c.42= | XM_017016207.2:c.42C>T | XM_017016207.2:c.42C>G |
| KCNMA1 transcript variant X1 | XM_017016207.1:c.42= | XM_017016207.1:c.42C>T | XM_017016207.1:c.42C>G |
| KCNMA1 transcript variant X2 | XM_017016208.3:c.42= | XM_017016208.3:c.42C>T | XM_017016208.3:c.42C>G |
| KCNMA1 transcript variant X2 | XM_017016208.2:c.42= | XM_017016208.2:c.42C>T | XM_017016208.2:c.42C>G |
| KCNMA1 transcript variant X2 | XM_017016208.1:c.42= | XM_017016208.1:c.42C>T | XM_017016208.1:c.42C>G |
| KCNMA1 transcript variant X4 | XM_011539773.3:c.42= | XM_011539773.3:c.42C>T | XM_011539773.3:c.42C>G |
| KCNMA1 transcript variant X4 | XM_011539773.2:c.42= | XM_011539773.2:c.42C>T | XM_011539773.2:c.42C>G |
| KCNMA1 transcript variant X4 | XM_011539773.1:c.42= | XM_011539773.1:c.42C>T | XM_011539773.1:c.42C>G |
| KCNMA1 transcript variant X5 | XM_017016210.3:c.42= | XM_017016210.3:c.42C>T | XM_017016210.3:c.42C>G |
| KCNMA1 transcript variant X5 | XM_017016210.2:c.42= | XM_017016210.2:c.42C>T | XM_017016210.2:c.42C>G |
| KCNMA1 transcript variant X5 | XM_017016210.1:c.42= | XM_017016210.1:c.42C>T | XM_017016210.1:c.42C>G |
| KCNMA1 transcript variant X7 | XM_011539775.3:c.42= | XM_011539775.3:c.42C>T | XM_011539775.3:c.42C>G |
| KCNMA1 transcript variant X7 | XM_011539775.2:c.42= | XM_011539775.2:c.42C>T | XM_011539775.2:c.42C>G |
| KCNMA1 transcript variant X7 | XM_011539775.1:c.42= | XM_011539775.1:c.42C>T | XM_011539775.1:c.42C>G |
| KCNMA1 transcript variant X10 | XM_017016211.3:c.42= | XM_017016211.3:c.42C>T | XM_017016211.3:c.42C>G |
| KCNMA1 transcript variant X10 | XM_017016211.2:c.42= | XM_017016211.2:c.42C>T | XM_017016211.2:c.42C>G |
| KCNMA1 transcript variant X11 | XM_017016211.1:c.42= | XM_017016211.1:c.42C>T | XM_017016211.1:c.42C>G |
| KCNMA1 transcript variant X13 | XM_017016213.3:c.42= | XM_017016213.3:c.42C>T | XM_017016213.3:c.42C>G |
| KCNMA1 transcript variant X13 | XM_017016213.2:c.42= | XM_017016213.2:c.42C>T | XM_017016213.2:c.42C>G |
| KCNMA1 transcript variant X14 | XM_017016213.1:c.42= | XM_017016213.1:c.42C>T | XM_017016213.1:c.42C>G |
| KCNMA1 transcript variant X15 | XM_011539780.3:c.42= | XM_011539780.3:c.42C>T | XM_011539780.3:c.42C>G |
| KCNMA1 transcript variant X15 | XM_011539780.2:c.42= | XM_011539780.2:c.42C>T | XM_011539780.2:c.42C>G |
| KCNMA1 transcript variant X16 | XM_011539780.1:c.42= | XM_011539780.1:c.42C>T | XM_011539780.1:c.42C>G |
| KCNMA1 transcript variant X16 | XM_005269778.3:c.42= | XM_005269778.3:c.42C>T | XM_005269778.3:c.42C>G |
| KCNMA1 transcript variant X16 | XM_005269778.2:c.42= | XM_005269778.2:c.42C>T | XM_005269778.2:c.42C>G |
| KCNMA1 transcript variant X17 | XM_005269778.1:c.42= | XM_005269778.1:c.42C>T | XM_005269778.1:c.42C>G |
| KCNMA1 transcript variant X17 | XM_005269781.3:c.42= | XM_005269781.3:c.42C>T | XM_005269781.3:c.42C>G |
| KCNMA1 transcript variant X18 | XM_005269781.2:c.42= | XM_005269781.2:c.42C>T | XM_005269781.2:c.42C>G |
| KCNMA1 transcript variant X10 | XM_005269781.1:c.42= | XM_005269781.1:c.42C>T | XM_005269781.1:c.42C>G |
| KCNMA1 transcript variant X24 | XM_005269789.3:c.42= | XM_005269789.3:c.42C>T | XM_005269789.3:c.42C>G |
| KCNMA1 transcript variant X24 | XM_005269789.2:c.42= | XM_005269789.2:c.42C>T | XM_005269789.2:c.42C>G |
| KCNMA1 transcript variant X14 | XM_005269789.1:c.42= | XM_005269789.1:c.42C>T | XM_005269789.1:c.42C>G |
| KCNMA1 transcript variant X38 | XM_011539785.3:c.42= | XM_011539785.3:c.42C>T | XM_011539785.3:c.42C>G |
| KCNMA1 transcript variant X38 | XM_011539785.2:c.42= | XM_011539785.2:c.42C>T | XM_011539785.2:c.42C>G |
| KCNMA1 transcript variant X36 | XM_011539785.1:c.42= | XM_011539785.1:c.42C>T | XM_011539785.1:c.42C>G |
| KCNMA1 transcript variant X25 | XM_005269792.3:c.42= | XM_005269792.3:c.42C>T | XM_005269792.3:c.42C>G |
| KCNMA1 transcript variant X25 | XM_005269792.2:c.42= | XM_005269792.2:c.42C>T | XM_005269792.2:c.42C>G |
| KCNMA1 transcript variant X15 | XM_005269792.1:c.42= | XM_005269792.1:c.42C>T | XM_005269792.1:c.42C>G |
| KCNMA1 transcript variant X29 | XM_005269796.3:c.42= | XM_005269796.3:c.42C>T | XM_005269796.3:c.42C>G |
| KCNMA1 transcript variant X42 | XM_017016222.3:c.42= | XM_017016222.3:c.42C>T | XM_017016222.3:c.42C>G |
| KCNMA1 transcript variant X42 | XM_017016222.2:c.42= | XM_017016222.2:c.42C>T | XM_017016222.2:c.42C>G |
| KCNMA1 transcript variant X37 | XM_017016222.1:c.42= | XM_017016222.1:c.42C>T | XM_017016222.1:c.42C>G |
| KCNMA1 transcript variant X31 | XM_017016219.3:c.42= | XM_017016219.3:c.42C>T | XM_017016219.3:c.42C>G |
| KCNMA1 transcript variant X31 | XM_017016219.2:c.42= | XM_017016219.2:c.42C>T | XM_017016219.2:c.42C>G |
| KCNMA1 transcript variant X30 | XM_017016219.1:c.42= | XM_017016219.1:c.42C>T | XM_017016219.1:c.42C>G |
| KCNMA1 transcript variant X3 | XM_017016209.3:c.42= | XM_017016209.3:c.42C>T | XM_017016209.3:c.42C>G |
| KCNMA1 transcript variant X3 | XM_017016209.2:c.42= | XM_017016209.2:c.42C>T | XM_017016209.2:c.42C>G |
| KCNMA1 transcript variant X3 | XM_017016209.1:c.42= | XM_017016209.1:c.42C>T | XM_017016209.1:c.42C>G |
| KCNMA1 transcript variant X6 | XM_011539774.3:c.42= | XM_011539774.3:c.42C>T | XM_011539774.3:c.42C>G |
| KCNMA1 transcript variant X6 | XM_011539774.2:c.42= | XM_011539774.2:c.42C>T | XM_011539774.2:c.42C>G |
| KCNMA1 transcript variant X6 | XM_011539774.1:c.42= | XM_011539774.1:c.42C>T | XM_011539774.1:c.42C>G |
| KCNMA1 transcript variant X8 | XM_011539777.3:c.42= | XM_011539777.3:c.42C>T | XM_011539777.3:c.42C>G |
| KCNMA1 transcript variant X8 | XM_011539777.2:c.42= | XM_011539777.2:c.42C>T | XM_011539777.2:c.42C>G |
| KCNMA1 transcript variant X9 | XM_011539777.1:c.42= | XM_011539777.1:c.42C>T | XM_011539777.1:c.42C>G |
| KCNMA1 transcript variant X9 | XM_011539778.3:c.42= | XM_011539778.3:c.42C>T | XM_011539778.3:c.42C>G |
| KCNMA1 transcript variant X9 | XM_011539778.2:c.42= | XM_011539778.2:c.42C>T | XM_011539778.2:c.42C>G |
| KCNMA1 transcript variant X6 | XM_011539778.1:c.42= | XM_011539778.1:c.42C>T | XM_011539778.1:c.42C>G |
| KCNMA1 transcript variant X14 | XM_017016214.3:c.42= | XM_017016214.3:c.42C>T | XM_017016214.3:c.42C>G |
| KCNMA1 transcript variant X14 | XM_017016214.2:c.42= | XM_017016214.2:c.42C>T | XM_017016214.2:c.42C>G |
| KCNMA1 transcript variant X15 | XM_017016214.1:c.42= | XM_017016214.1:c.42C>T | XM_017016214.1:c.42C>G |
| KCNMA1 transcript variant X21 | XM_011539782.3:c.42= | XM_011539782.3:c.42C>T | XM_011539782.3:c.42C>G |
| KCNMA1 transcript variant X21 | XM_011539782.2:c.42= | XM_011539782.2:c.42C>T | XM_011539782.2:c.42C>G |
| KCNMA1 transcript variant X12 | XM_011539782.1:c.42= | XM_011539782.1:c.42C>T | XM_011539782.1:c.42C>G |
| KCNMA1 transcript variant X23 | XM_011539783.3:c.42= | XM_011539783.3:c.42C>T | XM_011539783.3:c.42C>G |
| KCNMA1 transcript variant X23 | XM_011539783.2:c.42= | XM_011539783.2:c.42C>T | XM_011539783.2:c.42C>G |
| KCNMA1 transcript variant X24 | XM_011539783.1:c.42= | XM_011539783.1:c.42C>T | XM_011539783.1:c.42C>G |
| KCNMA1 transcript variant X27 | XM_006717826.3:c.42= | XM_006717826.3:c.42C>T | XM_006717826.3:c.42C>G |
| KCNMA1 transcript variant X26 | XM_006717826.2:c.42= | XM_006717826.2:c.42C>T | XM_006717826.2:c.42C>G |
| KCNMA1 transcript variant X16 | XM_006717826.1:c.42= | XM_006717826.1:c.42C>T | XM_006717826.1:c.42C>G |
| KCNMA1 transcript variant X32 | XM_011539784.3:c.42= | XM_011539784.3:c.42C>T | XM_011539784.3:c.42C>G |
| KCNMA1 transcript variant X32 | XM_011539784.2:c.42= | XM_011539784.2:c.42C>T | XM_011539784.2:c.42C>G |
| KCNMA1 transcript variant X31 | XM_011539784.1:c.42= | XM_011539784.1:c.42C>T | XM_011539784.1:c.42C>G |
| KCNMA1 transcript variant X36 | XM_024447987.2:c.42= | XM_024447987.2:c.42C>T | XM_024447987.2:c.42C>G |
| KCNMA1 transcript variant X36 | XM_024447987.1:c.42= | XM_024447987.1:c.42C>T | XM_024447987.1:c.42C>G |
| KCNMA1 transcript variant X18 | XM_024447984.2:c.42= | XM_024447984.2:c.42C>T | XM_024447984.2:c.42C>G |
| KCNMA1 transcript variant X19 | XM_024447984.1:c.42= | XM_024447984.1:c.42C>T | XM_024447984.1:c.42C>G |
| KCNMA1 transcript variant X22 | XM_017016217.2:c.42= | XM_017016217.2:c.42C>T | XM_017016217.2:c.42C>G |
| KCNMA1 transcript variant X22 | XM_017016217.1:c.42= | XM_017016217.1:c.42C>T | XM_017016217.1:c.42C>G |
| KCNMA1 transcript variant X40 | XM_024447989.2:c.42= | XM_024447989.2:c.42C>T | XM_024447989.2:c.42C>G |
| KCNMA1 transcript variant X40 | XM_024447989.1:c.42= | XM_024447989.1:c.42C>T | XM_024447989.1:c.42C>G |
| KCNMA1 transcript variant X39 | XM_024447988.2:c.42= | XM_024447988.2:c.42C>T | XM_024447988.2:c.42C>G |
| KCNMA1 transcript variant X39 | XM_024447988.1:c.42= | XM_024447988.1:c.42C>T | XM_024447988.1:c.42C>G |
| KCNMA1 transcript variant X41 | XM_024447990.2:c.42= | XM_024447990.2:c.42C>T | XM_024447990.2:c.42C>G |
| KCNMA1 transcript variant X41 | XM_024447990.1:c.42= | XM_024447990.1:c.42C>T | XM_024447990.1:c.42C>G |
| KCNMA1 transcript variant X28 | XM_024447985.2:c.42= | XM_024447985.2:c.42C>T | XM_024447985.2:c.42C>G |
| KCNMA1 transcript variant X27 | XM_024447985.1:c.42= | XM_024447985.1:c.42C>T | XM_024447985.1:c.42C>G |
| KCNMA1 transcript variant X12 | XM_047425196.1:c.42= | XM_047425196.1:c.42C>T | XM_047425196.1:c.42C>G |
| KCNMA1 transcript variant X26 | XM_047425199.1:c.42= | XM_047425199.1:c.42C>T | XM_047425199.1:c.42C>G |
| KCNMA1 transcript variant X11 | XM_047425195.1:c.42= | XM_047425195.1:c.42C>T | XM_047425195.1:c.42C>G |
| KCNMA1 transcript variant X19 | XM_047425197.1:c.42= | XM_047425197.1:c.42C>T | XM_047425197.1:c.42C>G |
| KCNMA1 transcript variant X33 | XM_047425201.1:c.42= | XM_047425201.1:c.42C>T | XM_047425201.1:c.42C>G |
| KCNMA1 transcript variant X34 | XR_007061964.1:n.208= | XR_007061964.1:n.208C>T | XR_007061964.1:n.208C>G |
| Calcium-activated potassium channel subunit alpha-1 isoform b | NP_002238.2:p.Gly14= | NP_002238.2:p.Gly14= | NP_002238.2:p.Gly14= |
| Calcium-activated potassium channel subunit alpha-1 isoform a | NP_001014797.1:p.Gly14= | NP_001014797.1:p.Gly14= | NP_001014797.1:p.Gly14= |
| Calcium-activated potassium channel subunit alpha-1 isoform h | NP_001309759.1:p.Gly14= | NP_001309759.1:p.Gly14= | NP_001309759.1:p.Gly14= |
| Calcium-activated potassium channel subunit alpha-1 isoform j | NP_001309764.1:p.Gly14= | NP_001309764.1:p.Gly14= | NP_001309764.1:p.Gly14= |
| Calcium-activated potassium channel subunit alpha-1 isoform g | NP_001309758.1:p.Gly14= | NP_001309758.1:p.Gly14= | NP_001309758.1:p.Gly14= |
| Calcium-activated potassium channel subunit alpha-1 isoform i | NP_001309761.1:p.Gly14= | NP_001309761.1:p.Gly14= | NP_001309761.1:p.Gly14= |
| Calcium-activated potassium channel subunit alpha-1 isoform e | NP_001258447.1:p.Gly14= | NP_001258447.1:p.Gly14= | NP_001258447.1:p.Gly14= |
| Calcium-activated potassium channel subunit alpha-1 isoform c | NP_001154824.1:p.Gly14= | NP_001154824.1:p.Gly14= | NP_001154824.1:p.Gly14= |
| Calcium-activated potassium channel subunit alpha-1 isoform d | NP_001154825.1:p.Gly14= | NP_001154825.1:p.Gly14= | NP_001154825.1:p.Gly14= |
| Calcium-activated potassium channel subunit alpha-1 isoform l | NP_001309766.1:p.Gly14= | NP_001309766.1:p.Gly14= | NP_001309766.1:p.Gly14= |
| Calcium-activated potassium channel subunit alpha-1 isoform f | NP_001258448.1:p.Gly14= | NP_001258448.1:p.Gly14= | NP_001258448.1:p.Gly14= |
| Calcium-activated potassium channel subunit alpha-1 isoform k | NP_001309765.1:p.Gly14= | NP_001309765.1:p.Gly14= | NP_001309765.1:p.Gly14= |
| Calcium-activated potassium channel subunit alpha-1 isoform short3 | NP_001258451.1:p.Gly14= | NP_001258451.1:p.Gly14= | NP_001258451.1:p.Gly14= |
| Calcium-activated potassium channel subunit alpha-1 isoform short1 | NP_001258449.1:p.Gly14= | NP_001258449.1:p.Gly14= | NP_001258449.1:p.Gly14= |
| Calcium-activated potassium channel subunit alpha-1 isoform short4 | NP_001309768.1:p.Gly14= | NP_001309768.1:p.Gly14= | NP_001309768.1:p.Gly14= |
| Calcium-activated potassium channel subunit alpha-1 isoform short2 | NP_001258450.1:p.Gly14= | NP_001258450.1:p.Gly14= | NP_001258450.1:p.Gly14= |
| calcium-activated potassium channel subunit alpha-1 isoform X34 | XP_005269833.1:p.Gly14= | XP_005269833.1:p.Gly14= | XP_005269833.1:p.Gly14= |
| calcium-activated potassium channel subunit alpha-1 isoform X36 | XP_005269844.1:p.Gly14= | XP_005269844.1:p.Gly14= | XP_005269844.1:p.Gly14= |
| calcium-activated potassium channel subunit alpha-1 isoform X20 | XP_011538083.1:p.Gly14= | XP_011538083.1:p.Gly14= | XP_011538083.1:p.Gly14= |
| calcium-activated potassium channel subunit alpha-1 isoform X1 | XP_016871696.1:p.Gly14= | XP_016871696.1:p.Gly14= | XP_016871696.1:p.Gly14= |
| calcium-activated potassium channel subunit alpha-1 isoform X2 | XP_016871697.1:p.Gly14= | XP_016871697.1:p.Gly14= | XP_016871697.1:p.Gly14= |
| calcium-activated potassium channel subunit alpha-1 isoform X4 | XP_011538075.1:p.Gly14= | XP_011538075.1:p.Gly14= | XP_011538075.1:p.Gly14= |
| calcium-activated potassium channel subunit alpha-1 isoform X5 | XP_016871699.1:p.Gly14= | XP_016871699.1:p.Gly14= | XP_016871699.1:p.Gly14= |
| calcium-activated potassium channel subunit alpha-1 isoform X7 | XP_011538077.1:p.Gly14= | XP_011538077.1:p.Gly14= | XP_011538077.1:p.Gly14= |
| calcium-activated potassium channel subunit alpha-1 isoform X10 | XP_016871700.1:p.Gly14= | XP_016871700.1:p.Gly14= | XP_016871700.1:p.Gly14= |
| calcium-activated potassium channel subunit alpha-1 isoform X13 | XP_016871702.1:p.Gly14= | XP_016871702.1:p.Gly14= | XP_016871702.1:p.Gly14= |
| calcium-activated potassium channel subunit alpha-1 isoform X15 | XP_011538082.1:p.Gly14= | XP_011538082.1:p.Gly14= | XP_011538082.1:p.Gly14= |
| calcium-activated potassium channel subunit alpha-1 isoform X16 | XP_005269835.1:p.Gly14= | XP_005269835.1:p.Gly14= | XP_005269835.1:p.Gly14= |
| calcium-activated potassium channel subunit alpha-1 isoform X17 | XP_005269838.1:p.Gly14= | XP_005269838.1:p.Gly14= | XP_005269838.1:p.Gly14= |
| calcium-activated potassium channel subunit alpha-1 isoform X24 | XP_005269846.1:p.Gly14= | XP_005269846.1:p.Gly14= | XP_005269846.1:p.Gly14= |
| calcium-activated potassium channel subunit alpha-1 isoform X37 | XP_011538087.1:p.Gly14= | XP_011538087.1:p.Gly14= | XP_011538087.1:p.Gly14= |
| calcium-activated potassium channel subunit alpha-1 isoform X25 | XP_005269849.1:p.Gly14= | XP_005269849.1:p.Gly14= | XP_005269849.1:p.Gly14= |
| calcium-activated potassium channel subunit alpha-1 isoform X29 | XP_005269853.1:p.Gly14= | XP_005269853.1:p.Gly14= | XP_005269853.1:p.Gly14= |
| calcium-activated potassium channel subunit alpha-1 isoform X41 | XP_016871711.2:p.Gly14= | XP_016871711.2:p.Gly14= | XP_016871711.2:p.Gly14= |
| calcium-activated potassium channel subunit alpha-1 isoform X31 | XP_016871708.1:p.Gly14= | XP_016871708.1:p.Gly14= | XP_016871708.1:p.Gly14= |
| calcium-activated potassium channel subunit alpha-1 isoform X3 | XP_016871698.1:p.Gly14= | XP_016871698.1:p.Gly14= | XP_016871698.1:p.Gly14= |
| calcium-activated potassium channel subunit alpha-1 isoform X6 | XP_011538076.1:p.Gly14= | XP_011538076.1:p.Gly14= | XP_011538076.1:p.Gly14= |
| calcium-activated potassium channel subunit alpha-1 isoform X8 | XP_011538079.1:p.Gly14= | XP_011538079.1:p.Gly14= | XP_011538079.1:p.Gly14= |
| calcium-activated potassium channel subunit alpha-1 isoform X9 | XP_011538080.1:p.Gly14= | XP_011538080.1:p.Gly14= | XP_011538080.1:p.Gly14= |
| calcium-activated potassium channel subunit alpha-1 isoform X14 | XP_016871703.1:p.Gly14= | XP_016871703.1:p.Gly14= | XP_016871703.1:p.Gly14= |
| calcium-activated potassium channel subunit alpha-1 isoform X21 | XP_011538084.1:p.Gly14= | XP_011538084.1:p.Gly14= | XP_011538084.1:p.Gly14= |
| calcium-activated potassium channel subunit alpha-1 isoform X23 | XP_011538085.1:p.Gly14= | XP_011538085.1:p.Gly14= | XP_011538085.1:p.Gly14= |
| calcium-activated potassium channel subunit alpha-1 isoform X27 | XP_006717889.1:p.Gly14= | XP_006717889.1:p.Gly14= | XP_006717889.1:p.Gly14= |
| calcium-activated potassium channel subunit alpha-1 isoform X32 | XP_011538086.1:p.Gly14= | XP_011538086.1:p.Gly14= | XP_011538086.1:p.Gly14= |
| calcium-activated potassium channel subunit alpha-1 isoform X35 | XP_024303755.1:p.Gly14= | XP_024303755.1:p.Gly14= | XP_024303755.1:p.Gly14= |
| calcium-activated potassium channel subunit alpha-1 isoform X18 | XP_024303752.1:p.Gly14= | XP_024303752.1:p.Gly14= | XP_024303752.1:p.Gly14= |
| calcium-activated potassium channel subunit alpha-1 isoform X22 | XP_016871706.1:p.Gly14= | XP_016871706.1:p.Gly14= | XP_016871706.1:p.Gly14= |
| calcium-activated potassium channel subunit alpha-1 isoform X39 | XP_024303757.1:p.Gly14= | XP_024303757.1:p.Gly14= | XP_024303757.1:p.Gly14= |
| calcium-activated potassium channel subunit alpha-1 isoform X38 | XP_024303756.1:p.Gly14= | XP_024303756.1:p.Gly14= | XP_024303756.1:p.Gly14= |
| calcium-activated potassium channel subunit alpha-1 isoform X40 | XP_024303758.1:p.Gly14= | XP_024303758.1:p.Gly14= | XP_024303758.1:p.Gly14= |
| calcium-activated potassium channel subunit alpha-1 isoform X28 | XP_024303753.1:p.Gly14= | XP_024303753.1:p.Gly14= | XP_024303753.1:p.Gly14= |
| calcium-activated potassium channel subunit alpha-1 isoform X12 | XP_047281152.1:p.Gly14= | XP_047281152.1:p.Gly14= | XP_047281152.1:p.Gly14= |
| calcium-activated potassium channel subunit alpha-1 isoform X26 | XP_047281155.1:p.Gly14= | XP_047281155.1:p.Gly14= | XP_047281155.1:p.Gly14= |
| calcium-activated potassium channel subunit alpha-1 isoform X11 | XP_047281151.1:p.Gly14= | XP_047281151.1:p.Gly14= | XP_047281151.1:p.Gly14= |
| calcium-activated potassium channel subunit alpha-1 isoform X19 | XP_047281153.1:p.Gly14= | XP_047281153.1:p.Gly14= | XP_047281153.1:p.Gly14= |
| calcium-activated potassium channel subunit alpha-1 isoform X33 | XP_047281157.1:p.Gly14= | XP_047281157.1:p.Gly14= | XP_047281157.1:p.Gly14= |
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Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.
3 SubSNP,
5 Frequency
submissions
| No | Submitter | Submission ID | Date (Build) |
|---|---|---|---|
| 1 | GNOMAD | ss2738349969 | Nov 08, 2017 (151) |
| 2 | GNOMAD | ss4221570420 | Apr 27, 2021 (155) |
| 3 | TOPMED | ss4858470847 | Apr 27, 2021 (155) |
| 4 | gnomAD - Genomes | NC_000010.11 - 77637601 | Apr 27, 2021 (155) |
| 5 |
gnomAD - Exomes
Submission ignored due to conflicting rows: |
- | Jul 13, 2019 (153) |
| 6 |
gnomAD - Exomes
Submission ignored due to conflicting rows: |
- | Jul 13, 2019 (153) |
| 7 | TopMed | NC_000010.11 - 77637601 | Apr 27, 2021 (155) |
| 8 | ALFA | NC_000010.11 - 77637601 | Apr 27, 2021 (155) |
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History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).
Added to this RefSNP Cluster:
| Submission IDs | Observation SPDI | Canonical SPDI | Source RSIDs |
|---|---|---|---|
| ss2738349969 | NC_000010.10:79397358:G:A | NC_000010.11:77637600:G:A | (self) |
| 357278670, 74016502, 999162151, ss4221570420, ss4858470847 | NC_000010.11:77637600:G:A | NC_000010.11:77637600:G:A | (self) |
| ss2738349969 | NC_000010.10:79397358:G:C | NC_000010.11:77637600:G:C | (self) |
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Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.
No publications for rs1469284538
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The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.
Genome context:
Select flank length:
Genomic regions, transcripts, and products
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NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.
NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.