Version: 8.0.0
Date: Tue Jan 28 2025
rs11537697
Variant overlaps PPP2R1A
Homo sapiens
SummaryVariant Molecular Consequences
Allele/Variant

rs11537697

Species
Homo sapiens
Symbol
rs11537697
Category
Variant
Variant type
SNP
Overlaps
PPP2R1A
Location
19:52212981
Nucleotide Change
G>A
Most Severe Consequence
  • synonymous variant
See all consequences
HGVS.g name
  • NC_000019.10:g.52212981G>A
HGVS.c name
  • ENSEMBL:ENST00000322088.11:c.678G>A
  • ENSEMBL:ENST00000454220.7:c.798G>A
HGVS.p name
  • ENSP00000324804:p.Glu226=
  • ENSP00000391905:p.Glu266=
Synonyms
Not Available
Notes
Not Available
Cross references
Not Available
References
Not Available
Genome location
Assembly version
Not Available
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Variant Molecular Consequences

Sequence feature
Sequence feature type
Associated gene
Location
Molecular consequence
Codon and amino acid change
ENSEMBL:ENST00000322088.11
protein_codingPPP2R1AExon 6/15
  • synonymous variant
676gaGN/A
[226]EN/A
=>
gaA
E
ENSEMBL:ENST00000454220.7
protein_codingPPP2R1AExon 6/15
  • synonymous variant
796gaGN/A
[266]EN/A
=>
gaA
E
ENSEMBL:ENST00000462047.1
transcriptPPP2R1AExon 2/3
  • non coding transcript exon variant
ENSEMBL:ENST00000462990.5
protein_codingPPP2R1AExon 6/15
  • synonymous variant
139gaGN/A
[47]EN/A
=>
gaA
E
ENSEMBL:ENST00000473820.1
transcriptPPP2R1AExon 1/5
  • non coding transcript exon variant
ENSEMBL:ENST00000703395.1
protein_codingPPP2R1AExon 6/15
  • synonymous variant
139gaGN/A
[47]EN/A
=>
gaA
E
ENSEMBL:ENST00000703397.1
protein_codingPPP2R1AExon 7/16
  • synonymous variant
139gaGN/A
[47]EN/A
=>
gaA
E
ENSEMBL:ENST00000703398.1
protein_codingPPP2R1AExon 6/15
  • synonymous variant
718gaGN/A
[240]EN/A
=>
gaA
E
ENSEMBL:ENST00000703421.1
transcriptPPP2R1AExon 5/5
  • non coding transcript exon variant
ENSEMBL:ENST00000703422.1
protein_codingPPP2R1AExon 6/15
  • synonymous variant
652gaGN/A
[218]EN/A
=>
gaA
E
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