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PPP1R15A RS557806
genetic variant
ARG251PRO
R251P
RS557806
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Statements
instance of
missense mutation
1 reference
stated in
CIViC database
retrieved
22 January 2022
reference URL
https://civic.genome.wustl.edu/links/variants/548
Polymorphic Sequence Variant
1 reference
stated in
CIViC database
retrieved
22 January 2022
reference URL
https://civic.genome.wustl.edu/links/variants/548
chromosome
human chromosome 19
genomic assembly
Genome assembly GRCh37
1 reference
stated in
CIViC database
retrieved
22 January 2022
reference URL
https://civic.genome.wustl.edu/links/variants/548
genomic start
49377242
genomic assembly
Genome assembly GRCh37
1 reference
stated in
CIViC database
retrieved
22 January 2022
reference URL
https://civic.genome.wustl.edu/links/variants/548
genomic end
49377242
genomic assembly
Genome assembly GRCh37
1 reference
stated in
CIViC database
retrieved
22 January 2022
reference URL
https://civic.genome.wustl.edu/links/variants/548
biological variant of
PPP1R15A
1 reference
stated in
CIViC database
retrieved
22 January 2022
reference URL
https://civic.genome.wustl.edu/links/variants/548
Identifiers
CIViC variant ID
548
1 reference
stated in
CIViC database
retrieved
22 January 2022
reference URL
https://civic.genome.wustl.edu/links/variants/548
dbSNP Reference SNP number
rs557806
1 reference
stated in
CIViC database
HGVS nomenclature
NM_014330.3:c.752G>C
1 reference
stated in
CIViC database
retrieved
22 January 2022
reference URL
https://civic.genome.wustl.edu/links/variants/548
NP_055145.3:p.Arg251Pro
1 reference
stated in
CIViC database
retrieved
22 January 2022
reference URL
https://civic.genome.wustl.edu/links/variants/548
ENST00000200453.5:c.752G>C
1 reference
stated in
CIViC database
retrieved
22 January 2022
reference URL
https://civic.genome.wustl.edu/links/variants/548
NC_000019.9:g.49377242G>C
1 reference
stated in
CIViC database
retrieved
22 January 2022
reference URL
https://civic.genome.wustl.edu/links/variants/548
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