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VHL G104V (c.311G>T)
genetic variant
G104V (c.311G>T)
C.311G>T
GLY104VAL
RS869025630
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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/2428
chromosome
human chromosome 3
genomic assembly
Genome assembly GRCh37
1 reference
stated in
CIViC database
retrieved
22 January 2022
reference URL
https://civic.genome.wustl.edu/links/variants/2428
genomic start
10183842
genomic assembly
Genome assembly GRCh37
1 reference
stated in
CIViC database
retrieved
22 January 2022
reference URL
https://civic.genome.wustl.edu/links/variants/2428
genomic end
10183842
genomic assembly
Genome assembly GRCh37
1 reference
stated in
CIViC database
retrieved
22 January 2022
reference URL
https://civic.genome.wustl.edu/links/variants/2428
biological variant of
VHL
1 reference
stated in
CIViC database
retrieved
22 January 2022
reference URL
https://civic.genome.wustl.edu/links/variants/2428
Identifiers
CIViC variant ID
2428
1 reference
stated in
CIViC database
retrieved
22 January 2022
reference URL
https://civic.genome.wustl.edu/links/variants/2428
dbSNP Reference SNP number
rs869025630
1 reference
stated in
CIViC database
HGVS nomenclature
ENST00000256474.2:c.311G>T
1 reference
stated in
CIViC database
retrieved
22 January 2022
reference URL
https://civic.genome.wustl.edu/links/variants/2428
NM_000551.3:c.311G>T
1 reference
stated in
CIViC database
retrieved
22 January 2022
reference URL
https://civic.genome.wustl.edu/links/variants/2428
NP_000542.1:p.Gly104Val
1 reference
stated in
CIViC database
retrieved
22 January 2022
reference URL
https://civic.genome.wustl.edu/links/variants/2428
NC_000003.11:g.10183842G>T
1 reference
stated in
CIViC database
retrieved
22 January 2022
reference URL
https://civic.genome.wustl.edu/links/variants/2428
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