ClinVar

NM_000071.3(CBS):c.1524C>T (p.Phe508=)

Gene:

CBS:cystathionine beta-synthase [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

21q22.3

Genomic location:

• Chr21: 43056831 (on Assembly GRCh38)
• Chr21: 44476941 (on Assembly GRCh37)

Preferred name:

NM_000071.3(CBS):c.1524C>T (p.Phe508=)

HGVS:

• NC_000021.9:g.43056831G>A
• NG_008938.1:g.24100C>T
• NM_000071.3:c.1524C>TMANE SELECT
• NM_001178008.3:c.1524C>T
• NM_001178009.3:c.1524C>T
• NM_001320298.2:c.1524C>T
• NM_001321072.1:c.1209C>T
• NP_000062.1:p.Phe508=
• NP_000062.1:p.Phe508=
• NP_001171479.1:p.Phe508=
• NP_001171480.1:p.Phe508=
• NP_001307227.1:p.Phe508=
• NP_001308001.1:p.Phe403=
• LRG_777t1:c.1524C>T
• LRG_777:g.24100C>T
• LRG_777p1:p.Phe508=
• NC_000021.8:g.44476941G>A
• NM_000071.2:c.1524C>T

This HGVS expression did not pass validation

Links:

dbSNP: rs748610628

NCBI 1000 Genomes Browser:

rs748610628

Molecular consequence:

• NM_000071.3:c.1524C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001178008.3:c.1524C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001178009.3:c.1524C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001320298.2:c.1524C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001321072.1:c.1209C>T - synonymous variant - [Sequence Ontology: SO:0001819]