ClinVar

NM_144997.7(FLCN):c.1068G>T (p.Leu356=)

Gene:

FLCN:folliculin [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

17p11.2

Genomic location:

• Chr17: 17217177 (on Assembly GRCh38)
• Chr17: 17120491 (on Assembly GRCh37)

Preferred name:

NM_144997.7(FLCN):c.1068G>T (p.Leu356=)

HGVS:

• NC_000017.11:g.17217177C>A
• NG_008001.2:g.25012G>T
• NM_001353229.2:c.1122G>T
• NM_001353230.2:c.1068G>T
• NM_001353231.2:c.1068G>T
• NM_144997.7:c.1068G>TMANE SELECT
• NP_001340158.1:p.Leu374=
• NP_001340159.1:p.Leu356=
• NP_001340160.1:p.Leu356=
• NP_659434.2:p.Leu356=
• LRG_325t1:c.1068G>T
• LRG_325:g.25012G>T
• NC_000017.10:g.17120491C>A
• NM_144997.5:c.1068G>T

This HGVS expression did not pass validation

Links:

dbSNP: rs534904034

NCBI 1000 Genomes Browser:

rs534904034

Molecular consequence:

• NM_001353229.2:c.1122G>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001353230.2:c.1068G>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001353231.2:c.1068G>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_144997.7:c.1068G>T - synonymous variant - [Sequence Ontology: SO:0001819]