ClinVar

NM_152564.5(VPS13B):c.11613C>T (p.Phe3871=)

Gene:

VPS13B:vacuolar protein sorting 13 homolog B [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

8q22.2

Genomic location:

• Chr8: 99871565 (on Assembly GRCh38)
• Chr8: 100883793 (on Assembly GRCh37)

Preferred name:

NM_152564.5(VPS13B):c.11613C>T (p.Phe3871=)

HGVS:

• NC_000008.11:g.99871565C>T
• NG_007098.2:g.863300C>T
• NM_017890.5:c.11688C>T
• NM_152564.5:c.11613C>TMANE SELECT
• NP_060360.3:p.Phe3896=
• NP_060360.3:p.Phe3896=
• NP_689777.3:p.Phe3871=
• LRG_351t1:c.11688C>T
• LRG_351:g.863300C>T
• LRG_351p1:p.Phe3896=
• NC_000008.10:g.100883793C>T
• NM_017890.3:c.11688C>T
• NM_017890.4:c.11688C>T
• NP_060360.3:p.(=)

This HGVS expression did not pass validation

Links:

dbSNP: rs139436386

NCBI 1000 Genomes Browser:

rs139436386

Molecular consequence:

• NM_017890.5:c.11688C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_152564.5:c.11613C>T - synonymous variant - [Sequence Ontology: SO:0001819]

Observations:

4