ClinVar

NM_002617.4(PEX10):c.279C>T (p.Gly93=)

Gene:

PEX10:peroxisomal biogenesis factor 10 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

1p36.32

Genomic location:

• Chr1: 2408773 (on Assembly GRCh38)
• Chr1: 2340212 (on Assembly GRCh37)

Preferred name:

NM_002617.4(PEX10):c.279C>T (p.Gly93=)

HGVS:

• NC_000001.11:g.2408773G>A
• NG_008342.1:g.8799C>T
• NM_001374425.1:c.279C>T
• NM_001374426.1:c.-154C>T
• NM_001374427.1:c.-154C>T
• NM_002617.4:c.279C>TMANE SELECT
• NM_153818.2:c.279C>T
• NP_001361354.1:p.Gly93=
• NP_002608.1:p.Gly93=
• NP_722540.1:p.Gly93=
• NP_722540.1:p.Gly93=
• NC_000001.10:g.2340212G>A
• NM_153818.1:c.279C>T
• NR_164636.1:n.398C>T

This HGVS expression did not pass validation

Links:

dbSNP: rs1143016

NCBI 1000 Genomes Browser:

rs1143016

Molecular consequence:

• NM_001374426.1:c.-154C>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
• NM_001374427.1:c.-154C>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
• NR_164636.1:n.398C>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]
• NM_001374425.1:c.279C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_002617.4:c.279C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_153818.2:c.279C>T - synonymous variant - [Sequence Ontology: SO:0001819]