ClinVar

NM_002617.4(PEX10):c.291A>G (p.Thr97=)

Gene:

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

Variant type:

single nucleotide variant

Cytogenetic location:

1p36.32

Genomic location:

• Chr1: 2408761 (on Assembly GRCh38)
• Chr1: 2340200 (on Assembly GRCh37)

Preferred name:

NM_002617.4(PEX10):c.291A>G (p.Thr97=)

HGVS:

• NC_000001.11:g.2408761T>C
• NG_008342.1:g.8811A>G
• NM_001374425.1:c.291A>G
• NM_001374426.1:c.-142A>G
• NM_001374427.1:c.-142A>G
• NM_002617.4:c.291A>GMANE SELECT
• NM_153818.2:c.291A>G
• NP_001361354.1:p.Thr97=
• NP_002608.1:p.Thr97=
• NP_722540.1:p.Thr97=
• NP_722540.1:p.Thr97=
• NC_000001.10:g.2340200T>C
• NM_153818.1:c.291A>G
• NR_164636.1:n.410A>G

This HGVS expression did not pass validation

Links:

dbSNP: rs2494598

NCBI 1000 Genomes Browser:

rs2494598

Molecular consequence:

• NM_001374426.1:c.-142A>G - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
• NM_001374427.1:c.-142A>G - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
• NR_164636.1:n.410A>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]
• NM_001374425.1:c.291A>G - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_002617.4:c.291A>G - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_153818.2:c.291A>G - synonymous variant - [Sequence Ontology: SO:0001819]