ClinVar

NM_003981.4(PRC1):c.282G>A (p.Thr94=)

Genes:

PRC1-AS1:PRC1 antisense RNA 1 [Gene - HGNC]
PRC1:protein regulator of cytokinesis 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

15q26.1

Genomic location:

• Chr15: 90981967 (on Assembly GRCh38)
• Chr15: 91525197 (on Assembly GRCh37)

Preferred name:

NM_003981.4(PRC1):c.282G>A (p.Thr94=)

HGVS:

• NC_000015.10:g.90981967C>T
• NG_050647.1:g.17685G>A
• NM_001267580.2:c.159G>A
• NM_003981.4:c.282G>AMANE SELECT
• NM_199413.3:c.282G>A
• NP_001254509.2:p.Thr53=
• NP_003972.2:p.Thr94=
• NP_955445.2:p.Thr94=
• NC_000015.9:g.91525197C>T
• NR_051984.1:n.323C>T

This HGVS expression did not pass validation

Links:

dbSNP: rs2301826

NCBI 1000 Genomes Browser:

rs2301826

Molecular consequence:

• NR_051984.1:n.323C>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]
• NM_001267580.2:c.159G>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_003981.4:c.282G>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_199413.3:c.282G>A - synonymous variant - [Sequence Ontology: SO:0001819]