ClinVar

NM_002691.4(POLD1):c.665C>T (p.Pro222Leu)

Gene:

POLD1:DNA polymerase delta 1, catalytic subunit [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

19q13.33

Genomic location:

• Chr19: 50402280 (on Assembly GRCh38)
• Chr19: 50905537 (on Assembly GRCh37)

Preferred name:

NM_002691.4(POLD1):c.665C>T (p.Pro222Leu)

HGVS:

• NC_000019.10:g.50402280C>T
• NG_033800.1:g.22958C>T
• NM_001256849.1:c.665C>T
• NM_001308632.1:c.665C>T
• NM_002691.4:c.665C>TMANE SELECT
• NP_001243778.1:p.Pro222Leu
• NP_001295561.1:p.Pro222Leu
• NP_002682.2:p.Pro222Leu
• LRG_785t1:c.665C>T
• LRG_785t2:c.665C>T
• LRG_785:g.22958C>T
• LRG_785p1:p.Pro222Leu
• LRG_785p2:p.Pro222Leu
• NC_000019.9:g.50905537C>T
• NM_002691.2:c.665C>T
• NM_002691.3:c.665C>T
• NR_046402.2:n.710C>T

This HGVS expression did not pass validation

Protein change:

P222L

Links:

dbSNP: rs368940099

NCBI 1000 Genomes Browser:

rs368940099

Molecular consequence:

• NM_001256849.1:c.665C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_001308632.1:c.665C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_002691.4:c.665C>T - missense variant - [Sequence Ontology: SO:0001583]
• NR_046402.2:n.710C>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]