ClinVar

NM_001135155.3(DPF1):c.-35C>A

Genes:

LOC130064339:ATAC-STARR-seq lymphoblastoid silent region 10563 [Gene]
DPF1:double PHD fingers 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

19q13.2

Genomic location:

• Chr19: 38224177 (on Assembly GRCh38)
• Chr19: 38714817 (on Assembly GRCh37)

Preferred name:

NM_001135155.3(DPF1):c.-35C>A

HGVS:

• NC_000019.10:g.38224177G>T
• NG_198756.1:g.291G>T
• NM_001135155.3:c.-35C>AMANE SELECT
• NM_001135156.3:c.-131-1474C>A
• NM_001289978.2:c.-35C>A
• NM_001363579.1:c.33-1469C>A
• NM_004647.4:c.-35C>A
• NC_000019.9:g.38714817G>T
• NM_001135155.1:c.47C>A

This HGVS expression did not pass validation

Molecular consequence:

• NM_001135155.3:c.-35C>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
• NM_001289978.2:c.-35C>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
• NM_004647.4:c.-35C>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
• NM_001135156.3:c.-131-1474C>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_001363579.1:c.33-1469C>A - intron variant - [Sequence Ontology: SO:0001627]