ClinVar

NM_016356.5(DCDC2):c.426-35T>C

Gene:

DCDC2:doublecortin domain containing 2 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

6p22.3

Genomic location:

• Chr6: 24301881 (on Assembly GRCh38)
• Chr6: 24302109 (on Assembly GRCh37)

Preferred name:

NM_016356.5(DCDC2):c.426-35T>C

HGVS:

• NC_000006.12:g.24301881A>G
• NG_012829.2:g.86412T>C
• NM_001195610.2:c.426-35T>C
• NM_016356.5:c.426-35T>CMANE SELECT
• NC_000006.11:g.24302109A>G

This HGVS expression did not pass validation

Links:

dbSNP: rs75393533

NCBI 1000 Genomes Browser:

rs75393533

Molecular consequence:

• NM_001195610.2:c.426-35T>C - intron variant - [Sequence Ontology: SO:0001627]
• NM_016356.5:c.426-35T>C - intron variant - [Sequence Ontology: SO:0001627]