ClinVar

NM_001195610.2(DCDC2):c.-97-408C>G

Genes:

DCDC2:doublecortin domain containing 2 [Gene - OMIM - HGNC]
KAAG1:kidney associated DCDC2 antisense RNA 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

6p22.3

Genomic location:

• Chr6: 24358255 (on Assembly GRCh38)
• Chr6: 24358483 (on Assembly GRCh37)

Preferred name:

NM_001195610.2(DCDC2):c.-97-408C>G

HGVS:

• NC_000006.12:g.24358255G>C
• NG_012829.2:g.30038C>G
• NM_001195610.2:c.-97-408C>G
• NC_000006.11:g.24358483G>C
• NR_174942.1:n.1353G>C

This HGVS expression did not pass validation

Links:

dbSNP: rs1277349

NCBI 1000 Genomes Browser:

rs1277349

Molecular consequence:

• NM_001195610.2:c.-97-408C>G - intron variant - [Sequence Ontology: SO:0001627]
• NR_174942.1:n.1353G>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]