ClinVar

NM_023036.6(DNAI2):c.865-11C>T

Gene:

DNAI2:dynein axonemal intermediate chain 2 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

17q25.1

Genomic location:

• Chr17: 74301035 (on Assembly GRCh38)
• Chr17: 72297174 (on Assembly GRCh37)

Preferred name:

NM_023036.6(DNAI2):c.865-11C>T

HGVS:

• NC_000017.11:g.74301035C>T
• NG_016865.1:g.31789C>T
• NM_001172810.3:c.865-11C>T
• NM_001353167.2:c.865-11C>T
• NM_023036.6:c.865-11C>TMANE SELECT
• NC_000017.10:g.72297174C>T

This HGVS expression did not pass validation

Links:

dbSNP: rs774483437

NCBI 1000 Genomes Browser:

rs774483437

Molecular consequence:

• NM_001172810.3:c.865-11C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001353167.2:c.865-11C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_023036.6:c.865-11C>T - intron variant - [Sequence Ontology: SO:0001627]