ClinVar

NM_001110.4(ADAM10):c.1804+115T>C

Gene:

ADAM10:ADAM metallopeptidase domain 10 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

15q21.3

Genomic location:

• Chr15: 58610884 (on Assembly GRCh38)
• Chr15: 58903083 (on Assembly GRCh37)

Preferred name:

NM_001110.4(ADAM10):c.1804+115T>C

HGVS:

• NC_000015.10:g.58610884A>G
• NG_033876.2:g.143824T>C
• NM_001110.4:c.1804+115T>CMANE SELECT
• NM_001320570.2:c.1711+115T>C
• NC_000015.9:g.58903083A>G

This HGVS expression did not pass validation

Links:

dbSNP: rs2305421

NCBI 1000 Genomes Browser:

rs2305421

Molecular consequence:

• NM_001110.4:c.1804+115T>C - intron variant - [Sequence Ontology: SO:0001627]
• NM_001320570.2:c.1711+115T>C - intron variant - [Sequence Ontology: SO:0001627]