ClinVar

NM_019032.6(ADAMTSL4):c.1131+15G>T

Genes:

ADAMTSL4:ADAMTS like 4 [Gene - OMIM - HGNC]
ADAMTSL4-AS2:ADAMTSL4 antisense RNA 2 [Gene - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

1q21.2

Genomic location:

• Chr1: 150554137 (on Assembly GRCh38)
• Chr1: 150526613 (on Assembly GRCh37)

Preferred name:

NM_019032.6(ADAMTSL4):c.1131+15G>T

HGVS:

• NC_000001.11:g.150554137G>T
• NG_012172.1:g.9716G>T
• NM_001288607.2:c.1131+15G>T
• NM_001288608.2:c.1131+15G>T
• NM_001378596.1:c.1131+15G>T
• NM_019032.6:c.1131+15G>TMANE SELECT
• NM_025008.5:c.1131+15G>T
• NC_000001.10:g.150526613G>T

This HGVS expression did not pass validation

Molecular consequence:

• NM_001288607.2:c.1131+15G>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001288608.2:c.1131+15G>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001378596.1:c.1131+15G>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_019032.6:c.1131+15G>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_025008.5:c.1131+15G>T - intron variant - [Sequence Ontology: SO:0001627]