ClinVar

NM_001145308.4(LRTOMT):c.-602G>A

Gene:

LRTOMT:leucine rich transmembrane and O-methyltransferase domain containing [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

11q13.4

Genomic location:

• Chr11: 72080605 (on Assembly GRCh38)
• Chr11: 71791651 (on Assembly GRCh37)

Preferred name:

NM_001145308.4(LRTOMT):c.-602G>A

HGVS:

• NC_000011.10:g.72080605G>A
• NG_021423.1:g.5270G>A
• NG_123420.1:g.753G>A
• NM_001145307.4:c.-420G>A
• NM_001145308.4:c.-602G>A
• NM_001145309.3:c.-823G>A
• NM_001145310.3:c.-823G>A
• NM_001205138.3:c.-337G>A
• NM_001271471.2:c.-420G>A
• NM_001286561.1:c.-348C>T
• NM_001318803.1:c.-377G>A
• NM_006185.3:c.-250C>T
• NM_145309.5:c.-420G>A
• NC_000011.9:g.71791651G>A
• NR_026886.3:n.275G>A
• NR_134858.1:n.275G>A

This HGVS expression did not pass validation

Links:

dbSNP: rs111537544

NCBI 1000 Genomes Browser:

rs111537544