ClinVar

NM_000045.4(ARG1):c.131-106C>T

Genes:

ARG1:arginase 1 [Gene - OMIM - HGNC]
MED23:mediator complex subunit 23 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

6q23.2

Genomic location:

• Chr6: 131579005 (on Assembly GRCh38)
• Chr6: 131900145 (on Assembly GRCh37)

Preferred name:

NM_000045.4(ARG1):c.131-106C>T

HGVS:

• NC_000006.12:g.131579005C>T
• NG_007086.2:g.10781C>T
• NG_031860.2:g.54219G>A
• NM_000045.4:c.131-106C>TMANE SELECT
• NM_001244438.2:c.131-82C>T
• NM_001270521.2:c.4078-4710G>A
• NM_001369020.1:c.131-106C>T
• NM_015979.4:c.4096-4710G>A
• NC_000006.11:g.131900145C>T

This HGVS expression did not pass validation

Links:

dbSNP: rs55706510

NCBI 1000 Genomes Browser:

rs55706510

Molecular consequence:

• NM_000045.4:c.131-106C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001244438.2:c.131-82C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001270521.2:c.4078-4710G>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_001369020.1:c.131-106C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_015979.4:c.4096-4710G>A - intron variant - [Sequence Ontology: SO:0001627]