ClinVar

NM_003476.5(CSRP3):c.113-3C>T

Gene:

CSRP3:cysteine and glycine rich protein 3 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

11p15.1

Genomic location:

• Chr11: 19188307 (on Assembly GRCh38)
• Chr11: 19209854 (on Assembly GRCh37)

Preferred name:

NM_003476.5(CSRP3):c.113-3C>T

HGVS:

• NC_000011.10:g.19188307G>A
• NG_011932.2:g.27267C>T
• NM_001369404.1:c.113-1959C>T
• NM_003476.5:c.113-3C>TMANE SELECT
• LRG_440:g.27267C>T
• NC_000011.9:g.19209854G>A
• NM_003476.4:c.113-3C>T

This HGVS expression did not pass validation

Links:

dbSNP: rs1310679270

NCBI 1000 Genomes Browser:

rs1310679270

Molecular consequence:

• NM_001369404.1:c.113-1959C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_003476.5:c.113-3C>T - intron variant - [Sequence Ontology: SO:0001627]