ClinVar

NM_018713.3(SLC30A10):c.*744G>T

Gene:

SLC30A10:solute carrier family 30 member 10 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

1q41

Genomic location:

• Chr1: 219914705 (on Assembly GRCh38)
• Chr1: 220088047 (on Assembly GRCh37)

Preferred name:

NM_018713.3(SLC30A10):c.*744G>T

HGVS:

• NC_000001.11:g.219914705C>A
• NG_032153.2:g.18947G>T
• NM_001376929.1:c.*744G>T
• NM_018713.3:c.*744G>TMANE SELECT
• NC_000001.10:g.220088047C>A
• NM_018713.2:c.*744G>T
• NR_046437.2:n.2357G>T
• NR_165031.1:n.2094G>T

This HGVS expression did not pass validation

Links:

dbSNP: rs2275707

NCBI 1000 Genomes Browser:

rs2275707

Molecular consequence:

• NM_001376929.1:c.*744G>T - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
• NM_018713.3:c.*744G>T - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
• NR_046437.2:n.2357G>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]
• NR_165031.1:n.2094G>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]