ClinVar

NM_001012631.1(IL32):c.114+13C>T

Gene:

IL32:interleukin 32 [Gene - OMIM]

Variant type:

single nucleotide variant

Cytogenetic location:

16p13.3

Genomic location:

• Chr16: 3067626 (on Assembly GRCh38)
• Chr16: 3117627 (on Assembly GRCh37)
• Chr16: 3057628 (on Assembly NCBI36)

Preferred name:

NM_001012631.1(IL32):c.114+13C>T

HGVS:

• NC_000016.10:g.3067626C>T
• NG_029254.1:g.7315C>T
• NM_001012631.1:c.114+13C>T
• NM_001012632.1:c.114+13C>T
• NM_001012633.1:c.114+13C>T
• NM_001012634.1:c.54+211C>T
• NM_001012635.1:c.54+211C>T
• NM_001012636.1:c.114+13C>T
• NM_001012718.1:c.114+13C>T
• NM_004221.4:c.114+13C>T
• NC_000016.8:g.3057628C>T
• NC_000016.9:g.3117627C>T
• XR_038594.1:c.2231+d4668G>A

This HGVS expression did not pass validation

Links:

dbSNP: rs202247796

NCBI 1000 Genomes Browser:

rs202247796

Molecular consequence:

• NM_001012631.1:c.114+13C>T - intron variant - [Sequence Ontology: SO:0001627]