ClinVar

NM_001136472.2(LITAF):c.377+261C>T

Gene:

LITAF:lipopolysaccharide induced TNF factor [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

16p13.13

Genomic location:

• Chr16: 11553272 (on Assembly GRCh38)
• Chr16: 11647128 (on Assembly GRCh37)

Preferred name:

NM_001136472.2(LITAF):c.377+261C>T

HGVS:

• NC_000016.10:g.11553272G>A
• NG_009008.1:g.38679C>T
• NM_001136472.2:c.377+261C>TMANE SELECT
• NM_001136473.1:c.377+261C>T
• NM_004862.4:c.377+261C>T
• LRG_253t1:c.377+261C>T
• LRG_253:g.38679C>T
• NC_000016.9:g.11647128G>A

This HGVS expression did not pass validation

Links:

dbSNP: rs115554638

NCBI 1000 Genomes Browser:

rs115554638

Molecular consequence:

• NM_001136472.2:c.377+261C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001136473.1:c.377+261C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_004862.4:c.377+261C>T - intron variant - [Sequence Ontology: SO:0001627]