ClinVar

NM_001321827.2(NIBAN3):c.1013G>T (p.Arg338Leu)

Gene:

NIBAN3:niban apoptosis regulator 3 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

19p13.11

Genomic location:

• Chr19: 17540425 (on Assembly GRCh38)
• Chr19: 17651234 (on Assembly GRCh37)

Preferred name:

NM_001321827.2(NIBAN3):c.1013G>T (p.Arg338Leu)

HGVS:

• NC_000019.10:g.17540425G>T
• NM_001098524.2:c.1106G>T
• NM_001321826.2:c.1013G>T
• NM_001321827.2:c.1013G>TMANE SELECT
• NM_001321828.1:c.284G>T
• NM_001363609.1:c.1013G>T
• NM_173544.5:c.1106G>T
• NP_001091994.2:p.Arg369Leu
• NP_001308755.2:p.Arg338Leu
• NP_001308756.2:p.Arg338Leu
• NP_001308757.1:p.Arg95Leu
• NP_001350538.1:p.Arg338Leu
• NP_775815.3:p.Arg369Leu
• NC_000019.9:g.17651234G>T
• NM_173544.4:c.1106G>T

This HGVS expression did not pass validation

Protein change:

R338L

Molecular consequence:

• NM_001098524.2:c.1106G>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_001321826.2:c.1013G>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_001321827.2:c.1013G>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_001321828.1:c.284G>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_001363609.1:c.1013G>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_173544.5:c.1106G>T - missense variant - [Sequence Ontology: SO:0001583]