ClinVar

NM_001267550.2(TTN):c.9955G>A (p.Val3319Ile)

Gene:

TTN:titin [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

2q31.2

Genomic location:

• Chr2: 178764560 (on Assembly GRCh38)
• Chr2: 179629287 (on Assembly GRCh37)

Preferred name:

NM_001267550.2(TTN):c.9955G>A (p.Val3319Ile)

HGVS:

• NC_000002.12:g.178764560C>T
• NG_011618.3:g.71243G>A
• NM_001256850.1:c.9955G>A
• NM_001267550.2:c.9955G>AMANE SELECT
• NM_003319.4:c.9817G>A
• NM_133378.4:c.9955G>A
• NM_133379.5:c.9955G>A
• NM_133432.3:c.9817G>A
• NM_133437.4:c.9817G>A
• NP_001243779.1:p.Val3319Ile
• NP_001254479.2:p.Val3319Ile
• NP_003310.4:p.Val3273Ile
• NP_596869.4:p.Val3319Ile
• NP_596870.2:p.Val3319Ile
• NP_597676.3:p.Val3273Ile
• NP_597681.4:p.Val3273Ile
• LRG_391:g.71243G>A
• NC_000002.11:g.179629287C>T

This HGVS expression did not pass validation

Protein change:

V3273I

Links:

dbSNP: rs375533809

NCBI 1000 Genomes Browser:

rs375533809

Molecular consequence:

• NM_001256850.1:c.9955G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001267550.2:c.9955G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_003319.4:c.9817G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_133378.4:c.9955G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_133379.5:c.9955G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_133432.3:c.9817G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_133437.4:c.9817G>A - missense variant - [Sequence Ontology: SO:0001583]

Observations:

1