ClinVar

NM_000363.5(TNNI3):c.303C>T (p.His101=)

Gene:

TNNI3:troponin I3, cardiac type [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

19q13.42

Genomic location:

• Chr19: 55154810 (on Assembly GRCh38)
• Chr19: 55666178 (on Assembly GRCh37)

Preferred name:

NM_000363.5(TNNI3):c.303C>T (p.His101=)

HGVS:

• NC_000019.10:g.55154810G>A
• NG_007866.2:g.7923C>T
• NM_000363.5:c.303C>TMANE SELECT
• NP_000354.4:p.His101=
• LRG_432t1:c.303C>T
• LRG_432:g.7923C>T
• NC_000019.9:g.55666178G>A
• NM_000363.4:c.303C>T
• c.303C>T
• p.His101His

This HGVS expression did not pass validation

Links:

dbSNP: rs199539066

NCBI 1000 Genomes Browser:

rs199539066

Molecular consequence:

• NM_000363.5:c.303C>T - synonymous variant - [Sequence Ontology: SO:0001819]

Observations:

1