ClinVar

NM_000051.4(ATM):c.6420C>A (p.Phe2140Leu)

Genes:

ATM:ATM serine/threonine kinase [Gene - OMIM - HGNC]
C11orf65:chromosome 11 open reading frame 65 [Gene - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

11q22.3

Genomic location:

• Chr11: 108320026 (on Assembly GRCh38)
• Chr11: 108190753 (on Assembly GRCh37)

Preferred name:

NM_000051.4(ATM):c.6420C>A (p.Phe2140Leu)

HGVS:

• NC_000011.10:g.108320026C>A
• NG_009830.1:g.102195C>A
• NG_054724.1:g.154807G>T
• NM_000051.4:c.6420C>AMANE SELECT
• NM_001330368.2:c.641-10955G>T
• NM_001351110.2:c.*39-10955G>T
• NM_001351834.2:c.6420C>A
• NP_000042.3:p.Phe2140Leu
• NP_000042.3:p.Phe2140Leu
• NP_001338763.1:p.Phe2140Leu
• LRG_135t1:c.6420C>A
• LRG_135:g.102195C>A
• LRG_135p1:p.Phe2140Leu
• NC_000011.9:g.108190753C>A
• NM_000051.3:c.6420C>A

This HGVS expression did not pass validation

Protein change:

F2140L

Links:

dbSNP: rs587780635

NCBI 1000 Genomes Browser:

rs587780635

Molecular consequence:

• NM_001330368.2:c.641-10955G>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001351110.2:c.*39-10955G>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_000051.4:c.6420C>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001351834.2:c.6420C>A - missense variant - [Sequence Ontology: SO:0001583]