ClinVar

NM_005591.4(MRE11):c.1341A>T (p.Ser447=)

Gene:

MRE11:MRE11 homolog, double strand break repair nuclease [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

11q21

Genomic location:

• Chr11: 94459567 (on Assembly GRCh38)
• Chr11: 94192733 (on Assembly GRCh37)

Preferred name:

NM_005591.4(MRE11):c.1341A>T (p.Ser447=)

HGVS:

• NC_000011.10:g.94459567T>A
• NG_007261.1:g.39308A>T
• NM_001330347.2:c.1341A>T
• NM_005590.4:c.1341A>T
• NM_005591.4:c.1341A>TMANE SELECT
• NP_001317276.1:p.Ser447=
• NP_005581.2:p.Ser447=
• NP_005582.1:p.Ser447=
• NP_005582.1:p.Ser447=
• LRG_85t1:c.1341A>T
• LRG_85:g.39308A>T
• LRG_85p1:p.Ser447=
• NC_000011.9:g.94192733T>A
• NM_005591.3:c.1341A>T

This HGVS expression did not pass validation

Links:

dbSNP: rs762323327

NCBI 1000 Genomes Browser:

rs762323327

Molecular consequence:

• NM_001330347.2:c.1341A>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_005590.4:c.1341A>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_005591.4:c.1341A>T - synonymous variant - [Sequence Ontology: SO:0001819]