ClinVar

NM_019591.4(ZNF26):c.1515C>T (p.Thr505=)

Genes:

ZNF84:zinc finger protein 84 [Gene - OMIM - HGNC]
ZNF26:zinc finger protein 26 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

12q24.33

Genomic location:

• Chr12: 133011394 (on Assembly GRCh38)
• Chr12: 133587980 (on Assembly GRCh37)

Preferred name:

NM_019591.4(ZNF26):c.1515C>T (p.Thr505=)

HGVS:

• NC_000012.12:g.133011394C>T
• NM_001256279.2:c.1614C>T
• NM_001256280.2:c.1419C>T
• NM_001330513.2:c.1455C>T
• NM_001330514.2:c.1455C>T
• NM_019591.4:c.1515C>TMANE SELECT
• NP_001243208.1:p.Thr538=
• NP_001243209.1:p.Thr473=
• NP_001317442.1:p.Thr485=
• NP_001317443.1:p.Thr485=
• NP_062537.2:p.Thr505=
• NC_000012.11:g.133587980C>T
• NM_019591.3:c.1515C>T

This HGVS expression did not pass validation

Links:

dbSNP: rs3825108

NCBI 1000 Genomes Browser:

rs3825108

Molecular consequence:

• NM_001256279.2:c.1614C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001256280.2:c.1419C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001330513.2:c.1455C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001330514.2:c.1455C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_019591.4:c.1515C>T - synonymous variant - [Sequence Ontology: SO:0001819]

Observations:

113