ClinVar

NM_001323342.2(AHCTF1):c.6115T>A (p.Ser2039Thr)

Gene:

AHCTF1:AT-hook containing transcription factor 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

1q44

Genomic location:

• Chr1: 246849891 (on Assembly GRCh38)
• Chr1: 247013193 (on Assembly GRCh37)

Preferred name:

NM_001323342.2(AHCTF1):c.6115T>A (p.Ser2039Thr)

HGVS:

• NC_000001.11:g.246849891A>T
• NM_001323342.2:c.6115T>AMANE SELECT
• NM_001323343.2:c.6115T>A
• NM_001410950.1:c.6220T>A
• NM_015446.5:c.6142T>A
• NP_001310271.1:p.Ser2039Thr
• NP_001310272.1:p.Ser2039Thr
• NP_001397879.1:p.Ser2074Thr
• NP_056261.4:p.Ser2048Thr
• NC_000001.10:g.247013193A>T
• NM_015446.4:c.6142T>A
• NR_136586.2:n.6627T>A

This HGVS expression did not pass validation

Protein change:

S2039T

Molecular consequence:

• NM_001323342.2:c.6115T>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001323343.2:c.6115T>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001410950.1:c.6220T>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_015446.5:c.6142T>A - missense variant - [Sequence Ontology: SO:0001583]
• NR_136586.2:n.6627T>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]