ClinVar

NM_206965.2(FTCD):c.906+15C>T

Gene:

FTCD:formimidoyltransferase cyclodeaminase [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

21q22.3

Genomic location:

• Chr21: 46150104 (on Assembly GRCh38)
• Chr21: 47570018 (on Assembly GRCh37)

Preferred name:

NM_206965.2(FTCD):c.906+15C>T

HGVS:

• NC_000021.9:g.46150104G>A
• NG_016191.1:g.10464C>T
• NM_001320412.2:c.906+15C>T
• NM_006657.3:c.906+15C>T
• NM_206965.2:c.906+15C>TMANE SELECT
• NC_000021.8:g.47570018G>A

This HGVS expression did not pass validation

Links:

dbSNP: rs76474184

NCBI 1000 Genomes Browser:

rs76474184

Molecular consequence:

• NM_001320412.2:c.906+15C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_006657.3:c.906+15C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_206965.2:c.906+15C>T - intron variant - [Sequence Ontology: SO:0001627]

Observations:

1