ClinVar

NM_001018115.3(FANCD2):c.3106-15C>A

Genes:

FANCD2:FA complementation group D2 [Gene - OMIM - HGNC]
FANCD2OS:FANCD2 opposite strand [Gene - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

3p25.3

Genomic location:

• Chr3: 10081331 (on Assembly GRCh38)
• Chr3: 10123015 (on Assembly GRCh37)

Preferred name:

NM_001018115.3(FANCD2):c.3106-15C>A

HGVS:

• NC_000003.12:g.10081331C>A
• NG_007311.1:g.59903C>A
• NG_042053.1:g.31901G>T
• NM_001018115.3:c.3106-15C>AMANE SELECT
• NM_001319984.2:c.3106-15C>A
• NM_001374253.1:c.2995-15C>A
• NM_001374254.1:c.3106-15C>A
• NM_033084.6:c.3106-15C>A
• NM_173472.2:c.*244G>T
• LRG_306:g.59903C>A
• NC_000003.11:g.10123015C>A

This HGVS expression did not pass validation

Molecular consequence:

• NM_173472.2:c.*244G>T - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
• NM_001018115.3:c.3106-15C>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_001319984.2:c.3106-15C>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_001374253.1:c.2995-15C>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_001374254.1:c.3106-15C>A - intron variant - [Sequence Ontology: SO:0001627]
• NM_033084.6:c.3106-15C>A - intron variant - [Sequence Ontology: SO:0001627]