ClinVar

NM_019616.4(F7):c.*561AT[1]

Gene:

F7:coagulation factor VII [Gene - OMIM - HGNC]

Variant type:

Microsatellite

Cytogenetic location:

13q34

Genomic location:

• Chr13: 113119569 - 113119570 (on Assembly GRCh38)
• Chr13: 113773883 - 113773884 (on Assembly GRCh37)

Preferred name:

NM_019616.4(F7):c.*561AT[1]

HGVS:

• NC_000013.11:g.113119569AT[1]
• NG_009258.1:g.1771AT[1]
• NG_009262.1:g.18779AT[1]
• NM_000131.4:c.*561AT[1]
• NM_001267554.2:c.*561AT[1]
• NM_019616.4:c.*561AT[1]MANE SELECT
• LRG_554t1:c.*561AT[1]
• LRG_548:g.1771AT[1]
• LRG_554:g.18779AT[1]
• NC_000013.10:g.113773883AT[1]
• NM_000131.4:c.*563_*564delAT
• NR_051961.2:n.1980AT[1]

This HGVS expression did not pass validation

Links:

dbSNP: rs886049992

NCBI 1000 Genomes Browser:

rs886049992

Molecular consequence:

• NM_000131.4:c.*561AT[1] - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
• NM_001267554.2:c.*561AT[1] - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
• NM_019616.4:c.*561AT[1] - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
• NR_051961.2:n.1980AT[1] - non-coding transcript variant - [Sequence Ontology: SO:0001619]