ClinVar

NM_005141.5(FGB):c.1203C>T (p.Asn401=)

Gene:

FGB:fibrinogen beta chain [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

4q31.3

Genomic location:

• Chr4: 154569758 (on Assembly GRCh38)
• Chr4: 155490910 (on Assembly GRCh37)

Preferred name:

NM_005141.5(FGB):c.1203C>T (p.Asn401=)

HGVS:

• NC_000004.12:g.154569758C>T
• NG_008833.1:g.11779C>T
• NM_001184741.1:c.1026C>T
• NM_001382759.1:c.1071C>T
• NM_001382760.1:c.1203C>T
• NM_001382761.1:c.1203C>T
• NM_001382762.1:c.903C>T
• NM_001382763.1:c.1194C>T
• NM_001382764.1:c.1081-15C>T
• NM_001382765.1:c.1203C>T
• NM_005141.5:c.1203C>TMANE SELECT
• NP_001171670.1:p.Asn342=
• NP_001369688.1:p.Asn357=
• NP_001369689.1:p.Asn401=
• NP_001369690.1:p.Asn401=
• NP_001369691.1:p.Asn301=
• NP_001369692.1:p.Asn398=
• NP_001369694.1:p.Asn401=
• NP_005132.2:p.Asn401=
• NP_005132.2:p.Asn401=
• LRG_558t1:c.1203C>T
• LRG_558:g.11779C>T
• LRG_558p1:p.Asn401=
• NC_000004.11:g.155490910C>T
• NM_005141.4:c.1203C>T

This HGVS expression did not pass validation

Molecular consequence:

• NM_001382764.1:c.1081-15C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001184741.1:c.1026C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001382759.1:c.1071C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001382760.1:c.1203C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001382761.1:c.1203C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001382762.1:c.903C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001382763.1:c.1194C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001382765.1:c.1203C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_005141.5:c.1203C>T - synonymous variant - [Sequence Ontology: SO:0001819]