ClinVar

NM_024301.5(FKRP):c.1397G>A (p.Arg466His)

Gene:

FKRP:fukutin related protein [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

19q13.32

Genomic location:

• Chr19: 46756847 (on Assembly GRCh38)
• Chr19: 47260104 (on Assembly GRCh37)

Preferred name:

NM_024301.5(FKRP):c.1397G>A (p.Arg466His)

HGVS:

• NC_000019.10:g.46756847G>A
• NG_008898.2:g.15802G>A
• NM_001039885.3:c.1397G>A
• NM_024301.5:c.1397G>AMANE SELECT
• NP_001034974.1:p.Arg466His
• NP_077277.1:p.Arg466His
• LRG_761t1:c.1397G>A
• LRG_761:g.15802G>A
• LRG_761p1:p.Arg466His
• NC_000019.9:g.47260104G>A
• NM_024301.4:c.1397G>A

This HGVS expression did not pass validation

Protein change:

R466H

Links:

dbSNP: rs763422045

NCBI 1000 Genomes Browser:

rs763422045

Molecular consequence:

• NM_001039885.3:c.1397G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_024301.5:c.1397G>A - missense variant - [Sequence Ontology: SO:0001583]

Observations:

1