ClinVar

NM_002230.4(JUP):c.1551G>A (p.Pro517=)

Gene:

JUP:junction plakoglobin [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

17q21.2

Genomic location:

• Chr17: 41758817 (on Assembly GRCh38)
• Chr17: 39915069 (on Assembly GRCh37)

Preferred name:

NM_002230.4(JUP):c.1551G>A (p.Pro517=)

HGVS:

• NC_000017.11:g.41758817C>T
• NG_009090.2:g.32896G>A
• NM_001352773.2:c.1551G>A
• NM_001352774.2:c.1551G>A
• NM_001352775.2:c.1551G>A
• NM_001352776.2:c.1551G>A
• NM_001352777.2:c.1551G>A
• NM_002230.4:c.1551G>AMANE SELECT
• NM_021991.4:c.1551G>A
• NP_001339702.1:p.Pro517=
• NP_001339703.1:p.Pro517=
• NP_001339704.1:p.Pro517=
• NP_001339705.1:p.Pro517=
• NP_001339706.1:p.Pro517=
• NP_002221.1:p.Pro517=
• NP_068831.1:p.Pro517=
• LRG_401t1:c.1551G>A
• LRG_401t2:c.1551G>A
• LRG_401:g.32896G>A
• NC_000017.10:g.39915069C>T
• NM_002230.2:c.1551G>A
• NM_021991.2:c.1551G>A

This HGVS expression did not pass validation

Links:

dbSNP: rs988891105

NCBI 1000 Genomes Browser:

rs988891105

Molecular consequence:

• NM_001352773.2:c.1551G>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001352774.2:c.1551G>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001352775.2:c.1551G>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001352776.2:c.1551G>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001352777.2:c.1551G>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_002230.4:c.1551G>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_021991.4:c.1551G>A - synonymous variant - [Sequence Ontology: SO:0001819]