ClinVar

NM_182548.4(LHFPL5):c.*425CA[19]

Gene:

LHFPL5:LHFPL tetraspan subfamily member 5 [Gene - OMIM - HGNC]

Variant type:

Microsatellite

Cytogenetic location:

6p21.31

Genomic location:

• Chr6: 35823388 - 35823389 (on Assembly GRCh38)
• Chr6: 35791165 - 35791166 (on Assembly GRCh37)

Preferred name:

NM_182548.4(LHFPL5):c.*425CA[19]

HGVS:

• NC_000006.12:g.35823390CA[19]
• NG_012184.3:g.31185CA[19]
• NM_182548.4:c.*425CA[19]MANE SELECT
• LRG_1352t1:c.*425CA[19]
• LRG_1352:g.31185CA[19]
• NC_000006.11:g.35791167CA[19]
• NG_012184.2:g.23097CA[19]
• NM_182548.3:c.*459_*460dupCA

This HGVS expression did not pass validation

Links:

dbSNP: rs67626900

NCBI 1000 Genomes Browser:

rs67626900

Molecular consequence:

• NM_182548.4:c.*425CA[19] - 3 prime UTR variant - [Sequence Ontology: SO:0001624]