ClinVar

NM_014629.4(ARHGEF10):c.37+5C>T

Genes:

LOC126860279:CDK7 strongly-dependent group 2 enhancer GRCh37_chr8:1791725-1792924 [Gene]
ARHGEF10:Rho guanine nucleotide exchange factor 10 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

8p23.3

Genomic location:

• Chr8: 1843441 (on Assembly GRCh38)
• Chr8: 1791607 (on Assembly GRCh37)

Preferred name:

NM_014629.4(ARHGEF10):c.37+5C>T

HGVS:

• NC_000008.11:g.1843441C>T
• NG_008480.1:g.24459C>T
• NG_084780.2:g.359C>T
• NM_001308152.2:c.37+5C>T
• NM_001308153.2:c.109+5C>T
• NM_014629.4:c.37+5C>TMANE SELECT
• LRG_234:g.24459C>T
• NC_000008.10:g.1791607C>T
• NM_014629.3:c.37+5C>T

This HGVS expression did not pass validation

Molecular consequence:

• NM_001308152.2:c.37+5C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_001308153.2:c.109+5C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_014629.4:c.37+5C>T - intron variant - [Sequence Ontology: SO:0001627]