Validation.variantvalidator.org

NM_138448.3:c.186-50189T: char 25: end of input

Enter variant description in the HGVS format:

Examples:

NM_000088.3:c.589G>T
NC_000017.10:g.48275363C>A
NG_007400.1:g.8638G>T
LRG_1:g.8638G>T
LRG_1t1:c.589G>T
17-50198002-C-A (Note: this variant is in the context of GRCh38 - select the genome build below)
chr17:50198002C>A ((Note: this variant is in the context of GRCh38 - select the genome build below)

Select Genome Build

GRCh38 GRCh37

Alignment method:

splign blat

Show exon boundary crossing