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VariantValidator.org_v0.1.0_dev_pre_a
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Invalid Variant description
Input variant description: NM_138448.3:c.186-50189T
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)
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GRCh38
GRCh37
Alignment method:
splign
blat
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