List of variants in gene BRAF reported as likely pathogenic for colorectal neoplasm

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_004333.6(BRAF):c.1397G>A (p.Gly466Glu)	rs121913351
NM_004333.6(BRAF):c.1397G>C (p.Gly466Ala)	rs121913351
NM_004333.6(BRAF):c.1405G>C (p.Gly469Arg)	rs121913357
NM_004333.6(BRAF):c.1454T>C (p.Leu485Ser)	rs397507475
NM_004333.6(BRAF):c.1741A>C (p.Asn581His)	rs180177040
NM_004333.6(BRAF):c.1742A>C (p.Asn581Thr)	rs121913370
NM_004333.6(BRAF):c.1742A>G (p.Asn581Ser)	rs121913370
NM_004333.6(BRAF):c.1780G>A (p.Asp594Asn)	rs397516896
NM_004333.6(BRAF):c.1780G>C (p.Asp594His)	rs397516896
NM_004333.6(BRAF):c.1799T>A (p.Val600Glu)	rs113488022
NM_004333.6(BRAF):c.1799_1800delinsAA (p.Val600Glu)	rs121913377
NM_004333.6(BRAF):c.2135C>A (p.Ala712Asp)	rs727502904

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