Related gene-specific medical variations for Gene (Select 673) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3361038	NM_004333.6(BRAF):c.1933_1935del (p.Val645del)	BRAF (V557del +7 more)	Deletion (inframe_deletion +1 more)	not provided	GUncertain significance
Select item 3359275	NM_004333.6(BRAF):c.1271G>A (p.Arg424Gln)	BRAF (R336Q +7 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3349476	NM_004333.6(BRAF):c.1018A>G (p.Ile340Val)	BRAF, LOC126860202 (I252V +4 more)	Single nucleotide variant (missense variant)	BRAF-related disorder	GUncertain significance
Select item 3340668	NM_004333.6(BRAF):c.1031A>G (p.Gln344Arg)	BRAF, LOC126860202 (Q256R +4 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3338728	NM_004333.6(BRAF):c.1099C>G (p.Pro367Ala)	BRAF, LOC126860202 (P279A +4 more)	Single nucleotide variant (missense variant)	not provided	GLikely pathogenic
Select item 3245839	NC_000007.13:g.(?_140434397)_(140534692_?)dup	BRAF	Duplication	RASopathy	GUncertain significance
Select item 3245838	NC_000007.13:g.(?_140476692)_(140494287_?)del	BRAF	Deletion	RASopathy	GUncertain significance
Select item 3017437	NM_004333.6(BRAF):c.981-16G>C	BRAF, LOC126860202	Single nucleotide variant (intron variant)	RASopathy	GLikely benign
Select item 3003504	NM_004333.6(BRAF):c.1077A>G (p.Gln359=)	BRAF, LOC126860202	Single nucleotide variant (synonymous variant)	RASopathy	GLikely benign
Select item 2996554	NM_004333.6(BRAF):c.1028C>T (p.Pro343Leu)	BRAF, LOC126860202 (P255L +4 more)	Single nucleotide variant (missense variant)	RASopathy	GUncertain significance
Select item 2904050	NM_004333.6(BRAF):c.1021C>G (p.Pro341Ala)	BRAF, LOC126860202 (P253A +4 more)	Single nucleotide variant (missense variant)	RASopathy	GUncertain significance
Select item 2867973	NM_004333.6(BRAF):c.1029A>G (p.Pro343=)	BRAF, LOC126860202	Single nucleotide variant (synonymous variant)	RASopathy	GLikely benign
Select item 2754449	NM_004333.6(BRAF):c.1012A>G (p.Lys338Glu)	BRAF, LOC126860202 (K341E +4 more)	Single nucleotide variant (missense variant)	RASopathy	GUncertain significance
Select item 2697291	NM_004333.6(BRAF):c.1117A>G (p.Thr373Ala)	BRAF, LOC126860202 (T285A +4 more)	Single nucleotide variant (missense variant)	RASopathy	GUncertain significance
Select item 2662761	NM_004333.6(BRAF):c.1081G>A (p.Asp361Asn)	BRAF, LOC126860202 (D273N +4 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2658071	NM_004333.6(BRAF):c.981-437A>G	BRAF, LOC126860202	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2658070	NM_004333.6(BRAF):c.981-261A>T	BRAF, LOC126860202	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2658069	NM_004333.6(BRAF):c.1140+188C>T	BRAF, LOC126860202	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2658068	NM_004333.6(BRAF):c.1140+475G>T	BRAF, LOC126860202	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2573928	NM_004333.6(BRAF):c.1085G>A (p.Arg362Gln)	BRAF, LOC126860202 (R274Q +4 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2499060	NM_004333.6(BRAF):c.981-200A>C	BRAF, LOC126860202	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2439552	NM_004333.6(BRAF):c.1084C>T (p.Arg362Ter)	BRAF, LOC126860202 (R274* +4 more)	Single nucleotide variant (nonsense)	not provided	GUncertain significance
Select item 2157460	NM_004333.6(BRAF):c.1140+13C>T	BRAF, LOC126860202	Single nucleotide variant (intron variant)	RASopathy	GLikely benign
Select item 2115052	NM_004333.6(BRAF):c.1076A>G (p.Gln359Arg)	BRAF, LOC126860202 (Q362R +4 more)	Single nucleotide variant (missense variant)	RASopathy	GUncertain significance
Select item 2080875	NM_004333.6(BRAF):c.1120A>G (p.Ile374Val)	BRAF, LOC126860202 (I374V +4 more)	Single nucleotide variant (missense variant)	RASopathy +1 more	GUncertain significance
Select item 1973400	NM_004333.6(BRAF):c.1087T>G (p.Ser363Ala)	BRAF, LOC126860202 (S366A +4 more)	Single nucleotide variant (missense variant)	RASopathy	GUncertain significance
Select item 1972615	NM_004333.6(BRAF):c.1085G>T (p.Arg362Leu)	BRAF, LOC126860202 (R310L +4 more)	Single nucleotide variant (missense variant)	RASopathy	GUncertain significance
Select item 1949185	NM_004333.6(BRAF):c.1004C>T (p.Ser335Phe)	BRAF, LOC126860202 (S247F +4 more)	Single nucleotide variant (missense variant)	RASopathy	GUncertain significance
Select item 1926048	NM_004333.6(BRAF):c.1040G>A (p.Arg347Gln)	BRAF, LOC126860202 (R259Q +4 more)	Single nucleotide variant (missense variant)	RASopathy	GUncertain significance
Select item 1772744	NM_004333.6(BRAF):c.1002G>A (p.Pro334=)	BRAF, LOC126860202	Single nucleotide variant (synonymous variant)	RASopathy +2 more	GLikely benign
Select item 1729849	NM_004333.6(BRAF):c.1136T>C (p.Ile379Thr)	BRAF, LOC126860202 (I327T +4 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 1727744	NM_004333.6(BRAF):c.1129G>A (p.Val377Ile)	BRAF, LOC126860202 (V380I +4 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype	GUncertain significance
Select item 1711831	NM_004333.6(BRAF):c.1432+141A>C	BRAF	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711830	NM_004333.6(BRAF):c.1695-10273A>G	BRAF	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711829	NM_004333.6(BRAF):c.1695-10233C>T	BRAF	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711828	NM_004333.6(BRAF):c.1695-10204C>T	BRAF	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711827	NM_004333.6(BRAF):c.1695-10155T>A	BRAF	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711826	NM_004333.6(BRAF):c.1389T>C (p.Ile463=)	BRAF	Single nucleotide variant (synonymous variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711825	NM_004333.6(BRAF):c.1432+230G>A	BRAF	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711824	NM_004333.6(BRAF):c.1351dup (p.Glu451fs)	BRAF (E363fs +7 more)	Duplication (frameshift variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711823	NM_004333.6(BRAF):c.1342_1343insT (p.Asp448fs)	BRAF (D360fs +7 more)	Insertion (frameshift variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711822	NM_004333.6(BRAF):c.1432+20A>C	BRAF	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711821	NM_004333.6(BRAF):c.1432+33T>C	BRAF	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711820	NM_004333.6(BRAF):c.1432+35A>G	BRAF	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711819	NM_004333.6(BRAF):c.1432+38A>C	BRAF	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711818	NM_004333.6(BRAF):c.1432+43A>T	BRAF	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711817	NM_004333.6(BRAF):c.1432+52A>T	BRAF	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711816	NM_004333.6(BRAF):c.1432+67T>C	BRAF	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711815	NM_004333.6(BRAF):c.1338G>T (p.Ser446=)	BRAF	Single nucleotide variant (synonymous variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711814	NM_004333.6(BRAF):c.1432+237T>C	BRAF	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711813	NM_004333.6(BRAF):c.1432+22A>T	BRAF	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711812	NM_004333.6(BRAF):c.1348_1349insC (p.Trp450fs)	BRAF (W362fs +7 more)	Insertion (frameshift variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711811	NM_004333.6(BRAF):c.1373del (p.Thr458fs)	BRAF (T370fs +7 more)	Deletion (frameshift variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711810	NM_004333.6(BRAF):c.1432+8T>C	BRAF	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711809	NM_004333.6(BRAF):c.1375dup (p.Val459fs)	BRAF (V371fs +7 more)	Duplication (frameshift variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711808	NM_004333.6(BRAF):c.1432+102C>A	BRAF	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711807	NM_004333.6(BRAF):c.1695-10472del	BRAF	Deletion (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711806	NM_004333.6(BRAF):c.1695-10468C>T	BRAF	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711805	NM_004333.6(BRAF):c.1695-10462T>G	BRAF	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711804	NM_004333.6(BRAF):c.1695-10455A>G	BRAF	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711803	NM_004333.6(BRAF):c.1432+276T>G	BRAF	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711802	NM_004333.6(BRAF):c.1695-10408A>G	BRAF	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711801	NM_004333.6(BRAF):c.1695-10396G>T	BRAF	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711800	NM_004333.6(BRAF):c.1695-10389T>C	BRAF	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711799	NM_004333.6(BRAF):c.1695-10377G>A	BRAF	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711798	NM_004333.6(BRAF):c.1695-10356G>A	BRAF	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711797	NM_004333.6(BRAF):c.1695-10345G>T	BRAF	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711796	NM_004333.6(BRAF):c.1695-10342T>A	BRAF	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711795	NM_004333.6(BRAF):c.1695-10335A>G	BRAF	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711794	NM_004333.6(BRAF):c.1695-10306G>A	BRAF	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711793	NM_004333.6(BRAF):c.1695-10295A>G	BRAF	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711792	NM_004333.6(BRAF):c.1432+282C>T	BRAF	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711791	NM_004333.6(BRAF):c.1695-10293G>A	BRAF	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711790	NM_004333.6(BRAF):c.1695-10286G>T	BRAF	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711789	NM_004333.6(BRAF):c.1695-10278G>A	BRAF	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711788	NM_004333.6(BRAF):c.1695-10229T>A	BRAF	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711787	NM_004333.6(BRAF):c.1695-10193A>T	BRAF	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711786	NM_004333.6(BRAF):c.1695-10145T>A	BRAF	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711785	NM_004333.6(BRAF):c.1367A>T (p.Gln456Leu)	BRAF (Q368L +7 more)	Single nucleotide variant (missense variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711784	NM_004333.6(BRAF):c.1377_1378insT (p.Gly460fs)	BRAF (G372fs +7 more)	Insertion (frameshift variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711783	NM_004333.6(BRAF):c.1432+65T>G	BRAF	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711782	NM_004333.6(BRAF):c.1432+296T>C	BRAF	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711781	NM_004333.6(BRAF):c.1432+95C>T	BRAF	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711780	NM_004333.6(BRAF):c.1333G>T (p.Asp445Tyr)	BRAF (D357Y +7 more)	Single nucleotide variant (missense variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711779	NM_004333.6(BRAF):c.1339A>T (p.Ser447Cys)	BRAF (S359C +7 more)	Single nucleotide variant (missense variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711778	NM_004333.6(BRAF):c.1430A>C (p.His477Pro)	BRAF (H389P +7 more)	Single nucleotide variant (missense variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711777	NM_004333.6(BRAF):c.1432+3A>T	BRAF	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711776	NM_004333.6(BRAF):c.1432+34C>T	BRAF	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711775	NM_004333.6(BRAF):c.1432+41G>A	BRAF	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711774	NM_004333.6(BRAF):c.1432+114A>G	BRAF	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711773	NM_004333.6(BRAF):c.1432+120A>T	BRAF	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711772	NM_004333.6(BRAF):c.1432+136C>T	BRAF	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711771	NM_004333.6(BRAF):c.1432+308T>A	BRAF	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711770	NM_004333.6(BRAF):c.1432+142A>C	BRAF	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711769	NM_004333.6(BRAF):c.1432+144G>A	BRAF	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711768	NM_004333.6(BRAF):c.1432+157A>G	BRAF	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711767	NM_004333.6(BRAF):c.1432+176G>C	BRAF	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711766	NM_004333.6(BRAF):c.1432+181C>T	BRAF	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711765	NM_004333.6(BRAF):c.1432+201A>T	BRAF	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance
Select item 1711764	NM_004333.6(BRAF):c.1432+234T>A	BRAF	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 1	GUncertain significance

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