List of variants reported as likely benign for benign neoplasm of skin

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Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 71

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HGVS	dbSNP	gnomAD frequency
NM_000142.5(FGFR3):c.348C>T (p.Arg116=)	rs2305179	0.01752
NM_015922.3(NSDHL):c.1054C>T (p.Leu352=)	rs142351862	0.00444
NM_000142.5(FGFR3):c.1150T>C (p.Phe384Leu)	rs17881656	0.00342
NM_002272.4(KRT4):c.205C>T (p.Arg69Ter)	rs200860840	0.00183
NM_000142.5(FGFR3):c.1959+15G>C	rs17886888	0.00158
NM_023110.3(FGFR1):c.336C>T (p.Thr112=)	rs148480919	0.00153
NM_015922.3(NSDHL):c.893G>T (p.Trp298Leu)	rs139186585	0.00143
NM_015922.3(NSDHL):c.306C>T (p.Phe102=)	rs141089248	0.00138
NM_005343.4(HRAS):c.357C>T (p.Asp119=)	rs111352454	0.00121
NM_033360.4(KRAS):c.5-18A>G	rs200189105	0.00100
NM_015922.3(NSDHL):c.834C>T (p.Phe278=)	rs149698967	0.00057
NM_015922.3(NSDHL):c.351T>C (p.Phe117=)	rs138711934	0.00045
NM_015922.3(NSDHL):c.678C>T (p.Phe226=)	rs147293409	0.00044
NM_023110.3(FGFR1):c.1398C>T (p.Pro466=)	rs150652786	0.00034
NM_023110.3(FGFR1):c.2424C>G (p.Pro808=)	rs374507681	0.00029
NM_153490.3(KRT13):c.-45C>A	rs367712050	0.00029
NM_004985.5(KRAS):c.24A>G (p.Val8=)	rs147406419	0.00025
NM_015922.3(NSDHL):c.987C>T (p.Val329=)	rs149122192	0.00017
NM_023110.3(FGFR1):c.2298C>T (p.Tyr766=)	rs376173540	0.00014
NM_005343.4(HRAS):c.330C>T (p.Pro110=)	rs200747280	0.00011
NM_033360.4(KRAS):c.90C>T (p.Asp30=)	rs113623140	0.00011
NM_023110.3(FGFR1):c.2331C>G (p.Ser777=)	rs763571736	0.00010
NM_153490.3(KRT13):c.1238A>T (p.Asp413Val)	rs200269035	0.00010
NM_002272.4(KRT4):c.1386G>A (p.Val462=)	rs373947229	0.00009
NM_023110.3(FGFR1):c.921T>C (p.Tyr307=)	rs377010221	0.00009
NM_023110.3(FGFR1):c.1888C>T (p.Leu630=)	rs746123129	0.00008
NM_002272.4(KRT4):c.364C>G (p.Leu122Val)	rs758695571	0.00007
NM_023110.3(FGFR1):c.359-13C>G	rs376369060	0.00007
NM_002272.4(KRT4):c.1192C>T (p.His398Tyr)	rs374654554	0.00006
NM_002272.4(KRT4):c.359C>A (p.Thr120Asn)	rs201805600	0.00006
NM_023110.3(FGFR1):c.1285-15C>T	rs760069564	0.00006
NM_023110.3(FGFR1):c.2049-13C>T	rs756845879	0.00006
NM_033360.4(KRAS):c.4+5G>A	rs201789109	0.00006
NM_000142.5(FGFR3):c.1827C>G (p.Ala609=)	rs750472969	0.00005
NM_002272.4(KRT4):c.466C>T (p.Gln156Ter)	rs535497819	0.00005
NM_002272.4(KRT4):c.1204G>A (p.Val402Ile)	rs772882487	0.00004
NM_002272.4(KRT4):c.954T>C (p.Ile318=)	rs770727989	0.00004
NM_004985.5(KRAS):c.451-5652C>T	rs727505314	0.00004
NM_005343.4(HRAS):c.520C>T (p.Pro174Ser)	rs397517144	0.00004
NM_023110.3(FGFR1):c.621+7G>T	rs377200873	0.00004
NM_023110.3(FGFR1):c.92-14C>T	rs547772178	0.00004
NM_002272.4(KRT4):c.513G>A (p.Leu171=)	rs774677002	0.00003
NM_002272.4(KRT4):c.527C>T (p.Thr176Met)	rs370759790	0.00003
NM_002272.4(KRT4):c.945C>T (p.Tyr315=)	rs778125368	0.00003
NM_023110.3(FGFR1):c.2106C>T (p.Pro702=)	rs777061347	0.00003
NM_023110.3(FGFR1):c.2186+19C>T	rs776791517	0.00003
NM_023110.3(FGFR1):c.456T>C (p.Ala152=)	rs369175953	0.00003
NM_153490.3(KRT13):c.291C>T (p.Gly97=)	rs747752896	0.00003
NM_000142.5(FGFR3):c.1935C>T (p.Leu645=)	rs104886006	0.00002
NM_002272.4(KRT4):c.1147G>A (p.Val383Met)	rs751984023	0.00002
NM_023110.3(FGFR1):c.1663+10G>A	rs901498652	0.00002
NM_023110.3(FGFR1):c.2238C>T (p.Thr746=)	rs774683007	0.00002
NM_023110.3(FGFR1):c.621+19G>A	rs945311072	0.00002
NM_002272.4(KRT4):c.-54A>T	rs369760401	0.00001
NM_015922.3(NSDHL):c.612C>T (p.Phe204=)	rs782252634	0.00001
NM_023110.3(FGFR1):c.1185C>T (p.Ile395=)	rs756104594	0.00001
NM_023110.3(FGFR1):c.1308C>T (p.Ser436=)	rs546318124	0.00001
NM_023110.3(FGFR1):c.1978-13G>A	rs761708658	0.00001
NM_023110.3(FGFR1):c.1978-16C>T	rs764971696	0.00001
NM_023110.3(FGFR1):c.2058C>T (p.Phe686=)	rs1193961883	0.00001
NM_023110.3(FGFR1):c.2271C>T (p.Ile757=)	rs369782405	0.00001
NM_153490.3(KRT13):c.844G>A (p.Glu282Lys)	rs202057977	0.00001
NM_153490.3(KRT13):c.9C>T (p.Leu3=)	rs185787290	0.00001
NM_002272.4(KRT4):c.1346+15A>T	rs931479
NM_002272.4(KRT4):c.801C>T (p.Asp267=)	rs369207280
NM_004985.5(KRAS):c.112-9C>T	rs727504298
NM_005343.4(HRAS):c.291-6T>G	rs766909143
NM_015922.3(NSDHL):c.268-15dup	rs782031217
NM_023110.3(FGFR1):c.2187-19C>T	rs376583717
NM_023110.3(FGFR1):c.381TGA[5] (p.Asp133del)	rs138489552
NM_153490.3(KRT13):c.610G>A (p.Val204Met)	rs138102206

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