List of variants in gene PALM reported as likely benign for not provided

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 91

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HGVS	dbSNP	gnomAD frequency
NM_002579.3(PALM):c.700G>A (p.Glu234Lys)	rs137941376	0.00092
NM_002579.3(PALM):c.81G>A (p.Glu27=)	rs200449881	0.00044
NM_002579.3(PALM):c.355C>T (p.Arg119Trp)	rs139966536	0.00034
NM_002579.3(PALM):c.720C>T (p.Asp240=)	rs142498012	0.00027
NM_002579.3(PALM):c.443-19G>A	rs375468860	0.00026
NM_002579.3(PALM):c.864G>A (p.Pro288=)	rs370324595	0.00024
NM_002579.3(PALM):c.936C>T (p.Ala312=)	rs142619819	0.00015
NM_002579.3(PALM):c.879C>A (p.Gly293=)	rs368736425	0.00014
NM_002579.3(PALM):c.336G>A (p.Ala112=)	rs550477288	0.00011
NM_002579.3(PALM):c.231C>T (p.Asp77=)	rs139932478	0.00009
NM_002579.3(PALM):c.228C>T (p.Asp76=)	rs556522898	0.00006
NM_002579.3(PALM):c.270-11C>T	rs370151535	0.00006
NM_002579.3(PALM):c.690C>T (p.Ser230=)	rs754671011	0.00006
NM_002579.3(PALM):c.975G>A (p.Thr325=)	rs376934419	0.00006
NM_002579.3(PALM):c.138+8C>T	rs750056429	0.00005
NM_002579.3(PALM):c.503-20C>T	rs778249420	0.00005
NM_002579.3(PALM):c.634+9A>G	rs773659099	0.00005
NM_002579.3(PALM):c.750G>A (p.Thr250=)	rs145938736	0.00005
NM_002579.3(PALM):c.273G>A (p.Leu91=)	rs765662362	0.00004
NM_002579.3(PALM):c.503-16G>A	rs754960807	0.00004
NM_002579.3(PALM):c.57+17C>T	rs748674089	0.00004
NM_002579.3(PALM):c.503-17C>T	rs754102497	0.00003
NM_002579.3(PALM):c.1032C>T (p.Asn344=)	rs747880907	0.00002
NM_002579.3(PALM):c.27G>A (p.Thr9=)	rs377213814	0.00002
NM_002579.3(PALM):c.288G>A (p.Glu96=)	rs752808504	0.00002
NM_002579.3(PALM):c.822C>T (p.Thr274=)	rs748378460	0.00002
NM_002579.3(PALM):c.1137C>T (p.His379=)	rs760803293	0.00001
NM_002579.3(PALM):c.1163G>A (p.Ter388=)	rs1049056291	0.00001
NM_002579.3(PALM):c.426G>T (p.Pro142=)	rs763743478	0.00001
NM_002579.3(PALM):c.5+9G>A	rs1246588804	0.00001
NM_002579.3(PALM):c.58-11C>T	rs1292766679	0.00001
NM_002579.3(PALM):c.635-9C>T	rs767203835	0.00001
NM_002579.3(PALM):c.1046A>T (p.Glu349Val)
NM_002579.3(PALM):c.1056G>A (p.Thr352=)
NM_002579.3(PALM):c.1086G>A (p.Ala362=)
NM_002579.3(PALM):c.111C>T (p.Asp37=)
NM_002579.3(PALM):c.138+11G>A
NM_002579.3(PALM):c.138+20C>T	rs2144880814
NM_002579.3(PALM):c.166C>T (p.Leu56=)
NM_002579.3(PALM):c.318_319inv (p.Thr107Ala)
NM_002579.3(PALM):c.333C>T (p.Asn111=)	rs374481450
NM_002579.3(PALM):c.421-11_421-9del	rs764916124
NM_002579.3(PALM):c.421-14C>T
NM_002579.3(PALM):c.421-19TC[2]	rs375076082
NM_002579.3(PALM):c.426G>A (p.Pro142=)
NM_002579.3(PALM):c.442+10C>T
NM_002579.3(PALM):c.442+9T>C
NM_002579.3(PALM):c.443-6G>A
NM_002579.3(PALM):c.456C>T (p.Ser152=)
NM_002579.3(PALM):c.477T>A (p.Val159=)
NM_002579.3(PALM):c.5+12C>G
NM_002579.3(PALM):c.5+15T>A
NM_002579.3(PALM):c.503-7G>A
NM_002579.3(PALM):c.503-8C>T
NM_002579.3(PALM):c.513G>A (p.Ser171=)
NM_002579.3(PALM):c.531G>A (p.Glu177=)
NM_002579.3(PALM):c.543G>C (p.Val181=)
NM_002579.3(PALM):c.57+10C>T
NM_002579.3(PALM):c.57+18C>T
NM_002579.3(PALM):c.57+20C>T
NM_002579.3(PALM):c.58-13G>T	rs1233749177
NM_002579.3(PALM):c.58-14G>C	rs1342223766
NM_002579.3(PALM):c.58-18A>C	rs1169108954
NM_002579.3(PALM):c.58-6C>T	rs1164178517
NM_002579.3(PALM):c.58-9T>C
NM_002579.3(PALM):c.6-10C>T	rs1485256889
NM_002579.3(PALM):c.6-4G>A
NM_002579.3(PALM):c.6-5C>T
NM_002579.3(PALM):c.618C>T (p.Tyr206=)
NM_002579.3(PALM):c.634+13C>T
NM_002579.3(PALM):c.635-7del
NM_002579.3(PALM):c.660C>T (p.Ala220=)	rs150589646
NM_002579.3(PALM):c.678C>G (p.Pro226=)
NM_002579.3(PALM):c.693G>A (p.Glu231=)
NM_002579.3(PALM):c.717G>A (p.Ala239=)
NM_002579.3(PALM):c.741A>C (p.Ala247=)
NM_002579.3(PALM):c.753C>T (p.Ala251=)
NM_002579.3(PALM):c.786G>T (p.Gly262=)
NM_002579.3(PALM):c.78G>A (p.Ala26=)
NM_002579.3(PALM):c.822C>G (p.Thr274=)	rs748378460
NM_002579.3(PALM):c.84C>T (p.Ile28=)	rs1036438626
NM_002579.3(PALM):c.861G>A (p.Pro287=)
NM_002579.3(PALM):c.891G>C (p.Pro297=)	rs140781313
NM_002579.3(PALM):c.921C>T (p.Asn307=)
NM_002579.3(PALM):c.933G>A (p.Glu311=)
NM_002579.3(PALM):c.952C>T (p.Leu318=)
NM_002579.3(PALM):c.963A>G (p.Gln321=)
NM_002579.3(PALM):c.974C>T (p.Thr325Met)
NM_002579.3(PALM):c.978G>A (p.Ala326=)
NM_002579.3(PALM):c.978G>C (p.Ala326=)
NM_002579.3(PALM):c.982C>T (p.Leu328=)

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