Pla2g1b Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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17 records found for search term Pla2g1b

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15194785	CV760105	single nucleotide variant	NM_000928.3(PLA2G1B):c.195-10C>T	not provided [RCV000911223]	likely benign	12	120325071	120325071	Human		name
8634535	CV89755	single nucleotide variant	NM_000928.2(PLA2G1B):c.7C>G (p.Leu3Val)	Malignant melanoma [RCV000069852]	not provided	12	120327747	120327747	Human		name
156298780	CV2252007	single nucleotide variant	NM_000928.3(PLA2G1B):c.43G>A (p.Ala15Thr)	not specified [RCV004121750]	uncertain significance	12	120326012	120326012	Human		name
329390926	CV2437436	single nucleotide variant	NM_000928.3(PLA2G1B):c.250A>G (p.Lys84Glu)	not specified [RCV004256302]	uncertain significance	12	120325006	120325006	Human		name
401884674	CV2755961	single nucleotide variant	NM_000928.3(PLA2G1B):c.208C>T (p.His70Tyr)	not specified [RCV004336046]	uncertain significance	12	120325048	120325048	Human		name
405656532	CV3375964	single nucleotide variant	NM_000928.3(PLA2G1B):c.164G>A (p.Gly55Asp)	not specified [RCV004511434]	uncertain significance	12	120325891	120325891	Human		name
405656529	CV3375965	single nucleotide variant	NM_000928.3(PLA2G1B):c.247T>C (p.Cys83Arg)	not specified [RCV004511435]	uncertain significance	12	120325009	120325009	Human		name
597704819	CV3569631	single nucleotide variant	NM_000928.3(PLA2G1B):c.269C>A (p.Pro90Gln)	not specified [RCV004840176]	uncertain significance	12	120324987	120324987	Human		name
598169429	CV4000209	single nucleotide variant	NM_000928.3(PLA2G1B):c.193A>G (p.Lys65Glu)	not specified [RCV005392068]	uncertain significance	12	120325862	120325862	Human		name
598169434	CV4000210	single nucleotide variant	NM_000928.3(PLA2G1B):c.272A>G (p.Tyr91Cys)	not specified [RCV005392069]	uncertain significance	12	120324984	120324984	Human		name
598169438	CV4000211	single nucleotide variant	NM_000928.3(PLA2G1B):c.173C>A (p.Thr58Asn)	not specified [RCV005392070]	uncertain significance	12	120325882	120325882	Human		name
598169446	CV4000213	single nucleotide variant	NM_000928.3(PLA2G1B):c.173C>T (p.Thr58Ile)	not specified [RCV005392072]	uncertain significance	12	120325882	120325882	Human		name
156272337	CV2297154	single nucleotide variant	NM_000928.3(PLA2G1B):c.368A>G (p.Asn123Ser)	not specified [RCV004151049]	uncertain significance	12	120322272	120322272	Human		name
401877314	CV2764590	single nucleotide variant	NM_000928.3(PLA2G1B):c.398A>G (p.Tyr133Cys)	not specified [RCV004339145]	uncertain significance	12	120322242	120322242	Human		name
598169442	CV4000212	single nucleotide variant	NM_000928.3(PLA2G1B):c.361G>T (p.Asp121Tyr)	not specified [RCV005392071]	uncertain significance	12	120322279	120322279	Human		name
15164436	CV738489	single nucleotide variant	NM_000928.3(PLA2G1B):c.365G>A (p.Arg122His)	not provided [RCV000904001]	benign	12	120322275	120322275	Human		name
8627199	CV82343	single nucleotide variant	NM_000928.3(PLA2G1B):c.305C>T (p.Ser102Leu)	not specified [RCV004840175]	uncertain significance\|not provided	12	120324951	120324951	Human		name