Abhd13 Variant Search Result - Rat Genome Database

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30 records found for search term Abhd13

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8582635	CV117188	single nucleotide variant	NM_032859.2(ABHD13):c.*4453C>T	Lung cancer [RCV000097709]	uncertain significance	13	108234685	108234685	Human		name
156263697	CV2375240	single nucleotide variant	NM_032859.3(ABHD13):c.31G>A (p.Val11Ile)	not specified [RCV004230272]	uncertain significance	13	108229249	108229249	Human		name
405676771	CV3283153	single nucleotide variant	NM_032859.3(ABHD13):c.95C>T (p.Pro32Leu)	not specified [RCV004420814]	uncertain significance	13	108229313	108229313	Human		name
407501639	CV3480695	single nucleotide variant	NM_032859.3(ABHD13):c.46A>G (p.Ile16Val)	not specified [RCV004669807]	uncertain significance	13	108229264	108229264	Human		name
597757316	CV3591119	single nucleotide variant	NM_032859.3(ABHD13):c.73C>A (p.Leu25Ile)	not specified [RCV004848301]	uncertain significance	13	108229291	108229291	Human		name
155991829	CV2253396	single nucleotide variant	NM_032859.3(ABHD13):c.239T>C (p.Met80Thr)	not specified [RCV004125128]	uncertain significance	13	108229457	108229457	Human		name
405676694	CV3283116	single nucleotide variant	NM_032859.3(ABHD13):c.293G>A (p.Arg98His)	not specified [RCV004420777]	uncertain significance	13	108229511	108229511	Human		name
407502796	CV3477100	single nucleotide variant	NM_032859.3(ABHD13):c.151A>G (p.Ile51Val)	not specified [RCV004670067]	likely benign	13	108229369	108229369	Human		name
597758157	CV3591325	single nucleotide variant	NM_032859.3(ABHD13):c.254C>T (p.Pro85Leu)	not specified [RCV004848474]	uncertain significance	13	108229472	108229472	Human		name
597758545	CV3591425	single nucleotide variant	NM_032859.3(ABHD13):c.265A>G (p.Ile89Val)	not specified [RCV004848557]	uncertain significance	13	108229483	108229483	Human		name
156287299	CV2229609	single nucleotide variant	NM_032859.3(ABHD13):c.947A>G (p.Lys316Arg)	not specified [RCV004103425]	uncertain significance	13	108230165	108230165	Human		name
155968960	CV2244389	single nucleotide variant	NM_032859.3(ABHD13):c.349A>G (p.Ile117Val)	not specified [RCV004100364]	uncertain significance	13	108229567	108229567	Human		name
156077709	CV2281683	single nucleotide variant	NM_032859.3(ABHD13):c.343C>G (p.Pro115Ala)	not specified [RCV004147836]	uncertain significance	13	108229561	108229561	Human		name
155920288	CV2343325	single nucleotide variant	NM_032859.3(ABHD13):c.323G>A (p.Gly108Glu)	not specified [RCV004194941]	uncertain significance	13	108229541	108229541	Human		name
329373713	CV2452623	single nucleotide variant	NM_032859.3(ABHD13):c.496T>C (p.Tyr166His)	not specified [RCV004275197]	uncertain significance	13	108229714	108229714	Human		name
401783375	CV2723505	single nucleotide variant	NM_032859.3(ABHD13):c.526G>A (p.Val176Met)	not specified [RCV004323911]	uncertain significance	13	108229744	108229744	Human		name
401863891	CV2770891	single nucleotide variant	NM_032859.3(ABHD13):c.926C>G (p.Thr309Ser)	not specified [RCV004343565]	uncertain significance	13	108230144	108230144	Human		name
405676743	CV3283124	single nucleotide variant	NM_032859.3(ABHD13):c.334C>T (p.Pro112Ser)	not specified [RCV004420785]	uncertain significance	13	108229552	108229552	Human		name
405677096	CV3283126	single nucleotide variant	NM_032859.3(ABHD13):c.335C>G (p.Pro112Arg)	not specified [RCV004420787]	uncertain significance	13	108229553	108229553	Human		name
405676993	CV3283146	single nucleotide variant	NM_032859.3(ABHD13):c.701C>T (p.Pro234Leu)	not specified [RCV004420807]	uncertain significance	13	108229919	108229919	Human		name
405676755	CV3283150	single nucleotide variant	NM_032859.3(ABHD13):c.955G>A (p.Val319Ile)	not specified [RCV004420811]	likely benign	13	108230173	108230173	Human		name
405676794	CV3283157	single nucleotide variant	NM_032859.3(ABHD13):c.960G>C (p.Lys320Asn)	not specified [RCV004420818]	uncertain significance	13	108230178	108230178	Human		name
407502415	CV3476943	single nucleotide variant	NM_032859.3(ABHD13):c.820G>T (p.Val274Leu)	not specified [RCV004669953]	uncertain significance	13	108230038	108230038	Human		name
407502596	CV3477016	single nucleotide variant	NM_032859.3(ABHD13):c.874A>G (p.Ile292Val)	not specified [RCV004670009]	uncertain significance	13	108230092	108230092	Human		name
407503063	CV3477197	single nucleotide variant	NM_032859.3(ABHD13):c.896A>G (p.Asn299Ser)	not specified [RCV004670136]	uncertain significance	13	108230114	108230114	Human		name
407519302	CV3480783	single nucleotide variant	NM_032859.3(ABHD13):c.850C>T (p.Pro284Ser)	not specified [RCV004676439]	uncertain significance	13	108230068	108230068	Human		name
597779296	CV3581082	single nucleotide variant	NM_032859.3(ABHD13):c.704T>C (p.Met235Thr)	not specified [RCV004853225]	uncertain significance	13	108229922	108229922	Human		name
597757670	CV3591221	single nucleotide variant	NM_032859.3(ABHD13):c.938A>T (p.Gln313Leu)	not specified [RCV004848370]	uncertain significance	13	108230156	108230156	Human		name
598247770	CV3901213	single nucleotide variant	NM_032859.3(ABHD13):c.926C>T (p.Thr309Ile)	not specified [RCV005258689]	uncertain significance	13	108230144	108230144	Human		name
598248402	CV3901304	single nucleotide variant	NM_032859.3(ABHD13):c.305T>C (p.Ile102Thr)	not specified [RCV005258779]	uncertain significance	13	108229523	108229523	Human		name

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