Tmem154 Variant Search Result - Rat Genome Database

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20 records found for search term Tmem154

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401928562	CV2820216	duplication	NM_152680.3(TMEM154):c.537-15_537-5dup	not provided [RCV003439518]	likely benign	4	152628565	152628566	Human		name
401928563	CV2820217	duplication	NM_152680.3(TMEM154):c.537-17_537-5dup	not provided [RCV003439519]	likely benign	4	152628565	152628566	Human		name
617153143	CV4021116	duplication	NM_152680.3(TMEM154):c.537-12_537-5dup	not provided [RCV005428869]	likely benign	4	152628565	152628566	Human		name
156375890	CV2210354	single nucleotide variant	NM_152680.3(TMEM154):c.7G>A (p.Ala3Thr)	not specified [RCV004089507]	uncertain significance	4	152679927	152679927	Human		name
156128948	CV2283945	single nucleotide variant	NM_152680.3(TMEM154):c.13C>G (p.Arg5Gly)	not specified [RCV004144256]	uncertain significance	4	152679921	152679921	Human		name
617152842	CV4020941	single nucleotide variant	NM_152680.3(TMEM154):c.498T>C (p.Pro166=)	not provided [RCV005428694]	likely benign	4	152640966	152640966	Human		name
155931116	CV2220978	single nucleotide variant	NM_152680.3(TMEM154):c.238G>T (p.Val80Leu)	not specified [RCV004092663]	uncertain significance	4	152652754	152652754	Human		name
156273612	CV2319833	single nucleotide variant	NM_152680.3(TMEM154):c.296C>T (p.Thr99Ile)	not specified [RCV004165893]	likely benign	4	152652696	152652696	Human		name
156351437	CV2323759	single nucleotide variant	NM_152680.3(TMEM154):c.280G>A (p.Val94Met)	not specified [RCV004176311]	uncertain significance	4	152652712	152652712	Human		name
405794497	CV3336018	single nucleotide variant	NM_152680.3(TMEM154):c.178G>A (p.Ala60Thr)	not specified [RCV004475263]	likely benign	4	152652814	152652814	Human		name
405794500	CV3336019	single nucleotide variant	NM_152680.3(TMEM154):c.206C>T (p.Pro69Leu)	not specified [RCV004475264]	uncertain significance	4	152652786	152652786	Human		name
597752938	CV3616905	single nucleotide variant	NM_152680.3(TMEM154):c.283G>A (p.Val95Ile)	not specified [RCV004867266]	likely benign	4	152652709	152652709	Human		name
597752942	CV3616906	single nucleotide variant	NM_152680.3(TMEM154):c.182A>G (p.Asn61Ser)	not specified [RCV004867267]	uncertain significance	4	152652810	152652810	Human		name
598178357	CV3917438	single nucleotide variant	NM_152680.3(TMEM154):c.277T>C (p.Ser93Pro)	not specified [RCV005285965]	uncertain significance	4	152652715	152652715	Human		name
329354080	CV2436915	single nucleotide variant	NM_152680.3(TMEM154):c.386T>C (p.Val129Ala)	not specified [RCV004260296]	uncertain significance	4	152644421	152644421	Human		name
329388419	CV2437391	single nucleotide variant	NM_152680.3(TMEM154):c.391G>C (p.Val131Leu)	not specified [RCV004256260]	uncertain significance	4	152644416	152644416	Human		name
329354178	CV2447289	single nucleotide variant	NM_152680.3(TMEM154):c.468G>A (p.Met156Ile)	not specified [RCV004262577]	uncertain significance	4	152643098	152643098	Human		name
405794503	CV3336020	single nucleotide variant	NM_152680.3(TMEM154):c.497C>T (p.Pro166Leu)	not specified [RCV004475265]	uncertain significance	4	152640967	152640967	Human		name
597752946	CV3616907	single nucleotide variant	NM_152680.3(TMEM154):c.409G>C (p.Asp137His)	not specified [RCV004867268]	uncertain significance	4	152643157	152643157	Human		name
598213199	CV3917437	single nucleotide variant	NM_152680.3(TMEM154):c.481G>A (p.Asp161Asn)	not specified [RCV005292271]	likely benign	4	152640983	152640983	Human		name

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable
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