ClinVar Miner

List of variants in gene TMEM138 reported as likely benign for Joubert syndrome 16

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Total variants: 44
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HGVS dbSNP gnomAD frequency
NM_016464.5(TMEM138):c.461G>A (p.Arg154His) rs147966742 0.00059
NM_016464.5(TMEM138):c.102T>A (p.Thr34=) rs139387935 0.00055
NM_016464.5(TMEM138):c.414C>T (p.Ala138=) rs151094420 0.00012
NM_016464.5(TMEM138):c.465G>A (p.Lys155=) rs141851191 0.00011
NM_016464.5(TMEM138):c.129-4A>G rs372877379 0.00009
NM_016464.5(TMEM138):c.128+7G>T rs560650147 0.00007
NM_016464.5(TMEM138):c.81C>T (p.Phe27=) rs149327827 0.00006
NM_016464.5(TMEM138):c.387G>A (p.Leu129=) rs553815473 0.00004
NM_016464.5(TMEM138):c.301-12C>T rs761355609 0.00003
NM_016464.5(TMEM138):c.288T>C (p.His96=) rs747609713 0.00002
NM_016464.5(TMEM138):c.459G>A (p.Leu153=) rs200771374 0.00002
NM_016464.5(TMEM138):c.129-10A>G rs767269480 0.00001
NM_016464.5(TMEM138):c.129-18T>A rs1181378192 0.00001
NM_016464.5(TMEM138):c.129-20A>T rs1477684645 0.00001
NM_016464.5(TMEM138):c.129-8G>T rs1438561210 0.00001
NM_016464.5(TMEM138):c.12C>T (p.Thr4=) rs376500080 0.00001
NM_016464.5(TMEM138):c.192C>T (p.Phe64=) rs199841349 0.00001
NM_016464.5(TMEM138):c.204T>C (p.Ala68=) rs2135158047 0.00001
NM_016464.5(TMEM138):c.276C>T (p.Ser92=) rs756828257 0.00001
NM_016464.5(TMEM138):c.300+17G>A rs1858147311 0.00001
NM_016464.5(TMEM138):c.301-13A>G rs565197509 0.00001
NM_016464.5(TMEM138):c.301-16C>T rs763842533 0.00001
NM_016464.5(TMEM138):c.301-18A>G rs760508736 0.00001
NM_016464.5(TMEM138):c.301-9C>A rs764884921 0.00001
NM_016464.5(TMEM138):c.420A>G (p.Arg140=) rs548368196 0.00001
NM_016464.5(TMEM138):c.426C>T (p.Gly142=) rs781330063 0.00001
NM_016464.5(TMEM138):c.435C>T (p.His145=) rs748095062 0.00001
NM_016464.5(TMEM138):c.482G>A (p.Arg161Gln) rs569659022 0.00001
NM_016464.5(TMEM138):c.105T>C (p.Pro35=) rs1370730016
NM_016464.5(TMEM138):c.128+19T>G rs746435246
NM_016464.5(TMEM138):c.128+8C>T rs769334895
NM_016464.5(TMEM138):c.129-10dup rs2135157730
NM_016464.5(TMEM138):c.129-19C>T rs2135157682
NM_016464.5(TMEM138):c.195C>T (p.Val65=) rs2135158008
NM_016464.5(TMEM138):c.207C>T (p.Gly69=) rs2539865620
NM_016464.5(TMEM138):c.231G>A (p.Lys77=) rs2135158146
NM_016464.5(TMEM138):c.24C>T (p.Ser8=) rs768366778
NM_016464.5(TMEM138):c.300+13G>A rs2135158448
NM_016464.5(TMEM138):c.303C>T (p.Asn101=) rs2135162983
NM_016464.5(TMEM138):c.377-10C>G
NM_016464.5(TMEM138):c.377-11C>T rs749034092
NM_016464.5(TMEM138):c.377-19T>C rs1858239048
NM_016464.5(TMEM138):c.384G>A (p.Val128=) rs2539872057
NM_016464.5(TMEM138):c.45C>T (p.Phe15=) rs2539860684

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