ClinVar Miner

List of variants in gene TECPR2 reported as likely benign by Natera, Inc.

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 58
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HGVS dbSNP gnomAD frequency
NM_014844.5(TECPR2):c.2941C>A (p.Gln981Lys) rs62000389 0.01415
NM_014844.5(TECPR2):c.1470C>T (p.Ser490=) rs149584733 0.00245
NM_014844.5(TECPR2):c.1605C>T (p.Asn535=) rs145715326 0.00080
NM_014844.5(TECPR2):c.606T>C (p.Ser202=) rs140791062 0.00061
NM_014844.5(TECPR2):c.754C>A (p.Gln252Lys) rs147010113 0.00061
NM_014844.5(TECPR2):c.2847G>A (p.Ala949=) rs145452704 0.00035
NM_014844.5(TECPR2):c.1546G>A (p.Val516Met) rs141697267 0.00032
NM_014844.5(TECPR2):c.3294C>T (p.His1098=) rs144141409 0.00031
NM_014844.5(TECPR2):c.2021C>T (p.Pro674Leu) rs149022686 0.00029
NM_014844.5(TECPR2):c.1677T>C (p.Ser559=) rs375017422 0.00024
NM_014844.5(TECPR2):c.3831C>T (p.Asn1277=) rs200792120 0.00024
NM_014844.5(TECPR2):c.672A>G (p.Gly224=) rs138689342 0.00024
NM_014844.5(TECPR2):c.3246G>C (p.Gly1082=) rs373876214 0.00023
NM_014844.5(TECPR2):c.4035C>T (p.Ala1345=) rs376614211 0.00023
NM_014844.5(TECPR2):c.2280C>T (p.His760=) rs61744796 0.00021
NM_014844.5(TECPR2):c.1248C>T (p.Thr416=) rs144313788 0.00013
NM_014844.5(TECPR2):c.3882C>T (p.Thr1294=) rs145556234 0.00011
NM_014844.5(TECPR2):c.1173G>A (p.Thr391=) rs747637703 0.00009
NM_014844.5(TECPR2):c.1926C>T (p.Val642=) rs770279871 0.00009
NM_014844.5(TECPR2):c.318T>C (p.Leu106=) rs769086551 0.00009
NM_014844.5(TECPR2):c.3873C>T (p.His1291=) rs377631259 0.00008
NM_014844.5(TECPR2):c.2250G>A (p.Thr750=) rs182655288 0.00007
NM_014844.5(TECPR2):c.4081+10C>T rs745954864 0.00007
NM_014844.5(TECPR2):c.1792G>A (p.Gly598Arg) rs772792595 0.00006
NM_014844.5(TECPR2):c.2970C>T (p.Leu990=) rs367970932 0.00006
NM_014844.5(TECPR2):c.3171C>T (p.Pro1057=) rs749964386 0.00006
NM_014844.5(TECPR2):c.3477G>A (p.Arg1159=) rs2295975 0.00006
NM_014844.5(TECPR2):c.4065C>T (p.Ser1355=) rs142318405 0.00006
NM_014844.5(TECPR2):c.3912C>T (p.Thr1304=) rs748689796 0.00005
NM_014844.5(TECPR2):c.72G>A (p.Pro24=) rs201004031 0.00005
NM_014844.5(TECPR2):c.1518G>A (p.Ser506=) rs370643085 0.00004
NM_014844.5(TECPR2):c.2933+9G>A rs549959695 0.00004
NM_014844.5(TECPR2):c.4119C>T (p.Pro1373=) rs536343745 0.00004
NM_014844.5(TECPR2):c.1803G>A (p.Pro601=) rs779281934 0.00003
NM_014844.5(TECPR2):c.1791C>T (p.Leu597=) rs757180768 0.00002
NM_014844.5(TECPR2):c.2697G>A (p.Leu899=) rs755040646 0.00002
NM_014844.5(TECPR2):c.3000C>T (p.Asp1000=) rs200626084 0.00002
NM_014844.5(TECPR2):c.3360T>A (p.Ala1120=) rs774314281 0.00002
NM_014844.5(TECPR2):c.4188C>T (p.Ala1396=) rs113941655 0.00002
NM_014844.5(TECPR2):c.1704T>G (p.Thr568=) rs749355080 0.00001
NM_014844.5(TECPR2):c.2694C>T (p.Ala898=) rs202031176 0.00001
NM_014844.5(TECPR2):c.3486G>A (p.Thr1162=) rs747983532 0.00001
NM_014844.5(TECPR2):c.3549G>A (p.Ala1183=) rs564868110 0.00001
NM_014844.5(TECPR2):c.3744C>T (p.Pro1248=) rs373973558 0.00001
NM_014844.5(TECPR2):c.3792C>T (p.Pro1264=) rs766197921 0.00001
NM_014844.5(TECPR2):c.816G>A (p.Pro272=) rs369410138 0.00001
NM_014844.5(TECPR2):c.1397AGA[5] (p.Lys471del) rs572609303
NM_014844.5(TECPR2):c.1606G>C (p.Gly536Arg) rs186595127
NM_014844.5(TECPR2):c.1785G>A (p.Thr595=) rs1367573550
NM_014844.5(TECPR2):c.1869G>C (p.Gly623=) rs45605932
NM_014844.5(TECPR2):c.1872G>T (p.Ala624=) rs145129878
NM_014844.5(TECPR2):c.1925T>A (p.Val642Asp) rs746442659
NM_014844.5(TECPR2):c.2979G>A (p.Gln993=) rs1889962080
NM_014844.5(TECPR2):c.3913G>T (p.Ala1305Ser) rs573719989
NM_014844.5(TECPR2):c.4116G>A (p.Pro1372=) rs777406369
NM_014844.5(TECPR2):c.4116G>T (p.Pro1372=) rs777406369
NM_014844.5(TECPR2):c.4194G>A (p.Met1398Ile) rs757191728
NM_014844.5(TECPR2):c.741C>T (p.Val247=) rs551933071

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