ClinVar Miner

List of variants in gene TNC reported by CeGaT Center for Human Genetics Tuebingen

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Gene type:
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Total variants: 38
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HGVS dbSNP gnomAD frequency
NM_002160.4(TNC):c.1642G>A (p.Val548Met) rs61729478 0.00984
NM_002160.4(TNC):c.96G>A (p.Lys32=) rs145367019 0.00396
NM_002160.4(TNC):c.1322A>G (p.Asn441Ser) rs142220270 0.00174
NM_002160.4(TNC):c.628G>A (p.Gly210Ser) rs144032672 0.00159
NM_002160.4(TNC):c.61G>A (p.Glu21Lys) rs141126037 0.00125
NM_002160.4(TNC):c.1297G>A (p.Asp433Asn) rs147990968 0.00052
NM_002160.4(TNC):c.2511C>T (p.Tyr837=) rs146641282 0.00023
NM_002160.4(TNC):c.4685C>T (p.Thr1562Met) rs145720474 0.00009
NM_002160.4(TNC):c.2960C>T (p.Thr987Met) rs778506429 0.00007
NM_002160.4(TNC):c.1312C>T (p.Arg438Trp) rs771475685 0.00006
NM_002160.4(TNC):c.3413C>T (p.Thr1138Met) rs371671996 0.00005
NM_002160.4(TNC):c.1726G>A (p.Gly576Ser) rs371055558 0.00004
NM_002160.4(TNC):c.2491G>A (p.Asp831Asn) rs199896561 0.00004
NM_002160.4(TNC):c.4472G>A (p.Arg1491Gln) rs189247379 0.00004
NM_002160.4(TNC):c.281G>A (p.Gly94Glu) rs138687252 0.00002
NM_002160.4(TNC):c.2805C>T (p.His935=) rs749996186 0.00001
NM_002160.4(TNC):c.408G>A (p.Leu136=) rs140689506 0.00001
NM_002160.4(TNC):c.421A>G (p.Thr141Ala) rs762858023 0.00001
NM_002160.4(TNC):c.1104C>T (p.Ala368=) rs201505515
NM_002160.4(TNC):c.1249C>T (p.Arg417Cys)
NM_002160.4(TNC):c.2860+3G>A
NM_002160.4(TNC):c.3140A>G (p.Gln1047Arg)
NM_002160.4(TNC):c.3153C>A (p.Val1051=)
NM_002160.4(TNC):c.3352C>T (p.Arg1118Trp)
NM_002160.4(TNC):c.4172A>G (p.Gln1391Arg) rs1057519148
NM_002160.4(TNC):c.4579+4208C>G
NM_002160.4(TNC):c.5093G>C (p.Arg1698Pro) rs61734387
NM_002160.4(TNC):c.5109T>C (p.Ser1703=)
NM_002160.4(TNC):c.5134T>A (p.Ser1712Thr)
NM_002160.4(TNC):c.5174C>T (p.Ser1725Leu)
NM_002160.4(TNC):c.5506G>A (p.Glu1836Lys)
NM_002160.4(TNC):c.5732G>A (p.Arg1911Gln)
NM_002160.4(TNC):c.5978C>T (p.Thr1993Met)
NM_002160.4(TNC):c.5987G>C (p.Gly1996Ala) rs2131648755
NM_002160.4(TNC):c.6078C>T (p.Phe2026=)
NM_002160.4(TNC):c.6187A>G (p.Lys2063Glu)
NM_002160.4(TNC):c.867C>T (p.Tyr289=)
NM_002160.4(TNC):c.969C>A (p.Gly323=) rs1834778495

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