ClinVar Miner

List of variants in gene TTC21B reported as likely benign for abdominal and pelvic region disorder

Included ClinVar conditions (961):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 31
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HGVS dbSNP
NM_024753.5(TTC21B):c.*1087A>T rs150328867
NM_024753.5(TTC21B):c.*1225C>T
NM_024753.5(TTC21B):c.*516C>T rs185578095
NM_024753.5(TTC21B):c.*656G>A rs180737925
NM_024753.5(TTC21B):c.*847A>C rs138656848
NM_024753.5(TTC21B):c.1571C>G (p.Ser524Cys) rs145436538
NM_024753.5(TTC21B):c.1650A>G (p.Glu550=) rs145926679
NM_024753.5(TTC21B):c.1697A>G (p.His566Arg) rs146320075
NM_024753.5(TTC21B):c.1846C>T (p.Arg616Cys) rs139441507
NM_024753.5(TTC21B):c.2046C>T (p.Ala682=)
NM_024753.5(TTC21B):c.2161A>C (p.Asn721His) rs146637219
NM_024753.5(TTC21B):c.2181C>T (p.Leu727=)
NM_024753.5(TTC21B):c.2258C>T (p.Pro753Leu) rs539769126
NM_024753.5(TTC21B):c.2322+3A>G rs79037278
NM_024753.5(TTC21B):c.2569-10dup rs144600502
NM_024753.5(TTC21B):c.2569G>A (p.Ala857Thr)
NM_024753.5(TTC21B):c.2600G>A (p.Arg867His) rs76726265
NM_024753.5(TTC21B):c.263-4C>A
NM_024753.5(TTC21B):c.2829A>G (p.Leu943=)
NM_024753.5(TTC21B):c.2895A>T (p.Lys965Asn) rs146201603
NM_024753.5(TTC21B):c.3004C>G (p.Leu1002Val) rs146496725
NM_024753.5(TTC21B):c.3114A>G (p.Glu1038=) rs1436732135
NM_024753.5(TTC21B):c.3162C>T (p.Asp1054=)
NM_024753.5(TTC21B):c.3450A>G (p.Ala1150=)
NM_024753.5(TTC21B):c.3797C>T (p.Pro1266Leu) rs140384742
NM_024753.5(TTC21B):c.468A>G (p.Gly156=)
NM_024753.5(TTC21B):c.553-5A>C
NM_024753.5(TTC21B):c.665A>T (p.Gln222Leu) rs80026831
NM_024753.5(TTC21B):c.724G>A (p.Asp242Asn) rs74447004
NM_024753.5(TTC21B):c.838A>G (p.Met280Val) rs112868646
NM_024753.5(TTC21B):c.895-8C>T

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