ClinVar Miner

List of variants in gene DYNC1H1 reported by CeGaT Praxis fuer Humangenetik Tuebingen

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 17
Download table as spreadsheet
HGVS dbSNP
NM_001376.5(DYNC1H1):c.11558C>G (p.Thr3853Arg) rs1567021411
NM_001376.5(DYNC1H1):c.12867C>T (p.Asp4289=) rs571858561
NM_001376.5(DYNC1H1):c.1288del (p.Leu430fs) rs1555408161
NM_001376.5(DYNC1H1):c.1312G>A (p.Val438Ile) rs1034508175
NM_001376.5(DYNC1H1):c.13360G>A (p.Glu4454Lys) rs1064797194
NM_001376.5(DYNC1H1):c.1741A>T (p.Met581Leu) rs1566999047
NM_001376.5(DYNC1H1):c.3804G>A (p.Thr1268=) rs757595764
NM_001376.5(DYNC1H1):c.5209A>G (p.Thr1737Ala) rs1064797192
NM_001376.5(DYNC1H1):c.5818-4C>T rs532720319
NM_001376.5(DYNC1H1):c.751C>T (p.Arg251Cys) rs879253979
NM_001376.5(DYNC1H1):c.7544G>A (p.Gly2515Asp) rs1064797193
NM_001376.5(DYNC1H1):c.7702G>T (p.Val2568Phe) rs765245789
NM_001376.5(DYNC1H1):c.7743G>T (p.Leu2581Phe) rs1236685924
NM_001376.5(DYNC1H1):c.8416A>G (p.Ile2806Val) rs777184216
NM_001376.5(DYNC1H1):c.8432G>T (p.Arg2811Ile) rs774929269
NM_001376.5(DYNC1H1):c.8703T>C (p.Tyr2901=) rs755411424
NM_001376.5(DYNC1H1):c.8771+4G>A rs1555410867

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.