ClinVar Miner

List of variants in gene SRGAP1 studied for cancer

Included ClinVar conditions (475):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 6
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_020762.4(SRGAP1):c.1849C>T (p.Arg617Cys) rs114817817 0.00101
NM_020762.4(SRGAP1):c.182C>T (p.Thr61Met) rs778174499 0.00009
NM_020762.4(SRGAP1):c.2225-7G>A rs375559876 0.00004
NM_020762.4(SRGAP1):c.447A>C (p.Gln149His) rs781626187 0.00001
NM_020762.4(SRGAP1):c.731_732insAG (p.Leu245fs) rs2035064004
NM_020762.4(SRGAP1):c.823G>A (p.Ala275Thr) rs797044990

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.