ClinVar Miner

List of variants in gene CRPPA reported as benign

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 53
Download table as spreadsheet
HGVS dbSNP
GRCh37/hg19 7p21.2(chr7:16085019-16127297)x1
GRCh37/hg19 7p21.2(chr7:16163218-16173482)x0
GRCh37/hg19 7p21.2(chr7:16168502-16173482)x0
GRCh37/hg19 7p21.2(chr7:16168708-16173590)x0
GRCh37/hg19 7p21.2(chr7:16319042-16445066)x1
GRCh37/hg19 7p21.2(chr7:16351568-16401190)x1
GRCh37/hg19 7p21.2(chr7:16436708-16440023)x3
GRCh38/hg38 7p21.2(chr7:16325260-16401680)x1
NC_000007.14:g.16258874_16258875del
NM_001101426.3(CRPPA):c.685-13_685-11dupGTT rs142647500
NM_001101426.3(CRPPA):c.836-9dupT rs3839757
NM_001101426.4(CRPPA):c.*1677A>G rs1528136
NM_001101426.4(CRPPA):c.*2106C>T rs11773533
NM_001101426.4(CRPPA):c.*2148T>C rs9691136
NM_001101426.4(CRPPA):c.*2167G>A rs28379235
NM_001101426.4(CRPPA):c.*2321_*2324dup rs138718602
NM_001101426.4(CRPPA):c.*2380G>A rs28444529
NM_001101426.4(CRPPA):c.*2566A>G rs76015838
NM_001101426.4(CRPPA):c.*3275_*3282del rs71549971
NM_001101426.4(CRPPA):c.*34C>G rs16878689
NM_001101426.4(CRPPA):c.*4023C>A rs12539174
NM_001101426.4(CRPPA):c.*60G>A rs1528137
NM_001101426.4(CRPPA):c.*988G>T rs1918859
NM_001101426.4(CRPPA):c.-145A>G
NM_001101426.4(CRPPA):c.1026+107A>C
NM_001101426.4(CRPPA):c.1026+111A>G
NM_001101426.4(CRPPA):c.1026+45_1026+46del rs139478143
NM_001101426.4(CRPPA):c.1059G>A (p.Lys353=) rs181099904
NM_001101426.4(CRPPA):c.1120-334C>T
NM_001101426.4(CRPPA):c.1220T>C (p.Leu407Ser) rs141625803
NM_001101426.4(CRPPA):c.1246C>T (p.Pro416Ser) rs373134516
NM_001101426.4(CRPPA):c.1251+18C>T rs201599524
NM_001101426.4(CRPPA):c.1251+50A>G rs78374272
NM_001101426.4(CRPPA):c.1251+89T>A
NM_001101426.4(CRPPA):c.257+164T>C
NM_001101426.4(CRPPA):c.257+203C>G
NM_001101426.4(CRPPA):c.258-125T>A
NM_001101426.4(CRPPA):c.32C>G (p.Pro11Arg) rs192925278
NM_001101426.4(CRPPA):c.346C>T (p.Arg116Cys) rs61744487
NM_001101426.4(CRPPA):c.360C>T (p.Val120=) rs183141256
NM_001101426.4(CRPPA):c.407C>T (p.Ala136Val) rs61734789
NM_001101426.4(CRPPA):c.534+13T>A rs6461252
NM_001101426.4(CRPPA):c.55A>C (p.Ser19Arg) rs7782939
NM_001101426.4(CRPPA):c.67G>T (p.Gly23Cys) rs187484645
NM_001101426.4(CRPPA):c.726A>G (p.Gln242=) rs61746966
NM_001101426.4(CRPPA):c.789+321T>A
NM_001101426.4(CRPPA):c.789+57T>G
NM_001101426.4(CRPPA):c.789+89A>G
NM_001101426.4(CRPPA):c.79A>C (p.Thr27Pro) rs558064127
NM_001101426.4(CRPPA):c.933+127A>G
NM_001101426.4(CRPPA):c.933+87A>G
NM_001101426.4(CRPPA):c.934-130_934-129insA
NM_001101426.4(CRPPA):c.947C>A (p.Thr316Lys) rs114363936

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.