List of variants in gene MAP4K4 reported by GeneDx

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 95

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001395002.1(MAP4K4):c.306+208G>A	rs7601576	0.92481
NM_001395002.1(MAP4K4):c.-106T>C	rs13430711	0.75577
NM_001395002.1(MAP4K4):c.181-224G>A	rs2286240	0.27326
NM_001395002.1(MAP4K4):c.3621+142A>G	rs57584884	0.25128
NM_001395002.1(MAP4K4):c.123+57A>G	rs1567385	0.24715
NM_001395002.1(MAP4K4):c.2454+112T>G	rs17745869	0.24674
NM_001395002.1(MAP4K4):c.2639+176A>G	rs6761844	0.22472
NM_001395002.1(MAP4K4):c.1022+125A>G	rs17801985	0.17229
NM_001395002.1(MAP4K4):c.1254A>G (p.Glu418=)	rs1139583	0.14395
NM_001395002.1(MAP4K4):c.1866+210G>A	rs62153660	0.13791
NM_001395002.1(MAP4K4):c.1234-81C>G	rs13407465	0.12014
NC_000002.12:g.101697473C>T	rs13430871	0.09890
NM_001395002.1(MAP4K4):c.2761-94A>T	rs9967668	0.09821
NM_001395002.1(MAP4K4):c.57+38del	rs375488010	0.06983
NM_001395002.1(MAP4K4):c.3931+164T>A	rs11895969	0.06925
NM_001395002.1(MAP4K4):c.4071+37A>G	rs79538056	0.06857
NM_001395002.1(MAP4K4):c.180+172C>T	rs6733385	0.06791
NM_001395002.1(MAP4K4):c.1866+5C>T	rs56378209	0.04141
NM_001395002.1(MAP4K4):c.3071-78C>T	rs6705854	0.03635
NM_001395002.1(MAP4K4):c.124-148A>G	rs13420267	0.03490
NM_001395002.1(MAP4K4):c.2356+136A>T	rs6713594	0.03344
NM_001395002.1(MAP4K4):c.3241+38G>C	rs7583833	0.02865
NM_001395002.1(MAP4K4):c.418-161T>G	rs79626224	0.02855
NM_001395002.1(MAP4K4):c.418-73A>G	rs55715763	0.02804
NM_001395002.1(MAP4K4):c.57+19G>A	rs142097566	0.02589
NM_001395002.1(MAP4K4):c.3931+40G>A	rs76906342	0.02240
NM_001395002.1(MAP4K4):c.3242-13G>A	rs114759280	0.02107
NM_001395002.1(MAP4K4):c.694+143G>A	rs56813602	0.01530
NM_001395002.1(MAP4K4):c.1234-214G>T	rs73943801	0.01442
NM_001395002.1(MAP4K4):c.773+92C>T	rs57968315	0.01423
NM_001395002.1(MAP4K4):c.57+163C>T	rs560675155	0.01326
NM_001395002.1(MAP4K4):c.124-3C>T	rs373459163	0.00019
NM_001395002.1(MAP4K4):c.-149GCC[5]	rs577276891
NM_001395002.1(MAP4K4):c.-363_-362dup	rs200434935
NM_001395002.1(MAP4K4):c.1011A>T (p.Glu337Asp)
NM_001395002.1(MAP4K4):c.1013G>C (p.Gly338Ala)
NM_001395002.1(MAP4K4):c.1060C>T (p.Arg354Ter)
NM_001395002.1(MAP4K4):c.106dup (p.Tyr36fs)	rs2466782013
NM_001395002.1(MAP4K4):c.1091A>G (p.Lys364Arg)
NM_001395002.1(MAP4K4):c.1298A>G (p.Glu433Gly)
NM_001395002.1(MAP4K4):c.1306_1308del (p.Arg437del)
NM_001395002.1(MAP4K4):c.1316A>G (p.Glu439Gly)
NM_001395002.1(MAP4K4):c.131A>T (p.His44Leu)	rs2470561483
NM_001395002.1(MAP4K4):c.163G>A (p.Val55Ile)
NM_001395002.1(MAP4K4):c.1752G>T (p.Gln584His)
NM_001395002.1(MAP4K4):c.1807T>C (p.Phe603Leu)
NM_001395002.1(MAP4K4):c.180G>A (p.Glu60=)
NM_001395002.1(MAP4K4):c.1853C>G (p.Pro618Arg)	rs2468033148
NM_001395002.1(MAP4K4):c.1867-1G>A
NM_001395002.1(MAP4K4):c.2008del (p.Leu670fs)
NM_001395002.1(MAP4K4):c.2019_2037dup (p.Ala680delinsLeuTer)
NM_001395002.1(MAP4K4):c.2178C>G (p.Ser726Arg)
NM_001395002.1(MAP4K4):c.2273C>T (p.Ser758Phe)
NM_001395002.1(MAP4K4):c.2286C>A (p.Ser762Arg)
NM_001395002.1(MAP4K4):c.2338G>A (p.Glu780Lys)
NM_001395002.1(MAP4K4):c.2454+2T>A
NM_001395002.1(MAP4K4):c.2639+174A>G	rs112366063
NM_001395002.1(MAP4K4):c.2741G>A (p.Gly914Asp)
NM_001395002.1(MAP4K4):c.281C>T (p.Pro94Leu)
NM_001395002.1(MAP4K4):c.2854TCC[2] (p.Ser954del)
NM_001395002.1(MAP4K4):c.2937G>T (p.Lys979Asn)
NM_001395002.1(MAP4K4):c.2952G>A (p.Glu984=)
NM_001395002.1(MAP4K4):c.2974del (p.Leu992fs)
NM_001395002.1(MAP4K4):c.3005C>T (p.Thr1002Ile)
NM_001395002.1(MAP4K4):c.3036T>G (p.Ile1012Met)
NM_001395002.1(MAP4K4):c.307-2A>G
NM_001395002.1(MAP4K4):c.3070+5G>A
NM_001395002.1(MAP4K4):c.3268A>T (p.Ser1090Cys)	rs2468661370
NM_001395002.1(MAP4K4):c.347T>C (p.Leu116Pro)
NM_001395002.1(MAP4K4):c.3481A>G (p.Thr1161Ala)
NM_001395002.1(MAP4K4):c.3514A>C (p.Lys1172Gln)
NM_001395002.1(MAP4K4):c.3521-137G>C	rs2072206
NM_001395002.1(MAP4K4):c.3521-60T>G	rs72991249
NM_001395002.1(MAP4K4):c.3590C>G (p.Pro1197Arg)
NM_001395002.1(MAP4K4):c.3622-44del	rs569902749
NM_001395002.1(MAP4K4):c.3622-45_3622-44del	rs569902749
NM_001395002.1(MAP4K4):c.3631G>T (p.Glu1211Ter)
NM_001395002.1(MAP4K4):c.3763C>T (p.Pro1255Ser)
NM_001395002.1(MAP4K4):c.3764C>G (p.Pro1255Arg)
NM_001395002.1(MAP4K4):c.3791C>T (p.Pro1264Leu)
NM_001395002.1(MAP4K4):c.3806T>C (p.Ile1269Thr)
NM_001395002.1(MAP4K4):c.3905A>C (p.Gln1302Pro)
NM_001395002.1(MAP4K4):c.3932-130T>A	rs10194704
NM_001395002.1(MAP4K4):c.4055G>A (p.Cys1352Tyr)
NM_001395002.1(MAP4K4):c.40G>A (p.Asp14Asn)
NM_001395002.1(MAP4K4):c.40G>T (p.Asp14Tyr)
NM_001395002.1(MAP4K4):c.52del (p.Leu18fs)
NM_001395002.1(MAP4K4):c.57+35GGCAGCC[4]	rs572189095
NM_001395002.1(MAP4K4):c.571A>C (p.Thr191Pro)	rs2466903970
NM_001395002.1(MAP4K4):c.584T>A (p.Met195Lys)	rs2466904177
NM_001395002.1(MAP4K4):c.60T>G (p.Asp20Glu)
NM_001395002.1(MAP4K4):c.640-140C>A	rs2301980
NM_001395002.1(MAP4K4):c.640-174_640-167dup	rs3216993
NM_001395002.1(MAP4K4):c.68G>C (p.Gly23Ala)	rs2466781417
NM_001395002.1(MAP4K4):c.940G>A (p.Gly314Ser)

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.