MLH1, mutL homolog 1, 4292

N. diseases: 526; N. variants: 757
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs878853787
rs878853787
3 37050630 stop gained -/A delins
Hereditary Nonpolyposis Colorectal Neoplasms
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Nutritional and Metabolic Diseases 0.700 1.000 9 1996 2016
dbSNP: rs1553665683
rs1553665683
3 37050540 stop gained -/TATAAAGCCTTGCGCTCACACATTCTGCCTC delins
Hereditary Nonpolyposis Colorectal Neoplasms
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Nutritional and Metabolic Diseases 0.700 1.000 6 1999 2014
dbSNP: rs1060500698
rs1060500698
3 37050639 frameshift variant T/- delins
Hereditary Nonpolyposis Colorectal Neoplasms
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Nutritional and Metabolic Diseases 0.700 1.000 4 2003 2012
dbSNP: rs1553665866
rs1553665866
3 37050594 stop gained G/T snv
Hereditary Nonpolyposis Colorectal Neoplasms
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Nutritional and Metabolic Diseases 0.700 1.000 4 1999 2010
dbSNP: rs1060500699
rs1060500699
3 37025702 frameshift variant -/T delins
Hereditary Nonpolyposis Colorectal Neoplasms
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Nutritional and Metabolic Diseases 0.700 1.000 3 2015 2017
dbSNP: rs1559597322
rs1559597322
3 37050642 frameshift variant AG/- delins
Hereditary Nonpolyposis Colorectal Neoplasms
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Nutritional and Metabolic Diseases 0.700 1.000 3 2003 2010
dbSNP: rs267607744
rs267607744
3 37006990 splice acceptor variant G/A;C snv
Hereditary Nonpolyposis Colorectal Neoplasms
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Nutritional and Metabolic Diseases 0.700 1.000 3 2005 2015
dbSNP: rs878853785
rs878853785
3 37048957 frameshift variant AT/- delins
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms 0.700 1.000 3 2014 2017
dbSNP: rs1416171624
rs1416171624
3 37047578 stop gained G/A;T snv 4.0E-06
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms 0.700 1.000 2 2005 2011
dbSNP: rs1553644277
rs1553644277
3 37012101 splice donor variant T/C snv
Hereditary Nonpolyposis Colorectal Neoplasms
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Nutritional and Metabolic Diseases 0.700 1.000 2 2005 2014
dbSNP: rs1553659500
rs1553659500
3 37042335 splice region variant A/G snv
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms 0.700 1.000 2 2009 2013
dbSNP: rs1553662800
rs1553662800
3 37047572 frameshift variant -/CCAGATAGTCCAGA ins
Hereditary Nonpolyposis Colorectal Neoplasms
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Nutritional and Metabolic Diseases 0.700 1.000 2 2005 2014
dbSNP: rs1553663834
rs1553663834
3 37048542 frameshift variant T/- delins
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms 0.700 1.000 2 2012 2015
dbSNP: rs1553664702
rs1553664702
3 37049012 stop gained C/T snv
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms 0.700 1.000 2 2010 2015
dbSNP: rs759680369
rs759680369
3 36993574 synonymous variant G/A;C;T snv 8.0E-06
Hereditary Nonpolyposis Colorectal Neoplasms
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Nutritional and Metabolic Diseases 0.700 1.000 2 2013 2018
dbSNP: rs786201990
rs786201990
3 37047675 frameshift variant -/T delins
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms 0.700 1.000 2 2011 2015
dbSNP: rs786202326
rs786202326
3 37050628 frameshift variant TA/- delins
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms 0.700 1.000 2 2013 2015
dbSNP: rs863225383
rs863225383
3 37011857 stop gained A/T snv
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms 0.700 1.000 2 2014 2015
dbSNP: rs878853785
rs878853785
3 37048957 frameshift variant AT/- delins
Hereditary Nonpolyposis Colorectal Neoplasms
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Nutritional and Metabolic Diseases 0.700 1.000 2 2014 2015
dbSNP: rs886039424
rs886039424
3 37048911 stop gained G/A;C snv
Hereditary Nonpolyposis Colorectal Neoplasms
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Nutritional and Metabolic Diseases 0.700 1.000 2 2002 2003
dbSNP: rs1305605404
rs1305605404
3 36996619 missense variant T/C;G snv
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms 0.700 1.000 1 2015 2015
dbSNP: rs1389945622
rs1389945622
3 36993560 missense variant G/A;C snv
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms
Neoplasms; Skin and Connective Tissue Diseases 0.010 1.000 1 2011 2011
dbSNP: rs1553640334
rs1553640334
3 37001052 missense variant A/C snv
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms 0.700 1.000 1 2011 2011
dbSNP: rs1553648149
rs1553648149
3 37020419 frameshift variant AAGC/- delins
Hereditary Nonpolyposis Colorectal Neoplasms
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Nutritional and Metabolic Diseases 0.700 1.000 1 2005 2005
dbSNP: rs1553648149
rs1553648149
3 37020419 frameshift variant AAGC/- delins
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms 0.700 1.000 1 2005 2005