regionname | pos | ref | alt | annotation | impact | samples | ahapids | achapids | acthapids | actghapids | ac | an | af | len | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length
|
cds cds pos length
|
aa aa pos length
|
distance | status | chr | external |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
TMEM132B_chr12_125181386_125667369 | 125316601 | A | ACTGAGTA others(3133): Show |
intron_variant | MODIFIER | HG01106.hp2 HG01358.hp1 HG01361.hp1 others(2): Show |
a0001a0002 | a0001c0004a0002c0001a0002c0006 | a0001c0004t0001a0002c0001t0013a0002c0006t0003 | a0001c0004t0001g0081a0002c0001t0013g0071a0002c0006t0003g0003others(2): Show | 5 | 128 | 0.0391 | 3140 | c.68- others(3157): Show |
TMEM132B | ENSG00000139364.11 | transcript | ENST00000682704.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TMEM132B_chr12_125181386_125667369 | 125316601 | A | ACTGAGTA others(3133): Show |
intron_variant | MODIFIER | HG03139.hp2 HG03209.hp1 |
a0001a0002 | a0001c0003a0002c0005 | a0001c0003t0027a0002c0005t0051 | a0001c0003t0027g0064a0002c0005t0051g0099 | 2 | 128 | 0.0156 | 3140 | c.68- others(3157): Show |
TMEM132B | ENSG00000139364.11 | transcript | ENST00000682704.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
TUBA4B_chr2_219248243_219277197 | 219270701 | C | CCCGTCCC others(3133): Show |
intron_variant | MODIFIER | HG01175.hp2 | a0005 | a0005c0005 | a0005c0005t0005 | a0005c0005t0005g0263 | 1 | 350 | 0.0029 | 3140 | c.192 others(3155): Show |
TUBA4B | ENSG00000243910.9 | transcript | ENST00000490341.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
HCN2_chr19_584881_622159 | 602415 | T | TCCTCCTC others(3134): Show |
intron_variant | MODIFIER | HG02647.hp1 | a0001 | a0001c0098 | a0001c0098t0006 | a0001c0098t0006g0064 | 1 | 408 | 0.0025 | 3141 | c.633 others(3158): Show |
HCN2 | ENSG00000099822.3 | transcript | ENST00000251287.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
LRCH1_chr13_46548170_46749898 | 46584009 | T | TAGAATAA others(3134): Show |
intron_variant | MODIFIER | NA18962.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0010 | 1 | 274 | 0.0037 | 3141 | c.307 others(3160): Show |
LRCH1 | ENSG00000136141.15 | transcript | ENST00000389797.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
NFATC3_chr16_68080370_68234259 | 68092609 | A | ATTAGCCG others(3134): Show |
intron_variant | MODIFIER | HG02572.hp2 HG02717.hp2 HG02886.hp2 others(1): Show |
a0002 | a0002c0002 | a0002c0002t0014a0002c0002t0036 | a0002c0002t0014g0177a0002c0002t0014g0178a0002c0002t0014g0180others(1): Show | 4 | 188 | 0.0213 | 3141 | c.103 others(3158): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
DCLK2_chr4_150073445_150262438 | 150251147 | C | CCCACACC others(3135): Show |
intron_variant | MODIFIER | HG00558.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0005 | 1 | 116 | 0.0086 | 3142 | c.207 others(3161): Show |
DCLK2 | ENSG00000170390.16 | transcript | ENST00000296550.12 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
EML6_chr2_54718662_54977025 | 54945186 | C | CCTCTCTC others(3135): Show |
intron_variant | MODIFIER | HG00639.hp1 | a0001 | a0001c0004 | a0001c0004t0008 | a0001c0004t0008g0099 | 1 | 264 | 0.0038 | 3142 | c.400 others(3161): Show |
EML6 | ENSG00000214595.13 | transcript | ENST00000356458.8 | protein_coding | 28/41 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
GALNT9_chr12_132191372_132334589 | 132241360 | G | GGCCCTCC others(3135): Show |
intron_variant | MODIFIER | HG00280.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0101 | 1 | 183 | 0.0055 | 3142 | c.107 others(3161): Show |
GALNT9 | ENSG00000182870.13 | transcript | ENST00000328957.13 | protein_coding | 6/10 | chr12 | TogoVar | ||||||
GALNT9_chr12_132191372_132334589 | 132241747 | A | ACCACACC others(3135): Show |
intron_variant | MODIFIER | NA20805.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0032 | 1 | 183 | 0.0055 | 3142 | c.107 others(3161): Show |
GALNT9 | ENSG00000182870.13 | transcript | ENST00000328957.13 | protein_coding | 6/10 | chr12 | TogoVar | ||||||
GALNT9_chr12_132191372_132334589 | 132241883 | A | ACACACCC others(3135): Show |
intron_variant | MODIFIER | HG02083.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0011 | 1 | 183 | 0.0055 | 3142 | c.107 others(3161): Show |
GALNT9 | ENSG00000182870.13 | transcript | ENST00000328957.13 | protein_coding | 6/10 | chr12 | TogoVar | ||||||
GALNT9_chr12_132191372_132334589 | 132241883 | A | ACACACCC others(3135): Show |
intron_variant | MODIFIER | NA19004.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0075 | 1 | 183 | 0.0055 | 3142 | c.107 others(3161): Show |
GALNT9 | ENSG00000182870.13 | transcript | ENST00000328957.13 | protein_coding | 6/10 | chr12 | TogoVar | ||||||
GALNT9_chr12_132191372_132334589 | 132242474 | C | CCCCTTCC others(3135): Show |
intron_variant | MODIFIER | HG01167.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0131 | 1 | 183 | 0.0055 | 3142 | c.107 others(3161): Show |
GALNT9 | ENSG00000182870.13 | transcript | ENST00000328957.13 | protein_coding | 6/10 | chr12 | TogoVar | ||||||
HHAT_chr1_210323902_210681290 | 210653965 | G | GGAATAGT others(3135): Show |
intron_variant | MODIFIER | HG02970.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0206 | 1 | 268 | 0.0037 | 3142 | c.139 others(3163): Show |
HHAT | ENSG00000054392.13 | transcript | ENST00000261458.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
PHF20_chr20_35767015_35955370 | 35829527 | G | GTAGAGAT others(3135): Show |
intron_variant | MODIFIER | HG02723.hp1 | a0001 | a0001c0001 | a0001c0001t0021 | a0001c0001t0021g0201 | 1 | 206 | 0.0049 | 3142 | c.84- others(3159): Show |
PHF20 | ENSG00000025293.17 | transcript | ENST00000374012.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | |||||
PHF20_chr20_35767015_35955370 | 35829527 | G | GTAGAGAT others(3135): Show |
intron_variant | MODIFIER | NA19067.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0197 | 1 | 206 | 0.0049 | 3142 | c.84- others(3159): Show |
PHF20 | ENSG00000025293.17 | transcript | ENST00000374012.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | |||||
LRCH1_chr13_46548170_46749898 | 46584009 | T | TAGAATAA others(3136): Show |
intron_variant | MODIFIER | NA18974.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0087 | 1 | 274 | 0.0037 | 3143 | c.307 others(3162): Show |
LRCH1 | ENSG00000136141.15 | transcript | ENST00000389797.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
MRPS36_chr5_69212760_69235158 | 69222008 | A | AGTACAAA others(3136): Show |
intron_variant | MODIFIER | HG02976.hp1 NA18522.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0048 | 2 | 409 | 0.0049 | 3143 | c.42+ others(3158): Show |
MRPS36 | ENSG00000134056.12 | transcript | ENST00000256441.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
MRPS36_chr5_69212760_69235158 | 69222008 | A | AGTACAAA others(3136): Show |
intron_variant | MODIFIER | HG02559.hp1 HG02602.hp1 HG02809.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0179a0001c0001t0001g0183a0001c0001t0001g0189others(3): Show | 6 | 409 | 0.0147 | 3143 | c.42+ others(3158): Show |
MRPS36 | ENSG00000134056.12 | transcript | ENST00000256441.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
MRPS36_chr5_69212760_69235158 | 69222008 | A | AGTACAAA others(3136): Show |
intron_variant | MODIFIER | HG01074.hp2 HG02486.hp2 HG02559.hp2 others(10): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0006a0001c0001t0001g0170a0001c0001t0001g0177others(6): Show | 13 | 409 | 0.0318 | 3143 | c.42+ others(3158): Show |
MRPS36 | ENSG00000134056.12 | transcript | ENST00000256441.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
MRPS36_chr5_69212760_69235158 | 69222008 | A | AGTACAAA others(3136): Show |
intron_variant | MODIFIER | HG00738.hp2 HG01123.hp1 HG01168.hp2 others(31): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0024others(19): Show | 34 | 409 | 0.0831 | 3143 | c.42+ others(3158): Show |
MRPS36 | ENSG00000134056.12 | transcript | ENST00000256441.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
MRPS36_chr5_69212760_69235158 | 69222008 | A | AGTACAAA others(3136): Show |
intron_variant | MODIFIER | HG00323.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0076 | 1 | 409 | 0.0024 | 3143 | c.42+ others(3158): Show |
MRPS36 | ENSG00000134056.12 | transcript | ENST00000256441.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
MRPS36_chr5_69212760_69235158 | 69222008 | A | AGTACAAA others(3136): Show |
intron_variant | MODIFIER | HG02258.hp2 HG02451.hp1 HG02572.hp1 others(8): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0009a0001c0001t0001g0025a0001c0001t0001g0058others(4): Show | 11 | 409 | 0.0269 | 3143 | c.42+ others(3158): Show |
MRPS36 | ENSG00000134056.12 | transcript | ENST00000256441.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
MRPS36_chr5_69212760_69235158 | 69222008 | A | AGTACAAA others(3136): Show |
intron_variant | MODIFIER | HG01167.hp2 HG01169.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0052 | 2 | 409 | 0.0049 | 3143 | c.42+ others(3158): Show |
MRPS36 | ENSG00000134056.12 | transcript | ENST00000256441.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
MRPS36_chr5_69212760_69235158 | 69222008 | A | AGTACAAA others(3136): Show |
intron_variant | MODIFIER | NA19043.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0077 | 1 | 409 | 0.0024 | 3143 | c.42+ others(3158): Show |
MRPS36 | ENSG00000134056.12 | transcript | ENST00000256441.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
NCF4_chr22_36856006_36883015 | 36863613 | A | AGCTGTGG others(3136): Show |
intron_variant | MODIFIER | HG00558.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0134 | 1 | 434 | 0.0023 | 3143 | c.33- others(3156): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
PHF20_chr20_35767015_35955370 | 35829527 | G | GTAGAGAT others(3136): Show |
intron_variant | MODIFIER | HG00544.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0196 | 1 | 206 | 0.0049 | 3143 | c.84- others(3160): Show |
PHF20 | ENSG00000025293.17 | transcript | ENST00000374012.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | |||||
PHF20_chr20_35767015_35955370 | 35829527 | G | GTAGAGAT others(3136): Show |
intron_variant | MODIFIER | HG00423.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0199 | 1 | 206 | 0.0049 | 3143 | c.84- others(3160): Show |
PHF20 | ENSG00000025293.17 | transcript | ENST00000374012.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | |||||
TNKS_chr8_9550912_9787346 | 9771917 | A | AGAGTGGA others(3136): Show |
intron_variant | MODIFIER | HG03831.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0253 | 1 | 272 | 0.0037 | 3143 | c.389 others(3162): Show |
TNKS | ENSG00000173273.17 | transcript | ENST00000310430.11 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
EML6_chr2_54718662_54977025 | 54945186 | C | CCTCTCTC others(3137): Show |
intron_variant | MODIFIER | HG03239.hp1 | a0001 | a0001c0004 | a0001c0004t0008 | a0001c0004t0008g0098 | 1 | 264 | 0.0038 | 3144 | c.400 others(3163): Show |
EML6 | ENSG00000214595.13 | transcript | ENST00000356458.8 | protein_coding | 28/41 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
LRRC27_chr10_132327193_132386508 | 132364409 | A | ACGCCCAC others(3137): Show |
intron_variant | MODIFIER | HG02572.hp1 | a0002 | a0002c0004 | a0002c0004t0011 | a0002c0004t0011g0010 | 1 | 290 | 0.0035 | 3144 | c.129 others(3163): Show |
LRRC27 | ENSG00000148814.18 | transcript | ENST00000368614.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
MRPS36_chr5_69212760_69235158 | 69222008 | A | AGTACAAA others(3137): Show |
intron_variant | MODIFIER | HG02280.hp2 HG02486.hp1 HG02809.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0045a0001c0001t0001g0194a0001c0001t0001g0207others(3): Show | 7 | 409 | 0.0171 | 3144 | c.42+ others(3159): Show |
MRPS36 | ENSG00000134056.12 | transcript | ENST00000256441.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
MRPS36_chr5_69212760_69235158 | 69222008 | A | AGTACAAA others(3137): Show |
intron_variant | MODIFIER | HG03927.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0195 | 1 | 409 | 0.0024 | 3144 | c.42+ others(3159): Show |
MRPS36 | ENSG00000134056.12 | transcript | ENST00000256441.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
MRPS36_chr5_69212760_69235158 | 69222008 | A | AGTACAAA others(3137): Show |
intron_variant | MODIFIER | HG00609.hp1 HG00642.hp2 HG01256.hp1 others(44): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0007a0001c0001t0001g0014a0001c0001t0001g0022others(29): Show | 47 | 409 | 0.1149 | 3144 | c.42+ others(3159): Show |
MRPS36 | ENSG00000134056.12 | transcript | ENST00000256441.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
MRPS36_chr5_69212760_69235158 | 69222008 | A | AGTACAAA others(3137): Show |
intron_variant | MODIFIER | HG00733.hp1 HG01243.hp2 HG02145.hp2 others(7): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0047a0001c0001t0001g0201a0001c0001t0001g0205others(6): Show | 10 | 409 | 0.0245 | 3144 | c.42+ others(3159): Show |
MRPS36 | ENSG00000134056.12 | transcript | ENST00000256441.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
MRPS36_chr5_69212760_69235158 | 69222008 | A | AGTACAAA others(3137): Show |
intron_variant | MODIFIER | NA18953.hp1 NA18987.hp1 NA18990.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0044a0001c0001t0001g0202 | 3 | 409 | 0.0073 | 3144 | c.42+ others(3159): Show |
MRPS36 | ENSG00000134056.12 | transcript | ENST00000256441.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
MRPS36_chr5_69212760_69235158 | 69222008 | A | AGTACAAA others(3137): Show |
intron_variant | MODIFIER | NA19064.hp2 | a0002 | a0002c0003 | a0002c0003t0001 | a0002c0003t0001g0157 | 1 | 409 | 0.0024 | 3144 | c.42+ others(3159): Show |
MRPS36 | ENSG00000134056.12 | transcript | ENST00000256441.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
MRPS36_chr5_69212760_69235158 | 69222008 | A | AGTACAAA others(3137): Show |
intron_variant | MODIFIER | HG03688.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0217 | 1 | 409 | 0.0024 | 3144 | c.42+ others(3159): Show |
MRPS36 | ENSG00000134056.12 | transcript | ENST00000256441.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
MRPS36_chr5_69212760_69235158 | 69222008 | A | AGTACAAA others(3137): Show |
intron_variant | MODIFIER | HG02273.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0176 | 1 | 409 | 0.0024 | 3144 | c.42+ others(3159): Show |
MRPS36 | ENSG00000134056.12 | transcript | ENST00000256441.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
MRPS36_chr5_69212760_69235158 | 69222008 | A | AGTACAAA others(3137): Show |
intron_variant | MODIFIER | HG01109.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0060 | 1 | 409 | 0.0024 | 3144 | c.42+ others(3159): Show |
MRPS36 | ENSG00000134056.12 | transcript | ENST00000256441.5 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
NCF4_chr22_36856006_36883015 | 36863613 | A | AGCTGTGG others(3137): Show |
intron_variant | MODIFIER | NA19066.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0124 | 1 | 434 | 0.0023 | 3144 | c.33- others(3157): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
NCF4_chr22_36856006_36883015 | 36863613 | A | AGCTGTGG others(3137): Show |
intron_variant | MODIFIER | NA18959.hp2 NA19066.hp1 NA19087.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0169 | 3 | 434 | 0.0069 | 3144 | c.33- others(3157): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
NCF4_chr22_36856006_36883015 | 36863613 | A | AGCTGTGG others(3137): Show |
intron_variant | MODIFIER | HG01109.hp1 NA18988.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0094a0001c0001t0001g0133 | 2 | 434 | 0.0046 | 3144 | c.33- others(3157): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
NCF4_chr22_36856006_36883015 | 36863613 | A | AGCTGTGG others(3137): Show |
intron_variant | MODIFIER | NA18970.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0135 | 1 | 434 | 0.0023 | 3144 | c.33- others(3157): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
NCF4_chr22_36856006_36883015 | 36863613 | A | AGCTGTGG others(3137): Show |
intron_variant | MODIFIER | HG02896.hp1 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0182 | 1 | 434 | 0.0023 | 3144 | c.33- others(3157): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
NCF4_chr22_36856006_36883015 | 36863613 | A | AGCTGTGG others(3137): Show |
intron_variant | MODIFIER | HG03710.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0297 | 1 | 434 | 0.0023 | 3144 | c.33- others(3157): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
NCF4_chr22_36856006_36883015 | 36863613 | A | AGCTGTGG others(3137): Show |
intron_variant | MODIFIER | HG01515.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0188 | 1 | 434 | 0.0023 | 3144 | c.33- others(3157): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
NCF4_chr22_36856006_36883015 | 36863616 | T | TGTGGCCT others(3137): Show |
intron_variant | MODIFIER | HG01891.hp1 HG03041.hp2 HG03225.hp1 |
a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0010 | 3 | 434 | 0.0069 | 3144 | c.33- others(3157): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | TogoVar | ||||||
NCF4_chr22_36856006_36883015 | 36863616 | T | TGTGGCCT others(3137): Show |
intron_variant | MODIFIER | HG00673.hp1 HG01123.hp2 HG01255.hp1 others(12): Show |
a0001 | a0001c0002a0001c0004 | a0001c0002t0001a0001c0002t0002a0001c0002t0004others(1): Show | a0001c0002t0001g0028a0001c0002t0001g0029a0001c0002t0001g0034others(9): Show | 15 | 434 | 0.0346 | 3144 | c.33- others(3157): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | TogoVar | ||||||
NCF4_chr22_36856006_36883015 | 36863616 | T | TGTGGCCT others(3137): Show |
intron_variant | MODIFIER | HG02280.hp1 HG03209.hp1 HG03209.hp2 others(2): Show |
a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0046a0001c0002t0001g0070a0001c0002t0001g0071others(1): Show | 5 | 434 | 0.0115 | 3144 | c.33- others(3157): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | TogoVar |