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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
NCF4_chr22_36856006_36883015 | 36863616 | T | TGTGGCCT others(3137): Show |
intron_variant | MODIFIER | HG02615.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0196 | 1 | 434 | 0.0023 | 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 | HG02257.hp1 HG03486.hp2 |
a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0072a0001c0002t0001g0221 | 2 | 434 | 0.0046 | 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 | HG02809.hp1 | a0001 | a0001c0004 | a0001c0004t0001 | a0001c0004t0001g0076 | 1 | 434 | 0.0023 | 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 | HG02572.hp2 HG02818.hp1 HG03516.hp1 others(3): Show |
a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0025a0001c0002t0001g0045a0001c0002t0001g0104others(1): Show | 6 | 434 | 0.0138 | 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 | HG02970.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0084 | 1 | 434 | 0.0023 | 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 | HG01975.hp1 NA18966.hp1 NA18975.hp2 others(4): Show |
a0001 | a0001c0002a0001c0004 | a0001c0002t0001a0001c0004t0001 | a0001c0002t0001g0136a0001c0002t0001g0158a0001c0002t0001g0253others(4): Show | 7 | 434 | 0.0161 | 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 | HG02647.hp2 HG02965.hp1 |
a0001 | a0001c0002 | a0001c0002t0003 | a0001c0002t0003g0067a0001c0002t0003g0068 | 2 | 434 | 0.0046 | 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 | HG02723.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0200 | 1 | 434 | 0.0023 | 3144 | c.33- others(3157): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | TogoVar | ||||||
PIEZO1_chr16_88710338_88790220 | 88731928 | C | CGGGGCGT others(3137): Show |
intron_variant | MODIFIER | HG00099.hp2 | a0012 | a0012c0035 | a0012c0035t0001 | a0012c0035t0001g0181 | 1 | 282 | 0.0036 | 3144 | c.299 others(3159): Show |
PIEZO1 | ENSG00000103335.22 | transcript | ENST00000301015.14 | protein_coding | 21/50 | chr16 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1223139 | T | TCTCCCTG others(3137): Show |
intron_variant | MODIFIER | HG01175.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0120 | 1 | 190 | 0.0053 | 3144 | c.719 others(3163): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
SPAAR_chr9_35904490_35916686 | 35913714 | G | GTGTGTGT others(3137): Show |
downstream_gene_variant | MODIFIER | HG02818.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0003 | 1 | 420 | 0.0024 | 3144 | c.*30 others(3155): Show |
SPAAR | ENSG00000235387.5 | transcript | ENST00000443779.3 | protein_coding | 2029 | chr9 | TogoVar | ||||||
TNKS_chr8_9550912_9787346 | 9771917 | A | AGAGTGGA others(3137): Show |
intron_variant | MODIFIER | HG02965.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0119 | 1 | 272 | 0.0037 | 3144 | c.389 others(3163): Show |
TNKS | ENSG00000173273.17 | transcript | ENST00000310430.11 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
TNKS_chr8_9550912_9787346 | 9771917 | A | AGAGTGGA others(3137): Show |
intron_variant | MODIFIER | HG03654.hp2 | a0001 | a0001c0003 | a0001c0003t0003 | a0001c0003t0003g0082 | 1 | 272 | 0.0037 | 3144 | c.389 others(3163): 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(3138): Show |
intron_variant | MODIFIER | NA18983.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0178 | 1 | 264 | 0.0038 | 3145 | c.400 others(3164): Show |
EML6 | ENSG00000214595.13 | transcript | ENST00000356458.8 | protein_coding | 28/41 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
F13A1_chr6_6139084_6325662 | 6262169 | G | GTGACCCT others(3138): Show |
intron_variant | MODIFIER | HG02896.hp1 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0178 | 1 | 292 | 0.0034 | 3145 | c.571 others(3162): Show |
F13A1 | ENSG00000124491.16 | transcript | ENST00000264870.8 | protein_coding | 4/14 | chr6 | TogoVar | ||||||
FAM227A_chr22_38573118_38661392 | 38644446 | A | ACTATGCT others(3138): Show |
intron_variant | MODIFIER | NA18960.hp2 | a0001 | a0001c0001 | a0001c0001t0055 | a0001c0001t0055g0243 | 1 | 328 | 0.0031 | 3145 | c.225 others(3162): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | TogoVar | ||||||
FAM227A_chr22_38573118_38661392 | 38644446 | A | ACTATGCT others(3138): Show |
intron_variant | MODIFIER | NA18974.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0308 | 1 | 328 | 0.0031 | 3145 | c.225 others(3162): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | TogoVar | ||||||
MRPS36_chr5_69212760_69235158 | 69222008 | A | AGTACAAA others(3138): Show |
intron_variant | MODIFIER | HG02080.hp2 NA18945.hp1 NA19091.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0180a0001c0001t0001g0192a0001c0001t0001g0193 | 3 | 409 | 0.0073 | 3145 | c.42+ others(3160): 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(3138): Show |
intron_variant | MODIFIER | HG00741.hp1 | a0001 | a0001c0004 | a0001c0004t0001 | a0001c0004t0001g0218 | 1 | 409 | 0.0024 | 3145 | c.42+ others(3160): 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(3138): Show |
intron_variant | MODIFIER | HG03041.hp1 HG03579.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0219a0001c0001t0001g0226 | 2 | 409 | 0.0049 | 3145 | c.42+ others(3160): 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(3138): Show |
intron_variant | MODIFIER | HG00423.hp1 HG04184.hp2 NA18944.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0017a0001c0001t0001g0096a0001c0001t0001g0097others(1): Show | 6 | 409 | 0.0147 | 3145 | c.42+ others(3160): 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(3138): Show |
intron_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(81): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0013others(34): Show | 84 | 409 | 0.2054 | 3145 | c.42+ others(3160): 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(3138): Show |
intron_variant | MODIFIER | HG00544.hp1 NA18943.hp2 NA18951.hp1 others(3): Show |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0001a0002c0003t0001 | a0001c0001t0001g0019a0001c0001t0001g0041a0002c0003t0001g0019others(2): Show | 6 | 409 | 0.0147 | 3145 | c.42+ others(3160): 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(3138): Show |
intron_variant | MODIFIER | HG02145.hp1 HG02895.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0238a0001c0001t0001g0239 | 2 | 409 | 0.0049 | 3145 | c.42+ others(3160): 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(3138): Show |
intron_variant | MODIFIER | HG02886.hp1 | a0001 | a0001c0014 | a0001c0014t0001 | a0001c0014t0001g0064 | 1 | 434 | 0.0023 | 3145 | c.33- others(3158): 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(3138): Show |
intron_variant | MODIFIER | HG02055.hp1 HG02055.hp2 HG02647.hp1 others(4): Show |
a0001 | a0001c0006a0001c0008 | a0001c0006t0001a0001c0008t0001 | a0001c0006t0001g0005a0001c0008t0001g0005 | 7 | 434 | 0.0161 | 3145 | c.33- others(3158): 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(3138): Show |
intron_variant | MODIFIER | HG02886.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0080 | 1 | 434 | 0.0023 | 3145 | c.33- others(3158): 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(3138): Show |
intron_variant | MODIFIER | NA19060.hp1 NA19082.hp2 NA19089.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0109a0001c0001t0001g0122a0001c0001t0002g0053 | 3 | 434 | 0.0069 | 3145 | c.33- others(3158): 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(3138): Show |
intron_variant | MODIFIER | NA18747.hp2 NA18964.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0123a0001c0001t0001g0212 | 2 | 434 | 0.0046 | 3145 | c.33- others(3158): 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(3138): Show |
intron_variant | MODIFIER | HG02056.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0213 | 1 | 434 | 0.0023 | 3145 | c.33- others(3158): 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(3138): Show |
intron_variant | MODIFIER | HG02451.hp2 | a0001 | a0001c0006 | a0001c0006t0001 | a0001c0006t0001g0081 | 1 | 434 | 0.0023 | 3145 | c.33- others(3158): 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(3138): Show |
intron_variant | MODIFIER | HG03579.hp1 | a0001 | a0001c0006 | a0001c0006t0003 | a0001c0006t0003g0065 | 1 | 434 | 0.0023 | 3145 | c.33- others(3158): 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(3138): Show |
intron_variant | MODIFIER | HG03834.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0279 | 1 | 434 | 0.0023 | 3145 | c.33- others(3158): 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(3138): Show |
intron_variant | MODIFIER | NA18973.hp1 NA18977.hp2 NA19003.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0030a0001c0001t0001g0127a0001c0001t0001g0168others(1): Show | 5 | 434 | 0.0115 | 3145 | c.33- others(3158): 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(3138): Show |
intron_variant | MODIFIER | NA18946.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0149 | 1 | 434 | 0.0023 | 3145 | c.33- others(3158): 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(3138): Show |
intron_variant | MODIFIER | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(91): Show |
a0001 | a0001c0001a0001c0005 | a0001c0001t0001a0001c0001t0002a0001c0005t0001 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(61): Show | 94 | 434 | 0.2166 | 3145 | c.33- others(3158): 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(3138): Show |
intron_variant | MODIFIER | HG02080.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0220 | 1 | 434 | 0.0023 | 3145 | c.33- others(3158): 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(3138): Show |
intron_variant | MODIFIER | NA18986.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0052 | 1 | 434 | 0.0023 | 3145 | c.33- others(3158): 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(3138): Show |
intron_variant | MODIFIER | HG02451.hp1 | a0001 | a0001c0006 | a0001c0006t0001 | a0001c0006t0001g0266 | 1 | 434 | 0.0023 | 3145 | c.33- others(3158): 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(3138): Show |
intron_variant | MODIFIER | HG03239.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0181 | 1 | 434 | 0.0023 | 3145 | c.33- others(3158): 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(3138): Show |
intron_variant | MODIFIER | NA21309.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0262 | 1 | 434 | 0.0023 | 3145 | c.33- others(3158): 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(3138): Show |
intron_variant | MODIFIER | NA18948.hp2 NA18971.hp1 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0022 | 2 | 434 | 0.0046 | 3145 | c.33- others(3158): 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(3138): Show |
intron_variant | MODIFIER | HG01891.hp2 HG02818.hp2 HG03139.hp2 others(1): Show |
a0001 | a0001c0001a0001c0005 | a0001c0001t0001a0001c0001t0003a0001c0005t0001 | a0001c0001t0001g0082a0001c0001t0003g0066a0001c0001t0003g0276others(1): Show | 4 | 434 | 0.0092 | 3145 | c.33- others(3158): 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(3138): Show |
intron_variant | MODIFIER | HG01175.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0100 | 1 | 434 | 0.0023 | 3145 | c.33- others(3158): 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(3138): Show |
intron_variant | MODIFIER | NA21309.hp2 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0291 | 1 | 434 | 0.0023 | 3145 | c.33- others(3158): 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(3138): Show |
intron_variant | MODIFIER | HG03579.hp2 NA20129.hp1 |
a0001 | a0001c0006 | a0001c0006t0001 | a0001c0006t0001g0073a0001c0006t0001g0198 | 2 | 434 | 0.0046 | 3145 | c.33- others(3158): 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(3138): Show |
intron_variant | MODIFIER | HG02074.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0157 | 1 | 434 | 0.0023 | 3145 | c.33- others(3158): 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(3138): Show |
intron_variant | MODIFIER | HG01516.hp2 HG02559.hp1 HG03195.hp1 |
a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0011 | 3 | 434 | 0.0069 | 3145 | c.33- others(3158): 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(3138): Show |
intron_variant | MODIFIER | HG01496.hp1 HG02572.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0263a0001c0001t0001g0264 | 2 | 434 | 0.0046 | 3145 | c.33- others(3158): 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(3138): Show |
intron_variant | MODIFIER | NA18989.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0183 | 1 | 434 | 0.0023 | 3145 | c.33- others(3158): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr22 | TogoVar |