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 | 36863613 | A | AGCTGTGG others(3138): Show |
intron_variant | MODIFIER | NA19012.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0226 | 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 | NA18951.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0101 | 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 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(70): Show |
a0001 | a0001c0001a0001c0005 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(2): Show | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0012others(41): Show | 73 | 434 | 0.1682 | 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 | NA19005.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0165 | 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 | HG01074.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0098 | 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 | HG00639.hp2 HG02615.hp1 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0001 | a0001c0001t0001g0233a0001c0003t0001g0096 | 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 | HG02965.hp2 | a0001 | a0001c0006 | a0001c0006t0001 | a0001c0006t0001g0278 | 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 | HG01099.hp1 HG02486.hp2 NA19240.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0235a0001c0001t0001g0265a0001c0001t0001g0284 | 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 | HG00642.hp1 HG03041.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0285a0001c0001t0001g0293 | 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 | NA20805.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0254 | 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 | HG04204.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0286 | 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 | 36863616 | T | TGTGGCCT others(3138): Show |
intron_variant | MODIFIER | NA18999.hp1 NA19012.hp2 |
a0001 | a0001c0002a0001c0004 | a0001c0002t0001a0001c0004t0001 | a0001c0002t0001g0166a0001c0004t0001g0125 | 2 | 434 | 0.0046 | 3145 | c.33- others(3158): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | TogoVar | ||||||
NCF4_chr22_36856006_36883015 | 36863616 | T | TGTGGCCT others(3138): Show |
intron_variant | MODIFIER | HG02622.hp1 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0208 | 1 | 434 | 0.0023 | 3145 | c.33- others(3158): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | TogoVar | ||||||
NCF4_chr22_36856006_36883015 | 36863616 | T | TGTGGCCT others(3138): Show |
intron_variant | MODIFIER | NA20300.hp1 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0078 | 1 | 434 | 0.0023 | 3145 | c.33- others(3158): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | TogoVar | ||||||
NCF4_chr22_36856006_36883015 | 36863616 | T | TGTGGCCT others(3138): Show |
intron_variant | MODIFIER | HG03130.hp1 | a0001 | a0001c0004 | a0001c0004t0001 | a0001c0004t0001g0222 | 1 | 434 | 0.0023 | 3145 | c.33- others(3158): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | TogoVar | ||||||
NCF4_chr22_36856006_36883015 | 36863616 | T | TGTGGCCT others(3138): Show |
intron_variant | MODIFIER | HG02922.hp2 NA18522.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0079a0001c0001t0001g0199 | 2 | 434 | 0.0046 | 3145 | c.33- others(3158): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | TogoVar | ||||||
NCF4_chr22_36856006_36883015 | 36863616 | T | TGTGGCCT others(3138): Show |
intron_variant | MODIFIER | HG01884.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0141 | 1 | 434 | 0.0023 | 3145 | c.33- others(3158): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | TogoVar | ||||||
PTGR1_chr9_111557567_111604647 | 111578316 | T | TTATTTCT others(3138): Show |
intron_variant | MODIFIER | NA19002.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0286 | 1 | 408 | 0.0025 | 3145 | c.651 others(3160): Show |
PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 7/9 | chr9 | TogoVar | ||||||
RPF2_chr6_110977038_111033263 | 111016638 | T | TAAAGAGT others(3138): Show |
intron_variant | MODIFIER | NA18998.hp2 | a0001 | a0001c0001 | a0001c0001t0020 | a0001c0001t0020g0203 | 1 | 360 | 0.0028 | 3145 | c.596 others(3160): Show |
RPF2 | ENSG00000197498.13 | transcript | ENST00000441448.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
TNKS_chr8_9550912_9787346 | 9771917 | A | AGAGTGGA others(3138): Show |
intron_variant | MODIFIER | HG02622.hp2 | a0001 | a0001c0002 | a0001c0002t0006 | a0001c0002t0006g0128 | 1 | 272 | 0.0037 | 3145 | c.389 others(3164): Show |
TNKS | ENSG00000173273.17 | transcript | ENST00000310430.11 | protein_coding | 26/26 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
TUBA4B_chr2_219248243_219277197 | 219270701 | C | CCCGTCCC others(3138): Show |
intron_variant | MODIFIER | HG03453.hp2 | a0004 | a0004c0004 | a0004c0004t0001 | a0004c0004t0001g0190 | 1 | 350 | 0.0029 | 3145 | c.192 others(3160): Show |
TUBA4B | ENSG00000243910.9 | transcript | ENST00000490341.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
TUBA4B_chr2_219248243_219277197 | 219270701 | C | CCCGTCCC others(3138): Show |
intron_variant | MODIFIER | HG02559.hp2 | a0004 | a0004c0004 | a0004c0004t0001 | a0004c0004t0001g0212 | 1 | 350 | 0.0029 | 3145 | c.192 others(3160): Show |
TUBA4B | ENSG00000243910.9 | transcript | ENST00000490341.3 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGEF16_chr1_3449665_3486113 | 3477303 | G | GTCACCCC others(3139): Show |
intron_variant | MODIFIER | HG01361.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0206 | 1 | 334 | 0.0030 | 3146 | c.147 others(3163): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
CLCN5_chrX_49917596_50104230 | 50057375 | G | GTCCTGGA others(3139): Show |
intron_variant | MODIFIER | HG02698.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0121 | 1 | 175 | 0.0057 | 3146 | c.164 others(3165): Show |
CLCN5 | ENSG00000171365.17 | transcript | ENST00000376091.8 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
MORN1_chr1_2316253_2396554 | 2325140 | C | CTTCCTTC others(3139): Show |
intron_variant | MODIFIER | HG03225.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0033 | 1 | 80 | 0.0125 | 3146 | c.125 others(3163): Show |
MORN1 | ENSG00000116151.14 | transcript | ENST00000378531.8 | protein_coding | 12/13 | chr1 | TogoVar | ||||||
MRPS36_chr5_69212760_69235158 | 69222008 | A | AGTACAAA others(3139): Show |
intron_variant | MODIFIER | NA18978.hp2 NA19090.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0138a0001c0001t0001g0139 | 2 | 409 | 0.0049 | 3146 | c.42+ others(3161): 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(3139): Show |
intron_variant | MODIFIER | NA18975.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0140 | 1 | 409 | 0.0024 | 3146 | c.42+ others(3161): 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(3139): Show |
intron_variant | MODIFIER | HG02523.hp1 NA18952.hp1 NA19065.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0134a0001c0001t0001g0141a0001c0001t0001g0142 | 3 | 409 | 0.0073 | 3146 | c.42+ others(3161): 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(3139): Show |
intron_variant | MODIFIER | HG01192.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0287 | 1 | 434 | 0.0023 | 3146 | c.33- others(3159): 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(3139): Show |
intron_variant | MODIFIER | HG03942.hp1 HG04115.hp1 NA18993.hp2 others(4): Show |
a0001a0004 | a0001c0001a0004c0013 | a0001c0001t0001a0001c0001t0005a0004c0013t0001 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0148others(4): Show | 7 | 434 | 0.0161 | 3146 | c.33- others(3159): 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(3139): Show |
intron_variant | MODIFIER | NA18981.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0117 | 1 | 434 | 0.0023 | 3146 | c.33- others(3159): 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(3139): Show |
intron_variant | MODIFIER | HG02071.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0118 | 1 | 434 | 0.0023 | 3146 | c.33- others(3159): 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(3139): Show |
intron_variant | MODIFIER | HG00738.hp2 HG01515.hp2 HG03688.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0015a0001c0001t0001g0108 | 4 | 434 | 0.0092 | 3146 | c.33- others(3159): 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(3139): Show |
intron_variant | MODIFIER | HG03831.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0062 | 1 | 434 | 0.0023 | 3146 | c.33- others(3159): 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(3139): Show |
intron_variant | MODIFIER | HG02683.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0089 | 1 | 434 | 0.0023 | 3146 | c.33- others(3159): 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(3139): Show |
intron_variant | MODIFIER | NA19081.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0160 | 1 | 434 | 0.0023 | 3146 | c.33- others(3159): 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(3139): Show |
intron_variant | MODIFIER | HG02109.hp2 HG02257.hp2 NA18959.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0119a0001c0001t0001g0137a0001c0001t0001g0195others(1): Show | 4 | 434 | 0.0092 | 3146 | c.33- others(3159): 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(3139): Show |
intron_variant | MODIFIER | HG03710.hp1 NA18991.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0139a0001c0001t0001g0256 | 2 | 434 | 0.0046 | 3146 | c.33- others(3159): 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(3139): Show |
intron_variant | MODIFIER | HG03490.hp1 HG03492.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0037 | 2 | 434 | 0.0046 | 3146 | c.33- others(3159): 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(3139): Show |
intron_variant | MODIFIER | HG02145.hp2 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0077 | 1 | 434 | 0.0023 | 3146 | c.33- others(3159): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | TogoVar | ||||||
NCF4_chr22_36856006_36883015 | 36863616 | T | TGTGGCCT others(3139): Show |
intron_variant | MODIFIER | HG03486.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0224 | 1 | 434 | 0.0023 | 3146 | c.33- others(3159): Show |
NCF4 | ENSG00000100365.16 | transcript | ENST00000248899.11 | protein_coding | 1/9 | chr22 | TogoVar | ||||||
NFATC3_chr16_68080370_68234259 | 68092609 | A | ATTAGCCG others(3139): Show |
intron_variant | MODIFIER | HG03041.hp2 HG03225.hp1 NA19240.hp2 |
a0003 | a0003c0003 | a0003c0003t0011 | a0003c0003t0011g0181a0003c0003t0011g0182a0003c0003t0011g0183 | 3 | 188 | 0.0160 | 3146 | c.103 others(3163): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
NFATC3_chr16_68080370_68234259 | 68092609 | A | ATTAGCCG others(3139): Show |
intron_variant | MODIFIER | HG01884.hp1 HG02280.hp2 HG02723.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0012a0001c0001t0016 | a0001c0001t0012g0185a0001c0001t0012g0187a0001c0001t0016g0184others(1): Show | 4 | 188 | 0.0213 | 3146 | c.103 others(3163): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
NFATC3_chr16_68080370_68234259 | 68092609 | A | ATTAGCCG others(3139): Show |
intron_variant | MODIFIER | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(39): Show |
a0001a0004 | a0001c0001a0004c0005 | a0001c0001t0002a0001c0001t0004a0001c0001t0019others(5): Show | a0001c0001t0002g0129a0001c0001t0002g0132a0001c0001t0002g0133others(39): Show | 42 | 188 | 0.2234 | 3146 | c.103 others(3163): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
NFATC3_chr16_68080370_68234259 | 68092609 | A | ATTAGCCG others(3139): Show |
intron_variant | MODIFIER | HG01169.hp2 | a0001 | a0001c0001 | a0001c0001t0021 | a0001c0001t0021g0158 | 1 | 188 | 0.0053 | 3146 | c.103 others(3163): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
NFATC3_chr16_68080370_68234259 | 68092609 | A | ATTAGCCG others(3139): Show |
intron_variant | MODIFIER | NA18975.hp1 | a0001 | a0001c0001 | a0001c0001t0026 | a0001c0001t0026g0159 | 1 | 188 | 0.0053 | 3146 | c.103 others(3163): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
NFATC3_chr16_68080370_68234259 | 68092609 | A | ATTAGCCG others(3139): Show |
intron_variant | MODIFIER | HG03098.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0160 | 1 | 188 | 0.0053 | 3146 | c.103 others(3163): Show |
NFATC3 | ENSG00000072736.19 | transcript | ENST00000346183.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
SULT2B1_chr19_48547172_48604423 | 48571207 | A | TTTTTTTT others(3139): Show |
intron_variant | MODIFIER | HG01433.hp1 HG03195.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0007a0001c0001t0001g0055 | 2 | 376 | 0.0053 | 3146 | c.72- others(3161): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | TogoVar | ||||||
SULT2B1_chr19_48547172_48604423 | 48571207 | A | TTTTTTTT others(3139): Show |
intron_variant | MODIFIER | HG01891.hp2 HG06807.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0031a0001c0001t0001g0367 | 2 | 376 | 0.0053 | 3146 | c.72- others(3161): Show |
SULT2B1 | ENSG00000088002.12 | transcript | ENST00000201586.7 | protein_coding | 1/6 | chr19 | TogoVar | ||||||
COL23A1_chr5_178232618_178595393 | 178585563 | G | GGGGGTAA others(3140): Show |
intron_variant | MODIFIER | HG00738.hp2 | a0001 | a0001c0004 | a0001c0004t0005 | a0001c0004t0005g0106 | 1 | 236 | 0.0042 | 3147 | c.294 others(3164): Show |
COL23A1 | ENSG00000050767.18 | transcript | ENST00000390654.8 | protein_coding | 1/28 | chr5 | TogoVar |