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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
NTAN1_chr16_15032857_15061074 | 15042718 | C | CTATTTAT others(13): Show |
intron_variant | MODIFIER | HG01081.hp1 HG02647.hp1 HG02896.hp1 others(3): Show |
a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0015a0002c0002t0001g0027 | 6 | 453 | 0.0133 | 20 | c.434 others(37): Show |
NTAN1 | ENSG00000157045.9 | transcript | ENST00000287706.8 | protein_coding | 5/9 | chr16 | TogoVar | ||||||
NTAQ1_chr8_123411774_123447240 | 123419733 | G | GCCCGCCC others(13): Show |
intron_variant | MODIFIER | HG02451.hp2 HG03139.hp2 |
a0001 | a0001c0001 | a0001c0001t0006a0001c0001t0007 | a0001c0001t0006g0070a0001c0001t0007g0069 | 2 | 366 | 0.0055 | 20 | c.83+ others(35): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
NTAQ1_chr8_123411774_123447240 | 123419733 | G | GCCCTCCC others(13): Show |
intron_variant | MODIFIER | HG03704.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0210 | 1 | 366 | 0.0027 | 20 | c.83+ others(35): Show |
NTAQ1 | ENSG00000156795.8 | transcript | ENST00000287387.7 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
NTMT2_chr1_170140959_170173866 | 170167779 | C | CTGGACTG others(13): Show |
3_prime_UTR_variant | MODIFIER | NA18972.hp2 | a0002 | a0002c0002 | a0002c0002t0020 | a0002c0002t0020g0079 | 1 | 356 | 0.0028 | 20 | c.*26 others(27): Show |
NTMT2 | ENSG00000203740.4 | transcript | ENST00000439373.3 | protein_coding | 4/4 | 46 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||
NTM_chr11_131365615_132341822 | 131401814 | A | ATATATAT others(13): Show |
intron_variant | MODIFIER | HG01496.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0017 | 1 | 86 | 0.0116 | 20 | c.82+ others(37): Show |
NTM | ENSG00000182667.15 | transcript | ENST00000683400.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
NTM_chr11_131365615_132341822 | 131424600 | C | CTTTTTTT others(13): Show |
intron_variant | MODIFIER | HG01978.hp1 HG01978.hp2 HG02258.hp1 others(2): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0002t0012 | a0001c0001t0001g0037a0001c0001t0001g0057a0001c0001t0001g0062others(2): Show | 5 | 86 | 0.0581 | 20 | c.82+ others(37): Show |
NTM | ENSG00000182667.15 | transcript | ENST00000683400.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
NTM_chr11_131365615_132341822 | 131616776 | G | GGTGTGTG others(13): Show |
intron_variant | MODIFIER | HG03041.hp2 | a0001 | a0001c0001 | a0001c0001t0010 | a0001c0001t0010g0019 | 1 | 86 | 0.0116 | 20 | c.82+ others(39): Show |
NTM | ENSG00000182667.15 | transcript | ENST00000683400.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
NTM_chr11_131365615_132341822 | 131812183 | C | CCTCTCTC others(13): Show |
intron_variant | MODIFIER | HG03098.hp1 HG03516.hp1 NA19240.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0004 | a0001c0001t0001g0083a0001c0001t0003g0051a0001c0001t0004g0043 | 3 | 86 | 0.0349 | 20 | c.83- others(37): Show |
NTM | ENSG00000182667.15 | transcript | ENST00000683400.1 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
NTM_chr11_131365615_132341822 | 131874029 | T | TTATATAT others(13): Show |
intron_variant | MODIFIER | HG01515.hp2 | a0001 | a0001c0002 | a0001c0002t0005 | a0001c0002t0005g0039 | 1 | 86 | 0.0116 | 20 | c.83- others(37): Show |
NTM | ENSG00000182667.15 | transcript | ENST00000683400.1 | protein_coding | 1/8 | chr11 | TogoVar | ||||||
NTM_chr11_131365615_132341822 | 131976116 | A | ATTCCTTC others(13): Show |
intron_variant | MODIFIER | HG02258.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0057 | 1 | 86 | 0.0116 | 20 | c.167 others(39): Show |
NTM | ENSG00000182667.15 | transcript | ENST00000683400.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
NTM_chr11_131365615_132341822 | 131987378 | C | CCTATTCT others(13): Show |
intron_variant | MODIFIER | HG03041.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0008 | 1 | 86 | 0.0116 | 20 | c.167 others(39): Show |
NTM | ENSG00000182667.15 | transcript | ENST00000683400.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
NTM_chr11_131365615_132341822 | 132015633 | A | ATATTTTA others(13): Show |
intron_variant | MODIFIER | HG02451.hp1 HG04184.hp2 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0013 | a0001c0001t0002g0035a0001c0001t0013g0048 | 2 | 86 | 0.0233 | 20 | c.167 others(41): Show |
NTM | ENSG00000182667.15 | transcript | ENST00000683400.1 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
NTN1_chr17_9016510_9249000 | 9114160 | A | AATATATA others(13): Show |
intron_variant | MODIFIER | NA19054.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0037 | 1 | 258 | 0.0039 | 20 | c.101 others(41): Show |
NTN1 | ENSG00000065320.9 | transcript | ENST00000173229.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
NTN1_chr17_9016510_9249000 | 9114162 | A | AATATATA others(13): Show |
intron_variant | MODIFIER | HG00733.hp1 | a0001 | a0001c0003 | a0001c0003t0007 | a0001c0003t0007g0087 | 1 | 258 | 0.0039 | 20 | c.101 others(41): Show |
NTN1 | ENSG00000065320.9 | transcript | ENST00000173229.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
NTN1_chr17_9016510_9249000 | 9114164 | A | AATATATA others(13): Show |
intron_variant | MODIFIER | HG03688.hp1 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0086 | 1 | 258 | 0.0039 | 20 | c.101 others(41): Show |
NTN1 | ENSG00000065320.9 | transcript | ENST00000173229.7 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
NTN1_chr17_9016510_9249000 | 9193920 | T | TAAAAAAA others(13): Show |
intron_variant | MODIFIER | HG02145.hp2 | a0001 | a0001c0001 | a0001c0001t0012 | a0001c0001t0012g0251 | 1 | 258 | 0.0039 | 20 | c.141 others(41): Show |
NTN1 | ENSG00000065320.9 | transcript | ENST00000173229.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
NTN1_chr17_9016510_9249000 | 9204176 | G | GTTCCTTC others(13): Show |
intron_variant | MODIFIER | HG00609.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0160 | 1 | 258 | 0.0039 | 20 | c.141 others(41): Show |
NTN1 | ENSG00000065320.9 | transcript | ENST00000173229.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
NTN1_chr17_9016510_9249000 | 9204193 | C | CTCCTTCC others(13): Show |
intron_variant | MODIFIER | HG01952.hp2 HG02109.hp2 HG02145.hp1 others(2): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0003a0001c0001t0013others(2): Show | a0001c0001t0001g0122a0001c0001t0003g0046a0001c0001t0013g0252others(2): Show | 5 | 258 | 0.0194 | 20 | c.141 others(41): Show |
NTN1 | ENSG00000065320.9 | transcript | ENST00000173229.7 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
NTN1_chr17_9016510_9249000 | 9225713 | C | CGGGCGGG others(13): Show |
intron_variant | MODIFIER | HG02055.hp2 HG02717.hp2 HG02818.hp1 others(5): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0001a0001c0001t0002a0001c0004t0002 | a0001c0001t0001g0076a0001c0001t0002g0008a0001c0001t0002g0088others(5): Show | 8 | 258 | 0.0310 | 20 | c.148 others(39): Show |
NTN1 | ENSG00000065320.9 | transcript | ENST00000173229.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
NTN4_chr12_95652807_95795764 | 95667863 | A | AAAATAAA others(13): Show |
intron_variant | MODIFIER | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0006a0001c0001t0012a0001c0001t0015others(1): Show | a0001c0001t0006g0147a0001c0001t0012g0068a0001c0001t0012g0069others(5): Show | 8 | 324 | 0.0247 | 20 | c.158 others(39): Show |
NTN4 | ENSG00000074527.13 | transcript | ENST00000343702.9 | protein_coding | 8/9 | chr12 | TogoVar | ||||||
NTN4_chr12_95652807_95795764 | 95700080 | A | ATTTTTTT others(13): Show |
intron_variant | MODIFIER | NA18961.hp2 NA18968.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0237a0001c0001t0001g0240 | 2 | 324 | 0.0062 | 20 | c.118 others(41): Show |
NTN4 | ENSG00000074527.13 | transcript | ENST00000343702.9 | protein_coding | 5/9 | chr12 | TogoVar | ||||||
NTN4_chr12_95652807_95795764 | 95770988 | A | ATTTTTTT others(13): Show |
intron_variant | MODIFIER | HG00639.hp2 HG02647.hp1 HG02895.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0004a0001c0001t0005a0001c0001t0006others(1): Show | a0001c0001t0004g0047a0001c0001t0005g0048a0001c0001t0006g0221others(2): Show | 5 | 324 | 0.0154 | 20 | c.585 others(39): Show |
NTN4 | ENSG00000074527.13 | transcript | ENST00000343702.9 | protein_coding | 2/9 | chr12 | TogoVar | ||||||
NTNG1_chr1_107136039_107489923 | 107280853 | C | CTTATTTT others(13): Show |
intron_variant | MODIFIER | HG06807.hp2 | a0001 | a0001c0002 | a0001c0002t0016 | a0001c0002t0016g0005 | 1 | 150 | 0.0067 | 20 | c.247 others(39): Show |
NTNG1 | ENSG00000162631.20 | transcript | ENST00000370068.6 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
NTNG2_chr9_132157058_132249526 | 132189068 | C | CTTTTTTT others(13): Show |
intron_variant | MODIFIER | HG01884.hp2 | a0001 | a0001c0001 | a0001c0001t0046 | a0001c0001t0046g0077 | 1 | 358 | 0.0028 | 20 | c.214 others(37): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
NTNG2_chr9_132157058_132249526 | 132216414 | C | CTCTCTCT others(13): Show |
intron_variant | MODIFIER | HG01943.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0289 | 1 | 358 | 0.0028 | 20 | c.858 others(39): Show |
NTNG2 | ENSG00000196358.12 | transcript | ENST00000393229.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
NTRK1_chr1_156855865_156886850 | 156869018 | C | CCCTTCCT others(13): Show |
intron_variant | MODIFIER | HG01175.hp2 HG01361.hp1 HG02132.hp2 others(4): Show |
a0001a0012 | a0001c0003a0001c0006a0001c0013others(1): Show | a0001c0003t0001a0001c0006t0001a0001c0013t0001others(1): Show | a0001c0003t0001g0145a0001c0003t0001g0146a0001c0003t0001g0147others(4): Show | 7 | 392 | 0.0179 | 20 | c.717 others(35): Show |
NTRK1 | ENSG00000198400.14 | transcript | ENST00000524377.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
NTRK2_chr9_84664729_85032054 | 84770153 | A | AACACACA others(13): Show |
intron_variant | MODIFIER | NA19077.hp2 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0049 | 1 | 170 | 0.0059 | 20 | c.139 others(41): Show |
NTRK2 | ENSG00000148053.18 | transcript | ENST00000277120.8 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
NTRK2_chr9_84664729_85032054 | 84798912 | C | CTATATAT others(13): Show |
intron_variant | MODIFIER | HG01168.hp1 HG01928.hp1 HG03098.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0028a0001c0001t0057 | a0001c0001t0002g0019a0001c0001t0002g0042a0001c0001t0028g0152others(1): Show | 4 | 170 | 0.0235 | 20 | c.139 others(41): Show |
NTRK2 | ENSG00000148053.18 | transcript | ENST00000277120.8 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
NTRK2_chr9_84664729_85032054 | 84836934 | G | GTATAATA others(13): Show |
intron_variant | MODIFIER | HG03669.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0120 | 1 | 170 | 0.0059 | 20 | c.139 others(41): Show |
NTRK2 | ENSG00000148053.18 | transcript | ENST00000277120.8 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
NTRK2_chr9_84664729_85032054 | 84870331 | G | GTGTGTGT others(13): Show |
intron_variant | MODIFIER | HG01175.hp2 HG01928.hp2 HG02602.hp1 others(5): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0003a0001c0001t0023others(2): Show | a0001c0001t0001g0139a0001c0001t0001g0163a0001c0001t0001g0164others(5): Show | 8 | 170 | 0.0471 | 20 | c.163 others(39): Show |
NTRK2 | ENSG00000148053.18 | transcript | ENST00000277120.8 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
NTRK2_chr9_84664729_85032054 | 84870331 | G | GTGTGTGT others(13): Show |
intron_variant | MODIFIER | HG03225.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0042 | 1 | 170 | 0.0059 | 20 | c.163 others(39): Show |
NTRK2 | ENSG00000148053.18 | transcript | ENST00000277120.8 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
NTRK2_chr9_84664729_85032054 | 84870331 | G | GTGTGTGT others(13): Show |
intron_variant | MODIFIER | HG03139.hp1 | a0001 | a0001c0001 | a0001c0001t0026 | a0001c0001t0026g0153 | 1 | 170 | 0.0059 | 20 | c.163 others(39): Show |
NTRK2 | ENSG00000148053.18 | transcript | ENST00000277120.8 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
NTRK2_chr9_84664729_85032054 | 84870331 | G | GTGTGTGT others(13): Show |
intron_variant | MODIFIER | HG01928.hp1 HG03130.hp2 HG03669.hp1 others(3): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0003a0001c0001t0004a0001c0001t0008others(2): Show | a0001c0001t0003g0120a0001c0001t0004g0049a0001c0001t0004g0168others(3): Show | 6 | 170 | 0.0353 | 20 | c.163 others(39): Show |
NTRK2 | ENSG00000148053.18 | transcript | ENST00000277120.8 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
NTRK2_chr9_84664729_85032054 | 84882719 | T | TGTGTGCG others(13): Show |
intron_variant | MODIFIER | HG02683.hp2 | a0001 | a0001c0001 | a0001c0001t0023 | a0001c0001t0023g0095 | 1 | 170 | 0.0059 | 20 | c.163 others(41): Show |
NTRK2 | ENSG00000148053.18 | transcript | ENST00000277120.8 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
NTRK2_chr9_84664729_85032054 | 84882719 | T | TGTGTGTG others(13): Show |
intron_variant | MODIFIER | HG02723.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0021 | 1 | 170 | 0.0059 | 20 | c.163 others(41): Show |
NTRK2 | ENSG00000148053.18 | transcript | ENST00000277120.8 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
NTRK2_chr9_84664729_85032054 | 84888982 | A | ATTTTTTT others(13): Show |
intron_variant | MODIFIER | HG03098.hp1 NA18999.hp1 NA19005.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0004a0001c0001t0007others(3): Show | a0001c0001t0002g0034a0001c0001t0004g0143a0001c0001t0007g0072others(3): Show | 6 | 170 | 0.0353 | 20 | c.163 others(41): Show |
NTRK2 | ENSG00000148053.18 | transcript | ENST00000277120.8 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
NTRK2_chr9_84664729_85032054 | 84901194 | G | GTTTTATT others(13): Show |
intron_variant | MODIFIER | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(6): Show |
a0001a0004 | a0001c0001a0001c0003a0001c0005others(1): Show | a0001c0001t0001a0001c0001t0006a0001c0001t0009others(6): Show | a0001c0001t0001g0009a0001c0001t0006g0008a0001c0001t0009g0130others(6): Show | 9 | 170 | 0.0529 | 20 | c.163 others(41): Show |
NTRK2 | ENSG00000148053.18 | transcript | ENST00000277120.8 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
NTRK2_chr9_84664729_85032054 | 84901199 | G | GTTTTATT others(13): Show |
intron_variant | MODIFIER | HG00621.hp2 HG01256.hp1 HG01928.hp1 others(9): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(6): Show | a0001c0001t0001g0169a0001c0001t0002g0144a0001c0001t0002g0147others(9): Show | 12 | 170 | 0.0706 | 20 | c.163 others(41): Show |
NTRK2 | ENSG00000148053.18 | transcript | ENST00000277120.8 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
NTRK2_chr9_84664729_85032054 | 84926169 | C | CCTTCCTT others(13): Show |
intron_variant | MODIFIER | HG01928.hp1 | a0001 | a0001c0001 | a0001c0001t0057 | a0001c0001t0057g0075 | 1 | 170 | 0.0059 | 20 | c.163 others(39): Show |
NTRK2 | ENSG00000148053.18 | transcript | ENST00000277120.8 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
NTRK2_chr9_84664729_85032054 | 84926169 | C | CCTTTCTT others(13): Show |
intron_variant | MODIFIER | HG01978.hp1 NA19066.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0010a0001c0002t0007 | a0001c0001t0010g0116a0001c0002t0007g0090 | 2 | 170 | 0.0118 | 20 | c.163 others(39): Show |
NTRK2 | ENSG00000148053.18 | transcript | ENST00000277120.8 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
NTRK2_chr9_84664729_85032054 | 85011958 | A | ATTATTTT others(13): Show |
intron_variant | MODIFIER | HG00597.hp1 HG02015.hp2 HG02109.hp2 others(11): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(6): Show | a0001c0001t0002g0034a0001c0001t0002g0144a0001c0001t0003g0092others(11): Show | 14 | 170 | 0.0824 | 20 | c.217 others(39): Show |
NTRK2 | ENSG00000148053.18 | transcript | ENST00000277120.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
NTRK3_chr15_87854751_88261739 | 87886676 | C | CTACATAT others(13): Show |
intron_variant | MODIFIER | HG00099.hp2 HG00735.hp1 NA18962.hp1 others(1): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0026a0001c0002t0012a0001c0002t0025others(1): Show | a0001c0001t0026g0061a0001c0002t0012g0123a0001c0002t0025g0063others(1): Show | 4 | 134 | 0.0299 | 20 | c.213 others(37): Show |
NTRK3 | ENSG00000140538.17 | transcript | ENST00000629765.3 | protein_coding | 17/19 | chr15 | TogoVar | ||||||
NTRK3_chr15_87854751_88261739 | 87886676 | C | CTATATAT others(13): Show |
intron_variant | MODIFIER | HG01346.hp2 HG02976.hp1 HG03209.hp2 others(1): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0011a0001c0002t0064a0001c0003t0075others(1): Show | a0001c0001t0011g0091a0001c0002t0064g0124a0001c0003t0075g0016others(1): Show | 4 | 134 | 0.0299 | 20 | c.213 others(37): Show |
NTRK3 | ENSG00000140538.17 | transcript | ENST00000629765.3 | protein_coding | 17/19 | chr15 | TogoVar | ||||||
NTRK3_chr15_87854751_88261739 | 87886699 | T | TATATATA others(13): Show |
intron_variant | MODIFIER | HG01884.hp1 | a0001 | a0001c0004 | a0001c0004t0070 | a0001c0004t0070g0070 | 1 | 134 | 0.0075 | 20 | c.213 others(37): Show |
NTRK3 | ENSG00000140538.17 | transcript | ENST00000629765.3 | protein_coding | 17/19 | chr15 | TogoVar | ||||||
NTRK3_chr15_87854751_88261739 | 87912929 | A | AATATATA others(13): Show |
intron_variant | MODIFIER | HG01070.hp2 | a0001 | a0001c0004 | a0001c0004t0058 | a0001c0004t0058g0115 | 1 | 134 | 0.0075 | 20 | c.213 others(41): Show |
NTRK3 | ENSG00000140538.17 | transcript | ENST00000629765.3 | protein_coding | 17/19 | chr15 | TogoVar | ||||||
NTRK3_chr15_87854751_88261739 | 87912931 | A | AATATATA others(13): Show |
intron_variant | MODIFIER | HG01952.hp2 NA18906.hp1 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0063a0001c0003t0060 | a0001c0001t0063g0049a0001c0003t0060g0048 | 2 | 134 | 0.0149 | 20 | c.213 others(41): Show |
NTRK3 | ENSG00000140538.17 | transcript | ENST00000629765.3 | protein_coding | 17/19 | chr15 | TogoVar | ||||||
NTRK3_chr15_87854751_88261739 | 88033176 | T | TTATATAT others(13): Show |
intron_variant | MODIFIER | HG01258.hp1 HG02258.hp1 |
a0001 | a0001c0002a0001c0005 | a0001c0002t0039a0001c0005t0007 | a0001c0002t0039g0081a0001c0005t0007g0109 | 2 | 134 | 0.0149 | 20 | c.139 others(37): Show |
NTRK3 | ENSG00000140538.17 | transcript | ENST00000629765.3 | protein_coding | 13/19 | chr15 | TogoVar | ||||||
NTRK3_chr15_87854751_88261739 | 88159943 | T | TACACACA others(13): Show |
intron_variant | MODIFIER | HG02922.hp2 HG03516.hp1 |
a0001 | a0001c0001 | a0001c0001t0020a0001c0001t0021 | a0001c0001t0020g0002a0001c0001t0021g0001 | 2 | 134 | 0.0149 | 20 | c.396 others(39): Show |
NTRK3 | ENSG00000140538.17 | transcript | ENST00000629765.3 | protein_coding | 5/19 | chr15 | TogoVar | ||||||
NTRK3_chr15_87854751_88261739 | 88191163 | C | CGTGTGTG others(13): Show |
intron_variant | MODIFIER | HG01109.hp1 HG03516.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0021a0001c0002t0072 | a0001c0001t0021g0001a0001c0002t0072g0045 | 2 | 134 | 0.0149 | 20 | c.249 others(37): Show |
NTRK3 | ENSG00000140538.17 | transcript | ENST00000629765.3 | protein_coding | 3/19 | chr15 | TogoVar | ||||||
NTSR1_chr20_62703836_62767771 | 62755813 | T | TCCTCCCT others(13): Show |
intron_variant | MODIFIER | HG00621.hp2 HG02735.hp2 HG03492.hp1 others(4): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0012a0001c0003t0031 | a0001c0001t0001g0007a0001c0001t0001g0054a0001c0003t0012g0122others(3): Show | 7 | 316 | 0.0222 | 20 | c.916 others(35): Show |
NTSR1 | ENSG00000101188.5 | transcript | ENST00000370501.4 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr20 | TogoVar |