view | regionname | pos | ref | alt | annotation | impact | samples | ahapids | chapids | thapids | thapids | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
NBPF19_chr1_149470045_149561361 | 149528945 | C | CTCTCTGT others(23): Show |
intron_variant | MODIFIER | NA19068.hp1 | a0205 | a0205c0169 | a0205c0169t0012 | a0205c0169t0012g0088 | 1 | 276 | 0.0036 | 30 | c.734 others(47): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
NBPF19_chr1_149470045_149561361 | 149528945 | C | CTCTGTGT others(23): Show |
intron_variant | MODIFIER | HG01257.hp2 | a0062 | a0062c0162 | a0062c0162t0001 | a0062c0162t0001g0107 | 1 | 276 | 0.0036 | 30 | c.734 others(47): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
NBPF19_chr1_149470045_149561361 | 149543186 | C | CTCTCTCT others(23): Show |
intron_variant | MODIFIER | HG02145.hp1 HG02896.hp1 HG02897.hp1 |
a0014a0089 | a0014c0036a0089c0193 | a0014c0036t0006a0089c0193t0006 | a0014c0036t0006g0004 a0089c0193t0006g0271 |
3 | 276 | 0.0109 | 30 | c.954 others(47): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
NBPF19_chr1_149470045_149561361 | 149543186 | C | CTCTGTGT others(23): Show |
intron_variant | MODIFIER | HG03710.hp2 | a0142 | a0142c0178 | a0142c0178t0003 | a0142c0178t0003g0110 | 1 | 276 | 0.0036 | 30 | c.954 others(47): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
NBPF19_chr1_149470045_149561361 | 149547923 | C | CTCTCTGT others(23): Show |
intron_variant | MODIFIER | NA18962.hp1 | a0171 | a0171c0204 | a0171c0204t0013 | a0171c0204t0013g0204 | 1 | 276 | 0.0036 | 30 | c.102 others(49): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 85/93 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
NBPF19_chr1_149470045_149561361 | 149547923 | C | CTCTCTGT others(23): Show |
intron_variant | MODIFIER | HG01081.hp1 HG01346.hp2 HG02129.hp2 others(9): Show |
a0004a0019a0028others(7): Show | a0004c0215a0004c0216a0019c0012others(8): Show | a0004c0215t0002a0004c0216t0002a0019c0012t0002others(8): Show | a0004c0215t0002g0224 a0004c0216t0002g0265 a0019c0012t0002g0232 others(9): Show |
12 | 276 | 0.0435 | 30 | c.102 others(49): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 85/93 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
NBPF3_chr1_21435137_21489900 | 21479820 | C | CTCTCTCT others(23): Show |
intron_variant | MODIFIER | HG01358.hp1 HG02071.hp1 HG02698.hp2 others(7): Show |
a0001a0012 | a0001c0001a0012c0011 | a0001c0001t0001a0001c0001t0007a0012c0011t0009 | a0001c0001t0001g0057 a0001c0001t0001g0219 a0001c0001t0001g0261 others(6): Show |
10 | 394 | 0.0254 | 30 | c.120 others(47): Show |
NBPF3 | ENSG00000142794.19 | transcript | ENST00000318249.10 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
NCAM1_chr11_112956420_113283436 | 113017635 | T | TTGTGTGT others(23): Show |
intron_variant | MODIFIER | HG00323.hp1 HG00597.hp1 HG02486.hp2 others(3): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0005a0001c0001t0009a0001c0001t0035others(2): Show | a0001c0001t0005g0194 a0001c0001t0009g0192 a0001c0001t0009g0203 others(3): Show |
6 | 242 | 0.0248 | 30 | c.52+ others(47): Show |
NCAM1 | ENSG00000149294.18 | transcript | ENST00000316851.12 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
NCAM1_chr11_112956420_113283436 | 113173591 | G | GATATATA others(23): Show |
intron_variant | MODIFIER | NA18973.hp1 NA19010.hp2 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0016 | a0001c0001t0002g0026 a0001c0001t0016g0241 |
2 | 242 | 0.0083 | 30 | c.53- others(47): Show |
NCAM1 | ENSG00000149294.18 | transcript | ENST00000316851.12 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
NCAM1_chr11_112956420_113283436 | 113185079 | T | TATATATA others(23): Show |
intron_variant | MODIFIER | HG02486.hp1 | a0001 | a0001c0013 | a0001c0013t0021 | a0001c0013t0021g0065 | 1 | 242 | 0.0041 | 30 | c.53- others(47): Show |
NCAM1 | ENSG00000149294.18 | transcript | ENST00000316851.12 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
NCAM1_chr11_112956420_113283436 | 113185079 | T | TATATATA others(23): Show |
intron_variant | MODIFIER | HG02735.hp2 HG02970.hp2 NA18961.hp1 others(1): Show |
a0001 | a0001c0001a0001c0009 | a0001c0001t0003a0001c0001t0016a0001c0001t0043others(1): Show | a0001c0001t0003g0139 a0001c0001t0016g0216 a0001c0001t0043g0209 others(1): Show |
4 | 242 | 0.0165 | 30 | c.53- others(47): Show |
NCAM1 | ENSG00000149294.18 | transcript | ENST00000316851.12 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
NCAM1_chr11_112956420_113283436 | 113185079 | T | TATATATA others(23): Show |
intron_variant | MODIFIER | HG01884.hp1 HG03453.hp1 |
a0001 | a0001c0001 | a0001c0001t0006a0001c0001t0010 | a0001c0001t0006g0059 a0001c0001t0010g0208 |
2 | 242 | 0.0083 | 30 | c.53- others(47): Show |
NCAM1 | ENSG00000149294.18 | transcript | ENST00000316851.12 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
NCAM1_chr11_112956420_113283436 | 113185079 | T | TATATATA others(23): Show |
intron_variant | MODIFIER | HG00423.hp1 | a0001 | a0001c0002 | a0001c0002t0003 | a0001c0002t0003g0103 | 1 | 242 | 0.0041 | 30 | c.53- others(47): Show |
NCAM1 | ENSG00000149294.18 | transcript | ENST00000316851.12 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
NCAM1_chr11_112956420_113283436 | 113185079 | T | TATATATA others(23): Show |
intron_variant | MODIFIER | HG01981.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0111 | 1 | 242 | 0.0041 | 30 | c.53- others(47): Show |
NCAM1 | ENSG00000149294.18 | transcript | ENST00000316851.12 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
NCAM2_chr21_20993409_21548329 | 21125489 | T | TATATGTA others(23): Show |
intron_variant | MODIFIER | HG00639.hp1 HG01243.hp2 HG02647.hp1 others(6): Show |
a0001a0002a0004 | a0001c0001a0001c0012a0002c0002others(3): Show | a0001c0001t0004a0001c0001t0005a0001c0001t0010others(6): Show | a0001c0001t0004g0028 a0001c0001t0005g0076 a0001c0001t0010g0056 others(6): Show |
9 | 132 | 0.0682 | 30 | c.55+ others(49): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | ||||||
NCAM2_chr21_20993409_21548329 | 21430394 | T | TTATATAT others(23): Show |
intron_variant | MODIFIER | HG00741.hp2 HG03540.hp2 |
a0002 | a0002c0002 | a0002c0002t0003a0002c0002t0015 | a0002c0002t0003g0020 a0002c0002t0015g0054 |
2 | 132 | 0.0152 | 30 | c.148 others(49): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | ||||||
NCAM2_chr21_20993409_21548329 | 21433742 | C | CAATAAAA others(23): Show |
intron_variant | MODIFIER | NA20129.hp1 | a0002 | a0002c0002 | a0002c0002t0004 | a0002c0002t0004g0073 | 1 | 132 | 0.0076 | 30 | c.165 others(49): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | ||||||
NCAPD2_chr12_6489102_6536955 | 6518504 | G | GTTTTTTT others(23): Show |
intron_variant | MODIFIER | HG00735.hp2 HG01261.hp2 |
a0003a0006 | a0003c0003a0006c0008 | a0003c0003t0003a0006c0008t0003 | a0003c0003t0003g0098 a0006c0008t0003g0051 |
2 | 432 | 0.0046 | 30 | c.158 others(47): Show |
NCAPD2 | ENSG00000010292.13 | transcript | ENST00000315579.10 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
NCAPD3_chr11_134145113_134228967 | 134165560 | T | TGTGAGAT others(23): Show |
intron_variant | MODIFIER | HG01981.hp2 | a0001 | a0001c0002 | a0001c0002t0008 | a0001c0002t0008g0212 | 1 | 370 | 0.0027 | 30 | c.357 others(49): Show |
NCAPD3 | ENSG00000151503.14 | transcript | ENST00000534548.7 | protein_coding | 27/34 | chr11 | TogoVar | |||||||
NCAPD3_chr11_134145113_134228967 | 134167034 | G | GGGGGAGG others(23): Show |
intron_variant | MODIFIER | NA18969.hp2 NA18992.hp2 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0002 | 2 | 370 | 0.0054 | 30 | c.357 others(47): Show |
NCAPD3 | ENSG00000151503.14 | transcript | ENST00000534548.7 | protein_coding | 27/34 | chr11 | TogoVar | |||||||
NCAPD3_chr11_134145113_134228967 | 134167117 | T | TCACTAGT others(23): Show |
intron_variant | MODIFIER | NA21309.hp1 | a0001 | a0001c0001 | a0001c0001t0035 | a0001c0001t0035g0288 | 1 | 370 | 0.0027 | 30 | c.357 others(47): Show |
NCAPD3 | ENSG00000151503.14 | transcript | ENST00000534548.7 | protein_coding | 27/34 | chr11 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158660401 | C | CTTTTTTT others(23): Show |
intron_variant | MODIFIER | NA18950.hp1 NA19007.hp2 NA19088.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0251 a0001c0001t0001g0269 a0001c0001t0001g0270 |
3 | 378 | 0.0079 | 30 | c.198 others(49): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 16/27 | chr7 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158667391 | T | TGGGTCCC others(23): Show |
intron_variant | MODIFIER | HG02630.hp1 HG03139.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0010 a0001c0001t0001g0011 |
2 | 378 | 0.0053 | 30 | c.148 others(49): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158667406 | T | TCCCTTAC others(23): Show |
intron_variant | MODIFIER | NA18944.hp2 NA18950.hp1 NA19002.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0251 a0001c0001t0001g0257 a0001c0001t0001g0269 others(2): Show |
5 | 378 | 0.0132 | 30 | c.148 others(49): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158667493 | G | GCCTTACC others(23): Show |
intron_variant | MODIFIER | HG02647.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0193 | 1 | 378 | 0.0027 | 30 | c.148 others(49): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158667522 | T | TCCCTTAC others(23): Show |
intron_variant | MODIFIER | NA19086.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0373 | 1 | 378 | 0.0027 | 30 | c.148 others(49): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158667532 | C | CTACTGGG others(23): Show |
intron_variant | MODIFIER | NA18957.hp2 NA18998.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0307 a0001c0001t0001g0308 |
2 | 378 | 0.0053 | 30 | c.148 others(49): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158667532 | C | CTACTGGG others(23): Show |
intron_variant | MODIFIER | HG01433.hp1 HG01952.hp2 HG02148.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0264 a0001c0001t0001g0281 a0001c0001t0001g0290 others(1): Show |
4 | 378 | 0.0106 | 30 | c.148 others(49): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158667618 | C | CTACTGGG others(23): Show |
intron_variant | MODIFIER | HG02273.hp2 NA18943.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0250 a0001c0001t0001g0255 |
2 | 378 | 0.0053 | 30 | c.148 others(49): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158667636 | T | TCCTTACC others(23): Show |
intron_variant | MODIFIER | HG02723.hp2 HG04115.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0302 a0001c0001t0001g0341 |
2 | 378 | 0.0053 | 30 | c.148 others(49): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158667664 | T | TCCTTACC others(23): Show |
intron_variant | MODIFIER | HG02615.hp2 | a0015 | a0015c0013 | a0015c0013t0002 | a0015c0013t0002g0016 | 1 | 378 | 0.0027 | 30 | c.148 others(49): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158667732 | C | CTACTGGG others(23): Show |
intron_variant | MODIFIER | HG02004.hp1 HG03195.hp2 |
a0001a0006 | a0001c0001a0006c0009 | a0001c0001t0001a0006c0009t0002 | a0001c0001t0001g0312 a0006c0009t0002g0317 |
2 | 378 | 0.0053 | 30 | c.148 others(49): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158667809 | C | CGCCTTAC others(23): Show |
intron_variant | MODIFIER | HG03654.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0359 | 1 | 378 | 0.0027 | 30 | c.148 others(49): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158667810 | T | TCCCTTAC others(23): Show |
intron_variant | MODIFIER | HG01934.hp1 NA20805.hp1 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0058 a0001c0001t0002g0238 |
2 | 378 | 0.0053 | 30 | c.148 others(49): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158667869 | T | TCCTTACC others(23): Show |
intron_variant | MODIFIER | HG03491.hp2 HG04228.hp1 |
a0001 | a0001c0004 | a0001c0004t0001a0001c0004t0002 | a0001c0004t0001g0191 a0001c0004t0002g0190 |
2 | 378 | 0.0053 | 30 | c.148 others(49): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158667897 | C | CGCCTTAC others(23): Show |
intron_variant | MODIFIER | NA19085.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0284 | 1 | 378 | 0.0027 | 30 | c.148 others(49): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158667898 | T | TCCCTTAC others(23): Show |
intron_variant | MODIFIER | HG00323.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0051 | 1 | 378 | 0.0027 | 30 | c.148 others(49): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158668012 | T | TCCCTTAC others(23): Show |
intron_variant | MODIFIER | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(23): Show |
a0001a0019 | a0001c0001a0001c0018a0019c0011 | a0001c0001t0001a0001c0001t0002a0001c0018t0002others(1): Show | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0066 others(23): Show |
26 | 378 | 0.0688 | 30 | c.148 others(49): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158668099 | C | CGCCTTAC others(23): Show |
intron_variant | MODIFIER | NA18993.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0226 | 1 | 378 | 0.0027 | 30 | c.148 others(49): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158668239 | G | GCCCGCCT others(23): Show |
intron_variant | MODIFIER | NA18967.hp2 | a0018 | a0018c0012 | a0018c0012t0002 | a0018c0012t0002g0042 | 1 | 378 | 0.0027 | 30 | c.147 others(49): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158668243 | T | TCCTTACC others(23): Show |
intron_variant | MODIFIER | NA19009.hp1 NA19063.hp2 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0069 a0001c0001t0002g0124 |
2 | 378 | 0.0053 | 30 | c.147 others(49): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCAPG2_chr7_158626169_158709804 | 158668298 | C | CCTCCCTT others(23): Show |
intron_variant | MODIFIER | HG02055.hp2 HG03209.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0344 a0001c0001t0001g0345 |
2 | 378 | 0.0053 | 30 | c.147 others(49): Show |
NCAPG2 | ENSG00000146918.20 | transcript | ENST00000356309.8 | protein_coding | 13/27 | chr7 | TogoVar | |||||||
NCBP2L_chrX_107772733_107800829 | 107781692 | C | CTCTCTCT others(23): Show |
intron_variant | MODIFIER | HG03540.hp2 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0064 | 1 | 303 | 0.0033 | 30 | c.-73 others(47): Show |
NCBP2L | ENSG00000170935.8 | transcript | ENST00000509000.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
NCF1_chr7_74769011_74794315 | 74776707 | G | GCCCCTCC others(23): Show |
intron_variant | MODIFIER | HG02145.hp1 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0042 | 1 | 330 | 0.0030 | 30 | c.73- others(43): Show |
NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
NCF1_chr7_74769011_74794315 | 74776716 | G | GTCCCCTC others(23): Show |
intron_variant | MODIFIER | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(203): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0003a0001c0013others(12): Show | a0001c0001t0001a0001c0001t0002a0001c0003t0001others(14): Show | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(86): Show |
206 | 330 | 0.6242 | 30 | c.73- others(43): Show |
NCF1 | ENSG00000158517.16 | transcript | ENST00000289473.11 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
NCK2_chr2_105739912_105899272 | 105750037 | A | AACACACA others(23): Show |
intron_variant | MODIFIER | NA18964.hp1 NA19083.hp2 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0177 a0001c0001t0002g0178 |
2 | 334 | 0.0060 | 30 | c.-20 others(49): Show |
NCK2 | ENSG00000071051.14 | transcript | ENST00000233154.9 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
NCK2_chr2_105739912_105899272 | 105835393 | A | ATATATAT others(23): Show |
intron_variant | MODIFIER | HG00609.hp2 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0069 | 1 | 334 | 0.0030 | 30 | c.-17 others(49): Show |
NCK2 | ENSG00000071051.14 | transcript | ENST00000233154.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
NCK2_chr2_105739912_105899272 | 105835393 | A | ATATATAT others(23): Show |
intron_variant | MODIFIER | HG00544.hp2 NA19086.hp1 |
a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0039 a0001c0001t0004g0047 |
2 | 334 | 0.0060 | 30 | c.-17 others(49): Show |
NCK2 | ENSG00000071051.14 | transcript | ENST00000233154.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
NCKAP1L_chr12_54492752_54553243 | 54506796 | A | AATATATA others(23): Show |
intron_variant | MODIFIER | HG01515.hp2 | a0001 | a0001c0002 | a0001c0002t0029 | a0001c0002t0029g0296 | 1 | 350 | 0.0029 | 30 | c.307 others(47): Show |
NCKAP1L | ENSG00000123338.13 | transcript | ENST00000293373.11 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
NCKAP5_chr2_132666788_133573463 | 133210173 | A | AATAATAT others(23): Show |
intron_variant | MODIFIER | HG03130.hp2 HG03453.hp2 |
a0001a0015 | a0001c0001a0015c0017 | a0001c0001t0001a0015c0017t0003 | a0001c0001t0001g0015 a0015c0017t0003g0033 |
2 | 70 | 0.0286 | 30 | c.207 others(47): Show |
NCKAP5 | ENSG00000176771.18 | transcript | ENST00000409261.6 | protein_coding | 5/19 | chr2 | TogoVar |