| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| NBPF19_chr1_149470045_149561361 | 149528945 | C | CTCTCTGT others(23): Show |
intron_variant | MODIFIER | NA19068.hp1 | a0129 | a0129c0167 | a0129c0167t0012 | a0129c0167t0012g0088 | 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 | a0150 | a0150c0160 | a0150c0160t0001 | a0150c0160t0001g0107 | 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 |
a0015a0173 | a0015c0036a0173c0191 | a0015c0036t0006a0173c0191t0006 | a0015c0036t0006g0004a0173c0191t0006g0271 | 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 | a0146 | a0146c0176 | a0146c0176t0003 | a0146c0176t0003g0110 | 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 | a0174 | a0174c0202 | a0174c0202t0013 | a0174c0202t0013g0204 | 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 |
a0006a0032a0035others(7): Show | a0006c0213a0006c0214a0032c0012others(8): Show | a0006c0213t0002a0006c0214t0002a0032c0012t0002others(8): Show | a0006c0213t0002g0224a0006c0214t0002g0265a0032c0012t0002g0232others(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 |
a0001a0013 | a0001c0001a0013c0011 | a0001c0001t0001a0001c0001t0007a0013c0011t0009 | a0001c0001t0001g0057a0001c0001t0001g0219a0001c0001t0001g0261others(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 | a0001c0001t0005g0194a0001c0001t0009g0192a0001c0001t0009g0203others(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 | a0001c0001t0002g0026a0001c0001t0016g0241 | 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 | a0001c0010 | a0001c0010t0021 | a0001c0010t0021g0065 | 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 | a0001c0001a0001c0008 | a0001c0001t0003a0001c0001t0016a0001c0001t0043others(1): Show | a0001c0001t0003g0139a0001c0001t0016g0216a0001c0001t0043g0209others(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 | a0001c0001t0006g0059a0001c0001t0010g0208 | 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 | a0001c0001t0004g0028a0001c0001t0005g0076a0001c0001t0010g0056others(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 | a0002c0002t0003g0020a0002c0002t0015g0054 | 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 | a0003c0003t0003g0098a0006c0008t0003g0051 | 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 | a0001c0001t0001g0251a0001c0001t0001g0269a0001c0001t0001g0270 | 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 | a0001c0001t0001g0010a0001c0001t0001g0011 | 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 | a0001c0001t0001g0251a0001c0001t0001g0257a0001c0001t0001g0269others(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 | a0001c0001t0001g0307a0001c0001t0001g0308 | 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 | a0001c0001t0001g0264a0001c0001t0001g0281a0001c0001t0001g0290others(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 | a0001c0001t0001g0250a0001c0001t0001g0255 | 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 | a0001c0001t0001g0302a0001c0001t0001g0341 | 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 |
a0001a0005 | a0001c0001a0005c0009 | a0001c0001t0001a0005c0009t0002 | a0001c0001t0001g0312a0005c0009t0002g0317 | 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 | a0001c0001t0002g0058a0001c0001t0002g0238 | 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 | a0001c0004t0001g0191a0001c0004t0002g0190 | 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 |
a0001a0017 | a0001c0001a0001c0018a0017c0011 | a0001c0001t0001a0001c0001t0002a0001c0018t0002others(1): Show | a0001c0001t0001g0025a0001c0001t0001g0034a0001c0001t0001g0066others(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 | a0016 | a0016c0012 | a0016c0012t0002 | a0016c0012t0002g0042 | 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 | a0001c0001t0002g0069a0001c0001t0002g0124 | 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 | a0001c0001t0001g0344a0001c0001t0001g0345 | 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 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(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 | a0001c0001t0002g0177a0001c0001t0002g0178 | 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 | a0001c0001t0004g0039a0001c0001t0004g0047 | 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 |
a0001a0016 | a0001c0001a0016c0017 | a0001c0001t0001a0016c0017t0003 | a0001c0001t0001g0015a0016c0017t0003g0033 | 2 | 70 | 0.0286 | 30 | c.207 others(47): Show |
NCKAP5 | ENSG00000176771.18 | transcript | ENST00000409261.6 | protein_coding | 5/19 | chr2 | TogoVar |