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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
NAV2_chr11_19707837_20126601 | 20106175 | A | ATATATAT others(17): Show |
intron_variant | MODIFIER | HG01168.hp2 HG01169.hp2 HG01261.hp2 others(5): Show |
a0002a0004a0005others(1): Show | a0002c0004a0002c0011a0002c0013others(4): Show | a0002c0004t0001a0002c0011t0006a0002c0013t0001others(4): Show | a0002c0004t0001g0100 a0002c0011t0006g0096 a0002c0013t0001g0144 others(5): Show |
8 | 166 | 0.0482 | 24 | c.684 others(41): Show |
NAV2 | ENSG00000166833.23 | transcript | ENST00000349880.9 | protein_coding | 35/37 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
NAV2_chr11_19707837_20126601 | 20106175 | A | ATATATAT others(17): Show |
intron_variant | MODIFIER | HG01169.hp1 | a0004 | a0004c0134 | a0004c0134t0001 | a0004c0134t0001g0050 | 1 | 166 | 0.0060 | 24 | c.684 others(41): Show |
NAV2 | ENSG00000166833.23 | transcript | ENST00000349880.9 | protein_coding | 35/37 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
NAV2_chr11_19707837_20126601 | 20106187 | A | ATATATAT others(17): Show |
intron_variant | MODIFIER | HG01243.hp2 | a0001 | a0001c0003 | a0001c0003t0023 | a0001c0003t0023g0132 | 1 | 166 | 0.0060 | 24 | c.684 others(41): Show |
NAV2 | ENSG00000166833.23 | transcript | ENST00000349880.9 | protein_coding | 35/37 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
NAV2_chr11_19707837_20126601 | 20106626 | G | GTTGTTTT others(17): Show |
intron_variant | MODIFIER | HG02886.hp2 | a0019 | a0019c0092 | a0019c0092t0045 | a0019c0092t0045g0076 | 1 | 166 | 0.0060 | 24 | c.684 others(41): Show |
NAV2 | ENSG00000166833.23 | transcript | ENST00000349880.9 | protein_coding | 35/37 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
NAV3_chr12_77825894_78218010 | 77873744 | G | GTGTGTGT others(17): Show |
intron_variant | MODIFIER | HG02886.hp1 | a0003 | a0003c0027 | a0003c0027t0027 | a0003c0027t0027g0009 | 1 | 186 | 0.0054 | 24 | c.243 others(43): Show |
NAV3 | ENSG00000067798.16 | transcript | ENST00000397909.7 | protein_coding | 1/39 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
NAV3_chr12_77825894_78218010 | 78064426 | T | TCTGTCTG others(17): Show |
intron_variant | MODIFIER | HG02895.hp2 | a0004 | a0004c0017 | a0004c0017t0021 | a0004c0017t0021g0176 | 1 | 186 | 0.0054 | 24 | c.263 others(43): Show |
NAV3 | ENSG00000067798.16 | transcript | ENST00000397909.7 | protein_coding | 12/39 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
NAV3_chr12_77825894_78218010 | 78154256 | T | TATAATAT others(17): Show |
intron_variant | MODIFIER | HG02293.hp2 HG03130.hp1 HG03704.hp1 others(7): Show |
a0001 | a0001c0001a0001c0004a0001c0007 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(7): Show | a0001c0001t0001g0126 a0001c0001t0002g0170 a0001c0001t0004g0038 others(7): Show |
10 | 186 | 0.0538 | 24 | c.478 others(43): Show |
NAV3 | ENSG00000067798.16 | transcript | ENST00000397909.7 | protein_coding | 22/39 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
NAV3_chr12_77825894_78218010 | 78160406 | T | TGTGTGTG others(17): Show |
intron_variant | MODIFIER | NA18945.hp2 | a0001 | a0001c0001 | a0001c0001t0070 | a0001c0001t0070g0172 | 1 | 186 | 0.0054 | 24 | c.486 others(43): Show |
NAV3 | ENSG00000067798.16 | transcript | ENST00000397909.7 | protein_coding | 23/39 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
NBAS_chr2_15161916_15566334 | 15247726 | C | CTATCTAT others(17): Show |
intron_variant | MODIFIER | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(112): Show |
a0001a0002a0003others(24): Show | a0001c0001a0001c0003a0001c0040others(34): Show | a0001c0001t0001a0001c0003t0001a0001c0040t0001others(34): Show | a0001c0001t0001g0013 a0001c0001t0001g0018 a0001c0001t0001g0035 others(112): Show |
115 | 224 | 0.5134 | 24 | c.572 others(43): Show |
NBAS | ENSG00000151779.14 | transcript | ENST00000281513.10 | protein_coding | 44/51 | chr2 | TogoVar | |||||||
NBEAL1_chr2_203009875_203230194 | 203119424 | C | CTTTTTTT others(17): Show |
intron_variant | MODIFIER | HG02135.hp1 HG02135.hp2 NA18965.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0040 | a0001c0001t0001g0009 a0001c0001t0001g0255 a0001c0001t0040g0012 |
3 | 292 | 0.0103 | 24 | c.259 others(43): Show |
NBEAL1 | ENSG00000144426.19 | transcript | ENST00000683969.1 | protein_coding | 18/55 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
NBEA_chr13_34937270_35677736 | 35373707 | A | AAATAATA others(17): Show |
intron_variant | MODIFIER | HG02735.hp2 HG03098.hp2 HG04204.hp2 |
a0001 | a0001c0003 | a0001c0003t0005a0001c0003t0008 | a0001c0003t0005g0009 a0001c0003t0008g0007 a0001c0003t0008g0008 |
3 | 122 | 0.0246 | 24 | c.617 others(45): Show |
NBEA | ENSG00000172915.20 | transcript | ENST00000379939.7 | protein_coding | 38/58 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
NBPF10_chr1_146059711_146149804 | 146074633 | C | CAGACAGA others(17): Show |
intron_variant | MODIFIER | HG02280.hp2 HG03834.hp1 NA19085.hp2 |
a0009a0064a0069 | a0009c0046a0064c0038a0069c0067 | a0009c0046t0001a0064c0038t0001a0069c0067t0001 | a0009c0046t0001g0084 a0064c0038t0001g0039 a0069c0067t0001g0070 |
3 | 283 | 0.0106 | 24 | c.990 others(41): Show |
NBPF10 | ENSG00000271425.9 | transcript | ENST00000583866.9 | protein_coding | 79/89 | chr1 | TogoVar | |||||||
NBPF10_chr1_146059711_146149804 | 146079369 | C | CAGACAGA others(17): Show |
intron_variant | MODIFIER | HG02257.hp2 HG02258.hp1 NA18940.hp1 |
a0043a0059a0063 | a0043c0034a0059c0047a0063c0037 | a0043c0034t0001a0059c0047t0001a0063c0037t0001 | a0043c0034t0001g0086 a0059c0047t0001g0038 a0063c0037t0001g0036 |
3 | 283 | 0.0106 | 24 | c.917 others(41): Show |
NBPF10 | ENSG00000271425.9 | transcript | ENST00000583866.9 | protein_coding | 73/89 | chr1 | TogoVar | |||||||
NBPF10_chr1_146059711_146149804 | 146088826 | C | CAGACAGA others(17): Show |
intron_variant | MODIFIER | HG03017.hp1 | a0062 | a0062c0036 | a0062c0036t0001 | a0062c0036t0001g0037 | 1 | 283 | 0.0035 | 24 | c.771 others(41): Show |
NBPF10 | ENSG00000271425.9 | transcript | ENST00000583866.9 | protein_coding | 61/89 | chr1 | TogoVar | |||||||
NBPF10_chr1_146059711_146149804 | 146093544 | C | CAGACAGA others(17): Show |
intron_variant | MODIFIER | HG02280.hp2 | a0009 | a0009c0046 | a0009c0046t0001 | a0009c0046t0001g0084 | 1 | 283 | 0.0035 | 24 | c.697 others(41): Show |
NBPF10 | ENSG00000271425.9 | transcript | ENST00000583866.9 | protein_coding | 55/89 | chr1 | TogoVar | |||||||
NBPF10_chr1_146059711_146149804 | 146109343 | C | CACACACA others(17): Show |
intron_variant | MODIFIER | NA19240.hp2 | a0138 | a0138c0149 | a0138c0149t0001 | a0138c0149t0001g0151 | 1 | 283 | 0.0035 | 24 | c.450 others(41): Show |
NBPF10 | ENSG00000271425.9 | transcript | ENST00000583866.9 | protein_coding | 35/89 | chr1 | TogoVar | |||||||
NBPF14_chr1_148526385_148601011 | 148552375 | C | CACACACA others(17): Show |
intron_variant | MODIFIER | NA18970.hp1 | a0099 | a0099c0056 | a0099c0056t0001 | a0099c0056t0001g0100 | 1 | 222 | 0.0045 | 24 | c.573 others(41): Show |
NBPF14 | ENSG00000270629.7 | transcript | ENST00000619423.4 | protein_coding | 46/70 | chr1 | TogoVar | |||||||
NBPF14_chr1_148526385_148601011 | 148566558 | C | CAGAGAGA others(17): Show |
intron_variant | MODIFIER | HG02109.hp2 | a0121 | a0121c0151 | a0121c0151t0001 | a0121c0151t0001g0209 | 1 | 222 | 0.0045 | 24 | c.354 others(41): Show |
NBPF14 | ENSG00000270629.7 | transcript | ENST00000619423.4 | protein_coding | 28/70 | chr1 | TogoVar | |||||||
NBPF19_chr1_149470045_149561361 | 149528945 | C | CTCTCTCT others(17): Show |
intron_variant | MODIFIER | NA20129.hp2 | a0006 | a0006c0214 | a0006c0214t0002 | a0006c0214t0002g0265 | 1 | 276 | 0.0036 | 24 | c.734 others(41): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
NBPF19_chr1_149470045_149561361 | 149528945 | C | CTCTCTCT others(17): Show |
intron_variant | MODIFIER | HG00544.hp1 HG00735.hp1 HG01978.hp1 others(6): Show |
a0003a0027a0050others(5): Show | a0003c0003a0027c0029a0050c0080others(5): Show | a0003c0003t0001a0027c0029t0001a0050c0080t0001others(5): Show | a0003c0003t0001g0170 a0027c0029t0001g0061 a0027c0029t0001g0062 others(6): Show |
9 | 276 | 0.0326 | 24 | c.734 others(41): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
NBPF19_chr1_149470045_149561361 | 149528945 | C | CTCTCTGT others(17): Show |
intron_variant | MODIFIER | HG00544.hp2 HG01123.hp1 NA19088.hp1 |
a0011a0108a0165 | a0011c0010a0108c0143a0165c0200 | a0011c0010t0001a0108c0143t0001a0165c0200t0005 | a0011c0010t0001g0011 a0108c0143t0001g0027 a0165c0200t0005g0212 |
3 | 276 | 0.0109 | 24 | c.734 others(41): 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(17): Show |
intron_variant | MODIFIER | HG02155.hp1 HG04204.hp1 NA18961.hp1 others(1): Show |
a0034a0180a0200 | a0034c0013a0180c0072a0200c0062 | a0034c0013t0002a0180c0072t0002a0200c0062t0002 | a0034c0013t0002g0220 a0034c0013t0002g0221 a0180c0072t0002g0218 others(1): Show |
4 | 276 | 0.0145 | 24 | c.734 others(41): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
NBPF19_chr1_149470045_149561361 | 149528946 | T | TCTCTCTC others(17): Show |
intron_variant | MODIFIER | HG02109.hp2 | a0167 | a0167c0203 | a0167c0203t0028 | a0167c0203t0028g0269 | 1 | 276 | 0.0036 | 24 | c.734 others(41): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | chr1 | TogoVar | |||||||
NBPF19_chr1_149470045_149561361 | 149528946 | T | TCTCTGTG others(17): Show |
intron_variant | MODIFIER | HG00558.hp2 HG00735.hp2 HG01516.hp1 |
a0161a0162a0163 | a0161c0197a0162c0196a0163c0199 | a0161c0197t0005a0162c0196t0005a0163c0199t0005 | a0161c0197t0005g0214 a0162c0196t0005g0213 a0163c0199t0005g0215 |
3 | 276 | 0.0109 | 24 | c.734 others(41): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 61/93 | chr1 | TogoVar | |||||||
NBPF19_chr1_149470045_149561361 | 149543186 | C | CTCTCTCT others(17): Show |
intron_variant | MODIFIER | HG02109.hp2 | a0167 | a0167c0203 | a0167c0203t0028 | a0167c0203t0028g0269 | 1 | 276 | 0.0036 | 24 | c.954 others(41): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
NBPF19_chr1_149470045_149561361 | 149543186 | C | CTCTCTGT others(17): Show |
intron_variant | MODIFIER | HG04115.hp1 | a0169 | a0169c0205 | a0169c0205t0004 | a0169c0205t0004g0209 | 1 | 276 | 0.0036 | 24 | c.954 others(41): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
NBPF19_chr1_149470045_149561361 | 149543186 | C | CTCTCTGT others(17): Show |
intron_variant | MODIFIER | HG00423.hp2 HG00642.hp2 HG01071.hp1 others(27): Show |
a0002a0011a0014others(17): Show | a0002c0002a0011c0010a0014c0008others(17): Show | a0002c0002t0003a0002c0002t0007a0011c0010t0001others(18): Show | a0002c0002t0003g0182 a0002c0002t0003g0189 a0002c0002t0003g0196 others(27): Show |
30 | 276 | 0.1087 | 24 | c.954 others(41): 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(17): Show |
intron_variant | MODIFIER | HG00733.hp2 HG01978.hp2 HG02135.hp2 others(4): Show |
a0028a0059a0095others(4): Show | a0028c0032a0059c0091a0095c0126others(4): Show | a0028c0032t0001a0059c0091t0001a0095c0126t0001others(4): Show | a0028c0032t0001g0036 a0059c0091t0001g0130 a0095c0126t0001g0140 others(4): Show |
7 | 276 | 0.0254 | 24 | c.954 others(41): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 79/93 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
NBPF19_chr1_149470045_149561361 | 149543186 | C | CTGTGTGT others(17): Show |
intron_variant | MODIFIER | NA18981.hp1 NA19082.hp1 |
a0039a0178 | a0039c0219a0178c0070 | a0039c0219t0002a0178c0070t0002 | a0039c0219t0002g0227 a0178c0070t0002g0253 |
2 | 276 | 0.0073 | 24 | c.954 others(41): 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(17): Show |
intron_variant | MODIFIER | HG01952.hp2 NA18972.hp2 NA19088.hp2 |
a0031a0210 | a0031c0028a0210c0068 | a0031c0028t0003a0210c0068t0016 | a0031c0028t0003g0180 a0031c0028t0003g0194 a0210c0068t0016g0233 |
3 | 276 | 0.0109 | 24 | c.102 others(43): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 85/93 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
NBPF19_chr1_149470045_149561361 | 149547923 | C | CTCTGTGT others(17): Show |
intron_variant | MODIFIER | HG00733.hp2 HG00735.hp1 HG03225.hp2 |
a0107a0137a0164 | a0107c0138a0137c0173a0164c0201 | a0107c0138t0001a0137c0173t0001a0164c0201t0004 | a0107c0138t0001g0072 a0137c0173t0001g0159 a0164c0201t0004g0205 |
3 | 276 | 0.0109 | 24 | c.102 others(43): Show |
NBPF19 | ENSG00000271383.9 | transcript | ENST00000651566.2 | protein_coding | 85/93 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
NBPF20_chr1_145285005_145430603 | 145371351 | G | GACACACA others(17): Show |
intron_variant | MODIFIER | homoSapiens_chm13v2.hp1 | a0004 | a0004c0003 | a0004c0003t0001 | a0004c0003t0001g0001 | 1 | 6 | 0.1667 | 24 | c.441 others(41): Show |
NBPF20 | ENSG00000162825.18 | transcript | ENST00000698833.1 | protein_coding | 42/142 | chr1 | TogoVar | |||||||
NBPF3_chr1_21435137_21489900 | 21479820 | C | CTCTCTCT others(17): Show |
intron_variant | MODIFIER | HG00609.hp1 HG00621.hp2 HG01070.hp2 others(20): Show |
a0001a0012 | a0001c0001a0012c0012 | a0001c0001t0001a0001c0001t0007a0001c0001t0014others(2): Show | a0001c0001t0001g0018 a0001c0001t0001g0196 a0001c0001t0001g0207 others(17): Show |
23 | 394 | 0.0584 | 24 | c.120 others(41): Show |
NBPF3 | ENSG00000142794.19 | transcript | ENST00000318249.10 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
NBPF3_chr1_21435137_21489900 | 21479820 | C | CTCTGTGT others(17): Show |
intron_variant | MODIFIER | HG00438.hp2 HG00558.hp2 HG00738.hp1 others(2): Show |
a0003a0005a0024 | a0003c0003a0005c0005a0024c0016 | a0003c0003t0003a0005c0005t0004a0024c0016t0004 | a0003c0003t0003g0138 a0003c0003t0003g0144 a0005c0005t0004g0288 others(2): Show |
5 | 394 | 0.0127 | 24 | c.120 others(41): Show |
NBPF3 | ENSG00000142794.19 | transcript | ENST00000318249.10 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
NBPF4_chr1_108217464_108249076 | 108244901 | G | GATATATA others(17): Show |
upstream_gene_variant | MODIFIER | HG02523.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0022 | 1 | 134 | 0.0075 | 24 | c.-10 others(35): Show |
NBPF4 | ENSG00000196427.14 | transcript | ENST00000415641.8 | protein_coding | 826 | chr1 | TogoVar | |||||||
NCALD_chr8_101681542_101795969 | 101705224 | A | AAAATAAA others(17): Show |
intron_variant | MODIFIER | HG02258.hp2 HG02809.hp2 HG02886.hp1 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0007a0001c0001t0009 | a0001c0001t0001g0267 a0001c0001t0007g0291 a0001c0001t0009g0001 others(3): Show |
8 | 300 | 0.0267 | 24 | c.379 others(43): Show |
NCALD | ENSG00000104490.18 | transcript | ENST00000220931.11 | protein_coding | 2/3 | chr8 | TogoVar | |||||||
NCAM1_chr11_112956420_113283436 | 113017635 | T | TTGTGTGT others(17): Show |
intron_variant | MODIFIER | HG00140.hp2 HG00408.hp1 HG00621.hp2 others(28): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(19): Show | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0155 others(28): Show |
31 | 242 | 0.1281 | 24 | c.52+ others(41): Show |
NCAM1 | ENSG00000149294.18 | transcript | ENST00000316851.12 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
NCAM1_chr11_112956420_113283436 | 113095326 | G | GTGTGTGT others(17): Show |
intron_variant | MODIFIER | HG03453.hp2 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0009 | 1 | 242 | 0.0041 | 24 | c.53- others(43): 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(17): Show |
intron_variant | MODIFIER | HG01975.hp2 HG02040.hp2 HG03491.hp1 others(4): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0001t0047a0001c0001t0054others(2): Show | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0047g0141 others(4): Show |
7 | 242 | 0.0289 | 24 | c.53- others(41): Show |
NCAM1 | ENSG00000149294.18 | transcript | ENST00000316851.12 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
NCAM1_chr11_112956420_113283436 | 113185068 | T | TTATATTT others(17): Show |
intron_variant | MODIFIER | HG02895.hp2 | a0001 | a0001c0002 | a0001c0002t0048 | a0001c0002t0048g0142 | 1 | 242 | 0.0041 | 24 | c.53- others(41): 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(17): Show |
intron_variant | MODIFIER | HG01516.hp2 HG02015.hp2 HG02083.hp2 others(2): Show |
a0001 | a0001c0001a0001c0002a0001c0005 | a0001c0001t0001a0001c0001t0011a0001c0002t0001others(1): Show | a0001c0001t0001g0110 a0001c0001t0001g0181 a0001c0001t0011g0145 others(2): Show |
5 | 242 | 0.0207 | 24 | c.53- others(41): 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(17): Show |
intron_variant | MODIFIER | NA19070.hp2 | a0001 | a0001c0002 | a0001c0002t0009 | a0001c0002t0009g0217 | 1 | 242 | 0.0041 | 24 | c.53- others(41): Show |
NCAM1 | ENSG00000149294.18 | transcript | ENST00000316851.12 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
NCAM1_chr11_112956420_113283436 | 113210775 | A | AACACACA others(17): Show |
intron_variant | MODIFIER | NA18993.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0168 | 1 | 242 | 0.0041 | 24 | c.916 others(41): Show |
NCAM1 | ENSG00000149294.18 | transcript | ENST00000316851.12 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
NCAM2_chr21_20993409_21548329 | 21106314 | C | CAAAAAAA others(17): Show |
intron_variant | MODIFIER | NA19062.hp2 | a0002 | a0002c0002 | a0002c0002t0006 | a0002c0002t0006g0042 | 1 | 132 | 0.0076 | 24 | c.55+ others(43): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | ||||||
NCAM2_chr21_20993409_21548329 | 21214746 | T | TATATATA others(17): Show |
intron_variant | MODIFIER | NA19062.hp2 | a0002 | a0002c0002 | a0002c0002t0006 | a0002c0002t0006g0042 | 1 | 132 | 0.0076 | 24 | c.56- others(41): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | ||||||
NCAM2_chr21_20993409_21548329 | 21214746 | T | TATATATA others(17): Show |
intron_variant | MODIFIER | HG00639.hp2 HG02293.hp1 HG03471.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0029 | a0001c0001t0001g0017 a0001c0001t0002g0072 a0001c0001t0029g0061 |
3 | 132 | 0.0227 | 24 | c.56- others(41): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | ||||||
NCAM2_chr21_20993409_21548329 | 21272934 | T | TCACACAC others(17): Show |
intron_variant | MODIFIER | HG02559.hp2 HG03540.hp1 NA21309.hp2 |
a0001a0002 | a0001c0001a0002c0002a0002c0003 | a0001c0001t0039a0002c0002t0009a0002c0003t0013 | a0001c0001t0039g0108 a0002c0002t0009g0002 a0002c0003t0013g0118 |
3 | 132 | 0.0227 | 24 | c.56- others(39): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | ||||||
NCAM2_chr21_20993409_21548329 | 21331517 | C | CTCTCTCT others(17): Show |
intron_variant | MODIFIER | HG02965.hp1 | a0002 | a0002c0003 | a0002c0003t0008 | a0002c0003t0008g0009 | 1 | 132 | 0.0076 | 24 | c.738 others(41): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | ||||||
NCAM2_chr21_20993409_21548329 | 21331517 | C | CTCTCTCT others(17): Show |
intron_variant | MODIFIER | NA18979.hp1 | a0002 | a0002c0002 | a0002c0002t0019 | a0002c0002t0019g0034 | 1 | 132 | 0.0076 | 24 | c.738 others(41): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | ||||||
NCAM2_chr21_20993409_21548329 | 21431123 | T | TTGTGTGT others(17): Show |
intron_variant | MODIFIER | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(2): Show |
a0002 | a0002c0002 | a0002c0002t0001a0002c0002t0003a0002c0002t0037 | a0002c0002t0001g0057 a0002c0002t0001g0086 a0002c0002t0003g0020 others(2): Show |
5 | 132 | 0.0379 | 24 | c.148 others(41): Show |
NCAM2 | ENSG00000154654.15 | transcript | ENST00000400546.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr21 | TogoVar |