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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
B4GALT7_chr5_177595132_177615330 | 177598537 | A | ATAGT | upstream_gene_variant | MODIFIER | HG02055.hp2 HG02622.hp2 HG02630.hp1 others(1): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0039a0001c0002t0001g0088 | 4 | 458 | 0.0087 | 4 | c.-16 others(15): Show |
B4GALT7 | ENSG00000027847.14 | transcript | ENST00000029410.10 | protein_coding | 1594 | chr5 | TogoVar | ||||||
B4GALT7_chr5_177595132_177615330 | 177613493 | C | CTAAA | downstream_gene_variant | MODIFIER | HG02074.hp1 HG02723.hp1 HG02976.hp1 others(4): Show |
a0001 | a0001c0001a0001c0002a0001c0004 | a0001c0001t0001a0001c0002t0001a0001c0004t0003 | a0001c0001t0001g0001a0001c0001t0001g0032a0001c0002t0001g0008others(2): Show | 7 | 458 | 0.0153 | 4 | c.*37 others(15): Show |
B4GALT7 | ENSG00000027847.14 | transcript | ENST00000029410.10 | protein_coding | 3164 | chr5 | TogoVar | ||||||
B4GAT1_chr11_66340374_66352629 | 66347802 | A | ACGCC | upstream_gene_variant | MODIFIER | HG02055.hp1 HG02717.hp1 HG02818.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | 5 | 412 | 0.0121 | 4 | c.-25 others(13): Show |
B4GAT1 | ENSG00000174684.7 | transcript | ENST00000311181.5 | protein_coding | 174 | chr11 | TogoVar | ||||||
B9D1_chr17_19338175_19367723 | 19340033 | A | ACCCC | downstream_gene_variant | MODIFIER | HG00738.hp1 HG01981.hp1 HG02027.hp1 others(11): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0005a0001c0001t0007 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(5): Show | 14 | 354 | 0.0396 | 4 | c.*32 others(15): Show |
B9D1 | ENSG00000108641.20 | transcript | ENST00000261499.11 | protein_coding | 3141 | chr17 | TogoVar | ||||||
BAALC_chr8_103135725_103235305 | 103140445 | C | CGGAT | upstream_gene_variant | MODIFIER | HG00642.hp2 HG01109.hp2 HG01192.hp2 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0007 | a0001c0001t0001g0193a0001c0001t0002g0205a0001c0001t0002g0209others(5): Show | 9 | 332 | 0.0271 | 4 | c.-45 others(13): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 279 | chr8 | TogoVar | ||||||
BAALC_chr8_103135725_103235305 | 103154920 | C | CTATA | intron_variant | MODIFIER | HG02630.hp2 HG02886.hp2 HG03540.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0010 | a0001c0001t0001g0251a0001c0001t0010g0088a0001c0001t0010g0089 | 3 | 332 | 0.0090 | 4 | c.160 others(23): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
BAALC_chr8_103135725_103235305 | 103158685 | A | AATAC | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(97): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(12): Show | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0017others(87): Show | 100 | 332 | 0.3012 | 4 | c.160 others(23): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
BAALC_chr8_103135725_103235305 | 103171283 | A | AAGAG | intron_variant | MODIFIER | HG00099.hp2 HG00323.hp2 HG00738.hp1 others(38): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(8): Show | a0001c0001t0001g0044a0001c0001t0001g0062a0001c0001t0001g0063others(33): Show | 41 | 332 | 0.1235 | 4 | c.160 others(23): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
BAALC_chr8_103135725_103235305 | 103174260 | C | CAAAA | intron_variant | MODIFIER | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(104): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(7): Show | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0067others(91): Show | 107 | 332 | 0.3223 | 4 | c.160 others(23): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
BAALC_chr8_103135725_103235305 | 103205538 | T | TGATA | intron_variant | MODIFIER | HG00280.hp2 HG01884.hp2 NA18953.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0005 | a0001c0001t0001g0037a0001c0001t0001g0102a0001c0001t0001g0106others(4): Show | 7 | 332 | 0.0211 | 4 | c.161 others(21): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
BABAM1_chr19_17262443_17284337 | 17266585 | A | AAAAT | upstream_gene_variant | MODIFIER | HG00735.hp2 HG01081.hp1 HG01255.hp1 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0004a0001c0001t0001g0140a0001c0001t0001g0153others(2): Show | 9 | 424 | 0.0212 | 4 | c.-95 others(13): Show |
BABAM1 | ENSG00000105393.16 | transcript | ENST00000598188.6 | protein_coding | 857 | chr19 | TogoVar | ||||||
BABAM2_chr2_27885729_28343901 | 27942791 | A | AATTT | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(57): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(2): Show | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0017others(57): Show | 60 | 158 | 0.3798 | 4 | c.205 others(23): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
BABAM2_chr2_27885729_28343901 | 27982844 | T | TACAC | intron_variant | MODIFIER | HG01192.hp1 HG01496.hp1 HG01934.hp1 others(17): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0094others(17): Show | 20 | 158 | 0.1266 | 4 | c.206 others(21): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
BABAM2_chr2_27885729_28343901 | 27982844 | T | TATAC | intron_variant | MODIFIER | HG00140.hp2 HG00735.hp2 HG01081.hp2 others(23): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(1): Show | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(23): Show | 26 | 158 | 0.1646 | 4 | c.206 others(21): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
BABAM2_chr2_27885729_28343901 | 27985057 | A | ATGTG | intron_variant | MODIFIER | HG00639.hp2 HG01069.hp2 HG01081.hp2 others(44): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(2): Show | a0001c0001t0001g0023a0001c0001t0001g0025a0001c0001t0001g0034others(44): Show | 47 | 158 | 0.2975 | 4 | c.206 others(21): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
BABAM2_chr2_27885729_28343901 | 28013694 | T | TACAC | intron_variant | MODIFIER | HG00140.hp2 HG00639.hp1 HG00735.hp2 others(14): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0002c0002t0001 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0053others(14): Show | 17 | 158 | 0.1076 | 4 | c.301 others(23): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
BABAM2_chr2_27885729_28343901 | 28020952 | G | GACAC | intron_variant | MODIFIER | HG00733.hp1 HG00735.hp1 HG00738.hp2 others(31): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003 | a0001c0001t0001g0015a0001c0001t0001g0027a0001c0001t0001g0058others(31): Show | 34 | 158 | 0.2152 | 4 | c.301 others(21): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
BABAM2_chr2_27885729_28343901 | 28026822 | T | TTATA | intron_variant | MODIFIER | HG01109.hp1 HG01109.hp2 HG01346.hp1 others(10): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0023others(10): Show | 13 | 158 | 0.0823 | 4 | c.495 others(21): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
BABAM2_chr2_27885729_28343901 | 28026894 | A | ATATT | intron_variant | MODIFIER | HG00639.hp1 HG01167.hp1 HG01934.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0029a0001c0001t0002g0046a0001c0001t0002g0047others(4): Show | 7 | 158 | 0.0443 | 4 | c.495 others(21): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
BABAM2_chr2_27885729_28343901 | 28075528 | T | TTCTC | intron_variant | MODIFIER | HG00639.hp2 HG00741.hp2 HG01109.hp1 others(9): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(9): Show | 12 | 158 | 0.0760 | 4 | c.570 others(23): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
BABAM2_chr2_27885729_28343901 | 28075558 | A | ATGTG | intron_variant | MODIFIER | HG00738.hp1 HG02280.hp1 HG02280.hp2 others(15): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0088others(15): Show | 18 | 158 | 0.1139 | 4 | c.570 others(23): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
BABAM2_chr2_27885729_28343901 | 28076473 | T | TTTAG | intron_variant | MODIFIER | HG00140.hp2 HG00639.hp1 HG00733.hp1 others(58): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(1): Show | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0031others(58): Show | 61 | 158 | 0.3861 | 4 | c.570 others(23): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
BABAM2_chr2_27885729_28343901 | 28076481 | T | TTTAG | intron_variant | MODIFIER | HG02615.hp2 HG03486.hp2 NA20129.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0004g0118 | 3 | 158 | 0.0190 | 4 | c.570 others(23): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
BABAM2_chr2_27885729_28343901 | 28092749 | C | CCTCT | intron_variant | MODIFIER | HG00140.hp2 HG02165.hp1 HG03098.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0082a0001c0001t0001g0139a0001c0001t0002g0110 | 3 | 158 | 0.0190 | 4 | c.571 others(23): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
BABAM2_chr2_27885729_28343901 | 28112083 | C | CTCTT | intron_variant | MODIFIER | HG00140.hp1 HG01069.hp1 HG01099.hp1 others(20): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0005 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0040others(20): Show | 23 | 158 | 0.1456 | 4 | c.571 others(23): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
BABAM2_chr2_27885729_28343901 | 28115182 | A | AACAC | intron_variant | MODIFIER | HG02135.hp1 HG02572.hp1 HG02698.hp1 others(7): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0057a0001c0001t0001g0070a0001c0001t0001g0074others(7): Show | 10 | 158 | 0.0633 | 4 | c.571 others(23): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
BABAM2_chr2_27885729_28343901 | 28143144 | A | AATAT | intron_variant | MODIFIER | HG03209.hp2 NA19030.hp1 |
a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0089a0001c0001t0003g0090 | 2 | 158 | 0.0127 | 4 | c.680 others(23): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
BABAM2_chr2_27885729_28343901 | 28151677 | A | ATACT | intron_variant | MODIFIER | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(101): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(1): Show | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0013others(101): Show | 104 | 158 | 0.6582 | 4 | c.680 others(23): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
BABAM2_chr2_27885729_28343901 | 28167693 | C | CAAAA | intron_variant | MODIFIER | HG00140.hp2 HG00733.hp1 HG01243.hp1 others(4): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0001 | a0001c0001t0001g0017a0001c0001t0001g0040a0001c0001t0001g0066others(4): Show | 7 | 158 | 0.0443 | 4 | c.680 others(23): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
BABAM2_chr2_27885729_28343901 | 28167697 | A | AAAAT | intron_variant | MODIFIER | HG00735.hp1 HG00738.hp1 HG00741.hp1 others(30): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003 | a0001c0001t0001g0057a0001c0001t0001g0065a0001c0001t0001g0069others(30): Show | 33 | 158 | 0.2089 | 4 | c.680 others(23): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
BABAM2_chr2_27885729_28343901 | 28171112 | A | AATAT | intron_variant | MODIFIER | HG02572.hp1 HG02698.hp1 HG03209.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0002g0012others(2): Show | 5 | 158 | 0.0317 | 4 | c.680 others(23): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
BABAM2_chr2_27885729_28343901 | 28176569 | C | CAAAA | intron_variant | MODIFIER | HG00733.hp2 HG00741.hp2 HG01167.hp2 others(9): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0023others(9): Show | 12 | 158 | 0.0760 | 4 | c.680 others(23): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
BABAM2_chr2_27885729_28343901 | 28184263 | C | CCTCT | intron_variant | MODIFIER | HG00140.hp2 HG00733.hp1 HG00735.hp2 others(27): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(27): Show | 30 | 158 | 0.1899 | 4 | c.681 others(23): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
BABAM2_chr2_27885729_28343901 | 28187662 | A | ATTTT | intron_variant | MODIFIER | HG01433.hp2 HG01934.hp1 HG02040.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0004 | a0001c0001t0001g0097a0001c0001t0001g0125a0001c0001t0001g0127others(2): Show | 5 | 158 | 0.0317 | 4 | c.681 others(23): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
BABAM2_chr2_27885729_28343901 | 28196836 | C | CTTTT | intron_variant | MODIFIER | HG01168.hp1 HG02818.hp1 HG02897.hp1 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003 | a0001c0001t0001g0035a0001c0001t0001g0093a0001c0001t0001g0142others(5): Show | 8 | 158 | 0.0506 | 4 | c.681 others(23): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
BABAM2_chr2_27885729_28343901 | 28200758 | T | TTTTG | intron_variant | MODIFIER | HG00733.hp2 HG01167.hp2 HG01346.hp1 others(18): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(18): Show | 21 | 158 | 0.1329 | 4 | c.681 others(23): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
BABAM2_chr2_27885729_28343901 | 28208029 | C | CTGTG | intron_variant | MODIFIER | HG02897.hp1 HG03195.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0043a0001c0001t0002g0020 | 2 | 158 | 0.0127 | 4 | c.681 others(23): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
BABAM2_chr2_27885729_28343901 | 28230560 | C | CAAAA | intron_variant | MODIFIER | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(14): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0027others(14): Show | 17 | 158 | 0.1076 | 4 | c.681 others(21): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
BABAM2_chr2_27885729_28343901 | 28235646 | T | TTTTG | intron_variant | MODIFIER | HG01891.hp2 HG02486.hp1 HG02572.hp1 others(10): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015others(10): Show | 13 | 158 | 0.0823 | 4 | c.681 others(21): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
BABAM2_chr2_27885729_28343901 | 28248209 | T | TTTTC | intron_variant | MODIFIER | HG01069.hp1 HG02027.hp1 HG02109.hp2 others(10): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(1): Show | a0001c0001t0001g0057a0001c0001t0001g0099a0001c0001t0001g0113others(10): Show | 13 | 158 | 0.0823 | 4 | c.934 others(21): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
BABAM2_chr2_27885729_28343901 | 28259074 | C | CTTTT | intron_variant | MODIFIER | HG00738.hp2 HG01069.hp1 HG01192.hp1 others(24): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003 | a0001c0001t0001g0008a0001c0001t0001g0058a0001c0001t0001g0072others(24): Show | 27 | 158 | 0.1709 | 4 | c.934 others(23): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
BABAM2_chr2_27885729_28343901 | 28267438 | T | TACAC | intron_variant | MODIFIER | HG01496.hp1 HG02572.hp2 HG02647.hp2 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0003 | a0001c0001t0002g0122a0001c0001t0002g0140a0001c0001t0003g0121 | 3 | 158 | 0.0190 | 4 | c.934 others(23): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
BABAM2_chr2_27885729_28343901 | 28315232 | T | TTTTG | intron_variant | MODIFIER | HG02572.hp2 HG02647.hp2 HG03139.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0003 | a0001c0001t0002g0010a0001c0001t0002g0016a0001c0001t0002g0112others(2): Show | 5 | 158 | 0.0317 | 4 | c.108 others(25): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
BABAM2_chr2_27885729_28343901 | 28315421 | T | TTTTC | intron_variant | MODIFIER | HG01099.hp2 HG02040.hp2 HG02622.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0027a0001c0001t0001g0052a0001c0001t0001g0080others(3): Show | 6 | 158 | 0.0380 | 4 | c.108 others(25): Show |
BABAM2 | ENSG00000158019.21 | transcript | ENST00000379624.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
BACE2_chr21_41163160_41287530 | 41198849 | T | TTTTA | intron_variant | MODIFIER | HG00733.hp2 HG01109.hp1 HG01496.hp2 others(36): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(20): Show | a0001c0001t0002g0154a0001c0001t0004g0023a0001c0001t0004g0104others(36): Show | 39 | 272 | 0.1434 | 4 | c.313 others(23): Show |
BACE2 | ENSG00000182240.16 | transcript | ENST00000330333.11 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | |||||
BACE2_chr21_41163160_41287530 | 41221827 | C | CAAAA | intron_variant | MODIFIER | HG00741.hp2 HG01106.hp2 HG02109.hp1 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0007a0001c0001t0011a0001c0001t0012others(5): Show | a0001c0001t0007g0002a0001c0001t0011g0264a0001c0001t0012g0137others(5): Show | 8 | 272 | 0.0294 | 4 | c.313 others(21): Show |
BACE2 | ENSG00000182240.16 | transcript | ENST00000330333.11 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | |||||
BACE2_chr21_41163160_41287530 | 41235854 | A | AAATG | intron_variant | MODIFIER | HG00280.hp1 HG00738.hp1 HG00741.hp2 others(62): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(27): Show | a0001c0001t0002g0001a0001c0001t0002g0070a0001c0001t0005g0140others(61): Show | 65 | 272 | 0.2390 | 4 | c.402 others(21): Show |
BACE2 | ENSG00000182240.16 | transcript | ENST00000330333.11 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | |||||
BACE2_chr21_41163160_41287530 | 41244863 | C | CTGTG | intron_variant | MODIFIER | HG00408.hp1 HG01109.hp1 HG01167.hp2 others(19): Show |
a0001 | a0001c0001 | a0001c0001t0004a0001c0001t0008a0001c0001t0012others(6): Show | a0001c0001t0004g0023a0001c0001t0004g0038a0001c0001t0004g0072others(19): Show | 22 | 272 | 0.0809 | 4 | c.883 others(21): Show |
BACE2 | ENSG00000182240.16 | transcript | ENST00000330333.11 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | |||||
BACE2_chr21_41163160_41287530 | 41286119 | T | TATAG | downstream_gene_variant | MODIFIER | HG00642.hp2 HG00738.hp2 HG01069.hp1 others(21): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0003a0001c0001t0004a0001c0001t0006others(11): Show | a0001c0001t0003g0178a0001c0001t0003g0230a0001c0001t0004g0074others(21): Show | 24 | 272 | 0.0882 | 4 | c.*10 others(17): Show |
BACE2 | ENSG00000182240.16 | transcript | ENST00000330333.11 | protein_coding | 3590 | chr21 | TogoVar | ||||||
BACH1_chr21_29293922_29351148 | 29306169 | A | AGTGT | intron_variant | MODIFIER | HG00099.hp1 HG00438.hp1 HG01975.hp1 others(29): Show |
a0001 | a0001c0001a0001c0002a0001c0005 | a0001c0001t0002a0001c0001t0011a0001c0001t0012others(9): Show | a0001c0001t0002g0010a0001c0001t0002g0044a0001c0001t0002g0046others(23): Show | 32 | 368 | 0.0870 | 4 | c.-61 others(21): Show |
BACH1 | ENSG00000156273.16 | transcript | ENST00000286800.8 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr21 | TogoVar |