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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
SMS_chrX_21935709_21999837 | 21966212 | CT | C | intron_variant | MODIFIER | NA18997.hp2 | a0001 | a0001c0001 | a0001c0001t0009 | a0001c0001t0009g0047 | 1 | 298 | 0.0034 | -1 | c.50- others(7): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21968555 | CG | C | intron_variant | MODIFIER | NA19058.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0245 | 1 | 298 | 0.0034 | -1 | c.170 others(9): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21969177 | AC | A | intron_variant | MODIFIER | NA19074.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0049 | 1 | 298 | 0.0034 | -1 | c.170 others(9): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21970123 | TA | T | intron_variant | MODIFIER | NA19089.hp2 | a0002 | a0002c0003 | a0002c0003t0002 | a0002c0003t0002g0193 | 1 | 298 | 0.0034 | -1 | c.171 others(9): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21970718 | GC | G | intron_variant | MODIFIER | NA19089.hp2 | a0002 | a0002c0003 | a0002c0003t0002 | a0002c0003t0002g0193 | 1 | 298 | 0.0034 | -1 | c.171 others(9): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21970745 | GT | G | intron_variant | MODIFIER | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(12): Show |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(1): Show | a0001c0001t0001g0077a0001c0001t0001g0089a0001c0001t0001g0245others(12): Show | 15 | 298 | 0.0503 | -1 | c.171 others(9): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21971199 | GA | G | intron_variant | MODIFIER | NA19089.hp2 | a0002 | a0002c0003 | a0002c0003t0002 | a0002c0003t0002g0193 | 1 | 298 | 0.0034 | -1 | c.171 others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21971343 | TA | T | intron_variant | MODIFIER | NA18953.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0039 | 1 | 298 | 0.0034 | -1 | c.171 others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21971372 | TA | T | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(86): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0005others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(10): Show | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0105others(86): Show | 89 | 298 | 0.2987 | -1 | c.171 others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21971692 | TA | T | intron_variant | MODIFIER | NA19089.hp2 | a0002 | a0002c0003 | a0002c0003t0002 | a0002c0003t0002g0193 | 1 | 298 | 0.0034 | -1 | c.171 others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21971792 | TA | T | intron_variant | MODIFIER | NA19089.hp2 | a0002 | a0002c0003 | a0002c0003t0002 | a0002c0003t0002g0193 | 1 | 298 | 0.0034 | -1 | c.171 others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21971852 | GC | G | intron_variant | MODIFIER | NA19089.hp2 | a0002 | a0002c0003 | a0002c0003t0002 | a0002c0003t0002g0193 | 1 | 298 | 0.0034 | -1 | c.171 others(7): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21972104 | TC | T | intron_variant | MODIFIER | NA19089.hp2 | a0002 | a0002c0003 | a0002c0003t0002 | a0002c0003t0002g0193 | 1 | 298 | 0.0034 | -1 | c.264 others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21972327 | AG | A | intron_variant | MODIFIER | NA18978.hp1 | a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0058 | 1 | 298 | 0.0034 | -1 | c.265 others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21972480 | GC | G | intron_variant | MODIFIER | HG02809.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0115 | 1 | 298 | 0.0034 | -1 | c.265 others(7): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21972570 | CG | C | splice_donor_variant others(1): Show |
HIGH | NA19089.hp2 | a0002 | a0002c0003 | a0002c0003t0002 | a0002c0003t0002g0193 | 1 | 298 | 0.0034 | -1 | c.329 others(6): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21972893 | TG | T | intron_variant | MODIFIER | HG02809.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0115 | 1 | 298 | 0.0034 | -1 | c.329 others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21972916 | CA | C | intron_variant | MODIFIER | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(42): Show |
a0001a0003 | a0001c0001a0001c0005a0003c0006 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(5): Show | a0001c0001t0001g0081a0001c0001t0001g0108a0001c0001t0001g0117others(42): Show | 45 | 298 | 0.1510 | -1 | c.329 others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21973527 | GT | G | intron_variant | MODIFIER | NA19089.hp2 | a0002 | a0002c0003 | a0002c0003t0002 | a0002c0003t0002g0193 | 1 | 298 | 0.0034 | -1 | c.329 others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21973678 | GA | G | intron_variant | MODIFIER | NA19089.hp2 | a0002 | a0002c0003 | a0002c0003t0002 | a0002c0003t0002g0193 | 1 | 298 | 0.0034 | -1 | c.329 others(9): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21973738 | TA | T | intron_variant | MODIFIER | NA19089.hp2 | a0002 | a0002c0003 | a0002c0003t0002 | a0002c0003t0002g0193 | 1 | 298 | 0.0034 | -1 | c.329 others(9): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21973868 | TG | T | intron_variant | MODIFIER | NA19089.hp2 | a0002 | a0002c0003 | a0002c0003t0002 | a0002c0003t0002g0193 | 1 | 298 | 0.0034 | -1 | c.329 others(9): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21974038 | TC | T | intron_variant | MODIFIER | NA19089.hp2 | a0002 | a0002c0003 | a0002c0003t0002 | a0002c0003t0002g0193 | 1 | 298 | 0.0034 | -1 | c.329 others(9): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21974856 | CT | C | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(223): Show |
a0001a0002a0004 | a0001c0001a0001c0002a0001c0005others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(13): Show | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(222): Show | 226 | 298 | 0.7584 | -1 | c.330 others(9): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21975085 | TA | T | intron_variant | MODIFIER | NA19089.hp2 | a0002 | a0002c0003 | a0002c0003t0002 | a0002c0003t0002g0193 | 1 | 298 | 0.0034 | -1 | c.330 others(9): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21975328 | TA | T | intron_variant | MODIFIER | NA19089.hp2 | a0002 | a0002c0003 | a0002c0003t0002 | a0002c0003t0002g0193 | 1 | 298 | 0.0034 | -1 | c.330 others(9): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21975562 | GC | G | intron_variant | MODIFIER | NA19089.hp2 | a0002 | a0002c0003 | a0002c0003t0002 | a0002c0003t0002g0193 | 1 | 298 | 0.0034 | -1 | c.330 others(9): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21975774 | CG | C | intron_variant | MODIFIER | NA19089.hp2 | a0002 | a0002c0003 | a0002c0003t0002 | a0002c0003t0002g0193 | 1 | 298 | 0.0034 | -1 | c.330 others(9): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21975791 | GT | G | intron_variant | MODIFIER | HG00408.hp2 HG02027.hp1 NA19011.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0188a0001c0001t0002g0183a0001c0001t0002g0203 | 3 | 298 | 0.0101 | -1 | c.330 others(9): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21976226 | TG | T | intron_variant | MODIFIER | NA19089.hp2 | a0002 | a0002c0003 | a0002c0003t0002 | a0002c0003t0002g0193 | 1 | 298 | 0.0034 | -1 | c.330 others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21976588 | GA | G | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
a0001a0003a0004 | a0001c0001a0001c0002a0001c0005others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(12): Show | a0001c0001t0001g0040a0001c0001t0001g0045a0001c0001t0001g0070others(169): Show | 172 | 298 | 0.5772 | -1 | c.330 others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21977486 | TA | T | intron_variant | MODIFIER | HG01070.hp2 HG02109.hp2 HG02647.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0145a0001c0001t0002g0130a0001c0001t0002g0131others(2): Show | 5 | 298 | 0.0168 | -1 | c.505 others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21979931 | CA | C | intron_variant | MODIFIER | HG00735.hp1 HG01081.hp1 HG01081.hp2 others(28): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(2): Show | a0001c0001t0001g0041a0001c0001t0001g0117a0001c0001t0001g0188others(28): Show | 31 | 298 | 0.1040 | -1 | c.750 others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21979953 | TA | T | intron_variant | MODIFIER | HG02109.hp2 HG02647.hp1 HG03195.hp2 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0136 | 3 | 298 | 0.0101 | -1 | c.750 others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21981376 | AG | A | intron_variant | MODIFIER | NA18997.hp2 | a0001 | a0001c0001 | a0001c0001t0009 | a0001c0001t0009g0047 | 1 | 298 | 0.0034 | -1 | c.750 others(9): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21982051 | AG | A | intron_variant | MODIFIER | NA19075.hp1 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0282 | 1 | 298 | 0.0034 | -1 | c.751 others(9): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21982336 | CA | C | intron_variant | MODIFIER | HG02976.hp2 NA18951.hp2 NA19086.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0005 | a0001c0001t0001g0117a0001c0001t0001g0227a0001c0001t0005g0275 | 3 | 298 | 0.0101 | -1 | c.751 others(9): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21983035 | CT | C | intron_variant | MODIFIER | NA19075.hp1 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0282 | 1 | 298 | 0.0034 | -1 | c.751 others(9): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21983322 | TG | T | intron_variant | MODIFIER | NA19075.hp1 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0282 | 1 | 298 | 0.0034 | -1 | c.751 others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21983402 | AT | A | intron_variant | MODIFIER | HG01891.hp2 HG02970.hp2 |
a0001 | a0001c0001a0001c0005 | a0001c0001t0003a0001c0005t0001 | a0001c0001t0003g0285a0001c0005t0001g0219 | 2 | 298 | 0.0067 | -1 | c.751 others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21984513 | GT | G | intron_variant | MODIFIER | NA18997.hp2 | a0001 | a0001c0001 | a0001c0001t0009 | a0001c0001t0009g0047 | 1 | 298 | 0.0034 | -1 | c.865 others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21984585 | GC | G | intron_variant | MODIFIER | NA19075.hp1 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0282 | 1 | 298 | 0.0034 | -1 | c.865 others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21984866 | GC | G | intron_variant | MODIFIER | NA19075.hp1 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0282 | 1 | 298 | 0.0034 | -1 | c.866 others(8): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21985044 | CT | C | intron_variant | MODIFIER | NA19075.hp1 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0282 | 1 | 298 | 0.0034 | -1 | c.866 others(7): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21986230 | TC | T | intron_variant | MODIFIER | NA19075.hp1 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0282 | 1 | 298 | 0.0034 | -1 | c.945 others(9): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21986347 | CA | C | intron_variant | MODIFIER | HG00544.hp2 HG00735.hp2 HG01070.hp2 others(14): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0038others(14): Show | 17 | 298 | 0.0571 | -1 | c.945 others(9): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21986995 | GT | G | intron_variant | MODIFIER | NA19077.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0250 | 1 | 298 | 0.0034 | -1 | c.945 others(9): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21987253 | TC | T | intron_variant | MODIFIER | NA18997.hp2 | a0001 | a0001c0001 | a0001c0001t0009 | a0001c0001t0009g0047 | 1 | 298 | 0.0034 | -1 | c.945 others(9): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21988320 | AC | A | intron_variant | MODIFIER | HG00597.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0180 | 1 | 298 | 0.0034 | -1 | c.945 others(9): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
SMS_chrX_21935709_21999837 | 21988662 | CA | C | intron_variant | MODIFIER | HG06807.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0166 | 1 | 298 | 0.0034 | -1 | c.945 others(9): Show |
SMS | ENSG00000102172.16 | transcript | ENST00000404933.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | TogoVar |