Item | Value |
---|---|
geneid | 150365 |
ensemblid | ENSG00000167077.13 |
hgncid | 28613 |
symbol | MEI1 |
name | meiotic double-stranded break formation protein 1 |
refseq_nuc | NM_152513.4 |
refseq_prot | NP_689726.3 |
ensembl_nuc | ENST00000401548.8 |
ensembl_prot | ENSP00000384115.3 |
mane_status | MANE Select |
chr | chr22 |
start | 41699503 |
end | 41799454 |
strand | + |
ver | v1.2 |
region | chr22:41699503-41799454 |
region5000 | chr22:41694503-41804454 |
regionname0 | MEI1_chr22_41699503_41799454 |
regionname5000 | MEI1_chr22_41694503_41804454 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1274 | 219 | 61 | 46 | 73 | 12 | 25 | 50 | MEI1_chr22_41694503_41804454 | MEI1 | MAVRQ others(1269): Show |
chr22 | 41694503 | 41804454 |
a0002 | 0/0 | 1274 | 13 | 1 | 4 | 7 | 0 | 1 | 4 | MEI1_chr22_41694503_41804454 | MEI1 | MAVRQ others(1269): Show |
chr22 | 41694503 | 41804454 |
a0003 | 0/0 | 1274 | 9 | 8 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | MAVRQ others(1269): Show |
chr22 | 41694503 | 41804454 |
a0004 | 0/0 | 1274 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | MAVRQ others(1269): Show |
chr22 | 41694503 | 41804454 |
a0005 | 0/0 | 1274 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | MAVRQ others(1269): Show |
chr22 | 41694503 | 41804454 |
a0006 | 0/0 | 1274 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | MAVRQ others(1269): Show |
chr22 | 41694503 | 41804454 |
a0007 | 0/0 | 1274 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | MAVRQ others(1269): Show |
chr22 | 41694503 | 41804454 |
a0008 | 0/0 | 1274 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | MAVRQ others(1269): Show |
chr22 | 41694503 | 41804454 |
a0009 | 0/0 | 1274 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | MAVRQ others(1269): Show |
chr22 | 41694503 | 41804454 |
a0010 | 0/0 | 1274 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | MAVRQ others(1269): Show |
chr22 | 41694503 | 41804454 |
a0011 | 0/0 | 1274 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | MAVRQ others(1269): Show |
chr22 | 41694503 | 41804454 |
a0012 | 0/0 | 1274 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | MAVRQ others(1269): Show |
chr22 | 41694503 | 41804454 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 3822 | 121 | 15 | 22 | 58 | 9 | 16 | MEI1_chr22_41694503_41804454 | MEI1 | ATGGC others(3817): Show |
chr22 | 41694503 | 41804454 | ||
a0001c0002 | 1/0 | 3822 | 49 | 2 | 21 | 13 | 3 | 9 | MEI1_chr22_41694503_41804454 | MEI1 | ATGGC others(3817): Show |
chr22 | 41694503 | 41804454 | ||
a0001c0003 | 0/0 | 3822 | 20 | 17 | 3 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | ATGGC others(3817): Show |
chr22 | 41694503 | 41804454 | ||
a0001c0004 | 0/0 | 3822 | 16 | 16 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | ATGGC others(3817): Show |
chr22 | 41694503 | 41804454 | ||
a0001c0008 | 0/0 | 3822 | 5 | 5 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | ATGGC others(3817): Show |
chr22 | 41694503 | 41804454 | ||
a0001c0011 | 0/0 | 3822 | 2 | 2 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | ATGGC others(3817): Show |
chr22 | 41694503 | 41804454 | ||
a0001c0012 | 0/0 | 3822 | 2 | 2 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | ATGGC others(3817): Show |
chr22 | 41694503 | 41804454 | ||
a0001c0015 | 0/0 | 3822 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | ATGGC others(3817): Show |
chr22 | 41694503 | 41804454 | ||
a0001c0017 | 0/0 | 3822 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | ATGGC others(3817): Show |
chr22 | 41694503 | 41804454 | ||
a0001c0018 | 0/0 | 3822 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | ATGGC others(3817): Show |
chr22 | 41694503 | 41804454 | ||
a0001c0022 | 0/0 | 3822 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | ATGGC others(3817): Show |
chr22 | 41694503 | 41804454 | ||
a0002c0005 | 0/0 | 3822 | 13 | 1 | 4 | 7 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 | ATGGC others(3817): Show |
chr22 | 41694503 | 41804454 | ||
a0003c0006 | 0/0 | 3822 | 9 | 8 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | ATGGC others(3817): Show |
chr22 | 41694503 | 41804454 | ||
a0004c0009 | 0/0 | 3822 | 5 | 4 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | ATGGC others(3817): Show |
chr22 | 41694503 | 41804454 | ||
a0005c0007 | 0/0 | 3822 | 5 | 5 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | ATGGC others(3817): Show |
chr22 | 41694503 | 41804454 | ||
a0006c0010 | 0/0 | 3822 | 3 | 2 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | ATGGC others(3817): Show |
chr22 | 41694503 | 41804454 | ||
a0007c0020 | 0/0 | 3822 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | ATGGC others(3817): Show |
chr22 | 41694503 | 41804454 | ||
a0008c0021 | 0/0 | 3822 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | ATGGC others(3817): Show |
chr22 | 41694503 | 41804454 | ||
a0009c0019 | 0/0 | 3822 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | ATGGC others(3817): Show |
chr22 | 41694503 | 41804454 | ||
a0010c0016 | 0/0 | 3822 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | ATGGC others(3817): Show |
chr22 | 41694503 | 41804454 | ||
a0011c0014 | 0/0 | 3822 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | ATGGC others(3817): Show |
chr22 | 41694503 | 41804454 | ||
a0012c0013 | 0/0 | 3822 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | ATGGC others(3817): Show |
chr22 | 41694503 | 41804454 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 4016 | 117 | 12 | 21 | 58 | 9 | 16 | MEI1_chr22_41694503_41804454 | MEI1 | GAAAG others(4011): Show |
chr22 | 41694503 | 41804454 |
a0001c0001t0002 | 0/0 | 4016 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | GAAAG others(4011): Show |
chr22 | 41694503 | 41804454 |
a0001c0001t0005 | 0/0 | 4016 | 3 | 3 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | GAAAG others(4011): Show |
chr22 | 41694503 | 41804454 |
a0001c0002t0001 | 1/0 | 4016 | 1 | 0 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | GAAAG others(4011): Show |
chr22 | 41694503 | 41804454 |
a0001c0002t0002 | 0/0 | 4016 | 48 | 2 | 21 | 13 | 3 | 9 | MEI1_chr22_41694503_41804454 | MEI1 | GAAAG others(4011): Show |
chr22 | 41694503 | 41804454 |
a0001c0003t0001 | 0/0 | 4016 | 3 | 3 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | GAAAG others(4011): Show |
chr22 | 41694503 | 41804454 |
a0001c0003t0004 | 0/0 | 4013 | 17 | 14 | 3 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | GAAAG others(4008): Show |
chr22 | 41694503 | 41804454 |
a0001c0004t0003 | 0/0 | 4018 | 15 | 15 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | GAAAG others(4013): Show |
chr22 | 41694503 | 41804454 |
a0001c0004t0006 | 0/0 | 4015 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | GAAAG others(4010): Show |
chr22 | 41694503 | 41804454 |
a0001c0008t0003 | 0/0 | 4018 | 5 | 5 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | GAAAG others(4013): Show |
chr22 | 41694503 | 41804454 |
a0001c0011t0003 | 0/0 | 4018 | 2 | 2 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | GAAAG others(4013): Show |
chr22 | 41694503 | 41804454 |
a0001c0012t0001 | 0/0 | 4016 | 2 | 2 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | GAAAG others(4011): Show |
chr22 | 41694503 | 41804454 |
a0001c0015t0003 | 0/0 | 4018 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | GAAAG others(4013): Show |
chr22 | 41694503 | 41804454 |
a0001c0017t0001 | 0/0 | 4016 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | GAAAG others(4011): Show |
chr22 | 41694503 | 41804454 |
a0001c0018t0001 | 0/0 | 4016 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | GAAAG others(4011): Show |
chr22 | 41694503 | 41804454 |
a0001c0022t0001 | 0/0 | 4016 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | GAAAG others(4011): Show |
chr22 | 41694503 | 41804454 |
a0002c0005t0001 | 0/0 | 4016 | 13 | 1 | 4 | 7 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 | GAAAG others(4011): Show |
chr22 | 41694503 | 41804454 |
a0003c0006t0001 | 0/0 | 4016 | 9 | 8 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | GAAAG others(4011): Show |
chr22 | 41694503 | 41804454 |
a0004c0009t0001 | 0/0 | 4016 | 5 | 4 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | GAAAG others(4011): Show |
chr22 | 41694503 | 41804454 |
a0005c0007t0004 | 0/0 | 4013 | 5 | 5 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | GAAAG others(4008): Show |
chr22 | 41694503 | 41804454 |
a0006c0010t0001 | 0/0 | 4016 | 3 | 2 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | GAAAG others(4011): Show |
chr22 | 41694503 | 41804454 |
a0007c0020t0001 | 0/0 | 4016 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | GAAAG others(4011): Show |
chr22 | 41694503 | 41804454 |
a0008c0021t0001 | 0/0 | 4016 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | GAAAG others(4011): Show |
chr22 | 41694503 | 41804454 |
a0009c0019t0001 | 0/0 | 4016 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | GAAAG others(4011): Show |
chr22 | 41694503 | 41804454 |
a0010c0016t0003 | 0/0 | 4018 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | GAAAG others(4013): Show |
chr22 | 41694503 | 41804454 |
a0011c0014t0004 | 0/0 | 4013 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | GAAAG others(4008): Show |
chr22 | 41694503 | 41804454 |
a0012c0013t0001 | 0/0 | 4016 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | GAAAG others(4011): Show |
chr22 | 41694503 | 41804454 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0241 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0005g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0005g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0001t0005g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0002t0001g0081 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0002t0002g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0002t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0002t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0002t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0002t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0002t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0002t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0002t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0002t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0002t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0002t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0002t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0002t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0002t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0002t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0002t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0002t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0002t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0002t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0002t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0002t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0002t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0003t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0003t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0003t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0003t0004g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0003t0004g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0003t0004g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0003t0004g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0003t0004g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0003t0004g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0003t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0003t0004g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0003t0004g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0003t0004g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0003t0004g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0003t0004g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0003t0004g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0003t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0003t0004g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0003t0004g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0003t0004g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0004t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0004t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0004t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0004t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0004t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0004t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0004t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0004t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0004t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0004t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0004t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0004t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0004t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0004t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0004t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0004t0006g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0008t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0008t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0008t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0008t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0008t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0011t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0011t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0012t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0012t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0015t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0017t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0018t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0001c0022t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0002c0005t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0002c0005t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0002c0005t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0002c0005t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0002c0005t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0002c0005t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0002c0005t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0002c0005t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0002c0005t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0002c0005t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0002c0005t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0002c0005t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0002c0005t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0003c0006t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0003c0006t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0003c0006t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0003c0006t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0003c0006t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0003c0006t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0003c0006t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0003c0006t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0004c0009t0001g0004 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0004c0009t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0004c0009t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0004c0009t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0005c0007t0004g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0005c0007t0004g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0005c0007t0004g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0005c0007t0004g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0005c0007t0004g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0006c0010t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0006c0010t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0006c0010t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0007c0020t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0008c0021t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0009c0019t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0010c0016t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0011c0014t0004g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
a0012c0013t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0159 | EUR | GBR | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0239 | EUR | GBR | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0229 | EUR | GBR | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0164 | EUR | GBR | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG00280 | hp1 | a0001 | c0002 | t0002 | g0075 | EUR | FIN | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0194 | EUR | FIN | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0175 | EUR | FIN | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG00323 | hp2 | a0001 | c0002 | t0002 | g0074 | EUR | FIN | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG00408 | hp1 | a0002 | c0005 | t0001 | g0038 | EAS | CHS | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | CHS | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | CHS | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG00423 | hp2 | a0002 | c0005 | t0001 | g0036 | EAS | CHS | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | CHS | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | CHS | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | CHS | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | CHS | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG00597 | hp2 | a0001 | c0002 | t0002 | g0064 | EAS | CHS | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | CHS | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG00609 | hp2 | a0001 | c0002 | t0002 | g0060 | EAS | CHS | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG00621 | hp1 | a0001 | c0002 | t0002 | g0058 | EAS | CHS | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | CHS | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG00639 | hp1 | a0001 | c0003 | t0004 | g0026 | AMR | PUR | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG00639 | hp2 | a0001 | c0002 | t0002 | g0056 | AMR | PUR | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | CHS | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG00673 | hp2 | a0002 | c0005 | t0001 | g0039 | EAS | CHS | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG00735 | hp2 | a0001 | c0002 | t0002 | g0046 | AMR | PUR | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG00738 | hp1 | a0001 | c0002 | t0002 | g0052 | AMR | PUR | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG00741 | hp1 | a0001 | c0002 | t0002 | g0073 | AMR | PUR | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG01070 | hp2 | a0001 | c0002 | t0002 | g0055 | AMR | PUR | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG01099 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG01106 | hp2 | a0001 | c0002 | t0002 | g0053 | AMR | PUR | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG01109 | hp1 | a0003 | c0006 | t0001 | g0091 | AMR | PUR | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG01109 | hp2 | a0002 | c0005 | t0001 | g0031 | AMR | PUR | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG01167 | hp1 | a0001 | c0002 | t0002 | g0077 | AMR | PUR | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG01175 | hp1 | a0001 | c0002 | t0002 | g0102 | AMR | PUR | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG01243 | hp1 | a0001 | c0003 | t0004 | g0019 | AMR | PUR | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG01243 | hp2 | a0006 | c0010 | t0001 | g0177 | AMR | PUR | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG01255 | hp1 | a0001 | c0002 | t0002 | g0051 | AMR | CLM | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG01255 | hp2 | a0001 | c0002 | t0002 | g0083 | AMR | CLM | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | CLM | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG01257 | hp2 | a0001 | c0002 | t0002 | g0070 | AMR | CLM | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG01258 | hp1 | a0001 | c0002 | t0002 | g0071 | AMR | CLM | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | CLM | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG01261 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | CLM | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG01346 | hp1 | a0001 | c0002 | t0002 | g0087 | AMR | CLM | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG01358 | hp2 | a0001 | c0002 | t0002 | g0103 | AMR | CLM | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | CLM | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG01496 | hp1 | a0001 | c0003 | t0004 | g0021 | AMR | CLM | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | CLM | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG01884 | hp1 | a0001 | c0004 | t0003 | g0114 | AFR | ACB | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG01884 | hp2 | a0001 | c0001 | t0005 | g0189 | AFR | ACB | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG01934 | hp1 | a0004 | c0009 | t0001 | g0004 | AMR | PEL | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG01934 | hp2 | a0002 | c0005 | t0001 | g0029 | AMR | PEL | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG01943 | hp2 | a0002 | c0005 | t0001 | g0028 | AMR | PEL | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG01981 | hp1 | a0001 | c0002 | t0002 | g0049 | AMR | PEL | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG01981 | hp2 | a0007 | c0020 | t0001 | g0208 | AMR | PEL | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG02004 | hp1 | a0002 | c0005 | t0001 | g0030 | AMR | PEL | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG02004 | hp2 | a0001 | c0002 | t0002 | g0047 | AMR | PEL | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | KHV | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG02027 | hp2 | a0001 | c0002 | t0002 | g0101 | EAS | KHV | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | KHV | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG02145 | hp1 | a0008 | c0021 | t0001 | g0129 | AFR | ACB | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG02148 | hp1 | a0001 | c0002 | t0002 | g0050 | AMR | PEL | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0201 | AMR | PEL | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | ACB | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG02257 | hp2 | a0001 | c0003 | t0001 | g0096 | AFR | ACB | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG02258 | hp1 | a0001 | c0001 | t0005 | g0181 | AFR | ACB | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG02258 | hp2 | a0003 | c0006 | t0001 | g0069 | AFR | ACB | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG02280 | hp1 | a0001 | c0004 | t0003 | g0044 | AFR | ACB | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG02280 | hp2 | a0004 | c0009 | t0001 | g0004 | AFR | ACB | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG02293 | hp2 | a0001 | c0002 | t0002 | g0054 | AMR | PEL | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG02300 | hp1 | a0001 | c0002 | t0002 | g0048 | AMR | PEL | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PEL | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG02451 | hp1 | a0001 | c0002 | t0002 | g0079 | AFR | ACB | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG02451 | hp2 | a0005 | c0007 | t0004 | g0012 | AFR | ACB | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG02572 | hp1 | a0001 | c0008 | t0003 | g0109 | AFR | GWD | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG02572 | hp2 | a0001 | c0003 | t0004 | g0018 | AFR | GWD | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG02602 | hp1 | a0001 | c0002 | t0002 | g0085 | SAS | PJL | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG02615 | hp1 | a0001 | c0012 | t0001 | g0182 | AFR | GWD | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG02615 | hp2 | a0001 | c0003 | t0004 | g0007 | AFR | GWD | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG02622 | hp1 | a0001 | c0003 | t0004 | g0022 | AFR | GWD | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG02622 | hp2 | a0001 | c0003 | t0001 | g0097 | AFR | GWD | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG02630 | hp1 | a0009 | c0019 | t0001 | g0104 | AFR | GWD | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | GWD | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG02683 | hp1 | a0001 | c0002 | t0002 | g0082 | SAS | PJL | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG02698 | hp1 | a0001 | c0002 | t0002 | g0088 | SAS | PJL | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG02717 | hp1 | a0001 | c0003 | t0004 | g0023 | AFR | GWD | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG02717 | hp2 | a0001 | c0012 | t0001 | g0190 | AFR | GWD | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG02723 | hp1 | a0001 | c0004 | t0003 | g0043 | AFR | GWD | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG02723 | hp2 | a0001 | c0004 | t0003 | g0112 | AFR | GWD | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG02809 | hp1 | a0001 | c0003 | t0004 | g0010 | AFR | GWD | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG02809 | hp2 | a0005 | c0007 | t0004 | g0011 | AFR | GWD | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG02818 | hp1 | a0010 | c0016 | t0003 | g0117 | AFR | GWD | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG02818 | hp2 | a0001 | c0001 | t0005 | g0188 | AFR | GWD | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | GWD | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG02886 | hp2 | a0001 | c0004 | t0003 | g0113 | AFR | GWD | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG02895 | hp2 | a0001 | c0004 | t0003 | g0123 | AFR | GWD | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG02896 | hp1 | a0001 | c0004 | t0003 | g0122 | AFR | GWD | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG02896 | hp2 | a0001 | c0008 | t0003 | g0108 | AFR | GWD | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG02897 | hp1 | a0001 | c0008 | t0003 | g0106 | AFR | GWD | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | GWD | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG02965 | hp1 | a0003 | c0006 | t0001 | g0092 | AFR | ESN | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG02965 | hp2 | a0004 | c0009 | t0001 | g0142 | AFR | ESN | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG02970 | hp1 | a0001 | c0003 | t0004 | g0025 | AFR | ESN | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG02970 | hp2 | a0003 | c0006 | t0001 | g0090 | AFR | ESN | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG02976 | hp1 | a0001 | c0004 | t0003 | g0118 | AFR | ESN | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG02976 | hp2 | a0001 | c0011 | t0003 | g0115 | AFR | ESN | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG03041 | hp1 | a0001 | c0004 | t0003 | g0042 | AFR | GWD | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG03041 | hp2 | a0001 | c0003 | t0004 | g0005 | AFR | GWD | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | MSL | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG03098 | hp2 | a0011 | c0014 | t0004 | g0014 | AFR | MSL | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG03130 | hp1 | a0003 | c0006 | t0001 | g0094 | AFR | ESN | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG03130 | hp2 | a0004 | c0009 | t0001 | g0256 | AFR | ESN | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG03139 | hp1 | a0001 | c0003 | t0004 | g0020 | AFR | ESN | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG03139 | hp2 | a0001 | c0004 | t0003 | g0041 | AFR | ESN | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG03195 | hp1 | a0001 | c0003 | t0004 | g0009 | AFR | ESN | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG03195 | hp2 | a0001 | c0003 | t0004 | g0017 | AFR | ESN | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG03225 | hp1 | a0001 | c0004 | t0003 | g0119 | AFR | MSL | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG03225 | hp2 | a0002 | c0005 | t0001 | g0040 | AFR | MSL | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG03453 | hp1 | a0001 | c0003 | t0001 | g0098 | AFR | MSL | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG03453 | hp2 | a0012 | c0013 | t0001 | g0099 | AFR | MSL | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG03486 | hp1 | a0004 | c0009 | t0001 | g0237 | AFR | MSL | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG03486 | hp2 | a0001 | c0004 | t0006 | g0124 | AFR | MSL | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | PJL | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG03490 | hp2 | a0001 | c0002 | t0002 | g0057 | SAS | PJL | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG03540 | hp2 | a0001 | c0004 | t0003 | g0045 | AFR | GWD | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG03579 | hp1 | a0005 | c0007 | t0004 | g0016 | AFR | MSL | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | MSL | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0254 | SAS | PJL | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG03704 | hp1 | a0002 | c0005 | t0001 | g0032 | SAS | PJL | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG03710 | hp2 | a0001 | c0002 | t0002 | g0105 | SAS | PJL | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG03927 | hp1 | a0001 | c0002 | t0002 | g0076 | SAS | BEB | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG03927 | hp2 | a0001 | c0002 | t0002 | g0086 | SAS | BEB | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG03942 | hp1 | a0001 | c0002 | t0002 | g0084 | SAS | BEB | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | BEB | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | BEB | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0235 | SAS | BEB | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG04199 | hp1 | a0001 | c0002 | t0002 | g0078 | SAS | STU | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | STU | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | STU | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | STU | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA18522 | hp1 | a0003 | c0006 | t0001 | g0095 | AFR | YRI | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA18522 | hp2 | a0001 | c0004 | t0003 | g0116 | AFR | YRI | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | CHB | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA18747 | hp2 | a0001 | c0002 | t0002 | g0061 | EAS | CHB | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA18906 | hp1 | a0005 | c0007 | t0004 | g0015 | AFR | YRI | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA18906 | hp2 | a0001 | c0018 | t0001 | g0089 | AFR | YRI | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA18969 | hp1 | a0001 | c0002 | t0002 | g0059 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA18969 | hp2 | a0001 | c0017 | t0001 | g0198 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA18975 | hp1 | a0001 | c0002 | t0002 | g0065 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA18975 | hp2 | a0002 | c0005 | t0001 | g0033 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA18982 | hp2 | a0001 | c0002 | t0002 | g0067 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA18984 | hp1 | a0001 | c0002 | t0002 | g0063 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA18991 | hp1 | a0001 | c0022 | t0001 | g0238 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA18992 | hp1 | a0001 | c0002 | t0002 | g0100 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA18994 | hp1 | a0002 | c0005 | t0001 | g0037 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA19000 | hp1 | a0001 | c0002 | t0002 | g0068 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA19000 | hp2 | a0002 | c0005 | t0001 | g0035 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA19030 | hp1 | a0001 | c0008 | t0003 | g0111 | AFR | LWK | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA19030 | hp2 | a0006 | c0010 | t0001 | g0234 | AFR | LWK | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | LWK | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA19043 | hp2 | a0001 | c0003 | t0004 | g0024 | AFR | LWK | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA19074 | hp1 | a0001 | c0002 | t0002 | g0062 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA19087 | hp2 | a0001 | c0002 | t0002 | g0066 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA19088 | hp2 | a0002 | c0005 | t0001 | g0034 | EAS | JPT | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA19240 | hp1 | a0003 | c0006 | t0001 | g0002 | AFR | YRI | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA19240 | hp2 | a0001 | c0011 | t0003 | g0121 | AFR | YRI | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA20129 | hp1 | a0001 | c0004 | t0003 | g0120 | AFR | ASW | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA20129 | hp2 | a0003 | c0006 | t0001 | g0093 | AFR | ASW | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0155 | EUR | TSI | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0230 | EUR | TSI | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0192 | EUR | TSI | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA20805 | hp2 | a0001 | c0002 | t0002 | g0080 | EUR | TSI | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0244 | SAS | GIH | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | GIH | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG02109 | hp1 | a0006 | c0010 | t0001 | g0218 | AFR | ACB | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG02109 | hp2 | a0001 | c0003 | t0004 | g0006 | AFR | ACB | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG02559 | hp1 | a0001 | c0015 | t0003 | g0107 | AFR | ACB | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG02559 | hp2 | a0001 | c0003 | t0004 | g0027 | AFR | ACB | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG03471 | hp1 | a0001 | c0003 | t0004 | g0008 | AFR | MSL | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG03471 | hp2 | a0001 | c0008 | t0003 | g0110 | AFR | MSL | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG06807 | hp1 | a0001 | c0002 | t0002 | g0072 | AFR | USA | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
HG06807 | hp2 | a0003 | c0006 | t0001 | g0002 | AFR | USA | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | USA | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | USA | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA21309 | hp1 | a0001 | c0004 | t0003 | g0125 | AFR | LWK | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
NA21309 | hp2 | a0005 | c0007 | t0004 | g0013 | AFR | LWK | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0241 | REF | REF | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0081 | REF | REF | MEI1_chr22_41694503_41804454 | MEI1 | chr22 | 41694503 | 41804454 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | 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 | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:41699535 | G | GGA | 2 | a0001 a0010 |
25 | HG01884.hp1 HG02280.hp1 HG02559.hp1 others(22): Show |
frameshift_variant&start_lost | HIGH | c.-1_1dupGA | p.Met1fs | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/31 | 38/4016 | 2/3825 | 1/1274 | INFO_REALIGN_3_PRIME | chr22 | 41699535 | ||
chr22:41699599 | G | A | 2 | a0003 a0012 |
10 | HG01109.hp1 HG02258.hp2 HG02965.hp1 others(7): Show |
missense_variant | MODERATE | c.61G>A | p.Ala21Thr | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/31 | 97/4016 | 61/3825 | 21/1274 | chr22 | 41699599 | |||
chr22:41699651 | C | T | 1 | a0008 | 1 | HG02145.hp1 | missense_variant | MODERATE | c.113C>T | p.Pro38Leu | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/31 | 149/4016 | 113/3825 | 38/1274 | chr22 | 41699651 | |||
chr22:41699707 | G | C | 1 | a0002 | 13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
missense_variant | MODERATE | c.169G>C | p.Val57Leu | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/31 | 205/4016 | 169/3825 | 57/1274 | chr22 | 41699707 | |||
chr22:41753975 | C | G | 1 | a0007 | 1 | HG01981.hp2 | missense_variant | MODERATE | c.1880C>G | p.Ser627Cys | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/31 | 1916/4016 | 1880/3825 | 627/1274 | chr22 | 41753975 | |||
chr22:41758382 | G | C | 2 | a0005 a0011 |
6 | HG02451.hp2 HG02809.hp2 HG03098.hp2 others(3): Show |
missense_variant | MODERATE | c.1969G>C | p.Glu657Gln | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/31 | 2005/4016 | 1969/3825 | 657/1274 | chr22 | 41758382 | |||
chr22:41758467 | G | T | 1 | a0009 | 1 | HG02630.hp1 | missense_variant | MODERATE | c.2054G>T | p.Gly685Val | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/31 | 2090/4016 | 2054/3825 | 685/1274 | chr22 | 41758467 | |||
chr22:41763250 | C | T | 1 | a0010 | 1 | HG02818.hp1 | missense_variant | MODERATE | c.2197C>T | p.Pro733Ser | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/31 | 2233/4016 | 2197/3825 | 733/1274 | chr22 | 41763250 | |||
chr22:41770720 | G | A | 2 | a0003 a0012 |
10 | HG01109.hp1 HG02258.hp2 HG02965.hp1 others(7): Show |
missense_variant | MODERATE | c.2303G>A | p.Gly768Asp | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/31 | 2339/4016 | 2303/3825 | 768/1274 | chr22 | 41770720 | |||
chr22:41776114 | T | A | 1 | a0004 | 5 | HG01934.hp1 HG02280.hp2 HG02965.hp2 others(2): Show |
missense_variant | MODERATE | c.2557T>A | p.Ser853Thr | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 21/31 | 2593/4016 | 2557/3825 | 853/1274 | chr22 | 41776114 | |||
chr22:41781313 | A | G | 1 | a0002 | 13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
missense_variant | MODERATE | c.2845A>G | p.Thr949Ala | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 23/31 | 2881/4016 | 2845/3825 | 949/1274 | chr22 | 41781313 | |||
chr22:41784640 | C | G | 1 | a0012 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.3202C>G | p.Arg1068Gly | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/31 | 3238/4016 | 3202/3825 | 1068/1274 | chr22 | 41784640 | |||
chr22:41795817 | C | T | 1 | a0011 | 1 | HG03098.hp2 | missense_variant | MODERATE | c.3749C>T | p.Ser1250Phe | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/31 | 3785/4016 | 3749/3825 | 1250/1274 | chr22 | 41795817 | |||
chr22:41795840 | G | T | 1 | a0006 | 3 | HG01243.hp2 HG02109.hp1 NA19030.hp2 |
missense_variant | MODERATE | c.3772G>T | p.Asp1258Tyr | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/31 | 3808/4016 | 3772/3825 | 1258/1274 | chr22 | 41795840 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | 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 | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:41699640 | C | T | 1 | a0001c0022 | 1 | NA18991.hp1 | synonymous_variant | LOW | c.102C>T | p.Arg34Arg | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/31 | 138/4016 | 102/3825 | 34/1274 | chr22 | 41699640 | |||
chr22:41732339 | G | C | 2 | a0003c0006 a0012c0013 |
10 | HG01109.hp1 HG02258.hp2 HG02965.hp1 others(7): Show |
synonymous_variant | LOW | c.1191G>C | p.Leu397Leu | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 10/31 | 1227/4016 | 1191/3825 | 397/1274 | chr22 | 41732339 | |||
chr22:41758405 | C | G | 1 | a0001c0012 | 2 | HG02615.hp1 HG02717.hp2 |
synonymous_variant | LOW | c.1992C>G | p.Pro664Pro | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/31 | 2028/4016 | 1992/3825 | 664/1274 | chr22 | 41758405 | |||
chr22:41758426 | T | C | 5 | a0001c0004 a0001c0008 a0001c0011 others(2): Show |
25 | HG01884.hp1 HG02280.hp1 HG02559.hp1 others(22): Show |
synonymous_variant | LOW | c.2013T>C | p.Pro671Pro | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/31 | 2049/4016 | 2013/3825 | 671/1274 | chr22 | 41758426 | |||
chr22:41758456 | G | A | 1 | a0001c0015 | 1 | HG02559.hp1 | synonymous_variant | LOW | c.2043G>A | p.Gln681Gln | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/31 | 2079/4016 | 2043/3825 | 681/1274 | chr22 | 41758456 | |||
chr22:41763225 | G | T | 21 | a0001c0001 a0001c0003 a0001c0004 others(18): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
synonymous_variant | LOW | c.2172G>T | p.Ser724Ser | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/31 | 2208/4016 | 2172/3825 | 724/1274 | chr22 | 41763225 | |||
chr22:41770952 | C | T | 1 | a0001c0018 | 1 | NA18906.hp2 | synonymous_variant | LOW | c.2535C>T | p.Leu845Leu | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/31 | 2571/4016 | 2535/3825 | 845/1274 | chr22 | 41770952 | |||
chr22:41776125 | G | A | 1 | a0009c0019 | 1 | HG02630.hp1 | synonymous_variant | LOW | c.2568G>A | p.Val856Val | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 21/31 | 2604/4016 | 2568/3825 | 856/1274 | chr22 | 41776125 | |||
chr22:41776224 | C | A | 1 | a0009c0019 | 1 | HG02630.hp1 | synonymous_variant | LOW | c.2667C>A | p.Ile889Ile | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 21/31 | 2703/4016 | 2667/3825 | 889/1274 | chr22 | 41776224 | |||
chr22:41778775 | A | G | 1 | a0001c0011 | 2 | HG02976.hp2 NA19240.hp2 |
synonymous_variant | LOW | c.2778A>G | p.Gln926Gln | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/31 | 2814/4016 | 2778/3825 | 926/1274 | chr22 | 41778775 | |||
chr22:41781812 | C | A | 9 | a0001c0003 a0001c0004 a0001c0011 others(6): Show |
60 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(57): Show |
synonymous_variant | LOW | c.3054C>A | p.Ser1018Ser | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 24/31 | 3090/4016 | 3054/3825 | 1018/1274 | chr22 | 41781812 | |||
chr22:41795503 | G | A | 1 | a0001c0017 | 1 | NA18969.hp2 | synonymous_variant | LOW | c.3627G>A | p.Ser1209Ser | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 29/31 | 3663/4016 | 3627/3825 | 1209/1274 | chr22 | 41795503 | |||
chr22:41795536 | C | T | 9 | a0001c0003 a0001c0004 a0001c0011 others(6): Show |
60 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(57): Show |
synonymous_variant | LOW | c.3660C>T | p.Phe1220Phe | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 29/31 | 3696/4016 | 3660/3825 | 1220/1274 | chr22 | 41795536 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | 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 | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:41699513 | C | T | 1 | a0001c0001t0005 | 3 | HG01884.hp2 HG02258.hp1 HG02818.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-26C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/31 | chr22 | 41699513 | |||||||
chr22:41799360 | ATTG | A | 4 | a0001c0003t0004 a0001c0004t0006 a0005c0007t0004 others(1): Show |
24 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*65_*67delTTG | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 31/31 | 65 | INFO_REALIGN_3_PRIME | chr22 | 41799360 | |||||
chr22:41799406 | T | C | 2 | a0001c0001t0002 a0001c0002t0002 |
49 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*107T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 31/31 | 107 | chr22 | 41799406 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:41699721 | G | A | 23 | a0001c0003t0004g0005 a0001c0003t0004g0006 a0001c0003t0004g0007 others(20): Show |
23 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.174+9G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41699721 | |||||||
chr22:41699900 | A | C | 132 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(129): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.174+188A>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41699900 | |||||||
chr22:41699908 | C | A | 13 | a0002c0005t0001g0028 a0002c0005t0001g0029 a0002c0005t0001g0030 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.174+196C>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41699908 | |||||||
chr22:41699945 | G | C | 5 | a0001c0004t0003g0041 a0001c0004t0003g0042 a0001c0004t0003g0043 others(2): Show |
5 | HG02280.hp1 HG02723.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.174+233G>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41699945 | |||||||
chr22:41700057 | C | T | 25 | a0001c0004t0003g0041 a0001c0004t0003g0042 a0001c0004t0003g0043 others(22): Show |
25 | HG01884.hp1 HG02280.hp1 HG02559.hp1 others(22): Show |
intron_variant | MODIFIER | c.174+345C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41700057 | |||||||
chr22:41700079 | GCTCCCGC others(9): Show |
G | 7 | a0001c0001t0001g0126 a0001c0008t0003g0106 a0001c0008t0003g0108 others(4): Show |
7 | HG02559.hp1 HG02572.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.174+388_174+403del others(16): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr22 | 41700079 | ||||||
chr22:41700098 | C | T | 13 | a0002c0005t0001g0028 a0002c0005t0001g0029 a0002c0005t0001g0030 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.174+386C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41700098 | |||||||
chr22:41700101 | G | C | 6 | a0001c0003t0004g0005 a0001c0003t0004g0006 a0001c0003t0004g0007 others(3): Show |
6 | HG02109.hp2 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.174+389G>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41700101 | |||||||
chr22:41700111 | C | A | 13 | a0002c0005t0001g0028 a0002c0005t0001g0029 a0002c0005t0001g0030 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.174+399C>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41700111 | |||||||
chr22:41700143 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.174+431G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41700143 | |||||||
chr22:41700226 | G | T | 1 | a0001c0002t0002g0105 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.174+514G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41700226 | |||||||
chr22:41700563 | T | G | 1 | a0001c0001t0001g0128 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.174+851T>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41700563 | |||||||
chr22:41700579 | CCTCGGCT others(10): Show |
C | 132 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(129): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.174+870_174+886del others(17): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr22 | 41700579 | ||||||
chr22:41700619 | C | T | 7 | a0001c0003t0004g0005 a0001c0003t0004g0006 a0001c0003t0004g0007 others(4): Show |
7 | HG02109.hp2 HG02559.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.174+907C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41700619 | |||||||
chr22:41700749 | A | AT | 5 | a0001c0002t0002g0100 a0001c0002t0002g0101 a0001c0002t0002g0102 others(2): Show |
5 | HG01175.hp1 HG01358.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.174+1063dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr22 | 41700749 | ||||||
chr22:41700749 | A | ATT | 12 | a0001c0003t0004g0026 a0001c0004t0003g0041 a0001c0004t0003g0042 others(9): Show |
12 | HG00639.hp1 HG01884.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.174+1062_174+1063d others(4): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr22 | 41700749 | ||||||
chr22:41700749 | A | ATTT | 7 | a0001c0004t0003g0045 a0001c0004t0003g0116 a0001c0004t0003g0118 others(4): Show |
7 | HG02818.hp1 HG02976.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.174+1061_174+1063d others(5): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr22 | 41700749 | ||||||
chr22:41700749 | A | ATTTT | 5 | a0001c0004t0003g0122 a0001c0004t0003g0123 a0001c0004t0003g0125 others(2): Show |
5 | HG02895.hp2 HG02896.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.174+1060_174+1063d others(6): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr22 | 41700749 | ||||||
chr22:41700749 | AT | A | 9 | a0001c0002t0002g0055 a0001c0002t0002g0056 a0001c0002t0002g0057 others(6): Show |
9 | HG00639.hp2 HG01070.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.174+1063delT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr22 | 41700749 | ||||||
chr22:41700749 | ATTTT | A | 12 | a0002c0005t0001g0028 a0002c0005t0001g0029 a0002c0005t0001g0030 others(9): Show |
12 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(9): Show |
intron_variant | MODIFIER | c.174+1060_174+1063d others(6): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr22 | 41700749 | ||||||
chr22:41700749 | ATTTTTTT others(2): Show |
A | 129 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(126): Show |
131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.174+1055_174+1063d others(11): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr22 | 41700749 | ||||||
chr22:41700749 | ATTTTTTT others(3): Show |
A | 1 | a0008c0021t0001g0129 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.174+1054_174+1063d others(12): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr22 | 41700749 | ||||||
chr22:41700749 | ATTTTTTT others(5): Show |
A | 10 | a0001c0002t0002g0001 a0001c0002t0002g0046 a0001c0002t0002g0047 others(7): Show |
11 | HG00735.hp2 HG00738.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.174+1052_174+1063d others(14): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr22 | 41700749 | ||||||
chr22:41700751 | T | TA | 9 | a0003c0006t0001g0002 a0003c0006t0001g0069 a0003c0006t0001g0090 others(6): Show |
10 | HG01109.hp1 HG02258.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.174+1039_174+1040i others(3): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41700751 | |||||||
chr22:41700775 | T | C | 3 | a0002c0005t0001g0028 a0002c0005t0001g0029 a0002c0005t0001g0030 |
3 | HG01934.hp2 HG01943.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.174+1063T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41700775 | |||||||
chr22:41700789 | C | T | 13 | a0002c0005t0001g0028 a0002c0005t0001g0029 a0002c0005t0001g0030 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.174+1077C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41700789 | |||||||
chr22:41700921 | A | G | 23 | a0001c0003t0004g0005 a0001c0003t0004g0006 a0001c0003t0004g0007 others(20): Show |
23 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.174+1209A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41700921 | |||||||
chr22:41700939 | C | CT | 13 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(10): Show |
13 | HG00544.hp1 HG02109.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.174+1244dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr22 | 41700939 | ||||||
chr22:41700939 | C | CTT | 13 | a0002c0005t0001g0028 a0002c0005t0001g0029 a0002c0005t0001g0030 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.174+1243_174+1244d others(4): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr22 | 41700939 | ||||||
chr22:41700939 | CT | C | 15 | a0001c0002t0002g0058 a0001c0002t0002g0059 a0001c0002t0002g0060 others(12): Show |
15 | HG00597.hp2 HG00609.hp2 HG00621.hp1 others(12): Show |
intron_variant | MODIFIER | c.174+1244delT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr22 | 41700939 | ||||||
chr22:41700999 | G | A | 1 | a0008c0021t0001g0129 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.174+1287G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41700999 | |||||||
chr22:41701065 | G | C | 12 | a0002c0005t0001g0028 a0002c0005t0001g0029 a0002c0005t0001g0030 others(9): Show |
12 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(9): Show |
intron_variant | MODIFIER | c.174+1353G>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41701065 | |||||||
chr22:41701127 | C | T | 1 | a0001c0003t0004g0025 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.174+1415C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41701127 | |||||||
chr22:41701234 | C | T | 132 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(129): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.174+1522C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41701234 | |||||||
chr22:41701237 | C | A | 1 | a0001c0001t0001g0130 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.174+1525C>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41701237 | |||||||
chr22:41701396 | C | T | 1 | a0001c0004t0003g0113 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.174+1684C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41701396 | |||||||
chr22:41701458 | A | T | 207 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(204): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.174+1746A>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41701458 | |||||||
chr22:41701459 | A | T | 1 | a0012c0013t0001g0099 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.174+1747A>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41701459 | |||||||
chr22:41701839 | C | G | 4 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0098 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.175-1492C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41701839 | |||||||
chr22:41702082 | A | C | 3 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0001g0251 |
3 | HG02027.hp1 HG02080.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.175-1249A>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41702082 | |||||||
chr22:41702150 | C | T | 11 | a0001c0002t0002g0001 a0001c0002t0002g0046 a0001c0002t0002g0047 others(8): Show |
12 | HG00735.hp2 HG00738.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.175-1181C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41702150 | |||||||
chr22:41702285 | C | T | 13 | a0002c0005t0001g0028 a0002c0005t0001g0029 a0002c0005t0001g0030 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.175-1046C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41702285 | |||||||
chr22:41702330 | G | T | 25 | a0001c0004t0003g0041 a0001c0004t0003g0042 a0001c0004t0003g0043 others(22): Show |
25 | HG01884.hp1 HG02280.hp1 HG02559.hp1 others(22): Show |
intron_variant | MODIFIER | c.175-1001G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41702330 | |||||||
chr22:41702435 | G | A | 7 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(4): Show |
7 | HG04204.hp1 NA18965.hp1 NA18980.hp2 others(4): Show |
intron_variant | MODIFIER | c.175-896G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41702435 | |||||||
chr22:41702455 | C | CT | 6 | a0001c0003t0004g0005 a0001c0003t0004g0006 a0001c0003t0004g0007 others(3): Show |
6 | HG02109.hp2 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.175-863dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr22 | 41702455 | ||||||
chr22:41702488 | C | A | 2 | a0001c0011t0003g0115 a0001c0011t0003g0121 |
2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.175-843C>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41702488 | |||||||
chr22:41702683 | G | A | 13 | a0002c0005t0001g0028 a0002c0005t0001g0029 a0002c0005t0001g0030 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.175-648G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41702683 | |||||||
chr22:41702740 | C | T | 13 | a0002c0005t0001g0028 a0002c0005t0001g0029 a0002c0005t0001g0030 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.175-591C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41702740 | |||||||
chr22:41702741 | G | A | 2 | a0001c0001t0001g0138 a0001c0001t0001g0252 |
2 | HG00544.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.175-590G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41702741 | |||||||
chr22:41702759 | T | G | 132 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(129): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.175-572T>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41702759 | |||||||
chr22:41702875 | A | C | 1 | a0001c0001t0001g0248 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.175-456A>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41702875 | |||||||
chr22:41702880 | C | T | 25 | a0001c0004t0003g0041 a0001c0004t0003g0042 a0001c0004t0003g0043 others(22): Show |
25 | HG01884.hp1 HG02280.hp1 HG02559.hp1 others(22): Show |
intron_variant | MODIFIER | c.175-451C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41702880 | |||||||
chr22:41702936 | T | C | 1 | a0001c0004t0003g0116 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.175-395T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41702936 | |||||||
chr22:41703013 | C | T | 1 | a0002c0005t0001g0040 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.175-318C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41703013 | |||||||
chr22:41703053 | A | G | 4 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0098 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.175-278A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41703053 | |||||||
chr22:41703215 | C | T | 4 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0098 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.175-116C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41703215 | |||||||
chr22:41703296 | G | A | 1 | a0001c0018t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.175-35G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 1/30 | chr22 | 41703296 | |||||||
chr22:41703684 | A | G | 194 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(191): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.298+230A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 2/30 | chr22 | 41703684 | |||||||
chr22:41703719 | C | G | 13 | a0002c0005t0001g0028 a0002c0005t0001g0029 a0002c0005t0001g0030 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.298+265C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 2/30 | chr22 | 41703719 | |||||||
chr22:41703977 | G | C | 207 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(204): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.298+523G>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 2/30 | chr22 | 41703977 | |||||||
chr22:41704167 | C | T | 2 | a0001c0001t0001g0247 a0001c0003t0004g0027 |
2 | HG00621.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.298+713C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 2/30 | chr22 | 41704167 | |||||||
chr22:41704271 | A | G | 207 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(204): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.298+817A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 2/30 | chr22 | 41704271 | |||||||
chr22:41704362 | C | G | 2 | a0001c0001t0001g0245 a0001c0001t0001g0246 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.298+908C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 2/30 | chr22 | 41704362 | |||||||
chr22:41704396 | G | A | 13 | a0002c0005t0001g0028 a0002c0005t0001g0029 a0002c0005t0001g0030 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.298+942G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 2/30 | chr22 | 41704396 | |||||||
chr22:41704407 | T | A | 5 | a0001c0004t0003g0041 a0001c0004t0003g0042 a0001c0004t0003g0043 others(2): Show |
5 | HG02280.hp1 HG02723.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.298+953T>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 2/30 | chr22 | 41704407 | |||||||
chr22:41704414 | CT | C | 46 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(43): Show |
47 | HG00423.hp2 HG01109.hp1 HG01109.hp2 others(44): Show |
intron_variant | MODIFIER | c.298+977delT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr22 | 41704414 | ||||||
chr22:41704414 | CTT | C | 23 | a0001c0003t0004g0005 a0001c0003t0004g0006 a0001c0003t0004g0007 others(20): Show |
23 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.298+976_298+977del others(2): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr22 | 41704414 | ||||||
chr22:41704445 | G | A | 2 | a0001c0001t0001g0139 a0001c0001t0001g0140 |
2 | HG03669.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.298+991G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 2/30 | chr22 | 41704445 | |||||||
chr22:41704461 | C | T | 1 | a0001c0003t0004g0027 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.298+1007C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 2/30 | chr22 | 41704461 | |||||||
chr22:41704677 | A | G | 207 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(204): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.299-827A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 2/30 | chr22 | 41704677 | |||||||
chr22:41704949 | C | T | 1 | a0001c0001t0001g0244 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.299-555C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 2/30 | chr22 | 41704949 | |||||||
chr22:41705003 | C | T | 1 | a0005c0007t0004g0015 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.299-501C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 2/30 | chr22 | 41705003 | |||||||
chr22:41705005 | C | T | 4 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0001g0245 others(1): Show |
4 | HG02630.hp2 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-499C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 2/30 | chr22 | 41705005 | |||||||
chr22:41705176 | C | CT | 16 | a0001c0002t0002g0068 a0001c0002t0002g0087 a0001c0018t0001g0089 others(13): Show |
16 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(13): Show |
intron_variant | MODIFIER | c.299-312dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr22 | 41705176 | ||||||
chr22:41705333 | G | A | 6 | a0001c0003t0004g0005 a0001c0003t0004g0006 a0001c0003t0004g0007 others(3): Show |
6 | HG02109.hp2 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.299-171G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 2/30 | chr22 | 41705333 | |||||||
chr22:41705369 | G | A | 7 | a0001c0003t0004g0005 a0001c0003t0004g0006 a0001c0003t0004g0007 others(4): Show |
7 | HG02109.hp2 HG02559.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.299-135G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 2/30 | chr22 | 41705369 | |||||||
chr22:41705430 | C | T | 4 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0098 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-74C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 2/30 | chr22 | 41705430 | |||||||
chr22:41705461 | C | T | 9 | a0003c0006t0001g0002 a0003c0006t0001g0069 a0003c0006t0001g0090 others(6): Show |
10 | HG01109.hp1 HG02258.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.299-43C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 2/30 | chr22 | 41705461 | |||||||
chr22:41705694 | A | G | 6 | a0001c0003t0004g0005 a0001c0003t0004g0006 a0001c0003t0004g0007 others(3): Show |
6 | HG02109.hp2 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.349+140A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41705694 | |||||||
chr22:41705708 | CT | C | 5 | a0001c0001t0001g0128 a0001c0002t0002g0070 a0004c0009t0001g0142 others(2): Show |
5 | HG01257.hp2 HG02145.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.349+171delT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr22 | 41705708 | ||||||
chr22:41705708 | CTT | C | 73 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0098 others(70): Show |
74 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.349+170_349+171del others(2): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr22 | 41705708 | ||||||
chr22:41705771 | A | G | 16 | a0001c0003t0004g0017 a0001c0003t0004g0018 a0001c0003t0004g0019 others(13): Show |
16 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.349+217A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41705771 | |||||||
chr22:41705811 | G | A | 130 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(127): Show |
132 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.349+257G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41705811 | |||||||
chr22:41706060 | C | T | 1 | a0001c0003t0004g0027 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.349+506C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41706060 | |||||||
chr22:41706088 | A | G | 5 | a0001c0004t0003g0112 a0001c0004t0003g0122 a0001c0004t0003g0123 others(2): Show |
5 | HG02723.hp2 HG02895.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.349+534A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41706088 | |||||||
chr22:41706131 | G | A | 5 | a0001c0004t0003g0112 a0001c0004t0003g0122 a0001c0004t0003g0123 others(2): Show |
5 | HG02723.hp2 HG02895.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.349+577G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41706131 | |||||||
chr22:41706265 | T | C | 1 | a0001c0001t0001g0131 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.349+711T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41706265 | |||||||
chr22:41706269 | T | C | 13 | a0002c0005t0001g0028 a0002c0005t0001g0029 a0002c0005t0001g0030 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.349+715T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41706269 | |||||||
chr22:41706364 | G | A | 4 | a0001c0008t0003g0106 a0001c0008t0003g0108 a0001c0008t0003g0109 others(1): Show |
4 | HG02559.hp1 HG02572.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.349+810G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41706364 | |||||||
chr22:41706607 | G | A | 1 | a0001c0004t0003g0119 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.349+1053G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41706607 | |||||||
chr22:41706690 | G | C | 1 | a0001c0004t0003g0114 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.349+1136G>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41706690 | |||||||
chr22:41706707 | C | G | 23 | a0001c0003t0004g0005 a0001c0003t0004g0006 a0001c0003t0004g0007 others(20): Show |
23 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.349+1153C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41706707 | |||||||
chr22:41706726 | A | C | 1 | a0001c0003t0004g0026 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.349+1172A>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41706726 | |||||||
chr22:41706857 | G | A | 1 | a0002c0005t0001g0031 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.349+1303G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41706857 | |||||||
chr22:41706917 | G | T | 1 | a0001c0022t0001g0238 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.349+1363G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41706917 | |||||||
chr22:41707028 | C | CA | 10 | a0001c0002t0002g0046 a0001c0002t0002g0068 a0001c0002t0002g0071 others(7): Show |
10 | HG00735.hp2 HG00741.hp1 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.349+1499dupA | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr22 | 41707028 | ||||||
chr22:41707028 | C | CAA | 5 | a0001c0003t0001g0096 a0002c0005t0001g0028 a0002c0005t0001g0029 others(2): Show |
5 | HG01934.hp2 HG01943.hp2 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.349+1498_349+1499d others(4): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr22 | 41707028 | ||||||
chr22:41707028 | C | CAAA | 7 | a0002c0005t0001g0032 a0002c0005t0001g0033 a0002c0005t0001g0034 others(4): Show |
7 | HG00408.hp1 HG00673.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.349+1497_349+1499d others(5): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr22 | 41707028 | ||||||
chr22:41707028 | CA | C | 6 | a0001c0003t0004g0006 a0001c0003t0004g0007 a0001c0003t0004g0008 others(3): Show |
6 | HG02109.hp2 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.349+1499delA | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr22 | 41707028 | ||||||
chr22:41707028 | CAAAAAA | C | 9 | a0003c0006t0001g0002 a0003c0006t0001g0069 a0003c0006t0001g0090 others(6): Show |
10 | HG01109.hp1 HG02258.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.349+1494_349+1499d others(8): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr22 | 41707028 | ||||||
chr22:41707028 | CAAAAAAA | C | 8 | a0001c0008t0003g0106 a0001c0008t0003g0108 a0001c0008t0003g0109 others(5): Show |
8 | HG01109.hp2 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.349+1493_349+1499d others(9): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr22 | 41707028 | ||||||
chr22:41707028 | CAAAAAAA others(1): Show |
C | 47 | a0001c0001t0001g0130 a0001c0001t0001g0132 a0001c0001t0001g0133 others(44): Show |
47 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.349+1492_349+1499d others(10): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr22 | 41707028 | ||||||
chr22:41707028 | CAAAAAAA others(2): Show |
C | 85 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(82): Show |
87 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.349+1491_349+1499d others(11): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr22 | 41707028 | ||||||
chr22:41707090 | C | G | 1 | a0004c0009t0001g0256 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.349+1536C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41707090 | |||||||
chr22:41707161 | C | T | 3 | a0002c0005t0001g0028 a0002c0005t0001g0029 a0002c0005t0001g0030 |
3 | HG01934.hp2 HG01943.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.349+1607C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41707161 | |||||||
chr22:41707452 | A | G | 4 | a0004c0009t0001g0004 a0004c0009t0001g0142 a0004c0009t0001g0237 others(1): Show |
5 | HG01934.hp1 HG02280.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.349+1898A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41707452 | |||||||
chr22:41707482 | A | G | 1 | a0001c0001t0001g0236 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.349+1928A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41707482 | |||||||
chr22:41707618 | G | A | 1 | a0001c0001t0001g0179 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.349+2064G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41707618 | |||||||
chr22:41707642 | T | TA | 7 | a0001c0004t0003g0113 a0001c0004t0003g0116 a0001c0004t0003g0118 others(4): Show |
7 | HG02886.hp2 HG02976.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.349+2097dupA | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr22 | 41707642 | ||||||
chr22:41707665 | A | G | 1 | a0001c0001t0001g0178 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.349+2111A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41707665 | |||||||
chr22:41707690 | T | C | 1 | a0001c0001t0001g0180 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.349+2136T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41707690 | |||||||
chr22:41708303 | G | A | 1 | a0010c0016t0003g0117 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.349+2749G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41708303 | |||||||
chr22:41708741 | G | C | 22 | a0001c0004t0003g0041 a0001c0004t0003g0042 a0001c0004t0003g0043 others(19): Show |
22 | HG01884.hp1 HG02280.hp1 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.349+3187G>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41708741 | |||||||
chr22:41708925 | A | G | 194 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(191): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.349+3371A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41708925 | |||||||
chr22:41709344 | C | T | 2 | a0001c0001t0001g0139 a0001c0001t0001g0140 |
2 | HG03669.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.349+3790C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41709344 | |||||||
chr22:41709509 | G | C | 23 | a0001c0003t0004g0005 a0001c0003t0004g0006 a0001c0003t0004g0007 others(20): Show |
23 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.349+3955G>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41709509 | |||||||
chr22:41709538 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.349+3984C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41709538 | |||||||
chr22:41709554 | G | A | 1 | a0001c0002t0002g0055 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.349+4000G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41709554 | |||||||
chr22:41709556 | C | T | 1 | a0001c0003t0001g0096 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.349+4002C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41709556 | |||||||
chr22:41709558 | G | A | 1 | a0001c0003t0004g0025 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.349+4004G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41709558 | |||||||
chr22:41709827 | A | C | 1 | a0001c0018t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.350-4175A>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41709827 | |||||||
chr22:41709860 | A | G | 16 | a0001c0002t0002g0058 a0001c0002t0002g0059 a0001c0002t0002g0060 others(13): Show |
16 | HG00597.hp2 HG00609.hp2 HG00621.hp1 others(13): Show |
intron_variant | MODIFIER | c.350-4142A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41709860 | |||||||
chr22:41709970 | A | AC | 8 | a0001c0001t0001g0176 a0001c0001t0001g0251 a0001c0002t0002g0084 others(5): Show |
8 | HG01243.hp2 HG02027.hp1 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.350-4026dupC | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr22 | 41709970 | ||||||
chr22:41709998 | G | A | 7 | a0001c0003t0004g0005 a0001c0003t0004g0006 a0001c0003t0004g0007 others(4): Show |
7 | HG02109.hp2 HG02559.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.350-4004G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41709998 | |||||||
chr22:41710205 | G | A | 13 | a0002c0005t0001g0028 a0002c0005t0001g0029 a0002c0005t0001g0030 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.350-3797G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41710205 | |||||||
chr22:41710212 | G | A | 207 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(204): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.350-3790G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41710212 | |||||||
chr22:41710671 | T | C | 25 | a0001c0004t0003g0041 a0001c0004t0003g0042 a0001c0004t0003g0043 others(22): Show |
25 | HG01884.hp1 HG02280.hp1 HG02559.hp1 others(22): Show |
intron_variant | MODIFIER | c.350-3331T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41710671 | |||||||
chr22:41710889 | G | T | 1 | a0001c0002t0002g0054 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.350-3113G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41710889 | |||||||
chr22:41710992 | T | C | 207 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(204): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.350-3010T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41710992 | |||||||
chr22:41711222 | G | A | 2 | a0001c0001t0001g0239 a0001c0001t0001g0240 |
2 | HG00099.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.350-2780G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41711222 | |||||||
chr22:41711258 | T | C | 207 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(204): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.350-2744T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41711258 | |||||||
chr22:41711480 | A | G | 3 | a0001c0008t0003g0106 a0001c0008t0003g0108 a0001c0008t0003g0109 |
3 | HG02572.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.350-2522A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41711480 | |||||||
chr22:41711482 | C | T | 1 | a0006c0010t0001g0234 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.350-2520C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41711482 | |||||||
chr22:41711515 | T | C | 1 | a0010c0016t0003g0117 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.350-2487T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41711515 | |||||||
chr22:41711651 | G | A | 1 | a0005c0007t0004g0015 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.350-2351G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41711651 | |||||||
chr22:41711740 | C | T | 7 | a0001c0003t0004g0005 a0001c0003t0004g0006 a0001c0003t0004g0007 others(4): Show |
7 | HG02109.hp2 HG02559.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.350-2262C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41711740 | |||||||
chr22:41711741 | A | G | 207 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(204): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.350-2261A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41711741 | |||||||
chr22:41711854 | CT | C | 13 | a0002c0005t0001g0028 a0002c0005t0001g0029 a0002c0005t0001g0030 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.350-2139delT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr22 | 41711854 | ||||||
chr22:41711976 | C | T | 24 | a0001c0003t0004g0005 a0001c0003t0004g0006 a0001c0003t0004g0007 others(21): Show |
24 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.350-2026C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41711976 | |||||||
chr22:41712097 | G | A | 25 | a0001c0004t0003g0041 a0001c0004t0003g0042 a0001c0004t0003g0043 others(22): Show |
25 | HG01884.hp1 HG02280.hp1 HG02559.hp1 others(22): Show |
intron_variant | MODIFIER | c.350-1905G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41712097 | |||||||
chr22:41712184 | A | G | 6 | a0001c0003t0004g0005 a0001c0003t0004g0006 a0001c0003t0004g0007 others(3): Show |
6 | HG02109.hp2 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-1818A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41712184 | |||||||
chr22:41712204 | C | CA | 45 | a0001c0002t0002g0001 a0001c0002t0002g0046 a0001c0002t0002g0047 others(42): Show |
46 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.350-1786dupA | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr22 | 41712204 | ||||||
chr22:41712204 | C | CAAA | 13 | a0002c0005t0001g0028 a0002c0005t0001g0029 a0002c0005t0001g0030 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.350-1788_350-1786d others(5): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr22 | 41712204 | ||||||
chr22:41712204 | C | CAAAAAAA others(5): Show |
7 | a0001c0001t0001g0128 a0001c0001t0001g0173 a0001c0001t0001g0174 others(4): Show |
7 | HG00323.hp1 HG01167.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.350-1797_350-1786d others(14): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr22 | 41712204 | ||||||
chr22:41712204 | C | CAAAAAAA others(6): Show |
139 | a0001c0001t0001g0003 a0001c0001t0001g0127 a0001c0001t0001g0130 others(136): Show |
142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.350-1786_350-1785i others(15): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr22 | 41712204 | ||||||
chr22:41712204 | C | CAAAAAAA others(7): Show |
44 | a0001c0001t0001g0126 a0001c0001t0001g0143 a0001c0001t0001g0144 others(41): Show |
44 | HG00408.hp2 HG00423.hp1 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.350-1786_350-1785i others(16): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr22 | 41712204 | ||||||
chr22:41712204 | C | CAAAAAAA others(8): Show |
3 | a0001c0004t0003g0041 a0001c0004t0003g0113 a0001c0004t0003g0114 |
3 | HG01884.hp1 HG02886.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.350-1786_350-1785i others(17): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr22 | 41712204 | ||||||
chr22:41712204 | C | CAAAAAAA others(1081): Show |
1 | a0001c0001t0001g0244 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.350-1786_350-1785i others(1090): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr22 | 41712204 | ||||||
chr22:41712224 | G | GT | 24 | a0001c0004t0003g0041 a0001c0004t0003g0042 a0001c0004t0003g0043 others(21): Show |
24 | HG02280.hp1 HG02559.hp1 HG02572.hp1 others(21): Show |
intron_variant | MODIFIER | c.350-1770dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr22 | 41712224 | ||||||
chr22:41712229 | TTTTG | T | 8 | a0002c0005t0001g0028 a0002c0005t0001g0029 a0002c0005t0001g0030 others(5): Show |
8 | HG00673.hp2 HG01109.hp2 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.350-1757_350-1754d others(6): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr22 | 41712229 | ||||||
chr22:41712245 | G | T | 1 | a0001c0018t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.350-1757G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41712245 | |||||||
chr22:41712249 | C | T | 207 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(204): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.350-1753C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41712249 | |||||||
chr22:41712276 | C | T | 1 | a0001c0003t0004g0022 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.350-1726C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41712276 | |||||||
chr22:41712363 | TA | T | 2 | a0001c0001t0001g0003 a0001c0001t0001g0231 |
3 | HG01433.hp2 NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.350-1638delA | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41712363 | |||||||
chr22:41712460 | C | T | 4 | a0001c0001t0001g0228 a0001c0001t0001g0229 a0001c0001t0001g0230 others(1): Show |
4 | HG00140.hp1 HG01070.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.350-1542C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41712460 | |||||||
chr22:41712470 | C | T | 13 | a0002c0005t0001g0028 a0002c0005t0001g0029 a0002c0005t0001g0030 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.350-1532C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41712470 | |||||||
chr22:41712494 | C | T | 1 | a0001c0002t0002g0087 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.350-1508C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41712494 | |||||||
chr22:41712594 | A | C | 2 | a0001c0001t0001g0148 a0001c0001t0001g0175 |
2 | HG00323.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.350-1408A>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41712594 | |||||||
chr22:41712671 | G | GGT | 5 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0098 others(2): Show |
5 | HG01884.hp1 HG02257.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.350-1331_350-1330i others(4): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41712671 | |||||||
chr22:41712671 | G | GGTGT | 9 | a0001c0004t0003g0041 a0001c0004t0003g0042 a0001c0004t0003g0043 others(6): Show |
9 | HG02280.hp1 HG02630.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.350-1331_350-1330i others(6): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41712671 | |||||||
chr22:41712671 | G | GGTGTGT | 11 | a0001c0004t0003g0045 a0001c0004t0003g0113 a0001c0004t0003g0118 others(8): Show |
11 | HG02559.hp1 HG02886.hp2 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.350-1331_350-1330i others(8): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41712671 | |||||||
chr22:41712671 | G | GGTGTGTG others(1): Show |
5 | a0001c0004t0003g0116 a0001c0004t0003g0119 a0001c0004t0003g0120 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.350-1331_350-1330i others(10): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41712671 | |||||||
chr22:41712671 | GATGTGTG others(9): Show |
G | 1 | a0001c0018t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.350-1330_350-1315d others(18): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41712671 | |||||||
chr22:41712672 | A | ATG | 13 | a0001c0002t0002g0001 a0001c0002t0002g0046 a0001c0002t0002g0047 others(10): Show |
14 | HG00735.hp2 HG01099.hp1 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.350-1301_350-1300d others(4): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr22 | 41712672 | ||||||
chr22:41712672 | A | ATGTG | 88 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0128 others(85): Show |
89 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(86): Show |
intron_variant | MODIFIER | c.350-1303_350-1300d others(6): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr22 | 41712672 | ||||||
chr22:41712672 | A | ATGTGTG | 43 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0138 others(40): Show |
43 | HG00423.hp1 HG00544.hp1 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.350-1305_350-1300d others(8): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr22 | 41712672 | ||||||
chr22:41712672 | A | ATGTGTGT others(1): Show |
7 | a0001c0001t0001g0147 a0001c0003t0004g0027 a0005c0007t0004g0011 others(4): Show |
7 | HG02451.hp2 HG02559.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.350-1307_350-1300d others(10): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr22 | 41712672 | ||||||
chr22:41712672 | A | ATGTGTGT others(3): Show |
4 | a0002c0005t0001g0028 a0002c0005t0001g0029 a0002c0005t0001g0040 others(1): Show |
4 | HG01934.hp2 HG01943.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.350-1309_350-1300d others(12): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr22 | 41712672 | ||||||
chr22:41712672 | A | ATGTGTGT others(5): Show |
13 | a0001c0001t0001g0003 a0001c0001t0001g0231 a0001c0003t0004g0005 others(10): Show |
14 | HG00673.hp2 HG01243.hp1 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.350-1311_350-1300d others(14): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr22 | 41712672 | ||||||
chr22:41712672 | A | ATGTGTGT others(7): Show |
12 | a0001c0003t0004g0010 a0001c0003t0004g0017 a0001c0003t0004g0018 others(9): Show |
12 | HG00408.hp1 HG01109.hp2 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.350-1313_350-1300d others(16): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr22 | 41712672 | ||||||
chr22:41712672 | A | ATGTGTGT others(9): Show |
2 | a0001c0003t0004g0021 a0002c0005t0001g0036 |
2 | HG00423.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.350-1315_350-1300d others(18): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr22 | 41712672 | ||||||
chr22:41712672 | A | G | 38 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0098 others(35): Show |
39 | HG01109.hp1 HG01884.hp1 HG02257.hp2 others(36): Show |
intron_variant | MODIFIER | c.350-1330A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41712672 | |||||||
chr22:41712672 | ATGTGTGT others(3): Show |
A | 1 | a0001c0003t0004g0026 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.350-1309_350-1300d others(12): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr22 | 41712672 | ||||||
chr22:41712703 | G | T | 18 | a0001c0004t0003g0041 a0001c0004t0003g0042 a0001c0004t0003g0043 others(15): Show |
18 | HG02280.hp1 HG02723.hp1 HG02723.hp2 others(15): Show |
intron_variant | MODIFIER | c.350-1299G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41712703 | |||||||
chr22:41712771 | G | A | 3 | a0001c0001t0005g0181 a0001c0001t0005g0188 a0001c0001t0005g0189 |
3 | HG01884.hp2 HG02258.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.350-1231G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41712771 | |||||||
chr22:41712809 | G | GT | 11 | a0001c0001t0001g0140 a0001c0001t0001g0146 a0001c0001t0001g0235 others(8): Show |
11 | HG01109.hp2 HG02257.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.350-1177dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr22 | 41712809 | ||||||
chr22:41712826 | A | T | 252 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(249): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.350-1176A>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41712826 | |||||||
chr22:41712878 | G | A | 1 | a0001c0001t0001g0149 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.350-1124G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41712878 | |||||||
chr22:41713483 | G | GA | 206 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(203): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.350-507dupA | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr22 | 41713483 | ||||||
chr22:41713628 | A | G | 1 | a0001c0003t0001g0098 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.350-374A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41713628 | |||||||
chr22:41713763 | G | A | 6 | a0001c0003t0004g0005 a0001c0003t0004g0006 a0001c0003t0004g0007 others(3): Show |
6 | HG02109.hp2 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-239G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41713763 | |||||||
chr22:41713793 | C | A | 1 | a0008c0021t0001g0129 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.350-209C>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41713793 | |||||||
chr22:41713793 | C | T | 6 | a0001c0003t0004g0005 a0001c0003t0004g0006 a0001c0003t0004g0007 others(3): Show |
6 | HG02109.hp2 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-209C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41713793 | |||||||
chr22:41713840 | G | T | 194 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(191): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.350-162G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41713840 | |||||||
chr22:41713913 | A | G | 194 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(191): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.350-89A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41713913 | |||||||
chr22:41713939 | C | T | 1 | a0001c0018t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.350-63C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 3/30 | chr22 | 41713939 | |||||||
chr22:41714353 | G | A | 23 | a0001c0003t0004g0005 a0001c0003t0004g0006 a0001c0003t0004g0007 others(20): Show |
23 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.423+278G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 4/30 | chr22 | 41714353 | |||||||
chr22:41714525 | G | A | 4 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0098 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.423+450G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 4/30 | chr22 | 41714525 | |||||||
chr22:41714568 | G | A | 9 | a0003c0006t0001g0002 a0003c0006t0001g0069 a0003c0006t0001g0090 others(6): Show |
10 | HG01109.hp1 HG02258.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.423+493G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 4/30 | chr22 | 41714568 | |||||||
chr22:41714591 | C | T | 1 | a0001c0001t0001g0145 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.423+516C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 4/30 | chr22 | 41714591 | |||||||
chr22:41714600 | A | G | 6 | a0001c0003t0004g0005 a0001c0003t0004g0006 a0001c0003t0004g0007 others(3): Show |
6 | HG02109.hp2 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.423+525A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 4/30 | chr22 | 41714600 | |||||||
chr22:41714638 | A | T | 1 | a0008c0021t0001g0129 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.423+563A>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 4/30 | chr22 | 41714638 | |||||||
chr22:41714716 | CA | C | 199 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(196): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.423+656delA | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr22 | 41714716 | ||||||
chr22:41714716 | CAA | C | 6 | a0001c0003t0004g0005 a0001c0003t0004g0006 a0001c0003t0004g0007 others(3): Show |
6 | HG02109.hp2 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.423+655_423+656del others(2): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr22 | 41714716 | ||||||
chr22:41714835 | C | T | 1 | a0001c0002t0002g0055 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.423+760C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 4/30 | chr22 | 41714835 | |||||||
chr22:41714907 | A | G | 1 | a0001c0001t0001g0175 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.423+832A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 4/30 | chr22 | 41714907 | |||||||
chr22:41714999 | C | G | 6 | a0001c0003t0004g0005 a0001c0003t0004g0006 a0001c0003t0004g0007 others(3): Show |
6 | HG02109.hp2 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.423+924C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 4/30 | chr22 | 41714999 | |||||||
chr22:41715386 | T | C | 6 | a0001c0003t0004g0005 a0001c0003t0004g0006 a0001c0003t0004g0007 others(3): Show |
6 | HG02109.hp2 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.424-655T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 4/30 | chr22 | 41715386 | |||||||
chr22:41715397 | AT | A | 8 | a0001c0001t0001g0141 a0001c0002t0002g0074 a0001c0004t0003g0125 others(5): Show |
8 | HG00323.hp2 HG01109.hp1 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.424-628delT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr22 | 41715397 | ||||||
chr22:41715597 | G | T | 1 | a0010c0016t0003g0117 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.424-444G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 4/30 | chr22 | 41715597 | |||||||
chr22:41715689 | T | C | 207 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(204): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.424-352T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 4/30 | chr22 | 41715689 | |||||||
chr22:41715892 | A | T | 132 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(129): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.424-149A>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 4/30 | chr22 | 41715892 | |||||||
chr22:41715909 | A | C | 1 | a0001c0001t0001g0137 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.424-132A>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 4/30 | chr22 | 41715909 | |||||||
chr22:41715913 | A | T | 1 | a0001c0001t0001g0209 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.424-128A>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 4/30 | chr22 | 41715913 | |||||||
chr22:41716037 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG00597.hp1 | splice_region_variant&intron_variant | LOW | c.424-4G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 4/30 | chr22 | 41716037 | |||||||
chr22:41716355 | C | CT | 17 | a0001c0002t0002g0050 a0001c0002t0002g0051 a0001c0002t0002g0052 others(14): Show |
17 | HG00738.hp1 HG00741.hp1 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.529+247dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 5/30 | INFO_REALIGN_3_PRIME | chr22 | 41716355 | ||||||
chr22:41716355 | CTTTTTT | C | 5 | a0001c0003t0004g0006 a0001c0003t0004g0007 a0001c0003t0004g0009 others(2): Show |
5 | HG01109.hp1 HG02109.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.529+242_529+247del others(6): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 5/30 | INFO_REALIGN_3_PRIME | chr22 | 41716355 | ||||||
chr22:41716355 | CTTTTTTT | C | 10 | a0001c0003t0001g0098 a0001c0003t0004g0005 a0003c0006t0001g0002 others(7): Show |
11 | HG02965.hp1 HG02970.hp2 HG03041.hp2 others(8): Show |
intron_variant | MODIFIER | c.529+241_529+247del others(7): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 5/30 | INFO_REALIGN_3_PRIME | chr22 | 41716355 | ||||||
chr22:41716355 | CTTTTTTT others(1): Show |
C | 6 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0004g0018 others(3): Show |
6 | HG02257.hp2 HG02258.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.529+240_529+247del others(8): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 5/30 | INFO_REALIGN_3_PRIME | chr22 | 41716355 | ||||||
chr22:41716355 | CTTTTTTT others(2): Show |
C | 16 | a0001c0002t0002g0072 a0001c0002t0002g0074 a0001c0002t0002g0084 others(13): Show |
16 | HG00323.hp2 HG00639.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.529+239_529+247del others(9): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 5/30 | INFO_REALIGN_3_PRIME | chr22 | 41716355 | ||||||
chr22:41716355 | CTTTTTTT others(3): Show |
C | 5 | a0001c0002t0002g0055 a0001c0002t0002g0070 a0001c0002t0002g0071 others(2): Show |
5 | HG01070.hp2 HG01257.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.529+238_529+247del others(10): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 5/30 | INFO_REALIGN_3_PRIME | chr22 | 41716355 | ||||||
chr22:41716355 | CTTTTTTT others(8): Show |
C | 1 | a0001c0002t0002g0058 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.529+233_529+247del others(15): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 5/30 | INFO_REALIGN_3_PRIME | chr22 | 41716355 | ||||||
chr22:41716355 | CTTTTTTT others(9): Show |
C | 13 | a0002c0005t0001g0028 a0002c0005t0001g0029 a0002c0005t0001g0030 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.529+232_529+247del others(16): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 5/30 | INFO_REALIGN_3_PRIME | chr22 | 41716355 | ||||||
chr22:41716355 | CTTTTTTT others(17): Show |
C | 155 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(152): Show |
157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.529+224_529+247del others(24): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 5/30 | INFO_REALIGN_3_PRIME | chr22 | 41716355 | ||||||
chr22:41716355 | CTTTTTTT others(18): Show |
C | 2 | a0001c0001t0001g0191 a0001c0001t0001g0211 |
2 | HG01943.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.529+223_529+247del others(25): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 5/30 | INFO_REALIGN_3_PRIME | chr22 | 41716355 | ||||||
chr22:41716420 | A | G | 1 | a0001c0002t0002g0057 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.529+274A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 5/30 | chr22 | 41716420 | |||||||
chr22:41716433 | A | G | 2 | a0001c0002t0002g0070 a0001c0002t0002g0071 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.529+287A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 5/30 | chr22 | 41716433 | |||||||
chr22:41716564 | C | T | 16 | a0001c0003t0004g0017 a0001c0003t0004g0018 a0001c0003t0004g0019 others(13): Show |
16 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.529+418C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 5/30 | chr22 | 41716564 | |||||||
chr22:41716595 | T | C | 207 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(204): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.529+449T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 5/30 | chr22 | 41716595 | |||||||
chr22:41716686 | CT | C | 135 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(132): Show |
137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.529+558delT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 5/30 | INFO_REALIGN_3_PRIME | chr22 | 41716686 | ||||||
chr22:41716713 | C | T | 15 | a0001c0002t0002g0052 a0001c0002t0002g0053 a0002c0005t0001g0028 others(12): Show |
15 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(12): Show |
intron_variant | MODIFIER | c.529+567C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 5/30 | chr22 | 41716713 | |||||||
chr22:41716790 | C | T | 6 | a0001c0003t0004g0005 a0001c0003t0004g0006 a0001c0003t0004g0007 others(3): Show |
6 | HG02109.hp2 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.529+644C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 5/30 | chr22 | 41716790 | |||||||
chr22:41716814 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.529+668C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 5/30 | chr22 | 41716814 | |||||||
chr22:41717075 | C | CT | 25 | a0001c0004t0003g0041 a0001c0004t0003g0042 a0001c0004t0003g0043 others(22): Show |
25 | HG01884.hp1 HG02280.hp1 HG02559.hp1 others(22): Show |
intron_variant | MODIFIER | c.529+935dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 5/30 | INFO_REALIGN_3_PRIME | chr22 | 41717075 | ||||||
chr22:41717161 | T | C | 6 | a0001c0002t0002g0055 a0001c0002t0002g0070 a0001c0002t0002g0071 others(3): Show |
6 | HG00323.hp2 HG01070.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.530-910T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 5/30 | chr22 | 41717161 | |||||||
chr22:41717224 | A | G | 13 | a0002c0005t0001g0028 a0002c0005t0001g0029 a0002c0005t0001g0030 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.530-847A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 5/30 | chr22 | 41717224 | |||||||
chr22:41717272 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.530-799C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 5/30 | chr22 | 41717272 | |||||||
chr22:41717311 | C | T | 25 | a0001c0004t0003g0041 a0001c0004t0003g0042 a0001c0004t0003g0043 others(22): Show |
25 | HG01884.hp1 HG02280.hp1 HG02559.hp1 others(22): Show |
intron_variant | MODIFIER | c.530-760C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 5/30 | chr22 | 41717311 | |||||||
chr22:41717359 | C | T | 5 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0098 others(2): Show |
5 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.530-712C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 5/30 | chr22 | 41717359 | |||||||
chr22:41717456 | C | G | 1 | a0007c0020t0001g0208 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.530-615C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 5/30 | chr22 | 41717456 | |||||||
chr22:41717618 | C | CT | 19 | a0001c0001t0001g0176 a0001c0004t0003g0041 a0001c0004t0003g0042 others(16): Show |
19 | HG01884.hp1 HG02280.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.530-438dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 5/30 | INFO_REALIGN_3_PRIME | chr22 | 41717618 | ||||||
chr22:41717618 | C | CTT | 7 | a0001c0004t0003g0113 a0001c0004t0003g0116 a0001c0004t0003g0118 others(4): Show |
7 | HG02886.hp2 HG02976.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.530-439_530-438dup others(2): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 5/30 | INFO_REALIGN_3_PRIME | chr22 | 41717618 | ||||||
chr22:41717706 | C | T | 9 | a0003c0006t0001g0002 a0003c0006t0001g0069 a0003c0006t0001g0090 others(6): Show |
10 | HG01109.hp1 HG02258.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.530-365C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 5/30 | chr22 | 41717706 | |||||||
chr22:41717771 | A | C | 1 | a0001c0001t0001g0211 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.530-300A>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 5/30 | chr22 | 41717771 | |||||||
chr22:41717942 | A | G | 2 | a0001c0001t0001g0003 a0001c0001t0001g0231 |
3 | HG01433.hp2 NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.530-129A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 5/30 | chr22 | 41717942 | |||||||
chr22:41718023 | G | A | 4 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0098 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.530-48G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 5/30 | chr22 | 41718023 | |||||||
chr22:41718300 | G | T | 1 | a0001c0001t0001g0133 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.733+26G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41718300 | |||||||
chr22:41718398 | G | A | 1 | a0001c0003t0004g0027 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.733+124G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41718398 | |||||||
chr22:41718609 | C | G | 1 | a0010c0016t0003g0117 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.733+335C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41718609 | |||||||
chr22:41718805 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.733+531T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41718805 | |||||||
chr22:41718855 | T | C | 1 | a0001c0001t0001g0192 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.733+581T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41718855 | |||||||
chr22:41718856 | G | C | 1 | a0001c0001t0001g0133 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.733+582G>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41718856 | |||||||
chr22:41718943 | C | T | 1 | a0001c0003t0004g0025 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.733+669C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41718943 | |||||||
chr22:41718977 | T | C | 13 | a0002c0005t0001g0028 a0002c0005t0001g0029 a0002c0005t0001g0030 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.733+703T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41718977 | |||||||
chr22:41718979 | C | CT | 7 | a0001c0001t0001g0146 a0001c0001t0001g0172 a0001c0001t0001g0247 others(4): Show |
7 | HG00621.hp2 HG01109.hp2 HG04184.hp1 others(4): Show |
intron_variant | MODIFIER | c.733+726dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr22 | 41718979 | ||||||
chr22:41718979 | CT | C | 60 | a0001c0001t0001g0150 a0001c0001t0001g0180 a0001c0001t0001g0245 others(57): Show |
61 | HG00639.hp1 HG01109.hp1 HG01243.hp1 others(58): Show |
intron_variant | MODIFIER | c.733+726delT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr22 | 41718979 | ||||||
chr22:41719026 | A | G | 1 | a0001c0001t0001g0180 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.733+752A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41719026 | |||||||
chr22:41719046 | A | G | 207 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(204): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.733+772A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41719046 | |||||||
chr22:41719046 | A | T | 3 | a0001c0002t0002g0085 a0001c0002t0002g0086 a0001c0002t0002g0105 |
3 | HG02602.hp1 HG03710.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.733+772A>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41719046 | |||||||
chr22:41719075 | C | T | 1 | a0003c0006t0001g0069 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.733+801C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41719075 | |||||||
chr22:41719189 | A | G | 1 | a0003c0006t0001g0069 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.733+915A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41719189 | |||||||
chr22:41719218 | G | A | 3 | a0002c0005t0001g0028 a0002c0005t0001g0029 a0002c0005t0001g0030 |
3 | HG01934.hp2 HG01943.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.733+944G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41719218 | |||||||
chr22:41719228 | C | T | 1 | a0001c0001t0001g0145 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.733+954C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41719228 | |||||||
chr22:41719246 | G | T | 2 | a0001c0002t0002g0070 a0001c0002t0002g0071 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.733+972G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41719246 | |||||||
chr22:41719281 | G | A | 14 | a0001c0018t0001g0089 a0002c0005t0001g0028 a0002c0005t0001g0029 others(11): Show |
14 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(11): Show |
intron_variant | MODIFIER | c.733+1007G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41719281 | |||||||
chr22:41719346 | C | A | 1 | a0001c0018t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.733+1072C>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41719346 | |||||||
chr22:41719536 | C | T | 1 | a0001c0001t0001g0131 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.733+1262C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41719536 | |||||||
chr22:41720159 | G | A | 132 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(129): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.733+1885G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41720159 | |||||||
chr22:41720200 | G | C | 23 | a0001c0003t0004g0005 a0001c0003t0004g0006 a0001c0003t0004g0007 others(20): Show |
23 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.733+1926G>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41720200 | |||||||
chr22:41720387 | A | G | 2 | a0001c0001t0001g0207 a0001c0001t0001g0232 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.733+2113A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41720387 | |||||||
chr22:41720445 | T | C | 1 | a0001c0004t0003g0114 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.733+2171T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41720445 | |||||||
chr22:41720556 | G | T | 62 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0098 others(59): Show |
63 | HG00639.hp1 HG01109.hp1 HG01243.hp1 others(60): Show |
intron_variant | MODIFIER | c.733+2282G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41720556 | |||||||
chr22:41720580 | C | T | 13 | a0002c0005t0001g0028 a0002c0005t0001g0029 a0002c0005t0001g0030 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.733+2306C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41720580 | |||||||
chr22:41720597 | A | AT | 142 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0128 others(139): Show |
143 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.733+2341dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr22 | 41720597 | ||||||
chr22:41720597 | A | ATT | 52 | a0001c0001t0001g0003 a0001c0001t0001g0132 a0001c0001t0001g0133 others(49): Show |
54 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.733+2340_733+2341d others(4): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr22 | 41720597 | ||||||
chr22:41720706 | C | G | 13 | a0002c0005t0001g0028 a0002c0005t0001g0029 a0002c0005t0001g0030 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.733+2432C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41720706 | |||||||
chr22:41720858 | G | A | 4 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0001g0245 others(1): Show |
4 | HG02630.hp2 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.733+2584G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41720858 | |||||||
chr22:41720865 | A | G | 4 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0001g0245 others(1): Show |
4 | HG02630.hp2 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.733+2591A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41720865 | |||||||
chr22:41720873 | G | A | 4 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0001g0245 others(1): Show |
4 | HG02630.hp2 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.733+2599G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41720873 | |||||||
chr22:41721061 | A | G | 207 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(204): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.733+2787A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41721061 | |||||||
chr22:41721065 | C | A | 1 | a0001c0001t0001g0193 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.733+2791C>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41721065 | |||||||
chr22:41721071 | G | A | 1 | a0009c0019t0001g0104 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.733+2797G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41721071 | |||||||
chr22:41721089 | A | G | 1 | a0001c0001t0001g0149 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.733+2815A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41721089 | |||||||
chr22:41721160 | A | ATCTCGGC others(18): Show |
1 | a0001c0018t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.734-2782_734-2758d others(27): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr22 | 41721160 | ||||||
chr22:41721224 | C | T | 1 | a0001c0004t0003g0118 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.734-2719C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41721224 | |||||||
chr22:41721229 | C | T | 23 | a0001c0003t0004g0005 a0001c0003t0004g0006 a0001c0003t0004g0007 others(20): Show |
23 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.734-2714C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41721229 | |||||||
chr22:41721237 | C | CT | 25 | a0001c0001t0001g0136 a0001c0001t0001g0146 a0001c0001t0001g0167 others(22): Show |
25 | HG00597.hp2 HG00621.hp2 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.734-2681dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr22 | 41721237 | ||||||
chr22:41721237 | C | CTTTTT | 9 | a0001c0003t0004g0021 a0001c0003t0004g0024 a0001c0003t0004g0025 others(6): Show |
9 | HG00639.hp1 HG01496.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.734-2685_734-2681d others(7): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr22 | 41721237 | ||||||
chr22:41721237 | C | CTTTTTT | 7 | a0001c0003t0004g0017 a0001c0003t0004g0018 a0001c0003t0004g0019 others(4): Show |
7 | HG01243.hp1 HG02572.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.734-2686_734-2681d others(8): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr22 | 41721237 | ||||||
chr22:41721237 | CT | C | 44 | a0001c0001t0001g0150 a0001c0001t0001g0193 a0001c0001t0001g0194 others(41): Show |
44 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.734-2681delT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr22 | 41721237 | ||||||
chr22:41721237 | CTT | C | 15 | a0001c0003t0004g0005 a0001c0004t0003g0041 a0001c0004t0003g0042 others(12): Show |
15 | HG01109.hp1 HG02258.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.734-2682_734-2681d others(4): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr22 | 41721237 | ||||||
chr22:41721237 | CTTT | C | 6 | a0001c0011t0003g0115 a0003c0006t0001g0002 a0003c0006t0001g0090 others(3): Show |
7 | HG02965.hp1 HG02970.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.734-2683_734-2681d others(5): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr22 | 41721237 | ||||||
chr22:41721278 | T | C | 25 | a0001c0004t0003g0041 a0001c0004t0003g0042 a0001c0004t0003g0043 others(22): Show |
25 | HG01884.hp1 HG02280.hp1 HG02559.hp1 others(22): Show |
intron_variant | MODIFIER | c.734-2665T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41721278 | |||||||
chr22:41721293 | G | A | 1 | a0008c0021t0001g0129 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.734-2650G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41721293 | |||||||
chr22:41721318 | C | T | 49 | a0001c0001t0001g0003 a0001c0001t0001g0132 a0001c0001t0001g0133 others(46): Show |
51 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.734-2625C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41721318 | |||||||
chr22:41721382 | C | G | 1 | a0008c0021t0001g0129 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.734-2561C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41721382 | |||||||
chr22:41721446 | G | A | 1 | a0001c0002t0002g0059 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.734-2497G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41721446 | |||||||
chr22:41721560 | A | G | 13 | a0002c0005t0001g0028 a0002c0005t0001g0029 a0002c0005t0001g0030 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.734-2383A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41721560 | |||||||
chr22:41721564 | AT | A | 207 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(204): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.734-2370delT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr22 | 41721564 | ||||||
chr22:41721566 | T | A | 1 | a0001c0018t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.734-2377T>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41721566 | |||||||
chr22:41721701 | C | T | 3 | a0001c0002t0002g0079 a0001c0002t0002g0080 a0001c0002t0002g0087 |
3 | HG01346.hp1 HG02451.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.734-2242C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41721701 | |||||||
chr22:41721715 | A | AC | 14 | a0001c0002t0002g0046 a0001c0002t0002g0066 a0001c0002t0002g0070 others(11): Show |
14 | HG00408.hp1 HG00673.hp2 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.734-2224dupC | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr22 | 41721715 | ||||||
chr22:41721719 | C | CCT | 4 | a0001c0001t0001g0139 a0001c0001t0001g0183 a0001c0001t0001g0186 others(1): Show |
4 | HG00423.hp1 HG01934.hp2 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.734-2224_734-2223i others(4): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41721719 | |||||||
chr22:41721719 | C | CT | 133 | a0001c0001t0001g0003 a0001c0001t0001g0127 a0001c0001t0001g0128 others(130): Show |
135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.734-2204dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr22 | 41721719 | ||||||
chr22:41721719 | C | CTT | 37 | a0001c0001t0001g0126 a0001c0001t0001g0136 a0001c0001t0001g0148 others(34): Show |
37 | HG00639.hp1 HG01175.hp2 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.734-2205_734-2204d others(4): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr22 | 41721719 | ||||||
chr22:41721719 | C | CTTTTT | 6 | a0003c0006t0001g0002 a0003c0006t0001g0091 a0003c0006t0001g0092 others(3): Show |
7 | HG01109.hp1 HG02965.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.734-2208_734-2204d others(7): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr22 | 41721719 | ||||||
chr22:41721720 | T | C | 1 | a0001c0002t0002g0102 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.734-2223T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41721720 | |||||||
chr22:41721952 | C | G | 2 | a0001c0011t0003g0115 a0001c0011t0003g0121 |
2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.734-1991C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41721952 | |||||||
chr22:41722004 | C | T | 1 | a0001c0001t0001g0135 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.734-1939C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41722004 | |||||||
chr22:41722018 | C | G | 13 | a0002c0005t0001g0028 a0002c0005t0001g0029 a0002c0005t0001g0030 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.734-1925C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41722018 | |||||||
chr22:41722020 | C | CT | 129 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(126): Show |
131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
intron_variant | MODIFIER | c.734-1908dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr22 | 41722020 | ||||||
chr22:41722225 | G | C | 1 | a0009c0019t0001g0104 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.734-1718G>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41722225 | |||||||
chr22:41722245 | G | A | 207 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(204): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.734-1698G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41722245 | |||||||
chr22:41722467 | A | AT | 16 | a0001c0001t0001g0168 a0001c0001t0001g0223 a0001c0001t0001g0225 others(13): Show |
17 | HG00741.hp2 HG01109.hp1 HG02300.hp1 others(14): Show |
intron_variant | MODIFIER | c.734-1455dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr22 | 41722467 | ||||||
chr22:41722467 | AT | A | 27 | a0001c0001t0001g0130 a0001c0001t0001g0153 a0001c0001t0001g0228 others(24): Show |
27 | HG00639.hp1 HG01070.hp1 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.734-1455delT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr22 | 41722467 | ||||||
chr22:41722467 | ATT | A | 13 | a0002c0005t0001g0028 a0002c0005t0001g0029 a0002c0005t0001g0030 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.734-1456_734-1455d others(4): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr22 | 41722467 | ||||||
chr22:41722623 | C | T | 2 | a0001c0012t0001g0182 a0001c0012t0001g0190 |
2 | HG02615.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.734-1320C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41722623 | |||||||
chr22:41722724 | G | T | 1 | a0001c0002t0002g0051 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.734-1219G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41722724 | |||||||
chr22:41722743 | G | C | 4 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0098 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.734-1200G>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41722743 | |||||||
chr22:41722969 | T | C | 1 | a0001c0004t0003g0114 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.734-974T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41722969 | |||||||
chr22:41723062 | G | A | 1 | a0001c0001t0001g0242 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.734-881G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41723062 | |||||||
chr22:41723121 | C | G | 1 | a0001c0004t0003g0118 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.734-822C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41723121 | |||||||
chr22:41723218 | GT | G | 207 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(204): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.734-713delT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr22 | 41723218 | ||||||
chr22:41723473 | C | G | 5 | a0001c0004t0003g0041 a0001c0004t0003g0042 a0001c0004t0003g0043 others(2): Show |
5 | HG02280.hp1 HG02723.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.734-470C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41723473 | |||||||
chr22:41723695 | C | T | 9 | a0003c0006t0001g0002 a0003c0006t0001g0069 a0003c0006t0001g0090 others(6): Show |
10 | HG01109.hp1 HG02258.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.734-248C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41723695 | |||||||
chr22:41723824 | A | G | 1 | a0010c0016t0003g0117 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.734-119A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41723824 | |||||||
chr22:41723837 | G | C | 4 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0001g0245 others(1): Show |
4 | HG02630.hp2 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.734-106G>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41723837 | |||||||
chr22:41723874 | G | A | 1 | a0001c0001t0001g0242 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.734-69G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 6/30 | chr22 | 41723874 | |||||||
chr22:41724117 | G | T | 7 | a0001c0003t0004g0005 a0001c0003t0004g0006 a0001c0003t0004g0007 others(4): Show |
7 | HG02109.hp2 HG02559.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.864+44G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41724117 | |||||||
chr22:41724124 | A | G | 1 | a0001c0001t0001g0223 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.864+51A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41724124 | |||||||
chr22:41724160 | A | T | 1 | a0001c0001t0001g0130 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.864+87A>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41724160 | |||||||
chr22:41724201 | T | C | 1 | a0001c0001t0001g0186 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.864+128T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41724201 | |||||||
chr22:41724392 | G | A | 1 | a0001c0002t0002g0055 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.864+319G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41724392 | |||||||
chr22:41724571 | C | A | 2 | a0001c0008t0003g0110 a0001c0008t0003g0111 |
2 | HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.864+498C>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41724571 | |||||||
chr22:41724574 | C | T | 2 | a0001c0001t0001g0165 a0001c0001t0001g0206 |
2 | HG00558.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.864+501C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41724574 | |||||||
chr22:41724616 | C | CA | 19 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0148 others(16): Show |
19 | HG00140.hp1 HG00741.hp2 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.864+562dupA | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | INFO_REALIGN_3_PRIME | chr22 | 41724616 | ||||||
chr22:41724616 | CAAAA | C | 13 | a0002c0005t0001g0028 a0002c0005t0001g0029 a0002c0005t0001g0030 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.864+559_864+562del others(4): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | INFO_REALIGN_3_PRIME | chr22 | 41724616 | ||||||
chr22:41724694 | G | A | 1 | a0001c0002t0002g0077 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.864+621G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41724694 | |||||||
chr22:41724803 | C | CT | 5 | a0001c0003t0004g0025 a0004c0009t0001g0004 a0004c0009t0001g0142 others(2): Show |
6 | HG01934.hp1 HG02280.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.864+745dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | INFO_REALIGN_3_PRIME | chr22 | 41724803 | ||||||
chr22:41724803 | CT | C | 16 | a0001c0001t0001g0152 a0001c0001t0001g0196 a0001c0001t0001g0209 others(13): Show |
16 | HG01109.hp1 HG01169.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.864+745delT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | INFO_REALIGN_3_PRIME | chr22 | 41724803 | ||||||
chr22:41724826 | G | A | 1 | a0001c0003t0004g0026 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.864+753G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41724826 | |||||||
chr22:41724860 | G | A | 54 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0128 others(51): Show |
54 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.864+787G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41724860 | |||||||
chr22:41724873 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.864+800G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41724873 | |||||||
chr22:41724903 | A | G | 1 | a0001c0008t0003g0109 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.864+830A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41724903 | |||||||
chr22:41724984 | G | A | 1 | a0001c0018t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.864+911G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41724984 | |||||||
chr22:41725074 | T | A | 3 | a0001c0008t0003g0106 a0001c0008t0003g0108 a0001c0008t0003g0109 |
3 | HG02572.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.864+1001T>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41725074 | |||||||
chr22:41725118 | A | AT | 8 | a0001c0001t0001g0203 a0001c0003t0004g0005 a0001c0003t0004g0006 others(5): Show |
8 | HG02109.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.864+1047dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | INFO_REALIGN_3_PRIME | chr22 | 41725118 | ||||||
chr22:41725121 | A | AT | 17 | a0001c0004t0003g0041 a0001c0004t0003g0042 a0001c0004t0003g0043 others(14): Show |
17 | HG02280.hp1 HG02723.hp1 HG02723.hp2 others(14): Show |
intron_variant | MODIFIER | c.864+1058dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | INFO_REALIGN_3_PRIME | chr22 | 41725121 | ||||||
chr22:41725121 | A | T | 168 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(165): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.864+1048A>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41725121 | |||||||
chr22:41725197 | C | T | 7 | a0001c0001t0001g0131 a0001c0001t0001g0134 a0001c0001t0001g0135 others(4): Show |
7 | NA18965.hp1 NA18977.hp2 NA18980.hp2 others(4): Show |
intron_variant | MODIFIER | c.864+1124C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41725197 | |||||||
chr22:41725242 | G | A | 1 | a0007c0020t0001g0208 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.864+1169G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41725242 | |||||||
chr22:41725256 | C | T | 1 | a0001c0001t0001g0152 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.864+1183C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41725256 | |||||||
chr22:41725257 | G | A | 23 | a0001c0003t0004g0005 a0001c0003t0004g0006 a0001c0003t0004g0007 others(20): Show |
23 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.864+1184G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41725257 | |||||||
chr22:41725274 | G | A | 132 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(129): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.864+1201G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41725274 | |||||||
chr22:41725476 | G | T | 13 | a0002c0005t0001g0028 a0002c0005t0001g0029 a0002c0005t0001g0030 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.864+1403G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41725476 | |||||||
chr22:41725606 | C | A | 1 | a0001c0002t0002g0078 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.864+1533C>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41725606 | |||||||
chr22:41725717 | A | C | 14 | a0001c0018t0001g0089 a0002c0005t0001g0028 a0002c0005t0001g0029 others(11): Show |
14 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(11): Show |
intron_variant | MODIFIER | c.864+1644A>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41725717 | |||||||
chr22:41725785 | T | G | 54 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0128 others(51): Show |
54 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.864+1712T>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41725785 | |||||||
chr22:41725862 | C | T | 1 | a0002c0005t0001g0038 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.864+1789C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41725862 | |||||||
chr22:41725905 | C | T | 25 | a0001c0004t0003g0041 a0001c0004t0003g0042 a0001c0004t0003g0043 others(22): Show |
25 | HG01884.hp1 HG02280.hp1 HG02559.hp1 others(22): Show |
intron_variant | MODIFIER | c.864+1832C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41725905 | |||||||
chr22:41725985 | A | C | 9 | a0003c0006t0001g0002 a0003c0006t0001g0069 a0003c0006t0001g0090 others(6): Show |
10 | HG01109.hp1 HG02258.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.864+1912A>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41725985 | |||||||
chr22:41726029 | C | G | 4 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0098 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.864+1956C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41726029 | |||||||
chr22:41726138 | C | T | 23 | a0001c0003t0004g0005 a0001c0003t0004g0006 a0001c0003t0004g0007 others(20): Show |
23 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.864+2065C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41726138 | |||||||
chr22:41726242 | AC | A | 39 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0098 others(36): Show |
40 | HG01109.hp1 HG01884.hp1 HG02257.hp2 others(37): Show |
intron_variant | MODIFIER | c.864+2170delC | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41726242 | |||||||
chr22:41726363 | T | C | 16 | a0001c0003t0004g0017 a0001c0003t0004g0018 a0001c0003t0004g0019 others(13): Show |
16 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.864+2290T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41726363 | |||||||
chr22:41726750 | TA | T | 132 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(129): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.864+2681delA | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | INFO_REALIGN_3_PRIME | chr22 | 41726750 | ||||||
chr22:41726778 | C | CT | 10 | a0001c0001t0001g0196 a0001c0001t0001g0247 a0001c0003t0004g0005 others(7): Show |
10 | HG00621.hp2 HG02109.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.864+2718dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | INFO_REALIGN_3_PRIME | chr22 | 41726778 | ||||||
chr22:41726865 | C | T | 4 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0098 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.864+2792C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41726865 | |||||||
chr22:41726922 | C | T | 132 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(129): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.865-2743C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41726922 | |||||||
chr22:41726974 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.865-2691C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41726974 | |||||||
chr22:41727049 | T | G | 1 | a0005c0007t0004g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.865-2616T>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41727049 | |||||||
chr22:41727095 | A | T | 207 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(204): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.865-2570A>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41727095 | |||||||
chr22:41727395 | C | T | 132 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(129): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.865-2270C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41727395 | |||||||
chr22:41727559 | A | G | 2 | a0002c0005t0001g0033 a0002c0005t0001g0036 |
2 | HG00423.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.865-2106A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41727559 | |||||||
chr22:41727611 | CA | C | 207 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(204): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.865-2051delA | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | INFO_REALIGN_3_PRIME | chr22 | 41727611 | ||||||
chr22:41727733 | A | G | 194 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(191): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.865-1932A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41727733 | |||||||
chr22:41727866 | G | A | 1 | a0001c0003t0004g0025 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.865-1799G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41727866 | |||||||
chr22:41728007 | G | T | 1 | a0001c0001t0001g0244 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.865-1658G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41728007 | |||||||
chr22:41728092 | C | T | 1 | a0001c0003t0004g0017 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.865-1573C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41728092 | |||||||
chr22:41728103 | T | C | 1 | a0002c0005t0001g0032 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.865-1562T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41728103 | |||||||
chr22:41728133 | T | C | 1 | a0002c0005t0001g0034 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.865-1532T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41728133 | |||||||
chr22:41728261 | C | T | 207 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(204): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.865-1404C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41728261 | |||||||
chr22:41728311 | C | G | 39 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0098 others(36): Show |
40 | HG01109.hp1 HG01884.hp1 HG02257.hp2 others(37): Show |
intron_variant | MODIFIER | c.865-1354C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41728311 | |||||||
chr22:41728365 | T | A | 25 | a0001c0004t0003g0041 a0001c0004t0003g0042 a0001c0004t0003g0043 others(22): Show |
25 | HG01884.hp1 HG02280.hp1 HG02559.hp1 others(22): Show |
intron_variant | MODIFIER | c.865-1300T>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41728365 | |||||||
chr22:41728613 | C | G | 2 | a0001c0008t0003g0106 a0001c0008t0003g0108 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.865-1052C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41728613 | |||||||
chr22:41728816 | A | G | 1 | a0001c0002t0002g0101 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.865-849A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41728816 | |||||||
chr22:41728860 | C | CA | 31 | a0001c0001t0001g0229 a0001c0001t0001g0248 a0001c0003t0001g0096 others(28): Show |
32 | HG00140.hp1 HG01109.hp1 HG02109.hp2 others(29): Show |
intron_variant | MODIFIER | c.865-796dupA | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | INFO_REALIGN_3_PRIME | chr22 | 41728860 | ||||||
chr22:41728860 | C | CAA | 17 | a0001c0003t0004g0017 a0001c0003t0004g0018 a0001c0003t0004g0019 others(14): Show |
17 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.865-797_865-796dup others(2): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | INFO_REALIGN_3_PRIME | chr22 | 41728860 | ||||||
chr22:41728870 | C | A | 207 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(204): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.865-795C>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41728870 | |||||||
chr22:41728891 | C | T | 1 | a0002c0005t0001g0031 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.865-774C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41728891 | |||||||
chr22:41728921 | T | A | 1 | a0001c0002t0002g0057 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.865-744T>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41728921 | |||||||
chr22:41728955 | G | C | 1 | a0001c0003t0004g0018 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.865-710G>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41728955 | |||||||
chr22:41728956 | G | T | 1 | a0001c0001t0001g0202 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.865-709G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41728956 | |||||||
chr22:41729078 | C | T | 1 | a0001c0002t0002g0078 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.865-587C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41729078 | |||||||
chr22:41729143 | C | T | 194 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(191): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.865-522C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41729143 | |||||||
chr22:41729164 | C | CA | 29 | a0001c0002t0002g0068 a0001c0003t0001g0096 a0001c0003t0001g0097 others(26): Show |
30 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.865-482dupA | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | INFO_REALIGN_3_PRIME | chr22 | 41729164 | ||||||
chr22:41729164 | C | CAA | 23 | a0001c0001t0001g0128 a0001c0001t0001g0175 a0001c0003t0004g0005 others(20): Show |
23 | HG00323.hp1 HG01243.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.865-483_865-482dup others(2): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | INFO_REALIGN_3_PRIME | chr22 | 41729164 | ||||||
chr22:41729164 | C | CAAA | 145 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(142): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.865-484_865-482dup others(3): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | INFO_REALIGN_3_PRIME | chr22 | 41729164 | ||||||
chr22:41729164 | C | CAAAA | 11 | a0001c0001t0001g0130 a0001c0001t0001g0140 a0001c0001t0001g0143 others(8): Show |
11 | HG00735.hp1 HG02027.hp1 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.865-485_865-482dup others(4): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | INFO_REALIGN_3_PRIME | chr22 | 41729164 | ||||||
chr22:41729206 | G | T | 4 | a0003c0006t0001g0090 a0003c0006t0001g0091 a0003c0006t0001g0095 others(1): Show |
4 | HG01109.hp1 HG02970.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.865-459G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41729206 | |||||||
chr22:41729313 | C | G | 1 | a0002c0005t0001g0029 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.865-352C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 7/30 | chr22 | 41729313 | |||||||
chr22:41729933 | G | A | 13 | a0002c0005t0001g0028 a0002c0005t0001g0029 a0002c0005t0001g0030 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.979+154G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 8/30 | chr22 | 41729933 | |||||||
chr22:41730003 | A | G | 1 | a0001c0001t0001g0164 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.979+224A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 8/30 | chr22 | 41730003 | |||||||
chr22:41730189 | T | A | 1 | a0001c0001t0001g0213 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.980-332T>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 8/30 | chr22 | 41730189 | |||||||
chr22:41730275 | C | T | 6 | a0001c0003t0004g0005 a0001c0003t0004g0006 a0001c0003t0004g0007 others(3): Show |
6 | HG02109.hp2 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.980-246C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 8/30 | chr22 | 41730275 | |||||||
chr22:41730297 | C | G | 58 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0128 others(55): Show |
59 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.980-224C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 8/30 | chr22 | 41730297 | |||||||
chr22:41730405 | T | C | 2 | a0001c0003t0004g0008 a0001c0003t0004g0009 |
2 | HG03195.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.980-116T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 8/30 | chr22 | 41730405 | |||||||
chr22:41730679 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1096+42C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 9/30 | chr22 | 41730679 | |||||||
chr22:41730704 | C | T | 13 | a0002c0005t0001g0028 a0002c0005t0001g0029 a0002c0005t0001g0030 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.1096+67C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 9/30 | chr22 | 41730704 | |||||||
chr22:41730712 | T | TG | 25 | a0001c0004t0003g0041 a0001c0004t0003g0042 a0001c0004t0003g0043 others(22): Show |
25 | HG01884.hp1 HG02280.hp1 HG02559.hp1 others(22): Show |
intron_variant | MODIFIER | c.1096+81dupG | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 9/30 | INFO_REALIGN_3_PRIME | chr22 | 41730712 | ||||||
chr22:41730815 | C | G | 9 | a0003c0006t0001g0002 a0003c0006t0001g0069 a0003c0006t0001g0090 others(6): Show |
10 | HG01109.hp1 HG02258.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.1096+178C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 9/30 | chr22 | 41730815 | |||||||
chr22:41731023 | T | G | 1 | a0001c0018t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1096+386T>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 9/30 | chr22 | 41731023 | |||||||
chr22:41731051 | C | CT | 63 | a0001c0001t0001g0164 a0001c0001t0001g0225 a0001c0001t0001g0247 others(60): Show |
64 | HG00140.hp2 HG00621.hp2 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.1096+434dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 9/30 | INFO_REALIGN_3_PRIME | chr22 | 41731051 | ||||||
chr22:41731051 | C | CTT | 15 | a0001c0003t0004g0024 a0002c0005t0001g0028 a0002c0005t0001g0029 others(12): Show |
15 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(12): Show |
intron_variant | MODIFIER | c.1096+433_1096+434d others(4): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 9/30 | INFO_REALIGN_3_PRIME | chr22 | 41731051 | ||||||
chr22:41731090 | G | A | 1 | a0001c0003t0004g0025 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1096+453G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 9/30 | chr22 | 41731090 | |||||||
chr22:41731135 | C | T | 62 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0098 others(59): Show |
63 | HG00639.hp1 HG01109.hp1 HG01243.hp1 others(60): Show |
intron_variant | MODIFIER | c.1096+498C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 9/30 | chr22 | 41731135 | |||||||
chr22:41731207 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1096+570C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 9/30 | chr22 | 41731207 | |||||||
chr22:41731343 | C | T | 1 | a0001c0003t0001g0098 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1096+706C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 9/30 | chr22 | 41731343 | |||||||
chr22:41731368 | A | G | 16 | a0001c0003t0004g0017 a0001c0003t0004g0018 a0001c0003t0004g0019 others(13): Show |
16 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.1096+731A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 9/30 | chr22 | 41731368 | |||||||
chr22:41731440 | T | C | 3 | a0002c0005t0001g0033 a0002c0005t0001g0036 a0002c0005t0001g0038 |
3 | HG00408.hp1 HG00423.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.1096+803T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 9/30 | chr22 | 41731440 | |||||||
chr22:41731521 | A | AT | 132 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(129): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.1097-717dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 9/30 | INFO_REALIGN_3_PRIME | chr22 | 41731521 | ||||||
chr22:41731622 | T | C | 1 | a0001c0001t0001g0197 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1097-623T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 9/30 | chr22 | 41731622 | |||||||
chr22:41731661 | T | C | 25 | a0001c0004t0003g0041 a0001c0004t0003g0042 a0001c0004t0003g0043 others(22): Show |
25 | HG01884.hp1 HG02280.hp1 HG02559.hp1 others(22): Show |
intron_variant | MODIFIER | c.1097-584T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 9/30 | chr22 | 41731661 | |||||||
chr22:41731777 | T | C | 75 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0098 others(72): Show |
76 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.1097-468T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 9/30 | chr22 | 41731777 | |||||||
chr22:41731953 | C | A | 1 | a0001c0018t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1097-292C>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 9/30 | chr22 | 41731953 | |||||||
chr22:41731995 | T | C | 132 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(129): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.1097-250T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 9/30 | chr22 | 41731995 | |||||||
chr22:41732093 | G | A | 132 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(129): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.1097-152G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 9/30 | chr22 | 41732093 | |||||||
chr22:41732457 | T | A | 75 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0098 others(72): Show |
76 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.1197-12T>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 10/30 | chr22 | 41732457 | |||||||
chr22:41732774 | A | C | 1 | a0001c0001t0001g0248 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1331+171A>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41732774 | |||||||
chr22:41732776 | A | AT | 36 | a0001c0001t0001g0184 a0001c0001t0001g0203 a0001c0001t0001g0204 others(33): Show |
37 | HG00735.hp1 HG01109.hp1 HG01884.hp1 others(34): Show |
intron_variant | MODIFIER | c.1331+193dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr22 | 41732776 | ||||||
chr22:41732776 | A | ATT | 6 | a0001c0004t0003g0041 a0001c0004t0003g0042 a0001c0004t0003g0044 others(3): Show |
6 | HG02280.hp1 HG02886.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1331+192_1331+193d others(4): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr22 | 41732776 | ||||||
chr22:41732776 | AT | A | 10 | a0001c0002t0002g0059 a0001c0002t0002g0067 a0001c0003t0004g0005 others(7): Show |
10 | HG02109.hp2 HG02559.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1331+193delT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr22 | 41732776 | ||||||
chr22:41732959 | T | C | 1 | a0001c0018t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1331+356T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41732959 | |||||||
chr22:41732969 | C | T | 6 | a0001c0008t0003g0106 a0001c0008t0003g0108 a0001c0008t0003g0109 others(3): Show |
6 | HG02559.hp1 HG02572.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1331+366C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41732969 | |||||||
chr22:41733005 | G | A | 1 | a0009c0019t0001g0104 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1331+402G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41733005 | |||||||
chr22:41733183 | C | T | 13 | a0002c0005t0001g0028 a0002c0005t0001g0029 a0002c0005t0001g0030 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.1331+580C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41733183 | |||||||
chr22:41733353 | G | T | 132 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(129): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.1331+750G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41733353 | |||||||
chr22:41733506 | C | G | 39 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0098 others(36): Show |
40 | HG01109.hp1 HG01884.hp1 HG02257.hp2 others(37): Show |
intron_variant | MODIFIER | c.1331+903C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41733506 | |||||||
chr22:41733770 | A | G | 1 | a0001c0002t0002g0086 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1331+1167A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41733770 | |||||||
chr22:41733794 | A | G | 4 | a0001c0001t0001g0152 a0001c0001t0001g0161 a0001c0001t0001g0162 others(1): Show |
4 | NA18947.hp2 NA18970.hp2 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.1331+1191A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41733794 | |||||||
chr22:41733960 | T | C | 207 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(204): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.1331+1357T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41733960 | |||||||
chr22:41734060 | G | A | 1 | a0009c0019t0001g0104 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1331+1457G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41734060 | |||||||
chr22:41734129 | A | AAAAAT | 38 | a0001c0003t0004g0005 a0001c0003t0004g0006 a0001c0003t0004g0007 others(35): Show |
38 | HG01884.hp1 HG02109.hp2 HG02280.hp1 others(35): Show |
intron_variant | MODIFIER | c.1331+1550_1331+155 others(9): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr22 | 41734129 | ||||||
chr22:41734129 | A | AAAAATAA others(3): Show |
8 | a0001c0003t0004g0018 a0001c0003t0004g0019 a0001c0003t0004g0020 others(5): Show |
8 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.1331+1545_1331+155 others(14): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr22 | 41734129 | ||||||
chr22:41734129 | A | AAAAATAA others(8): Show |
4 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0098 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1331+1540_1331+155 others(19): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr22 | 41734129 | ||||||
chr22:41734129 | A | AAAAATAA others(13): Show |
9 | a0003c0006t0001g0002 a0003c0006t0001g0069 a0003c0006t0001g0090 others(6): Show |
10 | HG01109.hp1 HG02258.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.1331+1535_1331+155 others(24): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr22 | 41734129 | ||||||
chr22:41734274 | A | T | 6 | a0005c0007t0004g0011 a0005c0007t0004g0012 a0005c0007t0004g0013 others(3): Show |
6 | HG02451.hp2 HG02809.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1331+1671A>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41734274 | |||||||
chr22:41734320 | C | T | 62 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0098 others(59): Show |
63 | HG00639.hp1 HG01109.hp1 HG01243.hp1 others(60): Show |
intron_variant | MODIFIER | c.1331+1717C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41734320 | |||||||
chr22:41734379 | A | G | 132 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(129): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.1331+1776A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41734379 | |||||||
chr22:41734405 | C | T | 25 | a0001c0004t0003g0041 a0001c0004t0003g0042 a0001c0004t0003g0043 others(22): Show |
25 | HG01884.hp1 HG02280.hp1 HG02559.hp1 others(22): Show |
intron_variant | MODIFIER | c.1331+1802C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41734405 | |||||||
chr22:41734533 | C | G | 1 | a0001c0004t0003g0114 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1331+1930C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41734533 | |||||||
chr22:41734553 | A | G | 1 | a0001c0001t0001g0185 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1331+1950A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41734553 | |||||||
chr22:41734626 | A | C | 1 | a0001c0018t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1331+2023A>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41734626 | |||||||
chr22:41734627 | G | T | 1 | a0001c0018t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1331+2024G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41734627 | |||||||
chr22:41734674 | G | C | 2 | a0001c0002t0002g0070 a0001c0002t0002g0071 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1331+2071G>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41734674 | |||||||
chr22:41734839 | G | A | 50 | a0001c0001t0001g0003 a0001c0001t0001g0132 a0001c0001t0001g0133 others(47): Show |
52 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.1331+2236G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41734839 | |||||||
chr22:41734929 | C | G | 3 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0098 |
3 | HG02257.hp2 HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1331+2326C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41734929 | |||||||
chr22:41734957 | T | A | 1 | a0001c0002t0002g0102 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1331+2354T>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41734957 | |||||||
chr22:41735075 | C | T | 4 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0098 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1331+2472C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41735075 | |||||||
chr22:41735107 | G | A | 1 | a0001c0002t0002g0083 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1331+2504G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41735107 | |||||||
chr22:41735153 | G | A | 6 | a0001c0003t0004g0005 a0001c0003t0004g0006 a0001c0003t0004g0007 others(3): Show |
6 | HG02109.hp2 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1331+2550G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41735153 | |||||||
chr22:41735183 | C | T | 1 | a0005c0007t0004g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1331+2580C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41735183 | |||||||
chr22:41735227 | G | GT | 36 | a0001c0001t0001g0126 a0001c0001t0001g0133 a0001c0001t0001g0134 others(33): Show |
36 | HG00597.hp1 HG00609.hp1 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.1331+2645dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr22 | 41735227 | ||||||
chr22:41735227 | GT | G | 44 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0098 others(41): Show |
45 | HG00408.hp1 HG00423.hp2 HG01109.hp1 others(42): Show |
intron_variant | MODIFIER | c.1331+2645delT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr22 | 41735227 | ||||||
chr22:41735406 | G | C | 1 | a0001c0002t0002g0001 | 2 | HG01099.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.1331+2803G>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41735406 | |||||||
chr22:41735426 | G | A | 9 | a0003c0006t0001g0002 a0003c0006t0001g0069 a0003c0006t0001g0090 others(6): Show |
10 | HG01109.hp1 HG02258.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.1331+2823G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41735426 | |||||||
chr22:41735443 | G | A | 50 | a0001c0001t0001g0003 a0001c0001t0001g0132 a0001c0001t0001g0133 others(47): Show |
52 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.1331+2840G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41735443 | |||||||
chr22:41735758 | C | T | 207 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(204): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.1331+3155C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41735758 | |||||||
chr22:41735977 | G | A | 13 | a0002c0005t0001g0028 a0002c0005t0001g0029 a0002c0005t0001g0030 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.1331+3374G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41735977 | |||||||
chr22:41736103 | C | T | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | HG00099.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1331+3500C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41736103 | |||||||
chr22:41736254 | CT | C | 184 | a0001c0001t0001g0003 a0001c0001t0001g0127 a0001c0001t0001g0130 others(181): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.1331+3664delT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr22 | 41736254 | ||||||
chr22:41736477 | T | C | 132 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(129): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.1331+3874T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41736477 | |||||||
chr22:41736506 | G | A | 3 | a0001c0001t0001g0150 a0001c0001t0001g0158 a0001c0001t0001g0159 |
3 | HG00099.hp1 HG01257.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1331+3903G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41736506 | |||||||
chr22:41736681 | C | T | 17 | a0001c0004t0003g0041 a0001c0004t0003g0042 a0001c0004t0003g0043 others(14): Show |
17 | HG02280.hp1 HG02723.hp1 HG02723.hp2 others(14): Show |
intron_variant | MODIFIER | c.1331+4078C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41736681 | |||||||
chr22:41736884 | C | A | 132 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(129): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.1331+4281C>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41736884 | |||||||
chr22:41737056 | T | C | 132 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(129): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.1331+4453T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41737056 | |||||||
chr22:41737371 | G | T | 1 | a0001c0001t0001g0243 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1331+4768G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41737371 | |||||||
chr22:41737439 | G | A | 207 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(204): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.1331+4836G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41737439 | |||||||
chr22:41737548 | C | T | 207 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(204): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.1331+4945C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41737548 | |||||||
chr22:41737549 | T | G | 25 | a0001c0004t0003g0041 a0001c0004t0003g0042 a0001c0004t0003g0043 others(22): Show |
25 | HG01884.hp1 HG02280.hp1 HG02559.hp1 others(22): Show |
intron_variant | MODIFIER | c.1331+4946T>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41737549 | |||||||
chr22:41737563 | T | C | 6 | a0001c0002t0002g0055 a0001c0002t0002g0070 a0001c0002t0002g0071 others(3): Show |
6 | HG00323.hp2 HG01070.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1331+4960T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41737563 | |||||||
chr22:41737704 | G | A | 1 | a0001c0001t0001g0250 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1331+5101G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41737704 | |||||||
chr22:41737771 | T | A | 1 | a0001c0002t0002g0102 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1331+5168T>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41737771 | |||||||
chr22:41737824 | A | G | 1 | a0001c0002t0002g0082 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1331+5221A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41737824 | |||||||
chr22:41737910 | T | TA | 39 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0098 others(36): Show |
40 | HG01109.hp1 HG01884.hp1 HG02257.hp2 others(37): Show |
intron_variant | MODIFIER | c.1332-5164dupA | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr22 | 41737910 | ||||||
chr22:41737917 | T | A | 197 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(194): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.1332-5163T>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41737917 | |||||||
chr22:41737920 | T | A | 1 | a0001c0001t0001g0146 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1332-5160T>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41737920 | |||||||
chr22:41737979 | C | A | 1 | a0009c0019t0001g0104 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1332-5101C>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41737979 | |||||||
chr22:41738107 | G | A | 1 | a0001c0001t0001g0132 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1332-4973G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41738107 | |||||||
chr22:41738385 | G | A | 1 | a0001c0002t0002g0049 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1332-4695G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41738385 | |||||||
chr22:41738392 | G | A | 1 | a0001c0003t0004g0027 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1332-4688G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41738392 | |||||||
chr22:41738490 | G | C | 1 | a0001c0001t0001g0143 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1332-4590G>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41738490 | |||||||
chr22:41738535 | C | T | 21 | a0001c0001t0001g0127 a0001c0001t0001g0130 a0001c0001t0001g0131 others(18): Show |
21 | HG00099.hp2 HG00621.hp2 HG01981.hp2 others(18): Show |
intron_variant | MODIFIER | c.1332-4545C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41738535 | |||||||
chr22:41738632 | C | T | 1 | a0001c0001t0001g0247 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1332-4448C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41738632 | |||||||
chr22:41738770 | C | CA | 9 | a0001c0003t0004g0017 a0001c0003t0004g0018 a0001c0003t0004g0019 others(6): Show |
9 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.1332-4299dupA | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr22 | 41738770 | ||||||
chr22:41738778 | A | T | 6 | a0001c0002t0002g0058 a0001c0002t0002g0060 a0001c0002t0002g0061 others(3): Show |
6 | HG00597.hp2 HG00609.hp2 HG00621.hp1 others(3): Show |
intron_variant | MODIFIER | c.1332-4302A>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41738778 | |||||||
chr22:41738779 | AAATAAAT | A | 6 | a0001c0003t0004g0005 a0001c0003t0004g0006 a0001c0003t0004g0007 others(3): Show |
6 | HG02109.hp2 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1332-4298_1332-429 others(11): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr22 | 41738779 | ||||||
chr22:41738780 | A | C | 1 | a0001c0001t0001g0153 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1332-4300A>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41738780 | |||||||
chr22:41738782 | T | A | 1 | a0001c0004t0003g0114 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1332-4298T>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41738782 | |||||||
chr22:41738786 | T | A | 176 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(173): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.1332-4294T>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41738786 | |||||||
chr22:41738809 | A | G | 3 | a0001c0001t0001g0170 a0001c0001t0001g0210 a0001c0001t0001g0221 |
3 | HG00597.hp1 HG02129.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.1332-4271A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41738809 | |||||||
chr22:41738810 | T | TAAAATA | 207 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(204): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.1332-4267_1332-426 others(10): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr22 | 41738810 | ||||||
chr22:41738891 | T | C | 207 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(204): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.1332-4189T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41738891 | |||||||
chr22:41738927 | G | A | 75 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0098 others(72): Show |
76 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.1332-4153G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41738927 | |||||||
chr22:41738986 | A | C | 2 | a0001c0002t0002g0073 a0001c0002t0002g0103 |
2 | HG00741.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.1332-4094A>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41738986 | |||||||
chr22:41739033 | G | A | 1 | a0001c0001t0001g0196 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1332-4047G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41739033 | |||||||
chr22:41739140 | CA | C | 173 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(170): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.1332-3926delA | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr22 | 41739140 | ||||||
chr22:41739155 | T | C | 1 | a0001c0004t0003g0118 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1332-3925T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41739155 | |||||||
chr22:41739357 | C | G | 1 | a0002c0005t0001g0040 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1332-3723C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41739357 | |||||||
chr22:41739381 | C | G | 1 | a0001c0004t0006g0124 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1332-3699C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41739381 | |||||||
chr22:41739481 | T | A | 36 | a0001c0003t0004g0005 a0001c0003t0004g0006 a0001c0003t0004g0007 others(33): Show |
36 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.1332-3599T>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41739481 | |||||||
chr22:41739548 | T | TAAAAATT others(315): Show |
1 | a0001c0004t0003g0118 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1332-3519_1332-351 others(326): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr22 | 41739548 | ||||||
chr22:41739548 | T | TAAAAATT others(316): Show |
8 | a0001c0004t0003g0113 a0001c0004t0003g0116 a0001c0004t0003g0119 others(5): Show |
8 | HG02886.hp2 HG02895.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1332-3519_1332-351 others(327): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr22 | 41739548 | ||||||
chr22:41739548 | T | TAAAAATT others(317): Show |
12 | a0001c0004t0003g0041 a0001c0004t0003g0042 a0001c0004t0003g0043 others(9): Show |
12 | HG01884.hp1 HG02280.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1332-3519_1332-351 others(328): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr22 | 41739548 | ||||||
chr22:41739548 | T | TAAAAATT others(318): Show |
4 | a0001c0008t0003g0111 a0001c0011t0003g0115 a0001c0011t0003g0121 others(1): Show |
4 | HG02559.hp1 HG02976.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1332-3519_1332-351 others(329): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr22 | 41739548 | ||||||
chr22:41739747 | T | C | 207 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(204): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.1332-3333T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41739747 | |||||||
chr22:41740036 | G | A | 2 | a0001c0001t0001g0003 a0001c0001t0001g0231 |
3 | HG01433.hp2 NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1332-3044G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41740036 | |||||||
chr22:41740036 | G | C | 1 | a0003c0006t0001g0069 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1332-3044G>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41740036 | |||||||
chr22:41740036 | G | T | 2 | a0001c0001t0001g0172 a0001c0001t0001g0224 |
2 | NA18968.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.1332-3044G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41740036 | |||||||
chr22:41740038 | G | A | 25 | a0001c0004t0003g0041 a0001c0004t0003g0042 a0001c0004t0003g0043 others(22): Show |
25 | HG01884.hp1 HG02280.hp1 HG02559.hp1 others(22): Show |
intron_variant | MODIFIER | c.1332-3042G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41740038 | |||||||
chr22:41740062 | C | T | 75 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0098 others(72): Show |
76 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.1332-3018C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41740062 | |||||||
chr22:41740089 | G | A | 3 | a0001c0001t0001g0196 a0001c0001t0001g0247 a0001c0001t0001g0248 |
3 | HG00621.hp2 NA18747.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1332-2991G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41740089 | |||||||
chr22:41740144 | C | A | 36 | a0001c0003t0004g0005 a0001c0003t0004g0006 a0001c0003t0004g0007 others(33): Show |
36 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.1332-2936C>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41740144 | |||||||
chr22:41740145 | G | A | 2 | a0001c0001t0001g0167 a0001c0004t0003g0114 |
2 | HG01884.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.1332-2935G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41740145 | |||||||
chr22:41740314 | G | A | 5 | a0001c0004t0003g0041 a0001c0004t0003g0042 a0001c0004t0003g0043 others(2): Show |
5 | HG02280.hp1 HG02723.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1332-2766G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41740314 | |||||||
chr22:41740596 | G | C | 6 | a0001c0003t0004g0005 a0001c0003t0004g0006 a0001c0003t0004g0007 others(3): Show |
6 | HG02109.hp2 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1332-2484G>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41740596 | |||||||
chr22:41740614 | C | T | 75 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0098 others(72): Show |
76 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.1332-2466C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41740614 | |||||||
chr22:41740645 | G | T | 1 | a0001c0018t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1332-2435G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41740645 | |||||||
chr22:41740715 | G | C | 1 | a0001c0001t0001g0138 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1332-2365G>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41740715 | |||||||
chr22:41740728 | T | TCAAAAA | 13 | a0001c0003t0004g0005 a0001c0003t0004g0006 a0001c0003t0004g0007 others(10): Show |
13 | HG02109.hp2 HG02451.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1332-2329_1332-232 others(10): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr22 | 41740728 | ||||||
chr22:41740728 | TCAAAAAC others(5): Show |
T | 1 | a0001c0001t0001g0222 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1332-2335_1332-232 others(16): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr22 | 41740728 | ||||||
chr22:41740764 | A | C | 16 | a0001c0003t0004g0017 a0001c0003t0004g0018 a0001c0003t0004g0019 others(13): Show |
16 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.1332-2316A>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41740764 | |||||||
chr22:41740926 | T | C | 207 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(204): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.1332-2154T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41740926 | |||||||
chr22:41741178 | C | T | 8 | a0002c0005t0001g0028 a0002c0005t0001g0029 a0002c0005t0001g0030 others(5): Show |
8 | HG00673.hp2 HG01109.hp2 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.1332-1902C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41741178 | |||||||
chr22:41741179 | G | A | 1 | a0001c0001t0001g0169 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1332-1901G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41741179 | |||||||
chr22:41741456 | T | C | 3 | a0001c0002t0002g0058 a0001c0002t0002g0060 a0001c0002t0002g0064 |
3 | HG00597.hp2 HG00609.hp2 HG00621.hp1 |
intron_variant | MODIFIER | c.1332-1624T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41741456 | |||||||
chr22:41741688 | G | C | 1 | a0001c0018t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1332-1392G>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41741688 | |||||||
chr22:41741747 | G | A | 1 | a0001c0004t0003g0118 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1332-1333G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41741747 | |||||||
chr22:41741869 | G | A | 1 | a0001c0018t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1332-1211G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41741869 | |||||||
chr22:41741942 | C | CA | 50 | a0001c0002t0002g0078 a0001c0003t0001g0096 a0001c0003t0001g0097 others(47): Show |
51 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(48): Show |
intron_variant | MODIFIER | c.1332-1120dupA | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr22 | 41741942 | ||||||
chr22:41741942 | CA | C | 127 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(124): Show |
129 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(126): Show |
intron_variant | MODIFIER | c.1332-1120delA | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr22 | 41741942 | ||||||
chr22:41741942 | CAAAAAAA | C | 20 | a0001c0003t0004g0005 a0001c0003t0004g0006 a0001c0003t0004g0007 others(17): Show |
20 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(17): Show |
intron_variant | MODIFIER | c.1332-1126_1332-112 others(11): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr22 | 41741942 | ||||||
chr22:41741997 | A | G | 1 | a0001c0018t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1332-1083A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41741997 | |||||||
chr22:41742102 | G | A | 201 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(198): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.1332-978G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41742102 | |||||||
chr22:41742102 | G | T | 6 | a0001c0003t0004g0005 a0001c0003t0004g0006 a0001c0003t0004g0007 others(3): Show |
6 | HG02109.hp2 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1332-978G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41742102 | |||||||
chr22:41742142 | C | T | 1 | a0008c0021t0001g0129 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1332-938C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41742142 | |||||||
chr22:41742175 | G | A | 4 | a0003c0006t0001g0090 a0003c0006t0001g0091 a0003c0006t0001g0095 others(1): Show |
4 | HG01109.hp1 HG02970.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1332-905G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41742175 | |||||||
chr22:41742176 | C | T | 4 | a0003c0006t0001g0090 a0003c0006t0001g0091 a0003c0006t0001g0095 others(1): Show |
4 | HG01109.hp1 HG02970.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1332-904C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41742176 | |||||||
chr22:41742196 | G | T | 132 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(129): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.1332-884G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41742196 | |||||||
chr22:41742264 | T | C | 9 | a0003c0006t0001g0002 a0003c0006t0001g0069 a0003c0006t0001g0090 others(6): Show |
10 | HG01109.hp1 HG02258.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.1332-816T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41742264 | |||||||
chr22:41742489 | A | T | 4 | a0004c0009t0001g0004 a0004c0009t0001g0142 a0004c0009t0001g0237 others(1): Show |
5 | HG01934.hp1 HG02280.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1332-591A>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41742489 | |||||||
chr22:41742525 | C | T | 5 | a0003c0006t0001g0002 a0003c0006t0001g0069 a0003c0006t0001g0092 others(2): Show |
6 | HG02258.hp2 HG02965.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1332-555C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41742525 | |||||||
chr22:41742852 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1332-228C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41742852 | |||||||
chr22:41743039 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1332-41G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41743039 | |||||||
chr22:41743050 | G | A | 207 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(204): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.1332-30G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41743050 | |||||||
chr22:41743074 | A | G | 207 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(204): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
splice_region_variant&intron_variant | LOW | c.1332-6A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 11/30 | chr22 | 41743074 | |||||||
chr22:41743211 | C | T | 4 | a0003c0006t0001g0090 a0003c0006t0001g0091 a0003c0006t0001g0095 others(1): Show |
4 | HG01109.hp1 HG02970.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1446+17C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 12/30 | chr22 | 41743211 | |||||||
chr22:41743264 | A | G | 1 | a0001c0018t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1446+70A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 12/30 | chr22 | 41743264 | |||||||
chr22:41743457 | GA | G | 207 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(204): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.1446+265delA | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 12/30 | INFO_REALIGN_3_PRIME | chr22 | 41743457 | ||||||
chr22:41743497 | A | G | 207 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(204): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.1446+303A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 12/30 | chr22 | 41743497 | |||||||
chr22:41743651 | G | C | 1 | a0001c0001t0001g0136 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1446+457G>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 12/30 | chr22 | 41743651 | |||||||
chr22:41743857 | G | T | 1 | a0001c0001t0001g0220 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1446+663G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 12/30 | chr22 | 41743857 | |||||||
chr22:41743879 | A | AT | 7 | a0001c0003t0004g0021 a0005c0007t0004g0011 a0005c0007t0004g0012 others(4): Show |
7 | HG01496.hp1 HG02451.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1446+696dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 12/30 | INFO_REALIGN_3_PRIME | chr22 | 41743879 | ||||||
chr22:41743940 | G | A | 1 | a0001c0003t0004g0017 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1446+746G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 12/30 | chr22 | 41743940 | |||||||
chr22:41744156 | C | T | 131 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(128): Show |
133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.1447-817C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 12/30 | chr22 | 41744156 | |||||||
chr22:41744361 | A | G | 5 | a0001c0004t0003g0112 a0001c0004t0003g0122 a0001c0004t0003g0123 others(2): Show |
5 | HG02723.hp2 HG02895.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1447-612A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 12/30 | chr22 | 41744361 | |||||||
chr22:41744474 | GCTATGAT others(315): Show |
G | 207 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(204): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.1447-485_1447-164d others(2): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 12/30 | INFO_REALIGN_3_PRIME | chr22 | 41744474 | ||||||
chr22:41744480 | A | AT | 17 | a0001c0002t0002g0001 a0001c0002t0002g0048 a0001c0002t0002g0049 others(14): Show |
17 | HG00597.hp2 HG00621.hp1 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.1447-458dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 12/30 | INFO_REALIGN_3_PRIME | chr22 | 41744480 | ||||||
chr22:41744480 | A | ATTT | 5 | a0001c0002t0002g0056 a0001c0002t0002g0073 a0001c0002t0002g0076 others(2): Show |
5 | HG00639.hp2 HG00741.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.1447-460_1447-458d others(5): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 12/30 | INFO_REALIGN_3_PRIME | chr22 | 41744480 | ||||||
chr22:41745129 | T | C | 1 | a0001c0018t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1538+65T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 13/30 | chr22 | 41745129 | |||||||
chr22:41745238 | C | T | 2 | a0001c0001t0001g0250 a0001c0001t0001g0251 |
2 | HG02027.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.1538+174C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 13/30 | chr22 | 41745238 | |||||||
chr22:41745322 | G | A | 1 | a0001c0001t0002g0201 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1538+258G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 13/30 | chr22 | 41745322 | |||||||
chr22:41745448 | A | G | 207 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(204): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.1538+384A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 13/30 | chr22 | 41745448 | |||||||
chr22:41745636 | G | A | 207 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(204): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.1539-249G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 13/30 | chr22 | 41745636 | |||||||
chr22:41745729 | C | T | 1 | a0001c0004t0003g0116 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1539-156C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 13/30 | chr22 | 41745729 | |||||||
chr22:41745867 | C | CA | 22 | a0001c0001t0001g0127 a0001c0001t0001g0130 a0001c0001t0001g0131 others(19): Show |
22 | HG00099.hp2 HG00621.hp2 HG01258.hp2 others(19): Show |
intron_variant | MODIFIER | c.1539-17dupA | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 13/30 | INFO_REALIGN_3_PRIME | chr22 | 41745867 | ||||||
chr22:41746244 | T | C | 5 | a0005c0007t0004g0011 a0005c0007t0004g0012 a0005c0007t0004g0013 others(2): Show |
5 | HG02451.hp2 HG02809.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1680+218T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 14/30 | chr22 | 41746244 | |||||||
chr22:41746302 | T | C | 207 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(204): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.1680+276T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 14/30 | chr22 | 41746302 | |||||||
chr22:41746382 | G | A | 206 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(203): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.1680+356G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 14/30 | chr22 | 41746382 | |||||||
chr22:41746389 | T | C | 1 | a0001c0001t0001g0164 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1680+363T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 14/30 | chr22 | 41746389 | |||||||
chr22:41746642 | T | C | 2 | a0001c0001t0001g0136 a0001c0001t0001g0137 |
2 | NA18980.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.1680+616T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 14/30 | chr22 | 41746642 | |||||||
chr22:41746713 | G | A | 1 | a0001c0018t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1680+687G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 14/30 | chr22 | 41746713 | |||||||
chr22:41746721 | G | A | 13 | a0002c0005t0001g0028 a0002c0005t0001g0029 a0002c0005t0001g0030 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.1680+695G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 14/30 | chr22 | 41746721 | |||||||
chr22:41746817 | G | C | 1 | a0001c0001t0001g0147 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1680+791G>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 14/30 | chr22 | 41746817 | |||||||
chr22:41746993 | CTTCT | C | 13 | a0002c0005t0001g0028 a0002c0005t0001g0029 a0002c0005t0001g0030 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.1680+972_1680+975d others(6): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 14/30 | INFO_REALIGN_3_PRIME | chr22 | 41746993 | ||||||
chr22:41747039 | A | G | 1 | a0001c0003t0004g0027 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1680+1013A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 14/30 | chr22 | 41747039 | |||||||
chr22:41747049 | T | TATAATA | 132 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(129): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.1680+1037_1681-103 others(10): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 14/30 | INFO_REALIGN_3_PRIME | chr22 | 41747049 | ||||||
chr22:41747049 | T | TATAATAA others(2): Show |
3 | a0001c0001t0001g0136 a0001c0001t0001g0179 a0001c0001t0001g0195 |
3 | NA18999.hp1 NA19060.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1680+1034_1681-103 others(13): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 14/30 | INFO_REALIGN_3_PRIME | chr22 | 41747049 | ||||||
chr22:41747237 | C | CT | 8 | a0001c0003t0004g0005 a0001c0003t0004g0006 a0001c0003t0004g0007 others(5): Show |
8 | HG01496.hp1 HG02109.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1681-855dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 14/30 | INFO_REALIGN_3_PRIME | chr22 | 41747237 | ||||||
chr22:41747237 | C | CTT | 15 | a0001c0003t0004g0017 a0001c0003t0004g0018 a0001c0003t0004g0019 others(12): Show |
15 | HG00639.hp1 HG01243.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1681-856_1681-855d others(4): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 14/30 | INFO_REALIGN_3_PRIME | chr22 | 41747237 | ||||||
chr22:41747237 | CT | C | 9 | a0001c0001t0001g0143 a0001c0001t0001g0152 a0001c0001t0001g0175 others(6): Show |
9 | HG00323.hp1 HG00738.hp1 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.1681-855delT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 14/30 | INFO_REALIGN_3_PRIME | chr22 | 41747237 | ||||||
chr22:41747425 | C | T | 13 | a0002c0005t0001g0028 a0002c0005t0001g0029 a0002c0005t0001g0030 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.1681-682C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 14/30 | chr22 | 41747425 | |||||||
chr22:41747524 | C | T | 1 | a0001c0003t0004g0017 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1681-583C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 14/30 | chr22 | 41747524 | |||||||
chr22:41747533 | G | A | 132 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(129): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.1681-574G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 14/30 | chr22 | 41747533 | |||||||
chr22:41747568 | A | G | 207 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(204): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.1681-539A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 14/30 | chr22 | 41747568 | |||||||
chr22:41747595 | C | G | 25 | a0001c0004t0003g0041 a0001c0004t0003g0042 a0001c0004t0003g0043 others(22): Show |
25 | HG01884.hp1 HG02280.hp1 HG02559.hp1 others(22): Show |
intron_variant | MODIFIER | c.1681-512C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 14/30 | chr22 | 41747595 | |||||||
chr22:41747645 | A | G | 3 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0098 |
3 | HG02257.hp2 HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1681-462A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 14/30 | chr22 | 41747645 | |||||||
chr22:41747736 | C | A | 206 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(203): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.1681-371C>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 14/30 | chr22 | 41747736 | |||||||
chr22:41747770 | A | G | 4 | a0003c0006t0001g0090 a0003c0006t0001g0091 a0003c0006t0001g0095 others(1): Show |
4 | HG01109.hp1 HG02970.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1681-337A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 14/30 | chr22 | 41747770 | |||||||
chr22:41747942 | C | T | 1 | a0001c0001t0001g0244 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1681-165C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 14/30 | chr22 | 41747942 | |||||||
chr22:41748368 | G | A | 7 | a0001c0001t0001g0197 a0001c0001t0001g0200 a0001c0001t0001g0236 others(4): Show |
7 | HG00099.hp2 HG01258.hp2 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.1792+150G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41748368 | |||||||
chr22:41748508 | A | AC | 157 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(154): Show |
159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.1792+294dupC | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr22 | 41748508 | ||||||
chr22:41748768 | C | T | 13 | a0002c0005t0001g0028 a0002c0005t0001g0029 a0002c0005t0001g0030 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.1792+550C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41748768 | |||||||
chr22:41748812 | T | G | 1 | a0001c0003t0004g0025 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1792+594T>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41748812 | |||||||
chr22:41748834 | C | T | 1 | a0009c0019t0001g0104 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1792+616C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41748834 | |||||||
chr22:41748835 | G | A | 2 | a0001c0001t0001g0199 a0001c0002t0002g0050 |
2 | HG02148.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1792+617G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41748835 | |||||||
chr22:41748922 | C | T | 9 | a0003c0006t0001g0002 a0003c0006t0001g0069 a0003c0006t0001g0090 others(6): Show |
10 | HG01109.hp1 HG02258.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.1792+704C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41748922 | |||||||
chr22:41748923 | G | A | 132 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(129): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.1792+705G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41748923 | |||||||
chr22:41749040 | G | A | 16 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0098 others(13): Show |
16 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(13): Show |
intron_variant | MODIFIER | c.1792+822G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41749040 | |||||||
chr22:41749151 | A | C | 2 | a0001c0012t0001g0182 a0001c0012t0001g0190 |
2 | HG02615.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1792+933A>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41749151 | |||||||
chr22:41749177 | A | G | 12 | a0001c0004t0003g0112 a0001c0004t0003g0113 a0001c0004t0003g0116 others(9): Show |
12 | HG02723.hp2 HG02886.hp2 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.1792+959A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41749177 | |||||||
chr22:41749249 | G | T | 1 | a0003c0006t0001g0090 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1792+1031G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41749249 | |||||||
chr22:41749256 | A | G | 12 | a0002c0005t0001g0028 a0002c0005t0001g0029 a0002c0005t0001g0030 others(9): Show |
12 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(9): Show |
intron_variant | MODIFIER | c.1792+1038A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41749256 | |||||||
chr22:41749279 | CT | C | 206 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(203): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.1792+1074delT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr22 | 41749279 | ||||||
chr22:41749292 | T | G | 6 | a0001c0003t0004g0005 a0001c0003t0004g0006 a0001c0003t0004g0007 others(3): Show |
6 | HG02109.hp2 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1792+1074T>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41749292 | |||||||
chr22:41749361 | C | T | 2 | a0001c0008t0003g0106 a0001c0008t0003g0108 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1792+1143C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41749361 | |||||||
chr22:41749368 | C | T | 9 | a0003c0006t0001g0002 a0003c0006t0001g0069 a0003c0006t0001g0090 others(6): Show |
10 | HG01109.hp1 HG02258.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.1792+1150C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41749368 | |||||||
chr22:41749600 | T | G | 2 | a0001c0003t0004g0008 a0001c0003t0004g0009 |
2 | HG03195.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1792+1382T>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41749600 | |||||||
chr22:41749887 | G | T | 1 | a0001c0002t0002g0102 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1792+1669G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41749887 | |||||||
chr22:41749932 | A | G | 3 | a0001c0001t0001g0150 a0001c0001t0001g0158 a0001c0001t0001g0159 |
3 | HG00099.hp1 HG01257.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1792+1714A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41749932 | |||||||
chr22:41749979 | CTG | C | 5 | a0001c0002t0002g0058 a0001c0002t0002g0060 a0001c0002t0002g0061 others(2): Show |
5 | HG00597.hp2 HG00609.hp2 HG00621.hp1 others(2): Show |
intron_variant | MODIFIER | c.1792+1765_1792+176 others(6): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr22 | 41749979 | ||||||
chr22:41750156 | A | C | 13 | a0002c0005t0001g0028 a0002c0005t0001g0029 a0002c0005t0001g0030 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.1792+1938A>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41750156 | |||||||
chr22:41750297 | C | T | 1 | a0001c0004t0003g0116 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1792+2079C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41750297 | |||||||
chr22:41750375 | A | G | 3 | a0005c0007t0004g0011 a0005c0007t0004g0013 a0011c0014t0004g0014 |
3 | HG02809.hp2 HG03098.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1792+2157A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41750375 | |||||||
chr22:41750672 | G | A | 25 | a0001c0004t0003g0041 a0001c0004t0003g0042 a0001c0004t0003g0043 others(22): Show |
25 | HG01884.hp1 HG02280.hp1 HG02559.hp1 others(22): Show |
intron_variant | MODIFIER | c.1793-1919G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41750672 | |||||||
chr22:41750912 | T | G | 4 | a0004c0009t0001g0004 a0004c0009t0001g0142 a0004c0009t0001g0237 others(1): Show |
5 | HG01934.hp1 HG02280.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1793-1679T>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41750912 | |||||||
chr22:41751071 | A | G | 4 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0098 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1793-1520A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41751071 | |||||||
chr22:41751073 | C | T | 1 | a0001c0001t0001g0227 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1793-1518C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41751073 | |||||||
chr22:41751175 | G | A | 47 | a0001c0001t0001g0003 a0001c0001t0001g0133 a0001c0001t0001g0139 others(44): Show |
49 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.1793-1416G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41751175 | |||||||
chr22:41751208 | C | T | 1 | a0001c0002t0002g0103 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1793-1383C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41751208 | |||||||
chr22:41751467 | GC | G | 62 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0098 others(59): Show |
63 | HG00639.hp1 HG01109.hp1 HG01243.hp1 others(60): Show |
intron_variant | MODIFIER | c.1793-1122delC | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr22 | 41751467 | ||||||
chr22:41751623 | T | C | 1 | a0001c0001t0001g0244 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1793-968T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41751623 | |||||||
chr22:41751641 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1793-950G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41751641 | |||||||
chr22:41751721 | A | G | 207 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(204): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.1793-870A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41751721 | |||||||
chr22:41751727 | G | A | 1 | a0001c0004t0003g0114 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1793-864G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41751727 | |||||||
chr22:41751772 | T | TA | 135 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(132): Show |
137 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.1793-802dupA | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr22 | 41751772 | ||||||
chr22:41751772 | T | TAA | 27 | a0001c0001t0001g0141 a0001c0001t0001g0153 a0001c0001t0001g0164 others(24): Show |
27 | HG00140.hp2 HG00639.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.1793-803_1793-802d others(4): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr22 | 41751772 | ||||||
chr22:41751776 | A | AG | 7 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0228 others(4): Show |
7 | HG00140.hp1 HG00735.hp1 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.1793-815_1793-814i others(3): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41751776 | |||||||
chr22:41752071 | G | GA | 9 | a0003c0006t0001g0002 a0003c0006t0001g0069 a0003c0006t0001g0090 others(6): Show |
10 | HG01109.hp1 HG02258.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.1793-507dupA | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr22 | 41752071 | ||||||
chr22:41752072 | A | G | 16 | a0001c0003t0004g0017 a0001c0003t0004g0018 a0001c0003t0004g0019 others(13): Show |
16 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.1793-519A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41752072 | |||||||
chr22:41752312 | T | C | 23 | a0001c0003t0004g0005 a0001c0003t0004g0006 a0001c0003t0004g0007 others(20): Show |
23 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.1793-279T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41752312 | |||||||
chr22:41752314 | T | C | 1 | a0001c0001t0001g0168 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1793-277T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41752314 | |||||||
chr22:41752463 | G | A | 207 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(204): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.1793-128G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 15/30 | chr22 | 41752463 | |||||||
chr22:41752674 | T | C | 1 | a0001c0018t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1853+23T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 16/30 | chr22 | 41752674 | |||||||
chr22:41752771 | G | A | 23 | a0001c0003t0004g0005 a0001c0003t0004g0006 a0001c0003t0004g0007 others(20): Show |
23 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.1853+120G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 16/30 | chr22 | 41752771 | |||||||
chr22:41753020 | A | AT | 11 | a0001c0001t0001g0127 a0001c0001t0001g0148 a0001c0001t0001g0164 others(8): Show |
11 | HG00140.hp2 HG00423.hp2 HG00639.hp2 others(8): Show |
intron_variant | MODIFIER | c.1853+385dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 16/30 | INFO_REALIGN_3_PRIME | chr22 | 41753020 | ||||||
chr22:41753364 | C | T | 1 | a0001c0003t0004g0027 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1854-585C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 16/30 | chr22 | 41753364 | |||||||
chr22:41753488 | A | G | 1 | a0001c0002t0002g0082 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1854-461A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 16/30 | chr22 | 41753488 | |||||||
chr22:41753566 | G | A | 3 | a0001c0001t0001g0207 a0001c0001t0001g0209 a0001c0018t0001g0089 |
3 | HG01169.hp1 HG01169.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1854-383G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 16/30 | chr22 | 41753566 | |||||||
chr22:41753636 | C | T | 1 | a0001c0018t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1854-313C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 16/30 | chr22 | 41753636 | |||||||
chr22:41754122 | A | G | 1 | a0001c0003t0004g0025 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1951+76A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | chr22 | 41754122 | |||||||
chr22:41754142 | C | T | 207 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(204): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.1951+96C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | chr22 | 41754142 | |||||||
chr22:41754390 | CTTCA | C | 9 | a0003c0006t0001g0002 a0003c0006t0001g0069 a0003c0006t0001g0090 others(6): Show |
10 | HG01109.hp1 HG02258.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.1951+353_1951+356d others(6): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr22 | 41754390 | ||||||
chr22:41754406 | A | C | 4 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0001g0245 others(1): Show |
4 | HG02630.hp2 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1951+360A>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | chr22 | 41754406 | |||||||
chr22:41754414 | TTTTTTC | T | 62 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0098 others(59): Show |
63 | HG00639.hp1 HG01109.hp1 HG01243.hp1 others(60): Show |
intron_variant | MODIFIER | c.1951+386_1951+391d others(8): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr22 | 41754414 | ||||||
chr22:41754624 | G | T | 1 | a0010c0016t0003g0117 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1951+578G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | chr22 | 41754624 | |||||||
chr22:41755057 | G | C | 1 | a0006c0010t0001g0234 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1951+1011G>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | chr22 | 41755057 | |||||||
chr22:41755068 | C | G | 1 | a0001c0002t0002g0086 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1951+1022C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | chr22 | 41755068 | |||||||
chr22:41755138 | A | T | 1 | a0001c0022t0001g0238 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1951+1092A>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | chr22 | 41755138 | |||||||
chr22:41755225 | C | T | 9 | a0003c0006t0001g0002 a0003c0006t0001g0069 a0003c0006t0001g0090 others(6): Show |
10 | HG01109.hp1 HG02258.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.1951+1179C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | chr22 | 41755225 | |||||||
chr22:41755334 | G | C | 4 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0098 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1951+1288G>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | chr22 | 41755334 | |||||||
chr22:41755347 | A | T | 13 | a0002c0005t0001g0028 a0002c0005t0001g0029 a0002c0005t0001g0030 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.1951+1301A>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | chr22 | 41755347 | |||||||
chr22:41755551 | C | T | 23 | a0001c0003t0004g0005 a0001c0003t0004g0006 a0001c0003t0004g0007 others(20): Show |
23 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.1951+1505C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | chr22 | 41755551 | |||||||
chr22:41755647 | G | T | 1 | a0001c0003t0004g0027 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1951+1601G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | chr22 | 41755647 | |||||||
chr22:41755676 | T | C | 3 | a0006c0010t0001g0177 a0006c0010t0001g0218 a0006c0010t0001g0234 |
3 | HG01243.hp2 HG02109.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1951+1630T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | chr22 | 41755676 | |||||||
chr22:41755943 | C | T | 36 | a0001c0003t0004g0005 a0001c0003t0004g0006 a0001c0003t0004g0007 others(33): Show |
36 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.1951+1897C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | chr22 | 41755943 | |||||||
chr22:41756176 | G | C | 1 | a0001c0002t0002g0073 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1951+2130G>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | chr22 | 41756176 | |||||||
chr22:41756181 | C | T | 9 | a0003c0006t0001g0002 a0003c0006t0001g0069 a0003c0006t0001g0090 others(6): Show |
10 | HG01109.hp1 HG02258.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.1951+2135C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | chr22 | 41756181 | |||||||
chr22:41756262 | A | G | 207 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(204): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.1952-2103A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | chr22 | 41756262 | |||||||
chr22:41756425 | C | T | 145 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(142): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.1952-1940C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | chr22 | 41756425 | |||||||
chr22:41756485 | T | C | 3 | a0001c0001t0005g0181 a0001c0001t0005g0188 a0001c0001t0005g0189 |
3 | HG01884.hp2 HG02258.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1952-1880T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | chr22 | 41756485 | |||||||
chr22:41756765 | C | T | 9 | a0003c0006t0001g0002 a0003c0006t0001g0069 a0003c0006t0001g0090 others(6): Show |
10 | HG01109.hp1 HG02258.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.1952-1600C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | chr22 | 41756765 | |||||||
chr22:41756984 | A | C | 55 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0128 others(52): Show |
55 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(52): Show |
intron_variant | MODIFIER | c.1952-1381A>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | chr22 | 41756984 | |||||||
chr22:41757093 | C | G | 2 | a0001c0001t0001g0186 a0001c0001t0001g0212 |
2 | HG00423.hp1 HG00558.hp1 |
intron_variant | MODIFIER | c.1952-1272C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | chr22 | 41757093 | |||||||
chr22:41757288 | T | G | 207 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(204): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.1952-1077T>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | chr22 | 41757288 | |||||||
chr22:41757365 | T | G | 3 | a0001c0001t0001g0196 a0001c0001t0001g0247 a0001c0001t0001g0248 |
3 | HG00621.hp2 NA18747.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1952-1000T>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | chr22 | 41757365 | |||||||
chr22:41757445 | C | T | 1 | a0001c0001t0001g0165 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1952-920C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | chr22 | 41757445 | |||||||
chr22:41757485 | G | A | 3 | a0001c0004t0003g0112 a0001c0004t0003g0122 a0001c0004t0003g0123 |
3 | HG02723.hp2 HG02895.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1952-880G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | chr22 | 41757485 | |||||||
chr22:41757506 | C | T | 13 | a0002c0005t0001g0028 a0002c0005t0001g0029 a0002c0005t0001g0030 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.1952-859C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | chr22 | 41757506 | |||||||
chr22:41757722 | A | G | 13 | a0002c0005t0001g0028 a0002c0005t0001g0029 a0002c0005t0001g0030 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.1952-643A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | chr22 | 41757722 | |||||||
chr22:41757783 | T | C | 30 | a0001c0001t0001g0138 a0001c0001t0001g0147 a0001c0001t0001g0169 others(27): Show |
30 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.1952-582T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | chr22 | 41757783 | |||||||
chr22:41757793 | G | T | 1 | a0001c0001t0001g0202 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1952-572G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | chr22 | 41757793 | |||||||
chr22:41757969 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1952-396G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | chr22 | 41757969 | |||||||
chr22:41758128 | G | A | 207 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(204): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.1952-237G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 17/30 | chr22 | 41758128 | |||||||
chr22:41758542 | A | G | 4 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0098 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.2120+9A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41758542 | |||||||
chr22:41758999 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2120+466C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41758999 | |||||||
chr22:41759040 | G | A | 7 | a0001c0003t0004g0005 a0001c0003t0004g0006 a0001c0003t0004g0007 others(4): Show |
7 | HG02109.hp2 HG02559.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.2120+507G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41759040 | |||||||
chr22:41759357 | C | T | 4 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0098 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.2120+824C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41759357 | |||||||
chr22:41759572 | G | A | 25 | a0001c0004t0003g0041 a0001c0004t0003g0042 a0001c0004t0003g0043 others(22): Show |
25 | HG01884.hp1 HG02280.hp1 HG02559.hp1 others(22): Show |
intron_variant | MODIFIER | c.2120+1039G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41759572 | |||||||
chr22:41759617 | G | A | 3 | a0001c0001t0001g0207 a0001c0001t0001g0209 a0009c0019t0001g0104 |
3 | HG01169.hp1 HG01169.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.2120+1084G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41759617 | |||||||
chr22:41759629 | C | CAATAAAT others(1): Show |
12 | a0001c0004t0003g0113 a0001c0004t0003g0116 a0001c0004t0003g0118 others(9): Show |
12 | HG02559.hp1 HG02572.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.2120+1098_2120+109 others(12): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | INFO_REALIGN_3_PRIME | chr22 | 41759629 | ||||||
chr22:41759629 | C | CAATAAAT others(5): Show |
4 | a0001c0004t0003g0112 a0001c0004t0003g0114 a0001c0004t0003g0123 others(1): Show |
4 | HG01884.hp1 HG02723.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.2120+1098_2120+109 others(16): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | INFO_REALIGN_3_PRIME | chr22 | 41759629 | ||||||
chr22:41759629 | C | CAATAAAT others(9): Show |
5 | a0001c0004t0003g0043 a0001c0004t0003g0122 a0001c0004t0006g0124 others(2): Show |
5 | HG02723.hp1 HG02896.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2120+1098_2120+109 others(20): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | INFO_REALIGN_3_PRIME | chr22 | 41759629 | ||||||
chr22:41759629 | C | CAATAAAT others(13): Show |
4 | a0001c0004t0003g0041 a0001c0004t0003g0042 a0001c0004t0003g0044 others(1): Show |
4 | HG02280.hp1 HG03041.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2120+1098_2120+109 others(24): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | INFO_REALIGN_3_PRIME | chr22 | 41759629 | ||||||
chr22:41759629 | CAAAA | C | 31 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0098 others(28): Show |
32 | HG00639.hp1 HG01109.hp1 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.2120+1099_2120+110 others(8): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | INFO_REALIGN_3_PRIME | chr22 | 41759629 | ||||||
chr22:41759632 | A | T | 31 | a0001c0004t0003g0041 a0001c0004t0003g0042 a0001c0004t0003g0043 others(28): Show |
31 | HG01884.hp1 HG02280.hp1 HG02451.hp2 others(28): Show |
intron_variant | MODIFIER | c.2120+1099A>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41759632 | |||||||
chr22:41759632 | AAAAT | A | 145 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(142): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.2120+1127_2120+113 others(8): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | INFO_REALIGN_3_PRIME | chr22 | 41759632 | ||||||
chr22:41759633 | A | AAATAAAT others(665): Show |
6 | a0005c0007t0004g0011 a0005c0007t0004g0012 a0005c0007t0004g0013 others(3): Show |
6 | HG02451.hp2 HG02809.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.2120+1126_2120+112 others(676): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | INFO_REALIGN_3_PRIME | chr22 | 41759633 | ||||||
chr22:41759681 | C | T | 1 | a0002c0005t0001g0040 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2120+1148C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41759681 | |||||||
chr22:41759895 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2120+1362C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41759895 | |||||||
chr22:41759896 | G | A | 1 | a0001c0001t0001g0149 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2120+1363G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41759896 | |||||||
chr22:41759904 | T | C | 1 | a0008c0021t0001g0129 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2120+1371T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41759904 | |||||||
chr22:41759940 | G | A | 23 | a0001c0003t0004g0005 a0001c0003t0004g0006 a0001c0003t0004g0007 others(20): Show |
23 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.2120+1407G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41759940 | |||||||
chr22:41760152 | A | G | 3 | a0002c0005t0001g0033 a0002c0005t0001g0036 a0002c0005t0001g0038 |
3 | HG00408.hp1 HG00423.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.2120+1619A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41760152 | |||||||
chr22:41760205 | G | T | 1 | a0003c0006t0001g0069 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2120+1672G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41760205 | |||||||
chr22:41760234 | T | A | 2 | a0001c0001t0001g0239 a0001c0001t0001g0240 |
2 | HG00099.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2120+1701T>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41760234 | |||||||
chr22:41760265 | G | A | 132 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(129): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.2120+1732G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41760265 | |||||||
chr22:41760339 | A | G | 23 | a0001c0003t0004g0005 a0001c0003t0004g0006 a0001c0003t0004g0007 others(20): Show |
23 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.2120+1806A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41760339 | |||||||
chr22:41760381 | C | T | 1 | a0001c0003t0004g0027 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2120+1848C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41760381 | |||||||
chr22:41760386 | G | A | 1 | a0001c0018t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2120+1853G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41760386 | |||||||
chr22:41760441 | G | A | 1 | a0001c0001t0001g0225 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2120+1908G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41760441 | |||||||
chr22:41760449 | C | G | 5 | a0003c0006t0001g0002 a0003c0006t0001g0069 a0003c0006t0001g0092 others(2): Show |
6 | HG02258.hp2 HG02965.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.2120+1916C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41760449 | |||||||
chr22:41760490 | C | T | 7 | a0001c0003t0004g0005 a0001c0003t0004g0006 a0001c0003t0004g0007 others(4): Show |
7 | HG02109.hp2 HG02559.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.2120+1957C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41760490 | |||||||
chr22:41760513 | A | G | 132 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(129): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.2120+1980A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41760513 | |||||||
chr22:41760544 | T | C | 35 | a0001c0004t0003g0041 a0001c0004t0003g0042 a0001c0004t0003g0043 others(32): Show |
36 | HG01109.hp1 HG01884.hp1 HG02258.hp2 others(33): Show |
intron_variant | MODIFIER | c.2120+2011T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41760544 | |||||||
chr22:41760557 | T | C | 207 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(204): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.2120+2024T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41760557 | |||||||
chr22:41760720 | G | C | 13 | a0002c0005t0001g0028 a0002c0005t0001g0029 a0002c0005t0001g0030 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.2120+2187G>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41760720 | |||||||
chr22:41760830 | G | T | 1 | a0001c0002t0002g0055 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.2120+2297G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41760830 | |||||||
chr22:41760852 | C | T | 1 | a0002c0005t0001g0036 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2120+2319C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41760852 | |||||||
chr22:41760960 | GT | G | 75 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0098 others(72): Show |
76 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.2121-2206delT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | INFO_REALIGN_3_PRIME | chr22 | 41760960 | ||||||
chr22:41761033 | C | T | 1 | a0008c0021t0001g0129 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2121-2141C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41761033 | |||||||
chr22:41761036 | G | T | 75 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0098 others(72): Show |
76 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.2121-2138G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41761036 | |||||||
chr22:41761040 | G | A | 1 | a0001c0001t0001g0215 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2121-2134G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41761040 | |||||||
chr22:41761077 | T | C | 207 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(204): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.2121-2097T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41761077 | |||||||
chr22:41761266 | G | C | 1 | a0001c0001t0001g0132 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2121-1908G>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41761266 | |||||||
chr22:41761306 | GTGTTTTT others(4): Show |
G | 2 | a0001c0002t0002g0072 a0001c0002t0002g0074 |
2 | HG00323.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2121-1855_2121-184 others(15): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | INFO_REALIGN_3_PRIME | chr22 | 41761306 | ||||||
chr22:41761308 | G | GT | 5 | a0001c0001t0001g0233 a0001c0002t0002g0058 a0001c0002t0002g0068 others(2): Show |
5 | HG00621.hp1 HG01175.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.2121-1856dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | INFO_REALIGN_3_PRIME | chr22 | 41761308 | ||||||
chr22:41761319 | G | T | 3 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0018t0001g0089 |
3 | HG00621.hp2 NA18906.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.2121-1855G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41761319 | |||||||
chr22:41761319 | GT | G | 174 | a0001c0001t0001g0003 a0001c0001t0001g0127 a0001c0001t0001g0131 others(171): Show |
176 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.2121-1842delT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | INFO_REALIGN_3_PRIME | chr22 | 41761319 | ||||||
chr22:41761320 | T | G | 1 | a0001c0018t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2121-1854T>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41761320 | |||||||
chr22:41761561 | G | T | 2 | a0001c0012t0001g0182 a0001c0012t0001g0190 |
2 | HG02615.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.2121-1613G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41761561 | |||||||
chr22:41761727 | A | T | 1 | a0001c0003t0004g0019 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2121-1447A>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41761727 | |||||||
chr22:41761731 | C | G | 25 | a0001c0004t0003g0041 a0001c0004t0003g0042 a0001c0004t0003g0043 others(22): Show |
25 | HG01884.hp1 HG02280.hp1 HG02559.hp1 others(22): Show |
intron_variant | MODIFIER | c.2121-1443C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41761731 | |||||||
chr22:41762150 | A | G | 1 | a0001c0004t0003g0118 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2121-1024A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41762150 | |||||||
chr22:41762198 | A | G | 1 | a0001c0004t0003g0118 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2121-976A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41762198 | |||||||
chr22:41762200 | T | C | 207 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(204): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.2121-974T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41762200 | |||||||
chr22:41762327 | T | C | 1 | a0001c0001t0001g0242 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2121-847T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41762327 | |||||||
chr22:41762416 | C | T | 23 | a0001c0003t0004g0005 a0001c0003t0004g0006 a0001c0003t0004g0007 others(20): Show |
23 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.2121-758C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41762416 | |||||||
chr22:41762549 | G | GT | 33 | a0001c0001t0001g0132 a0001c0001t0001g0138 a0001c0001t0001g0143 others(30): Show |
33 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.2121-625_2121-624i others(3): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41762549 | |||||||
chr22:41762549 | GA | G | 8 | a0001c0001t0001g0134 a0001c0001t0001g0151 a0001c0001t0001g0154 others(5): Show |
8 | HG01106.hp1 HG01358.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.2121-624delA | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41762549 | |||||||
chr22:41762550 | A | T | 199 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(196): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.2121-624A>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41762550 | |||||||
chr22:41762636 | C | A | 4 | a0002c0005t0001g0034 a0002c0005t0001g0035 a0002c0005t0001g0037 others(1): Show |
4 | HG00673.hp2 NA18994.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.2121-538C>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41762636 | |||||||
chr22:41763068 | A | G | 207 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(204): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.2121-106A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41763068 | |||||||
chr22:41763069 | T | C | 207 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(204): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.2121-105T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 18/30 | chr22 | 41763069 | |||||||
chr22:41763405 | T | C | 2 | a0001c0001t0001g0138 a0001c0001t0001g0252 |
2 | HG00544.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.2268+84T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41763405 | |||||||
chr22:41763438 | G | A | 2 | a0001c0004t0003g0113 a0001c0004t0006g0124 |
2 | HG02886.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2268+117G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41763438 | |||||||
chr22:41763530 | G | GATT | 207 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(204): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.2268+213_2268+215d others(5): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr22 | 41763530 | ||||||
chr22:41763577 | C | T | 5 | a0003c0006t0001g0002 a0003c0006t0001g0069 a0003c0006t0001g0092 others(2): Show |
6 | HG02258.hp2 HG02965.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.2268+256C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41763577 | |||||||
chr22:41763785 | C | A | 6 | a0001c0003t0004g0005 a0001c0003t0004g0006 a0001c0003t0004g0007 others(3): Show |
6 | HG02109.hp2 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2268+464C>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41763785 | |||||||
chr22:41763817 | A | G | 1 | a0001c0003t0004g0027 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2268+496A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41763817 | |||||||
chr22:41763943 | CT | C | 92 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(89): Show |
94 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(91): Show |
intron_variant | MODIFIER | c.2268+643delT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr22 | 41763943 | ||||||
chr22:41763943 | CTT | C | 50 | a0001c0001t0001g0135 a0001c0001t0001g0147 a0001c0001t0001g0153 others(47): Show |
50 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.2268+642_2268+643d others(4): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr22 | 41763943 | ||||||
chr22:41763943 | CTTT | C | 56 | a0001c0001t0001g0187 a0001c0003t0001g0096 a0001c0003t0001g0097 others(53): Show |
57 | HG01109.hp1 HG01243.hp1 HG01496.hp1 others(54): Show |
intron_variant | MODIFIER | c.2268+641_2268+643d others(5): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr22 | 41763943 | ||||||
chr22:41763970 | G | A | 13 | a0002c0005t0001g0028 a0002c0005t0001g0029 a0002c0005t0001g0030 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.2268+649G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41763970 | |||||||
chr22:41763977 | C | T | 3 | a0002c0005t0001g0033 a0002c0005t0001g0036 a0002c0005t0001g0038 |
3 | HG00408.hp1 HG00423.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.2268+656C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41763977 | |||||||
chr22:41764002 | AGTGGCAG others(7): Show |
A | 14 | a0001c0018t0001g0089 a0002c0005t0001g0028 a0002c0005t0001g0029 others(11): Show |
14 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(11): Show |
intron_variant | MODIFIER | c.2268+697_2268+710d others(16): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr22 | 41764002 | ||||||
chr22:41764046 | C | T | 132 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(129): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.2268+725C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41764046 | |||||||
chr22:41764150 | C | T | 4 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0098 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.2268+829C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41764150 | |||||||
chr22:41764378 | C | T | 1 | a0001c0001t0001g0172 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2268+1057C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41764378 | |||||||
chr22:41764508 | C | G | 1 | a0001c0004t0003g0116 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2268+1187C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41764508 | |||||||
chr22:41764596 | A | G | 1 | a0001c0001t0001g0157 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2268+1275A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41764596 | |||||||
chr22:41764799 | A | G | 9 | a0003c0006t0001g0002 a0003c0006t0001g0069 a0003c0006t0001g0090 others(6): Show |
10 | HG01109.hp1 HG02258.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.2268+1478A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41764799 | |||||||
chr22:41765030 | G | T | 1 | a0001c0002t0002g0076 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2268+1709G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41765030 | |||||||
chr22:41765109 | A | G | 6 | a0001c0001t0001g0147 a0001c0001t0001g0172 a0001c0001t0001g0174 others(3): Show |
6 | NA18947.hp1 NA18968.hp1 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.2268+1788A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41765109 | |||||||
chr22:41765132 | G | A | 1 | a0001c0002t0002g0073 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2268+1811G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41765132 | |||||||
chr22:41765423 | G | A | 9 | a0003c0006t0001g0002 a0003c0006t0001g0069 a0003c0006t0001g0090 others(6): Show |
10 | HG01109.hp1 HG02258.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.2268+2102G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41765423 | |||||||
chr22:41765684 | C | T | 1 | a0001c0003t0004g0024 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2268+2363C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41765684 | |||||||
chr22:41765794 | C | T | 9 | a0003c0006t0001g0002 a0003c0006t0001g0069 a0003c0006t0001g0090 others(6): Show |
10 | HG01109.hp1 HG02258.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.2268+2473C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41765794 | |||||||
chr22:41765883 | C | CT | 35 | a0001c0001t0001g0133 a0001c0001t0001g0141 a0001c0001t0001g0148 others(32): Show |
35 | HG00558.hp2 HG00609.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.2268+2587dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr22 | 41765883 | ||||||
chr22:41765883 | CT | C | 43 | a0001c0001t0001g0228 a0001c0002t0002g0057 a0001c0002t0002g0062 others(40): Show |
43 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(40): Show |
intron_variant | MODIFIER | c.2268+2587delT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr22 | 41765883 | ||||||
chr22:41765911 | A | G | 1 | a0005c0007t0004g0011 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2268+2590A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41765911 | |||||||
chr22:41765951 | C | T | 23 | a0001c0003t0004g0005 a0001c0003t0004g0006 a0001c0003t0004g0007 others(20): Show |
23 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.2268+2630C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41765951 | |||||||
chr22:41765976 | C | T | 1 | a0001c0004t0003g0114 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2268+2655C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41765976 | |||||||
chr22:41766127 | G | A | 9 | a0003c0006t0001g0002 a0003c0006t0001g0069 a0003c0006t0001g0090 others(6): Show |
10 | HG01109.hp1 HG02258.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.2268+2806G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41766127 | |||||||
chr22:41766169 | C | T | 1 | a0001c0001t0001g0248 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2268+2848C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41766169 | |||||||
chr22:41766185 | G | C | 206 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(203): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.2268+2864G>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41766185 | |||||||
chr22:41766185 | G | T | 1 | a0001c0001t0001g0160 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2268+2864G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41766185 | |||||||
chr22:41766186 | T | C | 1 | a0001c0001t0001g0160 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2268+2865T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41766186 | |||||||
chr22:41766297 | A | G | 4 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0098 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.2268+2976A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41766297 | |||||||
chr22:41766307 | G | A | 1 | a0001c0001t0001g0160 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2268+2986G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41766307 | |||||||
chr22:41766308 | A | T | 1 | a0001c0001t0001g0160 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2268+2987A>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41766308 | |||||||
chr22:41766310 | T | A | 1 | a0001c0001t0001g0160 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2268+2989T>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41766310 | |||||||
chr22:41766329 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2268+3008G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41766329 | |||||||
chr22:41766408 | G | T | 1 | a0001c0001t0001g0165 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2268+3087G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41766408 | |||||||
chr22:41766560 | T | G | 12 | a0001c0004t0003g0041 a0001c0004t0003g0042 a0001c0004t0003g0043 others(9): Show |
12 | HG02280.hp1 HG02723.hp1 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.2268+3239T>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41766560 | |||||||
chr22:41766665 | G | C | 1 | a0001c0001t0001g0131 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2268+3344G>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41766665 | |||||||
chr22:41766804 | T | A | 6 | a0001c0003t0004g0005 a0001c0003t0004g0006 a0001c0003t0004g0007 others(3): Show |
6 | HG02109.hp2 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2268+3483T>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41766804 | |||||||
chr22:41766856 | C | T | 13 | a0002c0005t0001g0028 a0002c0005t0001g0029 a0002c0005t0001g0030 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.2268+3535C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41766856 | |||||||
chr22:41767071 | G | A | 1 | a0008c0021t0001g0129 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2269-3615G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41767071 | |||||||
chr22:41767097 | A | G | 1 | a0005c0007t0004g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2269-3589A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41767097 | |||||||
chr22:41767255 | T | C | 26 | a0001c0001t0001g0202 a0001c0004t0003g0041 a0001c0004t0003g0042 others(23): Show |
26 | HG01099.hp2 HG01884.hp1 HG02280.hp1 others(23): Show |
intron_variant | MODIFIER | c.2269-3431T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41767255 | |||||||
chr22:41767301 | A | C | 1 | a0001c0002t0002g0078 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2269-3385A>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41767301 | |||||||
chr22:41767637 | T | C | 8 | a0001c0001t0001g0202 a0001c0004t0003g0113 a0001c0004t0003g0116 others(5): Show |
8 | HG01099.hp2 HG02886.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.2269-3049T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41767637 | |||||||
chr22:41768247 | C | T | 13 | a0002c0005t0001g0028 a0002c0005t0001g0029 a0002c0005t0001g0030 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.2269-2439C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41768247 | |||||||
chr22:41768301 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2269-2385G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41768301 | |||||||
chr22:41768361 | T | C | 13 | a0002c0005t0001g0028 a0002c0005t0001g0029 a0002c0005t0001g0030 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.2269-2325T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41768361 | |||||||
chr22:41768390 | CA | C | 200 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(197): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.2269-2280delA | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr22 | 41768390 | ||||||
chr22:41768501 | G | A | 1 | a0001c0004t0003g0114 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2269-2185G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41768501 | |||||||
chr22:41768507 | G | A | 1 | a0001c0018t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2269-2179G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41768507 | |||||||
chr22:41768512 | C | G | 207 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(204): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.2269-2174C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41768512 | |||||||
chr22:41768656 | T | C | 207 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(204): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.2269-2030T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41768656 | |||||||
chr22:41768720 | C | G | 13 | a0002c0005t0001g0028 a0002c0005t0001g0029 a0002c0005t0001g0030 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.2269-1966C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41768720 | |||||||
chr22:41768858 | A | G | 131 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(128): Show |
133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.2269-1828A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41768858 | |||||||
chr22:41769040 | C | G | 1 | a0005c0007t0004g0012 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2269-1646C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41769040 | |||||||
chr22:41769380 | A | T | 1 | a0001c0001t0001g0250 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2269-1306A>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41769380 | |||||||
chr22:41769476 | A | AT | 135 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(132): Show |
137 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(134): Show |
intron_variant | MODIFIER | c.2269-1197dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr22 | 41769476 | ||||||
chr22:41769476 | AT | A | 8 | a0001c0002t0002g0074 a0001c0008t0003g0106 a0001c0008t0003g0108 others(5): Show |
8 | HG00323.hp2 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2269-1197delT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr22 | 41769476 | ||||||
chr22:41769566 | G | A | 1 | a0001c0001t0001g0130 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2269-1120G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41769566 | |||||||
chr22:41769582 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2269-1104C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41769582 | |||||||
chr22:41769720 | C | A | 2 | a0001c0011t0003g0115 a0001c0011t0003g0121 |
2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2269-966C>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41769720 | |||||||
chr22:41769849 | A | G | 1 | a0001c0001t0001g0147 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2269-837A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41769849 | |||||||
chr22:41769922 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.2269-764G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41769922 | |||||||
chr22:41769929 | G | A | 1 | a0001c0002t0002g0052 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2269-757G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41769929 | |||||||
chr22:41769995 | A | G | 1 | a0001c0001t0001g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2269-691A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41769995 | |||||||
chr22:41770070 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2269-616G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41770070 | |||||||
chr22:41770083 | G | A | 1 | a0001c0018t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2269-603G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41770083 | |||||||
chr22:41770136 | G | GA | 13 | a0002c0005t0001g0028 a0002c0005t0001g0029 a0002c0005t0001g0030 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.2269-539dupA | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr22 | 41770136 | ||||||
chr22:41770185 | G | A | 1 | a0001c0018t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2269-501G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41770185 | |||||||
chr22:41770287 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2269-399A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41770287 | |||||||
chr22:41770412 | A | G | 48 | a0001c0001t0001g0003 a0001c0001t0001g0132 a0001c0001t0001g0133 others(45): Show |
50 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(47): Show |
intron_variant | MODIFIER | c.2269-274A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41770412 | |||||||
chr22:41770482 | G | A | 207 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(204): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.2269-204G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41770482 | |||||||
chr22:41770495 | CT | C | 3 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0098 |
3 | HG02257.hp2 HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2269-190delT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 19/30 | chr22 | 41770495 | |||||||
chr22:41771083 | T | C | 2 | a0001c0001t0001g0202 a0001c0004t0003g0116 |
2 | HG01099.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2544+122T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41771083 | |||||||
chr22:41771140 | T | G | 9 | a0003c0006t0001g0002 a0003c0006t0001g0069 a0003c0006t0001g0090 others(6): Show |
10 | HG01109.hp1 HG02258.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.2544+179T>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41771140 | |||||||
chr22:41771150 | C | A | 2 | a0001c0001t0001g0239 a0001c0001t0001g0240 |
2 | HG00099.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2544+189C>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41771150 | |||||||
chr22:41771256 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2544+295C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41771256 | |||||||
chr22:41771351 | G | T | 1 | a0001c0001t0001g0168 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2544+390G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41771351 | |||||||
chr22:41771358 | C | T | 2 | a0002c0005t0001g0033 a0002c0005t0001g0036 |
2 | HG00423.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.2544+397C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41771358 | |||||||
chr22:41771437 | C | T | 2 | a0001c0001t0001g0139 a0001c0001t0001g0140 |
2 | HG03669.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.2544+476C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41771437 | |||||||
chr22:41771460 | C | G | 207 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(204): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.2544+499C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41771460 | |||||||
chr22:41771537 | G | T | 1 | a0001c0004t0003g0116 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2544+576G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41771537 | |||||||
chr22:41771610 | C | CT | 205 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(202): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.2544+659dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | INFO_REALIGN_3_PRIME | chr22 | 41771610 | ||||||
chr22:41771650 | G | A | 1 | a0002c0005t0001g0032 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2544+689G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41771650 | |||||||
chr22:41771738 | G | A | 1 | a0003c0006t0001g0069 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2544+777G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41771738 | |||||||
chr22:41771770 | C | A | 4 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0098 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.2544+809C>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41771770 | |||||||
chr22:41771977 | T | C | 3 | a0001c0004t0003g0112 a0001c0004t0003g0122 a0001c0004t0003g0123 |
3 | HG02723.hp2 HG02895.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.2544+1016T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41771977 | |||||||
chr22:41772001 | T | G | 4 | a0004c0009t0001g0004 a0004c0009t0001g0142 a0004c0009t0001g0237 others(1): Show |
5 | HG01934.hp1 HG02280.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.2544+1040T>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41772001 | |||||||
chr22:41772177 | A | G | 207 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(204): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.2544+1216A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41772177 | |||||||
chr22:41772409 | G | A | 15 | a0001c0003t0004g0017 a0001c0003t0004g0018 a0001c0003t0004g0019 others(12): Show |
15 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.2544+1448G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41772409 | |||||||
chr22:41772482 | T | C | 2 | a0001c0012t0001g0182 a0001c0012t0001g0190 |
2 | HG02615.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.2544+1521T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41772482 | |||||||
chr22:41772553 | C | T | 9 | a0003c0006t0001g0002 a0003c0006t0001g0069 a0003c0006t0001g0090 others(6): Show |
10 | HG01109.hp1 HG02258.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.2544+1592C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41772553 | |||||||
chr22:41772657 | A | G | 3 | a0001c0002t0002g0076 a0001c0002t0002g0085 a0001c0002t0002g0105 |
3 | HG02602.hp1 HG03710.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.2544+1696A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41772657 | |||||||
chr22:41772763 | G | A | 207 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(204): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.2544+1802G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41772763 | |||||||
chr22:41772877 | A | C | 76 | a0001c0001t0001g0202 a0001c0003t0001g0096 a0001c0003t0001g0097 others(73): Show |
77 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.2544+1916A>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41772877 | |||||||
chr22:41773050 | C | T | 3 | a0001c0002t0002g0076 a0001c0002t0002g0085 a0001c0002t0002g0105 |
3 | HG02602.hp1 HG03710.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.2544+2089C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41773050 | |||||||
chr22:41773092 | C | T | 1 | a0001c0001t0001g0197 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2544+2131C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41773092 | |||||||
chr22:41773265 | T | G | 48 | a0001c0001t0001g0003 a0001c0001t0001g0132 a0001c0001t0001g0133 others(45): Show |
50 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(47): Show |
intron_variant | MODIFIER | c.2544+2304T>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41773265 | |||||||
chr22:41773472 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2544+2511G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41773472 | |||||||
chr22:41773560 | TA | T | 53 | a0001c0001t0001g0153 a0001c0001t0001g0163 a0001c0002t0002g0001 others(50): Show |
55 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.2545-2521delA | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | INFO_REALIGN_3_PRIME | chr22 | 41773560 | ||||||
chr22:41773560 | TAA | T | 90 | a0001c0001t0001g0003 a0001c0001t0001g0132 a0001c0001t0001g0133 others(87): Show |
92 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.2545-2522_2545-252 others(6): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | INFO_REALIGN_3_PRIME | chr22 | 41773560 | ||||||
chr22:41773560 | TAAA | T | 110 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0128 others(107): Show |
110 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.2545-2523_2545-252 others(7): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | INFO_REALIGN_3_PRIME | chr22 | 41773560 | ||||||
chr22:41773614 | G | A | 131 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(128): Show |
133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.2545-2488G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41773614 | |||||||
chr22:41773628 | C | T | 76 | a0001c0001t0001g0202 a0001c0003t0001g0096 a0001c0003t0001g0097 others(73): Show |
77 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.2545-2474C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41773628 | |||||||
chr22:41773649 | G | T | 5 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0098 others(2): Show |
5 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2545-2453G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41773649 | |||||||
chr22:41773699 | C | T | 4 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0098 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.2545-2403C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41773699 | |||||||
chr22:41773732 | G | A | 1 | a0001c0004t0006g0124 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2545-2370G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41773732 | |||||||
chr22:41773746 | G | A | 23 | a0001c0003t0004g0005 a0001c0003t0004g0006 a0001c0003t0004g0007 others(20): Show |
23 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.2545-2356G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41773746 | |||||||
chr22:41773870 | G | A | 13 | a0002c0005t0001g0028 a0002c0005t0001g0029 a0002c0005t0001g0030 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.2545-2232G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41773870 | |||||||
chr22:41773956 | A | G | 4 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0098 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.2545-2146A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41773956 | |||||||
chr22:41774021 | A | G | 207 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(204): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.2545-2081A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41774021 | |||||||
chr22:41774428 | A | C | 207 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(204): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.2545-1674A>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41774428 | |||||||
chr22:41774469 | G | A | 1 | a0005c0007t0004g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2545-1633G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41774469 | |||||||
chr22:41774506 | A | G | 1 | a0001c0001t0001g0178 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2545-1596A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41774506 | |||||||
chr22:41774670 | T | C | 3 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0098 |
3 | HG02257.hp2 HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2545-1432T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41774670 | |||||||
chr22:41774901 | C | A | 1 | a0001c0004t0003g0042 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2545-1201C>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41774901 | |||||||
chr22:41774931 | C | G | 1 | a0001c0001t0001g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2545-1171C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41774931 | |||||||
chr22:41775059 | A | C | 1 | a0001c0018t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2545-1043A>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41775059 | |||||||
chr22:41775067 | C | T | 13 | a0002c0005t0001g0028 a0002c0005t0001g0029 a0002c0005t0001g0030 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.2545-1035C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41775067 | |||||||
chr22:41775296 | T | C | 207 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(204): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.2545-806T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41775296 | |||||||
chr22:41775342 | C | T | 1 | a0001c0001t0001g0227 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2545-760C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41775342 | |||||||
chr22:41775594 | C | CT | 16 | a0001c0001t0001g0165 a0001c0001t0001g0236 a0002c0005t0001g0028 others(13): Show |
16 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(13): Show |
intron_variant | MODIFIER | c.2545-491dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | INFO_REALIGN_3_PRIME | chr22 | 41775594 | ||||||
chr22:41775594 | CT | C | 16 | a0001c0001t0001g0187 a0001c0003t0004g0017 a0001c0003t0004g0018 others(13): Show |
16 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.2545-491delT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | INFO_REALIGN_3_PRIME | chr22 | 41775594 | ||||||
chr22:41775613 | A | T | 35 | a0001c0001t0001g0127 a0001c0001t0001g0130 a0001c0001t0001g0131 others(32): Show |
35 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(32): Show |
intron_variant | MODIFIER | c.2545-489A>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41775613 | |||||||
chr22:41775742 | T | TG | 5 | a0003c0006t0001g0002 a0003c0006t0001g0069 a0003c0006t0001g0092 others(2): Show |
6 | HG02258.hp2 HG02965.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.2545-359dupG | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | INFO_REALIGN_3_PRIME | chr22 | 41775742 | ||||||
chr22:41775795 | C | T | 8 | a0002c0005t0001g0028 a0002c0005t0001g0029 a0002c0005t0001g0030 others(5): Show |
8 | HG00673.hp2 HG01109.hp2 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.2545-307C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41775795 | |||||||
chr22:41775813 | C | T | 27 | a0001c0001t0001g0138 a0001c0001t0001g0147 a0001c0001t0001g0169 others(24): Show |
27 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(24): Show |
intron_variant | MODIFIER | c.2545-289C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41775813 | |||||||
chr22:41776046 | C | T | 6 | a0001c0003t0004g0005 a0001c0003t0004g0006 a0001c0003t0004g0007 others(3): Show |
6 | HG02109.hp2 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2545-56C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41776046 | |||||||
chr22:41776076 | C | T | 97 | a0001c0001t0001g0127 a0001c0001t0001g0130 a0001c0001t0001g0131 others(94): Show |
98 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.2545-26C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 20/30 | chr22 | 41776076 | |||||||
chr22:41776322 | G | A | 1 | a0001c0022t0001g0238 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2710+55G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 21/30 | chr22 | 41776322 | |||||||
chr22:41776487 | G | A | 1 | a0002c0005t0001g0030 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2710+220G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 21/30 | chr22 | 41776487 | |||||||
chr22:41776560 | C | A | 5 | a0001c0004t0003g0041 a0001c0004t0003g0042 a0001c0004t0003g0043 others(2): Show |
5 | HG02280.hp1 HG02723.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2710+293C>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 21/30 | chr22 | 41776560 | |||||||
chr22:41776620 | C | T | 4 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0098 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.2710+353C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 21/30 | chr22 | 41776620 | |||||||
chr22:41776782 | GTATT | G | 75 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0098 others(72): Show |
76 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(73): Show |
intron_variant | MODIFIER | c.2710+525_2710+528d others(6): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 21/30 | INFO_REALIGN_3_PRIME | chr22 | 41776782 | ||||||
chr22:41777059 | C | T | 12 | a0001c0003t0004g0005 a0001c0004t0003g0041 a0001c0004t0003g0042 others(9): Show |
12 | HG02280.hp1 HG02723.hp1 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.2710+792C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 21/30 | chr22 | 41777059 | |||||||
chr22:41777108 | C | T | 1 | a0001c0001t0001g0215 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2710+841C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 21/30 | chr22 | 41777108 | |||||||
chr22:41777158 | A | AT | 150 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(147): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.2710+906dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 21/30 | INFO_REALIGN_3_PRIME | chr22 | 41777158 | ||||||
chr22:41777158 | A | T | 1 | a0001c0003t0004g0027 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2710+891A>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 21/30 | chr22 | 41777158 | |||||||
chr22:41777158 | AT | A | 10 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0098 others(7): Show |
10 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.2710+906delT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 21/30 | INFO_REALIGN_3_PRIME | chr22 | 41777158 | ||||||
chr22:41777180 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2710+913G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 21/30 | chr22 | 41777180 | |||||||
chr22:41777217 | G | A | 1 | a0001c0002t0002g0083 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2710+950G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 21/30 | chr22 | 41777217 | |||||||
chr22:41777244 | G | A | 1 | a0001c0003t0004g0027 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2710+977G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 21/30 | chr22 | 41777244 | |||||||
chr22:41777289 | G | A | 5 | a0003c0006t0001g0002 a0003c0006t0001g0069 a0003c0006t0001g0092 others(2): Show |
6 | HG02258.hp2 HG02965.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.2710+1022G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 21/30 | chr22 | 41777289 | |||||||
chr22:41777323 | T | A | 1 | a0002c0005t0001g0032 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2710+1056T>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 21/30 | chr22 | 41777323 | |||||||
chr22:41777371 | G | A | 1 | a0001c0004t0003g0119 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2710+1104G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 21/30 | chr22 | 41777371 | |||||||
chr22:41777479 | C | T | 1 | a0001c0003t0004g0027 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2710+1212C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 21/30 | chr22 | 41777479 | |||||||
chr22:41777829 | C | T | 5 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0098 others(2): Show |
5 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2711-879C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 21/30 | chr22 | 41777829 | |||||||
chr22:41777852 | GCTTC | G | 7 | a0001c0003t0004g0005 a0001c0003t0004g0006 a0001c0003t0004g0007 others(4): Show |
7 | HG02109.hp2 HG02615.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.2711-839_2711-836d others(6): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 21/30 | INFO_REALIGN_3_PRIME | chr22 | 41777852 | ||||||
chr22:41777875 | T | C | 36 | a0001c0001t0001g0127 a0001c0001t0001g0130 a0001c0001t0001g0131 others(33): Show |
36 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(33): Show |
intron_variant | MODIFIER | c.2711-833T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 21/30 | chr22 | 41777875 | |||||||
chr22:41778004 | CCTTCCTT others(10): Show |
C | 1 | a0001c0002t0002g0073 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2711-680_2711-664d others(19): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 21/30 | INFO_REALIGN_3_PRIME | chr22 | 41778004 | ||||||
chr22:41778213 | C | A | 1 | a0001c0003t0004g0027 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2711-495C>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 21/30 | chr22 | 41778213 | |||||||
chr22:41778223 | G | A | 3 | a0001c0001t0001g0185 a0001c0001t0001g0199 a0001c0001t0001g0203 |
3 | HG02145.hp2 HG03098.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2711-485G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 21/30 | chr22 | 41778223 | |||||||
chr22:41778227 | C | T | 24 | a0001c0004t0003g0041 a0001c0004t0003g0042 a0001c0004t0003g0043 others(21): Show |
24 | HG01884.hp1 HG02280.hp1 HG02559.hp1 others(21): Show |
intron_variant | MODIFIER | c.2711-481C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 21/30 | chr22 | 41778227 | |||||||
chr22:41778272 | C | T | 1 | a0001c0001t0001g0254 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2711-436C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 21/30 | chr22 | 41778272 | |||||||
chr22:41778301 | A | AT | 132 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(129): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.2711-405dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 21/30 | INFO_REALIGN_3_PRIME | chr22 | 41778301 | ||||||
chr22:41778555 | G | A | 5 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0098 others(2): Show |
5 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2711-153G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 21/30 | chr22 | 41778555 | |||||||
chr22:41778887 | T | G | 39 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0098 others(36): Show |
40 | HG01109.hp1 HG01884.hp1 HG02257.hp2 others(37): Show |
intron_variant | MODIFIER | c.2815+75T>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | chr22 | 41778887 | |||||||
chr22:41779144 | G | A | 1 | a0001c0018t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2815+332G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | chr22 | 41779144 | |||||||
chr22:41779227 | G | A | 131 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(128): Show |
133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.2815+415G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | chr22 | 41779227 | |||||||
chr22:41779283 | C | CA | 6 | a0001c0008t0003g0106 a0001c0008t0003g0108 a0001c0008t0003g0109 others(3): Show |
6 | HG02559.hp1 HG02572.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.2815+479dupA | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | INFO_REALIGN_3_PRIME | chr22 | 41779283 | ||||||
chr22:41779310 | T | C | 207 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(204): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.2815+498T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | chr22 | 41779310 | |||||||
chr22:41779314 | G | A | 1 | a0001c0001t0001g0239 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2815+502G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | chr22 | 41779314 | |||||||
chr22:41779361 | G | A | 132 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(129): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.2815+549G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | chr22 | 41779361 | |||||||
chr22:41779606 | A | G | 1 | a0001c0003t0004g0027 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2815+794A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | chr22 | 41779606 | |||||||
chr22:41779691 | A | G | 207 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(204): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.2815+879A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | chr22 | 41779691 | |||||||
chr22:41779828 | C | T | 16 | a0001c0003t0004g0017 a0001c0003t0004g0018 a0001c0003t0004g0019 others(13): Show |
16 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.2815+1016C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | chr22 | 41779828 | |||||||
chr22:41779947 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2815+1135C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | chr22 | 41779947 | |||||||
chr22:41780054 | C | T | 16 | a0001c0003t0004g0017 a0001c0003t0004g0018 a0001c0003t0004g0019 others(13): Show |
16 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.2816-1230C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | chr22 | 41780054 | |||||||
chr22:41780055 | G | A | 132 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0127 others(129): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.2816-1229G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | chr22 | 41780055 | |||||||
chr22:41780219 | C | T | 1 | a0001c0018t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2816-1065C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | chr22 | 41780219 | |||||||
chr22:41780279 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2816-1005G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | chr22 | 41780279 | |||||||
chr22:41780335 | G | A | 7 | a0001c0001t0001g0187 a0001c0001t0001g0211 a0001c0001t0001g0213 others(4): Show |
7 | HG00609.hp1 HG04184.hp2 NA18965.hp2 others(4): Show |
intron_variant | MODIFIER | c.2816-949G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | chr22 | 41780335 | |||||||
chr22:41780411 | G | T | 1 | a0001c0003t0004g0025 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2816-873G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | chr22 | 41780411 | |||||||
chr22:41780507 | C | T | 1 | a0001c0003t0004g0020 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2816-777C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | chr22 | 41780507 | |||||||
chr22:41780553 | T | C | 1 | a0001c0001t0001g0164 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2816-731T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | chr22 | 41780553 | |||||||
chr22:41780569 | T | A | 1 | a0001c0002t0002g0057 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2816-715T>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | chr22 | 41780569 | |||||||
chr22:41780576 | C | CT | 31 | a0001c0003t0004g0017 a0001c0003t0004g0018 a0001c0003t0004g0019 others(28): Show |
31 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.2816-704dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | INFO_REALIGN_3_PRIME | chr22 | 41780576 | ||||||
chr22:41780576 | C | CTT | 8 | a0001c0002t0002g0102 a0001c0003t0004g0005 a0001c0003t0004g0006 others(5): Show |
8 | HG01175.hp1 HG02109.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.2816-705_2816-704d others(4): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | INFO_REALIGN_3_PRIME | chr22 | 41780576 | ||||||
chr22:41780580 | T | C | 18 | a0001c0002t0002g0001 a0001c0002t0002g0046 a0001c0002t0002g0047 others(15): Show |
19 | HG00323.hp2 HG00735.hp2 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.2816-704T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | chr22 | 41780580 | |||||||
chr22:41780580 | TC | T | 12 | a0001c0002t0002g0100 a0001c0004t0003g0118 a0001c0004t0003g0123 others(9): Show |
13 | HG01109.hp1 HG02258.hp2 HG02895.hp2 others(10): Show |
intron_variant | MODIFIER | c.2816-703delC | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | chr22 | 41780580 | |||||||
chr22:41780581 | C | T | 94 | a0001c0002t0002g0001 a0001c0002t0002g0046 a0001c0002t0002g0047 others(91): Show |
95 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.2816-703C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | chr22 | 41780581 | |||||||
chr22:41780583 | T | C | 3 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0098 |
3 | HG02257.hp2 HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2816-701T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | chr22 | 41780583 | |||||||
chr22:41780681 | G | A | 1 | a0001c0018t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2816-603G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | chr22 | 41780681 | |||||||
chr22:41780751 | T | A | 1 | a0001c0001t0001g0128 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.2816-533T>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | chr22 | 41780751 | |||||||
chr22:41780865 | G | A | 1 | a0001c0002t0002g0073 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2816-419G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | chr22 | 41780865 | |||||||
chr22:41780865 | G | T | 1 | a0001c0002t0002g0061 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2816-419G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | chr22 | 41780865 | |||||||
chr22:41780867 | A | G | 9 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0148 others(6): Show |
9 | HG00323.hp1 HG01106.hp1 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.2816-417A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | chr22 | 41780867 | |||||||
chr22:41780904 | G | T | 1 | a0001c0002t0002g0078 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2816-380G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | chr22 | 41780904 | |||||||
chr22:41780906 | C | T | 18 | a0001c0004t0003g0041 a0001c0004t0003g0042 a0001c0004t0003g0043 others(15): Show |
18 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(15): Show |
intron_variant | MODIFIER | c.2816-378C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | chr22 | 41780906 | |||||||
chr22:41780913 | A | T | 122 | a0001c0002t0002g0001 a0001c0002t0002g0046 a0001c0002t0002g0047 others(119): Show |
124 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.2816-371A>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | chr22 | 41780913 | |||||||
chr22:41781133 | T | G | 1 | a0001c0001t0001g0244 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2816-151T>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 22/30 | chr22 | 41781133 | |||||||
chr22:41781449 | G | C | 122 | a0001c0002t0002g0001 a0001c0002t0002g0046 a0001c0002t0002g0047 others(119): Show |
124 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.2926+55G>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 23/30 | chr22 | 41781449 | |||||||
chr22:41781582 | CTGTT | C | 66 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0098 others(63): Show |
66 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.2927-95_2927-92del others(4): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 23/30 | INFO_REALIGN_3_PRIME | chr22 | 41781582 | ||||||
chr22:41781895 | A | G | 47 | a0001c0002t0002g0001 a0001c0002t0002g0046 a0001c0002t0002g0047 others(44): Show |
48 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.3087+50A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 24/30 | chr22 | 41781895 | |||||||
chr22:41782036 | C | T | 107 | a0001c0002t0002g0001 a0001c0002t0002g0046 a0001c0002t0002g0047 others(104): Show |
108 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.3087+191C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 24/30 | chr22 | 41782036 | |||||||
chr22:41782377 | G | A | 13 | a0002c0005t0001g0028 a0002c0005t0001g0029 a0002c0005t0001g0030 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.3087+532G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 24/30 | chr22 | 41782377 | |||||||
chr22:41782437 | G | A | 107 | a0001c0002t0002g0001 a0001c0002t0002g0046 a0001c0002t0002g0047 others(104): Show |
108 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.3087+592G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 24/30 | chr22 | 41782437 | |||||||
chr22:41782546 | T | C | 1 | a0001c0001t0001g0255 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.3087+701T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 24/30 | chr22 | 41782546 | |||||||
chr22:41782612 | G | A | 9 | a0003c0006t0001g0002 a0003c0006t0001g0069 a0003c0006t0001g0090 others(6): Show |
10 | HG01109.hp1 HG02258.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.3087+767G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 24/30 | chr22 | 41782612 | |||||||
chr22:41783107 | C | A | 11 | a0001c0004t0003g0041 a0001c0004t0003g0042 a0001c0004t0003g0043 others(8): Show |
11 | HG02280.hp1 HG02723.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.3088-1232C>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 24/30 | chr22 | 41783107 | |||||||
chr22:41783153 | C | CT | 9 | a0001c0003t0004g0017 a0001c0003t0004g0018 a0001c0003t0004g0019 others(6): Show |
9 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.3088-1178dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 24/30 | INFO_REALIGN_3_PRIME | chr22 | 41783153 | ||||||
chr22:41783327 | T | C | 1 | a0010c0016t0003g0117 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3088-1012T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 24/30 | chr22 | 41783327 | |||||||
chr22:41783384 | C | T | 1 | a0001c0008t0003g0109 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3088-955C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 24/30 | chr22 | 41783384 | |||||||
chr22:41783490 | C | A | 4 | a0001c0008t0003g0106 a0001c0008t0003g0108 a0001c0008t0003g0109 others(1): Show |
4 | HG02559.hp1 HG02572.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.3088-849C>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 24/30 | chr22 | 41783490 | |||||||
chr22:41783540 | C | A | 5 | a0001c0004t0003g0041 a0001c0004t0003g0042 a0001c0004t0003g0043 others(2): Show |
5 | HG02280.hp1 HG02723.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.3088-799C>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 24/30 | chr22 | 41783540 | |||||||
chr22:41783572 | G | A | 2 | a0001c0002t0002g0070 a0001c0002t0002g0071 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.3088-767G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 24/30 | chr22 | 41783572 | |||||||
chr22:41783658 | A | G | 48 | a0001c0001t0001g0003 a0001c0001t0001g0132 a0001c0001t0001g0133 others(45): Show |
50 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(47): Show |
intron_variant | MODIFIER | c.3088-681A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 24/30 | chr22 | 41783658 | |||||||
chr22:41784163 | C | G | 1 | a0001c0003t0004g0025 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3088-176C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 24/30 | chr22 | 41784163 | |||||||
chr22:41784280 | T | C | 1 | a0001c0003t0004g0026 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3088-59T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 24/30 | chr22 | 41784280 | |||||||
chr22:41784437 | C | A | 5 | a0001c0004t0003g0041 a0001c0004t0003g0042 a0001c0004t0003g0043 others(2): Show |
5 | HG02280.hp1 HG02723.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.3169+17C>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 25/30 | chr22 | 41784437 | |||||||
chr22:41784454 | C | T | 1 | a0001c0018t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3169+34C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 25/30 | chr22 | 41784454 | |||||||
chr22:41784580 | T | C | 60 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0098 others(57): Show |
60 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.3170-28T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 25/30 | chr22 | 41784580 | |||||||
chr22:41784850 | G | C | 2 | a0001c0001t0001g0003 a0001c0001t0001g0231 |
3 | HG01433.hp2 NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.3345+67G>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41784850 | |||||||
chr22:41784887 | T | TTGAG | 122 | a0001c0002t0002g0001 a0001c0002t0002g0046 a0001c0002t0002g0047 others(119): Show |
124 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.3345+105_3345+106i others(6): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr22 | 41784887 | ||||||
chr22:41784899 | T | A | 2 | a0001c0002t0002g0087 a0003c0006t0001g0090 |
2 | HG01346.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.3345+116T>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41784899 | |||||||
chr22:41784905 | A | T | 1 | a0001c0003t0004g0026 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3345+122A>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41784905 | |||||||
chr22:41784925 | T | TTTTA | 43 | a0001c0002t0002g0001 a0001c0002t0002g0046 a0001c0002t0002g0047 others(40): Show |
44 | HG00323.hp2 HG00639.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.3345+167_3345+170d others(6): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr22 | 41784925 | ||||||
chr22:41784925 | T | TTTTATTT others(1): Show |
5 | a0001c0002t0002g0051 a0001c0002t0002g0082 a0001c0002t0002g0085 others(2): Show |
5 | HG01175.hp1 HG01255.hp1 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.3345+163_3345+170d others(10): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr22 | 41784925 | ||||||
chr22:41784925 | T | TTTTATTT others(5): Show |
40 | a0001c0002t0002g0075 a0001c0003t0004g0005 a0001c0003t0004g0006 others(37): Show |
40 | HG00280.hp1 HG00639.hp1 HG01243.hp1 others(37): Show |
intron_variant | MODIFIER | c.3345+159_3345+170d others(14): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr22 | 41784925 | ||||||
chr22:41784925 | T | TTTTATTT others(9): Show |
2 | a0001c0003t0004g0008 a0001c0004t0003g0113 |
2 | HG02886.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.3345+155_3345+170d others(18): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr22 | 41784925 | ||||||
chr22:41784925 | T | TTTTATTT others(10): Show |
1 | a0001c0004t0003g0114 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3345+149_3345+150i others(19): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr22 | 41784925 | ||||||
chr22:41784925 | TTTTA | T | 16 | a0001c0002t0002g0058 a0001c0002t0002g0060 a0001c0002t0002g0064 others(13): Show |
16 | HG00408.hp1 HG00423.hp2 HG00597.hp2 others(13): Show |
intron_variant | MODIFIER | c.3345+167_3345+170d others(6): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr22 | 41784925 | ||||||
chr22:41784966 | C | T | 2 | a0001c0001t0001g0003 a0001c0001t0001g0231 |
3 | HG01433.hp2 NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.3345+183C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41784966 | |||||||
chr22:41785022 | C | T | 37 | a0001c0003t0004g0005 a0001c0003t0004g0006 a0001c0003t0004g0007 others(34): Show |
37 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.3345+239C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41785022 | |||||||
chr22:41785125 | C | T | 1 | a0001c0002t0002g0077 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.3345+342C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41785125 | |||||||
chr22:41785178 | G | A | 1 | a0001c0018t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3345+395G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41785178 | |||||||
chr22:41785187 | C | T | 17 | a0001c0004t0003g0041 a0001c0004t0003g0042 a0001c0004t0003g0043 others(14): Show |
17 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(14): Show |
intron_variant | MODIFIER | c.3345+404C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41785187 | |||||||
chr22:41785227 | G | A | 24 | a0001c0003t0004g0005 a0001c0003t0004g0006 a0001c0003t0004g0007 others(21): Show |
24 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.3345+444G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41785227 | |||||||
chr22:41785241 | T | TTTTA | 5 | a0002c0005t0001g0040 a0003c0006t0001g0090 a0003c0006t0001g0091 others(2): Show |
5 | HG01109.hp1 HG02970.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.3345+482_3345+485d others(6): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr22 | 41785241 | ||||||
chr22:41785241 | TTTTA | T | 70 | a0001c0002t0002g0001 a0001c0002t0002g0046 a0001c0002t0002g0047 others(67): Show |
71 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.3345+482_3345+485d others(6): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr22 | 41785241 | ||||||
chr22:41785285 | C | T | 1 | a0001c0002t0002g0101 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.3345+502C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41785285 | |||||||
chr22:41785293 | A | G | 1 | a0001c0003t0004g0025 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3345+510A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41785293 | |||||||
chr22:41785494 | T | C | 47 | a0001c0002t0002g0001 a0001c0002t0002g0046 a0001c0002t0002g0047 others(44): Show |
48 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.3345+711T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41785494 | |||||||
chr22:41785507 | C | T | 29 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0098 others(26): Show |
29 | HG01884.hp1 HG02257.hp2 HG02280.hp1 others(26): Show |
intron_variant | MODIFIER | c.3345+724C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41785507 | |||||||
chr22:41785698 | G | A | 13 | a0002c0005t0001g0028 a0002c0005t0001g0029 a0002c0005t0001g0030 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.3345+915G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41785698 | |||||||
chr22:41785725 | G | A | 3 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0098 |
3 | HG02257.hp2 HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.3345+942G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41785725 | |||||||
chr22:41785865 | ATTTTTAT others(1): Show |
A | 34 | a0001c0001t0001g0138 a0001c0001t0001g0147 a0001c0001t0001g0169 others(31): Show |
34 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.3345+1119_3345+112 others(12): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr22 | 41785865 | ||||||
chr22:41785865 | ATTTTTAT others(9): Show |
A | 2 | a0001c0001t0001g0164 a0001c0018t0001g0089 |
2 | HG00140.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3345+1111_3345+112 others(20): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr22 | 41785865 | ||||||
chr22:41785895 | A | AT | 47 | a0001c0002t0002g0001 a0001c0002t0002g0046 a0001c0002t0002g0047 others(44): Show |
48 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.3345+1119dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr22 | 41785895 | ||||||
chr22:41785906 | T | TA | 43 | a0001c0002t0002g0001 a0001c0002t0002g0046 a0001c0002t0002g0047 others(40): Show |
44 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.3345+1123_3345+112 others(5): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41785906 | |||||||
chr22:41785907 | T | A | 4 | a0001c0002t0002g0050 a0001c0002t0002g0076 a0001c0002t0002g0085 others(1): Show |
4 | HG02148.hp1 HG02602.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.3345+1124T>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41785907 | |||||||
chr22:41785910 | A | ATT | 6 | a0001c0002t0002g0058 a0001c0002t0002g0060 a0001c0002t0002g0064 others(3): Show |
6 | HG00280.hp1 HG00597.hp2 HG00609.hp2 others(3): Show |
intron_variant | MODIFIER | c.3345+1130_3345+113 others(6): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr22 | 41785910 | ||||||
chr22:41785910 | A | T | 4 | a0001c0002t0002g0050 a0001c0002t0002g0076 a0001c0002t0002g0085 others(1): Show |
4 | HG02148.hp1 HG02602.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.3345+1127A>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41785910 | |||||||
chr22:41785911 | T | A | 4 | a0001c0002t0002g0050 a0001c0002t0002g0076 a0001c0002t0002g0085 others(1): Show |
4 | HG02148.hp1 HG02602.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.3345+1128T>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41785911 | |||||||
chr22:41785912 | T | TTA | 36 | a0001c0002t0002g0001 a0001c0002t0002g0046 a0001c0002t0002g0047 others(33): Show |
37 | HG00323.hp2 HG00639.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.3345+1130_3345+113 others(6): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr22 | 41785912 | ||||||
chr22:41785915 | A | AT | 22 | a0001c0004t0003g0041 a0001c0004t0003g0042 a0001c0004t0003g0043 others(19): Show |
22 | HG01884.hp1 HG02280.hp1 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.3345+1145dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr22 | 41785915 | ||||||
chr22:41785915 | A | T | 43 | a0001c0002t0002g0001 a0001c0002t0002g0046 a0001c0002t0002g0047 others(40): Show |
44 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.3345+1132A>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41785915 | |||||||
chr22:41785920 | T | A | 35 | a0001c0001t0001g0127 a0001c0001t0001g0130 a0001c0001t0001g0131 others(32): Show |
35 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(32): Show |
intron_variant | MODIFIER | c.3345+1137T>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41785920 | |||||||
chr22:41785931 | G | A | 3 | a0001c0002t0002g0076 a0001c0002t0002g0085 a0001c0002t0002g0105 |
3 | HG02602.hp1 HG03710.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.3345+1148G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41785931 | |||||||
chr22:41785934 | G | A | 47 | a0001c0002t0002g0001 a0001c0002t0002g0046 a0001c0002t0002g0047 others(44): Show |
48 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.3345+1151G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41785934 | |||||||
chr22:41785941 | C | T | 16 | a0001c0003t0004g0017 a0001c0003t0004g0018 a0001c0003t0004g0019 others(13): Show |
16 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.3345+1158C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41785941 | |||||||
chr22:41785972 | G | A | 13 | a0002c0005t0001g0028 a0002c0005t0001g0029 a0002c0005t0001g0030 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.3345+1189G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41785972 | |||||||
chr22:41785996 | C | T | 13 | a0002c0005t0001g0028 a0002c0005t0001g0029 a0002c0005t0001g0030 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.3345+1213C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41785996 | |||||||
chr22:41786003 | C | T | 47 | a0001c0002t0002g0001 a0001c0002t0002g0046 a0001c0002t0002g0047 others(44): Show |
48 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.3345+1220C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41786003 | |||||||
chr22:41786011 | C | T | 4 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0001g0245 others(1): Show |
4 | HG02630.hp2 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.3345+1228C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41786011 | |||||||
chr22:41786012 | G | A | 1 | a0001c0002t0002g0057 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.3345+1229G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41786012 | |||||||
chr22:41786029 | G | C | 1 | a0001c0004t0003g0114 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3345+1246G>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41786029 | |||||||
chr22:41786132 | G | A | 14 | a0001c0001t0001g0138 a0001c0001t0001g0170 a0001c0001t0001g0210 others(11): Show |
15 | HG00544.hp1 HG00597.hp1 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.3345+1349G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41786132 | |||||||
chr22:41786135 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.3345+1352C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41786135 | |||||||
chr22:41786228 | A | G | 1 | a0001c0002t0002g0057 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.3345+1445A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41786228 | |||||||
chr22:41786295 | C | G | 1 | a0001c0001t0001g0130 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.3345+1512C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41786295 | |||||||
chr22:41786512 | T | C | 1 | a0002c0005t0001g0032 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3345+1729T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41786512 | |||||||
chr22:41787240 | G | A | 1 | a0001c0002t0002g0057 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.3345+2457G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41787240 | |||||||
chr22:41787286 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.3345+2503G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41787286 | |||||||
chr22:41787405 | T | C | 35 | a0001c0001t0001g0127 a0001c0001t0001g0130 a0001c0001t0001g0131 others(32): Show |
35 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(32): Show |
intron_variant | MODIFIER | c.3345+2622T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41787405 | |||||||
chr22:41787436 | C | A | 35 | a0001c0001t0001g0127 a0001c0001t0001g0130 a0001c0001t0001g0131 others(32): Show |
35 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(32): Show |
intron_variant | MODIFIER | c.3345+2653C>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41787436 | |||||||
chr22:41787464 | C | T | 59 | a0001c0001t0001g0127 a0001c0001t0001g0130 a0001c0001t0001g0131 others(56): Show |
59 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.3345+2681C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41787464 | |||||||
chr22:41787473 | C | A | 4 | a0001c0008t0003g0106 a0001c0008t0003g0108 a0001c0008t0003g0109 others(1): Show |
4 | HG02559.hp1 HG02572.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.3345+2690C>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41787473 | |||||||
chr22:41787513 | C | T | 4 | a0003c0006t0001g0090 a0003c0006t0001g0091 a0003c0006t0001g0095 others(1): Show |
4 | HG01109.hp1 HG02970.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.3345+2730C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41787513 | |||||||
chr22:41787584 | A | C | 1 | a0001c0002t0002g0061 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.3345+2801A>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41787584 | |||||||
chr22:41788135 | T | A | 24 | a0001c0003t0004g0005 a0001c0003t0004g0006 a0001c0003t0004g0007 others(21): Show |
24 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.3345+3352T>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41788135 | |||||||
chr22:41788139 | C | T | 3 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0200 |
3 | HG01258.hp2 HG01943.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.3345+3356C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41788139 | |||||||
chr22:41788216 | A | G | 1 | a0001c0001t0001g0244 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.3345+3433A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41788216 | |||||||
chr22:41788262 | C | G | 1 | a0001c0002t0002g0061 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.3345+3479C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41788262 | |||||||
chr22:41788525 | C | T | 9 | a0003c0006t0001g0002 a0003c0006t0001g0069 a0003c0006t0001g0090 others(6): Show |
10 | HG01109.hp1 HG02258.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.3345+3742C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41788525 | |||||||
chr22:41788572 | TTGGGATT others(128): Show |
T | 1 | a0001c0001t0001g0236 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.3345+3806_3345+394 others(4): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr22 | 41788572 | ||||||
chr22:41788955 | A | G | 2 | a0001c0004t0003g0044 a0001c0004t0003g0045 |
2 | HG02280.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.3345+4172A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41788955 | |||||||
chr22:41788977 | C | T | 9 | a0003c0006t0001g0002 a0003c0006t0001g0069 a0003c0006t0001g0090 others(6): Show |
10 | HG01109.hp1 HG02258.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.3345+4194C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41788977 | |||||||
chr22:41789040 | G | A | 13 | a0002c0005t0001g0028 a0002c0005t0001g0029 a0002c0005t0001g0030 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.3345+4257G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41789040 | |||||||
chr22:41789083 | C | T | 66 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0098 others(63): Show |
66 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.3345+4300C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41789083 | |||||||
chr22:41789139 | A | G | 1 | a0001c0003t0001g0098 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3345+4356A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41789139 | |||||||
chr22:41789181 | G | A | 25 | a0001c0004t0003g0041 a0001c0004t0003g0042 a0001c0004t0003g0043 others(22): Show |
25 | HG01884.hp1 HG02280.hp1 HG02559.hp1 others(22): Show |
intron_variant | MODIFIER | c.3345+4398G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41789181 | |||||||
chr22:41789182 | C | T | 109 | a0001c0001t0001g0003 a0001c0001t0001g0126 a0001c0001t0001g0128 others(106): Show |
111 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.3345+4399C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41789182 | |||||||
chr22:41789236 | C | T | 4 | a0001c0008t0003g0106 a0001c0008t0003g0108 a0001c0008t0003g0109 others(1): Show |
4 | HG02559.hp1 HG02572.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.3345+4453C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41789236 | |||||||
chr22:41789591 | C | G | 6 | a0001c0003t0004g0005 a0001c0003t0004g0006 a0001c0003t0004g0007 others(3): Show |
6 | HG02109.hp2 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.3346-4238C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41789591 | |||||||
chr22:41789679 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3346-4150C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41789679 | |||||||
chr22:41789965 | C | G | 24 | a0001c0003t0004g0005 a0001c0003t0004g0006 a0001c0003t0004g0007 others(21): Show |
24 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.3346-3864C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41789965 | |||||||
chr22:41790076 | T | C | 16 | a0001c0003t0004g0017 a0001c0003t0004g0018 a0001c0003t0004g0019 others(13): Show |
16 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.3346-3753T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41790076 | |||||||
chr22:41790262 | T | G | 36 | a0001c0001t0001g0127 a0001c0001t0001g0130 a0001c0001t0001g0131 others(33): Show |
36 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(33): Show |
intron_variant | MODIFIER | c.3346-3567T>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41790262 | |||||||
chr22:41790361 | A | G | 4 | a0003c0006t0001g0090 a0003c0006t0001g0091 a0003c0006t0001g0095 others(1): Show |
4 | HG01109.hp1 HG02970.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.3346-3468A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41790361 | |||||||
chr22:41790589 | T | A | 24 | a0001c0004t0003g0041 a0001c0004t0003g0042 a0001c0004t0003g0043 others(21): Show |
24 | HG01884.hp1 HG02280.hp1 HG02559.hp1 others(21): Show |
intron_variant | MODIFIER | c.3346-3240T>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41790589 | |||||||
chr22:41790834 | G | A | 47 | a0001c0002t0002g0001 a0001c0002t0002g0046 a0001c0002t0002g0047 others(44): Show |
48 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.3346-2995G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41790834 | |||||||
chr22:41790847 | C | T | 1 | a0001c0022t0001g0238 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3346-2982C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41790847 | |||||||
chr22:41791000 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.3346-2829G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41791000 | |||||||
chr22:41791011 | C | T | 47 | a0001c0002t0002g0001 a0001c0002t0002g0046 a0001c0002t0002g0047 others(44): Show |
48 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.3346-2818C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41791011 | |||||||
chr22:41791195 | C | T | 113 | a0001c0002t0002g0001 a0001c0002t0002g0046 a0001c0002t0002g0047 others(110): Show |
114 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.3346-2634C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41791195 | |||||||
chr22:41791323 | T | TA | 24 | a0001c0003t0004g0005 a0001c0003t0004g0006 a0001c0003t0004g0007 others(21): Show |
24 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.3346-2500dupA | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr22 | 41791323 | ||||||
chr22:41791324 | A | G | 1 | a0001c0018t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3346-2505A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41791324 | |||||||
chr22:41791378 | C | T | 28 | a0001c0001t0001g0138 a0001c0001t0001g0147 a0001c0001t0001g0169 others(25): Show |
28 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(25): Show |
intron_variant | MODIFIER | c.3346-2451C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41791378 | |||||||
chr22:41791480 | C | A | 7 | a0001c0008t0003g0106 a0001c0008t0003g0108 a0001c0008t0003g0109 others(4): Show |
7 | HG02559.hp1 HG02572.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.3346-2349C>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41791480 | |||||||
chr22:41791778 | G | A | 4 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0098 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.3346-2051G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41791778 | |||||||
chr22:41791786 | A | C | 4 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0098 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.3346-2043A>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41791786 | |||||||
chr22:41792065 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3346-1764G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41792065 | |||||||
chr22:41792148 | C | T | 13 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0098 others(10): Show |
13 | HG01884.hp1 HG02257.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.3346-1681C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41792148 | |||||||
chr22:41792320 | G | A | 1 | a0001c0001t0001g0230 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.3346-1509G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41792320 | |||||||
chr22:41792501 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.3346-1328C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41792501 | |||||||
chr22:41792518 | A | C | 1 | a0001c0003t0004g0025 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3346-1311A>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41792518 | |||||||
chr22:41792675 | T | A | 1 | a0003c0006t0001g0093 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3346-1154T>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41792675 | |||||||
chr22:41792718 | A | G | 3 | a0001c0001t0001g0134 a0001c0001t0001g0207 a0001c0001t0001g0232 |
3 | HG01167.hp2 HG01169.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.3346-1111A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41792718 | |||||||
chr22:41792865 | T | A | 1 | a0001c0001t0001g0196 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.3346-964T>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41792865 | |||||||
chr22:41792887 | C | G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0132 a0001c0001t0001g0133 others(54): Show |
60 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.3346-942C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41792887 | |||||||
chr22:41792891 | C | T | 1 | a0002c0005t0001g0038 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.3346-938C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41792891 | |||||||
chr22:41792918 | T | TA | 7 | a0001c0003t0004g0005 a0001c0003t0004g0006 a0001c0003t0004g0007 others(4): Show |
7 | HG02109.hp2 HG02615.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.3346-896dupA | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr22 | 41792918 | ||||||
chr22:41792918 | TA | T | 22 | a0001c0001t0001g0128 a0001c0001t0001g0150 a0001c0002t0002g0100 others(19): Show |
22 | HG00639.hp1 HG01109.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.3346-896delA | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr22 | 41792918 | ||||||
chr22:41792918 | TAA | T | 139 | a0001c0001t0001g0003 a0001c0001t0001g0127 a0001c0001t0001g0130 others(136): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.3346-897_3346-896d others(4): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr22 | 41792918 | ||||||
chr22:41792995 | G | T | 1 | a0001c0001t0001g0194 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.3346-834G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41792995 | |||||||
chr22:41793019 | G | C | 1 | a0001c0001t0001g0253 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.3346-810G>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41793019 | |||||||
chr22:41793032 | C | CT | 25 | a0001c0001t0001g0126 a0001c0001t0001g0133 a0001c0001t0001g0147 others(22): Show |
25 | HG00140.hp2 HG00423.hp1 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.3346-766dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr22 | 41793032 | ||||||
chr22:41793032 | C | CTTT | 8 | a0001c0001t0001g0127 a0001c0001t0001g0174 a0001c0001t0001g0196 others(5): Show |
8 | HG01981.hp2 HG03704.hp2 HG04184.hp2 others(5): Show |
intron_variant | MODIFIER | c.3346-768_3346-766d others(5): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr22 | 41793032 | ||||||
chr22:41793032 | C | CTTTT | 11 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0185 others(8): Show |
11 | HG00621.hp2 HG00673.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.3346-769_3346-766d others(6): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr22 | 41793032 | ||||||
chr22:41793032 | C | CTTTTT | 10 | a0001c0001t0001g0135 a0001c0001t0001g0137 a0001c0001t0001g0200 others(7): Show |
10 | HG01109.hp2 HG01258.hp2 HG03225.hp2 others(7): Show |
intron_variant | MODIFIER | c.3346-770_3346-766d others(7): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr22 | 41793032 | ||||||
chr22:41793032 | C | CTTTTTT | 7 | a0001c0001t0001g0134 a0001c0001t0001g0136 a0001c0001t0001g0180 others(4): Show |
7 | HG01943.hp2 HG02004.hp1 HG04204.hp2 others(4): Show |
intron_variant | MODIFIER | c.3346-771_3346-766d others(8): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr22 | 41793032 | ||||||
chr22:41793032 | CT | C | 24 | a0001c0001t0001g0003 a0001c0001t0001g0128 a0001c0001t0001g0132 others(21): Show |
26 | HG00099.hp1 HG00323.hp1 HG01257.hp1 others(23): Show |
intron_variant | MODIFIER | c.3346-766delT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr22 | 41793032 | ||||||
chr22:41793032 | CTTT | C | 17 | a0001c0001t0002g0201 a0001c0002t0002g0076 a0001c0002t0002g0085 others(14): Show |
17 | HG01175.hp1 HG02027.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.3346-768_3346-766d others(5): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr22 | 41793032 | ||||||
chr22:41793032 | CTTTT | C | 83 | a0001c0002t0002g0001 a0001c0002t0002g0046 a0001c0002t0002g0047 others(80): Show |
84 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.3346-769_3346-766d others(6): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr22 | 41793032 | ||||||
chr22:41793048 | T | C | 6 | a0001c0003t0004g0005 a0001c0003t0004g0006 a0001c0003t0004g0007 others(3): Show |
6 | HG02109.hp2 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.3346-781T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41793048 | |||||||
chr22:41793049 | T | C | 47 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0098 others(44): Show |
47 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(44): Show |
intron_variant | MODIFIER | c.3346-780T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41793049 | |||||||
chr22:41793073 | T | C | 1 | a0001c0002t0002g0056 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.3346-756T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41793073 | |||||||
chr22:41793086 | C | G | 37 | a0001c0001t0001g0127 a0001c0001t0001g0130 a0001c0001t0001g0131 others(34): Show |
37 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.3346-743C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41793086 | |||||||
chr22:41793131 | G | A | 53 | a0001c0001t0001g0003 a0001c0001t0001g0132 a0001c0001t0001g0133 others(50): Show |
56 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.3346-698G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41793131 | |||||||
chr22:41793142 | A | G | 1 | a0001c0002t0002g0082 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3346-687A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41793142 | |||||||
chr22:41793226 | T | C | 196 | a0001c0001t0001g0003 a0001c0001t0001g0127 a0001c0001t0001g0130 others(193): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.3346-603T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41793226 | |||||||
chr22:41793372 | G | A | 1 | a0001c0004t0006g0124 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3346-457G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41793372 | |||||||
chr22:41793380 | C | T | 53 | a0001c0001t0001g0003 a0001c0001t0001g0132 a0001c0001t0001g0133 others(50): Show |
56 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.3346-449C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41793380 | |||||||
chr22:41793382 | A | T | 6 | a0001c0008t0003g0106 a0001c0008t0003g0108 a0001c0008t0003g0109 others(3): Show |
6 | HG02559.hp1 HG02572.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.3346-447A>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41793382 | |||||||
chr22:41793403 | T | G | 195 | a0001c0001t0001g0003 a0001c0001t0001g0127 a0001c0001t0001g0130 others(192): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.3346-426T>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41793403 | |||||||
chr22:41793411 | C | T | 5 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0098 others(2): Show |
5 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.3346-418C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41793411 | |||||||
chr22:41793432 | G | A | 1 | a0008c0021t0001g0129 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3346-397G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41793432 | |||||||
chr22:41793547 | A | G | 195 | a0001c0001t0001g0003 a0001c0001t0001g0127 a0001c0001t0001g0130 others(192): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.3346-282A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41793547 | |||||||
chr22:41793758 | T | C | 6 | a0001c0004t0003g0113 a0001c0004t0003g0116 a0001c0004t0003g0118 others(3): Show |
6 | HG02886.hp2 HG02976.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.3346-71T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | chr22 | 41793758 | |||||||
chr22:41793806 | ATT | A | 18 | a0001c0003t0004g0017 a0001c0003t0004g0018 a0001c0003t0004g0019 others(15): Show |
18 | HG00639.hp1 HG01243.hp1 HG01496.hp1 others(15): Show |
splice_region_variant&intron_variant | LOW | c.3346-8_3346-7delTT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 26/30 | INFO_REALIGN_3_PRIME | chr22 | 41793806 | ||||||
chr22:41794192 | G | A | 1 | a0001c0018t0001g0089 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3428-179G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 27/30 | chr22 | 41794192 | |||||||
chr22:41794305 | A | G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0132 a0001c0001t0001g0133 others(54): Show |
60 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.3428-66A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 27/30 | chr22 | 41794305 | |||||||
chr22:41794544 | G | A | 1 | a0001c0003t0001g0096 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3534+67G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 28/30 | chr22 | 41794544 | |||||||
chr22:41795021 | C | T | 1 | a0001c0001t0001g0131 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.3535-390C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 28/30 | chr22 | 41795021 | |||||||
chr22:41795238 | C | A | 18 | a0001c0004t0003g0041 a0001c0004t0003g0042 a0001c0004t0003g0043 others(15): Show |
18 | HG01884.hp1 HG02280.hp1 HG02723.hp1 others(15): Show |
intron_variant | MODIFIER | c.3535-173C>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 28/30 | chr22 | 41795238 | |||||||
chr22:41795632 | A | G | 114 | a0001c0001t0002g0201 a0001c0002t0002g0001 a0001c0002t0002g0046 others(111): Show |
115 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.3666+90A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 29/30 | chr22 | 41795632 | |||||||
chr22:41796079 | A | G | 4 | a0001c0001t0001g0213 a0001c0001t0001g0216 a0001c0001t0001g0222 others(1): Show |
4 | HG00609.hp1 NA18965.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.3779+232A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | chr22 | 41796079 | |||||||
chr22:41796351 | G | GT | 6 | a0001c0001t0001g0204 a0001c0001t0001g0214 a0001c0003t0001g0096 others(3): Show |
6 | HG02109.hp2 HG02257.hp2 HG04204.hp2 others(3): Show |
intron_variant | MODIFIER | c.3779+520dupT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr22 | 41796351 | ||||||
chr22:41796351 | GT | G | 89 | a0001c0001t0001g0148 a0001c0001t0001g0152 a0001c0001t0002g0201 others(86): Show |
91 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.3779+520delT | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr22 | 41796351 | ||||||
chr22:41796351 | GTT | G | 61 | a0001c0001t0001g0003 a0001c0001t0001g0132 a0001c0001t0001g0133 others(58): Show |
63 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.3779+519_3779+520d others(4): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr22 | 41796351 | ||||||
chr22:41796430 | G | A | 13 | a0002c0005t0001g0028 a0002c0005t0001g0029 a0002c0005t0001g0030 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.3779+583G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | chr22 | 41796430 | |||||||
chr22:41796478 | G | A | 48 | a0001c0001t0002g0201 a0001c0002t0002g0001 a0001c0002t0002g0046 others(45): Show |
49 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.3779+631G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | chr22 | 41796478 | |||||||
chr22:41796546 | G | A | 1 | a0002c0005t0001g0032 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3779+699G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | chr22 | 41796546 | |||||||
chr22:41796590 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.3779+743G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | chr22 | 41796590 | |||||||
chr22:41796717 | G | A | 1 | a0001c0004t0003g0114 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3779+870G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | chr22 | 41796717 | |||||||
chr22:41796718 | G | A | 48 | a0001c0001t0002g0201 a0001c0002t0002g0001 a0001c0002t0002g0046 others(45): Show |
49 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.3779+871G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | chr22 | 41796718 | |||||||
chr22:41796932 | A | G | 1 | a0001c0004t0003g0118 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3779+1085A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | chr22 | 41796932 | |||||||
chr22:41797341 | G | A | 2 | a0001c0002t0002g0073 a0001c0002t0002g0103 |
2 | HG00741.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.3779+1494G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | chr22 | 41797341 | |||||||
chr22:41797350 | G | A | 1 | a0001c0003t0004g0026 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3779+1503G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | chr22 | 41797350 | |||||||
chr22:41797504 | T | G | 6 | a0001c0008t0003g0106 a0001c0008t0003g0108 a0001c0008t0003g0109 others(3): Show |
6 | HG02559.hp1 HG02572.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.3779+1657T>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | chr22 | 41797504 | |||||||
chr22:41797650 | G | T | 3 | a0001c0001t0001g0196 a0001c0001t0001g0247 a0001c0001t0001g0248 |
3 | HG00621.hp2 NA18747.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.3780-1604G>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | chr22 | 41797650 | |||||||
chr22:41797684 | T | C | 1 | a0001c0004t0006g0124 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3780-1570T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | chr22 | 41797684 | |||||||
chr22:41797737 | G | A | 61 | a0001c0001t0002g0201 a0001c0002t0002g0001 a0001c0002t0002g0046 others(58): Show |
62 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.3780-1517G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | chr22 | 41797737 | |||||||
chr22:41797893 | T | C | 1 | a0001c0001t0001g0195 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.3780-1361T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | chr22 | 41797893 | |||||||
chr22:41797909 | T | C | 48 | a0001c0001t0002g0201 a0001c0002t0002g0001 a0001c0002t0002g0046 others(45): Show |
49 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.3780-1345T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | chr22 | 41797909 | |||||||
chr22:41798116 | A | AAC | 15 | a0001c0001t0001g0135 a0001c0001t0001g0170 a0001c0001t0001g0172 others(12): Show |
15 | HG00140.hp1 HG00609.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.3780-1084_3780-108 others(6): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr22 | 41798116 | ||||||
chr22:41798116 | A | AACAC | 3 | a0001c0001t0001g0126 a0001c0001t0001g0213 a0001c0001t0001g0226 |
3 | HG04199.hp2 NA18982.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.3780-1086_3780-108 others(8): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr22 | 41798116 | ||||||
chr22:41798116 | A | AACACAC | 2 | a0001c0001t0001g0128 a0001c0001t0001g0216 |
2 | NA18992.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.3780-1088_3780-108 others(10): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr22 | 41798116 | ||||||
chr22:41798116 | A | AACACACA others(5): Show |
1 | a0001c0001t0001g0225 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.3780-1094_3780-108 others(16): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr22 | 41798116 | ||||||
chr22:41798116 | AAC | A | 26 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0136 others(23): Show |
26 | HG00280.hp2 HG00558.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.3780-1084_3780-108 others(6): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr22 | 41798116 | ||||||
chr22:41798116 | AACAC | A | 16 | a0001c0001t0001g0127 a0001c0001t0001g0196 a0001c0001t0001g0197 others(13): Show |
16 | HG00597.hp1 HG01099.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.3780-1086_3780-108 others(8): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr22 | 41798116 | ||||||
chr22:41798116 | AACACAC | A | 8 | a0001c0001t0001g0137 a0001c0001t0001g0248 a0001c0003t0004g0008 others(5): Show |
8 | HG01496.hp1 HG02886.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.3780-1088_3780-108 others(10): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr22 | 41798116 | ||||||
chr22:41798116 | AACACACA others(1): Show |
A | 6 | a0001c0003t0004g0017 a0001c0003t0004g0018 a0001c0003t0004g0019 others(3): Show |
6 | HG01243.hp1 HG02559.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.3780-1090_3780-108 others(12): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr22 | 41798116 | ||||||
chr22:41798116 | AACACACA others(3): Show |
A | 8 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0180 others(5): Show |
8 | HG00323.hp1 HG02723.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.3780-1092_3780-108 others(14): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr22 | 41798116 | ||||||
chr22:41798116 | AACACACA others(5): Show |
A | 6 | a0001c0001t0001g0255 a0001c0003t0004g0022 a0001c0003t0004g0025 others(3): Show |
6 | HG01981.hp2 HG02622.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.3780-1094_3780-108 others(16): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr22 | 41798116 | ||||||
chr22:41798116 | AACACACA others(7): Show |
A | 13 | a0001c0001t0001g0003 a0001c0001t0001g0143 a0001c0001t0001g0156 others(10): Show |
14 | HG01433.hp1 HG01433.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.3780-1096_3780-108 others(18): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr22 | 41798116 | ||||||
chr22:41798116 | AACACACA others(9): Show |
A | 43 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0139 others(40): Show |
44 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(41): Show |
intron_variant | MODIFIER | c.3780-1098_3780-108 others(20): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr22 | 41798116 | ||||||
chr22:41798116 | AACACACA others(11): Show |
A | 23 | a0001c0001t0001g0243 a0001c0001t0001g0245 a0001c0001t0001g0246 others(20): Show |
23 | HG00597.hp2 HG00609.hp2 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.3780-1100_3780-108 others(22): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr22 | 41798116 | ||||||
chr22:41798116 | AACACACA others(13): Show |
A | 51 | a0001c0001t0001g0176 a0001c0001t0001g0239 a0001c0001t0001g0240 others(48): Show |
52 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.3780-1102_3780-108 others(24): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr22 | 41798116 | ||||||
chr22:41798116 | AACACACA others(15): Show |
A | 1 | a0009c0019t0001g0104 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3780-1104_3780-108 others(26): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr22 | 41798116 | ||||||
chr22:41798154 | CACACACA others(11): Show |
C | 1 | a0002c0005t0001g0033 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.3780-1098_3780-108 others(22): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr22 | 41798154 | ||||||
chr22:41798162 | CACACACA others(3): Show |
C | 1 | a0010c0016t0003g0117 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3780-1090_3780-108 others(14): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr22 | 41798162 | ||||||
chr22:41798164 | CACACACA others(1): Show |
C | 3 | a0002c0005t0001g0028 a0002c0005t0001g0029 a0002c0005t0001g0030 |
3 | HG01934.hp2 HG01943.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.3780-1088_3780-108 others(12): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr22 | 41798164 | ||||||
chr22:41798168 | CACAT | C | 3 | a0002c0005t0001g0031 a0002c0005t0001g0036 a0002c0005t0001g0038 |
3 | HG00408.hp1 HG00423.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.3780-1084_3780-108 others(8): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr22 | 41798168 | ||||||
chr22:41798170 | CAT | C | 3 | a0002c0005t0001g0032 a0002c0005t0001g0034 a0002c0005t0001g0037 |
3 | HG03704.hp1 NA18994.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.3780-1082_3780-108 others(6): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr22 | 41798170 | ||||||
chr22:41798172 | T | C | 2 | a0001c0001t0001g0225 a0002c0005t0001g0035 |
2 | NA18965.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.3780-1082T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | chr22 | 41798172 | |||||||
chr22:41798225 | G | GCACA | 48 | a0001c0001t0002g0201 a0001c0002t0002g0001 a0001c0002t0002g0046 others(45): Show |
49 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.3780-1010_3780-100 others(8): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr22 | 41798225 | ||||||
chr22:41798310 | C | G | 4 | a0003c0006t0001g0090 a0003c0006t0001g0091 a0003c0006t0001g0095 others(1): Show |
4 | HG01109.hp1 HG02970.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.3780-944C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | chr22 | 41798310 | |||||||
chr22:41798535 | G | A | 15 | a0001c0001t0001g0144 a0001c0001t0001g0149 a0001c0001t0001g0152 others(12): Show |
15 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(12): Show |
intron_variant | MODIFIER | c.3780-719G>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | chr22 | 41798535 | |||||||
chr22:41798557 | A | G | 184 | a0001c0001t0001g0003 a0001c0001t0001g0127 a0001c0001t0001g0130 others(181): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.3780-697A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | chr22 | 41798557 | |||||||
chr22:41798563 | C | G | 192 | a0001c0001t0001g0003 a0001c0001t0001g0127 a0001c0001t0001g0130 others(189): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.3780-691C>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | chr22 | 41798563 | |||||||
chr22:41798576 | T | C | 34 | a0001c0001t0001g0127 a0001c0001t0001g0130 a0001c0001t0001g0131 others(31): Show |
34 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(31): Show |
intron_variant | MODIFIER | c.3780-678T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | chr22 | 41798576 | |||||||
chr22:41798623 | AATCCC | A | 4 | a0001c0003t0001g0096 a0001c0003t0001g0097 a0001c0003t0001g0098 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.3780-629_3780-625d others(7): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr22 | 41798623 | ||||||
chr22:41798720 | T | C | 34 | a0001c0001t0001g0127 a0001c0001t0001g0130 a0001c0001t0001g0131 others(31): Show |
34 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(31): Show |
intron_variant | MODIFIER | c.3780-534T>C | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | chr22 | 41798720 | |||||||
chr22:41798724 | C | T | 220 | a0001c0001t0001g0003 a0001c0001t0001g0127 a0001c0001t0001g0130 others(217): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.3780-530C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | chr22 | 41798724 | |||||||
chr22:41798728 | C | CA | 6 | a0001c0008t0003g0106 a0001c0008t0003g0108 a0001c0008t0003g0109 others(3): Show |
6 | HG02559.hp1 HG02572.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.3780-525dupA | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr22 | 41798728 | ||||||
chr22:41798778 | C | A | 1 | a0001c0017t0001g0198 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.3780-476C>A | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | chr22 | 41798778 | |||||||
chr22:41798868 | C | T | 2 | a0001c0001t0001g0139 a0001c0001t0001g0140 |
2 | HG03669.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.3780-386C>T | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | chr22 | 41798868 | |||||||
chr22:41798876 | C | CA | 11 | a0001c0001t0001g0149 a0001c0001t0001g0158 a0001c0001t0001g0159 others(8): Show |
11 | HG00099.hp1 HG00544.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.3780-361dupA | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr22 | 41798876 | ||||||
chr22:41798876 | C | CAA | 26 | a0001c0001t0001g0127 a0001c0001t0001g0130 a0001c0001t0001g0131 others(23): Show |
26 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.3780-362_3780-361d others(4): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr22 | 41798876 | ||||||
chr22:41798876 | C | CAAA | 9 | a0001c0001t0001g0134 a0001c0001t0001g0197 a0001c0001t0001g0248 others(6): Show |
9 | HG00408.hp1 HG01943.hp2 HG03942.hp2 others(6): Show |
intron_variant | MODIFIER | c.3780-363_3780-361d others(5): Show |
MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr22 | 41798876 | ||||||
chr22:41798958 | A | G | 48 | a0001c0001t0002g0201 a0001c0002t0002g0001 a0001c0002t0002g0046 others(45): Show |
49 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.3780-296A>G | MEI1 | ENSG00000167077.13 | transcript | ENST00000401548.8 | protein_coding | 30/30 | chr22 | 41798958 |