Item | Value |
---|---|
geneid | 23231 |
ensemblid | ENSG00000091490.11 |
hgncid | 29108 |
symbol | SEL1L3 |
name | SEL1L family member 3 |
refseq_nuc | NM_015187.5 |
refseq_prot | NP_056002.2 |
ensembl_nuc | ENST00000399878.8 |
ensembl_prot | ENSP00000382767.3 |
mane_status | MANE Select |
chr | chr4 |
start | 25747433 |
end | 25862988 |
strand | - |
ver | v1.2 |
region | chr4:25747433-25862988 |
region5000 | chr4:25742433-25867988 |
regionname0 | SEL1L3_chr4_25747433_25862988 |
regionname5000 | SEL1L3_chr4_25742433_25867988 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1132 | 258 | 57 | 52 | 102 | 9 | 36 | 70 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | MQRRG others(1127): Show |
chr4 | 25742433 | 25867988 |
a0002 | 0/0 | 1132 | 22 | 20 | 2 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | MQRRG others(1127): Show |
chr4 | 25742433 | 25867988 |
a0003 | 0/0 | 1132 | 8 | 0 | 0 | 8 | 0 | 0 | 8 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | MQRRG others(1127): Show |
chr4 | 25742433 | 25867988 |
a0004 | 0/0 | 1132 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | MQRRG others(1127): Show |
chr4 | 25742433 | 25867988 |
a0005 | 0/0 | 1132 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | MQRRG others(1127): Show |
chr4 | 25742433 | 25867988 |
a0006 | 0/0 | 1132 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | MQRRG others(1127): Show |
chr4 | 25742433 | 25867988 |
a0007 | 0/0 | 1132 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | MQRRG others(1127): Show |
chr4 | 25742433 | 25867988 |
a0008 | 0/0 | 1132 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | MQRRG others(1127): Show |
chr4 | 25742433 | 25867988 |
a0009 | 0/0 | 1132 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | MQRRG others(1127): Show |
chr4 | 25742433 | 25867988 |
a0010 | 0/0 | 1132 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | MQRRG others(1127): Show |
chr4 | 25742433 | 25867988 |
a0011 | 0/0 | 1132 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | MQRRG others(1127): Show |
chr4 | 25742433 | 25867988 |
a0012 | 0/0 | 1132 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | MQRRG others(1127): Show |
chr4 | 25742433 | 25867988 |
a0013 | 0/0 | 1132 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | MQRRG others(1127): Show |
chr4 | 25742433 | 25867988 |
a0014 | 0/0 | 1132 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | MQRRG others(1127): Show |
chr4 | 25742433 | 25867988 |
a0015 | 0/0 | 1132 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | MQRCG others(1127): Show |
chr4 | 25742433 | 25867988 |
a0016 | 0/0 | 1132 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | MQRRG others(1127): Show |
chr4 | 25742433 | 25867988 |
a0017 | 0/0 | 1132 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | MQRRG others(1127): Show |
chr4 | 25742433 | 25867988 |
a0018 | 0/0 | 1132 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | MQRRG others(1127): Show |
chr4 | 25742433 | 25867988 |
a0019 | 0/0 | 1132 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | MQRRG others(1127): Show |
chr4 | 25742433 | 25867988 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 3396 | 230 | 37 | 49 | 99 | 9 | 34 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | ATGCA others(3391): Show |
chr4 | 25742433 | 25867988 | ||
a0001c0003 | 0/0 | 3396 | 8 | 3 | 1 | 2 | 0 | 2 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | ATGCA others(3391): Show |
chr4 | 25742433 | 25867988 | ||
a0001c0006 | 0/0 | 3396 | 5 | 5 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | ATGCA others(3391): Show |
chr4 | 25742433 | 25867988 | ||
a0001c0008 | 0/0 | 3396 | 4 | 4 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | ATGCA others(3391): Show |
chr4 | 25742433 | 25867988 | ||
a0001c0010 | 0/0 | 3396 | 3 | 2 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | ATGCA others(3391): Show |
chr4 | 25742433 | 25867988 | ||
a0001c0011 | 0/0 | 3396 | 3 | 3 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | ATGCA others(3391): Show |
chr4 | 25742433 | 25867988 | ||
a0001c0014 | 0/0 | 3396 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | ATGCA others(3391): Show |
chr4 | 25742433 | 25867988 | ||
a0001c0017 | 0/0 | 3396 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | ATGCA others(3391): Show |
chr4 | 25742433 | 25867988 | ||
a0001c0025 | 0/0 | 3396 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | ATGCA others(3391): Show |
chr4 | 25742433 | 25867988 | ||
a0001c0027 | 0/0 | 3396 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | ATGCA others(3391): Show |
chr4 | 25742433 | 25867988 | ||
a0001c0034 | 0/0 | 3396 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | ATGCA others(3391): Show |
chr4 | 25742433 | 25867988 | ||
a0002c0002 | 0/0 | 3396 | 9 | 9 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | ATGCA others(3391): Show |
chr4 | 25742433 | 25867988 | ||
a0002c0005 | 0/0 | 3396 | 6 | 4 | 2 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | ATGCA others(3391): Show |
chr4 | 25742433 | 25867988 | ||
a0002c0009 | 0/0 | 3396 | 4 | 4 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | ATGCA others(3391): Show |
chr4 | 25742433 | 25867988 | ||
a0002c0013 | 0/0 | 3396 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | ATGCA others(3391): Show |
chr4 | 25742433 | 25867988 | ||
a0002c0015 | 0/0 | 3396 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | ATGCA others(3391): Show |
chr4 | 25742433 | 25867988 | ||
a0002c0018 | 0/0 | 3396 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | ATGCA others(3391): Show |
chr4 | 25742433 | 25867988 | ||
a0003c0004 | 0/0 | 3396 | 7 | 0 | 0 | 7 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | ATGCA others(3391): Show |
chr4 | 25742433 | 25867988 | ||
a0003c0028 | 0/0 | 3396 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | ATGCA others(3391): Show |
chr4 | 25742433 | 25867988 | ||
a0004c0007 | 0/0 | 3396 | 5 | 5 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | ATGCA others(3391): Show |
chr4 | 25742433 | 25867988 | ||
a0005c0019 | 0/0 | 3396 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | ATGCA others(3391): Show |
chr4 | 25742433 | 25867988 | ||
a0005c0021 | 0/0 | 3396 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | ATGCA others(3391): Show |
chr4 | 25742433 | 25867988 | ||
a0005c0022 | 0/0 | 3396 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | ATGCA others(3391): Show |
chr4 | 25742433 | 25867988 | ||
a0006c0012 | 0/0 | 3396 | 2 | 0 | 0 | 0 | 0 | 2 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | ATGCA others(3391): Show |
chr4 | 25742433 | 25867988 | ||
a0007c0031 | 0/0 | 3396 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | ATGCA others(3391): Show |
chr4 | 25742433 | 25867988 | ||
a0007c0033 | 0/0 | 3396 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | ATGCA others(3391): Show |
chr4 | 25742433 | 25867988 | ||
a0008c0023 | 0/0 | 3396 | 1 | 0 | 0 | 0 | 1 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | ATGCA others(3391): Show |
chr4 | 25742433 | 25867988 | ||
a0009c0037 | 0/0 | 3396 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | ATGCA others(3391): Show |
chr4 | 25742433 | 25867988 | ||
a0010c0016 | 0/0 | 3396 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | ATGCA others(3391): Show |
chr4 | 25742433 | 25867988 | ||
a0011c0029 | 0/0 | 3396 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | ATGCA others(3391): Show |
chr4 | 25742433 | 25867988 | ||
a0012c0020 | 0/0 | 3396 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | ATGCA others(3391): Show |
chr4 | 25742433 | 25867988 | ||
a0013c0036 | 0/0 | 3396 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | ATGCA others(3391): Show |
chr4 | 25742433 | 25867988 | ||
a0014c0026 | 0/0 | 3396 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | ATGCA others(3391): Show |
chr4 | 25742433 | 25867988 | ||
a0015c0038 | 0/0 | 3396 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | ATGCA others(3391): Show |
chr4 | 25742433 | 25867988 | ||
a0016c0032 | 0/0 | 3396 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | ATGCA others(3391): Show |
chr4 | 25742433 | 25867988 | ||
a0017c0030 | 0/0 | 3396 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | ATGCA others(3391): Show |
chr4 | 25742433 | 25867988 | ||
a0018c0035 | 0/0 | 3396 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | ATGCA others(3391): Show |
chr4 | 25742433 | 25867988 | ||
a0019c0024 | 0/0 | 3396 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | ATGCA others(3391): Show |
chr4 | 25742433 | 25867988 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4543 | 102 | 6 | 22 | 63 | 3 | 8 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4538): Show |
chr4 | 25742433 | 25867988 |
a0001c0001t0002 | 1/1 | 4543 | 92 | 22 | 20 | 22 | 5 | 21 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4538): Show |
chr4 | 25742433 | 25867988 |
a0001c0001t0003 | 0/0 | 4551 | 16 | 2 | 1 | 9 | 1 | 3 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4546): Show |
chr4 | 25742433 | 25867988 |
a0001c0001t0004 | 0/0 | 4543 | 2 | 1 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4538): Show |
chr4 | 25742433 | 25867988 |
a0001c0001t0005 | 0/0 | 4545 | 5 | 2 | 1 | 2 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4540): Show |
chr4 | 25742433 | 25867988 |
a0001c0001t0006 | 0/0 | 4541 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4536): Show |
chr4 | 25742433 | 25867988 |
a0001c0001t0008 | 0/0 | 4553 | 2 | 0 | 2 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4548): Show |
chr4 | 25742433 | 25867988 |
a0001c0001t0009 | 0/0 | 4551 | 2 | 2 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4546): Show |
chr4 | 25742433 | 25867988 |
a0001c0001t0010 | 0/0 | 4543 | 2 | 1 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4538): Show |
chr4 | 25742433 | 25867988 |
a0001c0001t0011 | 0/0 | 4543 | 2 | 0 | 0 | 0 | 0 | 2 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4538): Show |
chr4 | 25742433 | 25867988 |
a0001c0001t0016 | 0/0 | 4543 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4538): Show |
chr4 | 25742433 | 25867988 |
a0001c0001t0017 | 0/0 | 4545 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4540): Show |
chr4 | 25742433 | 25867988 |
a0001c0001t0018 | 0/0 | 4543 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4538): Show |
chr4 | 25742433 | 25867988 |
a0001c0001t0021 | 0/0 | 4543 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4538): Show |
chr4 | 25742433 | 25867988 |
a0001c0003t0002 | 0/0 | 4543 | 7 | 2 | 1 | 2 | 0 | 2 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4538): Show |
chr4 | 25742433 | 25867988 |
a0001c0003t0009 | 0/0 | 4551 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4546): Show |
chr4 | 25742433 | 25867988 |
a0001c0006t0002 | 0/0 | 4543 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4538): Show |
chr4 | 25742433 | 25867988 |
a0001c0006t0004 | 0/0 | 4543 | 3 | 3 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4538): Show |
chr4 | 25742433 | 25867988 |
a0001c0006t0007 | 0/0 | 4543 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4538): Show |
chr4 | 25742433 | 25867988 |
a0001c0008t0001 | 0/0 | 4543 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4538): Show |
chr4 | 25742433 | 25867988 |
a0001c0008t0002 | 0/0 | 4543 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4538): Show |
chr4 | 25742433 | 25867988 |
a0001c0008t0007 | 0/0 | 4543 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4538): Show |
chr4 | 25742433 | 25867988 |
a0001c0008t0012 | 0/0 | 4545 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4540): Show |
chr4 | 25742433 | 25867988 |
a0001c0010t0002 | 0/0 | 4543 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4538): Show |
chr4 | 25742433 | 25867988 |
a0001c0010t0022 | 0/0 | 4551 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4546): Show |
chr4 | 25742433 | 25867988 |
a0001c0010t0024 | 0/0 | 4543 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4538): Show |
chr4 | 25742433 | 25867988 |
a0001c0011t0002 | 0/0 | 4543 | 2 | 2 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4538): Show |
chr4 | 25742433 | 25867988 |
a0001c0011t0003 | 0/0 | 4551 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4546): Show |
chr4 | 25742433 | 25867988 |
a0001c0014t0001 | 0/0 | 4543 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4538): Show |
chr4 | 25742433 | 25867988 |
a0001c0017t0002 | 0/0 | 4543 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4538): Show |
chr4 | 25742433 | 25867988 |
a0001c0025t0001 | 0/0 | 4543 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4538): Show |
chr4 | 25742433 | 25867988 |
a0001c0027t0001 | 0/0 | 4543 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4538): Show |
chr4 | 25742433 | 25867988 |
a0001c0034t0002 | 0/0 | 4543 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4538): Show |
chr4 | 25742433 | 25867988 |
a0002c0002t0001 | 0/0 | 4543 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4538): Show |
chr4 | 25742433 | 25867988 |
a0002c0002t0002 | 0/0 | 4543 | 5 | 5 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4538): Show |
chr4 | 25742433 | 25867988 |
a0002c0002t0005 | 0/0 | 4545 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4540): Show |
chr4 | 25742433 | 25867988 |
a0002c0002t0006 | 0/0 | 4541 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4536): Show |
chr4 | 25742433 | 25867988 |
a0002c0002t0008 | 0/0 | 4553 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4548): Show |
chr4 | 25742433 | 25867988 |
a0002c0005t0001 | 0/0 | 4543 | 2 | 0 | 2 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4538): Show |
chr4 | 25742433 | 25867988 |
a0002c0005t0003 | 0/0 | 4551 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4546): Show |
chr4 | 25742433 | 25867988 |
a0002c0005t0006 | 0/0 | 4541 | 3 | 3 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4536): Show |
chr4 | 25742433 | 25867988 |
a0002c0009t0003 | 0/0 | 4551 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4546): Show |
chr4 | 25742433 | 25867988 |
a0002c0009t0004 | 0/0 | 4543 | 2 | 2 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4538): Show |
chr4 | 25742433 | 25867988 |
a0002c0009t0007 | 0/0 | 4543 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4538): Show |
chr4 | 25742433 | 25867988 |
a0002c0013t0014 | 0/0 | 4543 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4538): Show |
chr4 | 25742433 | 25867988 |
a0002c0015t0001 | 0/0 | 4543 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4538): Show |
chr4 | 25742433 | 25867988 |
a0002c0018t0002 | 0/0 | 4543 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4538): Show |
chr4 | 25742433 | 25867988 |
a0003c0004t0001 | 0/0 | 4543 | 7 | 0 | 0 | 7 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4538): Show |
chr4 | 25742433 | 25867988 |
a0003c0028t0001 | 0/0 | 4543 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4538): Show |
chr4 | 25742433 | 25867988 |
a0004c0007t0001 | 0/0 | 4543 | 3 | 3 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4538): Show |
chr4 | 25742433 | 25867988 |
a0004c0007t0002 | 0/0 | 4543 | 2 | 2 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4538): Show |
chr4 | 25742433 | 25867988 |
a0005c0019t0002 | 0/0 | 4543 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4538): Show |
chr4 | 25742433 | 25867988 |
a0005c0021t0003 | 0/0 | 4551 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4546): Show |
chr4 | 25742433 | 25867988 |
a0005c0022t0004 | 0/0 | 4543 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4538): Show |
chr4 | 25742433 | 25867988 |
a0006c0012t0002 | 0/0 | 4543 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4538): Show |
chr4 | 25742433 | 25867988 |
a0006c0012t0015 | 0/0 | 4545 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4540): Show |
chr4 | 25742433 | 25867988 |
a0007c0031t0020 | 0/0 | 4543 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4538): Show |
chr4 | 25742433 | 25867988 |
a0007c0033t0007 | 0/0 | 4543 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4538): Show |
chr4 | 25742433 | 25867988 |
a0008c0023t0002 | 0/0 | 4543 | 1 | 0 | 0 | 0 | 1 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4538): Show |
chr4 | 25742433 | 25867988 |
a0009c0037t0003 | 0/0 | 4551 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4546): Show |
chr4 | 25742433 | 25867988 |
a0010c0016t0002 | 0/0 | 4543 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4538): Show |
chr4 | 25742433 | 25867988 |
a0011c0029t0005 | 0/0 | 4545 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4540): Show |
chr4 | 25742433 | 25867988 |
a0012c0020t0002 | 0/0 | 4543 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4538): Show |
chr4 | 25742433 | 25867988 |
a0013c0036t0002 | 0/0 | 4543 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4538): Show |
chr4 | 25742433 | 25867988 |
a0014c0026t0013 | 0/0 | 4551 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4546): Show |
chr4 | 25742433 | 25867988 |
a0015c0038t0012 | 0/0 | 4545 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4540): Show |
chr4 | 25742433 | 25867988 |
a0016c0032t0019 | 0/0 | 4543 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4538): Show |
chr4 | 25742433 | 25867988 |
a0017c0030t0001 | 0/0 | 4543 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4538): Show |
chr4 | 25742433 | 25867988 |
a0018c0035t0001 | 0/0 | 4543 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4538): Show |
chr4 | 25742433 | 25867988 |
a0019c0024t0023 | 0/0 | 4543 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | AGTGG others(4538): Show |
chr4 | 25742433 | 25867988 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0002 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0052 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0189 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0002g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0003g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0003g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0004g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0005g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0005g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0005g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0005g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0005g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0006g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0008g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0008g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0009g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0009g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0010g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0010g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0011g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0011g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0016g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0017g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0018g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0001t0021g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0003t0002g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0003t0002g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0003t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0003t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0003t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0003t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0003t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0003t0009g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0006t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0006t0004g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0006t0004g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0006t0004g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0006t0007g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0008t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0008t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0008t0007g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0008t0012g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0010t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0010t0022g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0010t0024g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0011t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0011t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0011t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0014t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0017t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0025t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0027t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0001c0034t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0002c0002t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0002c0002t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0002c0002t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0002c0002t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0002c0002t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0002c0002t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0002c0002t0005g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0002c0002t0006g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0002c0002t0008g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0002c0005t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0002c0005t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0002c0005t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0002c0005t0006g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0002c0009t0003g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0002c0009t0004g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0002c0009t0004g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0002c0009t0007g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0002c0013t0014g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0002c0015t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0002c0018t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0003c0004t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0003c0004t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0003c0004t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0003c0004t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0003c0004t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0003c0004t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0003c0004t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0003c0028t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0004c0007t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0004c0007t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0004c0007t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0004c0007t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0004c0007t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0005c0019t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0005c0021t0003g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0005c0022t0004g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0006c0012t0002g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0006c0012t0015g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0007c0031t0020g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0007c0033t0007g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0008c0023t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0009c0037t0003g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0010c0016t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0011c0029t0005g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0012c0020t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0013c0036t0002g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0014c0026t0013g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0015c0038t0012g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0016c0032t0019g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0017c0030t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0018c0035t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
a0019c0024t0023g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0274 | EUR | GBR | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0046 | EUR | GBR | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0104 | EUR | GBR | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0102 | EUR | GBR | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG00438 | hp1 | a0001 | c0001 | t0003 | g0183 | EAS | CHS | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | CHS | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG00558 | hp2 | a0001 | c0003 | t0002 | g0103 | EAS | CHS | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | CHS | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | CHS | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG00609 | hp1 | a0001 | c0003 | t0002 | g0049 | EAS | CHS | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | CHS | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG00733 | hp2 | a0001 | c0027 | t0001 | g0197 | AMR | PUR | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0205 | AMR | PUR | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0191 | AMR | PUR | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0220 | AMR | PUR | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0264 | AMR | PUR | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG00741 | hp1 | a0001 | c0001 | t0010 | g0129 | AMR | PUR | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG01070 | hp1 | a0002 | c0005 | t0001 | g0156 | AMR | PUR | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG01071 | hp2 | a0002 | c0005 | t0001 | g0157 | AMR | PUR | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG01074 | hp1 | a0001 | c0001 | t0008 | g0114 | AMR | PUR | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG01081 | hp1 | a0001 | c0001 | t0003 | g0026 | AMR | PUR | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0247 | AMR | PUR | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0243 | AMR | PUR | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG01106 | hp2 | a0001 | c0003 | t0002 | g0025 | AMR | PUR | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG01109 | hp1 | a0001 | c0010 | t0024 | g0309 | AMR | PUR | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0291 | AMR | PUR | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0209 | AMR | PUR | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0261 | AMR | PUR | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG01192 | hp1 | a0001 | c0001 | t0018 | g0223 | AMR | PUR | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG01192 | hp2 | a0001 | c0001 | t0004 | g0123 | AMR | PUR | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0292 | AMR | CLM | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | CLM | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG01257 | hp2 | a0001 | c0001 | t0008 | g0290 | AMR | CLM | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | CLM | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | CLM | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0017 | AMR | CLM | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0106 | AMR | CLM | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | CLM | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0289 | AMR | CLM | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0062 | EUR | IBS | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG01515 | hp2 | a0008 | c0023 | t0002 | g0181 | EUR | IBS | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0072 | EUR | IBS | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0245 | EUR | IBS | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0296 | AFR | ACB | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | ACB | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG01891 | hp1 | a0001 | c0001 | t0009 | g0285 | AFR | ACB | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0297 | AFR | ACB | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | PEL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0053 | AMR | PEL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0064 | AMR | PEL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0251 | AMR | PEL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PEL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0066 | AMR | PEL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PEL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02040 | hp1 | a0001 | c0001 | t0003 | g0194 | EAS | KHV | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0196 | AFR | ACB | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02055 | hp2 | a0005 | c0019 | t0002 | g0010 | AFR | ACB | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | KHV | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | KHV | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02074 | hp2 | a0001 | c0001 | t0021 | g0306 | EAS | KHV | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | KHV | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | KHV | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0139 | AFR | ACB | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02145 | hp2 | a0009 | c0037 | t0003 | g0304 | AFR | ACB | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | PEL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PEL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02257 | hp1 | a0002 | c0005 | t0006 | g0001 | AFR | ACB | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0131 | AFR | ACB | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02258 | hp1 | a0002 | c0009 | t0007 | g0298 | AFR | ACB | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02258 | hp2 | a0010 | c0016 | t0002 | g0141 | AFR | ACB | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0063 | AMR | PEL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02280 | hp1 | a0001 | c0003 | t0009 | g0027 | AFR | ACB | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02280 | hp2 | a0002 | c0009 | t0004 | g0269 | AFR | ACB | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02293 | hp2 | a0001 | c0001 | t0005 | g0065 | AMR | PEL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02451 | hp1 | a0001 | c0001 | t0006 | g0150 | AFR | ACB | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02451 | hp2 | a0001 | c0006 | t0004 | g0299 | AFR | ACB | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02572 | hp1 | a0002 | c0009 | t0003 | g0278 | AFR | GWD | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0148 | AFR | GWD | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0111 | SAS | PJL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0163 | AFR | GWD | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02615 | hp2 | a0001 | c0006 | t0004 | g0132 | AFR | GWD | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0152 | AFR | GWD | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02622 | hp2 | a0001 | c0006 | t0004 | g0092 | AFR | GWD | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02630 | hp1 | a0001 | c0017 | t0002 | g0144 | AFR | GWD | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02630 | hp2 | a0001 | c0001 | t0010 | g0008 | AFR | GWD | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02647 | hp1 | a0002 | c0002 | t0002 | g0133 | AFR | GWD | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02647 | hp2 | a0001 | c0011 | t0002 | g0055 | AFR | GWD | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0192 | SAS | PJL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0054 | SAS | PJL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0099 | SAS | PJL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0249 | SAS | PJL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02717 | hp1 | a0005 | c0022 | t0004 | g0284 | AFR | GWD | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02717 | hp2 | a0011 | c0029 | t0005 | g0135 | AFR | GWD | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02723 | hp1 | a0001 | c0001 | t0004 | g0130 | AFR | GWD | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02723 | hp2 | a0001 | c0011 | t0002 | g0101 | AFR | GWD | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02735 | hp1 | a0006 | c0012 | t0002 | g0022 | SAS | PJL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02738 | hp2 | a0001 | c0003 | t0002 | g0024 | SAS | PJL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02809 | hp1 | a0012 | c0020 | t0002 | g0011 | AFR | GWD | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02809 | hp2 | a0002 | c0002 | t0008 | g0301 | AFR | GWD | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02818 | hp1 | a0002 | c0002 | t0002 | g0277 | AFR | GWD | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02818 | hp2 | a0001 | c0008 | t0002 | g0142 | AFR | GWD | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02886 | hp1 | a0001 | c0001 | t0003 | g0286 | AFR | GWD | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0302 | AFR | GWD | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02895 | hp1 | a0002 | c0002 | t0001 | g0279 | AFR | GWD | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | GWD | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02896 | hp1 | a0001 | c0003 | t0002 | g0096 | AFR | GWD | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0294 | AFR | GWD | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | GWD | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02897 | hp2 | a0001 | c0003 | t0002 | g0097 | AFR | GWD | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02922 | hp1 | a0001 | c0001 | t0005 | g0300 | AFR | ESN | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02922 | hp2 | a0005 | c0021 | t0003 | g0283 | AFR | ESN | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02965 | hp1 | a0004 | c0007 | t0001 | g0165 | AFR | ESN | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02965 | hp2 | a0002 | c0002 | t0006 | g0267 | AFR | ESN | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02970 | hp1 | a0004 | c0007 | t0001 | g0166 | AFR | ESN | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02970 | hp2 | a0001 | c0006 | t0002 | g0154 | AFR | ESN | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02976 | hp1 | a0001 | c0001 | t0009 | g0124 | AFR | ESN | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02976 | hp2 | a0001 | c0034 | t0002 | g0137 | AFR | ESN | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0174 | SAS | PJL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG03017 | hp2 | a0001 | c0001 | t0003 | g0265 | SAS | PJL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG03041 | hp1 | a0001 | c0010 | t0002 | g0173 | AFR | GWD | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG03041 | hp2 | a0001 | c0010 | t0022 | g0307 | AFR | GWD | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG03098 | hp1 | a0001 | c0014 | t0001 | g0159 | AFR | MSL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG03098 | hp2 | a0013 | c0036 | t0002 | g0303 | AFR | MSL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG03130 | hp1 | a0002 | c0005 | t0006 | g0001 | AFR | ESN | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0134 | AFR | ESN | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG03139 | hp1 | a0002 | c0002 | t0002 | g0281 | AFR | ESN | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0153 | AFR | ESN | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG03209 | hp1 | a0007 | c0031 | t0020 | g0169 | AFR | MSL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG03209 | hp2 | a0001 | c0006 | t0007 | g0125 | AFR | MSL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0295 | AFR | MSL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0128 | AFR | MSL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG03453 | hp1 | a0014 | c0026 | t0013 | g0280 | AFR | MSL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG03453 | hp2 | a0002 | c0015 | t0001 | g0160 | AFR | MSL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG03486 | hp1 | a0004 | c0007 | t0002 | g0168 | AFR | MSL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG03486 | hp2 | a0015 | c0038 | t0012 | g0305 | AFR | MSL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0266 | SAS | PJL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0214 | SAS | PJL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG03516 | hp1 | a0001 | c0008 | t0001 | g0162 | AFR | ESN | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG03516 | hp2 | a0002 | c0009 | t0004 | g0268 | AFR | ESN | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG03540 | hp1 | a0002 | c0002 | t0002 | g0282 | AFR | GWD | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0190 | AFR | GWD | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG03579 | hp2 | a0002 | c0002 | t0005 | g0187 | AFR | MSL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG03654 | hp2 | a0006 | c0012 | t0015 | g0073 | SAS | PJL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0176 | SAS | PJL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG03669 | hp2 | a0001 | c0001 | t0003 | g0215 | SAS | PJL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG03704 | hp1 | a0001 | c0003 | t0002 | g0013 | SAS | PJL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0031 | SAS | PJL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0178 | SAS | PJL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0018 | SAS | PJL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0069 | SAS | BEB | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG03942 | hp1 | a0001 | c0001 | t0011 | g0004 | SAS | BEB | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | BEB | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0233 | SAS | STU | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0032 | SAS | STU | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG04184 | hp1 | a0001 | c0001 | t0011 | g0005 | SAS | BEB | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | BEB | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | STU | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG04199 | hp2 | a0001 | c0001 | t0003 | g0091 | SAS | STU | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0020 | SAS | STU | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0199 | SAS | STU | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | STU | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0260 | SAS | STU | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA18522 | hp1 | a0002 | c0002 | t0002 | g0138 | AFR | YRI | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA18522 | hp2 | a0002 | c0005 | t0003 | g0122 | AFR | YRI | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA18747 | hp1 | a0001 | c0001 | t0003 | g0033 | EAS | CHB | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | CHB | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA18906 | hp1 | a0007 | c0033 | t0007 | g0171 | AFR | YRI | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0293 | AFR | YRI | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA18939 | hp2 | a0001 | c0001 | t0005 | g0234 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA18941 | hp2 | a0003 | c0004 | t0001 | g0239 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA18944 | hp2 | a0001 | c0001 | t0003 | g0276 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA18950 | hp2 | a0001 | c0001 | t0003 | g0273 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA18954 | hp1 | a0001 | c0025 | t0001 | g0232 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA18954 | hp2 | a0003 | c0028 | t0001 | g0185 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA18968 | hp1 | a0003 | c0004 | t0001 | g0110 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA18969 | hp1 | a0003 | c0004 | t0001 | g0195 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA18973 | hp2 | a0001 | c0001 | t0017 | g0089 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA18977 | hp2 | a0001 | c0001 | t0003 | g0093 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA18985 | hp1 | a0001 | c0001 | t0005 | g0211 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA18985 | hp2 | a0001 | c0001 | t0003 | g0210 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA19001 | hp1 | a0001 | c0001 | t0003 | g0179 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA19003 | hp1 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA19011 | hp1 | a0001 | c0001 | t0016 | g0090 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA19030 | hp1 | a0016 | c0032 | t0019 | g0170 | AFR | LWK | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA19030 | hp2 | a0002 | c0013 | t0014 | g0127 | AFR | LWK | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0140 | AFR | LWK | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA19043 | hp2 | a0001 | c0011 | t0003 | g0172 | AFR | LWK | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA19057 | hp1 | a0003 | c0004 | t0001 | g0208 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA19064 | hp2 | a0003 | c0004 | t0001 | g0202 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA19072 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA19072 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA19079 | hp1 | a0003 | c0004 | t0001 | g0212 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA19081 | hp1 | a0003 | c0004 | t0001 | g0146 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA19086 | hp1 | a0017 | c0030 | t0001 | g0045 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA19086 | hp2 | a0018 | c0035 | t0001 | g0255 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA19240 | hp1 | a0002 | c0018 | t0002 | g0158 | AFR | YRI | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA19240 | hp2 | a0019 | c0024 | t0023 | g0308 | AFR | YRI | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0272 | AFR | ASW | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA20129 | hp2 | a0004 | c0007 | t0002 | g0167 | AFR | ASW | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0262 | EUR | TSI | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0014 | EUR | TSI | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0071 | SAS | GIH | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | GIH | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02109 | hp1 | a0002 | c0005 | t0006 | g0001 | AFR | ACB | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0237 | AFR | ACB | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0259 | AFR | ACB | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0155 | AFR | ACB | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG03471 | hp1 | a0001 | c0008 | t0007 | g0161 | AFR | MSL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0151 | AFR | MSL | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG06807 | hp1 | a0001 | c0008 | t0012 | g0143 | AFR | USA | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | USA | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA20300 | hp1 | a0001 | c0001 | t0003 | g0149 | AFR | USA | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0126 | AFR | USA | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA21309 | hp1 | a0004 | c0007 | t0001 | g0164 | AFR | LWK | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
NA21309 | hp2 | a0001 | c0001 | t0005 | g0186 | AFR | LWK | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0189 | REF | REF | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0052 | REF | REF | SEL1L3_chr4_25742433_25867988 | SEL1L3 | chr4 | 25742433 | 25867988 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:25748460 | G | A | 1 | a0014 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.3364C>T | p.Pro1122Ser | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 24/24 | 3516/4543 | 3364/3399 | 1122/1132 | chr4 | 25748460 | |||
chr4:25757712 | C | G | 1 | a0003 | 8 | NA18941.hp2 NA18954.hp2 NA18968.hp1 others(5): Show |
missense_variant | MODERATE | c.3162G>C | p.Trp1054Cys | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 22/24 | 3314/4543 | 3162/3399 | 1054/1132 | chr4 | 25757712 | |||
chr4:25767594 | A | G | 1 | a0016 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.2776T>C | p.Tyr926His | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/24 | 2928/4543 | 2776/3399 | 926/1132 | chr4 | 25767594 | |||
chr4:25790562 | T | C | 2 | a0010 a0013 |
2 | HG02258.hp2 HG03098.hp2 |
missense_variant | MODERATE | c.1969A>G | p.Thr657Ala | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/24 | 2121/4543 | 1969/3399 | 657/1132 | chr4 | 25790562 | |||
chr4:25804657 | T | C | 6 | a0002 a0004 a0009 others(3): Show |
31 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(28): Show |
missense_variant | MODERATE | c.1660A>G | p.Ile554Val | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 10/24 | 1812/4543 | 1660/3399 | 554/1132 | chr4 | 25804657 | |||
chr4:25822001 | C | T | 1 | a0019 | 1 | NA19240.hp2 | missense_variant | MODERATE | c.1285G>A | p.Ala429Thr | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 7/24 | 1437/4543 | 1285/3399 | 429/1132 | chr4 | 25822001 | |||
chr4:25833099 | T | C | 1 | a0006 | 2 | HG02735.hp1 HG03654.hp2 |
missense_variant | MODERATE | c.994A>G | p.Ile332Val | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/24 | 1146/4543 | 994/3399 | 332/1132 | chr4 | 25833099 | |||
chr4:25833456 | G | A | 1 | a0011 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.974C>T | p.Thr325Met | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 4/24 | 1126/4543 | 974/3399 | 325/1132 | chr4 | 25833456 | |||
chr4:25833478 | C | T | 1 | a0008 | 1 | HG01515.hp2 | missense_variant | MODERATE | c.952G>A | p.Gly318Ser | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 4/24 | 1104/4543 | 952/3399 | 318/1132 | chr4 | 25833478 | |||
chr4:25835256 | G | T | 2 | a0005 a0012 |
4 | HG02055.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
missense_variant | MODERATE | c.801C>A | p.Phe267Leu | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 3/24 | 953/4543 | 801/3399 | 267/1132 | chr4 | 25835256 | |||
chr4:25847330 | G | A | 1 | a0017 | 1 | NA19086.hp1 | missense_variant | MODERATE | c.697C>T | p.Arg233Trp | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/24 | 849/4543 | 697/3399 | 233/1132 | chr4 | 25847330 | |||
chr4:25847707 | T | C | 3 | a0004 a0007 a0016 |
8 | HG02965.hp1 HG02970.hp1 HG03209.hp1 others(5): Show |
missense_variant | MODERATE | c.320A>G | p.Gln107Arg | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/24 | 472/4543 | 320/3399 | 107/1132 | chr4 | 25847707 | |||
chr4:25847855 | G | A | 1 | a0018 | 1 | NA19086.hp2 | missense_variant | MODERATE | c.172C>T | p.Pro58Ser | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/24 | 324/4543 | 172/3399 | 58/1132 | chr4 | 25847855 | |||
chr4:25862781 | G | A | 2 | a0009 a0013 |
2 | HG02145.hp2 HG03098.hp2 |
missense_variant | MODERATE | c.56C>T | p.Pro19Leu | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/24 | 208/4543 | 56/3399 | 19/1132 | chr4 | 25862781 | |||
chr4:25862827 | G | A | 1 | a0015 | 1 | HG03486.hp2 | missense_variant | MODERATE | c.10C>T | p.Arg4Cys | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/24 | 162/4543 | 10/3399 | 4/1132 | chr4 | 25862827 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:25757690 | G | A | 5 | a0001c0006 a0001c0011 a0002c0009 others(2): Show |
14 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(11): Show |
splice_region_variant&synonymous_variant | LOW | c.3184C>T | p.Leu1062Leu | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 22/24 | 3336/4543 | 3184/3399 | 1062/1132 | chr4 | 25757690 | |||
chr4:25765347 | G | A | 2 | a0007c0031 a0014c0026 |
2 | HG03209.hp1 HG03453.hp1 |
synonymous_variant | LOW | c.2934C>T | p.Ala978Ala | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/24 | 3086/4543 | 2934/3399 | 978/1132 | chr4 | 25765347 | |||
chr4:25779090 | A | G | 2 | a0002c0018 a0007c0031 |
2 | HG03209.hp1 NA19240.hp1 |
synonymous_variant | LOW | c.2571T>C | p.Pro857Pro | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 16/24 | 2723/4543 | 2571/3399 | 857/1132 | chr4 | 25779090 | |||
chr4:25788281 | G | A | 2 | a0001c0010 a0001c0014 |
4 | HG01109.hp1 HG03041.hp1 HG03041.hp2 others(1): Show |
synonymous_variant | LOW | c.2160C>T | p.Gly720Gly | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/24 | 2312/4543 | 2160/3399 | 720/1132 | chr4 | 25788281 | |||
chr4:25804697 | C | T | 1 | a0001c0027 | 1 | HG00733.hp2 | synonymous_variant | LOW | c.1620G>A | p.Lys540Lys | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 10/24 | 1772/4543 | 1620/3399 | 540/1132 | chr4 | 25804697 | |||
chr4:25804727 | T | C | 2 | a0005c0021 a0005c0022 |
2 | HG02717.hp1 HG02922.hp2 |
synonymous_variant | LOW | c.1590A>G | p.Val530Val | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 10/24 | 1742/4543 | 1590/3399 | 530/1132 | chr4 | 25804727 | |||
chr4:25819875 | A | G | 1 | a0001c0025 | 1 | NA18954.hp1 | synonymous_variant | LOW | c.1356T>C | p.Ala452Ala | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 8/24 | 1508/4543 | 1356/3399 | 452/1132 | chr4 | 25819875 | |||
chr4:25822002 | G | A | 7 | a0001c0003 a0001c0011 a0001c0017 others(4): Show |
16 | HG00558.hp2 HG00609.hp1 HG00733.hp2 others(13): Show |
synonymous_variant | LOW | c.1284C>T | p.Pro428Pro | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 7/24 | 1436/4543 | 1284/3399 | 428/1132 | chr4 | 25822002 | |||
chr4:25833109 | G | A | 2 | a0002c0005 a0002c0018 |
7 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(4): Show |
splice_region_variant&synonymous_variant | LOW | c.984C>T | p.Gly328Gly | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/24 | 1136/4543 | 984/3399 | 328/1132 | chr4 | 25833109 | |||
chr4:25847361 | A | G | 7 | a0001c0008 a0001c0014 a0001c0017 others(4): Show |
15 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(12): Show |
synonymous_variant | LOW | c.666T>C | p.Leu222Leu | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/24 | 818/4543 | 666/3399 | 222/1132 | chr4 | 25847361 | |||
chr4:25847727 | C | T | 1 | a0002c0013 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.300G>A | p.Ser100Ser | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/24 | 452/4543 | 300/3399 | 100/1132 | chr4 | 25847727 | |||
chr4:25847751 | G | A | 1 | a0001c0034 | 1 | HG02976.hp2 | synonymous_variant | LOW | c.276C>T | p.Asn92Asn | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/24 | 428/4543 | 276/3399 | 92/1132 | chr4 | 25847751 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:25747538 | A | T | 1 | a0002c0013t0014 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*887T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 24/24 | 887 | chr4 | 25747538 | ||||||
chr4:25747574 | T | A | 1 | a0007c0031t0020 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*851A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 24/24 | 851 | chr4 | 25747574 | ||||||
chr4:25747576 | T | A | 1 | a0007c0031t0020 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*849A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 24/24 | 849 | chr4 | 25747576 | ||||||
chr4:25747577 | A | AAC | 7 | a0001c0001t0005 a0001c0001t0017 a0001c0008t0012 others(4): Show |
11 | HG02293.hp2 HG02717.hp2 HG02922.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*846_*847dupGT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 24/24 | 847 | chr4 | 25747577 | ||||||
chr4:25747577 | A | AACACACA others(1): Show |
10 | a0001c0001t0003 a0001c0001t0009 a0001c0003t0009 others(7): Show |
26 | HG00438.hp1 HG01081.hp1 HG01516.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*840_*847dupGTGTGT others(2): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 24/24 | 847 | chr4 | 25747577 | ||||||
chr4:25747577 | A | AACACACA others(3): Show |
2 | a0001c0001t0008 a0002c0002t0008 |
3 | HG01074.hp1 HG01257.hp2 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*838_*847dupGTGTGT others(4): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 24/24 | 847 | chr4 | 25747577 | ||||||
chr4:25747577 | A | C | 1 | a0007c0031t0020 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*848T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 24/24 | 848 | chr4 | 25747577 | ||||||
chr4:25747577 | AAC | A | 3 | a0001c0001t0006 a0002c0002t0006 a0002c0005t0006 |
5 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*846_*847delGT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 24/24 | 846 | chr4 | 25747577 | ||||||
chr4:25747605 | T | C | 1 | a0006c0012t0015 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*820A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 24/24 | 820 | chr4 | 25747605 | ||||||
chr4:25747623 | C | T | 1 | a0001c0001t0016 | 1 | NA19011.hp1 | 3_prime_UTR_variant | MODIFIER | c.*802G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 24/24 | 802 | chr4 | 25747623 | ||||||
chr4:25747663 | C | T | 6 | a0001c0006t0007 a0001c0008t0007 a0001c0008t0012 others(3): Show |
6 | HG02258.hp1 HG03209.hp2 HG03471.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*762G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 24/24 | 762 | chr4 | 25747663 | ||||||
chr4:25747681 | C | A | 20 | a0001c0001t0001 a0001c0001t0010 a0001c0001t0016 others(17): Show |
131 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(128): Show |
3_prime_UTR_variant | MODIFIER | c.*744G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 24/24 | 744 | chr4 | 25747681 | ||||||
chr4:25747797 | T | C | 1 | a0001c0001t0018 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*628A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 24/24 | 628 | chr4 | 25747797 | ||||||
chr4:25747865 | C | T | 2 | a0001c0008t0012 a0015c0038t0012 |
2 | HG03486.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*560G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 24/24 | 560 | chr4 | 25747865 | ||||||
chr4:25747886 | A | G | 1 | a0014c0026t0013 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*539T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 24/24 | 539 | chr4 | 25747886 | ||||||
chr4:25748000 | C | T | 1 | a0014c0026t0013 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*425G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 24/24 | 425 | chr4 | 25748000 | ||||||
chr4:25748038 | C | G | 1 | a0001c0001t0011 | 2 | HG03942.hp1 HG04184.hp1 |
3_prime_UTR_variant | MODIFIER | c.*387G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 24/24 | 387 | chr4 | 25748038 | ||||||
chr4:25748065 | G | A | 1 | a0016c0032t0019 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*360C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 24/24 | 360 | chr4 | 25748065 | ||||||
chr4:25748128 | T | G | 3 | a0001c0001t0009 a0001c0003t0009 a0007c0031t0020 |
4 | HG01891.hp1 HG02280.hp1 HG02976.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*297A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 24/24 | 297 | chr4 | 25748128 | ||||||
chr4:25748268 | G | C | 4 | a0001c0001t0004 a0001c0006t0004 a0002c0009t0004 others(1): Show |
8 | HG01192.hp2 HG02280.hp2 HG02451.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*157C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 24/24 | 157 | chr4 | 25748268 | ||||||
chr4:25748378 | C | T | 1 | a0001c0001t0010 | 2 | HG00741.hp1 HG02630.hp2 |
3_prime_UTR_variant | MODIFIER | c.*47G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 24/24 | 47 | chr4 | 25748378 | ||||||
chr4:25862876 | G | C | 1 | a0001c0001t0021 | 1 | HG02074.hp2 | 5_prime_UTR_variant | MODIFIER | c.-40C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/24 | 40 | chr4 | 25862876 | ||||||
chr4:25862977 | G | A | 3 | a0001c0010t0022 a0001c0010t0024 a0019c0024t0023 |
3 | HG01109.hp1 HG03041.hp2 NA19240.hp2 |
5_prime_UTR_variant | MODIFIER | c.-141C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/24 | 141 | chr4 | 25862977 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:25748596 | T | A | 3 | a0001c0001t0002g0003 a0001c0003t0002g0013 a0006c0012t0015g0073 |
3 | HG03654.hp1 HG03654.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.3260-32A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25748596 | |||||||
chr4:25748639 | C | G | 65 | a0001c0001t0001g0012 a0001c0001t0001g0035 a0001c0001t0001g0036 others(62): Show |
65 | HG00597.hp2 HG00609.hp1 HG01074.hp2 others(62): Show |
intron_variant | MODIFIER | c.3260-75G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25748639 | |||||||
chr4:25748685 | T | G | 3 | a0001c0001t0003g0149 a0001c0010t0022g0307 a0002c0005t0003g0122 |
3 | HG03041.hp2 NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.3260-121A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25748685 | |||||||
chr4:25748846 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.3260-282T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25748846 | |||||||
chr4:25748867 | T | C | 93 | a0001c0001t0001g0293 a0001c0001t0002g0002 a0001c0001t0002g0014 others(90): Show |
96 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.3260-303A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25748867 | |||||||
chr4:25748912 | C | T | 15 | a0001c0001t0002g0053 a0001c0001t0002g0102 a0001c0001t0002g0106 others(12): Show |
15 | HG00140.hp2 HG00438.hp1 HG00558.hp2 others(12): Show |
intron_variant | MODIFIER | c.3260-348G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25748912 | |||||||
chr4:25748964 | G | C | 3 | a0001c0001t0003g0286 a0001c0011t0003g0172 a0002c0009t0003g0278 |
3 | HG02572.hp1 HG02886.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3260-400C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25748964 | |||||||
chr4:25749184 | C | T | 4 | a0001c0001t0001g0213 a0001c0001t0001g0227 a0001c0001t0001g0228 others(1): Show |
4 | HG02004.hp2 HG02148.hp2 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.3260-620G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25749184 | |||||||
chr4:25749205 | G | A | 2 | a0002c0005t0001g0156 a0002c0005t0001g0157 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.3260-641C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25749205 | |||||||
chr4:25749227 | T | G | 93 | a0001c0001t0001g0012 a0001c0001t0001g0035 a0001c0001t0001g0036 others(90): Show |
95 | HG00597.hp2 HG00609.hp1 HG01074.hp2 others(92): Show |
intron_variant | MODIFIER | c.3260-663A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25749227 | |||||||
chr4:25749495 | G | A | 1 | a0012c0020t0002g0011 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3260-931C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25749495 | |||||||
chr4:25749594 | T | C | 287 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0019 others(284): Show |
290 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.3260-1030A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25749594 | |||||||
chr4:25749656 | T | C | 285 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0019 others(282): Show |
288 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.3260-1092A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25749656 | |||||||
chr4:25749746 | G | A | 1 | a0014c0026t0013g0280 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3260-1182C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25749746 | |||||||
chr4:25749807 | T | C | 1 | a0001c0001t0009g0285 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3260-1243A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25749807 | |||||||
chr4:25749821 | G | A | 7 | a0001c0001t0003g0149 a0001c0001t0010g0008 a0001c0001t0010g0129 others(4): Show |
7 | HG00741.hp1 HG02630.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.3260-1257C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25749821 | |||||||
chr4:25750008 | C | A | 1 | a0001c0001t0017g0089 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.3260-1444G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25750008 | |||||||
chr4:25750234 | CA | C | 153 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0021 others(150): Show |
155 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.3260-1671delT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25750234 | |||||||
chr4:25750234 | CAAAAAAA others(6): Show |
C | 72 | a0001c0001t0001g0012 a0001c0001t0001g0035 a0001c0001t0001g0036 others(69): Show |
72 | HG00597.hp2 HG00609.hp1 HG01074.hp2 others(69): Show |
intron_variant | MODIFIER | c.3260-1683_3260-167 others(17): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25750234 | |||||||
chr4:25750306 | A | G | 1 | a0001c0001t0002g0241 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.3260-1742T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25750306 | |||||||
chr4:25750450 | G | A | 61 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0040 others(58): Show |
61 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(58): Show |
intron_variant | MODIFIER | c.3260-1886C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25750450 | |||||||
chr4:25750728 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.3260-2164G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25750728 | |||||||
chr4:25750735 | C | G | 1 | a0001c0006t0004g0092 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3260-2171G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25750735 | |||||||
chr4:25750805 | A | T | 1 | a0001c0006t0004g0092 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3260-2241T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25750805 | |||||||
chr4:25750892 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.3260-2328C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25750892 | |||||||
chr4:25751315 | A | T | 2 | a0001c0001t0002g0295 a0009c0037t0003g0304 |
2 | HG02145.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3260-2751T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25751315 | |||||||
chr4:25751374 | C | A | 2 | a0002c0002t0005g0187 a0004c0007t0002g0168 |
2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3260-2810G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25751374 | |||||||
chr4:25751378 | T | A | 2 | a0001c0001t0002g0007 a0001c0001t0002g0220 |
2 | HG00738.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.3260-2814A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25751378 | |||||||
chr4:25751396 | C | T | 1 | a0001c0001t0004g0123 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.3260-2832G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25751396 | |||||||
chr4:25751429 | C | T | 42 | a0001c0001t0002g0002 a0001c0001t0002g0015 a0001c0001t0002g0016 others(39): Show |
43 | HG00558.hp1 HG00733.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.3260-2865G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25751429 | |||||||
chr4:25751439 | A | G | 238 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0019 others(235): Show |
240 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.3260-2875T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25751439 | |||||||
chr4:25751478 | A | G | 1 | a0010c0016t0002g0141 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3260-2914T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25751478 | |||||||
chr4:25751511 | C | T | 4 | a0001c0001t0010g0008 a0001c0001t0010g0129 a0001c0008t0012g0143 others(1): Show |
4 | HG00741.hp1 HG02630.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.3260-2947G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25751511 | |||||||
chr4:25751613 | C | T | 2 | a0001c0008t0001g0162 a0002c0002t0001g0279 |
2 | HG02895.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3260-3049G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25751613 | |||||||
chr4:25751625 | A | G | 21 | a0001c0001t0001g0030 a0001c0001t0001g0077 a0001c0001t0001g0193 others(18): Show |
21 | HG00438.hp1 HG00558.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.3260-3061T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25751625 | |||||||
chr4:25751671 | G | A | 1 | a0001c0001t0001g0028 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.3260-3107C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25751671 | |||||||
chr4:25751754 | T | C | 14 | a0001c0001t0001g0293 a0001c0001t0002g0140 a0001c0001t0002g0196 others(11): Show |
16 | HG02055.hp1 HG02109.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.3260-3190A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25751754 | |||||||
chr4:25751832 | T | C | 238 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0019 others(235): Show |
240 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.3260-3268A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25751832 | |||||||
chr4:25751877 | A | G | 124 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0021 others(121): Show |
124 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.3260-3313T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25751877 | |||||||
chr4:25751983 | T | C | 238 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0019 others(235): Show |
240 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.3260-3419A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25751983 | |||||||
chr4:25752024 | G | A | 3 | a0001c0001t0001g0206 a0001c0008t0001g0162 a0002c0002t0001g0279 |
3 | HG02895.hp1 HG03516.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.3260-3460C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25752024 | |||||||
chr4:25752041 | G | A | 19 | a0001c0001t0001g0009 a0001c0001t0001g0104 a0001c0001t0001g0112 others(16): Show |
19 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(16): Show |
intron_variant | MODIFIER | c.3260-3477C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25752041 | |||||||
chr4:25752087 | C | T | 2 | a0001c0001t0010g0008 a0001c0001t0010g0129 |
2 | HG00741.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.3260-3523G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25752087 | |||||||
chr4:25752088 | G | A | 3 | a0001c0001t0002g0131 a0001c0001t0005g0211 a0001c0001t0005g0234 |
3 | HG02257.hp2 NA18939.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.3260-3524C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25752088 | |||||||
chr4:25752108 | C | CA | 6 | a0001c0001t0001g0047 a0001c0008t0001g0162 a0002c0002t0001g0279 others(3): Show |
6 | HG02056.hp1 HG02895.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.3260-3545dupT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25752108 | |||||||
chr4:25752108 | C | CAA | 11 | a0001c0001t0001g0293 a0001c0001t0002g0140 a0001c0001t0002g0196 others(8): Show |
13 | HG02055.hp1 HG02109.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.3260-3546_3260-354 others(6): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25752108 | |||||||
chr4:25752108 | C | CAAA | 9 | a0001c0006t0007g0125 a0001c0011t0003g0172 a0002c0002t0005g0187 others(6): Show |
9 | HG02258.hp1 HG02572.hp1 HG03209.hp2 others(6): Show |
intron_variant | MODIFIER | c.3260-3547_3260-354 others(7): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25752108 | |||||||
chr4:25752108 | C | CAAAAA | 60 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0042 others(57): Show |
60 | HG00597.hp2 HG00609.hp1 HG01074.hp2 others(57): Show |
intron_variant | MODIFIER | c.3260-3549_3260-354 others(9): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25752108 | |||||||
chr4:25752108 | C | CAAAAAA | 24 | a0001c0001t0001g0012 a0001c0001t0001g0204 a0001c0001t0001g0206 others(21): Show |
24 | HG01106.hp2 HG01256.hp2 HG01358.hp2 others(21): Show |
intron_variant | MODIFIER | c.3260-3550_3260-354 others(10): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25752108 | |||||||
chr4:25752108 | CA | C | 13 | a0001c0001t0001g0077 a0001c0001t0001g0253 a0001c0001t0002g0053 others(10): Show |
13 | HG00558.hp2 HG01070.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.3260-3545delT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25752108 | |||||||
chr4:25752188 | G | A | 3 | a0001c0001t0002g0067 a0001c0001t0002g0177 a0001c0001t0002g0235 |
3 | NA18941.hp1 NA19012.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.3260-3624C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25752188 | |||||||
chr4:25752335 | T | A | 87 | a0001c0001t0001g0012 a0001c0001t0001g0035 a0001c0001t0001g0036 others(84): Show |
87 | HG00597.hp2 HG00609.hp1 HG01074.hp2 others(84): Show |
intron_variant | MODIFIER | c.3260-3771A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25752335 | |||||||
chr4:25752404 | G | A | 98 | a0001c0001t0001g0012 a0001c0001t0001g0035 a0001c0001t0001g0036 others(95): Show |
100 | HG00597.hp2 HG00609.hp1 HG01074.hp2 others(97): Show |
intron_variant | MODIFIER | c.3260-3840C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25752404 | |||||||
chr4:25752418 | G | GA | 39 | a0001c0001t0001g0206 a0001c0001t0001g0293 a0001c0001t0002g0139 others(36): Show |
41 | HG00741.hp1 HG01192.hp2 HG01891.hp1 others(38): Show |
intron_variant | MODIFIER | c.3260-3855dupT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25752418 | |||||||
chr4:25752418 | G | GAA | 23 | a0001c0001t0001g0030 a0001c0001t0001g0077 a0001c0001t0001g0193 others(20): Show |
23 | HG00438.hp1 HG00558.hp2 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.3260-3856_3260-385 others(6): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25752418 | |||||||
chr4:25752418 | GA | G | 117 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0021 others(114): Show |
117 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.3260-3855delT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25752418 | |||||||
chr4:25752418 | GAA | G | 7 | a0001c0001t0001g0040 a0001c0001t0001g0296 a0001c0001t0003g0194 others(4): Show |
7 | HG01884.hp1 HG02040.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.3260-3856_3260-385 others(6): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25752418 | |||||||
chr4:25752441 | T | G | 2 | a0001c0001t0001g0287 a0001c0001t0001g0288 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.3260-3877A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25752441 | |||||||
chr4:25752444 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.3260-3880T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25752444 | |||||||
chr4:25752782 | C | T | 7 | a0001c0001t0002g0163 a0001c0001t0002g0259 a0001c0001t0002g0297 others(4): Show |
7 | HG01891.hp2 HG02559.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.3260-4218G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25752782 | |||||||
chr4:25752804 | A | G | 3 | a0001c0001t0001g0072 a0001c0001t0001g0221 a0001c0001t0002g0014 |
3 | HG01261.hp2 HG01516.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.3260-4240T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25752804 | |||||||
chr4:25752898 | C | A | 6 | a0001c0011t0003g0172 a0002c0002t0005g0187 a0002c0009t0003g0278 others(3): Show |
6 | HG02572.hp1 HG03453.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.3260-4334G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25752898 | |||||||
chr4:25752904 | C | T | 3 | a0001c0006t0007g0125 a0002c0009t0007g0298 a0007c0033t0007g0171 |
3 | HG02258.hp1 HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3260-4340G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25752904 | |||||||
chr4:25752905 | G | A | 2 | a0002c0002t0005g0187 a0004c0007t0002g0168 |
2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3260-4341C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25752905 | |||||||
chr4:25753031 | T | C | 1 | a0016c0032t0019g0170 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3260-4467A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25753031 | |||||||
chr4:25753069 | C | G | 235 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0019 others(232): Show |
237 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.3259+4465G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25753069 | |||||||
chr4:25753107 | C | T | 1 | a0001c0001t0002g0054 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3259+4427G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25753107 | |||||||
chr4:25753124 | G | A | 1 | a0009c0037t0003g0304 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3259+4410C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25753124 | |||||||
chr4:25753133 | G | A | 1 | a0001c0001t0002g0015 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.3259+4401C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25753133 | |||||||
chr4:25753176 | A | G | 1 | a0004c0007t0002g0168 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3259+4358T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25753176 | |||||||
chr4:25753231 | A | C | 1 | a0009c0037t0003g0304 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3259+4303T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25753231 | |||||||
chr4:25753419 | T | C | 112 | a0001c0001t0001g0012 a0001c0001t0001g0030 a0001c0001t0001g0035 others(109): Show |
114 | HG00438.hp1 HG00558.hp2 HG00609.hp1 others(111): Show |
intron_variant | MODIFIER | c.3259+4115A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25753419 | |||||||
chr4:25753517 | C | G | 5 | a0001c0011t0003g0172 a0002c0002t0005g0187 a0002c0009t0003g0278 others(2): Show |
5 | HG02572.hp1 HG03486.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.3259+4017G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25753517 | |||||||
chr4:25753530 | C | G | 1 | a0016c0032t0019g0170 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3259+4004G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25753530 | |||||||
chr4:25753628 | C | T | 1 | a0001c0001t0002g0068 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.3259+3906G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25753628 | |||||||
chr4:25753757 | G | A | 2 | a0001c0011t0002g0055 a0001c0011t0002g0101 |
2 | HG02647.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.3259+3777C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25753757 | |||||||
chr4:25753758 | T | C | 1 | a0010c0016t0002g0141 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3259+3776A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25753758 | |||||||
chr4:25753961 | G | A | 4 | a0001c0001t0010g0008 a0001c0001t0010g0129 a0001c0008t0012g0143 others(1): Show |
4 | HG00741.hp1 HG02630.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.3259+3573C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25753961 | |||||||
chr4:25753975 | C | G | 1 | a0001c0001t0001g0036 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.3259+3559G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25753975 | |||||||
chr4:25753984 | C | CATAA | 51 | a0001c0001t0001g0012 a0001c0001t0001g0077 a0001c0001t0001g0193 others(48): Show |
51 | HG00558.hp2 HG00741.hp1 HG01081.hp2 others(48): Show |
intron_variant | MODIFIER | c.3259+3546_3259+354 others(8): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25753984 | |||||||
chr4:25753984 | C | CATAAATA others(1): Show |
14 | a0001c0001t0001g0030 a0001c0001t0001g0293 a0001c0001t0003g0183 others(11): Show |
16 | HG00438.hp1 HG01891.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.3259+3542_3259+354 others(12): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25753984 | |||||||
chr4:25753984 | CATAA | C | 157 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0021 others(154): Show |
157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.3259+3546_3259+354 others(8): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25753984 | |||||||
chr4:25754004 | A | C | 10 | a0001c0001t0001g0136 a0001c0001t0001g0287 a0001c0001t0001g0288 others(7): Show |
10 | HG01109.hp1 HG01884.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.3259+3530T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25754004 | |||||||
chr4:25754173 | A | C | 1 | a0001c0001t0002g0249 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3259+3361T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25754173 | |||||||
chr4:25754227 | A | G | 278 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0019 others(275): Show |
281 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.3259+3307T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25754227 | |||||||
chr4:25754290 | G | A | 1 | a0001c0001t0002g0155 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3259+3244C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25754290 | |||||||
chr4:25754325 | T | G | 2 | a0001c0011t0002g0055 a0001c0011t0002g0101 |
2 | HG02647.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.3259+3209A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25754325 | |||||||
chr4:25754351 | CT | C | 107 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0021 others(104): Show |
107 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.3259+3182delA | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25754351 | |||||||
chr4:25754351 | CTT | C | 15 | a0001c0001t0001g0287 a0001c0001t0001g0293 a0001c0001t0002g0140 others(12): Show |
17 | HG01192.hp2 HG01891.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.3259+3181_3259+318 others(6): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25754351 | |||||||
chr4:25754401 | C | T | 112 | a0001c0001t0001g0012 a0001c0001t0001g0035 a0001c0001t0001g0036 others(109): Show |
114 | HG00609.hp1 HG00741.hp1 HG01074.hp2 others(111): Show |
intron_variant | MODIFIER | c.3259+3133G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25754401 | |||||||
chr4:25754416 | T | G | 1 | a0010c0016t0002g0141 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3259+3118A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25754416 | |||||||
chr4:25754420 | C | T | 1 | a0002c0002t0008g0301 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3259+3114G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25754420 | |||||||
chr4:25754566 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.3259+2968C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25754566 | |||||||
chr4:25755141 | T | C | 14 | a0001c0001t0001g0293 a0001c0001t0002g0140 a0001c0001t0002g0196 others(11): Show |
16 | HG01192.hp2 HG01891.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.3259+2393A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25755141 | |||||||
chr4:25755166 | C | T | 1 | a0013c0036t0002g0303 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3259+2368G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25755166 | |||||||
chr4:25755179 | G | C | 5 | a0001c0001t0002g0155 a0001c0001t0010g0008 a0001c0001t0010g0129 others(2): Show |
5 | HG00741.hp1 HG02559.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.3259+2355C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25755179 | |||||||
chr4:25755251 | T | TTTTTA | 19 | a0001c0001t0001g0030 a0001c0001t0001g0077 a0001c0001t0001g0193 others(16): Show |
19 | HG00438.hp1 HG00558.hp2 HG02083.hp2 others(16): Show |
intron_variant | MODIFIER | c.3259+2278_3259+228 others(9): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25755251 | |||||||
chr4:25755251 | T | TTTTTATT others(3): Show |
2 | a0001c0001t0002g0053 a0001c0001t0002g0106 |
2 | HG01358.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.3259+2273_3259+228 others(14): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25755251 | |||||||
chr4:25755251 | T | TTTTTATT others(8): Show |
1 | a0001c0001t0002g0247 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.3259+2268_3259+228 others(19): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25755251 | |||||||
chr4:25755251 | TTTTTA | T | 109 | a0001c0001t0001g0012 a0001c0001t0001g0035 a0001c0001t0001g0036 others(106): Show |
111 | HG00609.hp1 HG00741.hp1 HG01074.hp2 others(108): Show |
intron_variant | MODIFIER | c.3259+2278_3259+228 others(9): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25755251 | |||||||
chr4:25755385 | A | C | 1 | a0001c0001t0001g0057 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.3259+2149T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25755385 | |||||||
chr4:25755466 | G | A | 7 | a0001c0001t0001g0075 a0001c0001t0001g0080 a0001c0001t0001g0081 others(4): Show |
7 | HG02074.hp1 HG02083.hp1 NA18942.hp1 others(4): Show |
intron_variant | MODIFIER | c.3259+2068C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25755466 | |||||||
chr4:25755525 | T | G | 86 | a0001c0001t0001g0012 a0001c0001t0001g0035 a0001c0001t0001g0036 others(83): Show |
88 | HG00609.hp1 HG01074.hp2 HG01106.hp2 others(85): Show |
intron_variant | MODIFIER | c.3259+2009A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25755525 | |||||||
chr4:25755677 | G | A | 3 | a0007c0031t0020g0169 a0014c0026t0013g0280 a0016c0032t0019g0170 |
3 | HG03209.hp1 HG03453.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.3259+1857C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25755677 | |||||||
chr4:25755773 | T | C | 4 | a0001c0001t0001g0104 a0001c0001t0001g0112 a0001c0001t0001g0113 others(1): Show |
4 | HG00140.hp1 HG00733.hp2 HG01069.hp1 others(1): Show |
intron_variant | MODIFIER | c.3259+1761A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25755773 | |||||||
chr4:25755817 | T | C | 2 | a0001c0003t0002g0096 a0001c0003t0002g0097 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.3259+1717A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25755817 | |||||||
chr4:25755834 | A | G | 1 | a0001c0001t0001g0077 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.3259+1700T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25755834 | |||||||
chr4:25755875 | G | C | 4 | a0001c0001t0010g0008 a0001c0001t0010g0129 a0001c0008t0012g0143 others(1): Show |
4 | HG00741.hp1 HG02630.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.3259+1659C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25755875 | |||||||
chr4:25756146 | C | T | 1 | a0010c0016t0002g0141 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3259+1388G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25756146 | |||||||
chr4:25756147 | G | A | 1 | a0001c0001t0001g0044 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.3259+1387C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25756147 | |||||||
chr4:25756236 | C | T | 3 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0264 |
3 | HG00738.hp2 HG01928.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.3259+1298G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25756236 | |||||||
chr4:25756237 | G | A | 1 | a0001c0001t0001g0206 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.3259+1297C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25756237 | |||||||
chr4:25756452 | G | A | 2 | a0001c0001t0010g0008 a0001c0001t0010g0129 |
2 | HG00741.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.3259+1082C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25756452 | |||||||
chr4:25756474 | T | C | 1 | a0001c0001t0002g0275 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.3259+1060A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25756474 | |||||||
chr4:25756654 | G | A | 1 | a0001c0001t0002g0155 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3259+880C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25756654 | |||||||
chr4:25756734 | A | G | 1 | a0001c0001t0004g0123 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.3259+800T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25756734 | |||||||
chr4:25756797 | C | T | 1 | a0001c0001t0002g0155 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3259+737G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25756797 | |||||||
chr4:25756958 | G | A | 278 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0019 others(275): Show |
281 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.3259+576C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25756958 | |||||||
chr4:25757033 | T | C | 40 | a0001c0001t0002g0002 a0001c0001t0002g0015 a0001c0001t0002g0016 others(37): Show |
41 | HG00558.hp1 HG00733.hp1 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.3259+501A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25757033 | |||||||
chr4:25757104 | C | T | 1 | a0001c0001t0001g0118 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.3259+430G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25757104 | |||||||
chr4:25757291 | A | C | 1 | a0001c0001t0001g0217 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3259+243T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25757291 | |||||||
chr4:25757318 | A | G | 278 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0019 others(275): Show |
281 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.3259+216T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25757318 | |||||||
chr4:25757334 | C | T | 3 | a0001c0001t0001g0078 a0001c0001t0001g0244 a0001c0001t0001g0271 |
3 | NA18939.hp1 NA19007.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.3259+200G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25757334 | |||||||
chr4:25757342 | G | A | 171 | a0001c0001t0001g0012 a0001c0001t0001g0030 a0001c0001t0001g0035 others(168): Show |
174 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(171): Show |
intron_variant | MODIFIER | c.3259+192C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25757342 | |||||||
chr4:25757373 | T | C | 70 | a0001c0001t0001g0012 a0001c0001t0001g0035 a0001c0001t0001g0036 others(67): Show |
70 | HG00609.hp1 HG01074.hp2 HG01106.hp2 others(67): Show |
intron_variant | MODIFIER | c.3259+161A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25757373 | |||||||
chr4:25757455 | AC | A | 87 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0021 others(84): Show |
87 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(84): Show |
intron_variant | MODIFIER | c.3259+78delG | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25757455 | |||||||
chr4:25757457 | C | A | 18 | a0001c0001t0001g0029 a0001c0001t0001g0037 a0001c0001t0001g0047 others(15): Show |
18 | HG00438.hp2 HG00597.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.3259+77G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25757457 | |||||||
chr4:25757457 | C | CA | 13 | a0001c0001t0002g0032 a0001c0001t0002g0139 a0001c0001t0002g0148 others(10): Show |
13 | HG00738.hp1 HG00741.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.3259+76dupT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25757457 | |||||||
chr4:25757457 | CA | C | 85 | a0001c0001t0001g0030 a0001c0001t0001g0035 a0001c0001t0001g0042 others(82): Show |
85 | HG00558.hp2 HG00609.hp1 HG01074.hp2 others(82): Show |
intron_variant | MODIFIER | c.3259+76delT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25757457 | |||||||
chr4:25757457 | CAA | C | 22 | a0001c0001t0002g0155 a0001c0001t0002g0174 a0001c0001t0002g0176 others(19): Show |
22 | HG02258.hp2 HG02280.hp2 HG02451.hp2 others(19): Show |
intron_variant | MODIFIER | c.3259+75_3259+76del others(2): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25757457 | |||||||
chr4:25757487 | CT | C | 170 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0021 others(167): Show |
172 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.3259+46delA | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25757487 | |||||||
chr4:25757488 | T | C | 69 | a0001c0001t0001g0012 a0001c0001t0001g0035 a0001c0001t0001g0036 others(66): Show |
69 | HG00609.hp1 HG01074.hp2 HG01106.hp2 others(66): Show |
intron_variant | MODIFIER | c.3259+46A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 23/23 | chr4 | 25757488 | |||||||
chr4:25757676 | C | G | 44 | a0001c0001t0001g0030 a0001c0001t0001g0077 a0001c0001t0001g0084 others(41): Show |
46 | HG00438.hp1 HG00558.hp2 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.3186+12G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 22/23 | chr4 | 25757676 | |||||||
chr4:25757850 | A | T | 1 | a0001c0003t0002g0013 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3084-60T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 21/23 | chr4 | 25757850 | |||||||
chr4:25757862 | A | C | 4 | a0001c0001t0002g0126 a0004c0007t0001g0164 a0004c0007t0001g0165 others(1): Show |
4 | HG02965.hp1 HG02970.hp1 NA20300.hp2 others(1): Show |
intron_variant | MODIFIER | c.3084-72T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 21/23 | chr4 | 25757862 | |||||||
chr4:25758069 | A | T | 128 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0021 others(125): Show |
128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.3084-279T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 21/23 | chr4 | 25758069 | |||||||
chr4:25758153 | G | A | 1 | a0002c0002t0005g0187 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3084-363C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 21/23 | chr4 | 25758153 | |||||||
chr4:25758195 | G | A | 3 | a0001c0001t0009g0124 a0001c0001t0009g0285 a0001c0003t0009g0027 |
3 | HG01891.hp1 HG02280.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.3084-405C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 21/23 | chr4 | 25758195 | |||||||
chr4:25758361 | C | T | 3 | a0001c0006t0007g0125 a0002c0009t0007g0298 a0007c0033t0007g0171 |
3 | HG02258.hp1 HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3084-571G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 21/23 | chr4 | 25758361 | |||||||
chr4:25758388 | T | C | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3083+553A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 21/23 | chr4 | 25758388 | |||||||
chr4:25758559 | C | T | 9 | a0001c0001t0002g0002 a0001c0001t0002g0015 a0001c0001t0002g0016 others(6): Show |
10 | HG00733.hp1 HG00738.hp2 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.3083+382G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 21/23 | chr4 | 25758559 | |||||||
chr4:25758674 | CTT | C | 21 | a0001c0001t0001g0030 a0001c0001t0001g0077 a0001c0001t0001g0084 others(18): Show |
21 | HG00558.hp2 HG00741.hp1 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.3083+265_3083+266d others(4): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 21/23 | chr4 | 25758674 | |||||||
chr4:25758678 | T | C | 1 | a0001c0001t0002g0155 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3083+263A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 21/23 | chr4 | 25758678 | |||||||
chr4:25758761 | G | T | 20 | a0001c0001t0001g0030 a0001c0001t0001g0077 a0001c0001t0001g0084 others(17): Show |
20 | HG00438.hp1 HG00558.hp2 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.3083+180C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 21/23 | chr4 | 25758761 | |||||||
chr4:25758859 | G | T | 1 | a0001c0001t0017g0089 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.3083+82C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 21/23 | chr4 | 25758859 | |||||||
chr4:25758876 | C | T | 1 | a0001c0001t0002g0155 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3083+65G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 21/23 | chr4 | 25758876 | |||||||
chr4:25759071 | A | G | 70 | a0001c0001t0001g0012 a0001c0001t0001g0035 a0001c0001t0001g0036 others(67): Show |
70 | HG00609.hp1 HG01074.hp2 HG01106.hp2 others(67): Show |
splice_region_variant&intron_variant | LOW | c.2956-3T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25759071 | |||||||
chr4:25759158 | C | G | 1 | a0001c0017t0002g0144 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2956-90G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25759158 | |||||||
chr4:25759163 | AT | A | 9 | a0001c0006t0002g0154 a0001c0006t0004g0092 a0001c0006t0004g0132 others(6): Show |
9 | HG02280.hp2 HG02451.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.2956-96delA | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25759163 | |||||||
chr4:25759206 | T | C | 114 | a0001c0001t0001g0012 a0001c0001t0001g0035 a0001c0001t0001g0036 others(111): Show |
115 | HG00558.hp1 HG00609.hp1 HG00733.hp1 others(112): Show |
intron_variant | MODIFIER | c.2956-138A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25759206 | |||||||
chr4:25759236 | C | G | 20 | a0001c0001t0001g0030 a0001c0001t0001g0077 a0001c0001t0001g0084 others(17): Show |
20 | HG00438.hp1 HG00558.hp2 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.2956-168G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25759236 | |||||||
chr4:25759252 | CA | C | 20 | a0001c0001t0002g0002 a0001c0001t0002g0015 a0001c0001t0002g0016 others(17): Show |
21 | HG00558.hp1 HG00733.hp1 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.2956-185delT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25759252 | |||||||
chr4:25759263 | G | A | 41 | a0001c0001t0002g0002 a0001c0001t0002g0015 a0001c0001t0002g0016 others(38): Show |
42 | HG00558.hp1 HG00733.hp1 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.2956-195C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25759263 | |||||||
chr4:25759281 | C | T | 1 | a0001c0001t0002g0017 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2956-213G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25759281 | |||||||
chr4:25759322 | G | A | 22 | a0001c0001t0001g0030 a0001c0001t0001g0077 a0001c0001t0001g0084 others(19): Show |
22 | HG00438.hp1 HG00558.hp2 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.2956-254C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25759322 | |||||||
chr4:25759696 | C | T | 1 | a0001c0001t0002g0148 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2956-628G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25759696 | |||||||
chr4:25759783 | C | T | 1 | a0001c0010t0022g0307 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2956-715G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25759783 | |||||||
chr4:25759784 | A | G | 136 | a0001c0001t0001g0012 a0001c0001t0001g0030 a0001c0001t0001g0035 others(133): Show |
137 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(134): Show |
intron_variant | MODIFIER | c.2956-716T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25759784 | |||||||
chr4:25759797 | C | T | 2 | a0001c0003t0002g0096 a0001c0003t0002g0097 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2956-729G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25759797 | |||||||
chr4:25759798 | A | G | 264 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0019 others(261): Show |
265 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.2956-730T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25759798 | |||||||
chr4:25759877 | G | C | 1 | a0001c0001t0001g0012 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2956-809C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25759877 | |||||||
chr4:25760099 | T | C | 1 | a0004c0007t0001g0166 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2956-1031A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25760099 | |||||||
chr4:25760157 | G | A | 2 | a0002c0002t0005g0187 a0010c0016t0002g0141 |
2 | HG02258.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2956-1089C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25760157 | |||||||
chr4:25760241 | C | T | 3 | a0001c0001t0003g0149 a0001c0010t0022g0307 a0002c0005t0003g0122 |
3 | HG03041.hp2 NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2956-1173G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25760241 | |||||||
chr4:25760268 | T | C | 20 | a0001c0001t0001g0030 a0001c0001t0001g0077 a0001c0001t0001g0084 others(17): Show |
20 | HG00438.hp1 HG00558.hp2 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.2956-1200A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25760268 | |||||||
chr4:25760313 | G | A | 3 | a0007c0031t0020g0169 a0014c0026t0013g0280 a0016c0032t0019g0170 |
3 | HG03209.hp1 HG03453.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2956-1245C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25760313 | |||||||
chr4:25760695 | A | G | 1 | a0010c0016t0002g0141 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2956-1627T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25760695 | |||||||
chr4:25760760 | G | A | 1 | a0001c0001t0003g0194 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2956-1692C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25760760 | |||||||
chr4:25761298 | G | A | 113 | a0001c0001t0001g0012 a0001c0001t0001g0035 a0001c0001t0001g0036 others(110): Show |
114 | HG00558.hp1 HG00609.hp1 HG00733.hp1 others(111): Show |
intron_variant | MODIFIER | c.2956-2230C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25761298 | |||||||
chr4:25761301 | G | T | 1 | a0001c0001t0001g0258 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.2956-2233C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25761301 | |||||||
chr4:25761348 | G | C | 2 | a0001c0001t0010g0008 a0001c0001t0010g0129 |
2 | HG00741.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.2956-2280C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25761348 | |||||||
chr4:25761348 | G | T | 2 | a0001c0001t0001g0201 a0001c0001t0001g0218 |
2 | NA18993.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.2956-2280C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25761348 | |||||||
chr4:25761420 | T | C | 264 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0019 others(261): Show |
265 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.2956-2352A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25761420 | |||||||
chr4:25761421 | G | A | 2 | a0001c0001t0002g0295 a0009c0037t0003g0304 |
2 | HG02145.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2956-2353C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25761421 | |||||||
chr4:25761447 | C | T | 2 | a0001c0008t0012g0143 a0015c0038t0012g0305 |
2 | HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2956-2379G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25761447 | |||||||
chr4:25761623 | A | G | 3 | a0001c0001t0002g0295 a0002c0002t0005g0187 a0009c0037t0003g0304 |
3 | HG02145.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2956-2555T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25761623 | |||||||
chr4:25761669 | C | G | 1 | a0001c0001t0002g0295 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2956-2601G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25761669 | |||||||
chr4:25761770 | A | G | 1 | a0002c0009t0004g0268 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2956-2702T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25761770 | |||||||
chr4:25762138 | G | T | 1 | a0001c0001t0002g0237 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2956-3070C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25762138 | |||||||
chr4:25762431 | C | G | 265 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0019 others(262): Show |
266 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.2955+2895G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25762431 | |||||||
chr4:25762695 | C | T | 1 | a0001c0001t0002g0148 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2955+2631G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25762695 | |||||||
chr4:25762709 | G | T | 114 | a0001c0001t0001g0012 a0001c0001t0001g0035 a0001c0001t0001g0036 others(111): Show |
115 | HG00558.hp1 HG00609.hp1 HG00642.hp2 others(112): Show |
intron_variant | MODIFIER | c.2955+2617C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25762709 | |||||||
chr4:25762803 | C | G | 21 | a0001c0001t0001g0030 a0001c0001t0001g0077 a0001c0001t0001g0084 others(18): Show |
21 | HG00438.hp1 HG00558.hp2 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.2955+2523G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25762803 | |||||||
chr4:25762821 | C | G | 1 | a0001c0001t0001g0263 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2955+2505G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25762821 | |||||||
chr4:25762877 | G | A | 3 | a0001c0001t0002g0174 a0001c0001t0002g0176 a0001c0001t0002g0260 |
3 | HG03017.hp1 HG03669.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2955+2449C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25762877 | |||||||
chr4:25762953 | C | T | 2 | a0005c0019t0002g0010 a0010c0016t0002g0141 |
2 | HG02055.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.2955+2373G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25762953 | |||||||
chr4:25762974 | C | CA | 91 | a0001c0001t0001g0012 a0001c0001t0001g0035 a0001c0001t0001g0036 others(88): Show |
91 | HG00099.hp2 HG00609.hp1 HG00735.hp1 others(88): Show |
intron_variant | MODIFIER | c.2955+2351dupT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25762974 | |||||||
chr4:25762974 | CAA | C | 20 | a0001c0001t0001g0030 a0001c0001t0001g0077 a0001c0001t0001g0084 others(17): Show |
20 | HG00438.hp1 HG00558.hp2 HG01069.hp1 others(17): Show |
intron_variant | MODIFIER | c.2955+2350_2955+235 others(6): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25762974 | |||||||
chr4:25763037 | G | C | 1 | a0001c0001t0002g0148 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2955+2289C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25763037 | |||||||
chr4:25763185 | G | GA | 133 | a0001c0001t0001g0012 a0001c0001t0001g0035 a0001c0001t0001g0036 others(130): Show |
136 | HG00558.hp1 HG00609.hp1 HG00642.hp2 others(133): Show |
intron_variant | MODIFIER | c.2955+2140dupT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25763185 | |||||||
chr4:25763231 | C | G | 1 | a0001c0001t0002g0003 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2955+2095G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25763231 | |||||||
chr4:25763293 | T | C | 3 | a0001c0001t0010g0008 a0001c0001t0010g0129 a0010c0016t0002g0141 |
3 | HG00741.hp1 HG02258.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2955+2033A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25763293 | |||||||
chr4:25763376 | G | A | 1 | a0001c0001t0002g0196 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2955+1950C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25763376 | |||||||
chr4:25763690 | C | A | 235 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0021 others(232): Show |
238 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.2955+1636G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25763690 | |||||||
chr4:25763705 | G | A | 128 | a0001c0001t0001g0012 a0001c0001t0001g0035 a0001c0001t0001g0036 others(125): Show |
129 | HG00558.hp1 HG00609.hp1 HG00642.hp2 others(126): Show |
intron_variant | MODIFIER | c.2955+1621C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25763705 | |||||||
chr4:25763892 | G | C | 1 | a0001c0001t0002g0140 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2955+1434C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25763892 | |||||||
chr4:25763905 | G | A | 250 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0021 others(247): Show |
253 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.2955+1421C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25763905 | |||||||
chr4:25763911 | G | T | 1 | a0001c0001t0002g0153 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2955+1415C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25763911 | |||||||
chr4:25763942 | A | G | 8 | a0001c0006t0002g0154 a0001c0006t0004g0092 a0001c0006t0004g0132 others(5): Show |
8 | HG02280.hp2 HG02451.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.2955+1384T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25763942 | |||||||
chr4:25763996 | A | G | 5 | a0001c0001t0003g0149 a0001c0010t0022g0307 a0001c0011t0003g0172 others(2): Show |
5 | HG02572.hp1 HG03041.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.2955+1330T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25763996 | |||||||
chr4:25764021 | C | A | 8 | a0001c0006t0002g0154 a0001c0006t0004g0092 a0001c0006t0004g0132 others(5): Show |
8 | HG02280.hp2 HG02451.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.2955+1305G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25764021 | |||||||
chr4:25764064 | C | T | 1 | a0001c0001t0002g0176 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2955+1262G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25764064 | |||||||
chr4:25764065 | G | A | 5 | a0001c0001t0005g0300 a0001c0001t0009g0124 a0001c0001t0009g0285 others(2): Show |
5 | HG01891.hp1 HG02280.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2955+1261C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25764065 | |||||||
chr4:25764079 | G | T | 1 | a0001c0001t0001g0043 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2955+1247C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25764079 | |||||||
chr4:25764087 | C | T | 3 | a0001c0001t0010g0008 a0001c0001t0010g0129 a0010c0016t0002g0141 |
3 | HG00741.hp1 HG02258.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2955+1239G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25764087 | |||||||
chr4:25764088 | G | A | 48 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0226 others(45): Show |
49 | HG00558.hp1 HG00642.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.2955+1238C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25764088 | |||||||
chr4:25764190 | G | A | 1 | a0001c0001t0001g0012 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2955+1136C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25764190 | |||||||
chr4:25764262 | A | T | 72 | a0001c0001t0001g0012 a0001c0001t0001g0035 a0001c0001t0001g0036 others(69): Show |
72 | HG00609.hp1 HG01074.hp2 HG01106.hp2 others(69): Show |
intron_variant | MODIFIER | c.2955+1064T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25764262 | |||||||
chr4:25764357 | G | A | 1 | a0001c0001t0003g0215 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2955+969C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25764357 | |||||||
chr4:25764412 | G | A | 1 | a0001c0001t0002g0002 | 2 | HG00733.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.2955+914C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25764412 | |||||||
chr4:25764523 | G | T | 2 | a0005c0019t0002g0010 a0012c0020t0002g0011 |
2 | HG02055.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2955+803C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25764523 | |||||||
chr4:25764562 | G | A | 1 | a0001c0001t0002g0190 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2955+764C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25764562 | |||||||
chr4:25764603 | T | C | 1 | a0001c0001t0002g0261 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.2955+723A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25764603 | |||||||
chr4:25765029 | C | T | 1 | a0001c0001t0002g0139 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2955+297G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25765029 | |||||||
chr4:25765037 | C | T | 78 | a0001c0001t0001g0012 a0001c0001t0001g0035 a0001c0001t0001g0036 others(75): Show |
78 | HG00609.hp1 HG01074.hp2 HG01106.hp2 others(75): Show |
intron_variant | MODIFIER | c.2955+289G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25765037 | |||||||
chr4:25765063 | C | T | 6 | a0001c0006t0007g0125 a0001c0011t0002g0055 a0001c0011t0002g0101 others(3): Show |
6 | HG02258.hp1 HG02647.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.2955+263G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25765063 | |||||||
chr4:25765140 | G | A | 1 | a0002c0002t0008g0301 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2955+186C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25765140 | |||||||
chr4:25765269 | C | A | 13 | a0001c0001t0001g0293 a0001c0001t0002g0140 a0001c0001t0005g0300 others(10): Show |
15 | HG01891.hp1 HG02109.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.2955+57G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25765269 | |||||||
chr4:25765289 | C | G | 1 | a0001c0001t0004g0123 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2955+37G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 20/23 | chr4 | 25765289 | |||||||
chr4:25765442 | G | A | 3 | a0001c0001t0002g0295 a0002c0018t0002g0158 a0009c0037t0003g0304 |
3 | HG02145.hp2 HG03225.hp1 NA19240.hp1 |
splice_region_variant&intron_variant | LOW | c.2846-7C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25765442 | |||||||
chr4:25765497 | T | G | 4 | a0001c0001t0002g0128 a0001c0001t0002g0134 a0001c0001t0002g0151 others(1): Show |
4 | HG02630.hp1 HG03130.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2846-62A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25765497 | |||||||
chr4:25765511 | A | T | 107 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0030 others(104): Show |
107 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.2846-76T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25765511 | |||||||
chr4:25765561 | G | A | 205 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0021 others(202): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.2846-126C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25765561 | |||||||
chr4:25765752 | C | T | 1 | a0001c0001t0002g0131 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2846-317G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25765752 | |||||||
chr4:25766058 | G | T | 6 | a0001c0006t0007g0125 a0001c0011t0002g0055 a0001c0011t0002g0101 others(3): Show |
6 | HG02258.hp1 HG02647.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.2846-623C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25766058 | |||||||
chr4:25766154 | A | G | 1 | a0001c0001t0001g0041 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2846-719T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25766154 | |||||||
chr4:25766157 | G | T | 1 | a0001c0001t0001g0041 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2846-722C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25766157 | |||||||
chr4:25766158 | G | T | 1 | a0001c0001t0001g0041 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2846-723C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25766158 | |||||||
chr4:25766159 | C | A | 1 | a0001c0001t0001g0041 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2846-724G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25766159 | |||||||
chr4:25766160 | T | A | 1 | a0001c0001t0001g0041 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2846-725A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25766160 | |||||||
chr4:25766282 | A | G | 1 | a0006c0012t0002g0022 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2846-847T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25766282 | |||||||
chr4:25766344 | G | A | 1 | a0001c0001t0001g0250 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2846-909C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25766344 | |||||||
chr4:25766389 | G | A | 1 | a0001c0001t0002g0140 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2846-954C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25766389 | |||||||
chr4:25766439 | C | CA | 8 | a0001c0001t0001g0145 a0001c0001t0001g0246 a0001c0001t0002g0178 others(5): Show |
8 | HG01515.hp2 HG02055.hp1 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.2846-1005dupT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25766439 | |||||||
chr4:25766439 | CA | C | 80 | a0001c0001t0001g0012 a0001c0001t0001g0035 a0001c0001t0001g0036 others(77): Show |
80 | HG00609.hp1 HG01070.hp2 HG01074.hp2 others(77): Show |
intron_variant | MODIFIER | c.2846-1005delT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25766439 | |||||||
chr4:25766439 | CAA | C | 12 | a0001c0001t0001g0216 a0001c0001t0001g0293 a0001c0001t0002g0140 others(9): Show |
14 | HG00741.hp1 HG02109.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.2846-1006_2846-100 others(6): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25766439 | |||||||
chr4:25766459 | G | T | 1 | a0001c0001t0001g0077 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2846-1024C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25766459 | |||||||
chr4:25766500 | G | A | 1 | a0001c0001t0002g0174 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2845+1025C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25766500 | |||||||
chr4:25766508 | T | C | 8 | a0001c0001t0001g0293 a0001c0001t0002g0140 a0001c0001t0006g0150 others(5): Show |
10 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.2845+1017A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25766508 | |||||||
chr4:25766599 | G | C | 6 | a0001c0006t0007g0125 a0001c0011t0002g0055 a0001c0011t0002g0101 others(3): Show |
6 | HG02258.hp1 HG02647.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.2845+926C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25766599 | |||||||
chr4:25766627 | C | T | 1 | a0001c0001t0001g0240 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2845+898G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25766627 | |||||||
chr4:25766674 | A | G | 1 | a0002c0002t0008g0301 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2845+851T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25766674 | |||||||
chr4:25766855 | C | T | 1 | a0001c0001t0002g0105 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2845+670G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25766855 | |||||||
chr4:25766867 | G | T | 1 | a0001c0001t0003g0039 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2845+658C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25766867 | |||||||
chr4:25766868 | A | C | 1 | a0001c0001t0003g0039 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2845+657T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25766868 | |||||||
chr4:25766919 | G | A | 1 | a0012c0020t0002g0011 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2845+606C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25766919 | |||||||
chr4:25766957 | C | T | 1 | a0001c0001t0001g0078 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.2845+568G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25766957 | |||||||
chr4:25767002 | A | T | 1 | a0001c0001t0002g0297 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2845+523T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25767002 | |||||||
chr4:25767030 | G | A | 3 | a0001c0001t0002g0295 a0002c0018t0002g0158 a0009c0037t0003g0304 |
3 | HG02145.hp2 HG03225.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2845+495C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25767030 | |||||||
chr4:25767155 | G | A | 92 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0030 others(89): Show |
92 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(89): Show |
intron_variant | MODIFIER | c.2845+370C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25767155 | |||||||
chr4:25767160 | C | G | 1 | a0002c0018t0002g0158 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2845+365G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25767160 | |||||||
chr4:25767417 | C | A | 1 | a0002c0002t0008g0301 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2845+108G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25767417 | |||||||
chr4:25767419 | A | T | 3 | a0001c0001t0002g0295 a0002c0018t0002g0158 a0009c0037t0003g0304 |
3 | HG02145.hp2 HG03225.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2845+106T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25767419 | |||||||
chr4:25767507 | C | G | 71 | a0001c0001t0001g0012 a0001c0001t0001g0035 a0001c0001t0001g0036 others(68): Show |
71 | HG00609.hp1 HG01074.hp2 HG01106.hp2 others(68): Show |
intron_variant | MODIFIER | c.2845+18G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25767507 | |||||||
chr4:25767508 | C | G | 71 | a0001c0001t0001g0012 a0001c0001t0001g0035 a0001c0001t0001g0036 others(68): Show |
71 | HG00609.hp1 HG01074.hp2 HG01106.hp2 others(68): Show |
intron_variant | MODIFIER | c.2845+17G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25767508 | |||||||
chr4:25767513 | T | C | 160 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0030 others(157): Show |
161 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.2845+12A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 19/23 | chr4 | 25767513 | |||||||
chr4:25767614 | G | A | 1 | a0001c0001t0002g0243 | 1 | HG01106.hp1 | splice_region_variant&intron_variant | LOW | c.2761-5C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 18/23 | chr4 | 25767614 | |||||||
chr4:25767622 | G | A | 3 | a0001c0001t0010g0008 a0001c0001t0010g0129 a0010c0016t0002g0141 |
3 | HG00741.hp1 HG02258.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2761-13C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 18/23 | chr4 | 25767622 | |||||||
chr4:25767697 | T | C | 71 | a0001c0001t0001g0012 a0001c0001t0001g0035 a0001c0001t0001g0036 others(68): Show |
71 | HG00609.hp1 HG01074.hp2 HG01106.hp2 others(68): Show |
intron_variant | MODIFIER | c.2760+43A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 18/23 | chr4 | 25767697 | |||||||
chr4:25767705 | A | G | 71 | a0001c0001t0001g0012 a0001c0001t0001g0035 a0001c0001t0001g0036 others(68): Show |
71 | HG00609.hp1 HG01074.hp2 HG01106.hp2 others(68): Show |
intron_variant | MODIFIER | c.2760+35T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 18/23 | chr4 | 25767705 | |||||||
chr4:25767838 | T | C | 5 | a0001c0006t0007g0125 a0001c0011t0002g0055 a0001c0011t0002g0101 others(2): Show |
5 | HG02258.hp1 HG02647.hp2 HG02723.hp2 others(2): Show |
splice_region_variant&intron_variant | LOW | c.2670-8A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25767838 | |||||||
chr4:25767964 | T | A | 2 | a0001c0001t0001g0047 a0001c0001t0002g0196 |
2 | HG02055.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.2670-134A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25767964 | |||||||
chr4:25768011 | G | A | 1 | a0001c0001t0002g0155 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2670-181C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25768011 | |||||||
chr4:25768254 | C | T | 5 | a0001c0006t0007g0125 a0001c0011t0002g0055 a0001c0011t0002g0101 others(2): Show |
5 | HG02258.hp1 HG02647.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.2670-424G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25768254 | |||||||
chr4:25768349 | C | T | 107 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0040 others(104): Show |
107 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.2670-519G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25768349 | |||||||
chr4:25768460 | G | A | 1 | a0001c0001t0003g0039 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2670-630C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25768460 | |||||||
chr4:25768506 | C | T | 1 | a0001c0001t0002g0302 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2670-676G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25768506 | |||||||
chr4:25768612 | G | C | 1 | a0001c0001t0001g0084 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2670-782C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25768612 | |||||||
chr4:25768763 | G | A | 11 | a0001c0006t0002g0154 a0001c0006t0004g0092 a0001c0006t0004g0132 others(8): Show |
11 | HG02280.hp2 HG02451.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.2670-933C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25768763 | |||||||
chr4:25768830 | T | C | 2 | a0001c0008t0001g0162 a0002c0002t0001g0279 |
2 | HG02895.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2670-1000A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25768830 | |||||||
chr4:25768844 | T | C | 1 | a0002c0018t0002g0158 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2670-1014A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25768844 | |||||||
chr4:25768902 | G | C | 70 | a0001c0001t0001g0012 a0001c0001t0001g0035 a0001c0001t0001g0036 others(67): Show |
70 | HG00609.hp1 HG01074.hp2 HG01106.hp2 others(67): Show |
intron_variant | MODIFIER | c.2670-1072C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25768902 | |||||||
chr4:25769028 | A | AT | 239 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0021 others(236): Show |
241 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.2670-1199dupA | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25769028 | |||||||
chr4:25769266 | A | G | 5 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0291 others(2): Show |
5 | HG00099.hp2 HG00735.hp2 HG01069.hp1 others(2): Show |
intron_variant | MODIFIER | c.2670-1436T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25769266 | |||||||
chr4:25769493 | G | A | 254 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0021 others(251): Show |
256 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.2670-1663C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25769493 | |||||||
chr4:25769514 | T | G | 6 | a0001c0001t0003g0149 a0001c0001t0003g0286 a0001c0010t0022g0307 others(3): Show |
6 | HG02886.hp1 HG03041.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.2670-1684A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25769514 | |||||||
chr4:25769698 | G | A | 2 | a0001c0001t0002g0176 a0001c0001t0016g0090 |
2 | HG03669.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.2670-1868C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25769698 | |||||||
chr4:25769738 | T | C | 1 | a0002c0002t0008g0301 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2670-1908A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25769738 | |||||||
chr4:25769759 | C | T | 9 | a0001c0001t0001g0075 a0001c0001t0001g0080 a0001c0001t0001g0081 others(6): Show |
9 | HG02074.hp1 HG02083.hp1 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.2670-1929G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25769759 | |||||||
chr4:25769851 | C | A | 2 | a0002c0005t0001g0156 a0002c0005t0001g0157 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.2670-2021G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25769851 | |||||||
chr4:25769855 | T | G | 2 | a0002c0005t0001g0156 a0002c0005t0001g0157 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.2670-2025A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25769855 | |||||||
chr4:25769885 | T | C | 1 | a0002c0002t0008g0301 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2670-2055A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25769885 | |||||||
chr4:25769978 | A | T | 3 | a0001c0001t0006g0150 a0002c0002t0006g0267 a0002c0005t0006g0001 |
5 | HG02109.hp1 HG02257.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.2670-2148T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25769978 | |||||||
chr4:25770023 | G | A | 48 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0028 others(45): Show |
48 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.2670-2193C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25770023 | |||||||
chr4:25770168 | G | C | 2 | a0001c0001t0009g0285 a0001c0003t0009g0027 |
2 | HG01891.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.2670-2338C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25770168 | |||||||
chr4:25770169 | C | T | 89 | a0001c0001t0001g0012 a0001c0001t0001g0035 a0001c0001t0001g0036 others(86): Show |
90 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(87): Show |
intron_variant | MODIFIER | c.2670-2339G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25770169 | |||||||
chr4:25770257 | T | C | 1 | a0002c0002t0002g0133 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2670-2427A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25770257 | |||||||
chr4:25770274 | T | C | 2 | a0001c0001t0002g0259 a0001c0001t0002g0297 |
2 | HG01891.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.2670-2444A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25770274 | |||||||
chr4:25770336 | C | A | 1 | a0001c0011t0003g0172 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2670-2506G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25770336 | |||||||
chr4:25770351 | C | T | 176 | a0001c0001t0001g0012 a0001c0001t0001g0035 a0001c0001t0001g0036 others(173): Show |
179 | HG00140.hp2 HG00558.hp1 HG00642.hp1 others(176): Show |
intron_variant | MODIFIER | c.2670-2521G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25770351 | |||||||
chr4:25770461 | C | T | 24 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0002g0139 others(21): Show |
24 | HG02055.hp1 HG02055.hp2 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.2670-2631G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25770461 | |||||||
chr4:25770575 | G | A | 119 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0037 others(116): Show |
119 | HG00099.hp2 HG00597.hp1 HG00609.hp2 others(116): Show |
intron_variant | MODIFIER | c.2670-2745C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25770575 | |||||||
chr4:25770612 | C | T | 2 | a0001c0008t0007g0161 a0007c0031t0020g0169 |
2 | HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2670-2782G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25770612 | |||||||
chr4:25770671 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2670-2841G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25770671 | |||||||
chr4:25770739 | C | CA | 18 | a0001c0001t0001g0293 a0001c0001t0003g0149 a0001c0001t0003g0265 others(15): Show |
20 | HG01070.hp1 HG01071.hp2 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.2670-2910dupT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25770739 | |||||||
chr4:25770739 | CA | C | 13 | a0001c0001t0001g0184 a0001c0001t0001g0226 a0001c0001t0001g0238 others(10): Show |
13 | HG00642.hp2 HG01106.hp1 HG02071.hp1 others(10): Show |
intron_variant | MODIFIER | c.2670-2910delT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25770739 | |||||||
chr4:25770739 | CAA | C | 178 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0030 others(175): Show |
179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.2670-2911_2670-291 others(6): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25770739 | |||||||
chr4:25770739 | CAAA | C | 17 | a0001c0001t0002g0031 a0001c0001t0002g0139 a0001c0001t0002g0302 others(14): Show |
17 | HG02055.hp2 HG02145.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.2670-2912_2670-291 others(7): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25770739 | |||||||
chr4:25770760 | A | G | 1 | a0001c0001t0003g0039 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2670-2930T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25770760 | |||||||
chr4:25770837 | G | C | 226 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0030 others(223): Show |
229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.2670-3007C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25770837 | |||||||
chr4:25770855 | T | C | 205 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0030 others(202): Show |
206 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.2670-3025A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25770855 | |||||||
chr4:25770874 | G | A | 1 | a0002c0002t0008g0301 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2670-3044C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25770874 | |||||||
chr4:25771167 | C | A | 1 | a0016c0032t0019g0170 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2670-3337G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25771167 | |||||||
chr4:25771199 | C | A | 1 | a0019c0024t0023g0308 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2670-3369G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25771199 | |||||||
chr4:25771216 | T | C | 2 | a0001c0001t0002g0196 a0001c0034t0002g0137 |
2 | HG02055.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2670-3386A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25771216 | |||||||
chr4:25771344 | G | A | 2 | a0001c0008t0007g0161 a0007c0031t0020g0169 |
2 | HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2670-3514C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25771344 | |||||||
chr4:25771449 | C | A | 203 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0030 others(200): Show |
204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.2670-3619G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25771449 | |||||||
chr4:25771522 | C | T | 1 | a0001c0001t0002g0002 | 2 | HG00733.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.2670-3692G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25771522 | |||||||
chr4:25771575 | A | C | 97 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0037 others(94): Show |
97 | HG00099.hp2 HG00140.hp1 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.2670-3745T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25771575 | |||||||
chr4:25771743 | A | T | 2 | a0001c0001t0002g0259 a0001c0001t0002g0297 |
2 | HG01891.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.2670-3913T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25771743 | |||||||
chr4:25771828 | C | T | 95 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0037 others(92): Show |
95 | HG00099.hp2 HG00597.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.2670-3998G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25771828 | |||||||
chr4:25771838 | C | T | 1 | a0001c0008t0012g0143 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2670-4008G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25771838 | |||||||
chr4:25771888 | G | A | 4 | a0001c0001t0001g0051 a0001c0001t0001g0095 a0001c0001t0002g0147 others(1): Show |
4 | HG02040.hp2 NA18993.hp2 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.2670-4058C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25771888 | |||||||
chr4:25772356 | G | A | 2 | a0001c0001t0002g0237 a0001c0001t0003g0091 |
2 | HG02109.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.2669+3921C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25772356 | |||||||
chr4:25772641 | G | A | 11 | a0001c0001t0001g0136 a0001c0001t0001g0296 a0001c0001t0002g0139 others(8): Show |
11 | HG01109.hp1 HG01884.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.2669+3636C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25772641 | |||||||
chr4:25772811 | T | A | 17 | a0001c0001t0001g0226 a0001c0001t0001g0256 a0001c0001t0002g0002 others(14): Show |
18 | HG00642.hp2 HG00733.hp1 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.2669+3466A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25772811 | |||||||
chr4:25772922 | C | T | 2 | a0001c0001t0001g0203 a0001c0001t0001g0252 |
2 | NA18970.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.2669+3355G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25772922 | |||||||
chr4:25773085 | C | T | 1 | a0002c0002t0008g0301 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2669+3192G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25773085 | |||||||
chr4:25773279 | A | G | 1 | a0003c0004t0001g0146 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.2669+2998T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25773279 | |||||||
chr4:25773382 | G | T | 1 | a0001c0001t0002g0003 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2669+2895C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25773382 | |||||||
chr4:25773412 | T | C | 42 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0056 others(39): Show |
42 | HG00099.hp2 HG00597.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.2669+2865A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25773412 | |||||||
chr4:25773602 | A | T | 169 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0030 others(166): Show |
172 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.2669+2675T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25773602 | |||||||
chr4:25773628 | C | T | 20 | a0001c0001t0001g0136 a0001c0001t0001g0296 a0001c0001t0002g0126 others(17): Show |
20 | HG01192.hp2 HG01884.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.2669+2649G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25773628 | |||||||
chr4:25773666 | A | G | 111 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0035 others(108): Show |
114 | HG00140.hp1 HG00140.hp2 HG00609.hp1 others(111): Show |
intron_variant | MODIFIER | c.2669+2611T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25773666 | |||||||
chr4:25773718 | C | G | 5 | a0001c0001t0002g0302 a0002c0002t0002g0277 a0002c0002t0002g0281 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.2669+2559G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25773718 | |||||||
chr4:25773896 | C | T | 2 | a0001c0010t0002g0173 a0001c0010t0022g0307 |
2 | HG03041.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2669+2381G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25773896 | |||||||
chr4:25773985 | A | G | 2 | a0001c0001t0001g0080 a0001c0001t0001g0081 |
2 | NA18942.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.2669+2292T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25773985 | |||||||
chr4:25773996 | G | A | 56 | a0001c0001t0001g0117 a0001c0001t0001g0258 a0001c0001t0002g0014 others(53): Show |
56 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(53): Show |
intron_variant | MODIFIER | c.2669+2281C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25773996 | |||||||
chr4:25774169 | T | G | 14 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0082 others(11): Show |
14 | HG00673.hp2 HG02027.hp1 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.2669+2108A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25774169 | |||||||
chr4:25774208 | C | T | 2 | a0001c0010t0002g0173 a0001c0010t0022g0307 |
2 | HG03041.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2669+2069G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25774208 | |||||||
chr4:25774394 | T | C | 1 | a0001c0001t0002g0205 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2669+1883A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25774394 | |||||||
chr4:25774719 | G | A | 224 | a0001c0001t0001g0012 a0001c0001t0001g0030 a0001c0001t0001g0035 others(221): Show |
227 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.2669+1558C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25774719 | |||||||
chr4:25774919 | C | T | 2 | a0001c0010t0002g0173 a0001c0010t0022g0307 |
2 | HG03041.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2669+1358G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25774919 | |||||||
chr4:25775032 | G | A | 1 | a0001c0001t0002g0003 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2669+1245C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25775032 | |||||||
chr4:25775060 | G | C | 1 | a0001c0001t0002g0062 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2669+1217C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25775060 | |||||||
chr4:25775203 | T | A | 2 | a0001c0001t0001g0296 a0001c0008t0007g0161 |
2 | HG01884.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2669+1074A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25775203 | |||||||
chr4:25775441 | T | G | 3 | a0001c0001t0002g0237 a0001c0001t0003g0091 a0001c0001t0009g0285 |
3 | HG01891.hp1 HG02109.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.2669+836A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25775441 | |||||||
chr4:25775460 | G | T | 165 | a0001c0001t0001g0012 a0001c0001t0001g0030 a0001c0001t0001g0035 others(162): Show |
168 | HG00099.hp2 HG00140.hp2 HG00597.hp1 others(165): Show |
intron_variant | MODIFIER | c.2669+817C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25775460 | |||||||
chr4:25775527 | A | G | 221 | a0001c0001t0001g0012 a0001c0001t0001g0030 a0001c0001t0001g0035 others(218): Show |
224 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.2669+750T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25775527 | |||||||
chr4:25775655 | G | A | 17 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0056 others(14): Show |
17 | HG00099.hp2 HG00597.hp1 HG00609.hp2 others(14): Show |
intron_variant | MODIFIER | c.2669+622C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25775655 | |||||||
chr4:25775876 | C | T | 1 | a0001c0001t0004g0123 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2669+401G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25775876 | |||||||
chr4:25775905 | C | A | 1 | a0001c0001t0002g0295 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2669+372G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25775905 | |||||||
chr4:25776134 | G | C | 2 | a0001c0001t0001g0120 a0001c0027t0001g0197 |
2 | HG00733.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.2669+143C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25776134 | |||||||
chr4:25776180 | C | A | 8 | a0001c0001t0002g0302 a0001c0001t0008g0114 a0001c0001t0008g0290 others(5): Show |
8 | HG01074.hp1 HG01257.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2669+97G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 17/23 | chr4 | 25776180 | |||||||
chr4:25776645 | C | T | 4 | a0001c0001t0001g0040 a0001c0001t0001g0250 a0001c0001t0001g0271 others(1): Show |
4 | NA18939.hp1 NA18944.hp2 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.2586-285G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 16/23 | chr4 | 25776645 | |||||||
chr4:25776650 | A | G | 1 | a0003c0004t0001g0146 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.2586-290T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 16/23 | chr4 | 25776650 | |||||||
chr4:25776716 | T | C | 224 | a0001c0001t0001g0012 a0001c0001t0001g0030 a0001c0001t0001g0035 others(221): Show |
227 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.2586-356A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 16/23 | chr4 | 25776716 | |||||||
chr4:25776837 | AT | A | 53 | a0001c0001t0001g0104 a0001c0001t0001g0117 a0001c0001t0001g0258 others(50): Show |
53 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.2586-478delA | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 16/23 | chr4 | 25776837 | |||||||
chr4:25776886 | A | T | 3 | a0001c0001t0002g0237 a0001c0001t0003g0091 a0001c0001t0009g0285 |
3 | HG01891.hp1 HG02109.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.2586-526T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 16/23 | chr4 | 25776886 | |||||||
chr4:25776902 | A | C | 169 | a0001c0001t0001g0012 a0001c0001t0001g0030 a0001c0001t0001g0035 others(166): Show |
172 | HG00099.hp2 HG00140.hp2 HG00597.hp1 others(169): Show |
intron_variant | MODIFIER | c.2586-542T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 16/23 | chr4 | 25776902 | |||||||
chr4:25776984 | G | T | 1 | a0001c0001t0002g0014 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2586-624C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 16/23 | chr4 | 25776984 | |||||||
chr4:25777029 | C | A | 3 | a0001c0001t0002g0237 a0001c0001t0003g0091 a0001c0001t0009g0285 |
3 | HG01891.hp1 HG02109.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.2586-669G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 16/23 | chr4 | 25777029 | |||||||
chr4:25777045 | A | G | 1 | a0001c0001t0009g0285 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2586-685T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 16/23 | chr4 | 25777045 | |||||||
chr4:25777135 | A | G | 1 | a0002c0002t0005g0187 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2586-775T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 16/23 | chr4 | 25777135 | |||||||
chr4:25777191 | A | C | 1 | a0001c0001t0001g0216 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2586-831T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 16/23 | chr4 | 25777191 | |||||||
chr4:25777292 | C | T | 1 | a0003c0004t0001g0146 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.2586-932G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 16/23 | chr4 | 25777292 | |||||||
chr4:25777325 | T | C | 53 | a0001c0001t0001g0104 a0001c0001t0001g0117 a0001c0001t0001g0258 others(50): Show |
53 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.2586-965A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 16/23 | chr4 | 25777325 | |||||||
chr4:25777361 | A | G | 166 | a0001c0001t0001g0012 a0001c0001t0001g0030 a0001c0001t0001g0035 others(163): Show |
169 | HG00099.hp2 HG00140.hp2 HG00597.hp1 others(166): Show |
intron_variant | MODIFIER | c.2586-1001T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 16/23 | chr4 | 25777361 | |||||||
chr4:25777440 | G | T | 166 | a0001c0001t0001g0012 a0001c0001t0001g0030 a0001c0001t0001g0035 others(163): Show |
169 | HG00099.hp2 HG00140.hp2 HG00597.hp1 others(166): Show |
intron_variant | MODIFIER | c.2586-1080C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 16/23 | chr4 | 25777440 | |||||||
chr4:25777794 | G | T | 2 | a0001c0001t0002g0209 a0001c0001t0002g0249 |
2 | HG01169.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.2585+1282C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 16/23 | chr4 | 25777794 | |||||||
chr4:25777800 | A | G | 4 | a0001c0001t0001g0056 a0001c0001t0001g0058 a0001c0001t0001g0059 others(1): Show |
4 | NA18955.hp2 NA18973.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.2585+1276T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 16/23 | chr4 | 25777800 | |||||||
chr4:25777827 | C | T | 12 | a0001c0001t0002g0302 a0001c0001t0008g0114 a0001c0001t0008g0290 others(9): Show |
12 | HG01074.hp1 HG01257.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.2585+1249G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 16/23 | chr4 | 25777827 | |||||||
chr4:25777914 | T | C | 1 | a0009c0037t0003g0304 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2585+1162A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 16/23 | chr4 | 25777914 | |||||||
chr4:25778063 | G | A | 1 | a0001c0001t0002g0076 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2585+1013C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 16/23 | chr4 | 25778063 | |||||||
chr4:25778155 | C | T | 12 | a0001c0001t0002g0302 a0001c0001t0008g0114 a0001c0001t0008g0290 others(9): Show |
12 | HG01074.hp1 HG01257.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.2585+921G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 16/23 | chr4 | 25778155 | |||||||
chr4:25778363 | A | G | 166 | a0001c0001t0001g0012 a0001c0001t0001g0030 a0001c0001t0001g0035 others(163): Show |
169 | HG00099.hp2 HG00140.hp2 HG00597.hp1 others(166): Show |
intron_variant | MODIFIER | c.2585+713T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 16/23 | chr4 | 25778363 | |||||||
chr4:25778465 | A | T | 2 | a0001c0001t0002g0105 a0001c0001t0002g0180 |
2 | HG02135.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.2585+611T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 16/23 | chr4 | 25778465 | |||||||
chr4:25778525 | T | C | 224 | a0001c0001t0001g0012 a0001c0001t0001g0030 a0001c0001t0001g0035 others(221): Show |
227 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.2585+551A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 16/23 | chr4 | 25778525 | |||||||
chr4:25778925 | G | T | 166 | a0001c0001t0001g0012 a0001c0001t0001g0030 a0001c0001t0001g0035 others(163): Show |
169 | HG00099.hp2 HG00140.hp2 HG00597.hp1 others(166): Show |
intron_variant | MODIFIER | c.2585+151C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 16/23 | chr4 | 25778925 | |||||||
chr4:25778977 | C | T | 166 | a0001c0001t0001g0012 a0001c0001t0001g0030 a0001c0001t0001g0035 others(163): Show |
169 | HG00099.hp2 HG00140.hp2 HG00597.hp1 others(166): Show |
intron_variant | MODIFIER | c.2585+99G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 16/23 | chr4 | 25778977 | |||||||
chr4:25779269 | A | G | 224 | a0001c0001t0001g0012 a0001c0001t0001g0030 a0001c0001t0001g0035 others(221): Show |
227 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.2458-66T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 15/23 | chr4 | 25779269 | |||||||
chr4:25779389 | C | G | 1 | a0001c0001t0003g0033 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2458-186G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 15/23 | chr4 | 25779389 | |||||||
chr4:25779933 | T | A | 1 | a0001c0001t0001g0228 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2458-730A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 15/23 | chr4 | 25779933 | |||||||
chr4:25779938 | C | T | 1 | a0013c0036t0002g0303 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2458-735G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 15/23 | chr4 | 25779938 | |||||||
chr4:25780090 | T | A | 2 | a0002c0018t0002g0158 a0007c0031t0020g0169 |
2 | HG03209.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2458-887A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 15/23 | chr4 | 25780090 | |||||||
chr4:25780139 | G | A | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2458-936C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 15/23 | chr4 | 25780139 | |||||||
chr4:25780161 | C | G | 5 | a0001c0001t0001g0042 a0001c0001t0001g0057 a0001c0001t0001g0061 others(2): Show |
5 | HG01074.hp2 HG01257.hp1 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.2458-958G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 15/23 | chr4 | 25780161 | |||||||
chr4:25780290 | C | G | 1 | a0001c0001t0009g0285 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2458-1087G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 15/23 | chr4 | 25780290 | |||||||
chr4:25780541 | C | T | 5 | a0001c0001t0002g0237 a0001c0001t0003g0091 a0001c0001t0009g0285 others(2): Show |
5 | HG01891.hp1 HG02109.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.2458-1338G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 15/23 | chr4 | 25780541 | |||||||
chr4:25780824 | TTA | T | 166 | a0001c0001t0001g0012 a0001c0001t0001g0030 a0001c0001t0001g0035 others(163): Show |
169 | HG00099.hp2 HG00140.hp2 HG00597.hp1 others(166): Show |
intron_variant | MODIFIER | c.2457+1416_2457+141 others(6): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 15/23 | chr4 | 25780824 | |||||||
chr4:25780886 | C | T | 2 | a0001c0001t0002g0237 a0001c0001t0003g0091 |
2 | HG02109.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.2457+1356G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 15/23 | chr4 | 25780886 | |||||||
chr4:25780920 | G | A | 2 | a0001c0010t0002g0173 a0001c0010t0022g0307 |
2 | HG03041.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2457+1322C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 15/23 | chr4 | 25780920 | |||||||
chr4:25780959 | G | C | 1 | a0001c0001t0018g0223 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2457+1283C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 15/23 | chr4 | 25780959 | |||||||
chr4:25780969 | G | C | 166 | a0001c0001t0001g0012 a0001c0001t0001g0030 a0001c0001t0001g0035 others(163): Show |
169 | HG00099.hp2 HG00140.hp2 HG00597.hp1 others(166): Show |
intron_variant | MODIFIER | c.2457+1273C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 15/23 | chr4 | 25780969 | |||||||
chr4:25781213 | G | A | 53 | a0001c0001t0001g0104 a0001c0001t0001g0117 a0001c0001t0001g0258 others(50): Show |
53 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.2457+1029C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 15/23 | chr4 | 25781213 | |||||||
chr4:25781252 | A | T | 1 | a0001c0001t0001g0193 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2457+990T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 15/23 | chr4 | 25781252 | |||||||
chr4:25781366 | A | G | 1 | a0001c0001t0001g0121 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2457+876T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 15/23 | chr4 | 25781366 | |||||||
chr4:25781506 | T | G | 1 | a0001c0001t0001g0047 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2457+736A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 15/23 | chr4 | 25781506 | |||||||
chr4:25781543 | C | T | 2 | a0005c0019t0002g0010 a0012c0020t0002g0011 |
2 | HG02055.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2457+699G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 15/23 | chr4 | 25781543 | |||||||
chr4:25781676 | C | T | 1 | a0003c0004t0001g0208 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2457+566G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 15/23 | chr4 | 25781676 | |||||||
chr4:25781836 | T | G | 1 | a0001c0001t0001g0074 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2457+406A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 15/23 | chr4 | 25781836 | |||||||
chr4:25781859 | C | A | 2 | a0001c0001t0008g0114 a0001c0001t0008g0290 |
2 | HG01074.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.2457+383G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 15/23 | chr4 | 25781859 | |||||||
chr4:25781882 | T | C | 54 | a0001c0001t0001g0104 a0001c0001t0001g0117 a0001c0001t0001g0258 others(51): Show |
54 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.2457+360A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 15/23 | chr4 | 25781882 | |||||||
chr4:25782110 | C | T | 1 | a0005c0021t0003g0283 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2457+132G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 15/23 | chr4 | 25782110 | |||||||
chr4:25782178 | T | G | 1 | a0001c0001t0001g0226 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2457+64A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 15/23 | chr4 | 25782178 | |||||||
chr4:25782450 | T | G | 1 | a0001c0001t0002g0094 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.2281-32A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 14/23 | chr4 | 25782450 | |||||||
chr4:25782470 | A | C | 6 | a0001c0001t0001g0100 a0001c0001t0002g0003 a0001c0001t0002g0032 others(3): Show |
6 | HG02683.hp2 HG03654.hp1 HG03654.hp2 others(3): Show |
intron_variant | MODIFIER | c.2281-52T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 14/23 | chr4 | 25782470 | |||||||
chr4:25782495 | G | A | 12 | a0001c0001t0002g0302 a0001c0001t0008g0114 a0001c0001t0008g0290 others(9): Show |
12 | HG01074.hp1 HG01257.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.2281-77C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 14/23 | chr4 | 25782495 | |||||||
chr4:25782698 | C | T | 225 | a0001c0001t0001g0012 a0001c0001t0001g0030 a0001c0001t0001g0035 others(222): Show |
228 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.2281-280G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 14/23 | chr4 | 25782698 | |||||||
chr4:25782715 | C | T | 1 | a0001c0001t0002g0192 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2281-297G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 14/23 | chr4 | 25782715 | |||||||
chr4:25782932 | C | G | 128 | a0001c0001t0001g0012 a0001c0001t0001g0035 a0001c0001t0001g0036 others(125): Show |
131 | HG00140.hp2 HG00609.hp1 HG00642.hp2 others(128): Show |
intron_variant | MODIFIER | c.2281-514G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 14/23 | chr4 | 25782932 | |||||||
chr4:25782935 | T | G | 225 | a0001c0001t0001g0012 a0001c0001t0001g0030 a0001c0001t0001g0035 others(222): Show |
228 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.2281-517A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 14/23 | chr4 | 25782935 | |||||||
chr4:25783110 | A | G | 108 | a0001c0001t0001g0012 a0001c0001t0001g0035 a0001c0001t0001g0036 others(105): Show |
111 | HG00140.hp2 HG00609.hp1 HG00642.hp2 others(108): Show |
intron_variant | MODIFIER | c.2281-692T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 14/23 | chr4 | 25783110 | |||||||
chr4:25783204 | C | T | 55 | a0001c0001t0001g0104 a0001c0001t0001g0117 a0001c0001t0001g0258 others(52): Show |
55 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.2281-786G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 14/23 | chr4 | 25783204 | |||||||
chr4:25783357 | A | C | 55 | a0001c0001t0001g0104 a0001c0001t0001g0117 a0001c0001t0001g0258 others(52): Show |
55 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.2280+871T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 14/23 | chr4 | 25783357 | |||||||
chr4:25783501 | A | G | 1 | a0001c0001t0009g0285 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2280+727T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 14/23 | chr4 | 25783501 | |||||||
chr4:25783539 | C | A | 53 | a0001c0001t0001g0104 a0001c0001t0001g0117 a0001c0001t0001g0258 others(50): Show |
53 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.2280+689G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 14/23 | chr4 | 25783539 | |||||||
chr4:25783596 | G | A | 2 | a0001c0001t0010g0008 a0002c0002t0005g0187 |
2 | HG02630.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2280+632C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 14/23 | chr4 | 25783596 | |||||||
chr4:25783630 | T | G | 2 | a0001c0001t0010g0008 a0002c0002t0005g0187 |
2 | HG02630.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2280+598A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 14/23 | chr4 | 25783630 | |||||||
chr4:25783693 | T | C | 1 | a0010c0016t0002g0141 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2280+535A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 14/23 | chr4 | 25783693 | |||||||
chr4:25783824 | C | A | 53 | a0001c0001t0001g0104 a0001c0001t0001g0117 a0001c0001t0001g0258 others(50): Show |
53 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.2280+404G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 14/23 | chr4 | 25783824 | |||||||
chr4:25783966 | T | C | 1 | a0001c0001t0002g0233 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2280+262A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 14/23 | chr4 | 25783966 | |||||||
chr4:25784102 | G | A | 2 | a0001c0001t0010g0008 a0002c0002t0005g0187 |
2 | HG02630.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2280+126C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 14/23 | chr4 | 25784102 | |||||||
chr4:25784315 | T | C | 1 | a0009c0037t0003g0304 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2218-25A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25784315 | |||||||
chr4:25784322 | G | T | 1 | a0001c0001t0002g0237 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2218-32C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25784322 | |||||||
chr4:25784425 | T | G | 9 | a0001c0001t0002g0139 a0001c0001t0009g0124 a0001c0006t0007g0125 others(6): Show |
9 | HG02145.hp1 HG02965.hp1 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.2218-135A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25784425 | |||||||
chr4:25784470 | C | T | 1 | a0001c0001t0001g0019 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2218-180G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25784470 | |||||||
chr4:25784796 | T | C | 228 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0030 others(225): Show |
231 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.2218-506A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25784796 | |||||||
chr4:25785072 | T | C | 2 | a0005c0021t0003g0283 a0005c0022t0004g0284 |
2 | HG02717.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.2218-782A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25785072 | |||||||
chr4:25785274 | G | A | 2 | a0005c0019t0002g0010 a0012c0020t0002g0011 |
2 | HG02055.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2218-984C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25785274 | |||||||
chr4:25785512 | T | G | 15 | a0001c0001t0002g0126 a0001c0001t0002g0139 a0001c0001t0004g0123 others(12): Show |
15 | HG01192.hp2 HG02145.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.2218-1222A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25785512 | |||||||
chr4:25785723 | A | C | 6 | a0001c0001t0002g0237 a0001c0001t0003g0091 a0001c0001t0008g0114 others(3): Show |
6 | HG01074.hp1 HG01257.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.2218-1433T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25785723 | |||||||
chr4:25785723 | A | G | 213 | a0001c0001t0001g0012 a0001c0001t0001g0030 a0001c0001t0001g0035 others(210): Show |
216 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.2218-1433T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25785723 | |||||||
chr4:25785780 | T | C | 1 | a0009c0037t0003g0304 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2218-1490A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25785780 | |||||||
chr4:25785903 | T | A | 1 | a0001c0001t0002g0069 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2218-1613A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25785903 | |||||||
chr4:25786204 | T | C | 1 | a0019c0024t0023g0308 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2218-1914A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25786204 | |||||||
chr4:25786216 | A | G | 201 | a0001c0001t0001g0012 a0001c0001t0001g0030 a0001c0001t0001g0035 others(198): Show |
204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.2218-1926T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25786216 | |||||||
chr4:25786265 | C | T | 5 | a0001c0001t0002g0302 a0002c0002t0002g0277 a0002c0002t0002g0281 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.2217+1959G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25786265 | |||||||
chr4:25786328 | G | A | 1 | a0001c0010t0002g0173 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2217+1896C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25786328 | |||||||
chr4:25786426 | C | T | 20 | a0001c0001t0002g0126 a0001c0001t0002g0139 a0001c0001t0002g0302 others(17): Show |
20 | HG01192.hp2 HG02145.hp1 HG02572.hp1 others(17): Show |
intron_variant | MODIFIER | c.2217+1798G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25786426 | |||||||
chr4:25786564 | G | A | 2 | a0001c0001t0010g0008 a0002c0002t0005g0187 |
2 | HG02630.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2217+1660C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25786564 | |||||||
chr4:25786752 | C | T | 2 | a0005c0019t0002g0010 a0012c0020t0002g0011 |
2 | HG02055.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2217+1472G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25786752 | |||||||
chr4:25786891 | G | C | 4 | a0001c0001t0002g0006 a0001c0001t0002g0177 a0001c0001t0002g0235 others(1): Show |
4 | NA18941.hp1 NA19012.hp1 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.2217+1333C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25786891 | |||||||
chr4:25786980 | T | G | 49 | a0001c0001t0001g0104 a0001c0001t0001g0117 a0001c0001t0001g0258 others(46): Show |
49 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.2217+1244A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25786980 | |||||||
chr4:25786985 | G | C | 2 | a0005c0021t0003g0283 a0005c0022t0004g0284 |
2 | HG02717.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.2217+1239C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25786985 | |||||||
chr4:25787061 | T | C | 1 | a0001c0001t0002g0177 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2217+1163A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25787061 | |||||||
chr4:25787117 | T | C | 201 | a0001c0001t0001g0012 a0001c0001t0001g0030 a0001c0001t0001g0035 others(198): Show |
204 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.2217+1107A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25787117 | |||||||
chr4:25787163 | C | T | 2 | a0001c0001t0002g0153 a0001c0001t0002g0155 |
2 | HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2217+1061G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25787163 | |||||||
chr4:25787169 | C | A | 2 | a0001c0010t0002g0173 a0001c0010t0022g0307 |
2 | HG03041.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2217+1055G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25787169 | |||||||
chr4:25787246 | C | T | 1 | a0001c0001t0009g0285 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2217+978G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25787246 | |||||||
chr4:25787247 | G | A | 1 | a0001c0001t0002g0190 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2217+977C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25787247 | |||||||
chr4:25787383 | C | T | 26 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0056 others(23): Show |
26 | HG00099.hp2 HG00597.hp1 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.2217+841G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25787383 | |||||||
chr4:25787447 | G | A | 50 | a0001c0001t0001g0104 a0001c0001t0001g0117 a0001c0001t0001g0258 others(47): Show |
50 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.2217+777C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25787447 | |||||||
chr4:25787691 | T | C | 50 | a0001c0001t0001g0104 a0001c0001t0001g0117 a0001c0001t0001g0258 others(47): Show |
50 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.2217+533A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25787691 | |||||||
chr4:25787698 | C | G | 142 | a0001c0001t0001g0012 a0001c0001t0001g0030 a0001c0001t0001g0035 others(139): Show |
145 | HG00099.hp2 HG00140.hp2 HG00597.hp1 others(142): Show |
intron_variant | MODIFIER | c.2217+526G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25787698 | |||||||
chr4:25787700 | T | C | 50 | a0001c0001t0001g0104 a0001c0001t0001g0117 a0001c0001t0001g0258 others(47): Show |
50 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.2217+524A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25787700 | |||||||
chr4:25788132 | A | G | 1 | a0001c0003t0002g0025 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2217+92T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25788132 | |||||||
chr4:25788154 | C | T | 1 | a0009c0037t0003g0304 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2217+70G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 13/23 | chr4 | 25788154 | |||||||
chr4:25788406 | T | C | 2 | a0001c0001t0003g0215 a0001c0001t0003g0265 |
2 | HG03017.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.2077-42A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25788406 | |||||||
chr4:25788455 | G | A | 50 | a0001c0001t0001g0104 a0001c0001t0001g0117 a0001c0001t0001g0258 others(47): Show |
50 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.2077-91C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25788455 | |||||||
chr4:25788569 | C | CGT | 10 | a0001c0001t0001g0019 a0001c0001t0001g0028 a0001c0001t0001g0029 others(7): Show |
10 | HG00438.hp2 HG00673.hp1 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.2077-207_2077-206d others(4): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25788569 | |||||||
chr4:25788569 | CGT | C | 50 | a0001c0001t0001g0021 a0001c0001t0001g0040 a0001c0001t0001g0043 others(47): Show |
50 | HG00438.hp1 HG00558.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.2077-207_2077-206d others(4): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25788569 | |||||||
chr4:25788569 | CGTGT | C | 40 | a0001c0001t0001g0051 a0001c0001t0001g0077 a0001c0001t0001g0078 others(37): Show |
42 | HG01070.hp2 HG01109.hp1 HG01169.hp2 others(39): Show |
intron_variant | MODIFIER | c.2077-209_2077-206d others(6): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25788569 | |||||||
chr4:25788569 | CGTGTGT | C | 119 | a0001c0001t0001g0012 a0001c0001t0001g0035 a0001c0001t0001g0036 others(116): Show |
120 | HG00140.hp1 HG00140.hp2 HG00609.hp1 others(117): Show |
intron_variant | MODIFIER | c.2077-211_2077-206d others(8): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25788569 | |||||||
chr4:25788569 | CGTGTGTG others(1): Show |
C | 49 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0047 others(46): Show |
49 | HG00099.hp2 HG00597.hp1 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.2077-213_2077-206d others(10): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25788569 | |||||||
chr4:25788569 | CGTGTGTG others(3): Show |
C | 14 | a0001c0001t0002g0099 a0001c0001t0002g0126 a0001c0001t0002g0128 others(11): Show |
14 | HG02145.hp1 HG02630.hp1 HG02698.hp1 others(11): Show |
intron_variant | MODIFIER | c.2077-215_2077-206d others(12): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25788569 | |||||||
chr4:25788569 | CGTGTGTG others(5): Show |
C | 2 | a0001c0010t0002g0173 a0001c0010t0022g0307 |
2 | HG03041.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2077-217_2077-206d others(14): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25788569 | |||||||
chr4:25788569 | CGTGTGTG others(11): Show |
C | 1 | a0001c0001t0002g0205 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2077-223_2077-206d others(20): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25788569 | |||||||
chr4:25788592 | G | A | 3 | a0005c0021t0003g0283 a0005c0022t0004g0284 a0016c0032t0019g0170 |
3 | HG02717.hp1 HG02922.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2077-228C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25788592 | |||||||
chr4:25788594 | G | A | 11 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0002g0063 others(8): Show |
13 | HG02109.hp1 HG02257.hp1 HG02273.hp1 others(10): Show |
intron_variant | MODIFIER | c.2077-230C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25788594 | |||||||
chr4:25788596 | G | A | 98 | a0001c0001t0001g0012 a0001c0001t0001g0035 a0001c0001t0001g0036 others(95): Show |
99 | HG00140.hp2 HG00609.hp1 HG00642.hp2 others(96): Show |
intron_variant | MODIFIER | c.2077-232C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25788596 | |||||||
chr4:25788598 | G | A | 37 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0056 others(34): Show |
37 | HG00099.hp2 HG00597.hp1 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.2077-234C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25788598 | |||||||
chr4:25788615 | T | C | 27 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0056 others(24): Show |
27 | HG00099.hp2 HG00597.hp1 HG00609.hp2 others(24): Show |
intron_variant | MODIFIER | c.2077-251A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25788615 | |||||||
chr4:25788620 | G | A | 1 | a0001c0001t0002g0222 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2077-256C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25788620 | |||||||
chr4:25788809 | G | T | 11 | a0001c0001t0002g0139 a0001c0001t0009g0124 a0001c0003t0002g0096 others(8): Show |
11 | HG02145.hp1 HG02896.hp1 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.2077-445C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25788809 | |||||||
chr4:25788898 | C | G | 1 | a0014c0026t0013g0280 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2077-534G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25788898 | |||||||
chr4:25788899 | C | G | 1 | a0001c0001t0002g0140 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2077-535G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25788899 | |||||||
chr4:25788918 | C | A | 3 | a0001c0001t0008g0114 a0001c0001t0008g0290 a0011c0029t0005g0135 |
3 | HG01074.hp1 HG01257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2077-554G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25788918 | |||||||
chr4:25788936 | G | C | 3 | a0001c0001t0002g0128 a0001c0001t0002g0134 a0001c0001t0002g0151 |
3 | HG03130.hp2 HG03225.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2077-572C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25788936 | |||||||
chr4:25788982 | T | A | 1 | a0001c0001t0002g0094 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.2077-618A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25788982 | |||||||
chr4:25789021 | G | T | 1 | a0001c0001t0002g0094 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.2077-657C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25789021 | |||||||
chr4:25789090 | A | G | 199 | a0001c0001t0001g0012 a0001c0001t0001g0030 a0001c0001t0001g0035 others(196): Show |
202 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.2077-726T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25789090 | |||||||
chr4:25789096 | T | G | 225 | a0001c0001t0001g0012 a0001c0001t0001g0030 a0001c0001t0001g0035 others(222): Show |
228 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.2077-732A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25789096 | |||||||
chr4:25789133 | A | G | 50 | a0001c0001t0001g0104 a0001c0001t0001g0117 a0001c0001t0001g0258 others(47): Show |
50 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.2077-769T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25789133 | |||||||
chr4:25789242 | G | A | 1 | a0001c0003t0002g0024 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2077-878C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25789242 | |||||||
chr4:25789367 | G | A | 1 | a0001c0001t0001g0060 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.2077-1003C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25789367 | |||||||
chr4:25789584 | CA | C | 75 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0021 others(72): Show |
75 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.2076+870delT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25789584 | |||||||
chr4:25789584 | CAA | C | 111 | a0001c0001t0001g0012 a0001c0001t0001g0035 a0001c0001t0001g0036 others(108): Show |
114 | HG00609.hp1 HG00642.hp2 HG00733.hp1 others(111): Show |
intron_variant | MODIFIER | c.2076+869_2076+870d others(4): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25789584 | |||||||
chr4:25789584 | CAAA | C | 35 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0056 others(32): Show |
35 | HG00099.hp2 HG00140.hp2 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.2076+868_2076+870d others(5): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25789584 | |||||||
chr4:25789584 | CAAAA | C | 16 | a0001c0001t0002g0126 a0001c0001t0002g0139 a0001c0001t0009g0124 others(13): Show |
16 | HG02055.hp2 HG02145.hp1 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.2076+867_2076+870d others(6): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25789584 | |||||||
chr4:25789584 | CAAAAA | C | 55 | a0001c0001t0001g0104 a0001c0001t0001g0117 a0001c0001t0001g0258 others(52): Show |
55 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.2076+866_2076+870d others(7): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25789584 | |||||||
chr4:25789788 | C | A | 50 | a0001c0001t0001g0104 a0001c0001t0001g0117 a0001c0001t0001g0258 others(47): Show |
50 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.2076+667G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25789788 | |||||||
chr4:25789791 | C | A | 2 | a0002c0005t0001g0156 a0002c0005t0001g0157 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.2076+664G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25789791 | |||||||
chr4:25789807 | C | A | 1 | a0002c0013t0014g0127 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2076+648G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25789807 | |||||||
chr4:25789812 | G | A | 1 | a0001c0001t0002g0192 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2076+643C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25789812 | |||||||
chr4:25789849 | AG | A | 5 | a0001c0001t0002g0015 a0001c0001t0002g0017 a0001c0001t0002g0034 others(2): Show |
5 | HG01346.hp2 HG01928.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.2076+605delC | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25789849 | |||||||
chr4:25789855 | T | G | 1 | a0001c0001t0002g0094 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.2076+600A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25789855 | |||||||
chr4:25789968 | T | C | 3 | a0001c0001t0008g0114 a0001c0001t0008g0290 a0011c0029t0005g0135 |
3 | HG01074.hp1 HG01257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2076+487A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25789968 | |||||||
chr4:25789970 | T | C | 5 | a0001c0011t0002g0055 a0001c0011t0002g0101 a0005c0021t0003g0283 others(2): Show |
5 | HG02647.hp2 HG02717.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.2076+485A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25789970 | |||||||
chr4:25790013 | T | C | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2076+442A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25790013 | |||||||
chr4:25790204 | G | A | 2 | a0001c0011t0002g0055 a0001c0011t0002g0101 |
2 | HG02647.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.2076+251C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25790204 | |||||||
chr4:25790238 | C | T | 4 | a0001c0001t0005g0300 a0002c0002t0006g0267 a0002c0009t0004g0268 others(1): Show |
4 | HG02280.hp2 HG02922.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2076+217G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25790238 | |||||||
chr4:25790403 | C | T | 2 | a0001c0011t0002g0055 a0001c0011t0002g0101 |
2 | HG02647.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.2076+52G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 12/23 | chr4 | 25790403 | |||||||
chr4:25790610 | A | AGAAG | 6 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0072 others(3): Show |
6 | HG00597.hp2 HG01261.hp2 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.1957-40_1957-37dup others(4): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790610 | |||||||
chr4:25790610 | AGAAG | A | 12 | a0001c0001t0001g0080 a0001c0001t0002g0126 a0001c0001t0002g0302 others(9): Show |
12 | HG01074.hp1 HG01192.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1957-40_1957-37del others(4): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790610 | |||||||
chr4:25790610 | AGAAGGAA others(1): Show |
A | 5 | a0001c0001t0002g0139 a0002c0009t0003g0278 a0004c0007t0001g0165 others(2): Show |
5 | HG02145.hp1 HG02572.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1957-44_1957-37del others(8): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790610 | |||||||
chr4:25790610 | AGAAGGAA others(5): Show |
A | 7 | a0001c0001t0009g0124 a0001c0003t0002g0096 a0001c0003t0002g0097 others(4): Show |
7 | HG02896.hp1 HG02897.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1957-48_1957-37del others(12): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790610 | |||||||
chr4:25790610 | AGAAGGAA others(13): Show |
A | 2 | a0001c0001t0010g0008 a0002c0002t0005g0187 |
2 | HG02630.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1957-56_1957-37del others(20): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790610 | |||||||
chr4:25790610 | AGAAGGAA others(21): Show |
A | 3 | a0001c0001t0010g0129 a0005c0021t0003g0283 a0016c0032t0019g0170 |
3 | HG00741.hp1 HG02922.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1957-64_1957-37del others(28): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790610 | |||||||
chr4:25790610 | AGAAGGAA others(25): Show |
A | 47 | a0001c0001t0001g0104 a0001c0001t0001g0117 a0001c0001t0001g0258 others(44): Show |
47 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.1957-68_1957-37del others(32): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790610 | |||||||
chr4:25790621 | A | G | 1 | a0014c0026t0013g0280 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1957-47T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790621 | |||||||
chr4:25790626 | G | A | 1 | a0014c0026t0013g0280 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1957-52C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790626 | |||||||
chr4:25790632 | AAGGAAGG others(29): Show |
A | 2 | a0001c0001t0002g0233 a0015c0038t0012g0305 |
2 | HG03486.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1957-94_1957-59del others(36): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790632 | |||||||
chr4:25790632 | AAGGAAGG others(33): Show |
A | 1 | a0001c0001t0002g0266 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1957-98_1957-59del others(40): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790632 | |||||||
chr4:25790640 | AAGGAAGG others(21): Show |
A | 2 | a0001c0011t0002g0055 a0001c0011t0002g0101 |
2 | HG02647.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1957-94_1957-67del others(28): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790640 | |||||||
chr4:25790644 | AAGGAAGG others(17): Show |
A | 7 | a0001c0001t0001g0213 a0001c0001t0002g0063 a0001c0001t0002g0066 others(4): Show |
7 | HG02004.hp1 HG02148.hp2 HG02273.hp1 others(4): Show |
intron_variant | MODIFIER | c.1957-94_1957-71del others(24): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790644 | |||||||
chr4:25790644 | AAGGAAGG others(21): Show |
A | 2 | a0001c0001t0001g0204 a0001c0001t0018g0223 |
2 | HG01192.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1957-98_1957-71del others(28): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790644 | |||||||
chr4:25790644 | AAGGAAGG others(25): Show |
A | 1 | a0001c0001t0002g0131 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1957-102_1957-71de others(33): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790644 | |||||||
chr4:25790648 | AAGGAAGG others(13): Show |
A | 3 | a0001c0001t0002g0119 a0003c0004t0001g0110 a0006c0012t0002g0022 |
3 | HG02735.hp1 NA18968.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.1957-94_1957-75del others(20): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790648 | |||||||
chr4:25790648 | AAGGAAGG others(17): Show |
A | 57 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(54): Show |
57 | HG00140.hp2 HG00609.hp1 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.1957-98_1957-75del others(24): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790648 | |||||||
chr4:25790648 | AAGGAAGG others(21): Show |
A | 6 | a0001c0001t0001g0226 a0001c0001t0001g0256 a0001c0001t0002g0069 others(3): Show |
6 | HG00642.hp2 HG00738.hp2 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.1957-102_1957-75de others(29): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790648 | |||||||
chr4:25790652 | AAGGAAGG others(9): Show |
A | 3 | a0001c0010t0024g0309 a0001c0014t0001g0159 a0001c0027t0001g0197 |
3 | HG00733.hp2 HG01109.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1957-94_1957-79del others(16): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790652 | |||||||
chr4:25790652 | AAGGAAGG others(13): Show |
A | 20 | a0001c0001t0001g0012 a0001c0001t0001g0047 a0001c0001t0001g0057 others(17): Show |
20 | HG00741.hp2 HG01074.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.1957-98_1957-79del others(20): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790652 | |||||||
chr4:25790652 | AAGGAAGG others(17): Show |
A | 6 | a0001c0001t0001g0242 a0001c0001t0001g0246 a0001c0001t0002g0002 others(3): Show |
7 | HG00733.hp1 HG01169.hp1 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1957-102_1957-79de others(25): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790652 | |||||||
chr4:25790656 | AAGGAAGG others(5): Show |
A | 2 | a0001c0001t0001g0120 a0001c0001t0002g0190 |
2 | HG01069.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1957-94_1957-83del others(12): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790656 | |||||||
chr4:25790656 | AAGGAAGG others(9): Show |
A | 9 | a0001c0010t0002g0173 a0002c0002t0002g0133 a0002c0005t0003g0122 others(6): Show |
9 | HG02145.hp2 HG02647.hp1 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.1957-98_1957-83del others(16): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790656 | |||||||
chr4:25790656 | AAGGAAGG others(13): Show |
A | 20 | a0001c0001t0001g0009 a0001c0001t0001g0030 a0001c0001t0001g0041 others(17): Show |
20 | HG00609.hp2 HG00738.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1957-102_1957-83de others(21): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790656 | |||||||
chr4:25790660 | AAGGAAGG others(1): Show |
A | 4 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0002g0147 others(1): Show |
4 | HG00438.hp2 HG00673.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.1957-94_1957-87del others(8): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790660 | |||||||
chr4:25790660 | AAGGAAGG others(5): Show |
A | 3 | a0001c0010t0022g0307 a0002c0005t0006g0001 a0010c0016t0002g0141 |
5 | HG02109.hp1 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1957-98_1957-87del others(12): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790660 | |||||||
chr4:25790660 | AAGGAAGG others(9): Show |
A | 4 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0225 others(1): Show |
4 | HG00597.hp1 HG01069.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.1957-102_1957-87de others(17): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790660 | |||||||
chr4:25790664 | A | G | 8 | a0001c0001t0002g0083 a0001c0001t0004g0123 a0001c0001t0010g0008 others(5): Show |
8 | HG01192.hp2 HG02630.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1957-90T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790664 | |||||||
chr4:25790664 | AAGGG | A | 32 | a0001c0001t0001g0040 a0001c0001t0001g0051 a0001c0001t0001g0081 others(29): Show |
32 | HG00558.hp1 HG00558.hp2 HG01358.hp1 others(29): Show |
intron_variant | MODIFIER | c.1957-94_1957-91del others(4): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790664 | |||||||
chr4:25790664 | AAGGGAGG others(1): Show |
A | 6 | a0001c0001t0001g0075 a0001c0001t0002g0046 a0001c0001t0003g0091 others(3): Show |
6 | HG00099.hp2 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1957-98_1957-91del others(8): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790664 | |||||||
chr4:25790664 | AAGGGAGG others(5): Show |
A | 2 | a0001c0001t0001g0145 a0001c0001t0002g0191 |
2 | HG00735.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.1957-102_1957-91de others(13): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790664 | |||||||
chr4:25790668 | G | A | 32 | a0001c0001t0001g0021 a0001c0001t0001g0043 a0001c0001t0001g0072 others(29): Show |
32 | HG00099.hp1 HG00438.hp1 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.1957-94C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790668 | |||||||
chr4:25790672 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1957-98C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790672 | |||||||
chr4:25790676 | G | A | 1 | a0001c0001t0002g0046 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1957-102C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790676 | |||||||
chr4:25790705 | A | G | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1957-131T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790705 | |||||||
chr4:25790717 | A | C | 2 | a0001c0001t0001g0296 a0001c0008t0007g0161 |
2 | HG01884.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1957-143T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790717 | |||||||
chr4:25790782 | G | A | 1 | a0002c0013t0014g0127 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1957-208C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790782 | |||||||
chr4:25790881 | T | C | 1 | a0002c0013t0014g0127 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1957-307A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25790881 | |||||||
chr4:25791024 | G | T | 1 | a0001c0011t0003g0172 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1957-450C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25791024 | |||||||
chr4:25791094 | C | T | 50 | a0001c0001t0001g0104 a0001c0001t0001g0117 a0001c0001t0001g0258 others(47): Show |
50 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.1957-520G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25791094 | |||||||
chr4:25791095 | A | C | 228 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0030 others(225): Show |
231 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.1957-521T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25791095 | |||||||
chr4:25791273 | A | G | 2 | a0001c0001t0001g0296 a0001c0008t0007g0161 |
2 | HG01884.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1957-699T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25791273 | |||||||
chr4:25791436 | T | C | 145 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0030 others(142): Show |
148 | HG00099.hp2 HG00140.hp2 HG00597.hp1 others(145): Show |
intron_variant | MODIFIER | c.1957-862A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25791436 | |||||||
chr4:25791459 | C | T | 1 | a0010c0016t0002g0141 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1957-885G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25791459 | |||||||
chr4:25791472 | G | A | 2 | a0001c0011t0002g0055 a0001c0011t0002g0101 |
2 | HG02647.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1957-898C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25791472 | |||||||
chr4:25791492 | G | A | 1 | a0001c0001t0002g0272 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1957-918C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25791492 | |||||||
chr4:25791497 | C | T | 2 | a0001c0001t0002g0152 a0002c0002t0008g0301 |
2 | HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1957-923G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25791497 | |||||||
chr4:25791645 | T | C | 1 | a0001c0001t0003g0286 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1957-1071A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25791645 | |||||||
chr4:25791772 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1957-1198C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25791772 | |||||||
chr4:25791789 | G | A | 1 | a0001c0001t0005g0300 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1957-1215C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25791789 | |||||||
chr4:25791861 | C | G | 3 | a0001c0001t0004g0130 a0001c0001t0010g0129 a0002c0009t0007g0298 |
3 | HG00741.hp1 HG02258.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1957-1287G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25791861 | |||||||
chr4:25791911 | TA | T | 27 | a0001c0001t0001g0043 a0001c0001t0001g0136 a0001c0001t0001g0258 others(24): Show |
27 | HG01070.hp2 HG01433.hp2 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.1957-1338delT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25791911 | |||||||
chr4:25792053 | T | C | 1 | a0001c0001t0002g0196 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1957-1479A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25792053 | |||||||
chr4:25792116 | C | A | 31 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0030 others(28): Show |
31 | HG00099.hp2 HG00597.hp1 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.1957-1542G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25792116 | |||||||
chr4:25792179 | G | A | 70 | a0001c0001t0001g0104 a0001c0001t0001g0117 a0001c0001t0001g0136 others(67): Show |
72 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.1957-1605C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25792179 | |||||||
chr4:25792189 | G | GT | 4 | a0001c0001t0001g0145 a0001c0001t0001g0201 a0001c0001t0001g0206 others(1): Show |
4 | HG00597.hp2 HG02738.hp1 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.1957-1616dupA | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25792189 | |||||||
chr4:25792191 | A | T | 233 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0030 others(230): Show |
236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.1957-1617T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25792191 | |||||||
chr4:25792326 | C | A | 1 | a0001c0001t0002g0094 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1957-1752G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25792326 | |||||||
chr4:25792372 | G | A | 1 | a0001c0001t0004g0123 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1957-1798C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25792372 | |||||||
chr4:25792468 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1957-1894T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25792468 | |||||||
chr4:25792471 | G | T | 57 | a0001c0001t0001g0104 a0001c0001t0001g0117 a0001c0001t0001g0188 others(54): Show |
59 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.1957-1897C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25792471 | |||||||
chr4:25792485 | A | C | 101 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0030 others(98): Show |
103 | HG00099.hp2 HG00140.hp1 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.1957-1911T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25792485 | |||||||
chr4:25792679 | A | T | 1 | a0001c0001t0001g0109 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1957-2105T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25792679 | |||||||
chr4:25792823 | T | G | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1957-2249A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25792823 | |||||||
chr4:25792954 | G | A | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1957-2380C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25792954 | |||||||
chr4:25792959 | T | A | 1 | a0001c0001t0002g0251 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1957-2385A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25792959 | |||||||
chr4:25792961 | T | A | 4 | a0001c0001t0005g0300 a0002c0002t0006g0267 a0002c0009t0004g0268 others(1): Show |
4 | HG02280.hp2 HG02922.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1957-2387A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25792961 | |||||||
chr4:25792973 | G | A | 1 | a0001c0001t0001g0253 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1957-2399C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25792973 | |||||||
chr4:25793064 | C | T | 58 | a0001c0001t0001g0104 a0001c0001t0001g0117 a0001c0001t0001g0188 others(55): Show |
60 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.1957-2490G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25793064 | |||||||
chr4:25793083 | G | C | 3 | a0001c0001t0002g0071 a0001c0001t0002g0111 a0001c0001t0002g0261 |
3 | HG01169.hp2 HG02602.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1957-2509C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25793083 | |||||||
chr4:25793159 | C | T | 32 | a0001c0001t0001g0104 a0001c0001t0001g0117 a0001c0001t0001g0258 others(29): Show |
32 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.1957-2585G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25793159 | |||||||
chr4:25793220 | A | G | 33 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0030 others(30): Show |
33 | HG00099.hp2 HG00597.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.1957-2646T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25793220 | |||||||
chr4:25793247 | G | A | 95 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(92): Show |
96 | HG00140.hp2 HG00609.hp1 HG00642.hp2 others(93): Show |
intron_variant | MODIFIER | c.1957-2673C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25793247 | |||||||
chr4:25793256 | C | T | 1 | a0001c0006t0004g0092 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1957-2682G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25793256 | |||||||
chr4:25793290 | T | G | 1 | a0001c0001t0002g0094 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1957-2716A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25793290 | |||||||
chr4:25793438 | C | T | 4 | a0001c0001t0010g0008 a0005c0021t0003g0283 a0005c0022t0004g0284 others(1): Show |
4 | HG02630.hp2 HG02717.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1957-2864G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25793438 | |||||||
chr4:25793513 | T | C | 96 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(93): Show |
97 | HG00140.hp2 HG00597.hp2 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.1957-2939A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25793513 | |||||||
chr4:25793558 | GC | G | 95 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(92): Show |
96 | HG00140.hp2 HG00609.hp1 HG00642.hp2 others(93): Show |
intron_variant | MODIFIER | c.1957-2985delG | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25793558 | |||||||
chr4:25793685 | G | A | 2 | a0002c0005t0001g0156 a0002c0005t0001g0157 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1957-3111C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25793685 | |||||||
chr4:25793692 | T | A | 1 | a0001c0001t0001g0078 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1957-3118A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25793692 | |||||||
chr4:25793766 | T | G | 1 | a0002c0002t0005g0187 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1957-3192A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25793766 | |||||||
chr4:25793770 | C | T | 1 | a0001c0001t0002g0032 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1957-3196G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25793770 | |||||||
chr4:25793809 | G | T | 21 | a0001c0001t0001g0188 a0001c0001t0001g0287 a0001c0001t0001g0288 others(18): Show |
23 | HG01261.hp1 HG01891.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.1957-3235C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25793809 | |||||||
chr4:25793980 | A | T | 2 | a0005c0019t0002g0010 a0012c0020t0002g0011 |
2 | HG02055.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1957-3406T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25793980 | |||||||
chr4:25794013 | C | T | 54 | a0001c0001t0001g0104 a0001c0001t0001g0117 a0001c0001t0001g0188 others(51): Show |
56 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.1957-3439G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25794013 | |||||||
chr4:25794028 | G | A | 2 | a0001c0001t0002g0192 a0001c0001t0002g0262 |
2 | HG02683.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1957-3454C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25794028 | |||||||
chr4:25794228 | A | G | 32 | a0001c0001t0001g0104 a0001c0001t0001g0117 a0001c0001t0001g0258 others(29): Show |
32 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.1957-3654T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25794228 | |||||||
chr4:25794247 | T | C | 10 | a0001c0001t0001g0136 a0001c0001t0002g0148 a0001c0001t0002g0152 others(7): Show |
10 | HG02280.hp1 HG02451.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1957-3673A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25794247 | |||||||
chr4:25794251 | A | G | 1 | a0001c0001t0003g0183 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1957-3677T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25794251 | |||||||
chr4:25794271 | C | A | 2 | a0002c0002t0002g0133 a0002c0005t0003g0122 |
2 | HG02647.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1957-3697G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25794271 | |||||||
chr4:25794336 | C | A | 6 | a0001c0001t0004g0123 a0001c0001t0010g0008 a0002c0002t0008g0301 others(3): Show |
6 | HG01192.hp2 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1957-3762G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25794336 | |||||||
chr4:25794540 | C | A | 1 | a0001c0001t0001g0070 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1957-3966G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25794540 | |||||||
chr4:25794568 | A | G | 2 | a0001c0010t0002g0173 a0001c0010t0022g0307 |
2 | HG03041.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1957-3994T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25794568 | |||||||
chr4:25794574 | G | A | 22 | a0001c0001t0002g0015 a0001c0001t0002g0017 a0001c0001t0002g0034 others(19): Show |
22 | HG00741.hp1 HG01346.hp2 HG01928.hp1 others(19): Show |
intron_variant | MODIFIER | c.1957-4000C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25794574 | |||||||
chr4:25794591 | T | C | 4 | a0001c0010t0024g0309 a0001c0014t0001g0159 a0002c0002t0002g0133 others(1): Show |
4 | HG01109.hp1 HG02647.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1957-4017A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25794591 | |||||||
chr4:25794694 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1957-4120G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25794694 | |||||||
chr4:25794697 | A | C | 1 | a0001c0001t0008g0290 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1957-4123T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25794697 | |||||||
chr4:25794707 | T | C | 2 | a0001c0001t0002g0196 a0001c0034t0002g0137 |
2 | HG02055.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1957-4133A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25794707 | |||||||
chr4:25794892 | C | A | 73 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0030 others(70): Show |
75 | HG00099.hp2 HG00597.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.1957-4318G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25794892 | |||||||
chr4:25794892 | C | T | 1 | a0001c0001t0002g0053 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1957-4318G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25794892 | |||||||
chr4:25794894 | T | G | 5 | a0001c0001t0002g0302 a0002c0002t0002g0277 a0002c0002t0002g0281 others(2): Show |
5 | HG02572.hp1 HG02818.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1957-4320A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25794894 | |||||||
chr4:25794905 | G | A | 43 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0030 others(40): Show |
43 | HG00099.hp2 HG00597.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.1957-4331C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25794905 | |||||||
chr4:25795015 | T | C | 1 | a0002c0002t0008g0301 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1957-4441A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25795015 | |||||||
chr4:25795055 | G | A | 46 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0021 others(43): Show |
46 | HG00099.hp2 HG00597.hp1 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.1957-4481C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25795055 | |||||||
chr4:25795059 | G | A | 1 | a0010c0016t0002g0141 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1957-4485C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25795059 | |||||||
chr4:25795060 | T | TG | 14 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0002g0163 others(11): Show |
16 | HG01070.hp1 HG01071.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.1957-4487dupC | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25795060 | |||||||
chr4:25795154 | A | C | 7 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0002g0163 others(4): Show |
9 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1957-4580T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25795154 | |||||||
chr4:25795155 | CGT | C | 7 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0002g0163 others(4): Show |
9 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1957-4583_1957-458 others(6): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25795155 | |||||||
chr4:25795158 | T | C | 7 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0002g0163 others(4): Show |
9 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1957-4584A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25795158 | |||||||
chr4:25795191 | G | A | 1 | a0002c0005t0006g0001 | 3 | HG02109.hp1 HG02257.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1957-4617C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25795191 | |||||||
chr4:25795225 | A | G | 1 | a0001c0001t0002g0086 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1957-4651T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25795225 | |||||||
chr4:25795322 | C | T | 2 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
2 | HG00438.hp2 HG00673.hp1 |
intron_variant | MODIFIER | c.1957-4748G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25795322 | |||||||
chr4:25795393 | A | T | 1 | a0002c0002t0005g0187 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1957-4819T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25795393 | |||||||
chr4:25795463 | G | C | 73 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(70): Show |
73 | HG00140.hp2 HG00597.hp2 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.1957-4889C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25795463 | |||||||
chr4:25795595 | C | G | 1 | a0001c0001t0001g0221 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1957-5021G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25795595 | |||||||
chr4:25795825 | C | T | 1 | a0006c0012t0002g0022 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1957-5251G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25795825 | |||||||
chr4:25795826 | G | A | 29 | a0001c0001t0001g0104 a0001c0001t0001g0117 a0001c0001t0001g0188 others(26): Show |
30 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.1957-5252C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25795826 | |||||||
chr4:25795902 | G | A | 1 | a0001c0001t0001g0080 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1957-5328C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25795902 | |||||||
chr4:25795911 | C | T | 12 | a0001c0001t0001g0296 a0001c0001t0002g0302 a0001c0008t0007g0161 others(9): Show |
12 | HG01884.hp1 HG02280.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1957-5337G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25795911 | |||||||
chr4:25795924 | GA | G | 34 | a0001c0001t0001g0012 a0001c0001t0001g0100 a0001c0001t0001g0287 others(31): Show |
36 | HG00738.hp1 HG01070.hp1 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.1957-5351delT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25795924 | |||||||
chr4:25795924 | GAA | G | 25 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0042 others(22): Show |
25 | HG00099.hp2 HG00597.hp1 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.1957-5352_1957-535 others(6): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25795924 | |||||||
chr4:25795946 | C | T | 1 | a0003c0004t0001g0202 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1957-5372G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25795946 | |||||||
chr4:25795962 | G | C | 3 | a0002c0002t0008g0301 a0002c0009t0007g0298 a0009c0037t0003g0304 |
3 | HG02145.hp2 HG02258.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1957-5388C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25795962 | |||||||
chr4:25796043 | A | C | 3 | a0001c0001t0003g0286 a0001c0001t0004g0130 a0001c0001t0010g0129 |
3 | HG00741.hp1 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1957-5469T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25796043 | |||||||
chr4:25796096 | C | T | 3 | a0001c0001t0008g0114 a0001c0001t0008g0290 a0011c0029t0005g0135 |
3 | HG01074.hp1 HG01257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1957-5522G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25796096 | |||||||
chr4:25796239 | C | T | 1 | a0001c0010t0024g0309 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1957-5665G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25796239 | |||||||
chr4:25796253 | C | T | 1 | a0001c0001t0002g0102 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1957-5679G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25796253 | |||||||
chr4:25796315 | T | A | 1 | a0001c0001t0003g0183 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1957-5741A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25796315 | |||||||
chr4:25796321 | G | A | 3 | a0001c0001t0008g0114 a0001c0001t0008g0290 a0011c0029t0005g0135 |
3 | HG01074.hp1 HG01257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1957-5747C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25796321 | |||||||
chr4:25796342 | C | T | 7 | a0001c0001t0002g0196 a0001c0001t0009g0285 a0001c0014t0001g0159 others(4): Show |
7 | HG01891.hp1 HG02055.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1957-5768G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25796342 | |||||||
chr4:25796383 | C | T | 1 | a0001c0014t0001g0159 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1957-5809G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25796383 | |||||||
chr4:25796449 | A | ATG | 3 | a0001c0001t0001g0296 a0001c0001t0002g0192 a0001c0008t0007g0161 |
3 | HG01884.hp1 HG02683.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1956+5832_1956+583 others(6): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25796449 | |||||||
chr4:25796697 | T | C | 158 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0019 others(155): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.1956+5586A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25796697 | |||||||
chr4:25796713 | G | A | 1 | a0001c0003t0002g0024 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1956+5570C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25796713 | |||||||
chr4:25796730 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1956+5553C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25796730 | |||||||
chr4:25796864 | G | C | 1 | a0001c0001t0002g0140 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1956+5419C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25796864 | |||||||
chr4:25796868 | GA | G | 86 | a0001c0001t0001g0019 a0001c0001t0001g0104 a0001c0001t0001g0117 others(83): Show |
89 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.1956+5414delT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25796868 | |||||||
chr4:25796868 | GAA | G | 7 | a0001c0001t0002g0196 a0001c0001t0009g0285 a0001c0008t0002g0142 others(4): Show |
7 | HG01891.hp1 HG02055.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1956+5413_1956+541 others(6): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25796868 | |||||||
chr4:25796935 | G | C | 1 | a0001c0010t0002g0173 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1956+5348C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25796935 | |||||||
chr4:25797059 | G | A | 1 | a0001c0003t0002g0049 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1956+5224C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25797059 | |||||||
chr4:25797153 | T | C | 132 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0021 others(129): Show |
135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.1956+5130A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25797153 | |||||||
chr4:25797193 | C | CA | 79 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0100 others(76): Show |
82 | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.1956+5089dupT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25797193 | |||||||
chr4:25797250 | C | T | 32 | a0001c0001t0002g0126 a0001c0001t0002g0302 a0002c0002t0001g0279 others(29): Show |
34 | HG01070.hp1 HG01071.hp2 HG02055.hp2 others(31): Show |
intron_variant | MODIFIER | c.1956+5033G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25797250 | |||||||
chr4:25797330 | T | C | 118 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0019 others(115): Show |
121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
intron_variant | MODIFIER | c.1956+4953A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25797330 | |||||||
chr4:25797339 | C | T | 7 | a0001c0001t0001g0109 a0001c0001t0001g0240 a0001c0001t0002g0064 others(4): Show |
7 | HG01943.hp2 HG02004.hp1 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.1956+4944G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25797339 | |||||||
chr4:25797342 | T | C | 10 | a0001c0001t0002g0302 a0002c0002t0002g0277 a0002c0002t0002g0281 others(7): Show |
10 | HG02280.hp2 HG02572.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.1956+4941A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25797342 | |||||||
chr4:25797346 | A | T | 73 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0019 others(70): Show |
74 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(71): Show |
intron_variant | MODIFIER | c.1956+4937T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25797346 | |||||||
chr4:25797627 | A | G | 39 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0021 others(36): Show |
39 | HG00558.hp2 HG00597.hp1 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.1956+4656T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25797627 | |||||||
chr4:25797715 | C | A | 2 | a0001c0001t0001g0292 a0001c0001t0002g0220 |
2 | HG00738.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.1956+4568G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25797715 | |||||||
chr4:25797875 | A | C | 8 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0001g0296 others(5): Show |
8 | HG01074.hp1 HG01884.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1956+4408T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25797875 | |||||||
chr4:25797893 | G | A | 1 | a0001c0008t0007g0161 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1956+4390C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25797893 | |||||||
chr4:25798092 | G | A | 3 | a0001c0001t0001g0296 a0001c0001t0008g0114 a0011c0029t0005g0135 |
3 | HG01074.hp1 HG01884.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1956+4191C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25798092 | |||||||
chr4:25798130 | A | C | 156 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0019 others(153): Show |
157 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.1956+4153T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25798130 | |||||||
chr4:25798133 | G | A | 1 | a0001c0001t0002g0086 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1956+4150C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25798133 | |||||||
chr4:25798383 | T | C | 1 | a0001c0001t0002g0163 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1956+3900A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25798383 | |||||||
chr4:25798442 | CA | C | 11 | a0002c0002t0002g0133 a0002c0002t0002g0138 a0002c0002t0008g0301 others(8): Show |
13 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1956+3840delT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25798442 | |||||||
chr4:25798445 | A | G | 4 | a0001c0001t0001g0296 a0001c0001t0008g0114 a0001c0008t0007g0161 others(1): Show |
4 | HG01074.hp1 HG01884.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1956+3838T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25798445 | |||||||
chr4:25798476 | T | C | 1 | a0001c0001t0001g0250 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1956+3807A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25798476 | |||||||
chr4:25798545 | C | T | 21 | a0001c0001t0002g0196 a0001c0034t0002g0137 a0002c0002t0002g0133 others(18): Show |
23 | HG01070.hp1 HG01071.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.1956+3738G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25798545 | |||||||
chr4:25798657 | G | A | 1 | a0010c0016t0002g0141 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1956+3626C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25798657 | |||||||
chr4:25798870 | G | A | 1 | a0005c0019t0002g0010 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1956+3413C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25798870 | |||||||
chr4:25798957 | C | T | 1 | a0001c0001t0003g0276 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1956+3326G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25798957 | |||||||
chr4:25799077 | TTTG | T | 3 | a0001c0001t0001g0136 a0001c0001t0002g0131 a0001c0001t0002g0134 |
3 | HG02257.hp2 HG03130.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1956+3203_1956+320 others(7): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25799077 | |||||||
chr4:25799248 | C | T | 172 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0019 others(169): Show |
173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.1956+3035G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25799248 | |||||||
chr4:25799259 | G | C | 163 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0019 others(160): Show |
164 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.1956+3024C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25799259 | |||||||
chr4:25799267 | G | A | 1 | a0001c0001t0001g0043 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1956+3016C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25799267 | |||||||
chr4:25799519 | C | T | 2 | a0001c0001t0008g0114 a0011c0029t0005g0135 |
2 | HG01074.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1956+2764G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25799519 | |||||||
chr4:25799554 | G | A | 1 | a0001c0008t0001g0162 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1956+2729C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25799554 | |||||||
chr4:25799681 | T | C | 1 | a0007c0031t0020g0169 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1956+2602A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25799681 | |||||||
chr4:25799861 | T | C | 2 | a0001c0001t0002g0196 a0001c0034t0002g0137 |
2 | HG02055.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1956+2422A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25799861 | |||||||
chr4:25799906 | A | G | 2 | a0001c0001t0002g0302 a0001c0006t0004g0299 |
2 | HG02451.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1956+2377T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25799906 | |||||||
chr4:25799996 | G | T | 1 | a0001c0008t0007g0161 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1956+2287C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25799996 | |||||||
chr4:25800125 | G | A | 28 | a0002c0002t0001g0279 a0002c0002t0002g0133 a0002c0002t0002g0138 others(25): Show |
30 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.1956+2158C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25800125 | |||||||
chr4:25800255 | A | C | 1 | a0001c0001t0001g0088 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1956+2028T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25800255 | |||||||
chr4:25800315 | C | A | 183 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0019 others(180): Show |
186 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.1956+1968G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25800315 | |||||||
chr4:25800340 | C | G | 2 | a0001c0001t0002g0295 a0001c0008t0001g0162 |
2 | HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1956+1943G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25800340 | |||||||
chr4:25800358 | A | G | 2 | a0001c0001t0002g0032 a0006c0012t0015g0073 |
2 | HG03654.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1956+1925T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25800358 | |||||||
chr4:25800616 | T | C | 1 | a0005c0019t0002g0010 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1956+1667A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25800616 | |||||||
chr4:25800668 | T | A | 4 | a0001c0001t0001g0296 a0001c0001t0008g0114 a0001c0008t0007g0161 others(1): Show |
4 | HG01074.hp1 HG01884.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1956+1615A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25800668 | |||||||
chr4:25800669 | A | T | 1 | a0010c0016t0002g0141 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1956+1614T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25800669 | |||||||
chr4:25800754 | G | C | 34 | a0001c0001t0002g0196 a0001c0014t0001g0159 a0001c0034t0002g0137 others(31): Show |
36 | HG01070.hp1 HG01071.hp2 HG02055.hp1 others(33): Show |
intron_variant | MODIFIER | c.1956+1529C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25800754 | |||||||
chr4:25800776 | G | C | 4 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0002g0163 others(1): Show |
4 | HG02615.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1956+1507C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25800776 | |||||||
chr4:25800778 | A | G | 4 | a0001c0001t0001g0296 a0001c0001t0008g0114 a0001c0008t0007g0161 others(1): Show |
4 | HG01074.hp1 HG01884.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1956+1505T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25800778 | |||||||
chr4:25800867 | A | G | 35 | a0001c0001t0002g0196 a0001c0014t0001g0159 a0001c0034t0002g0137 others(32): Show |
37 | HG01070.hp1 HG01071.hp2 HG02055.hp1 others(34): Show |
intron_variant | MODIFIER | c.1956+1416T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25800867 | |||||||
chr4:25800885 | C | T | 1 | a0002c0002t0005g0187 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1956+1398G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25800885 | |||||||
chr4:25800930 | C | G | 6 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0002g0163 others(3): Show |
6 | HG02451.hp1 HG02615.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1956+1353G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25800930 | |||||||
chr4:25801030 | C | T | 1 | a0001c0027t0001g0197 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1956+1253G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25801030 | |||||||
chr4:25801141 | G | A | 1 | a0001c0014t0001g0159 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1956+1142C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25801141 | |||||||
chr4:25801262 | G | C | 2 | a0001c0001t0002g0067 a0001c0001t0002g0068 |
2 | NA18961.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1956+1021C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25801262 | |||||||
chr4:25801276 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1956+1007C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25801276 | |||||||
chr4:25801311 | G | A | 46 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0019 others(43): Show |
46 | HG00558.hp2 HG00597.hp1 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.1956+972C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25801311 | |||||||
chr4:25801346 | T | A | 1 | a0001c0001t0003g0091 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1956+937A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25801346 | |||||||
chr4:25801360 | G | T | 1 | a0001c0001t0002g0236 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1956+923C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25801360 | |||||||
chr4:25801534 | C | T | 28 | a0002c0002t0001g0279 a0002c0002t0002g0133 a0002c0002t0002g0138 others(25): Show |
30 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.1956+749G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25801534 | |||||||
chr4:25801602 | T | C | 1 | a0001c0001t0001g0203 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1956+681A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25801602 | |||||||
chr4:25802115 | A | C | 1 | a0001c0001t0001g0296 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1956+168T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25802115 | |||||||
chr4:25802208 | A | G | 202 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0019 others(199): Show |
205 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.1956+75T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 11/23 | chr4 | 25802208 | |||||||
chr4:25802486 | C | T | 28 | a0002c0002t0001g0279 a0002c0002t0002g0133 a0002c0002t0002g0138 others(25): Show |
30 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.1777-24G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 10/23 | chr4 | 25802486 | |||||||
chr4:25802621 | G | A | 28 | a0002c0002t0001g0279 a0002c0002t0002g0133 a0002c0002t0002g0138 others(25): Show |
30 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.1777-159C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 10/23 | chr4 | 25802621 | |||||||
chr4:25802726 | C | T | 1 | a0001c0001t0002g0295 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1777-264G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 10/23 | chr4 | 25802726 | |||||||
chr4:25802943 | C | T | 1 | a0001c0014t0001g0159 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1777-481G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 10/23 | chr4 | 25802943 | |||||||
chr4:25802959 | T | C | 1 | a0001c0001t0005g0300 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1777-497A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 10/23 | chr4 | 25802959 | |||||||
chr4:25803229 | C | T | 10 | a0001c0001t0002g0128 a0001c0001t0002g0148 a0001c0001t0002g0151 others(7): Show |
10 | HG01891.hp1 HG02280.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1777-767G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 10/23 | chr4 | 25803229 | |||||||
chr4:25803296 | CT | C | 12 | a0001c0001t0001g0038 a0001c0001t0001g0077 a0001c0001t0001g0084 others(9): Show |
12 | HG01358.hp1 HG01943.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.1777-835delA | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 10/23 | chr4 | 25803296 | |||||||
chr4:25803297 | T | G | 4 | a0001c0001t0001g0296 a0001c0001t0008g0114 a0001c0008t0007g0161 others(1): Show |
4 | HG01074.hp1 HG01884.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1777-835A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 10/23 | chr4 | 25803297 | |||||||
chr4:25803306 | C | A | 1 | a0019c0024t0023g0308 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1777-844G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 10/23 | chr4 | 25803306 | |||||||
chr4:25803327 | A | G | 158 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0019 others(155): Show |
159 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.1777-865T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 10/23 | chr4 | 25803327 | |||||||
chr4:25803398 | C | T | 2 | a0001c0001t0003g0149 a0001c0001t0006g0150 |
2 | HG02451.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1777-936G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 10/23 | chr4 | 25803398 | |||||||
chr4:25803435 | C | T | 1 | a0019c0024t0023g0308 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1777-973G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 10/23 | chr4 | 25803435 | |||||||
chr4:25803508 | G | A | 1 | a0001c0001t0002g0247 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1776+1033C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 10/23 | chr4 | 25803508 | |||||||
chr4:25803569 | C | T | 1 | a0001c0011t0003g0172 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1776+972G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 10/23 | chr4 | 25803569 | |||||||
chr4:25803638 | G | A | 38 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0002g0163 others(35): Show |
40 | HG01070.hp1 HG01071.hp2 HG02055.hp1 others(37): Show |
intron_variant | MODIFIER | c.1776+903C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 10/23 | chr4 | 25803638 | |||||||
chr4:25803781 | G | GT | 30 | a0001c0001t0002g0006 a0001c0001t0002g0177 a0001c0001t0002g0236 others(27): Show |
32 | HG00733.hp2 HG01070.hp1 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.1776+759dupA | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 10/23 | chr4 | 25803781 | |||||||
chr4:25803782 | T | G | 1 | a0001c0001t0002g0015 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1776+759A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 10/23 | chr4 | 25803782 | |||||||
chr4:25803790 | T | G | 9 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0002g0020 others(6): Show |
9 | HG02451.hp1 HG02615.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1776+751A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 10/23 | chr4 | 25803790 | |||||||
chr4:25803799 | G | T | 192 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0019 others(189): Show |
195 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.1776+742C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 10/23 | chr4 | 25803799 | |||||||
chr4:25803805 | G | T | 1 | a0017c0030t0001g0045 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1776+736C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 10/23 | chr4 | 25803805 | |||||||
chr4:25803928 | G | A | 1 | a0006c0012t0015g0073 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1776+613C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 10/23 | chr4 | 25803928 | |||||||
chr4:25804306 | G | A | 1 | a0019c0024t0023g0308 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1776+235C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 10/23 | chr4 | 25804306 | |||||||
chr4:25804778 | A | T | 2 | a0001c0001t0001g0080 a0001c0001t0002g0094 |
2 | NA18968.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.1565-26T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25804778 | |||||||
chr4:25804803 | T | C | 1 | a0001c0001t0002g0152 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1565-51A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25804803 | |||||||
chr4:25805224 | G | T | 1 | a0001c0001t0002g0235 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1565-472C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25805224 | |||||||
chr4:25805324 | C | A | 2 | a0001c0001t0001g0274 a0001c0001t0002g0178 |
2 | HG00099.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1565-572G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25805324 | |||||||
chr4:25805487 | C | G | 2 | a0001c0001t0002g0289 a0001c0001t0008g0290 |
2 | HG01257.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.1565-735G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25805487 | |||||||
chr4:25805496 | C | T | 1 | a0001c0006t0004g0299 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1565-744G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25805496 | |||||||
chr4:25805582 | A | G | 1 | a0001c0001t0002g0016 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1565-830T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25805582 | |||||||
chr4:25805592 | TC | T | 143 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0021 others(140): Show |
144 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.1565-841delG | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25805592 | |||||||
chr4:25805678 | TAG | T | 8 | a0001c0001t0002g0139 a0001c0001t0004g0123 a0001c0001t0009g0124 others(5): Show |
8 | HG01192.hp2 HG02145.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1565-928_1565-927d others(4): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25805678 | |||||||
chr4:25805698 | C | G | 1 | a0001c0001t0001g0252 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1565-946G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25805698 | |||||||
chr4:25805708 | C | T | 1 | a0013c0036t0002g0303 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1565-956G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25805708 | |||||||
chr4:25805897 | A | G | 1 | a0001c0001t0002g0192 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1565-1145T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25805897 | |||||||
chr4:25806041 | G | GT | 68 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(65): Show |
68 | HG00140.hp2 HG00558.hp1 HG00738.hp2 others(65): Show |
intron_variant | MODIFIER | c.1565-1290dupA | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25806041 | |||||||
chr4:25806041 | GT | G | 43 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0038 others(40): Show |
43 | HG00438.hp2 HG00642.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.1565-1290delA | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25806041 | |||||||
chr4:25806045 | T | G | 1 | a0001c0001t0002g0140 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1565-1293A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25806045 | |||||||
chr4:25806046 | T | G | 2 | a0001c0001t0003g0149 a0001c0001t0006g0150 |
2 | HG02451.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1565-1294A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25806046 | |||||||
chr4:25806196 | G | C | 1 | a0001c0001t0001g0050 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1565-1444C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25806196 | |||||||
chr4:25806205 | A | T | 1 | a0001c0001t0002g0205 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1565-1453T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25806205 | |||||||
chr4:25806251 | A | G | 1 | a0001c0014t0001g0159 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1565-1499T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25806251 | |||||||
chr4:25806294 | C | T | 1 | a0002c0002t0005g0187 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1565-1542G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25806294 | |||||||
chr4:25806478 | C | G | 2 | a0001c0001t0002g0196 a0001c0034t0002g0137 |
2 | HG02055.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1565-1726G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25806478 | |||||||
chr4:25806577 | G | A | 1 | a0001c0001t0004g0130 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1565-1825C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25806577 | |||||||
chr4:25806856 | T | TA | 12 | a0001c0001t0001g0296 a0001c0001t0002g0174 a0001c0001t0002g0196 others(9): Show |
12 | HG01074.hp1 HG01884.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.1565-2105dupT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25806856 | |||||||
chr4:25806991 | C | T | 2 | a0001c0001t0002g0209 a0001c0001t0002g0249 |
2 | HG01169.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.1565-2239G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25806991 | |||||||
chr4:25807070 | A | C | 159 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0019 others(156): Show |
160 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.1565-2318T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25807070 | |||||||
chr4:25807089 | G | A | 2 | a0001c0008t0007g0161 a0010c0016t0002g0141 |
2 | HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1565-2337C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25807089 | |||||||
chr4:25807152 | C | G | 1 | a0001c0001t0002g0071 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1565-2400G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25807152 | |||||||
chr4:25807155 | T | C | 31 | a0001c0001t0002g0302 a0001c0001t0005g0300 a0001c0006t0004g0299 others(28): Show |
33 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(30): Show |
intron_variant | MODIFIER | c.1565-2403A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25807155 | |||||||
chr4:25807280 | G | A | 1 | a0003c0004t0001g0195 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1565-2528C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25807280 | |||||||
chr4:25807448 | T | C | 1 | a0001c0001t0001g0250 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1565-2696A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25807448 | |||||||
chr4:25807580 | A | T | 1 | a0001c0011t0003g0172 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1565-2828T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25807580 | |||||||
chr4:25807641 | A | T | 3 | a0001c0001t0002g0264 a0001c0001t0003g0215 a0001c0001t0003g0265 |
3 | HG00738.hp2 HG03017.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1565-2889T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25807641 | |||||||
chr4:25807740 | C | T | 2 | a0001c0001t0002g0196 a0001c0034t0002g0137 |
2 | HG02055.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1565-2988G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25807740 | |||||||
chr4:25807783 | A | G | 1 | a0001c0001t0001g0047 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1565-3031T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25807783 | |||||||
chr4:25807812 | A | G | 1 | a0019c0024t0023g0308 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1565-3060T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25807812 | |||||||
chr4:25808202 | T | C | 1 | a0001c0001t0002g0016 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1565-3450A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808202 | |||||||
chr4:25808251 | A | C | 1 | a0001c0011t0003g0172 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1565-3499T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808251 | |||||||
chr4:25808318 | C | T | 1 | a0005c0019t0002g0010 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1565-3566G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808318 | |||||||
chr4:25808360 | A | G | 4 | a0001c0001t0001g0296 a0001c0001t0008g0114 a0001c0008t0007g0161 others(1): Show |
4 | HG01074.hp1 HG01884.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1565-3608T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808360 | |||||||
chr4:25808395 | T | C | 1 | a0005c0019t0002g0010 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1565-3643A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808395 | |||||||
chr4:25808396 | A | C | 1 | a0010c0016t0002g0141 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1565-3644T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808396 | |||||||
chr4:25808474 | G | A | 66 | a0001c0001t0001g0044 a0001c0001t0001g0048 a0001c0001t0001g0050 others(63): Show |
66 | HG00140.hp2 HG00558.hp1 HG00738.hp2 others(63): Show |
intron_variant | MODIFIER | c.1565-3722C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808474 | |||||||
chr4:25808725 | C | T | 1 | a0010c0016t0002g0141 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1565-3973G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808725 | |||||||
chr4:25808739 | T | C | 2 | a0001c0011t0002g0055 a0001c0011t0002g0101 |
2 | HG02647.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1565-3987A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808739 | |||||||
chr4:25808784 | T | C | 2 | a0001c0003t0002g0096 a0001c0003t0002g0097 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1565-4032A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808784 | |||||||
chr4:25808806 | A | ACGCCTGT others(129): Show |
3 | a0001c0001t0002g0196 a0001c0001t0002g0289 a0001c0034t0002g0137 |
3 | HG01433.hp2 HG02055.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1565-4055_1565-405 others(140): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808806 | |||||||
chr4:25808815 | A | ATCCCAGC others(129): Show |
2 | a0001c0001t0001g0201 a0001c0001t0001g0218 |
2 | NA18993.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.1565-4064_1565-406 others(140): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808815 | |||||||
chr4:25808836 | G | A | 2 | a0001c0003t0002g0096 a0001c0003t0002g0097 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1565-4084C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808836 | |||||||
chr4:25808836 | G | GAGGCGGG others(265): Show |
1 | a0001c0001t0002g0235 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1565-4085_1565-408 others(276): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808836 | |||||||
chr4:25808836 | G | GAGGCGGG others(129): Show |
226 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0030 others(223): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1565-4085_1565-408 others(140): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808836 | |||||||
chr4:25808836 | G | GAGGCGGG others(401): Show |
1 | a0001c0010t0024g0309 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1565-4085_1565-408 others(412): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808836 | |||||||
chr4:25808836 | G | GAGGCGGG others(265): Show |
1 | a0001c0001t0001g0038 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1565-4085_1565-408 others(276): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808836 | |||||||
chr4:25808836 | G | GAGGCGGG others(265): Show |
9 | a0001c0001t0001g0019 a0001c0001t0001g0047 a0001c0001t0001g0082 others(6): Show |
9 | HG00609.hp1 HG00673.hp2 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.1565-4085_1565-408 others(276): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808836 | |||||||
chr4:25808836 | G | GAGGCGGG others(265): Show |
28 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0051 others(25): Show |
28 | HG00438.hp2 HG00597.hp1 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.1565-4085_1565-408 others(276): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808836 | |||||||
chr4:25808836 | G | GAGGCGGG others(129): Show |
16 | a0001c0001t0001g0021 a0001c0001t0001g0041 a0001c0001t0001g0084 others(13): Show |
16 | HG00609.hp2 HG01074.hp1 HG02129.hp1 others(13): Show |
intron_variant | MODIFIER | c.1565-4085_1565-408 others(140): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808836 | |||||||
chr4:25808836 | G | GAGGCGGG others(265): Show |
1 | a0001c0001t0002g0248 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1565-4085_1565-408 others(276): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808836 | |||||||
chr4:25808836 | G | GAGGCGGG others(129): Show |
1 | a0001c0001t0002g0153 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1565-4085_1565-408 others(140): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808836 | |||||||
chr4:25808836 | G | GAGGCGGG others(129): Show |
1 | a0001c0001t0001g0246 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1565-4085_1565-408 others(140): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808836 | |||||||
chr4:25808841 | G | GGGCAGAT others(129): Show |
1 | a0001c0001t0002g0148 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1565-4090_1565-408 others(140): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808841 | |||||||
chr4:25808870 | A | C | 14 | a0001c0001t0003g0149 a0001c0001t0006g0150 a0001c0011t0003g0172 others(11): Show |
14 | HG02280.hp2 HG02451.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.1565-4118T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808870 | |||||||
chr4:25808873 | C | T | 14 | a0001c0001t0003g0149 a0001c0001t0006g0150 a0001c0011t0003g0172 others(11): Show |
14 | HG02280.hp2 HG02451.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.1565-4121G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808873 | |||||||
chr4:25808893 | C | CCCCCGTC others(128): Show |
1 | a0002c0002t0005g0187 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1565-4142_1565-414 others(139): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808893 | |||||||
chr4:25808897 | T | C | 6 | a0001c0001t0001g0040 a0001c0001t0001g0075 a0001c0001t0001g0193 others(3): Show |
6 | HG03579.hp2 NA18747.hp2 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.1565-4145A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808897 | |||||||
chr4:25808898 | A | C | 1 | a0001c0001t0001g0296 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1565-4146T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808898 | |||||||
chr4:25808898 | A | G | 9 | a0001c0001t0001g0040 a0001c0001t0001g0075 a0001c0001t0001g0193 others(6): Show |
9 | HG03098.hp1 HG03579.hp2 NA18747.hp2 others(6): Show |
intron_variant | MODIFIER | c.1565-4146T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808898 | |||||||
chr4:25808938 | T | A | 78 | a0001c0001t0001g0040 a0001c0001t0001g0048 a0001c0001t0001g0050 others(75): Show |
78 | HG00558.hp1 HG00558.hp2 HG00733.hp2 others(75): Show |
intron_variant | MODIFIER | c.1565-4186A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808938 | |||||||
chr4:25808943 | A | G | 1 | a0001c0001t0005g0211 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1565-4191T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808943 | |||||||
chr4:25808945 | T | C | 1 | a0001c0001t0005g0211 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1565-4193A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808945 | |||||||
chr4:25808965 | T | C | 2 | a0001c0010t0002g0173 a0003c0028t0001g0185 |
2 | HG03041.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.1565-4213A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808965 | |||||||
chr4:25808972 | G | C | 3 | a0001c0010t0002g0173 a0002c0002t0002g0138 a0003c0028t0001g0185 |
3 | HG03041.hp1 NA18522.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.1565-4220C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808972 | |||||||
chr4:25808990 | G | A | 2 | a0001c0001t0001g0029 a0001c0003t0002g0049 |
2 | HG00438.hp2 HG00609.hp1 |
intron_variant | MODIFIER | c.1565-4238C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25808990 | |||||||
chr4:25809005 | A | G | 1 | a0001c0001t0003g0091 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1565-4253T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25809005 | |||||||
chr4:25809012 | G | T | 1 | a0001c0001t0005g0234 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1565-4260C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25809012 | |||||||
chr4:25809022 | G | A | 63 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0001g0072 others(60): Show |
63 | HG00558.hp1 HG00558.hp2 HG00733.hp2 others(60): Show |
intron_variant | MODIFIER | c.1565-4270C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25809022 | |||||||
chr4:25809037 | C | T | 2 | a0001c0010t0024g0309 a0019c0024t0023g0308 |
2 | HG01109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1565-4285G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25809037 | |||||||
chr4:25809051 | C | T | 29 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0038 others(26): Show |
29 | HG00438.hp2 HG00597.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.1565-4299G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25809051 | |||||||
chr4:25809072 | C | CA | 21 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0095 others(18): Show |
21 | HG00597.hp1 HG00642.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.1565-4321dupT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25809072 | |||||||
chr4:25809289 | T | C | 1 | a0001c0001t0002g0178 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1565-4537A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25809289 | |||||||
chr4:25809308 | AT | A | 143 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0050 others(140): Show |
145 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(142): Show |
intron_variant | MODIFIER | c.1565-4557delA | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25809308 | |||||||
chr4:25809436 | C | T | 2 | a0001c0001t0003g0149 a0001c0001t0006g0150 |
2 | HG02451.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1565-4684G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25809436 | |||||||
chr4:25809609 | G | A | 1 | a0013c0036t0002g0303 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1565-4857C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25809609 | |||||||
chr4:25809629 | C | T | 29 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0051 others(26): Show |
29 | HG00438.hp2 HG00597.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.1565-4877G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25809629 | |||||||
chr4:25809770 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1565-5018A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25809770 | |||||||
chr4:25809771 | A | T | 7 | a0001c0010t0002g0173 a0002c0002t0002g0138 a0002c0005t0001g0156 others(4): Show |
9 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1565-5019T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25809771 | |||||||
chr4:25809853 | T | C | 17 | a0001c0001t0001g0121 a0001c0001t0001g0296 a0001c0010t0024g0309 others(14): Show |
17 | HG01109.hp1 HG01884.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.1565-5101A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25809853 | |||||||
chr4:25809920 | G | A | 1 | a0001c0001t0002g0017 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1565-5168C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25809920 | |||||||
chr4:25809982 | C | T | 4 | a0001c0001t0001g0296 a0002c0002t0008g0301 a0002c0009t0007g0298 others(1): Show |
4 | HG01884.hp1 HG02258.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1565-5230G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25809982 | |||||||
chr4:25810267 | C | A | 27 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0051 others(24): Show |
27 | HG00438.hp2 HG00597.hp1 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.1565-5515G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25810267 | |||||||
chr4:25810270 | C | T | 10 | a0002c0002t0001g0279 a0002c0002t0002g0277 a0002c0002t0002g0281 others(7): Show |
10 | HG02280.hp2 HG02572.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.1565-5518G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25810270 | |||||||
chr4:25810402 | A | C | 109 | a0001c0001t0001g0030 a0001c0001t0001g0035 a0001c0001t0001g0036 others(106): Show |
111 | HG00558.hp1 HG00735.hp1 HG00738.hp1 others(108): Show |
intron_variant | MODIFIER | c.1565-5650T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25810402 | |||||||
chr4:25810473 | G | A | 10 | a0002c0002t0001g0279 a0002c0002t0002g0277 a0002c0002t0002g0281 others(7): Show |
10 | HG02280.hp2 HG02572.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.1565-5721C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25810473 | |||||||
chr4:25810721 | C | G | 1 | a0001c0001t0001g0296 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1565-5969G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25810721 | |||||||
chr4:25810739 | G | A | 1 | a0001c0001t0002g0071 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1565-5987C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25810739 | |||||||
chr4:25810746 | G | A | 4 | a0001c0001t0001g0296 a0002c0002t0008g0301 a0002c0009t0007g0298 others(1): Show |
4 | HG01884.hp1 HG02258.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1565-5994C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25810746 | |||||||
chr4:25810765 | G | A | 2 | a0001c0001t0002g0067 a0001c0001t0002g0068 |
2 | NA18961.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1565-6013C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25810765 | |||||||
chr4:25810831 | G | A | 1 | a0012c0020t0002g0011 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1565-6079C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25810831 | |||||||
chr4:25810855 | G | A | 25 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0051 others(22): Show |
25 | HG00438.hp2 HG00597.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.1565-6103C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25810855 | |||||||
chr4:25810920 | C | T | 2 | a0006c0012t0002g0022 a0006c0012t0015g0073 |
2 | HG02735.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1565-6168G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25810920 | |||||||
chr4:25810994 | C | T | 1 | a0001c0010t0024g0309 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1565-6242G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25810994 | |||||||
chr4:25811075 | A | G | 64 | a0001c0001t0001g0121 a0001c0001t0001g0188 a0001c0001t0001g0293 others(61): Show |
66 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(63): Show |
intron_variant | MODIFIER | c.1565-6323T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25811075 | |||||||
chr4:25811090 | C | T | 16 | a0001c0001t0002g0128 a0001c0001t0002g0134 a0001c0001t0002g0139 others(13): Show |
16 | HG00741.hp1 HG01192.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.1565-6338G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25811090 | |||||||
chr4:25811091 | G | A | 2 | a0001c0001t0001g0081 a0001c0001t0003g0194 |
2 | HG02040.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.1565-6339C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25811091 | |||||||
chr4:25811360 | T | C | 3 | a0001c0001t0001g0121 a0001c0010t0024g0309 a0019c0024t0023g0308 |
3 | HG01109.hp1 HG02735.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1565-6608A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25811360 | |||||||
chr4:25811448 | G | A | 134 | a0001c0001t0001g0030 a0001c0001t0001g0035 a0001c0001t0001g0036 others(131): Show |
136 | HG00558.hp1 HG00558.hp2 HG00733.hp2 others(133): Show |
intron_variant | MODIFIER | c.1564+6690C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25811448 | |||||||
chr4:25811461 | GTCCATAG others(14): Show |
G | 1 | a0001c0008t0001g0162 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1564+6656_1564+667 others(25): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25811461 | |||||||
chr4:25811465 | A | G | 1 | a0001c0001t0003g0093 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1564+6673T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25811465 | |||||||
chr4:25811497 | A | G | 244 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0019 others(241): Show |
247 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(244): Show |
intron_variant | MODIFIER | c.1564+6641T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25811497 | |||||||
chr4:25811659 | C | T | 5 | a0004c0007t0001g0164 a0004c0007t0001g0165 a0004c0007t0001g0166 others(2): Show |
5 | HG02965.hp1 HG02970.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1564+6479G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25811659 | |||||||
chr4:25811748 | G | GT | 20 | a0001c0001t0001g0009 a0001c0001t0001g0042 a0001c0001t0001g0047 others(17): Show |
20 | HG00558.hp2 HG00642.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.1564+6389dupA | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25811748 | |||||||
chr4:25811748 | GT | G | 24 | a0001c0001t0001g0040 a0001c0001t0002g0140 a0001c0001t0002g0163 others(21): Show |
26 | HG01071.hp2 HG01074.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.1564+6389delA | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25811748 | |||||||
chr4:25811748 | GTT | G | 16 | a0001c0001t0001g0188 a0001c0001t0001g0296 a0001c0001t0002g0248 others(13): Show |
16 | HG01261.hp1 HG01884.hp1 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.1564+6388_1564+638 others(6): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25811748 | |||||||
chr4:25811761 | T | G | 1 | a0009c0037t0003g0304 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1564+6377A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25811761 | |||||||
chr4:25811761 | T | TG | 5 | a0001c0001t0002g0294 a0001c0001t0002g0302 a0001c0001t0004g0130 others(2): Show |
5 | HG02451.hp2 HG02723.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1564+6376_1564+637 others(5): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25811761 | |||||||
chr4:25811764 | T | G | 42 | a0001c0001t0001g0038 a0001c0001t0001g0041 a0001c0001t0001g0107 others(39): Show |
42 | HG00558.hp1 HG00609.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.1564+6374A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25811764 | |||||||
chr4:25811765 | TTG | T | 19 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0051 others(16): Show |
19 | HG00438.hp2 HG00597.hp1 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.1564+6371_1564+637 others(6): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25811765 | |||||||
chr4:25811766 | TG | T | 8 | a0001c0001t0001g0198 a0001c0001t0001g0230 a0001c0001t0001g0271 others(5): Show |
8 | HG01891.hp1 HG02027.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1564+6371delC | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25811766 | |||||||
chr4:25811767 | G | T | 20 | a0001c0001t0001g0293 a0001c0001t0002g0126 a0001c0001t0002g0128 others(17): Show |
20 | HG00741.hp1 HG01081.hp1 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.1564+6371C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25811767 | |||||||
chr4:25811770 | G | T | 2 | a0001c0001t0004g0123 a0015c0038t0012g0305 |
2 | HG01192.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1564+6368C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25811770 | |||||||
chr4:25811845 | A | C | 1 | a0001c0001t0005g0211 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1564+6293T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25811845 | |||||||
chr4:25811923 | A | G | 17 | a0001c0001t0001g0293 a0001c0001t0002g0128 a0001c0001t0002g0134 others(14): Show |
17 | HG00741.hp1 HG01192.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.1564+6215T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25811923 | |||||||
chr4:25811973 | T | G | 10 | a0002c0002t0001g0279 a0002c0002t0002g0277 a0002c0002t0002g0281 others(7): Show |
10 | HG02280.hp2 HG02572.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.1564+6165A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25811973 | |||||||
chr4:25812179 | CG | C | 5 | a0004c0007t0001g0164 a0004c0007t0001g0165 a0004c0007t0001g0166 others(2): Show |
5 | HG02965.hp1 HG02970.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1564+5958delC | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25812179 | |||||||
chr4:25812264 | T | C | 1 | a0001c0001t0002g0053 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1564+5874A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25812264 | |||||||
chr4:25812405 | T | C | 1 | a0001c0010t0024g0309 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1564+5733A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25812405 | |||||||
chr4:25812714 | G | GA | 7 | a0001c0001t0001g0048 a0001c0001t0001g0242 a0001c0001t0002g0126 others(4): Show |
7 | HG01109.hp1 HG02056.hp2 HG02129.hp2 others(4): Show |
intron_variant | MODIFIER | c.1564+5423dupT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25812714 | |||||||
chr4:25812714 | GA | G | 23 | a0001c0001t0001g0120 a0001c0001t0001g0224 a0001c0001t0001g0256 others(20): Show |
23 | HG00738.hp2 HG01069.hp2 HG01257.hp1 others(20): Show |
intron_variant | MODIFIER | c.1564+5423delT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25812714 | |||||||
chr4:25812762 | C | T | 1 | a0001c0011t0003g0172 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1564+5376G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25812762 | |||||||
chr4:25812815 | C | T | 1 | a0001c0001t0002g0249 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1564+5323G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25812815 | |||||||
chr4:25812882 | G | A | 26 | a0001c0001t0001g0293 a0001c0001t0002g0128 a0001c0001t0002g0134 others(23): Show |
28 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.1564+5256C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25812882 | |||||||
chr4:25812936 | C | T | 3 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0002g0196 |
3 | HG02055.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1564+5202G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25812936 | |||||||
chr4:25813107 | G | C | 5 | a0001c0003t0002g0024 a0001c0003t0002g0025 a0001c0003t0002g0103 others(2): Show |
5 | HG00558.hp2 HG00733.hp2 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.1564+5031C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25813107 | |||||||
chr4:25813198 | T | A | 82 | a0001c0001t0001g0030 a0001c0001t0001g0035 a0001c0001t0001g0036 others(79): Show |
82 | HG00558.hp1 HG00735.hp1 HG00738.hp1 others(79): Show |
intron_variant | MODIFIER | c.1564+4940A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25813198 | |||||||
chr4:25813396 | C | T | 77 | a0001c0001t0001g0030 a0001c0001t0001g0035 a0001c0001t0001g0036 others(74): Show |
77 | HG00558.hp1 HG00735.hp1 HG00738.hp1 others(74): Show |
intron_variant | MODIFIER | c.1564+4742G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25813396 | |||||||
chr4:25813470 | T | A | 17 | a0001c0001t0002g0126 a0001c0003t0002g0013 a0001c0003t0002g0024 others(14): Show |
17 | HG00558.hp2 HG00609.hp1 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.1564+4668A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25813470 | |||||||
chr4:25813541 | C | T | 2 | a0001c0001t0009g0285 a0001c0006t0004g0132 |
2 | HG01891.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1564+4597G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25813541 | |||||||
chr4:25813625 | C | T | 52 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0051 others(49): Show |
54 | HG00438.hp2 HG00597.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.1564+4513G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25813625 | |||||||
chr4:25813682 | G | A | 1 | a0001c0001t0001g0081 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1564+4456C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25813682 | |||||||
chr4:25813705 | G | A | 5 | a0004c0007t0001g0164 a0004c0007t0001g0165 a0004c0007t0001g0166 others(2): Show |
5 | HG02965.hp1 HG02970.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1564+4433C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25813705 | |||||||
chr4:25813803 | T | C | 1 | a0001c0001t0002g0053 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1564+4335A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25813803 | |||||||
chr4:25813922 | C | T | 1 | a0013c0036t0002g0303 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1564+4216G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25813922 | |||||||
chr4:25814032 | C | T | 11 | a0001c0001t0001g0121 a0001c0001t0001g0287 a0001c0001t0001g0288 others(8): Show |
11 | HG01109.hp1 HG02055.hp1 HG02735.hp2 others(8): Show |
intron_variant | MODIFIER | c.1564+4106G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25814032 | |||||||
chr4:25814046 | G | A | 10 | a0002c0002t0001g0279 a0002c0002t0002g0277 a0002c0002t0002g0281 others(7): Show |
10 | HG02280.hp2 HG02572.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.1564+4092C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25814046 | |||||||
chr4:25814182 | GA | G | 60 | a0001c0001t0001g0030 a0001c0001t0001g0072 a0001c0001t0001g0107 others(57): Show |
60 | HG00558.hp1 HG00735.hp1 HG00738.hp1 others(57): Show |
intron_variant | MODIFIER | c.1564+3955delT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25814182 | |||||||
chr4:25814350 | G | A | 3 | a0001c0001t0001g0121 a0001c0010t0024g0309 a0019c0024t0023g0308 |
3 | HG01109.hp1 HG02735.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1564+3788C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25814350 | |||||||
chr4:25814426 | A | G | 113 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0035 others(110): Show |
115 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(112): Show |
intron_variant | MODIFIER | c.1564+3712T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25814426 | |||||||
chr4:25814449 | T | A | 43 | a0001c0001t0001g0293 a0001c0001t0002g0126 a0001c0001t0002g0163 others(40): Show |
43 | HG00558.hp2 HG00609.hp1 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.1564+3689A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25814449 | |||||||
chr4:25814513 | T | C | 1 | a0001c0001t0001g0293 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1564+3625A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25814513 | |||||||
chr4:25814662 | G | GA | 35 | a0001c0001t0002g0126 a0001c0001t0002g0163 a0001c0001t0002g0259 others(32): Show |
35 | HG00558.hp2 HG00609.hp1 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.1564+3475dupT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25814662 | |||||||
chr4:25814745 | C | T | 3 | a0001c0001t0001g0121 a0001c0010t0024g0309 a0019c0024t0023g0308 |
3 | HG01109.hp1 HG02735.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1564+3393G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25814745 | |||||||
chr4:25814765 | AT | A | 5 | a0004c0007t0001g0164 a0004c0007t0001g0165 a0004c0007t0001g0166 others(2): Show |
5 | HG02965.hp1 HG02970.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1564+3372delA | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25814765 | |||||||
chr4:25814797 | G | GT | 69 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0035 others(66): Show |
71 | HG00438.hp2 HG00597.hp1 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.1564+3340dupA | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25814797 | |||||||
chr4:25814797 | G | GTT | 44 | a0001c0001t0001g0293 a0001c0001t0002g0126 a0001c0001t0002g0163 others(41): Show |
44 | HG00558.hp2 HG00609.hp1 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.1564+3339_1564+334 others(6): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25814797 | |||||||
chr4:25814862 | G | A | 1 | a0001c0001t0002g0032 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1564+3276C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25814862 | |||||||
chr4:25814970 | C | A | 1 | a0001c0011t0003g0172 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1564+3168G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25814970 | |||||||
chr4:25814990 | G | A | 1 | a0005c0019t0002g0010 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1564+3148C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25814990 | |||||||
chr4:25814991 | G | A | 4 | a0001c0001t0001g0056 a0001c0001t0001g0058 a0001c0001t0001g0059 others(1): Show |
4 | NA18955.hp2 NA18973.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.1564+3147C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25814991 | |||||||
chr4:25814996 | G | A | 43 | a0001c0001t0001g0293 a0001c0001t0002g0126 a0001c0001t0002g0163 others(40): Show |
43 | HG00558.hp2 HG00609.hp1 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.1564+3142C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25814996 | |||||||
chr4:25815013 | A | G | 175 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(172): Show |
177 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(174): Show |
intron_variant | MODIFIER | c.1564+3125T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25815013 | |||||||
chr4:25815036 | C | T | 2 | a0001c0003t0002g0024 a0001c0003t0002g0025 |
2 | HG01106.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.1564+3102G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25815036 | |||||||
chr4:25815069 | A | G | 1 | a0001c0034t0002g0137 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1564+3069T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25815069 | |||||||
chr4:25815198 | G | T | 54 | a0001c0001t0001g0030 a0001c0001t0001g0072 a0001c0001t0001g0107 others(51): Show |
54 | HG00558.hp1 HG00735.hp1 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.1564+2940C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25815198 | |||||||
chr4:25815387 | G | T | 5 | a0001c0001t0002g0294 a0001c0001t0002g0302 a0001c0001t0004g0130 others(2): Show |
5 | HG02451.hp2 HG02723.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1564+2751C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25815387 | |||||||
chr4:25815443 | A | G | 8 | a0001c0001t0001g0293 a0001c0001t0002g0295 a0001c0001t0003g0149 others(5): Show |
8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1564+2695T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25815443 | |||||||
chr4:25815526 | A | G | 1 | a0001c0001t0002g0126 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1564+2612T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25815526 | |||||||
chr4:25815660 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1564+2478C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25815660 | |||||||
chr4:25815718 | A | T | 1 | a0001c0001t0001g0115 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1564+2420T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25815718 | |||||||
chr4:25815805 | C | A | 7 | a0001c0003t0002g0013 a0001c0003t0002g0049 a0001c0003t0002g0096 others(4): Show |
7 | HG00609.hp1 HG02647.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1564+2333G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25815805 | |||||||
chr4:25815867 | T | TG | 54 | a0001c0001t0001g0030 a0001c0001t0001g0072 a0001c0001t0001g0107 others(51): Show |
54 | HG00558.hp1 HG00735.hp1 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.1564+2270dupC | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25815867 | |||||||
chr4:25815871 | G | T | 1 | a0001c0001t0001g0188 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1564+2267C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25815871 | |||||||
chr4:25816037 | A | C | 3 | a0001c0003t0002g0024 a0001c0003t0002g0025 a0001c0003t0002g0103 |
3 | HG00558.hp2 HG01106.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.1564+2101T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25816037 | |||||||
chr4:25816131 | CATAAT | C | 8 | a0001c0001t0001g0293 a0001c0001t0002g0295 a0001c0001t0003g0149 others(5): Show |
8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1564+2002_1564+200 others(9): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25816131 | |||||||
chr4:25816144 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1564+1994T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25816144 | |||||||
chr4:25816239 | T | A | 1 | a0001c0001t0001g0246 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1564+1899A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25816239 | |||||||
chr4:25816389 | G | C | 1 | a0007c0031t0020g0169 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1564+1749C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25816389 | |||||||
chr4:25816615 | C | A | 1 | a0001c0001t0002g0053 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1564+1523G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25816615 | |||||||
chr4:25816655 | C | T | 2 | a0001c0001t0003g0149 a0001c0001t0006g0150 |
2 | HG02451.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1564+1483G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25816655 | |||||||
chr4:25816775 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1564+1363G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25816775 | |||||||
chr4:25816851 | T | C | 176 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(173): Show |
178 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(175): Show |
intron_variant | MODIFIER | c.1564+1287A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25816851 | |||||||
chr4:25816942 | C | T | 3 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0002g0196 |
3 | HG02055.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1564+1196G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25816942 | |||||||
chr4:25816955 | A | G | 54 | a0001c0001t0001g0030 a0001c0001t0001g0072 a0001c0001t0001g0107 others(51): Show |
54 | HG00558.hp1 HG00735.hp1 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.1564+1183T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25816955 | |||||||
chr4:25817045 | C | G | 1 | a0001c0001t0003g0265 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1564+1093G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25817045 | |||||||
chr4:25817052 | A | G | 54 | a0001c0001t0001g0030 a0001c0001t0001g0072 a0001c0001t0001g0107 others(51): Show |
54 | HG00558.hp1 HG00735.hp1 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.1564+1086T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25817052 | |||||||
chr4:25817481 | C | T | 10 | a0001c0001t0001g0293 a0001c0001t0002g0163 a0001c0001t0002g0295 others(7): Show |
10 | HG02055.hp2 HG02258.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1564+657G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25817481 | |||||||
chr4:25817486 | G | A | 1 | a0001c0001t0002g0131 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1564+652C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25817486 | |||||||
chr4:25817572 | C | A | 10 | a0001c0001t0001g0293 a0001c0001t0002g0163 a0001c0001t0002g0295 others(7): Show |
10 | HG02055.hp2 HG02258.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1564+566G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25817572 | |||||||
chr4:25817596 | C | T | 5 | a0004c0007t0001g0164 a0004c0007t0001g0165 a0004c0007t0001g0166 others(2): Show |
5 | HG02965.hp1 HG02970.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1564+542G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25817596 | |||||||
chr4:25817632 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1564+506A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25817632 | |||||||
chr4:25817678 | C | G | 170 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(167): Show |
172 | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.1564+460G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25817678 | |||||||
chr4:25817706 | T | C | 3 | a0001c0001t0001g0121 a0001c0010t0024g0309 a0019c0024t0023g0308 |
3 | HG01109.hp1 HG02735.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1564+432A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25817706 | |||||||
chr4:25817812 | T | A | 66 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0035 others(63): Show |
68 | HG00438.hp2 HG00597.hp1 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.1564+326A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25817812 | |||||||
chr4:25817888 | G | A | 3 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0002g0196 |
3 | HG02055.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1564+250C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25817888 | |||||||
chr4:25817901 | A | G | 1 | a0001c0001t0002g0209 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1564+237T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 9/23 | chr4 | 25817901 | |||||||
chr4:25818369 | A | AAGAAGAG others(3): Show |
10 | a0001c0001t0001g0293 a0001c0001t0002g0163 a0001c0001t0002g0295 others(7): Show |
10 | HG02055.hp2 HG02258.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1424-92_1424-91ins others(10): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 8/23 | chr4 | 25818369 | |||||||
chr4:25818371 | G | A | 2 | a0001c0001t0002g0248 a0001c0001t0021g0306 |
2 | HG02074.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.1424-93C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 8/23 | chr4 | 25818371 | |||||||
chr4:25818491 | T | C | 2 | a0001c0001t0002g0302 a0001c0006t0004g0299 |
2 | HG02451.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1424-213A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 8/23 | chr4 | 25818491 | |||||||
chr4:25818535 | G | A | 3 | a0001c0001t0001g0296 a0001c0001t0002g0259 a0001c0001t0002g0297 |
3 | HG01884.hp1 HG01891.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1424-257C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 8/23 | chr4 | 25818535 | |||||||
chr4:25818536 | G | A | 6 | a0001c0001t0002g0294 a0001c0001t0002g0302 a0001c0001t0004g0130 others(3): Show |
6 | HG02451.hp2 HG02723.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1424-258C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 8/23 | chr4 | 25818536 | |||||||
chr4:25818538 | C | T | 3 | a0001c0001t0001g0056 a0001c0001t0001g0059 a0001c0001t0001g0060 |
3 | NA18955.hp2 NA18973.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1424-260G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 8/23 | chr4 | 25818538 | |||||||
chr4:25818584 | G | T | 1 | a0001c0001t0005g0186 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1424-306C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 8/23 | chr4 | 25818584 | |||||||
chr4:25818639 | C | T | 55 | a0001c0001t0001g0030 a0001c0001t0001g0072 a0001c0001t0001g0107 others(52): Show |
55 | HG00558.hp1 HG00735.hp1 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.1424-361G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 8/23 | chr4 | 25818639 | |||||||
chr4:25818694 | A | G | 55 | a0001c0001t0001g0030 a0001c0001t0001g0072 a0001c0001t0001g0107 others(52): Show |
55 | HG00558.hp1 HG00735.hp1 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.1424-416T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 8/23 | chr4 | 25818694 | |||||||
chr4:25818737 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1424-459G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 8/23 | chr4 | 25818737 | |||||||
chr4:25818973 | C | T | 1 | a0001c0001t0002g0151 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1424-695G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 8/23 | chr4 | 25818973 | |||||||
chr4:25818993 | C | T | 66 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0035 others(63): Show |
68 | HG00438.hp2 HG00597.hp1 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.1424-715G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 8/23 | chr4 | 25818993 | |||||||
chr4:25819180 | C | T | 55 | a0001c0001t0001g0030 a0001c0001t0001g0072 a0001c0001t0001g0107 others(52): Show |
55 | HG00558.hp1 HG00735.hp1 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.1423+628G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 8/23 | chr4 | 25819180 | |||||||
chr4:25819335 | AT | A | 55 | a0001c0001t0001g0030 a0001c0001t0001g0072 a0001c0001t0001g0107 others(52): Show |
55 | HG00558.hp1 HG00735.hp1 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.1423+472delA | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 8/23 | chr4 | 25819335 | |||||||
chr4:25819340 | A | T | 55 | a0001c0001t0001g0030 a0001c0001t0001g0072 a0001c0001t0001g0107 others(52): Show |
55 | HG00558.hp1 HG00735.hp1 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.1423+468T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 8/23 | chr4 | 25819340 | |||||||
chr4:25819421 | C | T | 8 | a0001c0001t0001g0293 a0001c0001t0002g0295 a0001c0001t0003g0149 others(5): Show |
8 | HG02258.hp1 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1423+387G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 8/23 | chr4 | 25819421 | |||||||
chr4:25819674 | A | AG | 17 | a0001c0001t0002g0126 a0001c0003t0002g0013 a0001c0003t0002g0024 others(14): Show |
17 | HG00558.hp2 HG00609.hp1 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.1423+133dupC | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 8/23 | chr4 | 25819674 | |||||||
chr4:25820009 | G | A | 1 | a0005c0021t0003g0283 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1291-69C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 7/23 | chr4 | 25820009 | |||||||
chr4:25820091 | C | T | 1 | a0001c0001t0008g0290 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1291-151G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 7/23 | chr4 | 25820091 | |||||||
chr4:25820147 | T | C | 1 | a0001c0008t0001g0162 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1291-207A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 7/23 | chr4 | 25820147 | |||||||
chr4:25820154 | G | C | 3 | a0001c0001t0001g0121 a0001c0010t0024g0309 a0019c0024t0023g0308 |
3 | HG01109.hp1 HG02735.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1291-214C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 7/23 | chr4 | 25820154 | |||||||
chr4:25820309 | AAG | A | 88 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0035 others(85): Show |
90 | HG00438.hp2 HG00597.hp1 HG00642.hp2 others(87): Show |
intron_variant | MODIFIER | c.1291-371_1291-370d others(4): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 7/23 | chr4 | 25820309 | |||||||
chr4:25820413 | G | A | 1 | a0001c0001t0002g0126 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1291-473C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 7/23 | chr4 | 25820413 | |||||||
chr4:25820422 | G | A | 1 | a0001c0001t0002g0152 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1291-482C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 7/23 | chr4 | 25820422 | |||||||
chr4:25820449 | T | G | 2 | a0001c0001t0003g0149 a0001c0001t0006g0150 |
2 | HG02451.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1291-509A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 7/23 | chr4 | 25820449 | |||||||
chr4:25820512 | G | A | 16 | a0001c0001t0002g0259 a0001c0001t0002g0297 a0001c0014t0001g0159 others(13): Show |
16 | HG01891.hp2 HG02280.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.1291-572C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 7/23 | chr4 | 25820512 | |||||||
chr4:25820564 | C | T | 1 | a0005c0019t0002g0010 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1291-624G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 7/23 | chr4 | 25820564 | |||||||
chr4:25820579 | A | G | 10 | a0001c0001t0001g0293 a0001c0001t0002g0163 a0001c0001t0002g0295 others(7): Show |
10 | HG02055.hp2 HG02258.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1291-639T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 7/23 | chr4 | 25820579 | |||||||
chr4:25820659 | G | A | 116 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0035 others(113): Show |
118 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(115): Show |
intron_variant | MODIFIER | c.1291-719C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 7/23 | chr4 | 25820659 | |||||||
chr4:25820721 | A | ATATATGT others(9): Show |
1 | a0001c0001t0002g0264 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1291-782_1291-781i others(18): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 7/23 | chr4 | 25820721 | |||||||
chr4:25820730 | T | C | 1 | a0001c0001t0002g0264 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1291-790A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 7/23 | chr4 | 25820730 | |||||||
chr4:25820889 | C | T | 80 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0035 others(77): Show |
82 | HG00438.hp2 HG00597.hp1 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.1291-949G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 7/23 | chr4 | 25820889 | |||||||
chr4:25820922 | G | T | 1 | a0001c0001t0002g0190 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1291-982C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 7/23 | chr4 | 25820922 | |||||||
chr4:25820970 | C | T | 1 | a0001c0001t0002g0190 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1290+1026G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 7/23 | chr4 | 25820970 | |||||||
chr4:25820992 | C | T | 1 | a0001c0001t0006g0150 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1290+1004G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 7/23 | chr4 | 25820992 | |||||||
chr4:25820994 | C | T | 26 | a0001c0001t0002g0126 a0001c0003t0002g0013 a0001c0003t0002g0024 others(23): Show |
26 | HG00558.hp2 HG00609.hp1 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.1290+1002G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 7/23 | chr4 | 25820994 | |||||||
chr4:25821209 | A | G | 1 | a0001c0001t0001g0042 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1290+787T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 7/23 | chr4 | 25821209 | |||||||
chr4:25821251 | T | C | 10 | a0001c0001t0002g0163 a0001c0001t0002g0295 a0001c0001t0003g0149 others(7): Show |
10 | HG02055.hp2 HG02258.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1290+745A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 7/23 | chr4 | 25821251 | |||||||
chr4:25821270 | C | T | 1 | a0001c0001t0001g0293 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1290+726G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 7/23 | chr4 | 25821270 | |||||||
chr4:25821337 | G | T | 1 | a0001c0001t0006g0150 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1290+659C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 7/23 | chr4 | 25821337 | |||||||
chr4:25821396 | T | G | 2 | a0001c0017t0002g0144 a0007c0033t0007g0171 |
2 | HG02630.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1290+600A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 7/23 | chr4 | 25821396 | |||||||
chr4:25821417 | C | T | 67 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0035 others(64): Show |
69 | HG00438.hp2 HG00597.hp1 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.1290+579G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 7/23 | chr4 | 25821417 | |||||||
chr4:25821453 | A | C | 4 | a0001c0001t0001g0204 a0001c0001t0001g0258 a0001c0001t0002g0174 others(1): Show |
4 | HG01070.hp2 HG01433.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.1290+543T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 7/23 | chr4 | 25821453 | |||||||
chr4:25821462 | C | T | 2 | a0001c0001t0001g0070 a0005c0022t0004g0284 |
2 | HG02717.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1290+534G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 7/23 | chr4 | 25821462 | |||||||
chr4:25821468 | C | T | 2 | a0001c0001t0001g0252 a0001c0001t0002g0264 |
2 | HG00738.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.1290+528G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 7/23 | chr4 | 25821468 | |||||||
chr4:25821469 | G | A | 6 | a0001c0001t0002g0294 a0001c0001t0002g0302 a0001c0001t0004g0130 others(3): Show |
6 | HG02451.hp2 HG02723.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1290+527C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 7/23 | chr4 | 25821469 | |||||||
chr4:25821692 | C | T | 66 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0035 others(63): Show |
68 | HG00438.hp2 HG00597.hp1 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.1290+304G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 7/23 | chr4 | 25821692 | |||||||
chr4:25822268 | G | A | 1 | a0013c0036t0002g0303 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1158-140C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25822268 | |||||||
chr4:25822292 | G | A | 2 | a0001c0001t0001g0120 a0001c0001t0002g0099 |
2 | HG01069.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.1158-164C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25822292 | |||||||
chr4:25822395 | C | G | 84 | a0001c0001t0001g0030 a0001c0001t0001g0072 a0001c0001t0001g0107 others(81): Show |
84 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.1158-267G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25822395 | |||||||
chr4:25822415 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1158-287G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25822415 | |||||||
chr4:25822487 | T | C | 7 | a0001c0010t0002g0173 a0002c0002t0002g0138 a0002c0005t0001g0156 others(4): Show |
9 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1158-359A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25822487 | |||||||
chr4:25822574 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1158-446G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25822574 | |||||||
chr4:25822606 | G | A | 1 | a0001c0001t0002g0062 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1158-478C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25822606 | |||||||
chr4:25822658 | G | A | 7 | a0002c0013t0014g0127 a0004c0007t0001g0164 a0004c0007t0001g0165 others(4): Show |
7 | HG02055.hp2 HG02965.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1158-530C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25822658 | |||||||
chr4:25822661 | G | A | 7 | a0002c0013t0014g0127 a0004c0007t0001g0164 a0004c0007t0001g0165 others(4): Show |
7 | HG02055.hp2 HG02965.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1158-533C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25822661 | |||||||
chr4:25822696 | C | T | 1 | a0001c0001t0005g0300 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1158-568G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25822696 | |||||||
chr4:25823117 | G | C | 1 | a0001c0001t0001g0293 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1158-989C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25823117 | |||||||
chr4:25823386 | G | A | 68 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0035 others(65): Show |
70 | HG00438.hp2 HG00597.hp1 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.1158-1258C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25823386 | |||||||
chr4:25823463 | G | A | 6 | a0001c0001t0001g0121 a0001c0001t0002g0163 a0001c0010t0022g0307 others(3): Show |
6 | HG01109.hp1 HG02055.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1158-1335C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25823463 | |||||||
chr4:25823478 | C | T | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1158-1350G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25823478 | |||||||
chr4:25823501 | C | T | 5 | a0001c0001t0001g0293 a0001c0001t0001g0296 a0005c0021t0003g0283 others(2): Show |
5 | HG01884.hp1 HG02717.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1158-1373G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25823501 | |||||||
chr4:25823509 | C | T | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1158-1381G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25823509 | |||||||
chr4:25823510 | A | G | 18 | a0001c0001t0001g0121 a0001c0001t0002g0163 a0001c0001t0002g0259 others(15): Show |
18 | HG01109.hp1 HG01891.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1158-1382T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25823510 | |||||||
chr4:25823606 | C | G | 25 | a0001c0001t0001g0121 a0001c0001t0001g0293 a0001c0001t0001g0296 others(22): Show |
27 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.1158-1478G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25823606 | |||||||
chr4:25823667 | C | T | 2 | a0001c0001t0002g0259 a0001c0001t0002g0297 |
2 | HG01891.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1158-1539G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25823667 | |||||||
chr4:25823707 | A | G | 21 | a0001c0001t0001g0121 a0001c0001t0001g0293 a0001c0001t0001g0296 others(18): Show |
21 | HG01109.hp1 HG01884.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.1158-1579T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25823707 | |||||||
chr4:25823793 | A | G | 57 | a0001c0001t0001g0030 a0001c0001t0001g0072 a0001c0001t0001g0107 others(54): Show |
57 | HG00558.hp1 HG00735.hp1 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.1158-1665T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25823793 | |||||||
chr4:25823833 | G | C | 1 | a0001c0001t0003g0245 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1158-1705C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25823833 | |||||||
chr4:25823874 | G | A | 1 | a0001c0001t0001g0263 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1158-1746C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25823874 | |||||||
chr4:25824158 | G | A | 1 | a0001c0001t0003g0286 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1158-2030C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25824158 | |||||||
chr4:25824177 | C | T | 2 | a0009c0037t0003g0304 a0013c0036t0002g0303 |
2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1158-2049G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25824177 | |||||||
chr4:25824661 | G | A | 1 | a0001c0001t0002g0176 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1158-2533C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25824661 | |||||||
chr4:25824695 | G | A | 1 | a0001c0001t0002g0196 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1158-2567C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25824695 | |||||||
chr4:25824721 | A | G | 9 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0001g0293 others(6): Show |
9 | HG02258.hp1 HG02809.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1158-2593T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25824721 | |||||||
chr4:25824772 | T | A | 1 | a0016c0032t0019g0170 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1158-2644A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25824772 | |||||||
chr4:25824772 | T | C | 3 | a0005c0021t0003g0283 a0005c0022t0004g0284 a0012c0020t0002g0011 |
3 | HG02717.hp1 HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1158-2644A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25824772 | |||||||
chr4:25824808 | T | A | 1 | a0001c0001t0003g0286 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1158-2680A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25824808 | |||||||
chr4:25824865 | A | G | 1 | a0001c0008t0001g0162 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1158-2737T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25824865 | |||||||
chr4:25824923 | T | C | 18 | a0001c0001t0001g0136 a0001c0001t0002g0126 a0001c0001t0002g0128 others(15): Show |
18 | HG00741.hp1 HG01074.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.1158-2795A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25824923 | |||||||
chr4:25824956 | G | A | 1 | a0001c0001t0003g0091 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1158-2828C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25824956 | |||||||
chr4:25824974 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1158-2846C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25824974 | |||||||
chr4:25825022 | G | T | 1 | a0001c0001t0003g0286 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1158-2894C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25825022 | |||||||
chr4:25825049 | T | C | 2 | a0001c0001t0002g0294 a0001c0001t0005g0300 |
2 | HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1158-2921A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25825049 | |||||||
chr4:25825057 | T | C | 2 | a0001c0001t0001g0287 a0001c0001t0001g0288 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1158-2929A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25825057 | |||||||
chr4:25825178 | C | T | 1 | a0016c0032t0019g0170 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1158-3050G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25825178 | |||||||
chr4:25825282 | G | A | 3 | a0005c0021t0003g0283 a0005c0022t0004g0284 a0012c0020t0002g0011 |
3 | HG02717.hp1 HG02809.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1158-3154C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25825282 | |||||||
chr4:25825343 | T | C | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1158-3215A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25825343 | |||||||
chr4:25825505 | A | G | 2 | a0001c0001t0010g0008 a0001c0034t0002g0137 |
2 | HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1158-3377T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25825505 | |||||||
chr4:25825506 | T | C | 1 | a0001c0001t0002g0259 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1158-3378A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25825506 | |||||||
chr4:25825665 | T | C | 4 | a0001c0001t0001g0056 a0001c0001t0001g0058 a0001c0001t0001g0059 others(1): Show |
4 | NA18955.hp2 NA18973.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.1158-3537A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25825665 | |||||||
chr4:25825666 | A | AT | 128 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0036 others(125): Show |
128 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(125): Show |
intron_variant | MODIFIER | c.1158-3539dupA | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25825666 | |||||||
chr4:25825666 | A | ATT | 20 | a0001c0001t0001g0029 a0001c0001t0001g0203 a0001c0001t0001g0206 others(17): Show |
20 | HG00438.hp2 HG00642.hp2 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.1158-3540_1158-353 others(6): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25825666 | |||||||
chr4:25825666 | AT | A | 32 | a0001c0001t0001g0136 a0001c0001t0002g0126 a0001c0001t0002g0128 others(29): Show |
34 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.1158-3539delA | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25825666 | |||||||
chr4:25825666 | ATTTT | A | 12 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0001g0293 others(9): Show |
12 | HG02055.hp2 HG02258.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1158-3542_1158-353 others(8): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25825666 | |||||||
chr4:25825666 | ATTTTT | A | 8 | a0001c0001t0001g0121 a0001c0001t0002g0163 a0001c0001t0002g0259 others(5): Show |
8 | HG01109.hp1 HG01891.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1158-3543_1158-353 others(9): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25825666 | |||||||
chr4:25825778 | G | A | 1 | a0001c0001t0003g0286 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1158-3650C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25825778 | |||||||
chr4:25825800 | G | A | 6 | a0002c0002t0002g0138 a0002c0005t0001g0156 a0002c0005t0001g0157 others(3): Show |
8 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1158-3672C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25825800 | |||||||
chr4:25825831 | C | T | 1 | a0001c0001t0002g0214 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1158-3703G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25825831 | |||||||
chr4:25826229 | G | A | 9 | a0001c0001t0001g0121 a0001c0001t0002g0163 a0001c0001t0002g0297 others(6): Show |
9 | HG01109.hp1 HG01891.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1157+3869C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25826229 | |||||||
chr4:25826231 | T | C | 2 | a0001c0001t0010g0008 a0001c0034t0002g0137 |
2 | HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1157+3867A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25826231 | |||||||
chr4:25826289 | C | A | 1 | a0001c0001t0003g0286 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1157+3809G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25826289 | |||||||
chr4:25826729 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1157+3369C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25826729 | |||||||
chr4:25826825 | G | A | 35 | a0001c0001t0001g0136 a0001c0001t0002g0126 a0001c0001t0002g0128 others(32): Show |
37 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.1157+3273C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25826825 | |||||||
chr4:25826861 | A | C | 12 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0001g0293 others(9): Show |
12 | HG02055.hp1 HG02258.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1157+3237T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25826861 | |||||||
chr4:25826943 | C | G | 9 | a0002c0002t0001g0279 a0002c0002t0002g0277 a0002c0002t0002g0281 others(6): Show |
9 | HG02280.hp2 HG02572.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.1157+3155G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25826943 | |||||||
chr4:25827066 | T | A | 1 | a0003c0004t0001g0212 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1157+3032A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25827066 | |||||||
chr4:25827162 | T | G | 57 | a0001c0001t0001g0072 a0001c0001t0001g0107 a0001c0001t0001g0175 others(54): Show |
57 | HG00558.hp1 HG00735.hp1 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.1157+2936A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25827162 | |||||||
chr4:25827409 | C | A | 13 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0001g0293 others(10): Show |
13 | HG02145.hp2 HG02258.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.1157+2689G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25827409 | |||||||
chr4:25827426 | C | T | 1 | a0001c0001t0001g0078 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1157+2672G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25827426 | |||||||
chr4:25827475 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1157+2623G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25827475 | |||||||
chr4:25827478 | T | C | 14 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0001g0293 others(11): Show |
14 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1157+2620A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25827478 | |||||||
chr4:25827694 | C | T | 2 | a0001c0001t0001g0108 a0001c0001t0002g0086 |
2 | HG02132.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.1157+2404G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25827694 | |||||||
chr4:25827756 | A | G | 2 | a0005c0021t0003g0283 a0005c0022t0004g0284 |
2 | HG02717.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1157+2342T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25827756 | |||||||
chr4:25827836 | G | C | 1 | a0012c0020t0002g0011 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1157+2262C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25827836 | |||||||
chr4:25827844 | A | AGAGGAAG others(149): Show |
1 | a0001c0027t0001g0197 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1157+2253_1157+225 others(160): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25827844 | |||||||
chr4:25828014 | T | C | 65 | a0001c0001t0001g0009 a0001c0001t0001g0121 a0001c0001t0001g0136 others(62): Show |
67 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(64): Show |
intron_variant | MODIFIER | c.1157+2084A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25828014 | |||||||
chr4:25828125 | CTA | C | 5 | a0001c0001t0002g0294 a0001c0001t0002g0302 a0001c0001t0004g0130 others(2): Show |
5 | HG02451.hp2 HG02723.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1157+1971_1157+197 others(6): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25828125 | |||||||
chr4:25828154 | C | T | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1157+1944G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25828154 | |||||||
chr4:25828156 | C | A | 3 | a0001c0001t0002g0148 a0001c0001t0002g0153 a0001c0001t0002g0155 |
3 | HG02559.hp2 HG02572.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1157+1942G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25828156 | |||||||
chr4:25828294 | AT | A | 14 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0001g0293 others(11): Show |
14 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1157+1803delA | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25828294 | |||||||
chr4:25828390 | G | GT | 26 | a0001c0001t0001g0085 a0001c0001t0001g0121 a0001c0001t0001g0246 others(23): Show |
28 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.1157+1707dupA | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25828390 | |||||||
chr4:25828393 | T | G | 3 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0034t0002g0137 |
3 | HG02895.hp2 HG02897.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1157+1705A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25828393 | |||||||
chr4:25828519 | G | C | 6 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0002g0196 others(3): Show |
6 | HG02055.hp1 HG02145.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1157+1579C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25828519 | |||||||
chr4:25828531 | C | T | 2 | a0005c0019t0002g0010 a0012c0020t0002g0011 |
2 | HG02055.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1157+1567G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25828531 | |||||||
chr4:25828533 | C | T | 1 | a0001c0008t0001g0162 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1157+1565G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25828533 | |||||||
chr4:25828575 | G | A | 1 | a0001c0001t0002g0196 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1157+1523C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25828575 | |||||||
chr4:25828616 | C | G | 1 | a0001c0001t0002g0148 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1157+1482G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25828616 | |||||||
chr4:25828651 | C | A | 7 | a0001c0001t0001g0121 a0001c0001t0002g0163 a0001c0001t0002g0297 others(4): Show |
7 | HG01109.hp1 HG01891.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1157+1447G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25828651 | |||||||
chr4:25828663 | G | A | 1 | a0001c0001t0002g0259 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1157+1435C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25828663 | |||||||
chr4:25828703 | A | AT | 5 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0034t0002g0137 others(2): Show |
5 | HG02145.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1157+1394dupA | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25828703 | |||||||
chr4:25829032 | G | T | 1 | a0001c0001t0003g0033 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1157+1066C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25829032 | |||||||
chr4:25829033 | C | T | 1 | a0001c0001t0002g0297 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1157+1065G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25829033 | |||||||
chr4:25829121 | C | A | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1157+977G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25829121 | |||||||
chr4:25829237 | C | T | 5 | a0002c0005t0001g0156 a0002c0005t0001g0157 a0002c0005t0003g0122 others(2): Show |
7 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1157+861G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25829237 | |||||||
chr4:25829252 | C | A | 13 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0001g0293 others(10): Show |
13 | HG01884.hp1 HG02145.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1157+846G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25829252 | |||||||
chr4:25829417 | G | A | 23 | a0001c0001t0001g0009 a0001c0001t0001g0136 a0001c0001t0002g0126 others(20): Show |
23 | HG00741.hp1 HG01192.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.1157+681C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25829417 | |||||||
chr4:25829535 | G | T | 37 | a0001c0001t0001g0009 a0001c0001t0001g0136 a0001c0001t0001g0287 others(34): Show |
37 | HG00741.hp1 HG01192.hp2 HG01884.hp1 others(34): Show |
intron_variant | MODIFIER | c.1157+563C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25829535 | |||||||
chr4:25829542 | C | T | 8 | a0001c0001t0002g0148 a0001c0001t0002g0151 a0001c0001t0002g0152 others(5): Show |
8 | HG02451.hp1 HG02559.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1157+556G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25829542 | |||||||
chr4:25829600 | G | A | 1 | a0002c0009t0007g0298 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1157+498C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25829600 | |||||||
chr4:25829613 | T | C | 1 | a0019c0024t0023g0308 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1157+485A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25829613 | |||||||
chr4:25829658 | A | G | 1 | a0003c0004t0001g0208 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1157+440T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25829658 | |||||||
chr4:25829936 | G | GA | 29 | a0001c0001t0001g0136 a0001c0001t0002g0126 a0001c0001t0002g0128 others(26): Show |
29 | HG00741.hp1 HG01192.hp2 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.1157+161dupT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25829936 | |||||||
chr4:25830053 | C | T | 1 | a0001c0003t0002g0013 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1157+45G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25830053 | |||||||
chr4:25830056 | G | A | 36 | a0001c0001t0001g0021 a0001c0001t0001g0047 a0001c0001t0001g0048 others(33): Show |
36 | HG00438.hp1 HG00597.hp2 HG01069.hp2 others(33): Show |
intron_variant | MODIFIER | c.1157+42C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 6/23 | chr4 | 25830056 | |||||||
chr4:25830331 | T | C | 6 | a0004c0007t0001g0164 a0004c0007t0001g0165 a0004c0007t0001g0166 others(3): Show |
6 | HG02965.hp1 HG02970.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1099-175A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25830331 | |||||||
chr4:25830568 | A | G | 22 | a0001c0001t0001g0009 a0001c0001t0001g0287 a0001c0001t0001g0288 others(19): Show |
22 | HG01884.hp1 HG02145.hp2 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.1099-412T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25830568 | |||||||
chr4:25830572 | T | A | 7 | a0001c0001t0001g0030 a0001c0001t0001g0271 a0001c0001t0002g0174 others(4): Show |
7 | HG00609.hp1 HG02083.hp2 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.1099-416A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25830572 | |||||||
chr4:25830767 | C | T | 29 | a0001c0001t0001g0136 a0001c0001t0002g0126 a0001c0001t0002g0128 others(26): Show |
29 | HG00741.hp1 HG01192.hp2 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.1099-611G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25830767 | |||||||
chr4:25831022 | T | C | 1 | a0001c0003t0009g0027 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1099-866A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25831022 | |||||||
chr4:25831071 | T | C | 6 | a0001c0001t0002g0294 a0001c0001t0002g0302 a0001c0001t0003g0286 others(3): Show |
6 | HG02451.hp2 HG02723.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1099-915A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25831071 | |||||||
chr4:25831149 | C | T | 1 | a0003c0004t0001g0202 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1099-993G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25831149 | |||||||
chr4:25831384 | G | A | 1 | a0001c0001t0003g0091 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1099-1228C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25831384 | |||||||
chr4:25831393 | G | C | 5 | a0002c0005t0001g0156 a0002c0005t0001g0157 a0002c0005t0003g0122 others(2): Show |
7 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1099-1237C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25831393 | |||||||
chr4:25831491 | A | AAAT | 23 | a0001c0001t0001g0012 a0001c0001t0001g0028 a0001c0001t0001g0029 others(20): Show |
23 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.1099-1338_1099-133 others(7): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25831491 | |||||||
chr4:25831491 | A | AAATAAT | 3 | a0001c0001t0001g0213 a0001c0001t0002g0016 a0016c0032t0019g0170 |
3 | HG02148.hp1 HG02148.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1099-1341_1099-133 others(10): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25831491 | |||||||
chr4:25831507 | AATAATT | A | 34 | a0001c0001t0001g0107 a0001c0001t0001g0175 a0001c0001t0001g0182 others(31): Show |
34 | HG00738.hp1 HG00738.hp2 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.1099-1357_1099-135 others(10): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25831507 | |||||||
chr4:25831507 | AATAATTA others(2): Show |
A | 3 | a0001c0001t0002g0294 a0001c0001t0004g0130 a0001c0001t0005g0300 |
3 | HG02723.hp1 HG02896.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1099-1360_1099-135 others(13): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25831507 | |||||||
chr4:25831510 | A | AATT | 6 | a0001c0001t0001g0080 a0001c0001t0001g0085 a0001c0001t0001g0219 others(3): Show |
6 | HG02074.hp1 HG02080.hp1 HG04199.hp2 others(3): Show |
intron_variant | MODIFIER | c.1099-1357_1099-135 others(7): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25831510 | |||||||
chr4:25831510 | A | T | 5 | a0001c0001t0001g0072 a0001c0001t0001g0088 a0001c0001t0002g0147 others(2): Show |
5 | HG01516.hp1 HG02071.hp2 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.1099-1354T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25831510 | |||||||
chr4:25831510 | AATT | A | 40 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0056 others(37): Show |
41 | HG00140.hp1 HG00438.hp1 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.1099-1357_1099-135 others(7): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25831510 | |||||||
chr4:25831510 | AATTATT | A | 70 | a0001c0001t0001g0050 a0001c0001t0001g0117 a0001c0001t0001g0136 others(67): Show |
70 | HG00099.hp1 HG00558.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.1099-1360_1099-135 others(10): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25831510 | |||||||
chr4:25831510 | AATTATTA others(2): Show |
A | 21 | a0001c0001t0002g0233 a0001c0001t0003g0286 a0001c0008t0002g0142 others(18): Show |
23 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.1099-1363_1099-135 others(13): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25831510 | |||||||
chr4:25831510 | AATTATTA others(5): Show |
A | 1 | a0001c0001t0002g0111 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1099-1366_1099-135 others(16): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25831510 | |||||||
chr4:25831513 | T | A | 97 | a0001c0001t0001g0012 a0001c0001t0001g0021 a0001c0001t0001g0028 others(94): Show |
97 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.1099-1357A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25831513 | |||||||
chr4:25831516 | T | A | 98 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0019 others(95): Show |
99 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.1099-1360A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25831516 | |||||||
chr4:25831519 | T | A | 93 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0021 others(90): Show |
94 | HG00099.hp2 HG00438.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.1099-1363A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25831519 | |||||||
chr4:25831522 | T | A | 48 | a0001c0001t0001g0021 a0001c0001t0001g0047 a0001c0001t0001g0048 others(45): Show |
50 | HG00597.hp2 HG01069.hp2 HG01070.hp1 others(47): Show |
intron_variant | MODIFIER | c.1099-1366A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25831522 | |||||||
chr4:25831525 | T | A | 13 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0121 others(10): Show |
15 | HG00597.hp2 HG01070.hp1 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.1099-1369A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25831525 | |||||||
chr4:25831679 | C | T | 6 | a0001c0001t0002g0148 a0001c0001t0002g0151 a0001c0001t0002g0152 others(3): Show |
6 | HG02559.hp2 HG02572.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1098+1316G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25831679 | |||||||
chr4:25831738 | T | A | 1 | a0016c0032t0019g0170 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1098+1257A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25831738 | |||||||
chr4:25831914 | C | A | 1 | a0001c0001t0002g0071 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1098+1081G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25831914 | |||||||
chr4:25831999 | G | A | 12 | a0001c0001t0002g0126 a0001c0001t0002g0128 a0001c0001t0002g0134 others(9): Show |
12 | HG01192.hp2 HG01891.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1098+996C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25831999 | |||||||
chr4:25832184 | C | T | 19 | a0001c0001t0002g0294 a0001c0001t0002g0302 a0001c0001t0003g0286 others(16): Show |
19 | HG02055.hp2 HG02280.hp2 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.1098+811G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25832184 | |||||||
chr4:25832302 | A | G | 5 | a0002c0005t0001g0156 a0002c0005t0001g0157 a0002c0005t0003g0122 others(2): Show |
7 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1098+693T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25832302 | |||||||
chr4:25832374 | T | C | 1 | a0001c0001t0001g0070 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1098+621A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25832374 | |||||||
chr4:25832562 | A | G | 1 | a0001c0008t0001g0162 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1098+433T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25832562 | |||||||
chr4:25832632 | C | G | 256 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0019 others(253): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.1098+363G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25832632 | |||||||
chr4:25832706 | A | G | 6 | a0004c0007t0001g0164 a0004c0007t0001g0165 a0004c0007t0001g0166 others(3): Show |
6 | HG02965.hp1 HG02970.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1098+289T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25832706 | |||||||
chr4:25832924 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1098+71C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25832924 | |||||||
chr4:25832961 | C | T | 1 | a0001c0001t0002g0222 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1098+34G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 5/23 | chr4 | 25832961 | |||||||
chr4:25833168 | G | A | 1 | a0001c0001t0002g0134 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.983-58C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 4/23 | chr4 | 25833168 | |||||||
chr4:25833422 | T | C | 2 | a0001c0001t0001g0009 a0001c0011t0003g0172 |
2 | HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.982+26A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 4/23 | chr4 | 25833422 | |||||||
chr4:25833687 | C | T | 1 | a0001c0001t0003g0149 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.861-118G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 3/23 | chr4 | 25833687 | |||||||
chr4:25833817 | A | G | 4 | a0005c0019t0002g0010 a0005c0021t0003g0283 a0005c0022t0004g0284 others(1): Show |
4 | HG02055.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.861-248T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 3/23 | chr4 | 25833817 | |||||||
chr4:25833892 | C | T | 4 | a0005c0019t0002g0010 a0005c0021t0003g0283 a0005c0022t0004g0284 others(1): Show |
4 | HG02055.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.861-323G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 3/23 | chr4 | 25833892 | |||||||
chr4:25833900 | A | T | 1 | a0001c0001t0004g0123 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.861-331T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 3/23 | chr4 | 25833900 | |||||||
chr4:25833985 | T | A | 4 | a0005c0019t0002g0010 a0005c0021t0003g0283 a0005c0022t0004g0284 others(1): Show |
4 | HG02055.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.861-416A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 3/23 | chr4 | 25833985 | |||||||
chr4:25834008 | C | T | 2 | a0005c0019t0002g0010 a0012c0020t0002g0011 |
2 | HG02055.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.861-439G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 3/23 | chr4 | 25834008 | |||||||
chr4:25834022 | A | G | 4 | a0005c0019t0002g0010 a0005c0021t0003g0283 a0005c0022t0004g0284 others(1): Show |
4 | HG02055.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.861-453T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 3/23 | chr4 | 25834022 | |||||||
chr4:25834084 | G | A | 1 | a0001c0001t0003g0093 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.861-515C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 3/23 | chr4 | 25834084 | |||||||
chr4:25834188 | C | A | 1 | a0001c0001t0002g0071 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.861-619G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 3/23 | chr4 | 25834188 | |||||||
chr4:25834622 | A | G | 2 | a0001c0001t0001g0080 a0001c0001t0001g0081 |
2 | NA18942.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.860+575T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 3/23 | chr4 | 25834622 | |||||||
chr4:25834847 | G | A | 1 | a0001c0001t0003g0026 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.860+350C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 3/23 | chr4 | 25834847 | |||||||
chr4:25834894 | C | G | 1 | a0001c0001t0002g0126 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.860+303G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 3/23 | chr4 | 25834894 | |||||||
chr4:25835074 | C | T | 14 | a0001c0001t0002g0294 a0001c0001t0002g0302 a0001c0001t0003g0286 others(11): Show |
14 | HG02280.hp2 HG02451.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.860+123G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 3/23 | chr4 | 25835074 | |||||||
chr4:25835095 | CAAG | C | 4 | a0005c0019t0002g0010 a0005c0021t0003g0283 a0005c0022t0004g0284 others(1): Show |
4 | HG02055.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.860+99_860+101delC others(2): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 3/23 | chr4 | 25835095 | |||||||
chr4:25835137 | T | C | 53 | a0001c0001t0001g0136 a0001c0001t0002g0126 a0001c0001t0002g0128 others(50): Show |
55 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(52): Show |
intron_variant | MODIFIER | c.860+60A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 3/23 | chr4 | 25835137 | |||||||
chr4:25835159 | C | T | 7 | a0004c0007t0001g0164 a0004c0007t0001g0165 a0004c0007t0001g0166 others(4): Show |
7 | HG02965.hp1 HG02970.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.860+38G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 3/23 | chr4 | 25835159 | |||||||
chr4:25835460 | T | G | 30 | a0001c0001t0001g0136 a0001c0001t0002g0126 a0001c0001t0002g0128 others(27): Show |
30 | HG00741.hp1 HG01192.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.734-137A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25835460 | |||||||
chr4:25835595 | G | A | 2 | a0009c0037t0003g0304 a0013c0036t0002g0303 |
2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.734-272C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25835595 | |||||||
chr4:25835602 | A | G | 4 | a0001c0001t0002g0294 a0001c0001t0002g0302 a0001c0001t0005g0300 others(1): Show |
4 | HG02451.hp2 HG02886.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.734-279T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25835602 | |||||||
chr4:25835688 | T | C | 140 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0019 others(137): Show |
143 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.734-365A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25835688 | |||||||
chr4:25835780 | A | G | 1 | a0001c0008t0002g0142 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.734-457T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25835780 | |||||||
chr4:25835847 | G | C | 4 | a0005c0019t0002g0010 a0005c0021t0003g0283 a0005c0022t0004g0284 others(1): Show |
4 | HG02055.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.734-524C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25835847 | |||||||
chr4:25835944 | T | C | 4 | a0005c0019t0002g0010 a0005c0021t0003g0283 a0005c0022t0004g0284 others(1): Show |
4 | HG02055.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.734-621A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25835944 | |||||||
chr4:25835950 | A | T | 30 | a0001c0001t0001g0136 a0001c0001t0002g0126 a0001c0001t0002g0128 others(27): Show |
30 | HG00741.hp1 HG01192.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.734-627T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25835950 | |||||||
chr4:25836017 | C | G | 15 | a0001c0001t0001g0009 a0001c0001t0001g0287 a0001c0001t0001g0288 others(12): Show |
15 | HG01884.hp1 HG02145.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.734-694G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25836017 | |||||||
chr4:25836096 | T | A | 1 | a0001c0001t0002g0191 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.734-773A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25836096 | |||||||
chr4:25836506 | G | A | 3 | a0001c0001t0002g0014 a0001c0003t0002g0024 a0001c0003t0002g0025 |
3 | HG01106.hp2 HG02738.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.734-1183C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25836506 | |||||||
chr4:25836509 | G | A | 1 | a0001c0001t0002g0106 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.734-1186C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25836509 | |||||||
chr4:25836533 | A | T | 215 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0019 others(212): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.734-1210T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25836533 | |||||||
chr4:25836693 | G | A | 1 | a0001c0001t0002g0003 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.734-1370C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25836693 | |||||||
chr4:25836792 | C | T | 4 | a0005c0019t0002g0010 a0005c0021t0003g0283 a0005c0022t0004g0284 others(1): Show |
4 | HG02055.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.734-1469G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25836792 | |||||||
chr4:25836806 | G | C | 4 | a0005c0019t0002g0010 a0005c0021t0003g0283 a0005c0022t0004g0284 others(1): Show |
4 | HG02055.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.734-1483C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25836806 | |||||||
chr4:25836859 | A | G | 2 | a0001c0001t0001g0221 a0001c0001t0002g0220 |
2 | HG00738.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.734-1536T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25836859 | |||||||
chr4:25836867 | T | G | 2 | a0001c0001t0002g0002 a0001c0001t0002g0023 |
3 | HG00733.hp1 HG01884.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.734-1544A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25836867 | |||||||
chr4:25836904 | T | C | 94 | a0001c0001t0001g0107 a0001c0001t0001g0175 a0001c0001t0001g0182 others(91): Show |
94 | HG00099.hp1 HG00558.hp1 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.734-1581A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25836904 | |||||||
chr4:25837192 | G | GA | 30 | a0001c0001t0001g0136 a0001c0001t0002g0126 a0001c0001t0002g0128 others(27): Show |
30 | HG00741.hp1 HG01192.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.734-1870dupT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25837192 | |||||||
chr4:25837279 | G | T | 1 | a0001c0001t0001g0293 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.734-1956C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25837279 | |||||||
chr4:25837391 | A | T | 2 | a0005c0021t0003g0283 a0005c0022t0004g0284 |
2 | HG02717.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.734-2068T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25837391 | |||||||
chr4:25837537 | C | T | 1 | a0001c0001t0002g0099 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.734-2214G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25837537 | |||||||
chr4:25837630 | G | A | 4 | a0001c0001t0002g0294 a0001c0001t0002g0302 a0001c0001t0005g0300 others(1): Show |
4 | HG02451.hp2 HG02886.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.734-2307C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25837630 | |||||||
chr4:25837784 | T | C | 2 | a0009c0037t0003g0304 a0013c0036t0002g0303 |
2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.734-2461A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25837784 | |||||||
chr4:25837856 | A | C | 1 | a0003c0004t0001g0212 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.734-2533T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25837856 | |||||||
chr4:25838106 | G | A | 3 | a0001c0001t0002g0014 a0001c0003t0002g0024 a0001c0003t0002g0025 |
3 | HG01106.hp2 HG02738.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.734-2783C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25838106 | |||||||
chr4:25838186 | C | T | 1 | a0003c0028t0001g0185 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.734-2863G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25838186 | |||||||
chr4:25838364 | G | A | 1 | a0001c0011t0003g0172 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.734-3041C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25838364 | |||||||
chr4:25838369 | A | T | 2 | a0001c0001t0003g0149 a0001c0001t0006g0150 |
2 | HG02451.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.734-3046T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25838369 | |||||||
chr4:25838954 | G | A | 3 | a0001c0001t0001g0074 a0001c0001t0002g0190 a0001c0001t0002g0191 |
3 | HG00735.hp2 HG02602.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.734-3631C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25838954 | |||||||
chr4:25839167 | A | G | 75 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0019 others(72): Show |
76 | HG00099.hp2 HG00438.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.734-3844T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25839167 | |||||||
chr4:25839413 | T | C | 4 | a0005c0019t0002g0010 a0005c0021t0003g0283 a0005c0022t0004g0284 others(1): Show |
4 | HG02055.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.734-4090A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25839413 | |||||||
chr4:25839426 | C | A | 7 | a0004c0007t0001g0164 a0004c0007t0001g0165 a0004c0007t0001g0166 others(4): Show |
7 | HG02965.hp1 HG02970.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.734-4103G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25839426 | |||||||
chr4:25839735 | C | T | 1 | a0001c0001t0002g0054 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.734-4412G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25839735 | |||||||
chr4:25839821 | C | CAA | 108 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(105): Show |
108 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.734-4500_734-4499d others(4): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25839821 | |||||||
chr4:25839950 | G | A | 1 | a0001c0001t0002g0126 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.734-4627C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25839950 | |||||||
chr4:25840377 | C | T | 14 | a0001c0001t0002g0294 a0001c0001t0002g0302 a0001c0001t0003g0286 others(11): Show |
14 | HG02280.hp2 HG02451.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.734-5054G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25840377 | |||||||
chr4:25840485 | T | C | 1 | a0001c0001t0001g0263 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.734-5162A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25840485 | |||||||
chr4:25840712 | T | C | 8 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0001g0293 others(5): Show |
8 | HG01884.hp1 HG01891.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.734-5389A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25840712 | |||||||
chr4:25840794 | T | C | 1 | a0001c0001t0001g0263 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.734-5471A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25840794 | |||||||
chr4:25840941 | A | G | 1 | a0001c0001t0002g0196 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.734-5618T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25840941 | |||||||
chr4:25841090 | TGG | T | 6 | a0001c0014t0001g0159 a0002c0005t0001g0156 a0002c0005t0001g0157 others(3): Show |
8 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.734-5769_734-5768d others(4): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25841090 | |||||||
chr4:25841132 | A | G | 1 | a0001c0001t0002g0105 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.734-5809T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25841132 | |||||||
chr4:25841218 | G | C | 1 | a0001c0001t0002g0155 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.734-5895C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25841218 | |||||||
chr4:25841281 | G | A | 1 | a0016c0032t0019g0170 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.734-5958C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25841281 | |||||||
chr4:25841388 | T | C | 1 | a0005c0022t0004g0284 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.733+5906A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25841388 | |||||||
chr4:25841445 | T | A | 3 | a0001c0008t0002g0142 a0001c0008t0012g0143 a0010c0016t0002g0141 |
3 | HG02258.hp2 HG02818.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.733+5849A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25841445 | |||||||
chr4:25841694 | C | T | 1 | a0002c0002t0008g0301 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.733+5600G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25841694 | |||||||
chr4:25842117 | T | C | 3 | a0001c0001t0002g0272 a0001c0003t0002g0096 a0001c0003t0002g0097 |
3 | HG02896.hp1 HG02897.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.733+5177A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25842117 | |||||||
chr4:25842171 | C | T | 1 | a0001c0027t0001g0197 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.733+5123G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25842171 | |||||||
chr4:25842245 | T | TA | 15 | a0001c0001t0001g0098 a0001c0001t0001g0182 a0001c0001t0001g0252 others(12): Show |
17 | HG01070.hp1 HG01071.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.733+5048dupT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25842245 | |||||||
chr4:25842246 | A | T | 2 | a0009c0037t0003g0304 a0013c0036t0002g0303 |
2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.733+5048T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25842246 | |||||||
chr4:25842308 | A | C | 10 | a0001c0014t0001g0159 a0002c0005t0001g0156 a0002c0005t0001g0157 others(7): Show |
12 | HG01070.hp1 HG01071.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.733+4986T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25842308 | |||||||
chr4:25842398 | G | A | 1 | a0001c0001t0002g0196 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.733+4896C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25842398 | |||||||
chr4:25842399 | C | T | 3 | a0001c0001t0001g0082 a0001c0001t0002g0083 a0001c0001t0002g0105 |
3 | HG00673.hp2 NA18961.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.733+4895G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25842399 | |||||||
chr4:25842437 | G | A | 4 | a0005c0019t0002g0010 a0005c0021t0003g0283 a0005c0022t0004g0284 others(1): Show |
4 | HG02055.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.733+4857C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25842437 | |||||||
chr4:25842535 | G | T | 4 | a0005c0019t0002g0010 a0005c0021t0003g0283 a0005c0022t0004g0284 others(1): Show |
4 | HG02055.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.733+4759C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25842535 | |||||||
chr4:25842550 | G | A | 11 | a0001c0001t0010g0008 a0001c0014t0001g0159 a0002c0005t0001g0156 others(8): Show |
13 | HG01070.hp1 HG01071.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.733+4744C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25842550 | |||||||
chr4:25842732 | G | A | 11 | a0001c0001t0010g0008 a0001c0014t0001g0159 a0002c0005t0001g0156 others(8): Show |
13 | HG01070.hp1 HG01071.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.733+4562C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25842732 | |||||||
chr4:25842757 | A | G | 11 | a0001c0001t0010g0008 a0001c0014t0001g0159 a0002c0005t0001g0156 others(8): Show |
13 | HG01070.hp1 HG01071.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.733+4537T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25842757 | |||||||
chr4:25842774 | G | A | 4 | a0001c0001t0002g0294 a0001c0001t0002g0302 a0001c0001t0005g0300 others(1): Show |
4 | HG02451.hp2 HG02886.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.733+4520C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25842774 | |||||||
chr4:25842783 | T | TC | 11 | a0001c0001t0010g0008 a0001c0014t0001g0159 a0002c0005t0001g0156 others(8): Show |
13 | HG01070.hp1 HG01071.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.733+4510dupG | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25842783 | |||||||
chr4:25842827 | T | C | 1 | a0001c0001t0003g0286 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.733+4467A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25842827 | |||||||
chr4:25842918 | C | T | 11 | a0001c0001t0010g0008 a0001c0014t0001g0159 a0002c0005t0001g0156 others(8): Show |
13 | HG01070.hp1 HG01071.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.733+4376G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25842918 | |||||||
chr4:25842953 | T | A | 10 | a0001c0001t0002g0128 a0001c0001t0002g0134 a0001c0001t0002g0139 others(7): Show |
10 | HG01192.hp2 HG02145.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.733+4341A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25842953 | |||||||
chr4:25842963 | G | A | 6 | a0001c0014t0001g0159 a0002c0005t0001g0156 a0002c0005t0001g0157 others(3): Show |
8 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.733+4331C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25842963 | |||||||
chr4:25842990 | G | A | 1 | a0001c0001t0002g0177 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.733+4304C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25842990 | |||||||
chr4:25843014 | A | T | 10 | a0001c0014t0001g0159 a0002c0005t0001g0156 a0002c0005t0001g0157 others(7): Show |
12 | HG01070.hp1 HG01071.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.733+4280T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25843014 | |||||||
chr4:25843068 | T | C | 11 | a0001c0001t0010g0008 a0001c0014t0001g0159 a0002c0005t0001g0156 others(8): Show |
13 | HG01070.hp1 HG01071.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.733+4226A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25843068 | |||||||
chr4:25843129 | G | A | 11 | a0001c0001t0010g0008 a0001c0014t0001g0159 a0002c0005t0001g0156 others(8): Show |
13 | HG01070.hp1 HG01071.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.733+4165C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25843129 | |||||||
chr4:25843174 | G | C | 3 | a0001c0001t0001g0100 a0001c0001t0002g0054 a0001c0001t0002g0099 |
3 | HG02683.hp2 HG02698.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.733+4120C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25843174 | |||||||
chr4:25843187 | G | A | 7 | a0001c0001t0010g0008 a0001c0014t0001g0159 a0002c0005t0001g0156 others(4): Show |
9 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.733+4107C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25843187 | |||||||
chr4:25843294 | C | T | 1 | a0001c0001t0011g0004 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.733+4000G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25843294 | |||||||
chr4:25843354 | C | T | 1 | a0007c0033t0007g0171 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.733+3940G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25843354 | |||||||
chr4:25843428 | C | T | 6 | a0004c0007t0001g0164 a0004c0007t0001g0165 a0004c0007t0001g0166 others(3): Show |
6 | HG02965.hp1 HG02970.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.733+3866G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25843428 | |||||||
chr4:25843436 | G | A | 1 | a0001c0001t0003g0026 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.733+3858C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25843436 | |||||||
chr4:25843648 | G | T | 7 | a0001c0001t0010g0008 a0001c0014t0001g0159 a0002c0005t0001g0156 others(4): Show |
9 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.733+3646C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25843648 | |||||||
chr4:25843751 | A | T | 1 | a0001c0001t0010g0129 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.733+3543T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25843751 | |||||||
chr4:25843796 | G | A | 7 | a0001c0001t0010g0008 a0001c0014t0001g0159 a0002c0005t0001g0156 others(4): Show |
9 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.733+3498C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25843796 | |||||||
chr4:25843829 | G | A | 2 | a0001c0011t0002g0055 a0001c0011t0002g0101 |
2 | HG02647.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.733+3465C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25843829 | |||||||
chr4:25843895 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.733+3399C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25843895 | |||||||
chr4:25844125 | C | T | 1 | a0014c0026t0013g0280 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.733+3169G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25844125 | |||||||
chr4:25844290 | C | G | 7 | a0001c0001t0010g0008 a0001c0014t0001g0159 a0002c0005t0001g0156 others(4): Show |
9 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.733+3004G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25844290 | |||||||
chr4:25844327 | T | C | 7 | a0001c0001t0010g0008 a0001c0014t0001g0159 a0002c0005t0001g0156 others(4): Show |
9 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.733+2967A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25844327 | |||||||
chr4:25844339 | G | A | 1 | a0001c0001t0009g0285 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.733+2955C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25844339 | |||||||
chr4:25844373 | T | C | 8 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0001g0293 others(5): Show |
8 | HG01884.hp1 HG01891.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.733+2921A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25844373 | |||||||
chr4:25844484 | G | A | 1 | a0001c0001t0002g0102 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.733+2810C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25844484 | |||||||
chr4:25844609 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.733+2685C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25844609 | |||||||
chr4:25844751 | C | T | 245 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0019 others(242): Show |
248 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(245): Show |
intron_variant | MODIFIER | c.733+2543G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25844751 | |||||||
chr4:25844755 | A | C | 95 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0021 others(92): Show |
98 | HG00597.hp2 HG00733.hp1 HG00741.hp1 others(95): Show |
intron_variant | MODIFIER | c.733+2539T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25844755 | |||||||
chr4:25845125 | C | T | 5 | a0001c0001t0002g0163 a0001c0010t0022g0307 a0001c0010t0024g0309 others(2): Show |
5 | HG01109.hp1 HG02615.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.733+2169G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25845125 | |||||||
chr4:25845166 | G | A | 1 | a0016c0032t0019g0170 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.733+2128C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25845166 | |||||||
chr4:25845372 | C | T | 7 | a0001c0001t0010g0008 a0001c0014t0001g0159 a0002c0005t0001g0156 others(4): Show |
9 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.733+1922G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25845372 | |||||||
chr4:25845412 | T | C | 7 | a0001c0001t0010g0008 a0001c0014t0001g0159 a0002c0005t0001g0156 others(4): Show |
9 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.733+1882A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25845412 | |||||||
chr4:25845426 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.733+1868C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25845426 | |||||||
chr4:25845636 | G | A | 7 | a0001c0001t0010g0008 a0001c0014t0001g0159 a0002c0005t0001g0156 others(4): Show |
9 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.733+1658C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25845636 | |||||||
chr4:25845693 | C | CAAGAAAT others(311): Show |
1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.733+1600_733+1601i others(320): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25845693 | |||||||
chr4:25845929 | T | C | 134 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0019 others(131): Show |
137 | HG00597.hp2 HG00733.hp1 HG00741.hp1 others(134): Show |
intron_variant | MODIFIER | c.733+1365A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25845929 | |||||||
chr4:25845983 | G | A | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.733+1311C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25845983 | |||||||
chr4:25845999 | T | C | 1 | a0001c0001t0002g0200 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.733+1295A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25845999 | |||||||
chr4:25846101 | T | C | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.733+1193A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25846101 | |||||||
chr4:25846240 | C | G | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.733+1054G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25846240 | |||||||
chr4:25846269 | G | A | 10 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0040 others(7): Show |
10 | HG00438.hp2 HG00673.hp1 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.733+1025C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25846269 | |||||||
chr4:25846434 | G | A | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.733+860C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25846434 | |||||||
chr4:25846603 | A | G | 2 | a0001c0001t0002g0297 a0002c0009t0007g0298 |
2 | HG01891.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.733+691T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25846603 | |||||||
chr4:25846649 | C | T | 1 | a0010c0016t0002g0141 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.733+645G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25846649 | |||||||
chr4:25846675 | A | G | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.733+619T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25846675 | |||||||
chr4:25846746 | T | C | 56 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0021 others(53): Show |
57 | HG00597.hp2 HG00733.hp1 HG01069.hp2 others(54): Show |
intron_variant | MODIFIER | c.733+548A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25846746 | |||||||
chr4:25846912 | C | CA | 200 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0019 others(197): Show |
203 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(200): Show |
intron_variant | MODIFIER | c.733+381dupT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25846912 | |||||||
chr4:25846912 | C | CAA | 26 | a0001c0001t0001g0253 a0001c0001t0001g0254 a0001c0001t0001g0296 others(23): Show |
26 | HG01884.hp1 HG02132.hp2 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.733+380_733+381dup others(2): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25846912 | |||||||
chr4:25846990 | G | A | 1 | a0001c0001t0001g0184 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.733+304C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25846990 | |||||||
chr4:25847015 | C | A | 1 | a0001c0001t0002g0261 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.733+279G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 2/23 | chr4 | 25847015 | |||||||
chr4:25847922 | C | A | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.163-58G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25847922 | |||||||
chr4:25848042 | C | G | 3 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0003c0004t0001g0146 |
3 | NA18942.hp1 NA18968.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.163-178G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25848042 | |||||||
chr4:25848402 | G | A | 6 | a0004c0007t0001g0164 a0004c0007t0001g0165 a0004c0007t0001g0166 others(3): Show |
6 | HG02965.hp1 HG02970.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.163-538C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25848402 | |||||||
chr4:25848456 | T | C | 6 | a0004c0007t0001g0164 a0004c0007t0001g0165 a0004c0007t0001g0166 others(3): Show |
6 | HG02965.hp1 HG02970.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.163-592A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25848456 | |||||||
chr4:25848487 | A | C | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.163-623T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25848487 | |||||||
chr4:25848497 | A | G | 1 | a0001c0001t0003g0273 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.163-633T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25848497 | |||||||
chr4:25848533 | T | G | 6 | a0001c0001t0002g0294 a0001c0001t0002g0297 a0001c0001t0002g0302 others(3): Show |
6 | HG01891.hp2 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.163-669A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25848533 | |||||||
chr4:25848580 | G | A | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.163-716C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25848580 | |||||||
chr4:25848651 | T | C | 2 | a0005c0021t0003g0283 a0005c0022t0004g0284 |
2 | HG02717.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.163-787A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25848651 | |||||||
chr4:25848702 | C | T | 40 | a0001c0001t0001g0136 a0001c0001t0001g0287 a0001c0001t0001g0288 others(37): Show |
42 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.163-838G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25848702 | |||||||
chr4:25848757 | C | G | 56 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0021 others(53): Show |
57 | HG00597.hp2 HG00733.hp1 HG01069.hp2 others(54): Show |
intron_variant | MODIFIER | c.163-893G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25848757 | |||||||
chr4:25848787 | G | A | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.163-923C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25848787 | |||||||
chr4:25848802 | G | A | 13 | a0001c0001t0001g0009 a0001c0001t0001g0293 a0001c0001t0001g0296 others(10): Show |
13 | HG01884.hp1 HG01891.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.163-938C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25848802 | |||||||
chr4:25848855 | C | T | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.163-991G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25848855 | |||||||
chr4:25848902 | G | A | 1 | a0012c0020t0002g0011 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.163-1038C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25848902 | |||||||
chr4:25848905 | C | A | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.163-1041G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25848905 | |||||||
chr4:25849001 | A | T | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.163-1137T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25849001 | |||||||
chr4:25849043 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.163-1179C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25849043 | |||||||
chr4:25849288 | C | T | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.163-1424G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25849288 | |||||||
chr4:25849290 | A | G | 42 | a0001c0001t0001g0136 a0001c0001t0001g0287 a0001c0001t0001g0288 others(39): Show |
44 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(41): Show |
intron_variant | MODIFIER | c.163-1426T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25849290 | |||||||
chr4:25849294 | A | T | 1 | a0001c0001t0001g0079 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.163-1430T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25849294 | |||||||
chr4:25849454 | G | A | 1 | a0002c0002t0002g0138 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.163-1590C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25849454 | |||||||
chr4:25849534 | G | A | 1 | a0002c0002t0002g0138 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.163-1670C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25849534 | |||||||
chr4:25849540 | A | G | 77 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0019 others(74): Show |
78 | HG00597.hp2 HG00733.hp1 HG01069.hp2 others(75): Show |
intron_variant | MODIFIER | c.163-1676T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25849540 | |||||||
chr4:25849641 | C | T | 93 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0019 others(90): Show |
94 | HG00597.hp2 HG00733.hp1 HG01069.hp2 others(91): Show |
intron_variant | MODIFIER | c.163-1777G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25849641 | |||||||
chr4:25849738 | T | C | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.163-1874A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25849738 | |||||||
chr4:25849826 | A | G | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.163-1962T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25849826 | |||||||
chr4:25849993 | C | T | 1 | a0001c0001t0001g0079 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.163-2129G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25849993 | |||||||
chr4:25849994 | G | A | 1 | a0001c0001t0001g0256 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.163-2130C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25849994 | |||||||
chr4:25850014 | G | C | 1 | a0001c0001t0002g0261 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.163-2150C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25850014 | |||||||
chr4:25850084 | T | G | 41 | a0001c0001t0001g0136 a0001c0001t0001g0287 a0001c0001t0001g0288 others(38): Show |
43 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(40): Show |
intron_variant | MODIFIER | c.163-2220A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25850084 | |||||||
chr4:25850097 | T | C | 41 | a0001c0001t0001g0136 a0001c0001t0001g0287 a0001c0001t0001g0288 others(38): Show |
43 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(40): Show |
intron_variant | MODIFIER | c.163-2233A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25850097 | |||||||
chr4:25850133 | A | G | 41 | a0001c0001t0001g0136 a0001c0001t0001g0287 a0001c0001t0001g0288 others(38): Show |
43 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(40): Show |
intron_variant | MODIFIER | c.163-2269T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25850133 | |||||||
chr4:25850144 | T | C | 1 | a0001c0001t0001g0256 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.163-2280A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25850144 | |||||||
chr4:25850166 | T | C | 15 | a0001c0001t0003g0286 a0001c0001t0009g0285 a0002c0002t0001g0279 others(12): Show |
15 | HG01891.hp1 HG02055.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.163-2302A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25850166 | |||||||
chr4:25850240 | G | C | 1 | a0001c0001t0002g0176 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.163-2376C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25850240 | |||||||
chr4:25850402 | C | A | 4 | a0001c0010t0022g0307 a0001c0010t0024g0309 a0015c0038t0012g0305 others(1): Show |
4 | HG01109.hp1 HG03041.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.163-2538G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25850402 | |||||||
chr4:25850503 | A | C | 1 | a0001c0010t0022g0307 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.163-2639T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25850503 | |||||||
chr4:25850721 | C | T | 2 | a0001c0001t0001g0206 a0001c0001t0002g0207 |
2 | NA19000.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.163-2857G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25850721 | |||||||
chr4:25850806 | G | T | 1 | a0001c0001t0002g0262 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.163-2942C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25850806 | |||||||
chr4:25850829 | T | A | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.163-2965A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25850829 | |||||||
chr4:25850857 | G | GT | 8 | a0001c0001t0001g0043 a0001c0001t0001g0056 a0001c0001t0001g0057 others(5): Show |
8 | HG00597.hp2 HG01074.hp2 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.163-2994dupA | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25850857 | |||||||
chr4:25850872 | T | A | 245 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0019 others(242): Show |
248 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(245): Show |
intron_variant | MODIFIER | c.163-3008A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25850872 | |||||||
chr4:25851012 | G | A | 6 | a0004c0007t0001g0164 a0004c0007t0001g0165 a0004c0007t0001g0166 others(3): Show |
6 | HG02965.hp1 HG02970.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.163-3148C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25851012 | |||||||
chr4:25851149 | C | T | 1 | a0001c0001t0002g0205 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.163-3285G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25851149 | |||||||
chr4:25851210 | A | G | 24 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0021 others(21): Show |
25 | HG00733.hp1 HG01081.hp1 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.163-3346T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25851210 | |||||||
chr4:25851430 | G | T | 2 | a0001c0001t0001g0050 a0001c0001t0001g0078 |
2 | NA18955.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.163-3566C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25851430 | |||||||
chr4:25851692 | C | T | 24 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0021 others(21): Show |
25 | HG00733.hp1 HG01081.hp1 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.163-3828G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25851692 | |||||||
chr4:25851714 | C | T | 1 | a0013c0036t0002g0303 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.163-3850G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25851714 | |||||||
chr4:25851717 | C | T | 24 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0021 others(21): Show |
25 | HG00733.hp1 HG01081.hp1 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.163-3853G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25851717 | |||||||
chr4:25851746 | G | A | 59 | a0001c0001t0001g0009 a0001c0001t0001g0136 a0001c0001t0001g0287 others(56): Show |
61 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(58): Show |
intron_variant | MODIFIER | c.163-3882C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25851746 | |||||||
chr4:25851772 | C | T | 6 | a0004c0007t0001g0164 a0004c0007t0001g0165 a0004c0007t0001g0166 others(3): Show |
6 | HG02965.hp1 HG02970.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.163-3908G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25851772 | |||||||
chr4:25851814 | G | A | 3 | a0001c0008t0002g0142 a0001c0008t0012g0143 a0010c0016t0002g0141 |
3 | HG02258.hp2 HG02818.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.163-3950C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25851814 | |||||||
chr4:25851846 | G | A | 1 | a0001c0001t0001g0256 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.163-3982C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25851846 | |||||||
chr4:25851887 | C | CA | 72 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0118 others(69): Show |
75 | HG00597.hp2 HG00733.hp1 HG00741.hp1 others(72): Show |
intron_variant | MODIFIER | c.163-4024dupT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25851887 | |||||||
chr4:25851887 | C | CAA | 7 | a0001c0001t0001g0012 a0001c0001t0001g0287 a0001c0001t0001g0288 others(4): Show |
7 | HG01358.hp2 HG01928.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.163-4025_163-4024d others(4): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25851887 | |||||||
chr4:25851908 | G | A | 59 | a0001c0001t0001g0009 a0001c0001t0001g0136 a0001c0001t0001g0287 others(56): Show |
61 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(58): Show |
intron_variant | MODIFIER | c.163-4044C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25851908 | |||||||
chr4:25852081 | G | A | 9 | a0002c0002t0001g0279 a0002c0002t0002g0277 a0002c0002t0002g0281 others(6): Show |
9 | HG02280.hp2 HG02572.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.163-4217C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25852081 | |||||||
chr4:25852152 | C | G | 1 | a0001c0001t0002g0126 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.163-4288G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25852152 | |||||||
chr4:25852414 | T | C | 60 | a0001c0001t0001g0009 a0001c0001t0001g0136 a0001c0001t0001g0287 others(57): Show |
62 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(59): Show |
intron_variant | MODIFIER | c.163-4550A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25852414 | |||||||
chr4:25852840 | A | G | 97 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0019 others(94): Show |
100 | HG00733.hp1 HG00741.hp1 HG01070.hp1 others(97): Show |
intron_variant | MODIFIER | c.163-4976T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25852840 | |||||||
chr4:25852844 | G | A | 1 | a0001c0011t0003g0172 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.163-4980C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25852844 | |||||||
chr4:25852916 | C | T | 60 | a0001c0001t0001g0009 a0001c0001t0001g0136 a0001c0001t0001g0287 others(57): Show |
62 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(59): Show |
intron_variant | MODIFIER | c.163-5052G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25852916 | |||||||
chr4:25853173 | C | A | 1 | a0001c0001t0001g0107 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.163-5309G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25853173 | |||||||
chr4:25853417 | G | A | 16 | a0001c0001t0001g0009 a0001c0001t0003g0286 a0001c0001t0009g0285 others(13): Show |
16 | HG01891.hp1 HG02055.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.163-5553C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25853417 | |||||||
chr4:25853488 | T | C | 60 | a0001c0001t0001g0009 a0001c0001t0001g0136 a0001c0001t0001g0287 others(57): Show |
62 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(59): Show |
intron_variant | MODIFIER | c.163-5624A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25853488 | |||||||
chr4:25853557 | A | G | 23 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0021 others(20): Show |
24 | HG00733.hp1 HG01081.hp1 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.163-5693T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25853557 | |||||||
chr4:25853632 | A | G | 1 | a0001c0011t0003g0172 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.163-5768T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25853632 | |||||||
chr4:25853633 | C | T | 1 | a0001c0001t0001g0077 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.163-5769G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25853633 | |||||||
chr4:25853664 | C | CT | 15 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0175 others(12): Show |
15 | HG00609.hp1 HG00741.hp2 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.163-5801dupA | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25853664 | |||||||
chr4:25853664 | CT | C | 130 | a0001c0001t0001g0009 a0001c0001t0001g0035 a0001c0001t0001g0036 others(127): Show |
132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.163-5801delA | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25853664 | |||||||
chr4:25853664 | CTT | C | 31 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0021 others(28): Show |
32 | HG00733.hp1 HG01081.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.163-5802_163-5801d others(4): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25853664 | |||||||
chr4:25853967 | C | T | 1 | a0001c0001t0001g0012 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.163-6103G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25853967 | |||||||
chr4:25854023 | G | A | 43 | a0001c0001t0001g0136 a0001c0001t0001g0287 a0001c0001t0001g0288 others(40): Show |
45 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(42): Show |
intron_variant | MODIFIER | c.163-6159C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25854023 | |||||||
chr4:25854104 | G | A | 96 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0019 others(93): Show |
99 | HG00733.hp1 HG00741.hp1 HG01070.hp1 others(96): Show |
intron_variant | MODIFIER | c.163-6240C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25854104 | |||||||
chr4:25854118 | T | C | 6 | a0004c0007t0001g0164 a0004c0007t0001g0165 a0004c0007t0001g0166 others(3): Show |
6 | HG02965.hp1 HG02970.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.163-6254A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25854118 | |||||||
chr4:25854262 | G | A | 10 | a0001c0001t0001g0293 a0001c0001t0001g0296 a0001c0001t0002g0294 others(7): Show |
10 | HG01884.hp1 HG01891.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.163-6398C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25854262 | |||||||
chr4:25854317 | G | A | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.163-6453C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25854317 | |||||||
chr4:25854410 | T | C | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.163-6546A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25854410 | |||||||
chr4:25854553 | C | T | 5 | a0001c0001t0002g0139 a0001c0001t0002g0140 a0001c0001t0004g0123 others(2): Show |
5 | HG01192.hp2 HG02145.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.163-6689G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25854553 | |||||||
chr4:25854659 | G | A | 60 | a0001c0001t0001g0009 a0001c0001t0001g0136 a0001c0001t0001g0287 others(57): Show |
62 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(59): Show |
intron_variant | MODIFIER | c.163-6795C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25854659 | |||||||
chr4:25854667 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.163-6803C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25854667 | |||||||
chr4:25854675 | T | A | 1 | a0003c0004t0001g0110 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.163-6811A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25854675 | |||||||
chr4:25855522 | G | A | 1 | a0001c0001t0009g0285 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.162+7153C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25855522 | |||||||
chr4:25855590 | T | C | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.162+7085A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25855590 | |||||||
chr4:25855636 | C | A | 1 | a0004c0007t0002g0168 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.162+7039G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25855636 | |||||||
chr4:25855693 | G | A | 2 | a0001c0001t0002g0139 a0001c0001t0002g0140 |
2 | HG02145.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.162+6982C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25855693 | |||||||
chr4:25855704 | T | C | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.162+6971A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25855704 | |||||||
chr4:25855779 | T | C | 22 | a0001c0001t0001g0009 a0001c0001t0003g0286 a0001c0001t0009g0285 others(19): Show |
22 | HG01891.hp1 HG02055.hp2 HG02280.hp2 others(19): Show |
intron_variant | MODIFIER | c.162+6896A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25855779 | |||||||
chr4:25855950 | C | T | 43 | a0001c0001t0001g0136 a0001c0001t0001g0287 a0001c0001t0001g0288 others(40): Show |
45 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(42): Show |
intron_variant | MODIFIER | c.162+6725G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25855950 | |||||||
chr4:25856018 | G | A | 83 | a0001c0001t0001g0175 a0001c0001t0001g0182 a0001c0001t0001g0198 others(80): Show |
83 | HG00099.hp1 HG00558.hp1 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.162+6657C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25856018 | |||||||
chr4:25856143 | C | A | 16 | a0001c0001t0001g0009 a0001c0001t0003g0286 a0001c0001t0009g0285 others(13): Show |
16 | HG01891.hp1 HG02055.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.162+6532G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25856143 | |||||||
chr4:25856230 | T | C | 16 | a0001c0001t0001g0009 a0001c0001t0003g0286 a0001c0001t0009g0285 others(13): Show |
16 | HG01891.hp1 HG02055.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.162+6445A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25856230 | |||||||
chr4:25856368 | G | A | 7 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0115 others(4): Show |
7 | HG00099.hp2 HG00642.hp1 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.162+6307C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25856368 | |||||||
chr4:25856399 | A | G | 1 | a0007c0033t0007g0171 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.162+6276T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25856399 | |||||||
chr4:25856483 | A | G | 12 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0001g0293 others(9): Show |
12 | HG01884.hp1 HG01891.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.162+6192T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25856483 | |||||||
chr4:25856593 | T | TA | 31 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0118 others(28): Show |
32 | HG00733.hp1 HG01081.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.162+6081dupT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25856593 | |||||||
chr4:25856593 | TA | T | 36 | a0001c0001t0001g0009 a0001c0001t0001g0043 a0001c0001t0001g0044 others(33): Show |
38 | HG00099.hp2 HG01070.hp1 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.162+6081delT | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25856593 | |||||||
chr4:25856593 | TAAA | T | 11 | a0001c0001t0003g0286 a0001c0001t0010g0008 a0002c0002t0001g0279 others(8): Show |
11 | HG02280.hp2 HG02572.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.162+6079_162+6081d others(5): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25856593 | |||||||
chr4:25856604 | A | C | 12 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0001g0293 others(9): Show |
12 | HG01884.hp1 HG01891.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.162+6071T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25856604 | |||||||
chr4:25856608 | A | C | 40 | a0001c0001t0001g0136 a0001c0001t0002g0126 a0001c0001t0002g0128 others(37): Show |
42 | HG00741.hp1 HG01070.hp1 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.162+6067T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25856608 | |||||||
chr4:25856609 | A | C | 6 | a0004c0007t0001g0164 a0004c0007t0001g0165 a0004c0007t0001g0166 others(3): Show |
6 | HG02965.hp1 HG02970.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.162+6066T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25856609 | |||||||
chr4:25856610 | A | C | 1 | a0001c0001t0002g0178 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.162+6065T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25856610 | |||||||
chr4:25856611 | A | C | 2 | a0005c0021t0003g0283 a0005c0022t0004g0284 |
2 | HG02717.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.162+6064T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25856611 | |||||||
chr4:25856801 | A | G | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.162+5874T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25856801 | |||||||
chr4:25857192 | A | G | 1 | a0001c0001t0002g0177 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.162+5483T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25857192 | |||||||
chr4:25857214 | A | T | 23 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0021 others(20): Show |
24 | HG00733.hp1 HG01081.hp1 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.162+5461T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25857214 | |||||||
chr4:25857517 | T | C | 1 | a0001c0001t0001g0120 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.162+5158A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25857517 | |||||||
chr4:25857527 | T | C | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.162+5148A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25857527 | |||||||
chr4:25858027 | G | A | 1 | a0002c0002t0008g0301 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.162+4648C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25858027 | |||||||
chr4:25858345 | C | T | 2 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
2 | HG00438.hp2 HG00673.hp1 |
intron_variant | MODIFIER | c.162+4330G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25858345 | |||||||
chr4:25858397 | T | C | 1 | a0001c0001t0002g0262 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.162+4278A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25858397 | |||||||
chr4:25858484 | A | C | 6 | a0002c0002t0001g0279 a0002c0002t0002g0277 a0002c0002t0002g0281 others(3): Show |
6 | HG02572.hp1 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.162+4191T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25858484 | |||||||
chr4:25858515 | T | C | 1 | a0001c0001t0001g0121 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.162+4160A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25858515 | |||||||
chr4:25858539 | T | G | 1 | a0001c0001t0001g0040 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.162+4136A>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25858539 | |||||||
chr4:25858822 | G | C | 2 | a0001c0011t0003g0172 a0016c0032t0019g0170 |
2 | NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.162+3853C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25858822 | |||||||
chr4:25859132 | A | G | 1 | a0001c0001t0002g0176 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.162+3543T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25859132 | |||||||
chr4:25859175 | G | A | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.162+3500C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25859175 | |||||||
chr4:25859328 | C | T | 16 | a0001c0001t0001g0009 a0001c0001t0003g0286 a0001c0001t0009g0285 others(13): Show |
16 | HG01891.hp1 HG02055.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.162+3347G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25859328 | |||||||
chr4:25859737 | T | C | 103 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0019 others(100): Show |
106 | HG00733.hp1 HG00741.hp1 HG01070.hp1 others(103): Show |
intron_variant | MODIFIER | c.162+2938A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25859737 | |||||||
chr4:25859790 | C | A | 12 | a0001c0008t0001g0162 a0001c0008t0002g0142 a0001c0008t0007g0161 others(9): Show |
14 | HG01070.hp1 HG01071.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.162+2885G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25859790 | |||||||
chr4:25859951 | A | C | 7 | a0004c0007t0001g0164 a0004c0007t0001g0165 a0004c0007t0001g0166 others(4): Show |
7 | HG02965.hp1 HG02970.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.162+2724T>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25859951 | |||||||
chr4:25859965 | G | A | 1 | a0001c0001t0002g0007 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.162+2710C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25859965 | |||||||
chr4:25860022 | G | A | 1 | a0001c0001t0009g0285 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.162+2653C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25860022 | |||||||
chr4:25860216 | T | C | 4 | a0001c0001t0001g0263 a0001c0001t0002g0264 a0001c0001t0002g0266 others(1): Show |
4 | HG00738.hp2 HG00741.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.162+2459A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25860216 | |||||||
chr4:25860567 | C | T | 1 | a0001c0001t0002g0174 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.162+2108G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25860567 | |||||||
chr4:25860586 | AAATGTGG others(12): Show |
A | 1 | a0001c0001t0010g0008 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.162+2070_162+2088d others(21): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25860586 | |||||||
chr4:25860844 | C | G | 1 | a0016c0032t0019g0170 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.162+1831G>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25860844 | |||||||
chr4:25860904 | T | A | 1 | a0001c0001t0002g0302 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.162+1771A>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25860904 | |||||||
chr4:25860974 | A | G | 1 | a0001c0001t0001g0042 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.162+1701T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25860974 | |||||||
chr4:25861086 | G | C | 52 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0019 others(49): Show |
53 | HG00733.hp1 HG01081.hp1 HG01106.hp2 others(50): Show |
intron_variant | MODIFIER | c.162+1589C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25861086 | |||||||
chr4:25861163 | G | A | 1 | a0001c0001t0003g0286 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.162+1512C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25861163 | |||||||
chr4:25861359 | A | G | 1 | a0001c0001t0001g0041 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.162+1316T>C | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25861359 | |||||||
chr4:25861498 | T | C | 1 | a0001c0001t0001g0270 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.162+1177A>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25861498 | |||||||
chr4:25861515 | A | T | 1 | a0001c0001t0002g0289 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.162+1160T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25861515 | |||||||
chr4:25861605 | A | T | 2 | a0001c0001t0001g0287 a0001c0001t0001g0288 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.162+1070T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25861605 | |||||||
chr4:25861630 | C | CT | 115 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0035 others(112): Show |
115 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.162+1044dupA | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25861630 | |||||||
chr4:25861630 | C | CTT | 9 | a0001c0001t0001g0030 a0001c0001t0001g0175 a0001c0001t0002g0174 others(6): Show |
9 | HG02083.hp2 HG02965.hp1 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.162+1043_162+1044d others(4): Show |
SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25861630 | |||||||
chr4:25861630 | CT | C | 30 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0001g0293 others(27): Show |
32 | HG01070.hp1 HG01071.hp2 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.162+1044delA | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25861630 | |||||||
chr4:25861753 | G | T | 146 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0019 others(143): Show |
147 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.162+922C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25861753 | |||||||
chr4:25861760 | A | T | 9 | a0001c0011t0003g0172 a0004c0007t0001g0164 a0004c0007t0001g0165 others(6): Show |
9 | HG02965.hp1 HG02970.hp1 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.162+915T>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25861760 | |||||||
chr4:25861837 | C | T | 1 | a0001c0010t0002g0173 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.162+838G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25861837 | |||||||
chr4:25861916 | G | T | 165 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0019 others(162): Show |
166 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(163): Show |
intron_variant | MODIFIER | c.162+759C>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25861916 | |||||||
chr4:25861940 | C | T | 1 | a0001c0001t0001g0293 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.162+735G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25861940 | |||||||
chr4:25862094 | C | T | 3 | a0001c0001t0002g0003 a0001c0001t0011g0004 a0001c0001t0011g0005 |
3 | HG03654.hp1 HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.162+581G>A | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25862094 | |||||||
chr4:25862275 | G | A | 1 | a0001c0001t0002g0163 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.162+400C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25862275 | |||||||
chr4:25862308 | G | C | 9 | a0001c0011t0003g0172 a0004c0007t0001g0164 a0004c0007t0001g0165 others(6): Show |
9 | HG02965.hp1 HG02970.hp1 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.162+367C>G | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25862308 | |||||||
chr4:25862384 | C | A | 132 | a0001c0001t0001g0175 a0001c0001t0001g0182 a0001c0001t0001g0184 others(129): Show |
132 | HG00099.hp1 HG00438.hp1 HG00558.hp1 others(129): Show |
intron_variant | MODIFIER | c.162+291G>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25862384 | |||||||
chr4:25862462 | G | A | 10 | a0001c0001t0001g0293 a0001c0001t0001g0296 a0001c0001t0002g0294 others(7): Show |
10 | HG01884.hp1 HG01891.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.162+213C>T | SEL1L3 | ENSG00000091490.11 | transcript | ENST00000399878.8 | protein_coding | 1/23 | chr4 | 25862462 |