Item | Value |
---|---|
geneid | 353299 |
ensemblid | ENSG00000121446.20 |
hgncid | 18636 |
symbol | RGSL1 |
name | regulator of G protein signaling like 1 |
refseq_nuc | NM_001137669.2 |
refseq_prot | NP_001131141.1 |
ensembl_nuc | ENST00000294854.13 |
ensembl_prot | ENSP00000457748.1 |
mane_status | MANE Select |
chr | chr1 |
start | 182450146 |
end | 182560597 |
strand | + |
ver | v1.2 |
region | chr1:182450146-182560597 |
region5000 | chr1:182445146-182565597 |
regionname0 | RGSL1_chr1_182450146_182560597 |
regionname5000 | RGSL1_chr1_182445146_182565597 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1076 | 170 | 53 | 36 | 54 | 10 | 15 | 38 | RGSL1_chr1_182445146_182565597 | RGSL1 | MSSAE others(1071): Show |
chr1 | 182445146 | 182565597 |
a0002 | 0/0 | 1076 | 76 | 8 | 12 | 46 | 2 | 8 | 37 | RGSL1_chr1_182445146_182565597 | RGSL1 | MSSAE others(1071): Show |
chr1 | 182445146 | 182565597 |
a0003 | 0/0 | 1076 | 68 | 12 | 10 | 40 | 1 | 5 | 31 | RGSL1_chr1_182445146_182565597 | RGSL1 | MSSAE others(1071): Show |
chr1 | 182445146 | 182565597 |
a0004 | 0/0 | 1076 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | MSSAD others(1071): Show |
chr1 | 182445146 | 182565597 |
a0005 | 0/0 | 1076 | 3 | 0 | 0 | 0 | 1 | 2 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | MSSAE others(1071): Show |
chr1 | 182445146 | 182565597 |
a0006 | 0/0 | 1076 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | MSSAE others(1071): Show |
chr1 | 182445146 | 182565597 |
a0007 | 0/0 | 1076 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | MSSAD others(1071): Show |
chr1 | 182445146 | 182565597 |
a0008 | 0/0 | 1076 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | MSSAE others(1071): Show |
chr1 | 182445146 | 182565597 |
a0009 | 0/0 | 1076 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | RGSL1_chr1_182445146_182565597 | RGSL1 | MSSAE others(1071): Show |
chr1 | 182445146 | 182565597 |
a0010 | 0/0 | 1076 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | MSSAE others(1071): Show |
chr1 | 182445146 | 182565597 |
a0011 | 0/0 | 1076 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | MSSAE others(1071): Show |
chr1 | 182445146 | 182565597 |
a0012 | 0/0 | 1076 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | MSSAE others(1071): Show |
chr1 | 182445146 | 182565597 |
a0013 | 0/0 | 1076 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | MSSAE others(1071): Show |
chr1 | 182445146 | 182565597 |
a0014 | 0/0 | 1076 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | MSSAE others(1071): Show |
chr1 | 182445146 | 182565597 |
a0015 | 0/0 | 1076 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | MSSAD others(1071): Show |
chr1 | 182445146 | 182565597 |
a0016 | 0/0 | 1076 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | MSSAE others(1071): Show |
chr1 | 182445146 | 182565597 |
a0017 | 0/0 | 1076 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | MSSAE others(1071): Show |
chr1 | 182445146 | 182565597 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 3228 | 93 | 21 | 21 | 37 | 6 | 8 | RGSL1_chr1_182445146_182565597 | RGSL1 | ATGAG others(3223): Show |
chr1 | 182445146 | 182565597 | ||
a0001c0004 | 1/1 | 3228 | 59 | 14 | 15 | 17 | 4 | 7 | RGSL1_chr1_182445146_182565597 | RGSL1 | ATGAG others(3223): Show |
chr1 | 182445146 | 182565597 | ||
a0001c0005 | 0/0 | 3228 | 8 | 8 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | ATGAG others(3223): Show |
chr1 | 182445146 | 182565597 | ||
a0001c0006 | 0/0 | 3228 | 5 | 5 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | ATGAG others(3223): Show |
chr1 | 182445146 | 182565597 | ||
a0001c0007 | 0/0 | 3228 | 4 | 4 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | ATGAG others(3223): Show |
chr1 | 182445146 | 182565597 | ||
a0001c0017 | 0/0 | 3228 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | ATGAG others(3223): Show |
chr1 | 182445146 | 182565597 | ||
a0002c0002 | 0/0 | 3228 | 76 | 8 | 12 | 46 | 2 | 8 | RGSL1_chr1_182445146_182565597 | RGSL1 | ATGAG others(3223): Show |
chr1 | 182445146 | 182565597 | ||
a0003c0003 | 0/0 | 3228 | 67 | 11 | 10 | 40 | 1 | 5 | RGSL1_chr1_182445146_182565597 | RGSL1 | ATGAG others(3223): Show |
chr1 | 182445146 | 182565597 | ||
a0003c0024 | 0/0 | 3228 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | ATGAG others(3223): Show |
chr1 | 182445146 | 182565597 | ||
a0004c0009 | 0/0 | 3228 | 3 | 2 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | ATGAG others(3223): Show |
chr1 | 182445146 | 182565597 | ||
a0004c0012 | 0/0 | 3228 | 2 | 2 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | ATGAG others(3223): Show |
chr1 | 182445146 | 182565597 | ||
a0005c0008 | 0/0 | 3228 | 3 | 0 | 0 | 0 | 1 | 2 | RGSL1_chr1_182445146_182565597 | RGSL1 | ATGAG others(3223): Show |
chr1 | 182445146 | 182565597 | ||
a0006c0011 | 0/0 | 3228 | 2 | 2 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | ATGAG others(3223): Show |
chr1 | 182445146 | 182565597 | ||
a0007c0013 | 0/0 | 3228 | 2 | 2 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | ATGAG others(3223): Show |
chr1 | 182445146 | 182565597 | ||
a0008c0010 | 0/0 | 3228 | 2 | 2 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | ATGAG others(3223): Show |
chr1 | 182445146 | 182565597 | ||
a0009c0018 | 0/0 | 3228 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | ATGAG others(3223): Show |
chr1 | 182445146 | 182565597 | ||
a0009c0020 | 0/0 | 3228 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | ATGAG others(3223): Show |
chr1 | 182445146 | 182565597 | ||
a0010c0016 | 0/0 | 3228 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | ATGAG others(3223): Show |
chr1 | 182445146 | 182565597 | ||
a0011c0021 | 0/0 | 3228 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | ATGAG others(3223): Show |
chr1 | 182445146 | 182565597 | ||
a0012c0019 | 0/0 | 3228 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | ATGAG others(3223): Show |
chr1 | 182445146 | 182565597 | ||
a0013c0015 | 0/0 | 3228 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | ATGAG others(3223): Show |
chr1 | 182445146 | 182565597 | ||
a0014c0014 | 0/0 | 3228 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | ATGAG others(3223): Show |
chr1 | 182445146 | 182565597 | ||
a0015c0025 | 0/0 | 3228 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | ATGAG others(3223): Show |
chr1 | 182445146 | 182565597 | ||
a0016c0022 | 0/0 | 3228 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | ATGAG others(3223): Show |
chr1 | 182445146 | 182565597 | ||
a0017c0023 | 0/0 | 3228 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | ATGAG others(3223): Show |
chr1 | 182445146 | 182565597 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3735 | 93 | 21 | 21 | 37 | 6 | 8 | RGSL1_chr1_182445146_182565597 | RGSL1 | GTCAG others(3730): Show |
chr1 | 182445146 | 182565597 |
a0001c0004t0001 | 1/1 | 3735 | 51 | 14 | 14 | 10 | 4 | 7 | RGSL1_chr1_182445146_182565597 | RGSL1 | GTCAG others(3730): Show |
chr1 | 182445146 | 182565597 |
a0001c0004t0002 | 0/0 | 3735 | 8 | 0 | 1 | 7 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | GTCAG others(3730): Show |
chr1 | 182445146 | 182565597 |
a0001c0005t0001 | 0/0 | 3735 | 8 | 8 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | GTCAG others(3730): Show |
chr1 | 182445146 | 182565597 |
a0001c0006t0001 | 0/0 | 3735 | 5 | 5 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | GTCAG others(3730): Show |
chr1 | 182445146 | 182565597 |
a0001c0007t0001 | 0/0 | 3735 | 4 | 4 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | GTCAG others(3730): Show |
chr1 | 182445146 | 182565597 |
a0001c0017t0001 | 0/0 | 3735 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | GTCAG others(3730): Show |
chr1 | 182445146 | 182565597 |
a0002c0002t0001 | 0/0 | 3735 | 74 | 8 | 11 | 46 | 2 | 7 | RGSL1_chr1_182445146_182565597 | RGSL1 | GTCAG others(3730): Show |
chr1 | 182445146 | 182565597 |
a0002c0002t0002 | 0/0 | 3735 | 2 | 0 | 1 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | GTCAG others(3730): Show |
chr1 | 182445146 | 182565597 |
a0003c0003t0001 | 0/0 | 3735 | 35 | 3 | 2 | 27 | 1 | 2 | RGSL1_chr1_182445146_182565597 | RGSL1 | GTCAG others(3730): Show |
chr1 | 182445146 | 182565597 |
a0003c0003t0002 | 0/0 | 3735 | 32 | 8 | 8 | 13 | 0 | 3 | RGSL1_chr1_182445146_182565597 | RGSL1 | GTCAG others(3730): Show |
chr1 | 182445146 | 182565597 |
a0003c0024t0001 | 0/0 | 3735 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | GTCAG others(3730): Show |
chr1 | 182445146 | 182565597 |
a0004c0009t0001 | 0/0 | 3735 | 3 | 2 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | GTCAG others(3730): Show |
chr1 | 182445146 | 182565597 |
a0004c0012t0001 | 0/0 | 3735 | 2 | 2 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | GTCAG others(3730): Show |
chr1 | 182445146 | 182565597 |
a0005c0008t0001 | 0/0 | 3735 | 3 | 0 | 0 | 0 | 1 | 2 | RGSL1_chr1_182445146_182565597 | RGSL1 | GTCAG others(3730): Show |
chr1 | 182445146 | 182565597 |
a0006c0011t0001 | 0/0 | 3735 | 2 | 2 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | GTCAG others(3730): Show |
chr1 | 182445146 | 182565597 |
a0007c0013t0001 | 0/0 | 3735 | 2 | 2 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | GTCAG others(3730): Show |
chr1 | 182445146 | 182565597 |
a0008c0010t0001 | 0/0 | 3735 | 2 | 2 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | GTCAG others(3730): Show |
chr1 | 182445146 | 182565597 |
a0009c0018t0001 | 0/0 | 3735 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | GTCAG others(3730): Show |
chr1 | 182445146 | 182565597 |
a0009c0020t0001 | 0/0 | 3735 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | GTCAG others(3730): Show |
chr1 | 182445146 | 182565597 |
a0010c0016t0002 | 0/0 | 3735 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | GTCAG others(3730): Show |
chr1 | 182445146 | 182565597 |
a0011c0021t0001 | 0/0 | 3735 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | GTCAG others(3730): Show |
chr1 | 182445146 | 182565597 |
a0012c0019t0001 | 0/0 | 3735 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | GTCAG others(3730): Show |
chr1 | 182445146 | 182565597 |
a0013c0015t0001 | 0/0 | 3735 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | GTCAG others(3730): Show |
chr1 | 182445146 | 182565597 |
a0014c0014t0001 | 0/0 | 3735 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | GTCAG others(3730): Show |
chr1 | 182445146 | 182565597 |
a0015c0025t0001 | 0/0 | 3735 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | GTCAG others(3730): Show |
chr1 | 182445146 | 182565597 |
a0016c0022t0001 | 0/0 | 3735 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | GTCAG others(3730): Show |
chr1 | 182445146 | 182565597 |
a0017c0023t0001 | 0/0 | 3735 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | GTCAG others(3730): Show |
chr1 | 182445146 | 182565597 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0004t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0004t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0004t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0004t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0004t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0004t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0004t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0004t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0004t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0004t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0004t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0004t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0004t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0004t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0004t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0004t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0004t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0004t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0004t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0004t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0004t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0004t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0004t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0004t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0004t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0004t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0004t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0004t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0004t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0004t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0004t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0004t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0004t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0004t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0004t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0004t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0004t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0004t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0004t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0004t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0004t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0004t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0004t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0004t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0004t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0004t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0004t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0004t0001g0321 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0004t0001g0322 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0004t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0004t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0004t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0004t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0004t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0004t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0004t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0004t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0004t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0005t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0005t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0005t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0005t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0005t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0005t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0005t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0005t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0006t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0006t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0006t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0006t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0006t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0007t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0007t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0007t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0007t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0001c0017t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0002c0002t0002g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0003c0003t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0003c0003t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0003c0003t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0003c0003t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0003c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0003c0003t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0003c0003t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0003c0003t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0003c0003t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0003c0003t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0003c0003t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0003c0003t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0003c0003t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0003c0003t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0003c0003t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0003c0003t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0003c0003t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0003c0003t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0003c0003t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0003c0003t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0003c0003t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0003c0003t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0003c0003t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0003c0003t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0003c0003t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0003c0003t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0003c0003t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0003c0003t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0003c0003t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0003c0003t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0003c0003t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0003c0003t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0003c0003t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0003c0003t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0003c0003t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0003c0003t0002g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0003c0003t0002g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0003c0003t0002g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0003c0003t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0003c0003t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0003c0003t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0003c0003t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0003c0003t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0003c0003t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0003c0003t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0003c0003t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0003c0003t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0003c0003t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0003c0003t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0003c0003t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0003c0003t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0003c0003t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0003c0003t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0003c0003t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0003c0003t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0003c0003t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0003c0003t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0003c0003t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0003c0003t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0003c0003t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0003c0003t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0003c0003t0002g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0003c0003t0002g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0003c0003t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0003c0024t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0004c0009t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0004c0009t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0004c0009t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0004c0012t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0004c0012t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0005c0008t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0005c0008t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0005c0008t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0006c0011t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0006c0011t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0007c0013t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0007c0013t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0008c0010t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0008c0010t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0009c0018t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0009c0020t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0010c0016t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0011c0021t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0012c0019t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0013c0015t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0014c0014t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0015c0025t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0016c0022t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
a0017c0023t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0004 | t0001 | g0314 | EUR | GBR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG00099 | hp2 | a0002 | c0002 | t0001 | g0033 | EUR | GBR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG00140 | hp1 | a0001 | c0004 | t0001 | g0220 | EUR | GBR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG00140 | hp2 | a0005 | c0008 | t0001 | g0085 | EUR | GBR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG00280 | hp1 | a0003 | c0003 | t0001 | g0156 | EUR | FIN | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0236 | EUR | FIN | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | CHS | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG00408 | hp2 | a0002 | c0002 | t0001 | g0037 | EAS | CHS | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG00423 | hp1 | a0010 | c0016 | t0002 | g0008 | EAS | CHS | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG00423 | hp2 | a0001 | c0004 | t0001 | g0284 | EAS | CHS | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG00438 | hp1 | a0002 | c0002 | t0001 | g0097 | EAS | CHS | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | CHS | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG00544 | hp1 | a0002 | c0002 | t0001 | g0035 | EAS | CHS | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG00544 | hp2 | a0003 | c0003 | t0001 | g0159 | EAS | CHS | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | CHS | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG00558 | hp2 | a0011 | c0021 | t0001 | g0170 | EAS | CHS | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG00609 | hp1 | a0002 | c0002 | t0001 | g0144 | EAS | CHS | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG00609 | hp2 | a0003 | c0003 | t0001 | g0043 | EAS | CHS | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG00639 | hp1 | a0003 | c0003 | t0002 | g0249 | AMR | PUR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG00642 | hp1 | a0001 | c0004 | t0001 | g0312 | AMR | PUR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG00642 | hp2 | a0002 | c0002 | t0001 | g0299 | AMR | PUR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG00673 | hp1 | a0003 | c0003 | t0001 | g0252 | EAS | CHS | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | CHS | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG00735 | hp1 | a0001 | c0004 | t0001 | g0316 | AMR | PUR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG00738 | hp2 | a0002 | c0002 | t0001 | g0099 | AMR | PUR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG00741 | hp2 | a0001 | c0004 | t0002 | g0131 | AMR | PUR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG01069 | hp2 | a0003 | c0003 | t0002 | g0006 | AMR | PUR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG01070 | hp2 | a0001 | c0004 | t0001 | g0112 | AMR | PUR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG01071 | hp1 | a0003 | c0003 | t0002 | g0006 | AMR | PUR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG01071 | hp2 | a0001 | c0004 | t0001 | g0130 | AMR | PUR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG01074 | hp1 | a0003 | c0003 | t0002 | g0214 | AMR | PUR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG01074 | hp2 | a0002 | c0002 | t0001 | g0069 | AMR | PUR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0279 | AMR | PUR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG01081 | hp2 | a0002 | c0002 | t0001 | g0288 | AMR | PUR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG01099 | hp1 | a0001 | c0004 | t0001 | g0191 | AMR | PUR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG01099 | hp2 | a0004 | c0009 | t0001 | g0261 | AMR | PUR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG01109 | hp1 | a0001 | c0004 | t0001 | g0188 | AMR | PUR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG01109 | hp2 | a0002 | c0002 | t0001 | g0136 | AMR | PUR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG01169 | hp1 | a0002 | c0002 | t0001 | g0074 | AMR | PUR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG01169 | hp2 | a0001 | c0004 | t0001 | g0278 | AMR | PUR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG01175 | hp1 | a0002 | c0002 | t0001 | g0083 | AMR | PUR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG01175 | hp2 | a0001 | c0004 | t0001 | g0315 | AMR | PUR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG01192 | hp1 | a0003 | c0003 | t0002 | g0309 | AMR | PUR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG01192 | hp2 | a0002 | c0002 | t0001 | g0259 | AMR | PUR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG01243 | hp2 | a0012 | c0019 | t0001 | g0216 | AMR | PUR | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG01255 | hp1 | a0001 | c0004 | t0001 | g0251 | AMR | CLM | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG01255 | hp2 | a0001 | c0004 | t0001 | g0221 | AMR | CLM | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG01258 | hp1 | a0002 | c0002 | t0002 | g0287 | AMR | CLM | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | CLM | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG01515 | hp2 | a0002 | c0002 | t0001 | g0274 | EUR | IBS | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG01516 | hp2 | a0001 | c0004 | t0001 | g0222 | EUR | IBS | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG01884 | hp1 | a0006 | c0011 | t0001 | g0187 | AFR | ACB | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | ACB | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG01891 | hp1 | a0001 | c0006 | t0001 | g0206 | AFR | ACB | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG01891 | hp2 | a0001 | c0004 | t0001 | g0181 | AFR | ACB | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG01928 | hp1 | a0002 | c0002 | t0001 | g0059 | AMR | PEL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | PEL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG01934 | hp1 | a0002 | c0002 | t0001 | g0225 | AMR | PEL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0276 | AMR | PEL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PEL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG01975 | hp2 | a0001 | c0004 | t0001 | g0285 | AMR | PEL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0293 | AMR | PEL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | PEL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG01981 | hp1 | a0003 | c0003 | t0001 | g0291 | AMR | PEL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG01981 | hp2 | a0003 | c0003 | t0002 | g0245 | AMR | PEL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PEL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG01993 | hp2 | a0001 | c0004 | t0001 | g0286 | AMR | PEL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PEL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02004 | hp2 | a0001 | c0004 | t0001 | g0311 | AMR | PEL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02015 | hp1 | a0002 | c0002 | t0001 | g0150 | EAS | KHV | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02015 | hp2 | a0003 | c0003 | t0002 | g0228 | EAS | KHV | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02027 | hp1 | a0003 | c0003 | t0002 | g0323 | EAS | KHV | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02027 | hp2 | a0002 | c0002 | t0001 | g0079 | EAS | KHV | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | ACB | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02071 | hp1 | a0001 | c0004 | t0001 | g0129 | EAS | KHV | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02071 | hp2 | a0002 | c0002 | t0001 | g0072 | EAS | KHV | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02074 | hp1 | a0003 | c0003 | t0001 | g0253 | EAS | KHV | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | KHV | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02129 | hp2 | a0001 | c0004 | t0001 | g0317 | EAS | KHV | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02135 | hp1 | a0003 | c0003 | t0002 | g0054 | EAS | KHV | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | ACB | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02145 | hp2 | a0002 | c0002 | t0001 | g0328 | AFR | ACB | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02148 | hp1 | a0003 | c0003 | t0002 | g0217 | AMR | PEL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02148 | hp2 | a0002 | c0002 | t0001 | g0082 | AMR | PEL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02155 | hp1 | a0002 | c0002 | t0001 | g0164 | EAS | CDX | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | CDX | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | CDX | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02165 | hp2 | a0002 | c0002 | t0001 | g0070 | EAS | CDX | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02257 | hp1 | a0004 | c0009 | t0001 | g0260 | AFR | ACB | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02257 | hp2 | a0001 | c0004 | t0001 | g0178 | AFR | ACB | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02258 | hp1 | a0001 | c0004 | t0001 | g0106 | AFR | ACB | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02258 | hp2 | a0001 | c0005 | t0001 | g0134 | AFR | ACB | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PEL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02273 | hp2 | a0003 | c0003 | t0001 | g0064 | AMR | PEL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02280 | hp1 | a0008 | c0010 | t0001 | g0204 | AFR | ACB | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02280 | hp2 | a0003 | c0003 | t0002 | g0029 | AFR | ACB | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02293 | hp1 | a0003 | c0003 | t0002 | g0290 | AMR | PEL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PEL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02451 | hp2 | a0001 | c0004 | t0001 | g0247 | AFR | ACB | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02523 | hp2 | a0003 | c0003 | t0002 | g0111 | EAS | KHV | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02572 | hp1 | a0001 | c0004 | t0001 | g0324 | AFR | GWD | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02572 | hp2 | a0001 | c0005 | t0001 | g0113 | AFR | GWD | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02602 | hp1 | a0002 | c0002 | t0001 | g0032 | SAS | PJL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02602 | hp2 | a0001 | c0004 | t0001 | g0282 | SAS | PJL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02615 | hp1 | a0002 | c0002 | t0001 | g0143 | AFR | GWD | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02615 | hp2 | a0003 | c0003 | t0002 | g0027 | AFR | GWD | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02622 | hp2 | a0001 | c0007 | t0001 | g0193 | AFR | GWD | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02630 | hp2 | a0002 | c0002 | t0001 | g0194 | AFR | GWD | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02647 | hp1 | a0001 | c0005 | t0001 | g0270 | AFR | GWD | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02698 | hp1 | a0002 | c0002 | t0001 | g0318 | SAS | PJL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02698 | hp2 | a0001 | c0004 | t0001 | g0023 | SAS | PJL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02717 | hp1 | a0001 | c0005 | t0001 | g0267 | AFR | GWD | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02717 | hp2 | a0001 | c0004 | t0001 | g0107 | AFR | GWD | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02809 | hp2 | a0003 | c0003 | t0001 | g0030 | AFR | GWD | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02818 | hp2 | a0003 | c0003 | t0001 | g0118 | AFR | GWD | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02895 | hp1 | a0001 | c0017 | t0001 | g0067 | AFR | GWD | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02895 | hp2 | a0003 | c0003 | t0002 | g0061 | AFR | GWD | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02896 | hp1 | a0002 | c0002 | t0001 | g0327 | AFR | GWD | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02896 | hp2 | a0004 | c0012 | t0001 | g0325 | AFR | GWD | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02897 | hp1 | a0004 | c0012 | t0001 | g0262 | AFR | GWD | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02897 | hp2 | a0003 | c0003 | t0002 | g0026 | AFR | GWD | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | ESN | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02922 | hp2 | a0003 | c0024 | t0001 | g0105 | AFR | ESN | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02965 | hp1 | a0001 | c0007 | t0001 | g0210 | AFR | ESN | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | ESN | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02970 | hp1 | a0001 | c0004 | t0001 | g0005 | AFR | ESN | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02970 | hp2 | a0013 | c0015 | t0001 | g0050 | AFR | ESN | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02976 | hp1 | a0014 | c0014 | t0001 | g0174 | AFR | ESN | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ESN | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0298 | SAS | PJL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG03017 | hp2 | a0003 | c0003 | t0001 | g0017 | SAS | PJL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG03041 | hp2 | a0001 | c0004 | t0001 | g0202 | AFR | GWD | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG03098 | hp1 | a0002 | c0002 | t0001 | g0195 | AFR | MSL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG03098 | hp2 | a0003 | c0003 | t0001 | g0209 | AFR | MSL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG03130 | hp1 | a0001 | c0007 | t0001 | g0021 | AFR | ESN | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG03130 | hp2 | a0001 | c0005 | t0001 | g0329 | AFR | ESN | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG03195 | hp1 | a0001 | c0006 | t0001 | g0138 | AFR | ESN | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG03195 | hp2 | a0001 | c0007 | t0001 | g0022 | AFR | ESN | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG03209 | hp1 | a0015 | c0025 | t0001 | g0266 | AFR | MSL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | MSL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG03225 | hp1 | a0004 | c0009 | t0001 | g0265 | AFR | MSL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG03225 | hp2 | a0001 | c0005 | t0001 | g0011 | AFR | MSL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG03239 | hp1 | a0005 | c0008 | t0001 | g0034 | SAS | PJL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0240 | SAS | PJL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG03453 | hp1 | a0001 | c0005 | t0001 | g0108 | AFR | MSL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG03453 | hp2 | a0001 | c0004 | t0001 | g0269 | AFR | MSL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG03486 | hp1 | a0008 | c0010 | t0001 | g0203 | AFR | MSL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG03486 | hp2 | a0003 | c0003 | t0002 | g0058 | AFR | MSL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG03490 | hp1 | a0002 | c0002 | t0001 | g0073 | SAS | PJL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG03490 | hp2 | a0001 | c0004 | t0001 | g0281 | SAS | PJL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG03579 | hp1 | a0002 | c0002 | t0001 | g0109 | AFR | MSL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG03579 | hp2 | a0001 | c0004 | t0001 | g0212 | AFR | MSL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG03688 | hp1 | a0002 | c0002 | t0001 | g0068 | SAS | STU | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG03688 | hp2 | a0003 | c0003 | t0001 | g0116 | SAS | STU | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0255 | SAS | PJL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG03704 | hp2 | a0001 | c0004 | t0001 | g0044 | SAS | PJL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG03710 | hp1 | a0002 | c0002 | t0002 | g0292 | SAS | PJL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG03710 | hp2 | a0002 | c0002 | t0001 | g0012 | SAS | PJL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG03831 | hp1 | a0003 | c0003 | t0002 | g0016 | SAS | BEB | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | BEB | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG03834 | hp1 | a0005 | c0008 | t0001 | g0014 | SAS | BEB | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG03834 | hp2 | a0001 | c0004 | t0001 | g0320 | SAS | BEB | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG03927 | hp1 | a0001 | c0004 | t0001 | g0227 | SAS | BEB | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG03927 | hp2 | a0001 | c0004 | t0001 | g0010 | SAS | BEB | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | BEB | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG04184 | hp2 | a0003 | c0003 | t0002 | g0250 | SAS | BEB | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG04204 | hp1 | a0003 | c0003 | t0002 | g0060 | SAS | STU | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG04204 | hp2 | a0002 | c0002 | t0001 | g0218 | SAS | STU | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | STU | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG04228 | hp2 | a0002 | c0002 | t0001 | g0117 | SAS | STU | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18522 | hp1 | a0007 | c0013 | t0001 | g0263 | AFR | YRI | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18522 | hp2 | a0001 | c0006 | t0001 | g0207 | AFR | YRI | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18612 | hp1 | a0003 | c0003 | t0001 | g0165 | EAS | CHB | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | CHB | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18906 | hp1 | a0001 | c0005 | t0001 | g0326 | AFR | YRI | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18906 | hp2 | a0006 | c0011 | t0001 | g0186 | AFR | YRI | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18939 | hp2 | a0003 | c0003 | t0002 | g0133 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18941 | hp1 | a0001 | c0004 | t0002 | g0019 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18941 | hp2 | a0002 | c0002 | t0001 | g0119 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18945 | hp1 | a0002 | c0002 | t0001 | g0171 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18946 | hp1 | a0003 | c0003 | t0001 | g0152 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18946 | hp2 | a0002 | c0002 | t0001 | g0075 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18947 | hp1 | a0001 | c0004 | t0001 | g0125 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18947 | hp2 | a0003 | c0003 | t0001 | g0256 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18949 | hp1 | a0002 | c0002 | t0001 | g0100 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18949 | hp2 | a0003 | c0003 | t0001 | g0151 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18950 | hp1 | a0002 | c0002 | t0001 | g0078 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18950 | hp2 | a0003 | c0003 | t0001 | g0157 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18951 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18951 | hp2 | a0003 | c0003 | t0001 | g0161 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18952 | hp1 | a0003 | c0003 | t0001 | g0160 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18952 | hp2 | a0002 | c0002 | t0001 | g0145 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18953 | hp1 | a0002 | c0002 | t0001 | g0122 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18953 | hp2 | a0003 | c0003 | t0001 | g0153 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18954 | hp1 | a0003 | c0003 | t0001 | g0051 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18954 | hp2 | a0002 | c0002 | t0001 | g0076 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18957 | hp1 | a0002 | c0002 | t0001 | g0036 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18962 | hp2 | a0001 | c0004 | t0001 | g0275 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18963 | hp1 | a0003 | c0003 | t0001 | g0158 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18965 | hp1 | a0001 | c0004 | t0002 | g0055 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18966 | hp1 | a0003 | c0003 | t0002 | g0025 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18966 | hp2 | a0016 | c0022 | t0001 | g0077 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18968 | hp1 | a0003 | c0003 | t0002 | g0063 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18968 | hp2 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18969 | hp1 | a0003 | c0003 | t0001 | g0229 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18969 | hp2 | a0001 | c0004 | t0001 | g0126 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18970 | hp2 | a0002 | c0002 | t0001 | g0254 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18973 | hp1 | a0002 | c0002 | t0001 | g0096 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18973 | hp2 | a0003 | c0003 | t0002 | g0092 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18974 | hp2 | a0003 | c0003 | t0001 | g0162 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18975 | hp1 | a0001 | c0004 | t0002 | g0280 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18975 | hp2 | a0002 | c0002 | t0001 | g0046 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18977 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18978 | hp2 | a0002 | c0002 | t0001 | g0141 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18979 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18979 | hp2 | a0003 | c0003 | t0001 | g0155 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18980 | hp1 | a0003 | c0003 | t0002 | g0002 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18980 | hp2 | a0002 | c0002 | t0001 | g0123 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18981 | hp1 | a0002 | c0002 | t0001 | g0084 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18982 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18986 | hp1 | a0002 | c0002 | t0001 | g0121 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18986 | hp2 | a0001 | c0004 | t0001 | g0283 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18989 | hp1 | a0009 | c0018 | t0001 | g0295 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18989 | hp2 | a0002 | c0002 | t0001 | g0098 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18994 | hp1 | a0002 | c0002 | t0001 | g0071 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA18994 | hp2 | a0003 | c0003 | t0002 | g0062 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA19000 | hp2 | a0003 | c0003 | t0001 | g0047 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA19004 | hp1 | a0002 | c0002 | t0001 | g0095 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA19004 | hp2 | a0001 | c0004 | t0002 | g0045 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA19006 | hp1 | a0002 | c0002 | t0001 | g0110 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA19010 | hp1 | a0002 | c0002 | t0001 | g0038 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA19010 | hp2 | a0003 | c0003 | t0001 | g0166 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA19011 | hp1 | a0002 | c0002 | t0001 | g0081 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA19011 | hp2 | a0002 | c0002 | t0001 | g0140 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA19012 | hp1 | a0002 | c0002 | t0001 | g0163 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA19030 | hp1 | a0001 | c0004 | t0001 | g0183 | AFR | LWK | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | LWK | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA19043 | hp1 | a0001 | c0004 | t0001 | g0177 | AFR | LWK | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA19043 | hp2 | a0003 | c0003 | t0002 | g0028 | AFR | LWK | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA19056 | hp1 | a0003 | c0003 | t0001 | g0294 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA19058 | hp1 | a0001 | c0004 | t0002 | g0169 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA19058 | hp2 | a0002 | c0002 | t0001 | g0179 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA19064 | hp1 | a0002 | c0002 | t0001 | g0089 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA19066 | hp1 | a0002 | c0002 | t0001 | g0128 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA19066 | hp2 | a0003 | c0003 | t0002 | g0002 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA19070 | hp1 | a0001 | c0004 | t0001 | g0087 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA19070 | hp2 | a0001 | c0004 | t0002 | g0056 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA19074 | hp1 | a0003 | c0003 | t0002 | g0167 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA19077 | hp2 | a0003 | c0003 | t0001 | g0154 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA19078 | hp1 | a0001 | c0004 | t0001 | g0093 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA19078 | hp2 | a0001 | c0004 | t0002 | g0124 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA19079 | hp1 | a0002 | c0002 | t0001 | g0120 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA19079 | hp2 | a0003 | c0003 | t0001 | g0039 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA19080 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA19081 | hp1 | a0002 | c0002 | t0001 | g0142 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA19081 | hp2 | a0003 | c0003 | t0001 | g0049 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA19082 | hp1 | a0003 | c0003 | t0002 | g0002 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA19082 | hp2 | a0001 | c0004 | t0001 | g0224 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA19084 | hp1 | a0009 | c0020 | t0001 | g0020 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA19084 | hp2 | a0003 | c0003 | t0001 | g0215 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA19086 | hp1 | a0017 | c0023 | t0001 | g0139 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA19087 | hp1 | a0003 | c0003 | t0001 | g0052 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA19087 | hp2 | a0002 | c0002 | t0001 | g0080 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA19089 | hp2 | a0003 | c0003 | t0001 | g0168 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA19091 | hp1 | a0003 | c0003 | t0001 | g0090 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA19091 | hp2 | a0002 | c0002 | t0001 | g0127 | EAS | JPT | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA19240 | hp1 | a0001 | c0006 | t0001 | g0208 | AFR | YRI | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA19240 | hp2 | a0001 | c0004 | t0001 | g0005 | AFR | YRI | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA20752 | hp1 | a0001 | c0004 | t0001 | g0313 | EUR | TSI | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0048 | EUR | TSI | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | CLM | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG01123 | hp2 | a0001 | c0004 | t0001 | g0102 | AMR | CLM | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02109 | hp1 | a0007 | c0013 | t0001 | g0264 | AFR | ACB | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | ACB | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02559 | hp1 | a0001 | c0006 | t0001 | g0137 | AFR | ACB | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG02559 | hp2 | a0001 | c0004 | t0001 | g0041 | AFR | ACB | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | MSL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | MSL | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG06807 | hp1 | a0003 | c0003 | t0002 | g0018 | AFR | USA | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
HG06807 | hp2 | a0002 | c0002 | t0001 | g0211 | AFR | USA | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | USA | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA20300 | hp2 | a0002 | c0002 | t0001 | g0289 | AFR | USA | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | LWK | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
NA21309 | hp2 | a0003 | c0003 | t0002 | g0180 | AFR | LWK | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
homoSapiens | chm13v2 | a0001 | c0004 | t0001 | g0322 | REF | REF | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
homoSapiens | grch38p0 | a0001 | c0004 | t0001 | g0321 | REF | REF | RGSL1_chr1_182445146_182565597 | RGSL1 | chr1 | 182445146 | 182565597 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:182453959 | G | T | 3 | a0004 a0007 a0015 |
8 | HG01099.hp2 HG02109.hp1 HG02257.hp1 others(5): Show |
missense_variant&splice_region_variant | MODERATE | c.15G>T | p.Glu5Asp | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/22 | 35/3735 | 15/3231 | 5/1076 | chr1 | 182453959 | |||
chr1:182454011 | G | A | 2 | a0005 a0014 |
4 | HG00140.hp2 HG02976.hp1 HG03239.hp1 others(1): Show |
missense_variant | MODERATE | c.67G>A | p.Asp23Asn | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/22 | 87/3735 | 67/3231 | 23/1076 | chr1 | 182454011 | |||
chr1:182472452 | A | C | 1 | a0017 | 1 | NA19086.hp1 | missense_variant | MODERATE | c.358A>C | p.Met120Leu | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 5/22 | 378/3735 | 358/3231 | 120/1076 | chr1 | 182472452 | |||
chr1:182472552 | A | G | 1 | a0016 | 1 | NA18966.hp2 | missense_variant | MODERATE | c.458A>G | p.Asn153Ser | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 5/22 | 478/3735 | 458/3231 | 153/1076 | chr1 | 182472552 | |||
chr1:182473626 | G | A | 1 | a0013 | 1 | HG02970.hp2 | missense_variant | MODERATE | c.515G>A | p.Arg172Lys | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/22 | 535/3735 | 515/3231 | 172/1076 | chr1 | 182473626 | |||
chr1:182473879 | G | C | 5 | a0003 a0010 a0013 others(2): Show |
72 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(69): Show |
missense_variant | MODERATE | c.768G>C | p.Trp256Cys | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/22 | 788/3735 | 768/3231 | 256/1076 | chr1 | 182473879 | |||
chr1:182474354 | A | T | 1 | a0006 | 2 | HG01884.hp1 NA18906.hp2 |
missense_variant | MODERATE | c.1243A>T | p.Asn415Tyr | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/22 | 1263/3735 | 1243/3231 | 415/1076 | chr1 | 182474354 | |||
chr1:182488987 | A | G | 1 | a0006 | 2 | HG01884.hp1 NA18906.hp2 |
missense_variant | MODERATE | c.1502A>G | p.Asn501Ser | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 8/22 | 1522/3735 | 1502/3231 | 501/1076 | chr1 | 182488987 | |||
chr1:182527656 | T | G | 1 | a0006 | 2 | HG01884.hp1 NA18906.hp2 |
missense_variant | MODERATE | c.2009T>G | p.Ile670Ser | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 11/22 | 2029/3735 | 2009/3231 | 670/1076 | chr1 | 182527656 | |||
chr1:182527694 | A | G | 6 | a0002 a0005 a0007 others(3): Show |
84 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(81): Show |
missense_variant | MODERATE | c.2047A>G | p.Ile683Val | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 11/22 | 2067/3735 | 2047/3231 | 683/1076 | chr1 | 182527694 | |||
chr1:182530295 | G | A | 1 | a0010 | 1 | HG00423.hp1 | missense_variant | MODERATE | c.2177G>A | p.Arg726His | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 12/22 | 2197/3735 | 2177/3231 | 726/1076 | chr1 | 182530295 | |||
chr1:182530808 | C | G | 1 | a0008 | 2 | HG02280.hp1 HG03486.hp1 |
missense_variant | MODERATE | c.2262C>G | p.Asp754Glu | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 13/22 | 2282/3735 | 2262/3231 | 754/1076 | chr1 | 182530808 | |||
chr1:182530821 | C | T | 1 | a0006 | 2 | HG01884.hp1 NA18906.hp2 |
missense_variant | MODERATE | c.2275C>T | p.His759Tyr | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 13/22 | 2295/3735 | 2275/3231 | 759/1076 | chr1 | 182530821 | |||
chr1:182530822 | A | G | 1 | a0006 | 2 | HG01884.hp1 NA18906.hp2 |
missense_variant | MODERATE | c.2276A>G | p.His759Arg | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 13/22 | 2296/3735 | 2276/3231 | 759/1076 | chr1 | 182530822 | |||
chr1:182540307 | G | A | 1 | a0011 | 1 | HG00558.hp2 | missense_variant | MODERATE | c.2555G>A | p.Ser852Asn | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/22 | 2575/3735 | 2555/3231 | 852/1076 | chr1 | 182540307 | |||
chr1:182548782 | C | G | 1 | a0012 | 1 | HG01243.hp2 | missense_variant | MODERATE | c.2891C>G | p.Ala964Gly | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/22 | 2911/3735 | 2891/3231 | 964/1076 | chr1 | 182548782 | |||
chr1:182553515 | G | A | 1 | a0009 | 2 | NA18989.hp1 NA19084.hp1 |
missense_variant | MODERATE | c.3104G>A | p.Arg1035Gln | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 19/22 | 3124/3735 | 3104/3231 | 1035/1076 | chr1 | 182553515 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:182472433 | C | T | 1 | a0003c0024 | 1 | HG02922.hp2 | synonymous_variant | LOW | c.339C>T | p.Asn113Asn | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 5/22 | 359/3735 | 339/3231 | 113/1076 | chr1 | 182472433 | |||
chr1:182473975 | G | A | 2 | a0001c0006 a0001c0017 |
6 | HG01891.hp1 HG02559.hp1 HG02895.hp1 others(3): Show |
synonymous_variant | LOW | c.864G>A | p.Val288Val | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/22 | 884/3735 | 864/3231 | 288/1076 | chr1 | 182473975 | |||
chr1:182474327 | T | C | 15 | a0001c0001 a0001c0005 a0001c0006 others(12): Show |
187 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(184): Show |
synonymous_variant | LOW | c.1216T>C | p.Leu406Leu | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/22 | 1236/3735 | 1216/3231 | 406/1076 | chr1 | 182474327 | |||
chr1:182532766 | C | T | 1 | a0006c0011 | 2 | HG01884.hp1 NA18906.hp2 |
synonymous_variant | LOW | c.2469C>T | p.His823His | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/22 | 2489/3735 | 2469/3231 | 823/1076 | chr1 | 182532766 | |||
chr1:182540254 | C | T | 3 | a0001c0005 a0001c0007 a0001c0017 |
13 | HG02258.hp2 HG02572.hp2 HG02622.hp2 others(10): Show |
synonymous_variant | LOW | c.2502C>T | p.Thr834Thr | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/22 | 2522/3735 | 2502/3231 | 834/1076 | chr1 | 182540254 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:182560449 | T | C | 4 | a0001c0004t0002 a0002c0002t0002 a0003c0003t0002 others(1): Show |
43 | HG00423.hp1 HG00639.hp1 HG00741.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*336T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 22/22 | 4392 | chr1 | 182560449 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:182450489 | T | C | 100 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0031 others(97): Show |
102 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.13+311T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182450489 | |||||||
chr1:182450505 | T | A | 76 | a0001c0001t0001g0001 a0001c0001t0001g0114 a0001c0001t0001g0115 others(73): Show |
80 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.13+327T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182450505 | |||||||
chr1:182450734 | A | C | 2 | a0001c0001t0001g0104 a0003c0024t0001g0105 |
2 | HG02922.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.13+556A>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182450734 | |||||||
chr1:182450809 | C | T | 1 | a0001c0001t0001g0103 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.13+631C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182450809 | |||||||
chr1:182450819 | T | C | 4 | a0001c0004t0001g0106 a0001c0004t0001g0107 a0001c0005t0001g0108 others(1): Show |
4 | HG02258.hp1 HG02717.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.13+641T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182450819 | |||||||
chr1:182450907 | G | C | 3 | a0001c0001t0001g0182 a0001c0004t0001g0181 a0003c0003t0002g0180 |
3 | HG01891.hp2 HG03041.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.13+729G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182450907 | |||||||
chr1:182451038 | G | T | 4 | a0001c0005t0001g0326 a0001c0005t0001g0329 a0002c0002t0001g0327 others(1): Show |
4 | HG02145.hp2 HG02896.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.13+860G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182451038 | |||||||
chr1:182451070 | T | G | 1 | a0002c0002t0001g0110 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.13+892T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182451070 | |||||||
chr1:182451087 | A | T | 1 | a0002c0002t0001g0110 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.13+909A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182451087 | |||||||
chr1:182451143 | C | A | 1 | a0003c0003t0002g0111 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.13+965C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182451143 | |||||||
chr1:182451143 | C | CA | 100 | a0001c0001t0001g0015 a0001c0001t0001g0031 a0001c0001t0001g0040 others(97): Show |
103 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.13+984dupA | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr1 | 182451143 | ||||||
chr1:182451143 | C | CAA | 9 | a0001c0001t0001g0009 a0001c0001t0001g0103 a0001c0001t0001g0184 others(6): Show |
9 | HG00423.hp1 HG01884.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.13+983_13+984dupAA | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr1 | 182451143 | ||||||
chr1:182451143 | CA | C | 77 | a0001c0001t0001g0001 a0001c0001t0001g0114 a0001c0001t0001g0115 others(74): Show |
81 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.13+984delA | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr1 | 182451143 | ||||||
chr1:182451209 | A | T | 1 | a0002c0002t0001g0110 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.13+1031A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182451209 | |||||||
chr1:182451258 | A | G | 1 | a0001c0004t0001g0324 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.13+1080A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182451258 | |||||||
chr1:182451283 | G | A | 1 | a0001c0005t0001g0011 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.13+1105G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182451283 | |||||||
chr1:182451313 | G | A | 247 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0015 others(244): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.13+1135G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182451313 | |||||||
chr1:182451340 | A | G | 1 | a0001c0004t0001g0320 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.13+1162A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182451340 | |||||||
chr1:182451356 | A | T | 1 | a0002c0002t0001g0179 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.13+1178A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182451356 | |||||||
chr1:182451422 | C | G | 1 | a0002c0002t0001g0110 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.13+1244C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182451422 | |||||||
chr1:182451455 | G | A | 3 | a0001c0007t0001g0193 a0002c0002t0001g0194 a0002c0002t0001g0195 |
3 | HG02622.hp2 HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.13+1277G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182451455 | |||||||
chr1:182451475 | G | GGATATAC others(102): Show |
30 | a0001c0001t0001g0190 a0001c0001t0001g0192 a0001c0001t0001g0296 others(27): Show |
30 | HG00099.hp1 HG00438.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.13+1297_13+1298ins others(109): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182451475 | |||||||
chr1:182451476 | C | T | 30 | a0001c0001t0001g0190 a0001c0001t0001g0192 a0001c0001t0001g0296 others(27): Show |
30 | HG00099.hp1 HG00438.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.13+1298C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182451476 | |||||||
chr1:182451478 | G | A | 30 | a0001c0001t0001g0190 a0001c0001t0001g0192 a0001c0001t0001g0296 others(27): Show |
30 | HG00099.hp1 HG00438.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.13+1300G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182451478 | |||||||
chr1:182451485 | C | T | 3 | a0001c0007t0001g0193 a0002c0002t0001g0194 a0002c0002t0001g0195 |
3 | HG02622.hp2 HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.13+1307C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182451485 | |||||||
chr1:182451499 | T | A | 30 | a0001c0001t0001g0190 a0001c0001t0001g0192 a0001c0001t0001g0296 others(27): Show |
30 | HG00099.hp1 HG00438.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.13+1321T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182451499 | |||||||
chr1:182451505 | A | G | 23 | a0001c0001t0001g0007 a0001c0001t0001g0189 a0001c0001t0001g0276 others(20): Show |
24 | HG00423.hp2 HG01081.hp1 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.13+1327A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182451505 | |||||||
chr1:182451705 | G | GGACATCA others(304): Show |
1 | a0002c0002t0001g0013 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.13+1544_13+1545ins others(311): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr1 | 182451705 | ||||||
chr1:182451705 | G | GGACATCA others(318): Show |
4 | a0001c0001t0001g0015 a0001c0005t0001g0011 a0003c0003t0002g0016 others(1): Show |
4 | HG03225.hp2 HG03831.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.13+1544_13+1545ins others(325): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr1 | 182451705 | ||||||
chr1:182451705 | G | GGACATCA others(319): Show |
30 | a0001c0001t0001g0031 a0001c0001t0001g0040 a0001c0001t0001g0042 others(27): Show |
30 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(27): Show |
intron_variant | MODIFIER | c.13+1544_13+1545ins others(326): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr1 | 182451705 | ||||||
chr1:182451705 | G | GGACATCA others(319): Show |
1 | a0001c0004t0002g0045 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.13+1544_13+1545ins others(326): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr1 | 182451705 | ||||||
chr1:182451705 | G | GGACATCA others(320): Show |
50 | a0001c0001t0001g0009 a0001c0001t0001g0048 a0001c0001t0001g0053 others(47): Show |
52 | HG00140.hp2 HG00735.hp2 HG01074.hp2 others(49): Show |
intron_variant | MODIFIER | c.13+1544_13+1545ins others(327): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr1 | 182451705 | ||||||
chr1:182451705 | G | GGACATCA others(321): Show |
8 | a0001c0001t0001g0091 a0001c0001t0001g0094 a0001c0004t0001g0010 others(5): Show |
8 | HG00438.hp1 HG00741.hp1 HG03927.hp2 others(5): Show |
intron_variant | MODIFIER | c.13+1544_13+1545ins others(328): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr1 | 182451705 | ||||||
chr1:182451705 | G | GGACATCA others(322): Show |
2 | a0002c0002t0001g0098 a0002c0002t0001g0099 |
2 | HG00738.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.13+1544_13+1545ins others(329): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr1 | 182451705 | ||||||
chr1:182451705 | G | GGACATCA others(323): Show |
1 | a0002c0002t0001g0100 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.13+1544_13+1545ins others(330): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr1 | 182451705 | ||||||
chr1:182451776 | G | A | 4 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0003c0003t0001g0294 others(1): Show |
4 | HG00438.hp2 NA18962.hp1 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.13+1598G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182451776 | |||||||
chr1:182451837 | T | C | 4 | a0001c0005t0001g0326 a0001c0005t0001g0329 a0002c0002t0001g0327 others(1): Show |
4 | HG02145.hp2 HG02896.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.13+1659T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182451837 | |||||||
chr1:182451923 | G | A | 3 | a0001c0007t0001g0193 a0002c0002t0001g0194 a0002c0002t0001g0195 |
3 | HG02622.hp2 HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.13+1745G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182451923 | |||||||
chr1:182452141 | G | T | 1 | a0003c0003t0001g0090 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.14-1817G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182452141 | |||||||
chr1:182452292 | G | A | 1 | a0001c0004t0001g0106 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.14-1666G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182452292 | |||||||
chr1:182452518 | T | C | 5 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0198 others(2): Show |
5 | HG01069.hp1 HG02055.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.14-1440T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182452518 | |||||||
chr1:182452556 | G | A | 5 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0004t0001g0183 others(2): Show |
5 | HG01884.hp1 HG02622.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.14-1402G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182452556 | |||||||
chr1:182452657 | T | C | 1 | a0001c0001t0001g0201 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.14-1301T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182452657 | |||||||
chr1:182453037 | T | C | 9 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0004t0001g0106 others(6): Show |
9 | HG01346.hp2 HG02258.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.14-921T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182453037 | |||||||
chr1:182453052 | A | G | 4 | a0001c0005t0001g0326 a0001c0005t0001g0329 a0002c0002t0001g0327 others(1): Show |
4 | HG02145.hp2 HG02896.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.14-906A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182453052 | |||||||
chr1:182453532 | G | A | 30 | a0001c0001t0001g0190 a0001c0001t0001g0192 a0001c0001t0001g0296 others(27): Show |
30 | HG00099.hp1 HG00438.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.14-426G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182453532 | |||||||
chr1:182453565 | G | A | 6 | a0002c0002t0001g0119 a0002c0002t0001g0120 a0002c0002t0001g0121 others(3): Show |
6 | NA18941.hp2 NA18953.hp1 NA18980.hp2 others(3): Show |
intron_variant | MODIFIER | c.14-393G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182453565 | |||||||
chr1:182453877 | T | C | 11 | a0001c0001t0001g0205 a0001c0001t0001g0213 a0001c0004t0001g0212 others(8): Show |
11 | HG01891.hp1 HG02280.hp1 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.14-81T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182453877 | |||||||
chr1:182453888 | G | C | 1 | a0003c0003t0001g0017 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.14-70G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182453888 | |||||||
chr1:182453920 | T | G | 1 | a0003c0003t0002g0214 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.14-38T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 1/21 | chr1 | 182453920 | |||||||
chr1:182454076 | C | T | 4 | a0001c0001t0001g0182 a0001c0007t0001g0193 a0002c0002t0001g0194 others(1): Show |
4 | HG02622.hp2 HG02630.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+36C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182454076 | |||||||
chr1:182454077 | A | G | 4 | a0001c0005t0001g0326 a0001c0005t0001g0329 a0002c0002t0001g0327 others(1): Show |
4 | HG02145.hp2 HG02896.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.96+37A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182454077 | |||||||
chr1:182454100 | A | C | 14 | a0001c0001t0001g0103 a0001c0001t0001g0182 a0001c0001t0001g0200 others(11): Show |
15 | HG01109.hp1 HG02109.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.96+60A>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182454100 | |||||||
chr1:182454163 | A | G | 1 | a0001c0001t0001g0103 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.96+123A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182454163 | |||||||
chr1:182454164 | T | TA | 14 | a0001c0001t0001g0103 a0001c0001t0001g0182 a0001c0001t0001g0200 others(11): Show |
15 | HG01109.hp1 HG02109.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.96+131dupA | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr1 | 182454164 | ||||||
chr1:182454323 | C | T | 9 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0004t0001g0181 others(6): Show |
9 | HG01884.hp1 HG01891.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.96+283C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182454323 | |||||||
chr1:182454441 | A | G | 31 | a0001c0001t0001g0190 a0001c0001t0001g0192 a0001c0001t0001g0296 others(28): Show |
31 | HG00099.hp1 HG00438.hp2 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.96+401A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182454441 | |||||||
chr1:182454446 | C | T | 1 | a0001c0004t0001g0178 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.96+406C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182454446 | |||||||
chr1:182454447 | G | A | 1 | a0001c0001t0001g0298 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.96+407G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182454447 | |||||||
chr1:182454524 | C | A | 1 | a0003c0003t0002g0180 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.96+484C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182454524 | |||||||
chr1:182454586 | A | ATG | 5 | a0001c0001t0001g0040 a0001c0001t0001g0104 a0001c0005t0001g0267 others(2): Show |
5 | HG00639.hp2 HG02148.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.96+585_96+586dupTG | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr1 | 182454586 | ||||||
chr1:182454586 | A | ATGTG | 9 | a0001c0001t0001g0200 a0001c0001t0001g0226 a0001c0001t0001g0238 others(6): Show |
9 | HG01258.hp2 HG02109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.96+583_96+586dupTG others(2): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr1 | 182454586 | ||||||
chr1:182454586 | A | ATGTGTG | 2 | a0001c0004t0001g0005 a0001c0004t0001g0188 |
3 | HG01109.hp1 HG02970.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.96+581_96+586dupTG others(4): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr1 | 182454586 | ||||||
chr1:182454586 | ATG | A | 32 | a0001c0001t0001g0009 a0001c0001t0001g0190 a0001c0001t0001g0296 others(29): Show |
32 | HG00438.hp2 HG00642.hp2 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.96+585_96+586delTG | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr1 | 182454586 | ||||||
chr1:182454586 | ATGTG | A | 108 | a0001c0001t0001g0015 a0001c0001t0001g0031 a0001c0001t0001g0048 others(105): Show |
110 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.96+583_96+586delTG others(2): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr1 | 182454586 | ||||||
chr1:182454586 | ATGTGTG | A | 71 | a0001c0001t0001g0042 a0001c0001t0001g0115 a0001c0001t0001g0132 others(68): Show |
73 | HG00280.hp1 HG00408.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.96+581_96+586delTG others(4): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr1 | 182454586 | ||||||
chr1:182454586 | ATGTGTGT others(1): Show |
A | 28 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0184 others(25): Show |
31 | HG00423.hp2 HG01070.hp1 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.96+579_96+586delTG others(6): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr1 | 182454586 | ||||||
chr1:182454586 | ATGTGTGT others(3): Show |
A | 11 | a0001c0001t0001g0103 a0001c0001t0001g0114 a0001c0001t0001g0182 others(8): Show |
11 | HG01069.hp1 HG01346.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.96+577_96+586delTG others(8): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr1 | 182454586 | ||||||
chr1:182454586 | ATGTGTGT others(5): Show |
A | 4 | a0001c0005t0001g0326 a0001c0005t0001g0329 a0002c0002t0001g0327 others(1): Show |
4 | HG02145.hp2 HG02896.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.96+575_96+586delTG others(10): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr1 | 182454586 | ||||||
chr1:182454602 | G | A | 10 | a0001c0001t0001g0103 a0001c0001t0001g0114 a0001c0001t0001g0182 others(7): Show |
10 | HG01069.hp1 HG01346.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.96+562G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182454602 | |||||||
chr1:182454630 | C | G | 1 | a0001c0004t0001g0005 | 2 | HG02970.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.96+590C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182454630 | |||||||
chr1:182454667 | A | C | 16 | a0001c0004t0001g0181 a0001c0005t0001g0326 a0001c0005t0001g0329 others(13): Show |
16 | HG01099.hp2 HG01891.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.96+627A>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182454667 | |||||||
chr1:182454753 | A | G | 17 | a0001c0001t0001g0115 a0001c0001t0001g0173 a0001c0001t0001g0175 others(14): Show |
17 | HG01123.hp2 HG01192.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.96+713A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182454753 | |||||||
chr1:182454887 | C | G | 1 | a0001c0001t0001g0297 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.96+847C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182454887 | |||||||
chr1:182454901 | C | T | 2 | a0001c0001t0001g0114 a0001c0001t0001g0199 |
2 | HG01069.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.96+861C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182454901 | |||||||
chr1:182454958 | C | T | 6 | a0004c0009t0001g0265 a0004c0012t0001g0262 a0004c0012t0001g0325 others(3): Show |
6 | HG02109.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.96+918C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182454958 | |||||||
chr1:182455350 | G | A | 86 | a0001c0001t0001g0007 a0001c0001t0001g0048 a0001c0001t0001g0091 others(83): Show |
89 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.96+1310G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182455350 | |||||||
chr1:182455439 | G | A | 1 | a0001c0005t0001g0267 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.96+1399G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182455439 | |||||||
chr1:182455479 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.96+1439G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182455479 | |||||||
chr1:182455591 | G | A | 1 | a0002c0002t0001g0110 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.96+1551G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182455591 | |||||||
chr1:182455591 | GA | G | 116 | a0001c0001t0001g0007 a0001c0001t0001g0042 a0001c0001t0001g0086 others(113): Show |
119 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(116): Show |
intron_variant | MODIFIER | c.96+1562delA | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr1 | 182455591 | ||||||
chr1:182455591 | GAA | G | 45 | a0001c0001t0001g0048 a0001c0001t0001g0088 a0001c0001t0001g0091 others(42): Show |
46 | HG00280.hp2 HG00558.hp1 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.96+1561_96+1562del others(2): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr1 | 182455591 | ||||||
chr1:182455592 | A | G | 1 | a0002c0002t0001g0110 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.96+1552A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182455592 | |||||||
chr1:182455612 | T | C | 5 | a0001c0001t0001g0103 a0001c0001t0001g0146 a0001c0001t0001g0198 others(2): Show |
5 | HG02055.hp1 HG02055.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.96+1572T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182455612 | |||||||
chr1:182455799 | G | A | 1 | a0003c0003t0002g0133 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.96+1759G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182455799 | |||||||
chr1:182455850 | C | T | 127 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0031 others(124): Show |
131 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.96+1810C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182455850 | |||||||
chr1:182455912 | C | T | 300 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0015 others(297): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.96+1872C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182455912 | |||||||
chr1:182455946 | G | A | 1 | a0001c0005t0001g0134 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.96+1906G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182455946 | |||||||
chr1:182455959 | C | T | 3 | a0001c0004t0001g0041 a0001c0004t0001g0107 a0001c0004t0001g0247 |
3 | HG02451.hp2 HG02559.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.96+1919C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182455959 | |||||||
chr1:182455980 | G | A | 2 | a0001c0007t0001g0021 a0001c0007t0001g0022 |
2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.96+1940G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182455980 | |||||||
chr1:182456063 | G | A | 28 | a0001c0001t0001g0009 a0001c0001t0001g0042 a0001c0001t0001g0057 others(25): Show |
28 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.96+2023G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182456063 | |||||||
chr1:182456063 | G | T | 1 | a0002c0002t0001g0012 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.96+2023G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182456063 | |||||||
chr1:182456221 | C | T | 158 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0015 others(155): Show |
164 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.97-2098C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182456221 | |||||||
chr1:182456299 | C | CT | 63 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0042 others(60): Show |
64 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.97-2005dupT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr1 | 182456299 | ||||||
chr1:182456539 | C | T | 1 | a0001c0001t0001g0293 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.97-1780C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182456539 | |||||||
chr1:182456564 | C | T | 1 | a0003c0003t0002g0006 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.97-1755C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182456564 | |||||||
chr1:182456582 | G | A | 1 | a0001c0007t0001g0021 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.97-1737G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182456582 | |||||||
chr1:182456617 | C | T | 2 | a0001c0004t0001g0278 a0002c0002t0002g0287 |
2 | HG01169.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.97-1702C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182456617 | |||||||
chr1:182456651 | A | T | 1 | a0002c0002t0001g0110 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.97-1668A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182456651 | |||||||
chr1:182456839 | G | A | 2 | a0003c0003t0002g0018 a0003c0003t0002g0214 |
2 | HG01074.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.97-1480G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182456839 | |||||||
chr1:182456912 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.97-1407C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182456912 | |||||||
chr1:182456913 | G | A | 1 | a0003c0003t0002g0058 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.97-1406G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182456913 | |||||||
chr1:182456934 | G | T | 99 | a0001c0001t0001g0009 a0001c0001t0001g0042 a0001c0001t0001g0053 others(96): Show |
99 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.97-1385G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182456934 | |||||||
chr1:182456994 | A | T | 1 | a0002c0002t0001g0110 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.97-1325A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182456994 | |||||||
chr1:182457148 | A | AAAAC | 131 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0042 others(128): Show |
132 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.97-1155_97-1152dup others(4): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr1 | 182457148 | ||||||
chr1:182457177 | T | C | 1 | a0001c0004t0001g0107 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.97-1142T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182457177 | |||||||
chr1:182457230 | G | C | 4 | a0001c0001t0001g0200 a0001c0001t0001g0271 a0001c0001t0001g0272 others(1): Show |
4 | HG02145.hp1 HG02630.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.97-1089G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182457230 | |||||||
chr1:182457336 | A | G | 1 | a0006c0011t0001g0187 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.97-983A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182457336 | |||||||
chr1:182457400 | G | T | 11 | a0001c0001t0001g0104 a0001c0001t0001g0182 a0001c0001t0001g0185 others(8): Show |
11 | HG01243.hp2 HG01884.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.97-919G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182457400 | |||||||
chr1:182457462 | C | A | 126 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0042 others(123): Show |
127 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.97-857C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182457462 | |||||||
chr1:182457487 | T | A | 1 | a0002c0002t0001g0110 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.97-832T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182457487 | |||||||
chr1:182457532 | G | T | 1 | a0003c0003t0001g0162 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.97-787G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182457532 | |||||||
chr1:182457570 | G | A | 130 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0042 others(127): Show |
131 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.97-749G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182457570 | |||||||
chr1:182457682 | G | A | 2 | a0001c0001t0001g0182 a0012c0019t0001g0216 |
2 | HG01243.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.97-637G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182457682 | |||||||
chr1:182457693 | G | A | 7 | a0001c0001t0001g0258 a0001c0006t0001g0137 a0001c0006t0001g0138 others(4): Show |
7 | HG01884.hp2 HG02559.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.97-626G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182457693 | |||||||
chr1:182457762 | G | T | 142 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0042 others(139): Show |
143 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.97-557G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182457762 | |||||||
chr1:182458097 | G | A | 2 | a0002c0002t0001g0096 a0002c0002t0001g0098 |
2 | NA18973.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.97-222G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182458097 | |||||||
chr1:182458220 | G | A | 51 | a0001c0001t0001g0053 a0001c0001t0001g0135 a0001c0001t0001g0148 others(48): Show |
51 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.97-99G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 2/21 | chr1 | 182458220 | |||||||
chr1:182458524 | C | T | 127 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0042 others(124): Show |
128 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.171+131C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 3/21 | chr1 | 182458524 | |||||||
chr1:182458627 | G | A | 66 | a0001c0001t0001g0053 a0001c0001t0001g0104 a0001c0001t0001g0135 others(63): Show |
66 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.171+234G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 3/21 | chr1 | 182458627 | |||||||
chr1:182458857 | G | A | 1 | a0003c0003t0001g0116 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.171+464G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 3/21 | chr1 | 182458857 | |||||||
chr1:182459205 | A | C | 1 | a0001c0001t0001g0310 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.172-799A>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 3/21 | chr1 | 182459205 | |||||||
chr1:182459470 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.172-534G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 3/21 | chr1 | 182459470 | |||||||
chr1:182459578 | A | G | 2 | a0001c0007t0001g0021 a0001c0007t0001g0022 |
2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.172-426A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 3/21 | chr1 | 182459578 | |||||||
chr1:182459657 | A | G | 2 | a0001c0001t0001g0296 a0009c0018t0001g0295 |
2 | NA18962.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.172-347A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 3/21 | chr1 | 182459657 | |||||||
chr1:182459659 | C | A | 1 | a0001c0005t0001g0113 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.172-345C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 3/21 | chr1 | 182459659 | |||||||
chr1:182459704 | G | A | 3 | a0001c0001t0001g0258 a0003c0003t0001g0118 a0014c0014t0001g0174 |
3 | HG01884.hp2 HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.172-300G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 3/21 | chr1 | 182459704 | |||||||
chr1:182459749 | G | T | 11 | a0001c0001t0001g0114 a0001c0001t0001g0146 a0001c0001t0001g0198 others(8): Show |
11 | HG01069.hp1 HG01346.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.172-255G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 3/21 | chr1 | 182459749 | |||||||
chr1:182459892 | T | G | 1 | a0001c0001t0001g0175 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.172-112T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 3/21 | chr1 | 182459892 | |||||||
chr1:182459945 | A | AT | 4 | a0001c0006t0001g0137 a0001c0006t0001g0138 a0002c0002t0001g0194 others(1): Show |
4 | HG02559.hp1 HG02630.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.172-52dupT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr1 | 182459945 | ||||||
chr1:182460160 | C | CTGTG | 3 | a0001c0001t0001g0042 a0001c0001t0001g0147 a0001c0001t0001g0246 |
3 | HG02040.hp2 HG02155.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.301+49_301+52dupGT others(2): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 182460160 | ||||||
chr1:182460160 | CTG | C | 208 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0031 others(205): Show |
215 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.301+51_301+52delGT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 182460160 | ||||||
chr1:182460160 | CTGTG | C | 5 | a0001c0001t0001g0088 a0001c0001t0001g0114 a0001c0001t0001g0146 others(2): Show |
5 | HG00735.hp2 HG01069.hp1 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.301+49_301+52delGT others(2): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 182460160 | ||||||
chr1:182460164 | GTGTGTGT others(57): Show |
G | 2 | a0001c0001t0001g0103 a0001c0001t0001g0205 |
2 | HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.301+51_301+114delG others(63): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 182460164 | ||||||
chr1:182460166 | GTGTGTGT others(55): Show |
G | 1 | a0001c0004t0001g0183 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.301+81_301+142delA others(61): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 182460166 | ||||||
chr1:182460184 | G | GTGTA | 7 | a0001c0001t0001g0104 a0001c0001t0001g0185 a0001c0001t0001g0200 others(4): Show |
7 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.301+52_301+53insGT others(2): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 182460184 | ||||||
chr1:182460184 | G | GTGTGTA | 4 | a0001c0001t0001g0182 a0006c0011t0001g0186 a0006c0011t0001g0187 others(1): Show |
4 | HG01243.hp2 HG01884.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.301+52_301+53insGT others(4): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 182460184 | ||||||
chr1:182460226 | GTA | G | 11 | a0001c0001t0001g0104 a0001c0001t0001g0182 a0001c0001t0001g0185 others(8): Show |
11 | HG01243.hp2 HG01884.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.301+95_301+96delAT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 182460226 | ||||||
chr1:182460228 | A | ATG | 3 | a0001c0001t0001g0048 a0001c0004t0001g0227 a0003c0003t0001g0090 |
3 | HG03927.hp1 NA19091.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.301+113_301+114dup others(2): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 182460228 | ||||||
chr1:182460228 | A | T | 3 | a0001c0001t0001g0258 a0003c0003t0001g0118 a0014c0014t0001g0174 |
3 | HG01884.hp2 HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.301+95A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182460228 | |||||||
chr1:182460240 | G | A | 32 | a0001c0001t0001g0009 a0001c0001t0001g0042 a0001c0001t0001g0057 others(29): Show |
32 | HG00438.hp2 HG00673.hp2 HG01123.hp1 others(29): Show |
intron_variant | MODIFIER | c.301+107G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182460240 | |||||||
chr1:182460338 | A | G | 1 | a0002c0002t0001g0084 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.301+205A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182460338 | |||||||
chr1:182460398 | G | T | 1 | a0002c0002t0001g0083 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.301+265G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182460398 | |||||||
chr1:182460437 | A | G | 2 | a0002c0002t0001g0194 a0002c0002t0001g0195 |
2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.301+304A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182460437 | |||||||
chr1:182460439 | T | C | 5 | a0001c0001t0001g0190 a0001c0001t0001g0300 a0001c0001t0001g0301 others(2): Show |
5 | NA18977.hp2 NA19000.hp1 NA19006.hp2 others(2): Show |
intron_variant | MODIFIER | c.301+306T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182460439 | |||||||
chr1:182460470 | C | A | 34 | a0001c0001t0001g0009 a0001c0001t0001g0042 a0001c0001t0001g0057 others(31): Show |
34 | HG00438.hp2 HG00673.hp2 HG01123.hp1 others(31): Show |
intron_variant | MODIFIER | c.301+337C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182460470 | |||||||
chr1:182460593 | T | C | 275 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(272): Show |
284 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.301+460T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182460593 | |||||||
chr1:182460650 | A | G | 5 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0080 others(2): Show |
7 | NA18951.hp1 NA18970.hp2 NA18977.hp1 others(4): Show |
intron_variant | MODIFIER | c.301+517A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182460650 | |||||||
chr1:182460752 | A | G | 1 | a0002c0002t0001g0254 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.301+619A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182460752 | |||||||
chr1:182460807 | G | A | 1 | a0001c0005t0001g0134 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.301+674G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182460807 | |||||||
chr1:182460860 | C | A | 43 | a0001c0001t0001g0048 a0001c0001t0001g0053 a0001c0001t0001g0086 others(40): Show |
43 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.301+727C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182460860 | |||||||
chr1:182460920 | G | C | 2 | a0004c0012t0001g0262 a0004c0012t0001g0325 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.301+787G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182460920 | |||||||
chr1:182460941 | G | C | 1 | a0001c0004t0001g0087 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.301+808G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182460941 | |||||||
chr1:182460992 | T | C | 1 | a0003c0003t0002g0133 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.301+859T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182460992 | |||||||
chr1:182461026 | G | A | 2 | a0001c0004t0001g0221 a0001c0004t0001g0222 |
2 | HG01255.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.301+893G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182461026 | |||||||
chr1:182461103 | A | G | 67 | a0001c0004t0001g0112 a0001c0004t0001g0130 a0003c0003t0001g0030 others(64): Show |
69 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.301+970A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182461103 | |||||||
chr1:182461136 | C | CT | 67 | a0001c0004t0001g0112 a0001c0004t0001g0130 a0003c0003t0001g0030 others(64): Show |
69 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.301+1013dupT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 182461136 | ||||||
chr1:182461200 | T | A | 1 | a0001c0001t0001g0009 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.301+1067T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182461200 | |||||||
chr1:182461313 | G | GTAA | 73 | a0001c0001t0001g0146 a0001c0001t0001g0199 a0001c0001t0001g0219 others(70): Show |
76 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.301+1199_301+1201d others(5): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 182461313 | ||||||
chr1:182461313 | G | GTAATAA | 6 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0003c0003t0001g0030 others(3): Show |
6 | HG02809.hp2 HG02922.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.301+1196_301+1201d others(8): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 182461313 | ||||||
chr1:182461359 | A | C | 2 | a0003c0003t0001g0209 a0003c0024t0001g0105 |
2 | HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.301+1226A>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182461359 | |||||||
chr1:182461366 | C | A | 1 | a0001c0001t0001g0279 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.301+1233C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182461366 | |||||||
chr1:182461395 | G | A | 70 | a0001c0004t0001g0112 a0001c0004t0001g0130 a0003c0003t0001g0030 others(67): Show |
73 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.301+1262G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182461395 | |||||||
chr1:182461544 | T | C | 46 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0015 others(43): Show |
48 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.301+1411T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182461544 | |||||||
chr1:182461581 | A | G | 3 | a0001c0001t0001g0184 a0001c0001t0001g0268 a0001c0005t0001g0267 |
3 | HG02109.hp2 HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.301+1448A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182461581 | |||||||
chr1:182461585 | T | C | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.301+1452T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182461585 | |||||||
chr1:182461663 | A | G | 7 | a0001c0001t0001g0114 a0001c0001t0001g0182 a0001c0001t0001g0219 others(4): Show |
8 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.301+1530A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182461663 | |||||||
chr1:182461780 | ATAGGACA others(8): Show |
A | 101 | a0001c0001t0001g0273 a0001c0004t0001g0041 a0001c0004t0001g0087 others(98): Show |
103 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.301+1650_301+1664d others(17): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 182461780 | ||||||
chr1:182461783 | G | A | 2 | a0008c0010t0001g0203 a0008c0010t0001g0204 |
2 | HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.301+1650G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182461783 | |||||||
chr1:182461896 | A | G | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.301+1763A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182461896 | |||||||
chr1:182461962 | G | A | 3 | a0001c0001t0001g0114 a0001c0001t0001g0182 a0012c0019t0001g0216 |
3 | HG01243.hp2 HG01346.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.301+1829G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182461962 | |||||||
chr1:182461963 | G | T | 66 | a0003c0003t0001g0017 a0003c0003t0001g0030 a0003c0003t0001g0039 others(63): Show |
69 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.301+1830G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182461963 | |||||||
chr1:182462030 | T | G | 6 | a0001c0006t0001g0137 a0001c0006t0001g0138 a0001c0006t0001g0206 others(3): Show |
6 | HG01891.hp1 HG02559.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.301+1897T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182462030 | |||||||
chr1:182462073 | T | C | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.301+1940T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182462073 | |||||||
chr1:182462182 | T | G | 1 | a0001c0001t0001g0219 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.301+2049T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182462182 | |||||||
chr1:182462309 | A | G | 1 | a0001c0001t0001g0244 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.301+2176A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182462309 | |||||||
chr1:182462459 | T | G | 1 | a0001c0005t0001g0113 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.301+2326T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182462459 | |||||||
chr1:182462560 | G | A | 12 | a0001c0001t0001g0173 a0001c0001t0001g0175 a0001c0001t0001g0176 others(9): Show |
12 | HG01884.hp2 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.301+2427G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182462560 | |||||||
chr1:182462578 | A | T | 71 | a0001c0004t0001g0112 a0001c0004t0001g0130 a0003c0003t0001g0017 others(68): Show |
74 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.301+2445A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182462578 | |||||||
chr1:182463029 | C | T | 6 | a0001c0006t0001g0137 a0001c0006t0001g0138 a0001c0006t0001g0206 others(3): Show |
6 | HG01891.hp1 HG02559.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.301+2896C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182463029 | |||||||
chr1:182463046 | A | C | 318 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(315): Show |
327 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(324): Show |
intron_variant | MODIFIER | c.301+2913A>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182463046 | |||||||
chr1:182463064 | C | T | 5 | a0001c0004t0001g0010 a0001c0004t0001g0251 a0001c0004t0001g0285 others(2): Show |
5 | HG00735.hp1 HG01255.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.301+2931C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182463064 | |||||||
chr1:182463110 | G | C | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.301+2977G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182463110 | |||||||
chr1:182463118 | C | A | 43 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0015 others(40): Show |
45 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.301+2985C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182463118 | |||||||
chr1:182463167 | G | A | 1 | a0001c0004t0001g0181 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.301+3034G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182463167 | |||||||
chr1:182463183 | A | C | 4 | a0003c0003t0001g0052 a0003c0003t0001g0160 a0003c0003t0001g0161 others(1): Show |
4 | NA18951.hp2 NA18952.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.301+3050A>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182463183 | |||||||
chr1:182463193 | T | C | 1 | a0002c0002t0001g0068 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.301+3060T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182463193 | |||||||
chr1:182463272 | C | T | 2 | a0003c0003t0001g0116 a0003c0003t0002g0016 |
2 | HG03688.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.301+3139C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182463272 | |||||||
chr1:182463293 | C | CA | 54 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0015 others(51): Show |
56 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.301+3178dupA | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 182463293 | ||||||
chr1:182463359 | C | A | 1 | a0001c0001t0001g0230 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.301+3226C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182463359 | |||||||
chr1:182463472 | A | G | 2 | a0001c0004t0001g0221 a0001c0004t0001g0222 |
2 | HG01255.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.301+3339A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182463472 | |||||||
chr1:182463515 | A | G | 2 | a0001c0001t0001g0182 a0012c0019t0001g0216 |
2 | HG01243.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.301+3382A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182463515 | |||||||
chr1:182463551 | T | G | 2 | a0001c0001t0001g0066 a0001c0001t0001g0273 |
2 | NA18944.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.301+3418T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182463551 | |||||||
chr1:182463680 | T | G | 3 | a0001c0001t0001g0184 a0001c0001t0001g0268 a0001c0005t0001g0267 |
3 | HG02109.hp2 HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.301+3547T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182463680 | |||||||
chr1:182463749 | A | T | 1 | a0001c0005t0001g0134 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.301+3616A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182463749 | |||||||
chr1:182464259 | T | C | 8 | a0001c0001t0001g0273 a0001c0004t0001g0087 a0001c0004t0001g0125 others(5): Show |
8 | HG02071.hp1 NA18947.hp1 NA18962.hp2 others(5): Show |
intron_variant | MODIFIER | c.301+4126T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182464259 | |||||||
chr1:182464365 | T | C | 1 | a0002c0002t0001g0032 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.301+4232T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182464365 | |||||||
chr1:182464462 | G | A | 1 | a0002c0002t0001g0080 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.301+4329G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182464462 | |||||||
chr1:182464727 | G | GA | 10 | a0001c0001t0001g0086 a0001c0001t0001g0230 a0001c0001t0001g0231 others(7): Show |
10 | HG00738.hp1 HG01243.hp1 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.301+4607dupA | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 182464727 | ||||||
chr1:182464761 | T | C | 2 | a0008c0010t0001g0203 a0008c0010t0001g0204 |
2 | HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.301+4628T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182464761 | |||||||
chr1:182464852 | T | C | 71 | a0001c0004t0001g0112 a0001c0004t0001g0130 a0003c0003t0001g0017 others(68): Show |
74 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.301+4719T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182464852 | |||||||
chr1:182464854 | G | C | 1 | a0001c0005t0001g0113 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.301+4721G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182464854 | |||||||
chr1:182464916 | G | A | 36 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0015 others(33): Show |
38 | HG00673.hp2 HG00735.hp2 HG01070.hp1 others(35): Show |
intron_variant | MODIFIER | c.301+4783G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182464916 | |||||||
chr1:182465082 | A | AATAATAA others(215): Show |
1 | a0001c0005t0001g0011 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.301+4961_301+4962i others(224): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 182465082 | ||||||
chr1:182465082 | A | AATAATAA others(213): Show |
2 | a0001c0001t0001g0199 a0001c0001t0001g0219 |
2 | HG01069.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.301+4961_301+4962i others(222): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 182465082 | ||||||
chr1:182465082 | A | AATAATAA others(211): Show |
2 | a0001c0001t0001g0196 a0001c0001t0001g0197 |
2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.301+4961_301+4962i others(220): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 182465082 | ||||||
chr1:182465082 | A | AATAATAA others(219): Show |
2 | a0008c0010t0001g0203 a0008c0010t0001g0204 |
2 | HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.301+4961_301+4962i others(228): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 182465082 | ||||||
chr1:182465082 | A | AATAATAA others(211): Show |
1 | a0001c0001t0001g0146 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.301+4961_301+4962i others(220): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 182465082 | ||||||
chr1:182465100 | A | G | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.301+4967A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182465100 | |||||||
chr1:182465190 | T | C | 1 | a0003c0003t0001g0151 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.301+5057T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182465190 | |||||||
chr1:182465196 | AGATAGAA others(1): Show |
A | 8 | a0001c0001t0001g0146 a0001c0001t0001g0196 a0001c0001t0001g0197 others(5): Show |
8 | HG01069.hp1 HG02055.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.301+5067_301+5074d others(10): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 182465196 | ||||||
chr1:182465351 | A | G | 69 | a0001c0004t0001g0112 a0001c0004t0001g0130 a0003c0003t0001g0017 others(66): Show |
72 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.301+5218A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182465351 | |||||||
chr1:182465380 | G | A | 35 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0015 others(32): Show |
37 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.301+5247G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182465380 | |||||||
chr1:182465469 | G | C | 9 | a0001c0001t0001g0173 a0001c0001t0001g0175 a0001c0001t0001g0176 others(6): Show |
9 | HG01884.hp2 HG02258.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.301+5336G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182465469 | |||||||
chr1:182465470 | G | A | 8 | a0001c0001t0001g0173 a0001c0001t0001g0175 a0001c0001t0001g0176 others(5): Show |
8 | HG01884.hp2 HG02451.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.301+5337G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182465470 | |||||||
chr1:182465606 | T | TATA | 2 | a0002c0002t0001g0004 a0002c0002t0001g0081 |
3 | NA18977.hp1 NA19011.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.301+5487_301+5489d others(5): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 182465606 | ||||||
chr1:182465647 | C | G | 45 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0015 others(42): Show |
47 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.301+5514C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182465647 | |||||||
chr1:182465702 | G | A | 69 | a0003c0003t0001g0017 a0003c0003t0001g0030 a0003c0003t0001g0039 others(66): Show |
72 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.301+5569G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182465702 | |||||||
chr1:182465870 | G | C | 1 | a0002c0002t0001g0119 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.301+5737G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182465870 | |||||||
chr1:182466039 | C | T | 69 | a0003c0003t0001g0017 a0003c0003t0001g0030 a0003c0003t0001g0039 others(66): Show |
72 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.301+5906C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182466039 | |||||||
chr1:182466103 | A | G | 1 | a0001c0001t0001g0308 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.301+5970A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182466103 | |||||||
chr1:182466123 | GA | G | 69 | a0003c0003t0001g0017 a0003c0003t0001g0030 a0003c0003t0001g0039 others(66): Show |
72 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.301+5999delA | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 182466123 | ||||||
chr1:182466217 | A | G | 3 | a0001c0006t0001g0206 a0001c0006t0001g0207 a0001c0006t0001g0208 |
3 | HG01891.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.301+6084A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182466217 | |||||||
chr1:182466539 | G | C | 69 | a0003c0003t0001g0017 a0003c0003t0001g0030 a0003c0003t0001g0039 others(66): Show |
72 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.302-5857G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182466539 | |||||||
chr1:182466577 | A | G | 1 | a0001c0001t0001g0273 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.302-5819A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182466577 | |||||||
chr1:182466586 | C | T | 1 | a0003c0003t0001g0116 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.302-5810C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182466586 | |||||||
chr1:182466603 | T | C | 1 | a0001c0001t0001g0175 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.302-5793T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182466603 | |||||||
chr1:182466621 | A | G | 67 | a0003c0003t0001g0017 a0003c0003t0001g0030 a0003c0003t0001g0039 others(64): Show |
70 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.302-5775A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182466621 | |||||||
chr1:182466649 | C | T | 3 | a0001c0001t0001g0114 a0001c0001t0001g0182 a0012c0019t0001g0216 |
3 | HG01243.hp2 HG01346.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.302-5747C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182466649 | |||||||
chr1:182466749 | A | C | 9 | a0001c0001t0001g0173 a0001c0001t0001g0175 a0001c0001t0001g0176 others(6): Show |
9 | HG01884.hp2 HG02258.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.302-5647A>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182466749 | |||||||
chr1:182466821 | T | C | 69 | a0003c0003t0001g0017 a0003c0003t0001g0030 a0003c0003t0001g0039 others(66): Show |
72 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.302-5575T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182466821 | |||||||
chr1:182466874 | T | A | 1 | a0002c0002t0001g0274 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.302-5522T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182466874 | |||||||
chr1:182466879 | A | G | 25 | a0001c0004t0001g0010 a0001c0004t0001g0023 a0001c0004t0001g0044 others(22): Show |
25 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.302-5517A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182466879 | |||||||
chr1:182466945 | T | C | 6 | a0001c0006t0001g0137 a0001c0006t0001g0138 a0001c0006t0001g0206 others(3): Show |
6 | HG01891.hp1 HG02559.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.302-5451T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182466945 | |||||||
chr1:182467021 | T | C | 1 | a0017c0023t0001g0139 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.302-5375T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182467021 | |||||||
chr1:182467023 | C | A | 1 | a0017c0023t0001g0139 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.302-5373C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182467023 | |||||||
chr1:182467056 | C | A | 43 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0015 others(40): Show |
45 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.302-5340C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182467056 | |||||||
chr1:182467103 | A | G | 1 | a0001c0001t0001g0065 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.302-5293A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182467103 | |||||||
chr1:182467135 | G | T | 1 | a0001c0004t0001g0107 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.302-5261G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182467135 | |||||||
chr1:182467268 | T | C | 2 | a0003c0003t0001g0209 a0003c0024t0001g0105 |
2 | HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.302-5128T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182467268 | |||||||
chr1:182467304 | C | T | 40 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(37): Show |
41 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.302-5092C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182467304 | |||||||
chr1:182467427 | C | T | 6 | a0001c0006t0001g0137 a0001c0006t0001g0138 a0001c0006t0001g0206 others(3): Show |
6 | HG01891.hp1 HG02559.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.302-4969C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182467427 | |||||||
chr1:182467431 | C | T | 135 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0015 others(132): Show |
140 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(137): Show |
intron_variant | MODIFIER | c.302-4965C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182467431 | |||||||
chr1:182467441 | C | A | 1 | a0001c0004t0001g0324 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.302-4955C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182467441 | |||||||
chr1:182467584 | G | T | 68 | a0003c0003t0001g0017 a0003c0003t0001g0030 a0003c0003t0001g0039 others(65): Show |
71 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.302-4812G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182467584 | |||||||
chr1:182467647 | C | T | 1 | a0002c0002t0001g0099 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.302-4749C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182467647 | |||||||
chr1:182467746 | T | C | 1 | a0003c0003t0002g0133 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.302-4650T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182467746 | |||||||
chr1:182467844 | A | G | 69 | a0003c0003t0001g0017 a0003c0003t0001g0030 a0003c0003t0001g0039 others(66): Show |
72 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.302-4552A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182467844 | |||||||
chr1:182467904 | C | A | 3 | a0002c0002t0001g0109 a0007c0013t0001g0263 a0007c0013t0001g0264 |
3 | HG02109.hp1 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.302-4492C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182467904 | |||||||
chr1:182467961 | A | G | 3 | a0001c0001t0001g0114 a0001c0001t0001g0182 a0012c0019t0001g0216 |
3 | HG01243.hp2 HG01346.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.302-4435A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182467961 | |||||||
chr1:182468071 | A | C | 144 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0015 others(141): Show |
149 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(146): Show |
intron_variant | MODIFIER | c.302-4325A>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182468071 | |||||||
chr1:182468094 | C | T | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.302-4302C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182468094 | |||||||
chr1:182468095 | G | A | 1 | a0001c0001t0001g0308 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.302-4301G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182468095 | |||||||
chr1:182468193 | G | T | 1 | a0003c0003t0001g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.302-4203G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182468193 | |||||||
chr1:182468275 | T | C | 69 | a0003c0003t0001g0017 a0003c0003t0001g0030 a0003c0003t0001g0039 others(66): Show |
72 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.302-4121T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182468275 | |||||||
chr1:182468307 | C | T | 1 | a0002c0002t0001g0012 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.302-4089C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182468307 | |||||||
chr1:182468333 | C | T | 28 | a0001c0004t0001g0010 a0001c0004t0001g0023 a0001c0004t0001g0044 others(25): Show |
28 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.302-4063C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182468333 | |||||||
chr1:182468374 | C | T | 1 | a0001c0005t0001g0113 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.302-4022C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182468374 | |||||||
chr1:182468422 | G | A | 1 | a0017c0023t0001g0139 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.302-3974G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182468422 | |||||||
chr1:182468424 | A | T | 1 | a0017c0023t0001g0139 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.302-3972A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182468424 | |||||||
chr1:182468425 | T | A | 1 | a0017c0023t0001g0139 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.302-3971T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182468425 | |||||||
chr1:182468488 | A | G | 1 | a0004c0009t0001g0265 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.302-3908A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182468488 | |||||||
chr1:182468778 | T | A | 3 | a0001c0001t0001g0189 a0001c0001t0001g0255 a0001c0001t0001g0293 |
3 | HG01978.hp1 HG02738.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.302-3618T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182468778 | |||||||
chr1:182468780 | A | T | 3 | a0001c0001t0001g0189 a0001c0001t0001g0255 a0001c0001t0001g0293 |
3 | HG01978.hp1 HG02738.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.302-3616A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182468780 | |||||||
chr1:182468808 | G | T | 1 | a0017c0023t0001g0139 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.302-3588G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182468808 | |||||||
chr1:182468835 | A | G | 135 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0015 others(132): Show |
140 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(137): Show |
intron_variant | MODIFIER | c.302-3561A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182468835 | |||||||
chr1:182468968 | G | A | 135 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0015 others(132): Show |
140 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(137): Show |
intron_variant | MODIFIER | c.302-3428G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182468968 | |||||||
chr1:182468971 | C | T | 1 | a0001c0004t0001g0324 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.302-3425C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182468971 | |||||||
chr1:182469001 | A | T | 1 | a0003c0003t0002g0245 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.302-3395A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182469001 | |||||||
chr1:182469032 | G | A | 3 | a0001c0001t0001g0184 a0001c0001t0001g0268 a0001c0005t0001g0267 |
3 | HG02109.hp2 HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.302-3364G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182469032 | |||||||
chr1:182469367 | C | A | 37 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(34): Show |
38 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.302-3029C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182469367 | |||||||
chr1:182469404 | C | A | 2 | a0001c0004t0001g0177 a0001c0004t0001g0269 |
2 | HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.302-2992C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182469404 | |||||||
chr1:182469422 | G | A | 6 | a0001c0006t0001g0137 a0001c0006t0001g0138 a0001c0006t0001g0206 others(3): Show |
6 | HG01891.hp1 HG02559.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.302-2974G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182469422 | |||||||
chr1:182469436 | G | A | 1 | a0002c0002t0001g0259 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.302-2960G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182469436 | |||||||
chr1:182469511 | G | A | 68 | a0003c0003t0001g0017 a0003c0003t0001g0030 a0003c0003t0001g0039 others(65): Show |
71 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.302-2885G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182469511 | |||||||
chr1:182469519 | G | T | 1 | a0011c0021t0001g0170 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.302-2877G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182469519 | |||||||
chr1:182469577 | A | T | 9 | a0001c0001t0001g0173 a0001c0001t0001g0175 a0001c0001t0001g0176 others(6): Show |
9 | HG01884.hp2 HG02258.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.302-2819A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182469577 | |||||||
chr1:182469593 | T | C | 2 | a0001c0004t0001g0311 a0001c0004t0001g0312 |
2 | HG00642.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.302-2803T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182469593 | |||||||
chr1:182469604 | C | T | 1 | a0008c0010t0001g0204 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.302-2792C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182469604 | |||||||
chr1:182469675 | G | A | 1 | a0003c0003t0001g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.302-2721G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182469675 | |||||||
chr1:182469895 | A | C | 2 | a0001c0001t0001g0057 a0001c0001t0001g0094 |
2 | NA18982.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.302-2501A>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182469895 | |||||||
chr1:182469951 | A | G | 67 | a0003c0003t0001g0017 a0003c0003t0001g0030 a0003c0003t0001g0039 others(64): Show |
70 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.302-2445A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182469951 | |||||||
chr1:182470007 | G | C | 2 | a0003c0003t0001g0209 a0003c0024t0001g0105 |
2 | HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.302-2389G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182470007 | |||||||
chr1:182470017 | GGCAGTGA others(2): Show |
G | 3 | a0001c0001t0001g0184 a0001c0001t0001g0268 a0001c0005t0001g0267 |
3 | HG02109.hp2 HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.302-2377_302-2369d others(11): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 182470017 | ||||||
chr1:182470018 | G | A | 18 | a0002c0002t0001g0024 a0002c0002t0001g0038 a0002c0002t0001g0046 others(15): Show |
18 | HG00438.hp1 HG01928.hp1 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.302-2378G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182470018 | |||||||
chr1:182470124 | A | G | 1 | a0001c0001t0001g0243 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.302-2272A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182470124 | |||||||
chr1:182470132 | G | A | 6 | a0001c0006t0001g0137 a0001c0006t0001g0138 a0001c0006t0001g0206 others(3): Show |
6 | HG01891.hp1 HG02559.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.302-2264G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182470132 | |||||||
chr1:182470161 | C | T | 10 | a0001c0001t0001g0086 a0001c0001t0001g0219 a0001c0001t0001g0230 others(7): Show |
10 | HG00738.hp1 HG01243.hp1 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.302-2235C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182470161 | |||||||
chr1:182470228 | C | T | 1 | a0001c0001t0001g0205 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.302-2168C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182470228 | |||||||
chr1:182470266 | A | G | 3 | a0001c0007t0001g0021 a0001c0007t0001g0022 a0001c0007t0001g0210 |
3 | HG02965.hp1 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.302-2130A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182470266 | |||||||
chr1:182470398 | C | T | 37 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(34): Show |
38 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.302-1998C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182470398 | |||||||
chr1:182470407 | T | G | 1 | a0001c0001t0001g0048 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.302-1989T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182470407 | |||||||
chr1:182470496 | CG | C | 3 | a0003c0003t0001g0064 a0003c0003t0001g0159 a0003c0003t0001g0291 |
3 | HG00544.hp2 HG01981.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.302-1899delG | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182470496 | |||||||
chr1:182470658 | T | C | 1 | a0002c0002t0001g0194 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.302-1738T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182470658 | |||||||
chr1:182470690 | T | C | 69 | a0003c0003t0001g0017 a0003c0003t0001g0030 a0003c0003t0001g0039 others(66): Show |
72 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.302-1706T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182470690 | |||||||
chr1:182470786 | T | C | 69 | a0003c0003t0001g0017 a0003c0003t0001g0030 a0003c0003t0001g0039 others(66): Show |
72 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.302-1610T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182470786 | |||||||
chr1:182471172 | A | G | 2 | a0002c0002t0001g0194 a0002c0002t0001g0195 |
2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.302-1224A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182471172 | |||||||
chr1:182471311 | C | A | 1 | a0017c0023t0001g0139 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.302-1085C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182471311 | |||||||
chr1:182471338 | G | C | 1 | a0001c0001t0001g0236 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.302-1058G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182471338 | |||||||
chr1:182471580 | C | T | 6 | a0001c0004t0001g0005 a0001c0004t0001g0102 a0001c0004t0001g0106 others(3): Show |
7 | HG01099.hp2 HG01109.hp1 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.302-816C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182471580 | |||||||
chr1:182471619 | T | C | 115 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0015 others(112): Show |
120 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.302-777T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182471619 | |||||||
chr1:182471719 | C | G | 1 | a0002c0002t0001g0288 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.302-677C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182471719 | |||||||
chr1:182471728 | C | T | 1 | a0001c0001t0001g0243 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.302-668C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182471728 | |||||||
chr1:182471788 | G | C | 4 | a0002c0002t0001g0140 a0002c0002t0001g0141 a0002c0002t0001g0142 others(1): Show |
4 | NA18978.hp2 NA19011.hp2 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.302-608G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182471788 | |||||||
chr1:182471865 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.302-531C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182471865 | |||||||
chr1:182471912 | G | T | 4 | a0003c0003t0001g0052 a0003c0003t0001g0160 a0003c0003t0001g0161 others(1): Show |
4 | NA18951.hp2 NA18952.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.302-484G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182471912 | |||||||
chr1:182471954 | C | T | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.302-442C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182471954 | |||||||
chr1:182471970 | C | A | 8 | a0001c0001t0001g0146 a0001c0001t0001g0196 a0001c0001t0001g0197 others(5): Show |
8 | HG01069.hp1 HG02055.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.302-426C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182471970 | |||||||
chr1:182472063 | G | GT | 71 | a0002c0002t0001g0195 a0003c0003t0001g0017 a0003c0003t0001g0030 others(68): Show |
74 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.302-326dupT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr1 | 182472063 | ||||||
chr1:182472140 | C | T | 1 | a0003c0003t0002g0217 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.302-256C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182472140 | |||||||
chr1:182472232 | C | T | 9 | a0001c0001t0001g0173 a0001c0001t0001g0175 a0001c0001t0001g0176 others(6): Show |
9 | HG01884.hp2 HG02258.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.302-164C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182472232 | |||||||
chr1:182472311 | G | A | 69 | a0003c0003t0001g0017 a0003c0003t0001g0030 a0003c0003t0001g0039 others(66): Show |
72 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.302-85G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 4/21 | chr1 | 182472311 | |||||||
chr1:182472676 | A | G | 1 | a0002c0002t0001g0117 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.463+119A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 5/21 | chr1 | 182472676 | |||||||
chr1:182472700 | C | A | 67 | a0003c0003t0001g0017 a0003c0003t0001g0030 a0003c0003t0001g0039 others(64): Show |
70 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.463+143C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 5/21 | chr1 | 182472700 | |||||||
chr1:182472797 | C | G | 43 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0015 others(40): Show |
45 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.463+240C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 5/21 | chr1 | 182472797 | |||||||
chr1:182473066 | G | C | 69 | a0003c0003t0001g0017 a0003c0003t0001g0030 a0003c0003t0001g0039 others(66): Show |
72 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.463+509G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 5/21 | chr1 | 182473066 | |||||||
chr1:182473128 | G | T | 1 | a0002c0002t0001g0119 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.464-447G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 5/21 | chr1 | 182473128 | |||||||
chr1:182473375 | T | C | 3 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0005t0001g0011 |
3 | HG02922.hp1 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.464-200T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 5/21 | chr1 | 182473375 | |||||||
chr1:182474625 | G | A | 3 | a0001c0001t0001g0114 a0001c0001t0001g0182 a0012c0019t0001g0216 |
3 | HG01243.hp2 HG01346.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1431+83G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182474625 | |||||||
chr1:182475076 | A | G | 6 | a0001c0006t0001g0137 a0001c0006t0001g0138 a0001c0006t0001g0206 others(3): Show |
6 | HG01891.hp1 HG02559.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1431+534A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182475076 | |||||||
chr1:182475435 | T | C | 2 | a0003c0003t0001g0209 a0003c0024t0001g0105 |
2 | HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1431+893T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182475435 | |||||||
chr1:182475439 | T | C | 1 | a0001c0004t0001g0129 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1431+897T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182475439 | |||||||
chr1:182475491 | G | T | 1 | a0001c0004t0001g0126 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1431+949G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182475491 | |||||||
chr1:182475610 | G | A | 1 | a0003c0003t0002g0060 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1431+1068G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182475610 | |||||||
chr1:182475695 | CCATCTCC others(13): Show |
C | 36 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0015 others(33): Show |
38 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.1431+1159_1431+117 others(24): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr1 | 182475695 | ||||||
chr1:182475867 | C | T | 2 | a0003c0003t0001g0051 a0003c0003t0001g0294 |
2 | NA18954.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.1431+1325C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182475867 | |||||||
chr1:182475869 | T | A | 69 | a0003c0003t0001g0017 a0003c0003t0001g0030 a0003c0003t0001g0039 others(66): Show |
72 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.1431+1327T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182475869 | |||||||
chr1:182476153 | C | G | 4 | a0001c0001t0001g0114 a0001c0001t0001g0182 a0002c0002t0001g0084 others(1): Show |
4 | HG01243.hp2 HG01346.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1431+1611C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182476153 | |||||||
chr1:182476377 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1431+1835A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182476377 | |||||||
chr1:182476394 | C | T | 9 | a0001c0001t0001g0173 a0001c0001t0001g0175 a0001c0001t0001g0176 others(6): Show |
9 | HG01884.hp2 HG02258.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1431+1852C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182476394 | |||||||
chr1:182476762 | C | T | 1 | a0001c0004t0001g0220 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1431+2220C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182476762 | |||||||
chr1:182476962 | C | A | 69 | a0003c0003t0001g0017 a0003c0003t0001g0030 a0003c0003t0001g0039 others(66): Show |
72 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.1431+2420C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182476962 | |||||||
chr1:182477053 | G | T | 33 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(30): Show |
34 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1431+2511G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182477053 | |||||||
chr1:182477059 | G | A | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1431+2517G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182477059 | |||||||
chr1:182477080 | C | A | 40 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0015 others(37): Show |
42 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1431+2538C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182477080 | |||||||
chr1:182477221 | G | A | 180 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(177): Show |
186 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.1431+2679G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182477221 | |||||||
chr1:182477361 | A | G | 180 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(177): Show |
186 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.1431+2819A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182477361 | |||||||
chr1:182477383 | T | C | 3 | a0001c0001t0001g0184 a0001c0001t0001g0268 a0001c0005t0001g0267 |
3 | HG02109.hp2 HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1431+2841T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182477383 | |||||||
chr1:182477390 | G | A | 1 | a0001c0001t0001g0048 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1431+2848G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182477390 | |||||||
chr1:182477446 | T | C | 69 | a0003c0003t0001g0017 a0003c0003t0001g0030 a0003c0003t0001g0039 others(66): Show |
72 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.1431+2904T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182477446 | |||||||
chr1:182477448 | G | A | 36 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(33): Show |
37 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.1431+2906G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182477448 | |||||||
chr1:182477743 | C | T | 1 | a0001c0005t0001g0134 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1431+3201C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182477743 | |||||||
chr1:182477883 | G | A | 67 | a0003c0003t0001g0017 a0003c0003t0001g0030 a0003c0003t0001g0039 others(64): Show |
70 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.1431+3341G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182477883 | |||||||
chr1:182477975 | C | A | 2 | a0001c0004t0001g0181 a0004c0009t0001g0265 |
2 | HG01891.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1431+3433C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182477975 | |||||||
chr1:182478039 | A | T | 67 | a0003c0003t0001g0017 a0003c0003t0001g0030 a0003c0003t0001g0039 others(64): Show |
70 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.1431+3497A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182478039 | |||||||
chr1:182478125 | C | G | 1 | a0003c0003t0002g0309 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1431+3583C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182478125 | |||||||
chr1:182478125 | C | T | 11 | a0001c0001t0001g0114 a0001c0001t0001g0173 a0001c0001t0001g0175 others(8): Show |
11 | HG01243.hp2 HG01346.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.1431+3583C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182478125 | |||||||
chr1:182478319 | C | A | 67 | a0003c0003t0001g0017 a0003c0003t0001g0030 a0003c0003t0001g0039 others(64): Show |
70 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.1431+3777C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182478319 | |||||||
chr1:182478653 | A | G | 2 | a0003c0003t0001g0209 a0003c0024t0001g0105 |
2 | HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1431+4111A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182478653 | |||||||
chr1:182478708 | A | G | 6 | a0001c0006t0001g0137 a0001c0006t0001g0138 a0001c0006t0001g0206 others(3): Show |
6 | HG01891.hp1 HG02559.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1431+4166A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182478708 | |||||||
chr1:182478877 | G | A | 113 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0015 others(110): Show |
118 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.1431+4335G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182478877 | |||||||
chr1:182478932 | A | G | 2 | a0003c0003t0001g0118 a0014c0014t0001g0174 |
2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1431+4390A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182478932 | |||||||
chr1:182479023 | A | T | 1 | a0001c0001t0001g0146 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1431+4481A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182479023 | |||||||
chr1:182479056 | G | T | 1 | a0001c0001t0001g0244 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1431+4514G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182479056 | |||||||
chr1:182479146 | G | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0015 others(127): Show |
135 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.1431+4604G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182479146 | |||||||
chr1:182479566 | C | T | 1 | a0002c0002t0001g0318 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1431+5024C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182479566 | |||||||
chr1:182479667 | C | T | 10 | a0001c0004t0001g0093 a0001c0004t0001g0283 a0001c0004t0001g0284 others(7): Show |
10 | HG00423.hp2 NA18941.hp1 NA18965.hp1 others(7): Show |
intron_variant | MODIFIER | c.1431+5125C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182479667 | |||||||
chr1:182479768 | G | A | 1 | a0001c0007t0001g0021 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1431+5226G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182479768 | |||||||
chr1:182480080 | A | G | 1 | a0002c0002t0001g0097 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1431+5538A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182480080 | |||||||
chr1:182480114 | G | T | 1 | a0001c0004t0001g0010 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1431+5572G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182480114 | |||||||
chr1:182480207 | C | T | 1 | a0004c0009t0001g0260 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1431+5665C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182480207 | |||||||
chr1:182480285 | G | T | 65 | a0003c0003t0001g0017 a0003c0003t0001g0030 a0003c0003t0001g0039 others(62): Show |
68 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.1431+5743G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182480285 | |||||||
chr1:182480460 | G | GT | 70 | a0001c0001t0001g0258 a0001c0001t0001g0272 a0003c0003t0001g0017 others(67): Show |
73 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.1431+5933dupT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr1 | 182480460 | ||||||
chr1:182480486 | C | T | 2 | a0003c0003t0001g0209 a0003c0024t0001g0105 |
2 | HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1431+5944C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182480486 | |||||||
chr1:182480516 | C | T | 67 | a0003c0003t0001g0017 a0003c0003t0001g0030 a0003c0003t0001g0039 others(64): Show |
70 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.1431+5974C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182480516 | |||||||
chr1:182480646 | G | T | 67 | a0003c0003t0001g0017 a0003c0003t0001g0030 a0003c0003t0001g0039 others(64): Show |
70 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.1431+6104G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182480646 | |||||||
chr1:182481210 | TA | T | 114 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0015 others(111): Show |
119 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.1431+6676delA | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr1 | 182481210 | ||||||
chr1:182481241 | A | G | 36 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(33): Show |
37 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.1431+6699A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182481241 | |||||||
chr1:182481487 | C | T | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1432-6798C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182481487 | |||||||
chr1:182481488 | G | A | 33 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(30): Show |
34 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1432-6797G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182481488 | |||||||
chr1:182481715 | G | C | 6 | a0001c0001t0001g0146 a0001c0001t0001g0196 a0001c0001t0001g0197 others(3): Show |
6 | HG01069.hp1 HG02055.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1432-6570G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182481715 | |||||||
chr1:182481742 | C | T | 1 | a0003c0003t0001g0049 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1432-6543C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182481742 | |||||||
chr1:182481754 | G | GGGA | 181 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(178): Show |
187 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.1432-6530_1432-652 others(7): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr1 | 182481754 | ||||||
chr1:182481930 | G | A | 2 | a0003c0003t0001g0209 a0003c0024t0001g0105 |
2 | HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1432-6355G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182481930 | |||||||
chr1:182482355 | A | G | 318 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(315): Show |
327 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(324): Show |
intron_variant | MODIFIER | c.1432-5930A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182482355 | |||||||
chr1:182482390 | T | C | 1 | a0001c0005t0001g0134 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1432-5895T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182482390 | |||||||
chr1:182482410 | T | TA | 38 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(35): Show |
39 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.1432-5867dupA | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr1 | 182482410 | ||||||
chr1:182482551 | G | A | 67 | a0003c0003t0001g0017 a0003c0003t0001g0030 a0003c0003t0001g0039 others(64): Show |
70 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.1432-5734G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182482551 | |||||||
chr1:182482681 | T | C | 67 | a0003c0003t0001g0017 a0003c0003t0001g0030 a0003c0003t0001g0039 others(64): Show |
70 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.1432-5604T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182482681 | |||||||
chr1:182482704 | A | T | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1432-5581A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182482704 | |||||||
chr1:182482886 | G | A | 114 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0015 others(111): Show |
119 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.1432-5399G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182482886 | |||||||
chr1:182483103 | C | A | 1 | a0001c0006t0001g0137 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1432-5182C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182483103 | |||||||
chr1:182483152 | G | A | 1 | a0001c0001t0001g0310 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1432-5133G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182483152 | |||||||
chr1:182483194 | G | A | 131 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0015 others(128): Show |
136 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.1432-5091G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182483194 | |||||||
chr1:182483227 | G | A | 67 | a0003c0003t0001g0017 a0003c0003t0001g0030 a0003c0003t0001g0039 others(64): Show |
70 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.1432-5058G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182483227 | |||||||
chr1:182483371 | A | G | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1432-4914A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182483371 | |||||||
chr1:182483501 | A | G | 1 | a0001c0004t0001g0282 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1432-4784A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182483501 | |||||||
chr1:182483548 | A | G | 67 | a0003c0003t0001g0017 a0003c0003t0001g0030 a0003c0003t0001g0039 others(64): Show |
70 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.1432-4737A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182483548 | |||||||
chr1:182483551 | C | T | 6 | a0001c0006t0001g0137 a0001c0006t0001g0138 a0001c0006t0001g0206 others(3): Show |
6 | HG01891.hp1 HG02559.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1432-4734C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182483551 | |||||||
chr1:182483694 | A | G | 3 | a0001c0001t0001g0042 a0001c0001t0001g0147 a0001c0001t0001g0246 |
3 | HG02040.hp2 HG02155.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.1432-4591A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182483694 | |||||||
chr1:182483702 | T | C | 1 | a0001c0001t0001g0304 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1432-4583T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182483702 | |||||||
chr1:182483768 | G | A | 1 | a0001c0005t0001g0270 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1432-4517G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182483768 | |||||||
chr1:182483978 | G | T | 47 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0015 others(44): Show |
49 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.1432-4307G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182483978 | |||||||
chr1:182484122 | T | C | 2 | a0003c0003t0001g0051 a0003c0003t0001g0294 |
2 | NA18954.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.1432-4163T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182484122 | |||||||
chr1:182484360 | A | C | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1432-3925A>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182484360 | |||||||
chr1:182484389 | G | A | 1 | a0001c0004t0001g0324 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1432-3896G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182484389 | |||||||
chr1:182484412 | G | A | 53 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0015 others(50): Show |
55 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.1432-3873G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182484412 | |||||||
chr1:182484484 | C | G | 1 | a0003c0003t0001g0161 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1432-3801C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182484484 | |||||||
chr1:182484498 | G | A | 52 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0015 others(49): Show |
54 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.1432-3787G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182484498 | |||||||
chr1:182484530 | A | G | 5 | a0003c0003t0001g0166 a0003c0003t0001g0168 a0003c0003t0002g0002 others(2): Show |
7 | HG02135.hp1 NA18980.hp1 NA19010.hp2 others(4): Show |
intron_variant | MODIFIER | c.1432-3755A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182484530 | |||||||
chr1:182484550 | A | G | 1 | a0001c0001t0001g0296 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1432-3735A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182484550 | |||||||
chr1:182484784 | C | T | 119 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0015 others(116): Show |
124 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.1432-3501C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182484784 | |||||||
chr1:182484820 | C | T | 67 | a0003c0003t0001g0017 a0003c0003t0001g0030 a0003c0003t0001g0039 others(64): Show |
70 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.1432-3465C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182484820 | |||||||
chr1:182485015 | C | T | 2 | a0001c0001t0001g0135 a0001c0001t0001g0319 |
2 | HG00408.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.1432-3270C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182485015 | |||||||
chr1:182485116 | C | G | 18 | a0001c0001t0001g0086 a0001c0001t0001g0101 a0001c0001t0001g0132 others(15): Show |
18 | HG00558.hp1 HG00738.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.1432-3169C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182485116 | |||||||
chr1:182485238 | G | A | 1 | a0001c0004t0001g0178 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1432-3047G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182485238 | |||||||
chr1:182485402 | A | G | 1 | a0003c0003t0002g0250 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1432-2883A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182485402 | |||||||
chr1:182485517 | A | G | 52 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0015 others(49): Show |
54 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.1432-2768A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182485517 | |||||||
chr1:182485582 | T | C | 67 | a0003c0003t0001g0017 a0003c0003t0001g0030 a0003c0003t0001g0039 others(64): Show |
70 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.1432-2703T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182485582 | |||||||
chr1:182485609 | T | G | 52 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0015 others(49): Show |
54 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.1432-2676T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182485609 | |||||||
chr1:182485795 | T | C | 1 | a0003c0003t0001g0165 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1432-2490T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182485795 | |||||||
chr1:182485817 | G | GA | 5 | a0001c0001t0001g0184 a0001c0001t0001g0268 a0001c0005t0001g0011 others(2): Show |
5 | HG02109.hp2 HG02572.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1432-2461dupA | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr1 | 182485817 | ||||||
chr1:182485937 | T | C | 36 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0015 others(33): Show |
38 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.1432-2348T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182485937 | |||||||
chr1:182486036 | C | T | 1 | a0001c0004t0001g0247 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1432-2249C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182486036 | |||||||
chr1:182486195 | C | T | 119 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0015 others(116): Show |
124 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.1432-2090C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182486195 | |||||||
chr1:182486285 | C | G | 2 | a0003c0003t0001g0118 a0014c0014t0001g0174 |
2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1432-2000C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182486285 | |||||||
chr1:182486310 | A | AT | 7 | a0001c0001t0001g0115 a0001c0001t0001g0184 a0001c0001t0001g0268 others(4): Show |
7 | HG02109.hp2 HG02257.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1432-1957dupT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr1 | 182486310 | ||||||
chr1:182486310 | AT | A | 20 | a0001c0001t0001g0042 a0001c0001t0001g0103 a0001c0001t0001g0114 others(17): Show |
20 | HG01243.hp2 HG01346.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.1432-1957delT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr1 | 182486310 | ||||||
chr1:182486398 | T | C | 8 | a0001c0001t0001g0173 a0001c0001t0001g0175 a0001c0001t0001g0176 others(5): Show |
8 | HG01884.hp2 HG02451.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1432-1887T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182486398 | |||||||
chr1:182486553 | G | A | 1 | a0001c0005t0001g0134 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1432-1732G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182486553 | |||||||
chr1:182486758 | C | T | 52 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0015 others(49): Show |
54 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.1432-1527C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182486758 | |||||||
chr1:182486762 | G | A | 8 | a0001c0001t0001g0173 a0001c0001t0001g0175 a0001c0001t0001g0176 others(5): Show |
8 | HG01884.hp2 HG02451.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1432-1523G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182486762 | |||||||
chr1:182486783 | C | G | 2 | a0001c0001t0001g0066 a0001c0001t0001g0273 |
2 | NA18944.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.1432-1502C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182486783 | |||||||
chr1:182486785 | C | T | 8 | a0001c0001t0001g0173 a0001c0001t0001g0175 a0001c0001t0001g0176 others(5): Show |
8 | HG01884.hp2 HG02451.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1432-1500C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182486785 | |||||||
chr1:182486994 | C | A | 7 | a0001c0001t0001g0146 a0001c0001t0001g0196 a0001c0001t0001g0197 others(4): Show |
7 | HG01069.hp1 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1432-1291C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182486994 | |||||||
chr1:182487002 | G | T | 7 | a0001c0001t0001g0146 a0001c0001t0001g0196 a0001c0001t0001g0197 others(4): Show |
7 | HG01069.hp1 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1432-1283G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182487002 | |||||||
chr1:182487012 | G | C | 7 | a0001c0001t0001g0146 a0001c0001t0001g0196 a0001c0001t0001g0197 others(4): Show |
7 | HG01069.hp1 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1432-1273G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182487012 | |||||||
chr1:182487288 | T | A | 50 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0015 others(47): Show |
52 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.1432-997T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182487288 | |||||||
chr1:182487312 | T | C | 9 | a0001c0001t0001g0146 a0001c0001t0001g0196 a0001c0001t0001g0197 others(6): Show |
9 | HG01069.hp1 HG02055.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1432-973T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182487312 | |||||||
chr1:182487485 | T | C | 1 | a0001c0005t0001g0134 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1432-800T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182487485 | |||||||
chr1:182487712 | A | G | 4 | a0002c0002t0001g0003 a0002c0002t0001g0004 a0002c0002t0001g0080 others(1): Show |
6 | NA18951.hp1 NA18977.hp1 NA18982.hp2 others(3): Show |
intron_variant | MODIFIER | c.1432-573A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182487712 | |||||||
chr1:182487717 | C | T | 28 | a0003c0003t0001g0039 a0003c0003t0001g0043 a0003c0003t0001g0047 others(25): Show |
28 | HG00280.hp1 HG00544.hp2 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.1432-568C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182487717 | |||||||
chr1:182487742 | A | G | 1 | a0003c0003t0001g0158 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1432-543A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182487742 | |||||||
chr1:182487807 | A | G | 52 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0015 others(49): Show |
54 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.1432-478A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182487807 | |||||||
chr1:182487812 | T | C | 67 | a0003c0003t0001g0017 a0003c0003t0001g0030 a0003c0003t0001g0039 others(64): Show |
70 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.1432-473T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182487812 | |||||||
chr1:182487894 | G | T | 52 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0015 others(49): Show |
54 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.1432-391G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182487894 | |||||||
chr1:182488147 | T | C | 1 | a0001c0001t0001g0192 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1432-138T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 6/21 | chr1 | 182488147 | |||||||
chr1:182488466 | ACCAAAGA others(4): Show |
A | 3 | a0001c0001t0001g0200 a0001c0001t0001g0271 a0001c0005t0001g0270 |
3 | HG02630.hp1 HG02647.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1494+121_1494+131d others(13): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr1 | 182488466 | ||||||
chr1:182488486 | C | G | 1 | a0003c0003t0002g0063 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1494+139C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 7/21 | chr1 | 182488486 | |||||||
chr1:182488582 | C | T | 1 | a0001c0005t0001g0134 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1494+235C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 7/21 | chr1 | 182488582 | |||||||
chr1:182488642 | T | C | 52 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0015 others(49): Show |
54 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.1494+295T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 7/21 | chr1 | 182488642 | |||||||
chr1:182488659 | G | T | 1 | a0002c0002t0001g0083 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1494+312G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 7/21 | chr1 | 182488659 | |||||||
chr1:182488725 | C | CA | 36 | a0001c0001t0001g0053 a0001c0001t0001g0146 a0001c0001t0001g0147 others(33): Show |
38 | HG00280.hp2 HG00438.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.1495-232dupA | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr1 | 182488725 | ||||||
chr1:182488725 | C | CAAAAAAA others(9): Show |
2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1495-247_1495-232d others(18): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr1 | 182488725 | ||||||
chr1:182488725 | CAAAAAAA | C | 6 | a0001c0006t0001g0137 a0001c0006t0001g0138 a0001c0006t0001g0206 others(3): Show |
6 | HG01891.hp1 HG02559.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1495-238_1495-232d others(9): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr1 | 182488725 | ||||||
chr1:182488725 | CAAAAAAA others(3): Show |
C | 4 | a0001c0001t0001g0184 a0001c0001t0001g0268 a0001c0005t0001g0113 others(1): Show |
4 | HG02109.hp2 HG02572.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1495-241_1495-232d others(12): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr1 | 182488725 | ||||||
chr1:182488725 | CAAAAAAA others(5): Show |
C | 2 | a0003c0003t0001g0209 a0003c0024t0001g0105 |
2 | HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1495-243_1495-232d others(14): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr1 | 182488725 | ||||||
chr1:182488824 | G | T | 1 | a0001c0004t0001g0212 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1495-156G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 7/21 | chr1 | 182488824 | |||||||
chr1:182489382 | C | T | 1 | a0002c0002t0001g0164 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1717+180C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 8/21 | chr1 | 182489382 | |||||||
chr1:182489625 | C | T | 5 | a0001c0001t0001g0184 a0001c0001t0001g0268 a0001c0005t0001g0011 others(2): Show |
5 | HG02109.hp2 HG02572.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1717+423C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 8/21 | chr1 | 182489625 | |||||||
chr1:182489641 | C | T | 9 | a0001c0001t0001g0146 a0001c0001t0001g0196 a0001c0001t0001g0197 others(6): Show |
9 | HG01069.hp1 HG02055.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1717+439C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 8/21 | chr1 | 182489641 | |||||||
chr1:182489643 | C | T | 1 | a0004c0009t0001g0265 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1717+441C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 8/21 | chr1 | 182489643 | |||||||
chr1:182489720 | C | T | 24 | a0001c0004t0001g0010 a0001c0004t0001g0023 a0001c0004t0001g0044 others(21): Show |
24 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.1717+518C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 8/21 | chr1 | 182489720 | |||||||
chr1:182489742 | T | C | 5 | a0001c0001t0001g0146 a0001c0001t0001g0196 a0001c0001t0001g0197 others(2): Show |
5 | HG01069.hp1 HG02055.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1717+540T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 8/21 | chr1 | 182489742 | |||||||
chr1:182489828 | T | A | 1 | a0001c0005t0001g0134 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1717+626T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 8/21 | chr1 | 182489828 | |||||||
chr1:182490455 | G | A | 1 | a0001c0004t0001g0087 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1717+1253G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 8/21 | chr1 | 182490455 | |||||||
chr1:182490484 | G | A | 1 | a0005c0008t0001g0014 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1717+1282G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 8/21 | chr1 | 182490484 | |||||||
chr1:182490670 | G | A | 7 | a0001c0001t0001g0104 a0001c0001t0001g0185 a0001c0001t0001g0200 others(4): Show |
7 | HG02145.hp1 HG02615.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1717+1468G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 8/21 | chr1 | 182490670 | |||||||
chr1:182490915 | C | CT | 190 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(187): Show |
194 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.1717+1731dupT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr1 | 182490915 | ||||||
chr1:182490915 | C | CTT | 111 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0031 others(108): Show |
116 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.1717+1730_1717+173 others(6): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr1 | 182490915 | ||||||
chr1:182491042 | C | A | 36 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0015 others(33): Show |
38 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.1717+1840C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 8/21 | chr1 | 182491042 | |||||||
chr1:182491057 | A | AT | 15 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0132 others(12): Show |
15 | HG01884.hp1 HG02145.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.1717+1867dupT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr1 | 182491057 | ||||||
chr1:182491318 | C | T | 10 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0185 others(7): Show |
10 | HG01884.hp1 HG02145.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1718-1704C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 8/21 | chr1 | 182491318 | |||||||
chr1:182491319 | A | G | 10 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0185 others(7): Show |
10 | HG01884.hp1 HG02145.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1718-1703A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 8/21 | chr1 | 182491319 | |||||||
chr1:182491411 | C | T | 1 | a0001c0005t0001g0113 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1718-1611C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 8/21 | chr1 | 182491411 | |||||||
chr1:182491490 | C | T | 1 | a0001c0005t0001g0134 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1718-1532C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 8/21 | chr1 | 182491490 | |||||||
chr1:182491685 | GTGA | G | 103 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0015 others(100): Show |
108 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.1718-1318_1718-131 others(7): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr1 | 182491685 | ||||||
chr1:182491727 | C | G | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1718-1295C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 8/21 | chr1 | 182491727 | |||||||
chr1:182491751 | A | T | 11 | a0001c0001t0001g0114 a0001c0001t0001g0173 a0001c0001t0001g0175 others(8): Show |
11 | HG01243.hp2 HG01346.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.1718-1271A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 8/21 | chr1 | 182491751 | |||||||
chr1:182491808 | A | G | 1 | a0004c0012t0001g0325 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1718-1214A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 8/21 | chr1 | 182491808 | |||||||
chr1:182491831 | GA | G | 10 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0185 others(7): Show |
10 | HG01884.hp1 HG02145.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1718-1189delA | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr1 | 182491831 | ||||||
chr1:182491852 | A | G | 103 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0015 others(100): Show |
108 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.1718-1170A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 8/21 | chr1 | 182491852 | |||||||
chr1:182492215 | T | C | 1 | a0001c0001t0001g0237 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1718-807T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 8/21 | chr1 | 182492215 | |||||||
chr1:182492320 | G | C | 1 | a0003c0003t0001g0116 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1718-702G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 8/21 | chr1 | 182492320 | |||||||
chr1:182492328 | A | G | 1 | a0001c0001t0001g0242 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1718-694A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 8/21 | chr1 | 182492328 | |||||||
chr1:182492483 | A | G | 2 | a0003c0003t0001g0209 a0003c0024t0001g0105 |
2 | HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1718-539A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 8/21 | chr1 | 182492483 | |||||||
chr1:182492531 | A | G | 181 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(178): Show |
187 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.1718-491A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 8/21 | chr1 | 182492531 | |||||||
chr1:182492628 | C | CT | 142 | a0001c0001t0001g0103 a0001c0001t0001g0205 a0001c0004t0001g0005 others(139): Show |
145 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.1718-380dupT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr1 | 182492628 | ||||||
chr1:182492704 | C | G | 2 | a0003c0003t0001g0209 a0003c0024t0001g0105 |
2 | HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1718-318C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 8/21 | chr1 | 182492704 | |||||||
chr1:182492773 | C | T | 1 | a0001c0001t0001g0031 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1718-249C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 8/21 | chr1 | 182492773 | |||||||
chr1:182493509 | A | C | 3 | a0001c0001t0001g0198 a0001c0005t0001g0326 a0001c0005t0001g0329 |
3 | HG02055.hp2 HG03130.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1825+380A>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182493509 | |||||||
chr1:182494110 | C | T | 1 | a0002c0002t0001g0070 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1825+981C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182494110 | |||||||
chr1:182494190 | G | C | 5 | a0001c0001t0001g0184 a0001c0001t0001g0268 a0001c0005t0001g0011 others(2): Show |
5 | HG02109.hp2 HG02572.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1825+1061G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182494190 | |||||||
chr1:182494309 | C | T | 1 | a0001c0005t0001g0134 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1825+1180C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182494309 | |||||||
chr1:182494373 | C | T | 1 | a0001c0005t0001g0011 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1825+1244C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182494373 | |||||||
chr1:182494548 | A | G | 2 | a0003c0003t0001g0157 a0003c0003t0001g0229 |
2 | NA18950.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.1825+1419A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182494548 | |||||||
chr1:182494580 | A | T | 1 | a0001c0001t0001g0298 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1825+1451A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182494580 | |||||||
chr1:182494740 | C | T | 1 | a0003c0024t0001g0105 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1825+1611C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182494740 | |||||||
chr1:182494769 | T | C | 103 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0015 others(100): Show |
108 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.1825+1640T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182494769 | |||||||
chr1:182494869 | A | C | 2 | a0003c0003t0001g0209 a0003c0024t0001g0105 |
2 | HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1825+1740A>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182494869 | |||||||
chr1:182494973 | A | G | 8 | a0001c0001t0001g0173 a0001c0001t0001g0175 a0001c0001t0001g0176 others(5): Show |
8 | HG01884.hp2 HG02451.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1825+1844A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182494973 | |||||||
chr1:182495107 | G | T | 6 | a0003c0003t0002g0006 a0003c0003t0002g0018 a0003c0003t0002g0214 others(3): Show |
7 | HG00639.hp1 HG01069.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1825+1978G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182495107 | |||||||
chr1:182495394 | A | G | 1 | a0001c0001t0001g0248 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1825+2265A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182495394 | |||||||
chr1:182495461 | T | G | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1825+2332T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182495461 | |||||||
chr1:182495524 | T | C | 7 | a0001c0001t0001g0146 a0001c0001t0001g0196 a0001c0001t0001g0197 others(4): Show |
7 | HG01069.hp1 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1825+2395T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182495524 | |||||||
chr1:182495623 | G | A | 1 | a0005c0008t0001g0014 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1825+2494G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182495623 | |||||||
chr1:182495776 | T | C | 3 | a0001c0001t0001g0114 a0001c0001t0001g0182 a0012c0019t0001g0216 |
3 | HG01243.hp2 HG01346.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1825+2647T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182495776 | |||||||
chr1:182496143 | G | T | 2 | a0001c0001t0001g0238 a0001c0001t0001g0277 |
2 | HG01258.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.1825+3014G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182496143 | |||||||
chr1:182496329 | T | C | 5 | a0001c0001t0001g0184 a0001c0001t0001g0268 a0001c0005t0001g0011 others(2): Show |
5 | HG02109.hp2 HG02572.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1825+3200T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182496329 | |||||||
chr1:182496517 | C | T | 1 | a0001c0007t0001g0210 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1825+3388C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182496517 | |||||||
chr1:182496615 | T | A | 7 | a0001c0001t0001g0146 a0001c0001t0001g0196 a0001c0001t0001g0197 others(4): Show |
7 | HG01069.hp1 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1825+3486T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182496615 | |||||||
chr1:182496762 | A | G | 6 | a0001c0006t0001g0137 a0001c0006t0001g0138 a0001c0006t0001g0206 others(3): Show |
6 | HG01891.hp1 HG02559.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1825+3633A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182496762 | |||||||
chr1:182496865 | C | A | 36 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0015 others(33): Show |
38 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.1825+3736C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182496865 | |||||||
chr1:182496882 | C | T | 3 | a0001c0006t0001g0206 a0001c0006t0001g0207 a0001c0006t0001g0208 |
3 | HG01891.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1825+3753C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182496882 | |||||||
chr1:182496888 | CCTTT | C | 224 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(221): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.1825+3764_1825+376 others(8): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182496888 | ||||||
chr1:182496904 | T | G | 5 | a0001c0001t0001g0184 a0001c0001t0001g0268 a0001c0005t0001g0011 others(2): Show |
5 | HG02109.hp2 HG02572.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1825+3775T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182496904 | |||||||
chr1:182497179 | G | C | 30 | a0001c0004t0001g0010 a0001c0004t0001g0023 a0001c0004t0001g0044 others(27): Show |
30 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.1825+4050G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182497179 | |||||||
chr1:182497224 | TAGAA | T | 15 | a0001c0001t0001g0146 a0001c0001t0001g0184 a0001c0001t0001g0196 others(12): Show |
15 | HG01069.hp1 HG01074.hp2 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.1825+4099_1825+410 others(8): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182497224 | ||||||
chr1:182497228 | A | T | 209 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(206): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.1825+4099A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182497228 | |||||||
chr1:182497228 | AAGAT | A | 39 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0015 others(36): Show |
41 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.1825+4121_1825+412 others(8): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182497228 | ||||||
chr1:182497232 | T | A | 209 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(206): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.1825+4103T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182497232 | |||||||
chr1:182497236 | T | A | 15 | a0001c0001t0001g0146 a0001c0001t0001g0184 a0001c0001t0001g0196 others(12): Show |
15 | HG01069.hp1 HG01074.hp2 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.1825+4107T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182497236 | |||||||
chr1:182497267 | ATG | A | 4 | a0001c0001t0001g0103 a0001c0001t0001g0205 a0006c0011t0001g0186 others(1): Show |
4 | HG01884.hp1 HG02965.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1825+4151_1825+415 others(6): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182497267 | ||||||
chr1:182497316 | GATATATA others(40): Show |
G | 1 | a0003c0003t0002g0111 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1825+4198_1825+424 others(51): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182497316 | ||||||
chr1:182497326 | T | TTA | 8 | a0001c0001t0001g0173 a0001c0001t0001g0175 a0001c0001t0001g0176 others(5): Show |
8 | HG01884.hp2 HG02451.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1825+4209_1825+421 others(6): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182497326 | ||||||
chr1:182497436 | G | A | 1 | a0001c0004t0001g0010 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1825+4307G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182497436 | |||||||
chr1:182497478 | A | AG | 5 | a0001c0001t0001g0053 a0001c0001t0001g0135 a0001c0001t0001g0148 others(2): Show |
5 | HG00408.hp1 HG02135.hp2 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.1825+4350dupG | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182497478 | ||||||
chr1:182497556 | G | T | 1 | a0003c0003t0002g0133 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1825+4427G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182497556 | |||||||
chr1:182497706 | C | T | 1 | a0003c0003t0002g0027 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1825+4577C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182497706 | |||||||
chr1:182497706 | CTT | C | 3 | a0001c0007t0001g0021 a0001c0007t0001g0022 a0001c0007t0001g0210 |
3 | HG02965.hp1 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1825+4580_1825+458 others(6): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182497706 | ||||||
chr1:182497783 | C | T | 1 | a0001c0001t0001g0042 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1825+4654C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182497783 | |||||||
chr1:182497828 | T | C | 2 | a0001c0001t0001g0103 a0001c0001t0001g0205 |
2 | HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1825+4699T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182497828 | |||||||
chr1:182498082 | T | G | 2 | a0003c0003t0001g0209 a0003c0024t0001g0105 |
2 | HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1825+4953T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182498082 | |||||||
chr1:182498265 | A | G | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1825+5136A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182498265 | |||||||
chr1:182498308 | T | TGTATATG others(12): Show |
188 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(185): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.1825+5180_1825+519 others(23): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182498308 | ||||||
chr1:182498309 | G | GTATATGC others(12): Show |
2 | a0001c0004t0001g0112 a0001c0004t0001g0130 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1825+5182_1825+520 others(23): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182498309 | ||||||
chr1:182498363 | C | A | 1 | a0001c0005t0001g0134 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1825+5234C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182498363 | |||||||
chr1:182498566 | C | T | 1 | a0002c0002t0001g0136 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1825+5437C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182498566 | |||||||
chr1:182498732 | A | G | 224 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(221): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.1825+5603A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182498732 | |||||||
chr1:182498796 | G | GT | 195 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(192): Show |
199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.1825+5670dupT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182498796 | ||||||
chr1:182498796 | G | GTT | 16 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0199 others(13): Show |
16 | HG01069.hp1 HG01891.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.1825+5669_1825+567 others(6): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182498796 | ||||||
chr1:182498800 | G | T | 222 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(219): Show |
226 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.1825+5671G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182498800 | |||||||
chr1:182498949 | C | A | 10 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0185 others(7): Show |
10 | HG01884.hp1 HG02145.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1825+5820C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182498949 | |||||||
chr1:182499158 | G | A | 3 | a0001c0001t0001g0114 a0001c0001t0001g0182 a0012c0019t0001g0216 |
3 | HG01243.hp2 HG01346.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1825+6029G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182499158 | |||||||
chr1:182499204 | T | G | 10 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0185 others(7): Show |
10 | HG01884.hp1 HG02145.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1825+6075T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182499204 | |||||||
chr1:182499250 | G | T | 1 | a0001c0005t0001g0011 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1825+6121G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182499250 | |||||||
chr1:182499296 | G | T | 1 | a0003c0003t0002g0063 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1825+6167G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182499296 | |||||||
chr1:182499316 | G | A | 8 | a0001c0001t0001g0173 a0001c0001t0001g0175 a0001c0001t0001g0176 others(5): Show |
8 | HG01884.hp2 HG02451.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1825+6187G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182499316 | |||||||
chr1:182499570 | T | C | 2 | a0001c0001t0001g0103 a0001c0001t0001g0205 |
2 | HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1825+6441T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182499570 | |||||||
chr1:182499634 | C | T | 2 | a0001c0001t0001g0184 a0001c0001t0001g0268 |
2 | HG02109.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1825+6505C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182499634 | |||||||
chr1:182499922 | C | T | 1 | a0001c0004t0001g0247 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1825+6793C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182499922 | |||||||
chr1:182500153 | C | A | 2 | a0001c0001t0001g0103 a0001c0001t0001g0205 |
2 | HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1825+7024C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182500153 | |||||||
chr1:182500359 | T | G | 2 | a0002c0002t0001g0059 a0002c0002t0001g0225 |
2 | HG01928.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.1825+7230T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182500359 | |||||||
chr1:182500531 | A | AT | 5 | a0001c0001t0001g0184 a0001c0001t0001g0268 a0001c0005t0001g0011 others(2): Show |
5 | HG02109.hp2 HG02572.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1825+7408dupT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182500531 | ||||||
chr1:182500604 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1825+7475G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182500604 | |||||||
chr1:182500801 | A | T | 1 | a0001c0004t0001g0275 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1825+7672A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182500801 | |||||||
chr1:182500950 | T | A | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1825+7821T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182500950 | |||||||
chr1:182501002 | C | T | 146 | a0001c0004t0001g0005 a0001c0004t0001g0010 a0001c0004t0001g0023 others(143): Show |
149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.1825+7873C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182501002 | |||||||
chr1:182501115 | T | C | 10 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0185 others(7): Show |
10 | HG01884.hp1 HG02145.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1825+7986T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182501115 | |||||||
chr1:182501245 | G | A | 1 | a0003c0003t0001g0157 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1825+8116G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182501245 | |||||||
chr1:182501245 | G | T | 262 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(259): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.1825+8116G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182501245 | |||||||
chr1:182501266 | C | CTCTT | 17 | a0001c0004t0001g0093 a0001c0004t0001g0224 a0001c0004t0001g0247 others(14): Show |
17 | HG00423.hp2 HG02027.hp2 HG02148.hp2 others(14): Show |
intron_variant | MODIFIER | c.1825+8147_1825+815 others(8): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182501266 | ||||||
chr1:182501280 | T | C | 205 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(202): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.1825+8151T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182501280 | |||||||
chr1:182501282 | TTTCTTTT others(6): Show |
T | 11 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0114 others(8): Show |
11 | HG01243.hp2 HG01346.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1825+8156_1825+816 others(17): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182501282 | ||||||
chr1:182501284 | TC | T | 193 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(190): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.1825+8156delC | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182501284 | |||||||
chr1:182501295 | CTT | C | 13 | a0001c0001t0001g0173 a0001c0001t0001g0175 a0001c0001t0001g0176 others(10): Show |
13 | HG01258.hp2 HG01884.hp2 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.1825+8171_1825+817 others(6): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182501295 | ||||||
chr1:182501300 | T | C | 180 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(177): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.1825+8171T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182501300 | |||||||
chr1:182501302 | C | T | 180 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(177): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.1825+8173C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182501302 | |||||||
chr1:182501307 | C | CT | 9 | a0003c0003t0001g0030 a0003c0003t0001g0047 a0003c0003t0001g0052 others(6): Show |
9 | HG00280.hp1 HG02280.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1825+8208dupT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182501307 | ||||||
chr1:182501307 | C | T | 13 | a0001c0001t0001g0173 a0001c0001t0001g0175 a0001c0001t0001g0176 others(10): Show |
13 | HG01258.hp2 HG01884.hp2 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.1825+8178C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182501307 | |||||||
chr1:182501307 | CT | C | 81 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(78): Show |
86 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.1825+8208delT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182501307 | ||||||
chr1:182501307 | CTT | C | 46 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0015 others(43): Show |
48 | HG00438.hp2 HG00735.hp2 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.1825+8207_1825+820 others(6): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182501307 | ||||||
chr1:182501307 | CTTT | C | 8 | a0001c0001t0001g0114 a0001c0001t0001g0182 a0001c0001t0001g0308 others(5): Show |
8 | HG00673.hp2 HG01243.hp2 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.1825+8206_1825+820 others(7): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182501307 | ||||||
chr1:182501307 | CTTTT | C | 15 | a0001c0004t0001g0093 a0001c0004t0001g0224 a0001c0004t0001g0247 others(12): Show |
15 | HG00423.hp2 HG02148.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1825+8205_1825+820 others(8): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182501307 | ||||||
chr1:182501309 | T | C | 13 | a0001c0001t0001g0173 a0001c0001t0001g0175 a0001c0001t0001g0176 others(10): Show |
13 | HG01258.hp2 HG01884.hp2 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.1825+8180T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182501309 | |||||||
chr1:182501312 | T | C | 117 | a0001c0001t0001g0091 a0001c0001t0001g0257 a0001c0004t0001g0005 others(114): Show |
119 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(116): Show |
intron_variant | MODIFIER | c.1825+8183T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182501312 | |||||||
chr1:182501313 | T | C | 61 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(58): Show |
63 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.1825+8184T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182501313 | |||||||
chr1:182501314 | T | C | 21 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0173 others(18): Show |
21 | HG01258.hp2 HG01884.hp2 HG01928.hp2 others(18): Show |
intron_variant | MODIFIER | c.1825+8185T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182501314 | |||||||
chr1:182501315 | T | C | 40 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0015 others(37): Show |
42 | HG00438.hp2 HG00735.hp2 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.1825+8186T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182501315 | |||||||
chr1:182501316 | T | C | 1 | a0001c0001t0001g0308 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1825+8187T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182501316 | |||||||
chr1:182501321 | T | C | 8 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0185 others(5): Show |
8 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1825+8192T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182501321 | |||||||
chr1:182501322 | T | C | 4 | a0001c0001t0001g0114 a0001c0001t0001g0182 a0001c0001t0001g0305 others(1): Show |
4 | HG01243.hp2 HG01346.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1825+8193T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182501322 | |||||||
chr1:182501326 | T | C | 8 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0185 others(5): Show |
8 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1825+8197T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182501326 | |||||||
chr1:182501327 | T | C | 3 | a0001c0001t0001g0114 a0001c0001t0001g0182 a0012c0019t0001g0216 |
3 | HG01243.hp2 HG01346.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1825+8198T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182501327 | |||||||
chr1:182501359 | G | A | 1 | a0001c0004t0001g0324 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1825+8230G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182501359 | |||||||
chr1:182501475 | C | A | 1 | a0002c0002t0001g0145 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1825+8346C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182501475 | |||||||
chr1:182501555 | G | C | 17 | a0001c0001t0001g0114 a0001c0001t0001g0173 a0001c0001t0001g0175 others(14): Show |
17 | HG01243.hp2 HG01346.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.1825+8426G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182501555 | |||||||
chr1:182501721 | G | A | 1 | a0001c0004t0001g0188 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1825+8592G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182501721 | |||||||
chr1:182501951 | C | A | 1 | a0001c0001t0001g0219 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1825+8822C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182501951 | |||||||
chr1:182502020 | G | T | 1 | a0001c0004t0001g0269 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1825+8891G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182502020 | |||||||
chr1:182502093 | T | C | 2 | a0001c0001t0001g0103 a0001c0001t0001g0205 |
2 | HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1825+8964T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182502093 | |||||||
chr1:182502195 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1825+9066C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182502195 | |||||||
chr1:182502237 | T | C | 1 | a0003c0003t0001g0116 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1825+9108T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182502237 | |||||||
chr1:182502386 | G | A | 2 | a0003c0003t0002g0026 a0003c0003t0002g0061 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1825+9257G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182502386 | |||||||
chr1:182502438 | C | A | 36 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(33): Show |
37 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.1825+9309C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182502438 | |||||||
chr1:182502563 | T | A | 224 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(221): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.1825+9434T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182502563 | |||||||
chr1:182502610 | G | C | 325 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(322): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.1825+9481G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182502610 | |||||||
chr1:182502812 | G | C | 2 | a0003c0003t0001g0118 a0014c0014t0001g0174 |
2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1825+9683G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182502812 | |||||||
chr1:182502847 | T | C | 1 | a0015c0025t0001g0266 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1825+9718T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182502847 | |||||||
chr1:182503140 | C | G | 1 | a0003c0003t0002g0060 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1825+10011C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182503140 | |||||||
chr1:182503184 | C | T | 214 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(211): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.1825+10055C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182503184 | |||||||
chr1:182503491 | G | A | 224 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(221): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.1825+10362G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182503491 | |||||||
chr1:182503521 | T | C | 16 | a0001c0001t0001g0114 a0001c0001t0001g0173 a0001c0001t0001g0175 others(13): Show |
16 | HG01243.hp2 HG01346.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.1825+10392T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182503521 | |||||||
chr1:182503769 | T | A | 1 | a0003c0003t0002g0228 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1825+10640T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182503769 | |||||||
chr1:182503837 | G | A | 36 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0015 others(33): Show |
38 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.1825+10708G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182503837 | |||||||
chr1:182503860 | A | G | 1 | a0001c0005t0001g0134 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1825+10731A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182503860 | |||||||
chr1:182503974 | C | CT | 91 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0015 others(88): Show |
96 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.1825+10869dupT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182503974 | ||||||
chr1:182503974 | C | CTT | 10 | a0001c0001t0001g0066 a0001c0001t0001g0147 a0001c0001t0001g0303 others(7): Show |
10 | HG02040.hp2 HG02135.hp1 HG02293.hp1 others(7): Show |
intron_variant | MODIFIER | c.1825+10868_1825+10 others(8): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182503974 | ||||||
chr1:182503974 | CT | C | 177 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(174): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.1825+10869delT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182503974 | ||||||
chr1:182503975 | T | TC | 9 | a0001c0001t0001g0104 a0001c0001t0001g0146 a0001c0001t0001g0185 others(6): Show |
9 | HG01884.hp1 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1825+10846_1825+10 others(7): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182503975 | |||||||
chr1:182503976 | T | C | 36 | a0001c0001t0001g0086 a0001c0001t0001g0103 a0001c0001t0001g0114 others(33): Show |
36 | HG00438.hp1 HG00558.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.1825+10847T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182503976 | |||||||
chr1:182503977 | T | C | 186 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(183): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.1825+10848T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182503977 | |||||||
chr1:182503978 | T | C | 36 | a0001c0001t0001g0086 a0001c0001t0001g0114 a0001c0001t0001g0173 others(33): Show |
36 | HG00438.hp1 HG00558.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.1825+10849T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182503978 | |||||||
chr1:182503979 | T | C | 177 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(174): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.1825+10850T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182503979 | |||||||
chr1:182503980 | T | C | 2 | a0002c0002t0001g0013 a0002c0002t0001g0078 |
2 | NA18950.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.1825+10851T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182503980 | |||||||
chr1:182504022 | C | T | 137 | a0001c0004t0001g0005 a0001c0004t0001g0010 a0001c0004t0001g0023 others(134): Show |
140 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.1825+10893C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182504022 | |||||||
chr1:182504073 | C | T | 1 | a0001c0001t0001g0205 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1825+10944C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182504073 | |||||||
chr1:182504127 | C | T | 1 | a0002c0002t0002g0287 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1825+10998C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182504127 | |||||||
chr1:182504200 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1825+11071C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182504200 | |||||||
chr1:182504472 | C | CT | 32 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0031 others(29): Show |
32 | HG00673.hp2 HG00735.hp2 HG01123.hp1 others(29): Show |
intron_variant | MODIFIER | c.1825+11370dupT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182504472 | ||||||
chr1:182504472 | C | CTT | 8 | a0001c0001t0001g0115 a0001c0001t0001g0147 a0001c0001t0001g0190 others(5): Show |
8 | HG02027.hp1 HG02040.hp2 HG03688.hp2 others(5): Show |
intron_variant | MODIFIER | c.1825+11369_1825+11 others(8): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182504472 | ||||||
chr1:182504472 | CTTTT | C | 18 | a0001c0001t0001g0173 a0001c0001t0001g0175 a0001c0001t0001g0176 others(15): Show |
18 | HG01891.hp1 HG02257.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.1825+11367_1825+11 others(10): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182504472 | ||||||
chr1:182504472 | CTTTTT | C | 81 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(78): Show |
82 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.1825+11366_1825+11 others(11): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182504472 | ||||||
chr1:182504472 | CTTTTTT | C | 111 | a0001c0001t0001g0184 a0001c0001t0001g0196 a0001c0001t0001g0197 others(108): Show |
114 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.1825+11365_1825+11 others(12): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182504472 | ||||||
chr1:182504472 | CTTTTTTT others(2): Show |
C | 6 | a0001c0001t0001g0104 a0001c0001t0001g0185 a0001c0001t0001g0200 others(3): Show |
6 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1825+11362_1825+11 others(15): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182504472 | ||||||
chr1:182504569 | G | T | 6 | a0003c0003t0001g0039 a0003c0003t0001g0051 a0003c0003t0001g0165 others(3): Show |
6 | HG00673.hp1 HG02074.hp1 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.1825+11440G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182504569 | |||||||
chr1:182504594 | C | T | 6 | a0001c0001t0001g0104 a0001c0001t0001g0185 a0001c0001t0001g0200 others(3): Show |
6 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1825+11465C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182504594 | |||||||
chr1:182504841 | A | G | 2 | a0001c0001t0001g0238 a0001c0001t0001g0277 |
2 | HG01258.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.1825+11712A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182504841 | |||||||
chr1:182504894 | C | T | 137 | a0001c0004t0001g0005 a0001c0004t0001g0010 a0001c0004t0001g0023 others(134): Show |
140 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.1825+11765C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182504894 | |||||||
chr1:182505025 | C | T | 214 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(211): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.1825+11896C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182505025 | |||||||
chr1:182505118 | A | G | 4 | a0002c0002t0001g0140 a0002c0002t0001g0141 a0002c0002t0001g0142 others(1): Show |
4 | NA18978.hp2 NA19011.hp2 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.1825+11989A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182505118 | |||||||
chr1:182505140 | A | G | 224 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(221): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.1825+12011A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182505140 | |||||||
chr1:182505224 | CT | C | 103 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0015 others(100): Show |
108 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.1825+12097delT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182505224 | ||||||
chr1:182505279 | A | G | 11 | a0001c0001t0001g0114 a0001c0001t0001g0173 a0001c0001t0001g0175 others(8): Show |
11 | HG01243.hp2 HG01346.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.1825+12150A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182505279 | |||||||
chr1:182505339 | G | T | 214 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(211): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.1825+12210G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182505339 | |||||||
chr1:182505382 | T | TG | 224 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(221): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.1825+12258dupG | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182505382 | ||||||
chr1:182505417 | C | T | 36 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(33): Show |
37 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.1825+12288C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182505417 | |||||||
chr1:182505469 | A | G | 1 | a0016c0022t0001g0077 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1825+12340A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182505469 | |||||||
chr1:182505527 | G | A | 9 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0173 others(6): Show |
9 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1825+12398G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182505527 | |||||||
chr1:182505546 | T | A | 1 | a0010c0016t0002g0008 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1825+12417T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182505546 | |||||||
chr1:182505569 | C | T | 214 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(211): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.1825+12440C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182505569 | |||||||
chr1:182505591 | T | A | 224 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(221): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.1825+12462T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182505591 | |||||||
chr1:182505930 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1825+12801C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182505930 | |||||||
chr1:182505965 | T | A | 1 | a0001c0001t0001g0244 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1825+12836T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182505965 | |||||||
chr1:182506285 | G | T | 214 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(211): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.1825+13156G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182506285 | |||||||
chr1:182506327 | G | A | 44 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(41): Show |
45 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.1825+13198G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182506327 | |||||||
chr1:182506459 | A | T | 224 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(221): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.1825+13330A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182506459 | |||||||
chr1:182506512 | GC | G | 214 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(211): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.1825+13384delC | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182506512 | |||||||
chr1:182506538 | A | G | 2 | a0001c0001t0001g0103 a0001c0001t0001g0205 |
2 | HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1825+13409A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182506538 | |||||||
chr1:182506550 | T | A | 214 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(211): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.1825+13421T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182506550 | |||||||
chr1:182506657 | A | G | 2 | a0001c0004t0001g0212 a0002c0002t0001g0328 |
2 | HG02145.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1825+13528A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182506657 | |||||||
chr1:182506841 | A | G | 1 | a0007c0013t0001g0263 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1825+13712A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182506841 | |||||||
chr1:182506870 | A | G | 7 | a0001c0001t0001g0146 a0001c0001t0001g0196 a0001c0001t0001g0197 others(4): Show |
7 | HG01069.hp1 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1825+13741A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182506870 | |||||||
chr1:182506983 | C | CT | 7 | a0003c0003t0001g0116 a0003c0003t0001g0151 a0003c0003t0001g0291 others(4): Show |
7 | HG00639.hp1 HG01981.hp1 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.1825+13877dupT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182506983 | ||||||
chr1:182506983 | C | T | 4 | a0003c0003t0001g0166 a0003c0003t0001g0168 a0003c0003t0002g0002 others(1): Show |
6 | HG02135.hp1 NA18980.hp1 NA19010.hp2 others(3): Show |
intron_variant | MODIFIER | c.1825+13854C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182506983 | |||||||
chr1:182506983 | CT | C | 39 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0015 others(36): Show |
41 | HG00438.hp2 HG00735.hp2 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.1825+13877delT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182506983 | ||||||
chr1:182506983 | CTTT | C | 52 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0053 others(49): Show |
53 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.1825+13875_1825+13 others(9): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182506983 | ||||||
chr1:182506983 | CTTTT | C | 159 | a0001c0001t0001g0114 a0001c0001t0001g0173 a0001c0001t0001g0175 others(156): Show |
161 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(158): Show |
intron_variant | MODIFIER | c.1825+13874_1825+13 others(10): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182506983 | ||||||
chr1:182506990 | T | C | 1 | a0001c0001t0001g0231 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1825+13861T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182506990 | |||||||
chr1:182506991 | T | C | 1 | a0001c0005t0001g0134 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1825+13862T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182506991 | |||||||
chr1:182507028 | T | C | 214 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(211): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.1825+13899T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182507028 | |||||||
chr1:182507050 | C | T | 10 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0185 others(7): Show |
10 | HG01884.hp1 HG02145.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1825+13921C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182507050 | |||||||
chr1:182507071 | A | G | 146 | a0001c0004t0001g0005 a0001c0004t0001g0010 a0001c0004t0001g0023 others(143): Show |
149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.1825+13942A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182507071 | |||||||
chr1:182507150 | T | C | 224 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(221): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.1825+14021T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182507150 | |||||||
chr1:182507178 | G | A | 1 | a0003c0003t0002g0018 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1825+14049G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182507178 | |||||||
chr1:182507216 | C | T | 1 | a0002c0002t0001g0038 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1825+14087C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182507216 | |||||||
chr1:182507285 | G | A | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1825+14156G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182507285 | |||||||
chr1:182507339 | A | G | 1 | a0003c0003t0002g0309 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1825+14210A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182507339 | |||||||
chr1:182507397 | C | T | 6 | a0001c0006t0001g0137 a0001c0006t0001g0138 a0001c0006t0001g0206 others(3): Show |
6 | HG01891.hp1 HG02559.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1825+14268C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182507397 | |||||||
chr1:182507539 | G | C | 1 | a0002c0002t0001g0145 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1825+14410G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182507539 | |||||||
chr1:182507690 | T | C | 1 | a0002c0002t0001g0072 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1826-14314T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182507690 | |||||||
chr1:182507701 | AT | A | 7 | a0001c0001t0001g0319 a0001c0006t0001g0137 a0001c0006t0001g0138 others(4): Show |
7 | HG01891.hp1 HG02165.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1826-14291delT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182507701 | ||||||
chr1:182508191 | T | G | 224 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(221): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.1826-13813T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182508191 | |||||||
chr1:182508201 | C | T | 1 | a0002c0002t0001g0327 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1826-13803C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182508201 | |||||||
chr1:182508231 | C | T | 5 | a0001c0001t0001g0184 a0001c0001t0001g0268 a0001c0005t0001g0011 others(2): Show |
5 | HG02109.hp2 HG02572.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1826-13773C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182508231 | |||||||
chr1:182508290 | G | GT | 139 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0042 others(136): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.1826-13689dupT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182508290 | ||||||
chr1:182508290 | G | GTT | 78 | a0001c0001t0001g0048 a0001c0001t0001g0172 a0001c0001t0001g0175 others(75): Show |
78 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.1826-13690_1826-13 others(8): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182508290 | ||||||
chr1:182508290 | G | GTTT | 18 | a0001c0001t0001g0104 a0001c0001t0001g0173 a0001c0001t0001g0185 others(15): Show |
18 | HG01175.hp1 HG01928.hp1 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.1826-13691_1826-13 others(9): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182508290 | ||||||
chr1:182508290 | G | GTTTT | 6 | a0001c0001t0001g0103 a0001c0001t0001g0205 a0001c0001t0001g0272 others(3): Show |
6 | HG02145.hp1 HG02647.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1826-13692_1826-13 others(10): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182508290 | ||||||
chr1:182508293 | T | C | 1 | a0001c0001t0001g0305 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1826-13711T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182508293 | |||||||
chr1:182508545 | C | T | 2 | a0002c0002t0001g0327 a0002c0002t0001g0328 |
2 | HG02145.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1826-13459C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182508545 | |||||||
chr1:182508594 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1826-13410C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182508594 | |||||||
chr1:182508668 | ATTTGTT | A | 6 | a0001c0001t0001g0184 a0001c0001t0001g0268 a0001c0005t0001g0113 others(3): Show |
6 | HG02109.hp2 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1826-13332_1826-13 others(12): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182508668 | ||||||
chr1:182508668 | ATTTGTTT | A | 74 | a0001c0004t0001g0093 a0001c0004t0001g0102 a0001c0004t0001g0125 others(71): Show |
76 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.1826-13332_1826-13 others(13): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182508668 | ||||||
chr1:182508668 | ATTTGTTT others(1): Show |
A | 108 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0053 others(105): Show |
110 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(107): Show |
intron_variant | MODIFIER | c.1826-13332_1826-13 others(14): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182508668 | ||||||
chr1:182508668 | ATTTGTTT others(2): Show |
A | 18 | a0001c0001t0001g0048 a0001c0001t0001g0114 a0001c0001t0001g0146 others(15): Show |
18 | HG01069.hp1 HG01243.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.1826-13332_1826-13 others(15): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182508668 | ||||||
chr1:182508668 | ATTTGTTT others(3): Show |
A | 4 | a0001c0006t0001g0137 a0001c0006t0001g0138 a0001c0007t0001g0210 others(1): Show |
4 | HG02559.hp1 HG02895.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1826-13332_1826-13 others(16): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182508668 | ||||||
chr1:182508668 | ATTTGTTT others(4): Show |
A | 3 | a0001c0006t0001g0206 a0001c0006t0001g0207 a0001c0006t0001g0208 |
3 | HG01891.hp1 NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1826-13332_1826-13 others(17): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182508668 | ||||||
chr1:182508672 | G | GT | 27 | a0001c0001t0001g0300 a0003c0003t0001g0039 a0003c0003t0001g0043 others(24): Show |
27 | HG00280.hp1 HG00544.hp2 HG00609.hp2 others(24): Show |
intron_variant | MODIFIER | c.1826-13312dupT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182508672 | ||||||
chr1:182508672 | GT | G | 15 | a0001c0001t0001g0185 a0001c0001t0001g0200 a0001c0001t0001g0271 others(12): Show |
15 | HG01884.hp1 HG02615.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.1826-13312delT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182508672 | ||||||
chr1:182508692 | T | A | 18 | a0001c0001t0001g0173 a0001c0001t0001g0175 a0001c0001t0001g0176 others(15): Show |
18 | HG00099.hp2 HG00642.hp2 HG01515.hp2 others(15): Show |
intron_variant | MODIFIER | c.1826-13312T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182508692 | |||||||
chr1:182508839 | C | T | 214 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(211): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.1826-13165C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182508839 | |||||||
chr1:182508904 | C | T | 3 | a0001c0001t0001g0198 a0001c0005t0001g0326 a0001c0005t0001g0329 |
3 | HG02055.hp2 HG03130.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1826-13100C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182508904 | |||||||
chr1:182509084 | T | C | 146 | a0001c0004t0001g0005 a0001c0004t0001g0010 a0001c0004t0001g0023 others(143): Show |
149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.1826-12920T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509084 | |||||||
chr1:182509141 | C | T | 8 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0185 others(5): Show |
8 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1826-12863C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509141 | |||||||
chr1:182509142 | G | C | 2 | a0008c0010t0001g0203 a0008c0010t0001g0204 |
2 | HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1826-12862G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509142 | |||||||
chr1:182509144 | C | T | 2 | a0008c0010t0001g0203 a0008c0010t0001g0204 |
2 | HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1826-12860C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509144 | |||||||
chr1:182509218 | G | A | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | NA18612.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.1826-12786G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509218 | |||||||
chr1:182509228 | G | A | 2 | a0002c0002t0002g0292 a0003c0003t0002g0323 |
2 | HG02027.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1826-12776G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509228 | |||||||
chr1:182509261 | G | A | 1 | a0001c0001t0001g0242 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1826-12743G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509261 | |||||||
chr1:182509274 | C | T | 10 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0185 others(7): Show |
10 | HG01884.hp1 HG02145.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1826-12730C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509274 | |||||||
chr1:182509284 | C | G | 5 | a0001c0001t0001g0184 a0001c0001t0001g0268 a0001c0005t0001g0011 others(2): Show |
5 | HG02109.hp2 HG02572.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1826-12720C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509284 | |||||||
chr1:182509292 | C | T | 1 | a0001c0001t0001g0237 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1826-12712C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509292 | |||||||
chr1:182509306 | G | A | 1 | a0001c0005t0001g0326 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1826-12698G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509306 | |||||||
chr1:182509309 | CAGGGGGC others(167): Show |
C | 1 | a0001c0005t0001g0326 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1826-12694_1826-12 others(6): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509309 | |||||||
chr1:182509310 | A | G | 212 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(209): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.1826-12694A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509310 | |||||||
chr1:182509313 | GGGCTGAC others(118): Show |
G | 211 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(208): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.1826-12688_1826-12 others(6): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182509313 | ||||||
chr1:182509314 | GGCTGACC others(117): Show |
G | 2 | a0001c0004t0001g0010 a0003c0003t0001g0209 |
2 | HG03098.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1826-12688_1826-12 others(6): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182509314 | ||||||
chr1:182509349 | TGGCCGGG others(30): Show |
T | 1 | a0003c0003t0002g0060 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1826-12641_1826-12 others(43): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182509349 | ||||||
chr1:182509386 | C | T | 10 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0185 others(7): Show |
10 | HG01884.hp1 HG02145.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1826-12618C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509386 | |||||||
chr1:182509415 | A | G | 8 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0185 others(5): Show |
8 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1826-12589A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509415 | |||||||
chr1:182509418 | C | T | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1826-12586C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509418 | |||||||
chr1:182509424 | G | A | 6 | a0001c0001t0001g0104 a0001c0001t0001g0185 a0001c0001t0001g0200 others(3): Show |
6 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1826-12580G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509424 | |||||||
chr1:182509432 | GGGCAGAG others(42): Show |
G | 2 | a0003c0003t0001g0118 a0014c0014t0001g0174 |
2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1826-12568_1826-12 others(55): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182509432 | ||||||
chr1:182509436 | A | G | 36 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0015 others(33): Show |
38 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.1826-12568A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509436 | |||||||
chr1:182509438 | A | G | 10 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0185 others(7): Show |
10 | HG01884.hp1 HG02145.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1826-12566A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509438 | |||||||
chr1:182509445 | AC | A | 8 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0185 others(5): Show |
8 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1826-12552delC | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182509445 | ||||||
chr1:182509467 | C | T | 1 | a0002c0002t0001g0109 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1826-12537C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509467 | |||||||
chr1:182509472 | C | CGGCTGGC others(71): Show |
2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1826-12524_1826-12 others(84): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182509472 | ||||||
chr1:182509472 | C | CGGCTGGC others(198): Show |
8 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0185 others(5): Show |
8 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1826-12524_1826-12 others(211): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182509472 | ||||||
chr1:182509481 | A | G | 46 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0015 others(43): Show |
48 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.1826-12523A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509481 | |||||||
chr1:182509484 | C | G | 1 | a0001c0005t0001g0326 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1826-12520C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509484 | |||||||
chr1:182509487 | G | A | 12 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0185 others(9): Show |
12 | HG01884.hp1 HG02145.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1826-12517G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509487 | |||||||
chr1:182509497 | C | T | 1 | a0003c0003t0002g0058 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1826-12507C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509497 | |||||||
chr1:182509498 | C | T | 5 | a0001c0001t0001g0184 a0001c0001t0001g0268 a0001c0005t0001g0011 others(2): Show |
5 | HG02109.hp2 HG02572.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1826-12506C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509498 | |||||||
chr1:182509522 | A | G | 224 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(221): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.1826-12482A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509522 | |||||||
chr1:182509531 | G | C | 1 | a0001c0001t0001g0304 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1826-12473G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509531 | |||||||
chr1:182509532 | GT | G | 10 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0185 others(7): Show |
10 | HG01884.hp1 HG02145.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1826-12471delT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509532 | |||||||
chr1:182509534 | G | C | 10 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0185 others(7): Show |
10 | HG01884.hp1 HG02145.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1826-12470G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509534 | |||||||
chr1:182509545 | C | T | 4 | a0002c0002t0001g0140 a0002c0002t0001g0141 a0002c0002t0001g0142 others(1): Show |
4 | NA18978.hp2 NA19011.hp2 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.1826-12459C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509545 | |||||||
chr1:182509546 | G | A | 1 | a0001c0005t0001g0134 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1826-12458G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509546 | |||||||
chr1:182509546 | G | C | 10 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0185 others(7): Show |
10 | HG01884.hp1 HG02145.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1826-12458G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509546 | |||||||
chr1:182509553 | T | C | 10 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0185 others(7): Show |
10 | HG01884.hp1 HG02145.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1826-12451T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509553 | |||||||
chr1:182509567 | G | C | 10 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0185 others(7): Show |
10 | HG01884.hp1 HG02145.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1826-12437G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509567 | |||||||
chr1:182509570 | G | T | 3 | a0001c0007t0001g0021 a0001c0007t0001g0022 a0001c0007t0001g0210 |
3 | HG02965.hp1 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1826-12434G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509570 | |||||||
chr1:182509571 | T | C | 10 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0185 others(7): Show |
10 | HG01884.hp1 HG02145.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1826-12433T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509571 | |||||||
chr1:182509575 | T | C | 1 | a0004c0009t0001g0261 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1826-12429T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509575 | |||||||
chr1:182509580 | A | G | 10 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0185 others(7): Show |
10 | HG01884.hp1 HG02145.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1826-12424A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509580 | |||||||
chr1:182509584 | T | A | 10 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0185 others(7): Show |
10 | HG01884.hp1 HG02145.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1826-12420T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509584 | |||||||
chr1:182509615 | C | A | 2 | a0008c0010t0001g0203 a0008c0010t0001g0204 |
2 | HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1826-12389C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509615 | |||||||
chr1:182509616 | T | C | 10 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0185 others(7): Show |
10 | HG01884.hp1 HG02145.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1826-12388T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509616 | |||||||
chr1:182509641 | G | A | 10 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0185 others(7): Show |
10 | HG01884.hp1 HG02145.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1826-12363G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509641 | |||||||
chr1:182509648 | GCGGCTGG others(42): Show |
G | 6 | a0003c0003t0001g0049 a0003c0003t0001g0064 a0003c0003t0001g0090 others(3): Show |
6 | HG01981.hp1 HG02273.hp2 NA18949.hp2 others(3): Show |
intron_variant | MODIFIER | c.1826-12332_1826-12 others(55): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182509648 | ||||||
chr1:182509658 | G | A | 1 | a0004c0009t0001g0260 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1826-12346G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509658 | |||||||
chr1:182509671 | AACCCCCC others(41): Show |
A | 1 | a0003c0003t0001g0159 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1826-12325_1826-12 others(54): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182509671 | ||||||
chr1:182509672 | ACCCCCCA others(42): Show |
A | 1 | a0003c0003t0001g0165 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1826-12311_1826-12 others(55): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182509672 | ||||||
chr1:182509697 | A | G | 1 | a0001c0006t0001g0208 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1826-12307A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509697 | |||||||
chr1:182509698 | C | T | 95 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0015 others(92): Show |
100 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.1826-12306C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509698 | |||||||
chr1:182509702 | T | C | 214 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(211): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.1826-12302T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509702 | |||||||
chr1:182509706 | C | T | 13 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0185 others(10): Show |
13 | HG01069.hp1 HG01884.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1826-12298C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509706 | |||||||
chr1:182509718 | T | A | 10 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0185 others(7): Show |
10 | HG01884.hp1 HG02145.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1826-12286T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509718 | |||||||
chr1:182509720 | A | C | 1 | a0003c0003t0001g0159 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1826-12284A>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509720 | |||||||
chr1:182509738 | C | A | 10 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0185 others(7): Show |
10 | HG01884.hp1 HG02145.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1826-12266C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509738 | |||||||
chr1:182509738 | C | T | 7 | a0001c0001t0001g0146 a0001c0001t0001g0196 a0001c0001t0001g0197 others(4): Show |
7 | HG01069.hp1 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1826-12266C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509738 | |||||||
chr1:182509765 | G | A | 2 | a0008c0010t0001g0203 a0008c0010t0001g0204 |
2 | HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1826-12239G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509765 | |||||||
chr1:182509765 | G | C | 1 | a0003c0003t0001g0039 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1826-12239G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509765 | |||||||
chr1:182509796 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1826-12208C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509796 | |||||||
chr1:182509818 | A | AC | 21 | a0001c0001t0001g0104 a0001c0001t0001g0189 a0001c0001t0001g0190 others(18): Show |
21 | HG00642.hp1 HG01099.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.1826-12177dupC | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182509818 | ||||||
chr1:182509818 | AC | A | 16 | a0001c0001t0001g0146 a0001c0001t0001g0173 a0001c0001t0001g0175 others(13): Show |
16 | HG01069.hp1 HG01884.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.1826-12177delC | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182509818 | ||||||
chr1:182509825 | C | G | 2 | a0001c0001t0001g0015 a0001c0001t0001g0031 |
2 | HG02129.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.1826-12179C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509825 | |||||||
chr1:182509825 | C | T | 4 | a0002c0002t0001g0037 a0002c0002t0001g0110 a0002c0002t0001g0150 others(1): Show |
4 | HG00408.hp2 HG02015.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1826-12179C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509825 | |||||||
chr1:182509827 | C | A | 1 | a0002c0002t0001g0123 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1826-12177C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509827 | |||||||
chr1:182509842 | C | T | 1 | a0003c0003t0001g0090 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1826-12162C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509842 | |||||||
chr1:182509843 | G | A | 1 | a0001c0001t0001g0257 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1826-12161G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509843 | |||||||
chr1:182509846 | G | T | 1 | a0001c0001t0001g0048 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1826-12158G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509846 | |||||||
chr1:182509848 | G | A | 5 | a0001c0001t0001g0184 a0001c0001t0001g0268 a0001c0005t0001g0011 others(2): Show |
5 | HG02109.hp2 HG02572.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1826-12156G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509848 | |||||||
chr1:182509854 | C | T | 214 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(211): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.1826-12150C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509854 | |||||||
chr1:182509857 | G | A | 1 | a0001c0004t0002g0019 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1826-12147G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509857 | |||||||
chr1:182509967 | C | T | 1 | a0001c0001t0001g0239 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1826-12037C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509967 | |||||||
chr1:182509971 | C | T | 1 | a0011c0021t0001g0170 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1826-12033C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182509971 | |||||||
chr1:182510007 | C | T | 146 | a0001c0004t0001g0005 a0001c0004t0001g0010 a0001c0004t0001g0023 others(143): Show |
149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.1826-11997C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510007 | |||||||
chr1:182510047 | C | T | 10 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0185 others(7): Show |
10 | HG01884.hp1 HG02145.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1826-11957C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510047 | |||||||
chr1:182510096 | A | G | 33 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(30): Show |
34 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1826-11908A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510096 | |||||||
chr1:182510097 | CG | C | 33 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(30): Show |
34 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1826-11906delG | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510097 | |||||||
chr1:182510101 | C | A | 33 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(30): Show |
34 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1826-11903C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510101 | |||||||
chr1:182510102 | C | CATGTGA | 33 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(30): Show |
34 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1826-11902_1826-11 others(12): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510102 | |||||||
chr1:182510111 | T | C | 1 | a0001c0004t0001g0181 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1826-11893T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510111 | |||||||
chr1:182510113 | G | C | 214 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(211): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.1826-11891G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510113 | |||||||
chr1:182510137 | C | T | 1 | a0001c0004t0001g0324 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1826-11867C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510137 | |||||||
chr1:182510146 | T | C | 224 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(221): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.1826-11858T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510146 | |||||||
chr1:182510164 | G | A | 1 | a0001c0005t0001g0134 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1826-11840G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510164 | |||||||
chr1:182510178 | G | A | 7 | a0001c0001t0001g0146 a0001c0001t0001g0196 a0001c0001t0001g0197 others(4): Show |
7 | HG01069.hp1 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1826-11826G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510178 | |||||||
chr1:182510215 | T | G | 224 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(221): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.1826-11789T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510215 | |||||||
chr1:182510223 | C | A | 1 | a0001c0004t0001g0010 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1826-11781C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510223 | |||||||
chr1:182510271 | C | CG | 15 | a0001c0001t0001g0009 a0001c0001t0001g0226 a0001c0001t0001g0232 others(12): Show |
15 | HG00738.hp1 HG01928.hp2 HG01978.hp2 others(12): Show |
intron_variant | MODIFIER | c.1826-11729dupG | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182510271 | ||||||
chr1:182510271 | C | T | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1826-11733C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510271 | |||||||
chr1:182510272 | G | A | 1 | a0003c0003t0002g0180 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1826-11732G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510272 | |||||||
chr1:182510321 | G | T | 11 | a0001c0001t0001g0114 a0001c0001t0001g0173 a0001c0001t0001g0175 others(8): Show |
11 | HG01243.hp2 HG01346.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.1826-11683G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510321 | |||||||
chr1:182510355 | C | G | 1 | a0001c0001t0001g0088 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1826-11649C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510355 | |||||||
chr1:182510409 | GACTCCGT | G | 8 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0185 others(5): Show |
8 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1826-11594_1826-11 others(13): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510409 | |||||||
chr1:182510417 | C | G | 8 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0185 others(5): Show |
8 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1826-11587C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510417 | |||||||
chr1:182510420 | CAATCCCG others(6): Show |
C | 8 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0185 others(5): Show |
8 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1826-11583_1826-11 others(19): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510420 | |||||||
chr1:182510487 | A | G | 224 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(221): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.1826-11517A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510487 | |||||||
chr1:182510536 | C | A | 7 | a0001c0001t0001g0146 a0001c0001t0001g0196 a0001c0001t0001g0197 others(4): Show |
7 | HG01069.hp1 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1826-11468C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510536 | |||||||
chr1:182510537 | A | G | 224 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(221): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.1826-11467A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510537 | |||||||
chr1:182510542 | C | T | 214 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(211): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.1826-11462C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510542 | |||||||
chr1:182510543 | C | T | 2 | a0003c0003t0002g0029 a0003c0003t0002g0058 |
2 | HG02280.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1826-11461C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510543 | |||||||
chr1:182510605 | G | C | 224 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(221): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.1826-11399G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510605 | |||||||
chr1:182510639 | A | G | 224 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(221): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.1826-11365A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510639 | |||||||
chr1:182510665 | T | G | 217 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(214): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.1826-11339T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510665 | |||||||
chr1:182510665 | T | TGAGAGG | 44 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0015 others(41): Show |
46 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.1826-11302_1826-11 others(12): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182510665 | ||||||
chr1:182510665 | T | TGAGAGGG others(5): Show |
1 | a0001c0001t0001g0192 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1826-11308_1826-11 others(18): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182510665 | ||||||
chr1:182510665 | TGAGAGG | T | 5 | a0003c0003t0001g0064 a0003c0003t0001g0116 a0003c0003t0001g0155 others(2): Show |
5 | HG00544.hp2 HG01981.hp1 HG02273.hp2 others(2): Show |
intron_variant | MODIFIER | c.1826-11302_1826-11 others(12): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182510665 | ||||||
chr1:182510667 | A | AGAGGGG | 5 | a0001c0001t0001g0146 a0001c0001t0001g0196 a0001c0001t0001g0197 others(2): Show |
5 | HG01069.hp1 HG02055.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1826-11332_1826-11 others(12): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182510667 | ||||||
chr1:182510667 | A | G | 2 | a0001c0001t0001g0104 a0001c0001t0001g0185 |
2 | HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1826-11337A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510667 | |||||||
chr1:182510669 | A | G | 2 | a0001c0001t0001g0103 a0001c0001t0001g0205 |
2 | HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1826-11335A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510669 | |||||||
chr1:182510673 | A | G | 13 | a0001c0001t0001g0104 a0001c0001t0001g0146 a0001c0001t0001g0185 others(10): Show |
13 | HG01069.hp1 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1826-11331A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510673 | |||||||
chr1:182510675 | A | AGGGGTAG others(7): Show |
34 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(31): Show |
35 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.1826-11326_1826-11 others(20): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182510675 | ||||||
chr1:182510675 | A | AGGGGTAG others(12): Show |
1 | a0001c0001t0001g0257 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1826-11326_1826-11 others(25): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182510675 | ||||||
chr1:182510675 | A | G | 5 | a0001c0001t0001g0104 a0001c0001t0001g0185 a0001c0005t0001g0270 others(2): Show |
5 | HG01884.hp1 HG02622.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1826-11329A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510675 | |||||||
chr1:182510679 | A | AGAGGGG | 8 | a0001c0001t0001g0173 a0001c0001t0001g0175 a0001c0001t0001g0176 others(5): Show |
8 | HG01884.hp2 HG02451.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1826-11320_1826-11 others(12): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182510679 | ||||||
chr1:182510679 | A | AGAGGGGG others(5): Show |
6 | a0001c0001t0001g0184 a0001c0001t0001g0268 a0001c0005t0001g0011 others(3): Show |
6 | HG02109.hp2 HG02258.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1826-11320_1826-11 others(18): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182510679 | ||||||
chr1:182510679 | A | AGAGGGGG others(11): Show |
4 | a0001c0001t0001g0114 a0001c0001t0001g0182 a0002c0002t0001g0318 others(1): Show |
4 | HG01243.hp2 HG01346.hp2 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.1826-11320_1826-11 others(24): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182510679 | ||||||
chr1:182510679 | A | G | 18 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0146 others(15): Show |
18 | HG01069.hp1 HG01884.hp1 HG01978.hp2 others(15): Show |
intron_variant | MODIFIER | c.1826-11325A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510679 | |||||||
chr1:182510681 | A | G | 39 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(36): Show |
40 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.1826-11323A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510681 | |||||||
chr1:182510685 | A | G | 189 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0114 others(186): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.1826-11319A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510685 | |||||||
chr1:182510687 | A | G | 35 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(32): Show |
36 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.1826-11317A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510687 | |||||||
chr1:182510691 | A | G | 189 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0114 others(186): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.1826-11313A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510691 | |||||||
chr1:182510693 | A | G | 35 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(32): Show |
36 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.1826-11311A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510693 | |||||||
chr1:182510694 | G | A | 1 | a0001c0001t0001g0257 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1826-11310G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510694 | |||||||
chr1:182510694 | G | GGGGGAGG others(11): Show |
151 | a0001c0004t0001g0005 a0001c0004t0001g0010 a0001c0004t0001g0023 others(148): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.1826-11308_1826-11 others(24): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182510694 | ||||||
chr1:182510694 | G | GGGGGAGG others(23): Show |
1 | a0005c0008t0001g0034 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1826-11308_1826-11 others(36): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182510694 | ||||||
chr1:182510694 | G | GGGGGAGG others(13): Show |
1 | a0001c0004t0001g0224 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1826-11308_1826-11 others(26): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182510694 | ||||||
chr1:182510697 | A | AAGGG | 34 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(31): Show |
35 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.1826-11307_1826-11 others(10): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510697 | |||||||
chr1:182510697 | A | AGGGGGAG others(27): Show |
1 | a0001c0001t0001g0241 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1826-11306_1826-11 others(40): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182510697 | ||||||
chr1:182510697 | A | G | 189 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0114 others(186): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.1826-11307A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510697 | |||||||
chr1:182510703 | A | G | 10 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0185 others(7): Show |
10 | HG01884.hp1 HG02145.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1826-11301A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510703 | |||||||
chr1:182510707 | G | C | 224 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(221): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.1826-11297G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510707 | |||||||
chr1:182510796 | C | T | 1 | a0001c0004t0001g0044 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1826-11208C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182510796 | |||||||
chr1:182511235 | G | A | 224 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(221): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.1826-10769G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182511235 | |||||||
chr1:182511283 | G | A | 214 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(211): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.1826-10721G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182511283 | |||||||
chr1:182511411 | G | A | 2 | a0001c0001t0001g0182 a0012c0019t0001g0216 |
2 | HG01243.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1826-10593G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182511411 | |||||||
chr1:182511422 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1826-10582C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182511422 | |||||||
chr1:182511462 | G | A | 4 | a0001c0001t0001g0184 a0001c0001t0001g0268 a0001c0005t0001g0113 others(1): Show |
4 | HG02109.hp2 HG02572.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1826-10542G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182511462 | |||||||
chr1:182511568 | G | T | 16 | a0001c0001t0001g0114 a0001c0001t0001g0173 a0001c0001t0001g0175 others(13): Show |
16 | HG01243.hp2 HG01346.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.1826-10436G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182511568 | |||||||
chr1:182511650 | T | A | 214 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(211): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.1826-10354T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182511650 | |||||||
chr1:182511660 | A | C | 1 | a0001c0004t0001g0278 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1826-10344A>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182511660 | |||||||
chr1:182511734 | T | C | 190 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(187): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.1826-10270T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182511734 | |||||||
chr1:182511787 | A | G | 1 | a0001c0001t0001g0219 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1826-10217A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182511787 | |||||||
chr1:182511800 | T | C | 1 | a0003c0003t0002g0111 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1826-10204T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182511800 | |||||||
chr1:182511889 | G | C | 1 | a0002c0002t0001g0083 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1826-10115G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182511889 | |||||||
chr1:182511945 | A | C | 3 | a0001c0001t0001g0114 a0001c0001t0001g0182 a0012c0019t0001g0216 |
3 | HG01243.hp2 HG01346.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1826-10059A>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182511945 | |||||||
chr1:182512008 | G | A | 1 | a0003c0003t0001g0160 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1826-9996G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182512008 | |||||||
chr1:182512501 | G | A | 3 | a0003c0003t0001g0165 a0003c0003t0001g0252 a0003c0003t0001g0253 |
3 | HG00673.hp1 HG02074.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.1826-9503G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182512501 | |||||||
chr1:182512553 | C | G | 2 | a0001c0001t0001g0196 a0001c0001t0001g0197 |
2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1826-9451C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182512553 | |||||||
chr1:182512579 | T | C | 224 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(221): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.1826-9425T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182512579 | |||||||
chr1:182512783 | T | C | 214 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(211): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.1826-9221T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182512783 | |||||||
chr1:182512787 | G | C | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1826-9217G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182512787 | |||||||
chr1:182512815 | T | C | 1 | a0001c0005t0001g0134 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1826-9189T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182512815 | |||||||
chr1:182512916 | T | C | 1 | a0002c0002t0001g0211 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1826-9088T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182512916 | |||||||
chr1:182513077 | A | G | 224 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(221): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.1826-8927A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182513077 | |||||||
chr1:182513123 | G | A | 25 | a0001c0004t0001g0010 a0001c0004t0001g0023 a0001c0004t0001g0044 others(22): Show |
25 | HG00140.hp1 HG00423.hp2 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.1826-8881G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182513123 | |||||||
chr1:182513147 | C | T | 1 | a0001c0001t0001g0149 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1826-8857C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182513147 | |||||||
chr1:182513206 | G | A | 147 | a0001c0001t0001g0175 a0001c0004t0001g0005 a0001c0004t0001g0010 others(144): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.1826-8798G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182513206 | |||||||
chr1:182513239 | G | A | 3 | a0002c0002t0001g0069 a0002c0002t0001g0143 a0002c0002t0001g0259 |
3 | HG01074.hp2 HG01192.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1826-8765G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182513239 | |||||||
chr1:182513378 | A | T | 225 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(222): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1826-8626A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182513378 | |||||||
chr1:182513383 | T | G | 214 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(211): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.1826-8621T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182513383 | |||||||
chr1:182513402 | G | A | 1 | a0002c0002t0001g0211 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1826-8602G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182513402 | |||||||
chr1:182513421 | C | A | 2 | a0001c0001t0001g0103 a0001c0001t0001g0205 |
2 | HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1826-8583C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182513421 | |||||||
chr1:182513816 | G | A | 190 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(187): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.1826-8188G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182513816 | |||||||
chr1:182513886 | T | C | 1 | a0001c0001t0001g0310 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1826-8118T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182513886 | |||||||
chr1:182513897 | C | CT | 155 | a0001c0001t0001g0189 a0001c0001t0001g0196 a0001c0001t0001g0197 others(152): Show |
158 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(155): Show |
intron_variant | MODIFIER | c.1826-8091dupT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182513897 | ||||||
chr1:182513897 | CT | C | 19 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0148 others(16): Show |
19 | HG01884.hp1 HG01891.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.1826-8091delT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182513897 | ||||||
chr1:182513981 | T | C | 1 | a0002c0002t0001g0068 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1826-8023T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182513981 | |||||||
chr1:182514082 | AG | A | 148 | a0001c0001t0001g0238 a0001c0001t0001g0277 a0001c0004t0001g0005 others(145): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.1826-7919delG | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182514082 | ||||||
chr1:182514164 | A | T | 190 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(187): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.1826-7840A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182514164 | |||||||
chr1:182514329 | G | C | 224 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(221): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.1826-7675G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182514329 | |||||||
chr1:182514339 | A | G | 1 | a0002c0002t0001g0099 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1826-7665A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182514339 | |||||||
chr1:182514375 | T | C | 1 | a0003c0003t0002g0029 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1826-7629T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182514375 | |||||||
chr1:182514530 | G | A | 28 | a0003c0003t0001g0039 a0003c0003t0001g0043 a0003c0003t0001g0047 others(25): Show |
28 | HG00280.hp1 HG00544.hp2 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.1826-7474G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182514530 | |||||||
chr1:182514562 | G | A | 1 | a0003c0003t0001g0155 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1826-7442G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182514562 | |||||||
chr1:182514567 | T | C | 262 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(259): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.1826-7437T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182514567 | |||||||
chr1:182514673 | A | G | 1 | a0001c0001t0001g0279 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1826-7331A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182514673 | |||||||
chr1:182514745 | G | T | 10 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0185 others(7): Show |
10 | HG01884.hp1 HG02145.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1826-7259G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182514745 | |||||||
chr1:182514806 | G | A | 34 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(31): Show |
35 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.1826-7198G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182514806 | |||||||
chr1:182514854 | A | T | 5 | a0001c0001t0001g0184 a0001c0001t0001g0268 a0001c0005t0001g0011 others(2): Show |
5 | HG02109.hp2 HG02572.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1826-7150A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182514854 | |||||||
chr1:182515037 | G | A | 6 | a0001c0001t0001g0101 a0001c0001t0001g0132 a0001c0001t0001g0239 others(3): Show |
6 | HG00558.hp1 HG02040.hp1 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.1826-6967G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182515037 | |||||||
chr1:182515168 | G | T | 42 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(39): Show |
43 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.1826-6836G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182515168 | |||||||
chr1:182515276 | C | T | 5 | a0001c0001t0001g0104 a0001c0001t0001g0185 a0001c0001t0001g0200 others(2): Show |
5 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1826-6728C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182515276 | |||||||
chr1:182515294 | C | T | 1 | a0001c0004t0001g0087 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1826-6710C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182515294 | |||||||
chr1:182515348 | T | C | 9 | a0001c0004t0001g0178 a0001c0004t0001g0181 a0001c0004t0001g0191 others(6): Show |
9 | HG00099.hp1 HG00642.hp1 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.1826-6656T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182515348 | |||||||
chr1:182515387 | G | A | 4 | a0002c0002t0001g0140 a0002c0002t0001g0141 a0002c0002t0001g0142 others(1): Show |
4 | NA18978.hp2 NA19011.hp2 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.1826-6617G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182515387 | |||||||
chr1:182515400 | T | C | 3 | a0001c0001t0001g0114 a0001c0001t0001g0182 a0012c0019t0001g0216 |
3 | HG01243.hp2 HG01346.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1826-6604T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182515400 | |||||||
chr1:182515496 | A | G | 1 | a0003c0003t0001g0052 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1826-6508A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182515496 | |||||||
chr1:182515552 | A | AG | 8 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0196 others(5): Show |
8 | HG02148.hp1 HG02630.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1826-6452_1826-645 others(5): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182515552 | |||||||
chr1:182515552 | A | AGG | 7 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0197 others(4): Show |
7 | HG01069.hp1 HG02145.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1826-6452_1826-645 others(6): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182515552 | |||||||
chr1:182515552 | A | AGGG | 3 | a0001c0001t0001g0146 a0001c0001t0001g0268 a0001c0004t0001g0315 |
3 | HG01175.hp2 HG02055.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1826-6452_1826-645 others(7): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182515552 | |||||||
chr1:182515552 | A | G | 2 | a0008c0010t0001g0203 a0008c0010t0001g0204 |
2 | HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1826-6452A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182515552 | |||||||
chr1:182515553 | A | AG | 106 | a0001c0001t0001g0173 a0001c0001t0001g0175 a0001c0001t0001g0176 others(103): Show |
109 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.1826-6443dupG | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182515553 | ||||||
chr1:182515553 | A | AGG | 47 | a0001c0001t0001g0007 a0001c0001t0001g0053 a0001c0001t0001g0101 others(44): Show |
48 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.1826-6444_1826-644 others(6): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182515553 | ||||||
chr1:182515553 | A | G | 28 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0146 others(25): Show |
28 | HG01069.hp1 HG01175.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.1826-6451A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182515553 | |||||||
chr1:182515570 | A | G | 8 | a0001c0001t0001g0173 a0001c0001t0001g0175 a0001c0001t0001g0176 others(5): Show |
8 | HG01884.hp2 HG02451.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1826-6434A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182515570 | |||||||
chr1:182515574 | CGT | C | 41 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(38): Show |
42 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.1826-6428_1826-642 others(6): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182515574 | ||||||
chr1:182515632 | C | T | 1 | a0001c0004t0001g0282 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1826-6372C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182515632 | |||||||
chr1:182515932 | G | A | 224 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(221): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.1826-6072G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182515932 | |||||||
chr1:182516132 | G | A | 1 | a0001c0005t0001g0134 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1826-5872G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182516132 | |||||||
chr1:182516286 | A | G | 222 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(219): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1826-5718A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182516286 | |||||||
chr1:182516614 | T | C | 222 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(219): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1826-5390T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182516614 | |||||||
chr1:182516664 | G | A | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1826-5340G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182516664 | |||||||
chr1:182516709 | A | AAAC | 222 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(219): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1826-5293_1826-529 others(7): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182516709 | ||||||
chr1:182516810 | T | C | 222 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(219): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1826-5194T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182516810 | |||||||
chr1:182516913 | T | C | 1 | a0001c0001t0001g0040 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1826-5091T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182516913 | |||||||
chr1:182517021 | G | A | 222 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(219): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1826-4983G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182517021 | |||||||
chr1:182517101 | G | C | 222 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(219): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1826-4903G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182517101 | |||||||
chr1:182517201 | T | G | 222 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(219): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1826-4803T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182517201 | |||||||
chr1:182517282 | G | GT | 163 | a0001c0001t0001g0042 a0001c0001t0001g0104 a0001c0001t0001g0146 others(160): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.1826-4711dupT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182517282 | ||||||
chr1:182517282 | G | GTT | 55 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(52): Show |
56 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.1826-4712_1826-471 others(6): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182517282 | ||||||
chr1:182517285 | T | TC | 6 | a0001c0004t0002g0019 a0001c0004t0002g0045 a0001c0004t0002g0055 others(3): Show |
6 | NA18941.hp1 NA18965.hp1 NA19004.hp2 others(3): Show |
intron_variant | MODIFIER | c.1826-4719_1826-471 others(5): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182517285 | |||||||
chr1:182517376 | G | C | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1826-4628G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182517376 | |||||||
chr1:182517397 | C | T | 222 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(219): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1826-4607C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182517397 | |||||||
chr1:182517446 | T | TG | 224 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(221): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.1826-4558_1826-455 others(5): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182517446 | |||||||
chr1:182517591 | T | A | 222 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(219): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1826-4413T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182517591 | |||||||
chr1:182517657 | TTGAGAGC others(9): Show |
T | 1 | a0001c0004t0001g0181 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1826-4346_1826-433 others(20): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182517657 | |||||||
chr1:182517678 | T | C | 1 | a0001c0004t0001g0181 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1826-4326T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182517678 | |||||||
chr1:182517771 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1826-4233C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182517771 | |||||||
chr1:182517929 | C | T | 33 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(30): Show |
34 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1826-4075C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182517929 | |||||||
chr1:182517948 | C | T | 222 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(219): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1826-4056C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182517948 | |||||||
chr1:182517953 | G | T | 2 | a0003c0003t0001g0118 a0014c0014t0001g0174 |
2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1826-4051G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182517953 | |||||||
chr1:182517993 | G | A | 2 | a0008c0010t0001g0203 a0008c0010t0001g0204 |
2 | HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1826-4011G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182517993 | |||||||
chr1:182518007 | G | GT | 3 | a0001c0004t0001g0221 a0001c0004t0001g0251 a0001c0004t0001g0286 |
3 | HG01255.hp1 HG01255.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.1826-3993dupT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182518007 | ||||||
chr1:182518071 | GCT | G | 222 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(219): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1826-3930_1826-392 others(6): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182518071 | ||||||
chr1:182518109 | G | A | 8 | a0001c0001t0001g0173 a0001c0001t0001g0175 a0001c0001t0001g0176 others(5): Show |
8 | HG01884.hp2 HG02451.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1826-3895G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182518109 | |||||||
chr1:182518187 | G | A | 1 | a0002c0002t0001g0117 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1826-3817G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182518187 | |||||||
chr1:182518262 | C | T | 5 | a0001c0001t0001g0104 a0001c0001t0001g0185 a0001c0001t0001g0200 others(2): Show |
5 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1826-3742C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182518262 | |||||||
chr1:182518303 | T | C | 222 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(219): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1826-3701T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182518303 | |||||||
chr1:182518358 | T | C | 222 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(219): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1826-3646T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182518358 | |||||||
chr1:182518420 | G | C | 2 | a0008c0010t0001g0203 a0008c0010t0001g0204 |
2 | HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1826-3584G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182518420 | |||||||
chr1:182518509 | C | A | 2 | a0003c0003t0001g0209 a0003c0024t0001g0105 |
2 | HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1826-3495C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182518509 | |||||||
chr1:182518523 | C | G | 1 | a0001c0001t0001g0232 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1826-3481C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182518523 | |||||||
chr1:182518543 | C | G | 222 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(219): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1826-3461C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182518543 | |||||||
chr1:182518767 | C | T | 1 | a0001c0005t0001g0134 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1826-3237C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182518767 | |||||||
chr1:182518816 | T | C | 10 | a0001c0004t0001g0178 a0001c0004t0001g0181 a0001c0004t0001g0191 others(7): Show |
10 | HG00099.hp1 HG00642.hp1 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.1826-3188T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182518816 | |||||||
chr1:182519010 | T | A | 1 | a0001c0001t0001g0298 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1826-2994T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182519010 | |||||||
chr1:182519010 | T | TG | 23 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0185 others(20): Show |
24 | HG00140.hp2 HG01069.hp1 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.1826-2985dupG | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182519010 | ||||||
chr1:182519027 | G | A | 222 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(219): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1826-2977G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182519027 | |||||||
chr1:182519099 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1826-2905G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182519099 | |||||||
chr1:182519167 | G | A | 222 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(219): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1826-2837G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182519167 | |||||||
chr1:182519252 | AT | A | 222 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(219): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1826-2744delT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182519252 | ||||||
chr1:182519494 | T | TC | 222 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(219): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1826-2507dupC | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182519494 | ||||||
chr1:182519515 | C | T | 11 | a0001c0001t0001g0114 a0001c0001t0001g0173 a0001c0001t0001g0175 others(8): Show |
11 | HG01243.hp2 HG01346.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.1826-2489C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182519515 | |||||||
chr1:182519598 | C | T | 3 | a0001c0005t0001g0134 a0006c0011t0001g0186 a0006c0011t0001g0187 |
3 | HG01884.hp1 HG02258.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1826-2406C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182519598 | |||||||
chr1:182519625 | G | A | 1 | a0001c0001t0001g0246 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1826-2379G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182519625 | |||||||
chr1:182519743 | T | G | 1 | a0003c0003t0002g0309 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1826-2261T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182519743 | |||||||
chr1:182519774 | C | A | 1 | a0001c0001t0001g0192 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1826-2230C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182519774 | |||||||
chr1:182519843 | C | T | 222 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(219): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1826-2161C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182519843 | |||||||
chr1:182519874 | T | G | 222 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(219): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1826-2130T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182519874 | |||||||
chr1:182519878 | A | C | 222 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(219): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1826-2126A>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182519878 | |||||||
chr1:182520002 | C | A | 222 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(219): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1826-2002C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182520002 | |||||||
chr1:182520039 | T | C | 1 | a0001c0004t0001g0087 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1826-1965T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182520039 | |||||||
chr1:182520071 | T | C | 1 | a0002c0002t0001g0289 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1826-1933T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182520071 | |||||||
chr1:182520080 | C | G | 2 | a0001c0001t0001g0103 a0001c0001t0001g0205 |
2 | HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1826-1924C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182520080 | |||||||
chr1:182520133 | C | T | 7 | a0001c0001t0001g0146 a0001c0001t0001g0196 a0001c0001t0001g0197 others(4): Show |
7 | HG01069.hp1 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1826-1871C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182520133 | |||||||
chr1:182520343 | C | G | 5 | a0001c0001t0001g0146 a0001c0001t0001g0196 a0001c0001t0001g0197 others(2): Show |
5 | HG01069.hp1 HG02055.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1826-1661C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182520343 | |||||||
chr1:182520350 | T | C | 105 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0015 others(102): Show |
110 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.1826-1654T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182520350 | |||||||
chr1:182520622 | T | A | 11 | a0001c0001t0001g0114 a0001c0001t0001g0173 a0001c0001t0001g0175 others(8): Show |
11 | HG01243.hp2 HG01346.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.1826-1382T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182520622 | |||||||
chr1:182520849 | G | A | 222 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(219): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1826-1155G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182520849 | |||||||
chr1:182520856 | G | A | 1 | a0003c0003t0001g0157 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1826-1148G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182520856 | |||||||
chr1:182521054 | A | G | 3 | a0002c0002t0001g0074 a0002c0002t0001g0136 a0002c0002t0001g0218 |
3 | HG01109.hp2 HG01169.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1826-950A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182521054 | |||||||
chr1:182521186 | C | T | 1 | a0002c0002t0001g0144 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1826-818C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182521186 | |||||||
chr1:182521229 | C | T | 222 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(219): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1826-775C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182521229 | |||||||
chr1:182521233 | T | G | 1 | a0001c0001t0001g0147 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1826-771T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182521233 | |||||||
chr1:182521334 | A | G | 222 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(219): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1826-670A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182521334 | |||||||
chr1:182521380 | A | G | 222 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(219): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1826-624A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182521380 | |||||||
chr1:182521402 | A | T | 1 | a0001c0004t0001g0010 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1826-602A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182521402 | |||||||
chr1:182521561 | T | G | 1 | a0003c0003t0002g0217 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1826-443T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182521561 | |||||||
chr1:182521630 | A | C | 8 | a0003c0003t0001g0030 a0003c0003t0002g0026 a0003c0003t0002g0027 others(5): Show |
8 | HG02280.hp2 HG02615.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1826-374A>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182521630 | |||||||
chr1:182521733 | G | A | 8 | a0001c0001t0001g0173 a0001c0001t0001g0175 a0001c0001t0001g0176 others(5): Show |
8 | HG01884.hp2 HG02451.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1826-271G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182521733 | |||||||
chr1:182521825 | G | A | 222 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(219): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1826-179G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182521825 | |||||||
chr1:182521832 | A | G | 7 | a0001c0001t0001g0146 a0001c0001t0001g0196 a0001c0001t0001g0197 others(4): Show |
7 | HG01069.hp1 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1826-172A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182521832 | |||||||
chr1:182521972 | A | C | 222 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(219): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1826-32A>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182521972 | |||||||
chr1:182521976 | T | C | 31 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(28): Show |
32 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.1826-28T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | chr1 | 182521976 | |||||||
chr1:182521991 | AT | A | 8 | a0001c0001t0001g0146 a0001c0001t0001g0196 a0001c0001t0001g0197 others(5): Show |
8 | HG00544.hp1 HG01069.hp1 HG02055.hp1 others(5): Show |
splice_region_variant&intron_variant | LOW | c.1826-3delT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr1 | 182521991 | ||||||
chr1:182522355 | T | A | 224 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(221): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.1931+246T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182522355 | |||||||
chr1:182522652 | T | C | 1 | a0002c0002t0001g0099 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1931+543T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182522652 | |||||||
chr1:182522793 | T | G | 1 | a0001c0005t0001g0134 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1931+684T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182522793 | |||||||
chr1:182522797 | T | C | 6 | a0001c0001t0001g0184 a0001c0001t0001g0268 a0001c0005t0001g0011 others(3): Show |
6 | HG02109.hp2 HG02572.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1931+688T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182522797 | |||||||
chr1:182522938 | T | C | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1931+829T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182522938 | |||||||
chr1:182522999 | G | T | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1931+890G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182522999 | |||||||
chr1:182523026 | C | CT | 222 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(219): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1931+925dupT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 182523026 | ||||||
chr1:182523040 | A | ATT | 221 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(218): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.1931+939_1931+940d others(4): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 182523040 | ||||||
chr1:182523100 | A | G | 222 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(219): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1931+991A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182523100 | |||||||
chr1:182523146 | C | T | 1 | a0001c0005t0001g0134 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1931+1037C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182523146 | |||||||
chr1:182523198 | G | GGC | 222 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(219): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1931+1089_1931+109 others(6): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182523198 | |||||||
chr1:182523199 | T | G | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1931+1090T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182523199 | |||||||
chr1:182523200 | T | C | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1931+1091T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182523200 | |||||||
chr1:182523206 | T | C | 222 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(219): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1931+1097T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182523206 | |||||||
chr1:182523208 | C | CT | 38 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0015 others(35): Show |
40 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.1931+1112dupT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 182523208 | ||||||
chr1:182523208 | C | T | 222 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(219): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1931+1099C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182523208 | |||||||
chr1:182523391 | T | C | 1 | a0003c0003t0002g0027 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1931+1282T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182523391 | |||||||
chr1:182523452 | A | G | 139 | a0001c0001t0001g0198 a0001c0001t0001g0238 a0001c0001t0001g0277 others(136): Show |
142 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.1931+1343A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182523452 | |||||||
chr1:182523509 | G | A | 222 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(219): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1931+1400G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182523509 | |||||||
chr1:182523545 | A | G | 222 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(219): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1931+1436A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182523545 | |||||||
chr1:182523649 | A | G | 222 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(219): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1931+1540A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182523649 | |||||||
chr1:182523972 | G | A | 3 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0199 |
3 | HG01069.hp1 HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1931+1863G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182523972 | |||||||
chr1:182524111 | A | T | 8 | a0001c0001t0001g0173 a0001c0001t0001g0175 a0001c0001t0001g0176 others(5): Show |
8 | HG01884.hp2 HG02451.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1931+2002A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182524111 | |||||||
chr1:182524113 | A | C | 1 | a0003c0003t0001g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1931+2004A>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182524113 | |||||||
chr1:182524133 | C | T | 222 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(219): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1931+2024C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182524133 | |||||||
chr1:182524167 | G | A | 2 | a0001c0001t0001g0103 a0001c0001t0001g0205 |
2 | HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1931+2058G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182524167 | |||||||
chr1:182524269 | T | C | 2 | a0002c0002t0001g0096 a0002c0002t0001g0098 |
2 | NA18973.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.1931+2160T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182524269 | |||||||
chr1:182524291 | GTA | G | 222 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(219): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1931+2187_1931+218 others(6): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 182524291 | ||||||
chr1:182524394 | C | G | 103 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0015 others(100): Show |
108 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.1931+2285C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182524394 | |||||||
chr1:182524630 | A | T | 222 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(219): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1931+2521A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182524630 | |||||||
chr1:182524650 | A | T | 15 | a0001c0001t0001g0086 a0001c0001t0001g0101 a0001c0001t0001g0132 others(12): Show |
15 | HG00558.hp1 HG00738.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.1931+2541A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182524650 | |||||||
chr1:182524830 | A | G | 224 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(221): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.1931+2721A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182524830 | |||||||
chr1:182524928 | G | A | 222 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(219): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1932-2651G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182524928 | |||||||
chr1:182525010 | A | G | 1 | a0001c0004t0001g0311 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1932-2569A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182525010 | |||||||
chr1:182525081 | C | T | 1 | a0001c0005t0001g0134 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1932-2498C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182525081 | |||||||
chr1:182525102 | G | A | 222 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(219): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1932-2477G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182525102 | |||||||
chr1:182525104 | G | A | 224 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(221): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.1932-2475G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182525104 | |||||||
chr1:182525380 | G | C | 222 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(219): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1932-2199G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182525380 | |||||||
chr1:182525404 | T | C | 1 | a0001c0001t0001g0185 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1932-2175T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182525404 | |||||||
chr1:182525463 | G | A | 1 | a0001c0017t0001g0067 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1932-2116G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182525463 | |||||||
chr1:182525512 | G | C | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1932-2067G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182525512 | |||||||
chr1:182525597 | A | C | 4 | a0001c0005t0001g0270 a0001c0007t0001g0021 a0001c0007t0001g0022 others(1): Show |
4 | HG02647.hp1 HG02965.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1932-1982A>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182525597 | |||||||
chr1:182525860 | CG | C | 222 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(219): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1932-1715delG | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 182525860 | ||||||
chr1:182525862 | G | A | 222 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(219): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1932-1717G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182525862 | |||||||
chr1:182526003 | A | G | 1 | a0002c0002t0001g0012 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1932-1576A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182526003 | |||||||
chr1:182526057 | A | G | 1 | a0013c0015t0001g0050 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1932-1522A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182526057 | |||||||
chr1:182526060 | A | C | 222 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(219): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1932-1519A>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182526060 | |||||||
chr1:182526127 | G | A | 222 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(219): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1932-1452G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182526127 | |||||||
chr1:182526205 | T | A | 222 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(219): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1932-1374T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182526205 | |||||||
chr1:182526217 | C | T | 222 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(219): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1932-1362C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182526217 | |||||||
chr1:182526337 | C | T | 7 | a0001c0001t0001g0146 a0001c0001t0001g0196 a0001c0001t0001g0197 others(4): Show |
7 | HG01069.hp1 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1932-1242C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182526337 | |||||||
chr1:182526391 | G | A | 222 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(219): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1932-1188G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182526391 | |||||||
chr1:182526497 | G | A | 224 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(221): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.1932-1082G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182526497 | |||||||
chr1:182526502 | T | TA | 84 | a0001c0001t0001g0146 a0001c0001t0001g0196 a0001c0001t0001g0197 others(81): Show |
86 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.1932-1066dupA | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 182526502 | ||||||
chr1:182526578 | A | G | 214 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(211): Show |
218 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.1932-1001A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182526578 | |||||||
chr1:182526594 | C | T | 222 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(219): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.1932-985C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182526594 | |||||||
chr1:182526698 | T | A | 1 | a0001c0001t0001g0091 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1932-881T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182526698 | |||||||
chr1:182526785 | GAC | G | 4 | a0001c0001t0001g0190 a0001c0001t0001g0300 a0001c0001t0001g0302 others(1): Show |
4 | NA18977.hp2 NA19000.hp1 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.1932-790_1932-789d others(4): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr1 | 182526785 | ||||||
chr1:182526789 | CAT | C | 6 | a0001c0001t0001g0114 a0001c0001t0001g0182 a0003c0003t0002g0214 others(3): Show |
6 | HG01074.hp1 HG01243.hp2 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.1932-789_1932-788d others(4): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182526789 | |||||||
chr1:182526813 | A | G | 2 | a0001c0001t0001g0103 a0001c0001t0001g0205 |
2 | HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1932-766A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182526813 | |||||||
chr1:182526873 | T | C | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1932-706T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 10/21 | chr1 | 182526873 | |||||||
chr1:182527853 | T | A | 2 | a0008c0010t0001g0203 a0008c0010t0001g0204 |
2 | HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2125+81T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 11/21 | chr1 | 182527853 | |||||||
chr1:182527886 | C | A | 147 | a0001c0001t0001g0198 a0001c0004t0001g0005 a0001c0004t0001g0010 others(144): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.2125+114C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 11/21 | chr1 | 182527886 | |||||||
chr1:182528117 | G | T | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2125+345G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 11/21 | chr1 | 182528117 | |||||||
chr1:182528168 | T | C | 1 | a0001c0001t0001g0233 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2125+396T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 11/21 | chr1 | 182528168 | |||||||
chr1:182528354 | T | C | 1 | a0001c0004t0001g0281 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2125+582T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 11/21 | chr1 | 182528354 | |||||||
chr1:182528535 | G | T | 5 | a0001c0001t0001g0104 a0001c0001t0001g0185 a0001c0001t0001g0200 others(2): Show |
5 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2125+763G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 11/21 | chr1 | 182528535 | |||||||
chr1:182528716 | C | G | 3 | a0001c0001t0001g0114 a0001c0001t0001g0182 a0012c0019t0001g0216 |
3 | HG01243.hp2 HG01346.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2125+944C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 11/21 | chr1 | 182528716 | |||||||
chr1:182528848 | C | T | 2 | a0001c0001t0001g0147 a0001c0001t0001g0246 |
2 | HG02040.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.2125+1076C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 11/21 | chr1 | 182528848 | |||||||
chr1:182528849 | G | A | 3 | a0003c0003t0002g0006 a0003c0003t0002g0018 a0003c0003t0002g0214 |
4 | HG01069.hp2 HG01071.hp1 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.2125+1077G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 11/21 | chr1 | 182528849 | |||||||
chr1:182528931 | T | C | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2125+1159T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 11/21 | chr1 | 182528931 | |||||||
chr1:182529028 | C | T | 5 | a0001c0001t0001g0104 a0001c0001t0001g0185 a0001c0001t0001g0200 others(2): Show |
5 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2126-1216C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 11/21 | chr1 | 182529028 | |||||||
chr1:182529289 | C | T | 2 | a0003c0003t0001g0209 a0003c0024t0001g0105 |
2 | HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2126-955C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 11/21 | chr1 | 182529289 | |||||||
chr1:182529492 | G | T | 1 | a0001c0005t0001g0134 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2126-752G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 11/21 | chr1 | 182529492 | |||||||
chr1:182529505 | A | G | 1 | a0001c0001t0001g0101 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2126-739A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 11/21 | chr1 | 182529505 | |||||||
chr1:182529524 | G | A | 1 | a0002c0002t0001g0074 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.2126-720G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 11/21 | chr1 | 182529524 | |||||||
chr1:182529759 | G | A | 2 | a0001c0005t0001g0326 a0001c0005t0001g0329 |
2 | HG03130.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2126-485G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 11/21 | chr1 | 182529759 | |||||||
chr1:182529776 | G | A | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2126-468G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 11/21 | chr1 | 182529776 | |||||||
chr1:182529801 | T | G | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2126-443T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 11/21 | chr1 | 182529801 | |||||||
chr1:182529832 | G | T | 9 | a0003c0003t0002g0025 a0003c0003t0002g0062 a0003c0003t0002g0063 others(6): Show |
9 | HG00423.hp1 HG01981.hp2 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.2126-412G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 11/21 | chr1 | 182529832 | |||||||
chr1:182529884 | T | A | 2 | a0003c0003t0001g0118 a0014c0014t0001g0174 |
2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2126-360T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 11/21 | chr1 | 182529884 | |||||||
chr1:182529910 | T | C | 2 | a0001c0004t0001g0093 a0001c0004t0001g0126 |
2 | NA18969.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.2126-334T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 11/21 | chr1 | 182529910 | |||||||
chr1:182529928 | C | T | 2 | a0001c0004t0001g0044 a0001c0004t0001g0320 |
2 | HG03704.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.2126-316C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 11/21 | chr1 | 182529928 | |||||||
chr1:182529930 | G | C | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2126-314G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 11/21 | chr1 | 182529930 | |||||||
chr1:182529985 | G | T | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2126-259G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 11/21 | chr1 | 182529985 | |||||||
chr1:182530036 | A | G | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2126-208A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 11/21 | chr1 | 182530036 | |||||||
chr1:182530111 | G | A | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2126-133G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 11/21 | chr1 | 182530111 | |||||||
chr1:182530237 | T | G | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
splice_region_variant&intron_variant | LOW | c.2126-7T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 11/21 | chr1 | 182530237 | |||||||
chr1:182530375 | A | G | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2243+14A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 12/21 | chr1 | 182530375 | |||||||
chr1:182530538 | T | TAC | 66 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(63): Show |
67 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.2243+203_2243+204d others(4): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr1 | 182530538 | ||||||
chr1:182530538 | T | TACAC | 10 | a0001c0001t0001g0173 a0001c0001t0001g0176 a0001c0001t0001g0213 others(7): Show |
10 | HG01255.hp1 HG01884.hp2 HG02004.hp2 others(7): Show |
intron_variant | MODIFIER | c.2243+201_2243+204d others(6): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr1 | 182530538 | ||||||
chr1:182530538 | T | TACACAC | 5 | a0001c0001t0001g0146 a0001c0001t0001g0175 a0001c0001t0001g0199 others(2): Show |
5 | HG01069.hp1 HG02055.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.2243+199_2243+204d others(8): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr1 | 182530538 | ||||||
chr1:182530538 | T | TACACACA others(1): Show |
28 | a0001c0001t0001g0230 a0001c0004t0001g0112 a0001c0004t0001g0130 others(25): Show |
28 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.2243+197_2243+204d others(10): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr1 | 182530538 | ||||||
chr1:182530538 | T | TACACACA others(3): Show |
102 | a0001c0001t0001g0198 a0001c0001t0001g0238 a0001c0001t0001g0277 others(99): Show |
104 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(101): Show |
intron_variant | MODIFIER | c.2243+195_2243+204d others(12): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr1 | 182530538 | ||||||
chr1:182530538 | T | TACACACA others(5): Show |
15 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0004t0001g0005 others(12): Show |
16 | HG00544.hp1 HG01109.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.2243+193_2243+204d others(14): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr1 | 182530538 | ||||||
chr1:182530538 | T | TACACACA others(7): Show |
3 | a0001c0004t0001g0183 a0001c0004t0001g0269 a0016c0022t0001g0077 |
3 | HG03453.hp2 NA18966.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2243+191_2243+204d others(16): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr1 | 182530538 | ||||||
chr1:182530538 | TAC | T | 23 | a0001c0001t0001g0057 a0001c0001t0001g0094 a0001c0001t0001g0103 others(20): Show |
24 | HG00423.hp1 HG00544.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.2243+203_2243+204d others(4): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr1 | 182530538 | ||||||
chr1:182530696 | G | C | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2244-94G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 12/21 | chr1 | 182530696 | |||||||
chr1:182530993 | C | T | 2 | a0001c0001t0001g0103 a0001c0001t0001g0205 |
2 | HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2364+83C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 13/21 | chr1 | 182530993 | |||||||
chr1:182531026 | A | G | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2364+116A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 13/21 | chr1 | 182531026 | |||||||
chr1:182531412 | G | A | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2364+502G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 13/21 | chr1 | 182531412 | |||||||
chr1:182531425 | A | G | 1 | a0001c0004t0001g0227 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2364+515A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 13/21 | chr1 | 182531425 | |||||||
chr1:182531453 | A | C | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2364+543A>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 13/21 | chr1 | 182531453 | |||||||
chr1:182531681 | C | T | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2364+771C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 13/21 | chr1 | 182531681 | |||||||
chr1:182531801 | A | C | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2365-861A>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 13/21 | chr1 | 182531801 | |||||||
chr1:182531831 | G | A | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2365-831G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 13/21 | chr1 | 182531831 | |||||||
chr1:182531964 | A | T | 2 | a0001c0001t0001g0103 a0001c0001t0001g0205 |
2 | HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2365-698A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 13/21 | chr1 | 182531964 | |||||||
chr1:182532021 | G | C | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2365-641G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 13/21 | chr1 | 182532021 | |||||||
chr1:182532025 | C | T | 1 | a0004c0009t0001g0260 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2365-637C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 13/21 | chr1 | 182532025 | |||||||
chr1:182532050 | C | T | 1 | a0002c0002t0001g0128 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2365-612C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 13/21 | chr1 | 182532050 | |||||||
chr1:182532311 | A | G | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2365-351A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 13/21 | chr1 | 182532311 | |||||||
chr1:182532311 | A | T | 2 | a0003c0003t0002g0026 a0003c0003t0002g0061 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2365-351A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 13/21 | chr1 | 182532311 | |||||||
chr1:182532373 | C | T | 36 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0015 others(33): Show |
38 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.2365-289C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 13/21 | chr1 | 182532373 | |||||||
chr1:182532374 | G | A | 148 | a0001c0001t0001g0198 a0001c0001t0001g0230 a0001c0004t0001g0005 others(145): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.2365-288G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 13/21 | chr1 | 182532374 | |||||||
chr1:182532392 | T | G | 1 | a0003c0003t0001g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2365-270T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 13/21 | chr1 | 182532392 | |||||||
chr1:182532503 | C | G | 1 | a0002c0002t0001g0099 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2365-159C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 13/21 | chr1 | 182532503 | |||||||
chr1:182532541 | T | A | 1 | a0001c0001t0001g0301 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.2365-121T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 13/21 | chr1 | 182532541 | |||||||
chr1:182532572 | G | A | 1 | a0004c0009t0001g0260 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2365-90G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 13/21 | chr1 | 182532572 | |||||||
chr1:182532798 | C | A | 148 | a0001c0001t0001g0198 a0001c0001t0001g0230 a0001c0004t0001g0005 others(145): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
splice_region_variant&intron_variant | LOW | c.2494+7C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182532798 | |||||||
chr1:182532808 | T | C | 1 | a0001c0001t0001g0219 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2494+17T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182532808 | |||||||
chr1:182532898 | G | T | 190 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(187): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.2494+107G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182532898 | |||||||
chr1:182533145 | G | A | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2494+354G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182533145 | |||||||
chr1:182533189 | A | G | 5 | a0001c0001t0001g0104 a0001c0001t0001g0185 a0001c0001t0001g0200 others(2): Show |
5 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2494+398A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182533189 | |||||||
chr1:182533270 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2494+479C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182533270 | |||||||
chr1:182533296 | C | CT | 10 | a0001c0001t0001g0184 a0001c0001t0001g0219 a0001c0001t0001g0268 others(7): Show |
10 | HG02015.hp1 HG02109.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.2494+522dupT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr1 | 182533296 | ||||||
chr1:182533296 | C | CTT | 7 | a0001c0001t0001g0104 a0001c0001t0001g0185 a0001c0001t0001g0200 others(4): Show |
7 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.2494+521_2494+522d others(4): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr1 | 182533296 | ||||||
chr1:182533296 | C | CTTT | 37 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0031 others(34): Show |
39 | HG00438.hp2 HG00544.hp2 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.2494+520_2494+522d others(5): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr1 | 182533296 | ||||||
chr1:182533296 | CT | C | 6 | a0001c0001t0001g0223 a0001c0001t0001g0226 a0001c0004t0001g0275 others(3): Show |
6 | HG01884.hp1 HG02602.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.2494+522delT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr1 | 182533296 | ||||||
chr1:182533300 | T | TTTTTTTT others(99): Show |
2 | a0001c0001t0001g0103 a0001c0001t0001g0205 |
2 | HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2494+523_2494+524i others(108): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr1 | 182533300 | ||||||
chr1:182533300 | T | TTTTTTTT others(98): Show |
27 | a0001c0001t0001g0104 a0001c0001t0001g0114 a0001c0001t0001g0173 others(24): Show |
27 | HG00544.hp2 HG01243.hp2 HG01346.hp2 others(24): Show |
intron_variant | MODIFIER | c.2494+512_2494+616d others(107): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr1 | 182533300 | ||||||
chr1:182533300 | T | TTTTTTTT others(100): Show |
1 | a0003c0003t0001g0294 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2494+522_2494+523i others(109): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr1 | 182533300 | ||||||
chr1:182533300 | T | TTTTTTTT others(101): Show |
62 | a0001c0001t0001g0244 a0003c0003t0001g0017 a0003c0003t0001g0030 others(59): Show |
65 | HG00280.hp1 HG00423.hp1 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.2494+522_2494+523i others(110): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr1 | 182533300 | ||||||
chr1:182533337 | C | G | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2494+546C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182533337 | |||||||
chr1:182533345 | G | A | 1 | a0001c0001t0001g0302 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2494+554G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182533345 | |||||||
chr1:182533470 | G | A | 1 | a0012c0019t0001g0216 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2494+679G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182533470 | |||||||
chr1:182533507 | T | C | 1 | a0001c0004t0001g0220 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2494+716T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182533507 | |||||||
chr1:182533565 | A | G | 1 | a0003c0003t0001g0090 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2494+774A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182533565 | |||||||
chr1:182533587 | G | A | 2 | a0001c0001t0001g0103 a0001c0001t0001g0205 |
2 | HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2494+796G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182533587 | |||||||
chr1:182533724 | A | T | 1 | a0002c0002t0001g0079 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2494+933A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182533724 | |||||||
chr1:182533772 | T | C | 1 | a0001c0004t0001g0281 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2494+981T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182533772 | |||||||
chr1:182533780 | A | T | 1 | a0002c0002t0001g0100 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.2494+989A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182533780 | |||||||
chr1:182533792 | G | A | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2494+1001G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182533792 | |||||||
chr1:182533794 | C | T | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2494+1003C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182533794 | |||||||
chr1:182533811 | T | G | 11 | a0001c0001t0001g0114 a0001c0001t0001g0173 a0001c0001t0001g0175 others(8): Show |
11 | HG01243.hp2 HG01346.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.2494+1020T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182533811 | |||||||
chr1:182533864 | A | G | 1 | a0002c0002t0001g0143 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2494+1073A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182533864 | |||||||
chr1:182534039 | G | A | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2494+1248G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182534039 | |||||||
chr1:182534163 | A | G | 2 | a0001c0001t0001g0182 a0012c0019t0001g0216 |
2 | HG01243.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2494+1372A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182534163 | |||||||
chr1:182534570 | G | A | 1 | a0001c0004t0001g0177 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2494+1779G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182534570 | |||||||
chr1:182534625 | C | T | 2 | a0008c0010t0001g0203 a0008c0010t0001g0204 |
2 | HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2494+1834C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182534625 | |||||||
chr1:182534734 | A | G | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2494+1943A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182534734 | |||||||
chr1:182534742 | A | T | 40 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(37): Show |
41 | HG00280.hp2 HG00408.hp1 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.2494+1951A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182534742 | |||||||
chr1:182534826 | C | CA | 6 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0241 others(3): Show |
6 | HG01978.hp1 HG02738.hp1 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.2494+2049dupA | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr1 | 182534826 | ||||||
chr1:182534848 | A | T | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2494+2057A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182534848 | |||||||
chr1:182535061 | T | C | 1 | a0002c0002t0001g0100 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.2494+2270T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182535061 | |||||||
chr1:182535263 | G | A | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2494+2472G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182535263 | |||||||
chr1:182535366 | AGT | A | 3 | a0001c0001t0001g0114 a0001c0001t0001g0182 a0012c0019t0001g0216 |
3 | HG01243.hp2 HG01346.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2494+2586_2494+258 others(6): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr1 | 182535366 | ||||||
chr1:182535508 | G | A | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2494+2717G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182535508 | |||||||
chr1:182535527 | A | G | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2494+2736A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182535527 | |||||||
chr1:182535764 | T | C | 2 | a0003c0003t0001g0118 a0014c0014t0001g0174 |
2 | HG02818.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2494+2973T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182535764 | |||||||
chr1:182535807 | T | C | 1 | a0002c0002t0001g0079 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2494+3016T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182535807 | |||||||
chr1:182536061 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2494+3270C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182536061 | |||||||
chr1:182536135 | C | T | 2 | a0003c0003t0001g0157 a0003c0003t0001g0229 |
2 | NA18950.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.2494+3344C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182536135 | |||||||
chr1:182536208 | A | G | 2 | a0008c0010t0001g0203 a0008c0010t0001g0204 |
2 | HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2494+3417A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182536208 | |||||||
chr1:182536247 | C | T | 2 | a0002c0002t0001g0096 a0002c0002t0001g0098 |
2 | NA18973.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.2494+3456C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182536247 | |||||||
chr1:182536279 | A | G | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2494+3488A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182536279 | |||||||
chr1:182536498 | G | A | 2 | a0002c0002t0001g0327 a0002c0002t0001g0328 |
2 | HG02145.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.2494+3707G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182536498 | |||||||
chr1:182536520 | A | G | 1 | a0001c0005t0001g0134 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2495-3727A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182536520 | |||||||
chr1:182536542 | A | G | 139 | a0001c0001t0001g0198 a0001c0001t0001g0230 a0001c0001t0001g0238 others(136): Show |
142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.2495-3705A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182536542 | |||||||
chr1:182536574 | C | A | 1 | a0001c0004t0001g0212 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2495-3673C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182536574 | |||||||
chr1:182536605 | G | C | 2 | a0001c0001t0001g0196 a0001c0001t0001g0197 |
2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2495-3642G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182536605 | |||||||
chr1:182536620 | C | T | 7 | a0001c0001t0001g0198 a0001c0004t0001g0005 a0001c0004t0001g0102 others(4): Show |
8 | HG01099.hp2 HG01109.hp1 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.2495-3627C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182536620 | |||||||
chr1:182536650 | C | T | 81 | a0001c0001t0001g0308 a0001c0004t0001g0178 a0001c0004t0001g0191 others(78): Show |
83 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.2495-3597C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182536650 | |||||||
chr1:182536656 | C | T | 14 | a0001c0001t0001g0173 a0001c0001t0001g0175 a0001c0001t0001g0176 others(11): Show |
14 | HG01884.hp1 HG01884.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.2495-3591C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182536656 | |||||||
chr1:182536791 | C | T | 5 | a0001c0001t0001g0007 a0001c0001t0001g0172 a0001c0001t0001g0236 others(2): Show |
6 | HG00280.hp2 HG01081.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.2495-3456C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182536791 | |||||||
chr1:182536792 | G | A | 4 | a0001c0001t0001g0184 a0001c0001t0001g0268 a0006c0011t0001g0186 others(1): Show |
4 | HG01884.hp1 HG02109.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.2495-3455G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182536792 | |||||||
chr1:182536849 | A | G | 1 | a0001c0017t0001g0067 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2495-3398A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182536849 | |||||||
chr1:182536872 | C | T | 9 | a0001c0001t0001g0103 a0001c0001t0001g0146 a0001c0001t0001g0184 others(6): Show |
9 | HG01884.hp1 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.2495-3375C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182536872 | |||||||
chr1:182536940 | T | C | 1 | a0002c0002t0001g0117 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2495-3307T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182536940 | |||||||
chr1:182536948 | G | A | 195 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(192): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.2495-3299G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182536948 | |||||||
chr1:182537010 | C | A | 202 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(199): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.2495-3237C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182537010 | |||||||
chr1:182537014 | T | A | 202 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(199): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.2495-3233T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182537014 | |||||||
chr1:182537036 | A | G | 12 | a0001c0005t0001g0011 a0001c0005t0001g0108 a0001c0005t0001g0113 others(9): Show |
12 | HG02258.hp2 HG02572.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.2495-3211A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182537036 | |||||||
chr1:182537121 | T | C | 1 | a0002c0002t0001g0171 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.2495-3126T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182537121 | |||||||
chr1:182537155 | T | A | 4 | a0001c0001t0001g0146 a0003c0003t0001g0209 a0006c0011t0001g0186 others(1): Show |
4 | HG01884.hp1 HG02055.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2495-3092T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182537155 | |||||||
chr1:182537186 | C | T | 4 | a0001c0001t0001g0146 a0003c0003t0001g0209 a0006c0011t0001g0186 others(1): Show |
4 | HG01884.hp1 HG02055.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2495-3061C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182537186 | |||||||
chr1:182537273 | C | T | 1 | a0001c0006t0001g0137 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2495-2974C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182537273 | |||||||
chr1:182537303 | T | G | 4 | a0001c0001t0001g0146 a0003c0003t0001g0209 a0006c0011t0001g0186 others(1): Show |
4 | HG01884.hp1 HG02055.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2495-2944T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182537303 | |||||||
chr1:182537322 | T | A | 1 | a0001c0001t0001g0146 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2495-2925T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182537322 | |||||||
chr1:182537342 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2495-2905G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182537342 | |||||||
chr1:182537345 | T | C | 4 | a0001c0001t0001g0146 a0003c0003t0001g0209 a0006c0011t0001g0186 others(1): Show |
4 | HG01884.hp1 HG02055.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2495-2902T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182537345 | |||||||
chr1:182537384 | A | G | 9 | a0001c0004t0001g0178 a0001c0004t0001g0181 a0001c0004t0001g0191 others(6): Show |
9 | HG00099.hp1 HG00642.hp1 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.2495-2863A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182537384 | |||||||
chr1:182537391 | C | G | 4 | a0001c0001t0001g0146 a0003c0003t0001g0209 a0006c0011t0001g0186 others(1): Show |
4 | HG01884.hp1 HG02055.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2495-2856C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182537391 | |||||||
chr1:182537450 | T | C | 4 | a0001c0001t0001g0146 a0003c0003t0001g0209 a0006c0011t0001g0186 others(1): Show |
4 | HG01884.hp1 HG02055.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2495-2797T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182537450 | |||||||
chr1:182537467 | A | G | 1 | a0003c0003t0002g0029 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2495-2780A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182537467 | |||||||
chr1:182537492 | C | T | 4 | a0001c0001t0001g0146 a0003c0003t0001g0209 a0006c0011t0001g0186 others(1): Show |
4 | HG01884.hp1 HG02055.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2495-2755C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182537492 | |||||||
chr1:182537588 | C | T | 4 | a0001c0001t0001g0146 a0003c0003t0001g0209 a0006c0011t0001g0186 others(1): Show |
4 | HG01884.hp1 HG02055.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2495-2659C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182537588 | |||||||
chr1:182537611 | T | C | 4 | a0001c0001t0001g0146 a0003c0003t0001g0209 a0006c0011t0001g0186 others(1): Show |
4 | HG01884.hp1 HG02055.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2495-2636T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182537611 | |||||||
chr1:182537687 | T | C | 9 | a0001c0004t0001g0178 a0001c0004t0001g0181 a0001c0004t0001g0191 others(6): Show |
9 | HG00099.hp1 HG00642.hp1 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.2495-2560T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182537687 | |||||||
chr1:182537739 | G | A | 5 | a0001c0001t0001g0104 a0001c0001t0001g0185 a0001c0001t0001g0200 others(2): Show |
5 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2495-2508G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182537739 | |||||||
chr1:182537774 | C | A | 4 | a0001c0001t0001g0146 a0003c0003t0001g0209 a0006c0011t0001g0186 others(1): Show |
4 | HG01884.hp1 HG02055.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2495-2473C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182537774 | |||||||
chr1:182537830 | T | C | 4 | a0001c0001t0001g0146 a0003c0003t0001g0209 a0006c0011t0001g0186 others(1): Show |
4 | HG01884.hp1 HG02055.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2495-2417T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182537830 | |||||||
chr1:182537840 | G | A | 3 | a0001c0001t0001g0114 a0001c0001t0001g0182 a0012c0019t0001g0216 |
3 | HG01243.hp2 HG01346.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2495-2407G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182537840 | |||||||
chr1:182537979 | G | A | 2 | a0001c0001t0001g0146 a0003c0003t0001g0209 |
2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2495-2268G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182537979 | |||||||
chr1:182538114 | C | G | 1 | a0003c0003t0001g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2495-2133C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182538114 | |||||||
chr1:182538229 | G | C | 1 | a0001c0004t0001g0181 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2495-2018G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182538229 | |||||||
chr1:182538246 | A | C | 2 | a0007c0013t0001g0263 a0007c0013t0001g0264 |
2 | HG02109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2495-2001A>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182538246 | |||||||
chr1:182538325 | C | G | 5 | a0001c0001t0001g0104 a0001c0001t0001g0185 a0001c0001t0001g0200 others(2): Show |
5 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2495-1922C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182538325 | |||||||
chr1:182538336 | T | C | 123 | a0001c0001t0001g0048 a0001c0001t0001g0198 a0001c0001t0001g0230 others(120): Show |
126 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.2495-1911T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182538336 | |||||||
chr1:182538370 | G | A | 6 | a0001c0001t0001g0146 a0001c0001t0001g0184 a0001c0001t0001g0268 others(3): Show |
6 | HG01884.hp1 HG02055.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.2495-1877G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182538370 | |||||||
chr1:182538436 | G | A | 36 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0053 others(33): Show |
37 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.2495-1811G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182538436 | |||||||
chr1:182538459 | C | T | 2 | a0008c0010t0001g0203 a0008c0010t0001g0204 |
2 | HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2495-1788C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182538459 | |||||||
chr1:182538460 | G | C | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2495-1787G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182538460 | |||||||
chr1:182538461 | G | T | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2495-1786G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182538461 | |||||||
chr1:182538484 | T | C | 6 | a0001c0001t0001g0146 a0001c0001t0001g0184 a0001c0001t0001g0268 others(3): Show |
6 | HG01884.hp1 HG02055.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.2495-1763T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182538484 | |||||||
chr1:182538527 | C | CA | 12 | a0001c0001t0001g0190 a0001c0001t0001g0306 a0001c0004t0001g0023 others(9): Show |
12 | HG00099.hp1 HG00642.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.2495-1706dupA | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr1 | 182538527 | ||||||
chr1:182538527 | CA | C | 8 | a0001c0001t0001g0146 a0001c0001t0001g0184 a0001c0001t0001g0268 others(5): Show |
8 | HG01884.hp1 HG02055.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.2495-1706delA | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr1 | 182538527 | ||||||
chr1:182538667 | G | GGGA | 7 | a0001c0004t0002g0019 a0001c0004t0002g0045 a0001c0004t0002g0055 others(4): Show |
7 | NA18941.hp1 NA18965.hp1 NA19004.hp2 others(4): Show |
intron_variant | MODIFIER | c.2495-1577_2495-157 others(7): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr1 | 182538667 | ||||||
chr1:182538670 | A | G | 5 | a0001c0001t0001g0184 a0001c0001t0001g0268 a0003c0003t0001g0209 others(2): Show |
5 | HG01884.hp1 HG02109.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2495-1577A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182538670 | |||||||
chr1:182538746 | G | A | 1 | a0001c0004t0001g0269 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2495-1501G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182538746 | |||||||
chr1:182538764 | C | T | 2 | a0001c0001t0001g0146 a0003c0003t0001g0209 |
2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2495-1483C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182538764 | |||||||
chr1:182538838 | C | T | 1 | a0011c0021t0001g0170 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2495-1409C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182538838 | |||||||
chr1:182538864 | T | A | 1 | a0001c0017t0001g0067 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2495-1383T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182538864 | |||||||
chr1:182538900 | A | G | 129 | a0001c0001t0001g0048 a0001c0001t0001g0146 a0001c0001t0001g0184 others(126): Show |
132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.2495-1347A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182538900 | |||||||
chr1:182538909 | A | G | 129 | a0001c0001t0001g0048 a0001c0001t0001g0146 a0001c0001t0001g0184 others(126): Show |
132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.2495-1338A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182538909 | |||||||
chr1:182539274 | CTT | C | 15 | a0001c0001t0001g0230 a0001c0004t0001g0010 a0001c0004t0001g0023 others(12): Show |
15 | HG00140.hp1 HG00735.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.2495-967_2495-966d others(4): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr1 | 182539274 | ||||||
chr1:182539447 | T | A | 127 | a0001c0001t0001g0048 a0001c0001t0001g0146 a0001c0001t0001g0184 others(124): Show |
130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.2495-800T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182539447 | |||||||
chr1:182539448 | A | G | 127 | a0001c0001t0001g0048 a0001c0001t0001g0146 a0001c0001t0001g0184 others(124): Show |
130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.2495-799A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182539448 | |||||||
chr1:182539474 | A | G | 1 | a0002c0002t0001g0096 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.2495-773A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182539474 | |||||||
chr1:182539580 | A | AC | 127 | a0001c0001t0001g0048 a0001c0001t0001g0146 a0001c0001t0001g0184 others(124): Show |
130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.2495-665dupC | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr1 | 182539580 | ||||||
chr1:182539626 | A | G | 127 | a0001c0001t0001g0048 a0001c0001t0001g0146 a0001c0001t0001g0184 others(124): Show |
130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.2495-621A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182539626 | |||||||
chr1:182539656 | C | T | 127 | a0001c0001t0001g0048 a0001c0001t0001g0146 a0001c0001t0001g0184 others(124): Show |
130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.2495-591C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182539656 | |||||||
chr1:182539801 | A | G | 127 | a0001c0001t0001g0048 a0001c0001t0001g0146 a0001c0001t0001g0184 others(124): Show |
130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.2495-446A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182539801 | |||||||
chr1:182539820 | T | A | 3 | a0001c0001t0001g0114 a0001c0001t0001g0182 a0012c0019t0001g0216 |
3 | HG01243.hp2 HG01346.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2495-427T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182539820 | |||||||
chr1:182539913 | T | C | 127 | a0001c0001t0001g0048 a0001c0001t0001g0146 a0001c0001t0001g0184 others(124): Show |
130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.2495-334T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182539913 | |||||||
chr1:182540026 | G | A | 127 | a0001c0001t0001g0048 a0001c0001t0001g0146 a0001c0001t0001g0184 others(124): Show |
130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.2495-221G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182540026 | |||||||
chr1:182540134 | G | A | 211 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(208): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.2495-113G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182540134 | |||||||
chr1:182540155 | A | G | 1 | a0001c0017t0001g0067 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2495-92A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182540155 | |||||||
chr1:182540157 | A | G | 127 | a0001c0001t0001g0048 a0001c0001t0001g0146 a0001c0001t0001g0184 others(124): Show |
130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.2495-90A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 14/21 | chr1 | 182540157 | |||||||
chr1:182540463 | T | C | 34 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0015 others(31): Show |
36 | HG00438.hp2 HG00735.hp2 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.2669+42T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182540463 | |||||||
chr1:182540481 | C | T | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2669+60C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182540481 | |||||||
chr1:182540482 | C | A | 121 | a0001c0001t0001g0048 a0001c0001t0001g0198 a0001c0001t0001g0230 others(118): Show |
124 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.2669+61C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182540482 | |||||||
chr1:182540482 | C | G | 6 | a0001c0001t0001g0146 a0001c0001t0001g0184 a0001c0001t0001g0268 others(3): Show |
6 | HG01884.hp1 HG02055.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.2669+61C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182540482 | |||||||
chr1:182540499 | A | G | 1 | a0003c0003t0001g0155 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2669+78A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182540499 | |||||||
chr1:182540511 | T | C | 127 | a0001c0001t0001g0048 a0001c0001t0001g0146 a0001c0001t0001g0184 others(124): Show |
130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.2669+90T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182540511 | |||||||
chr1:182540785 | G | A | 1 | a0001c0004t0001g0102 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2669+364G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182540785 | |||||||
chr1:182540936 | A | G | 127 | a0001c0001t0001g0048 a0001c0001t0001g0146 a0001c0001t0001g0184 others(124): Show |
130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.2669+515A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182540936 | |||||||
chr1:182540978 | T | G | 1 | a0003c0003t0001g0152 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.2669+557T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182540978 | |||||||
chr1:182540999 | T | C | 7 | a0001c0001t0001g0173 a0001c0001t0001g0175 a0001c0001t0001g0176 others(4): Show |
7 | HG01884.hp2 HG02451.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2669+578T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182540999 | |||||||
chr1:182541039 | T | A | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2669+618T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182541039 | |||||||
chr1:182541053 | C | T | 127 | a0001c0001t0001g0048 a0001c0001t0001g0146 a0001c0001t0001g0184 others(124): Show |
130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.2669+632C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182541053 | |||||||
chr1:182541134 | G | A | 125 | a0001c0001t0001g0048 a0001c0001t0001g0146 a0001c0001t0001g0184 others(122): Show |
128 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.2669+713G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182541134 | |||||||
chr1:182541175 | C | A | 127 | a0001c0001t0001g0048 a0001c0001t0001g0146 a0001c0001t0001g0184 others(124): Show |
130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.2669+754C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182541175 | |||||||
chr1:182541446 | T | C | 127 | a0001c0001t0001g0048 a0001c0001t0001g0146 a0001c0001t0001g0184 others(124): Show |
130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.2669+1025T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182541446 | |||||||
chr1:182541527 | A | G | 2 | a0008c0010t0001g0203 a0008c0010t0001g0204 |
2 | HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2669+1106A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182541527 | |||||||
chr1:182541581 | G | A | 1 | a0003c0003t0001g0209 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2669+1160G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182541581 | |||||||
chr1:182541765 | C | T | 2 | a0001c0005t0001g0108 a0001c0005t0001g0113 |
2 | HG02572.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2669+1344C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182541765 | |||||||
chr1:182541766 | G | C | 127 | a0001c0001t0001g0048 a0001c0001t0001g0146 a0001c0001t0001g0184 others(124): Show |
130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.2669+1345G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182541766 | |||||||
chr1:182541840 | G | A | 1 | a0001c0006t0001g0138 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2669+1419G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182541840 | |||||||
chr1:182542053 | C | T | 2 | a0001c0001t0001g0236 a0001c0001t0001g0237 |
2 | HG00280.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.2669+1632C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182542053 | |||||||
chr1:182542113 | T | C | 2 | a0008c0010t0001g0203 a0008c0010t0001g0204 |
2 | HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2669+1692T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182542113 | |||||||
chr1:182542114 | C | T | 127 | a0001c0001t0001g0048 a0001c0001t0001g0146 a0001c0001t0001g0184 others(124): Show |
130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.2669+1693C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182542114 | |||||||
chr1:182542250 | G | C | 2 | a0001c0001t0001g0184 a0001c0001t0001g0268 |
2 | HG02109.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2669+1829G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182542250 | |||||||
chr1:182542263 | T | G | 127 | a0001c0001t0001g0048 a0001c0001t0001g0146 a0001c0001t0001g0184 others(124): Show |
130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.2669+1842T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182542263 | |||||||
chr1:182542331 | C | T | 127 | a0001c0001t0001g0048 a0001c0001t0001g0146 a0001c0001t0001g0184 others(124): Show |
130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.2669+1910C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182542331 | |||||||
chr1:182542346 | C | G | 1 | a0001c0001t0001g0268 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2669+1925C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182542346 | |||||||
chr1:182542410 | T | C | 121 | a0001c0001t0001g0048 a0001c0001t0001g0198 a0001c0001t0001g0230 others(118): Show |
124 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.2669+1989T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182542410 | |||||||
chr1:182542537 | G | T | 3 | a0001c0001t0001g0114 a0001c0001t0001g0182 a0012c0019t0001g0216 |
3 | HG01243.hp2 HG01346.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2669+2116G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182542537 | |||||||
chr1:182542577 | AT | A | 127 | a0001c0001t0001g0048 a0001c0001t0001g0146 a0001c0001t0001g0184 others(124): Show |
130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.2669+2165delT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr1 | 182542577 | ||||||
chr1:182542599 | A | G | 2 | a0001c0001t0001g0066 a0001c0001t0001g0273 |
2 | NA18944.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.2669+2178A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182542599 | |||||||
chr1:182542634 | A | G | 127 | a0001c0001t0001g0048 a0001c0001t0001g0146 a0001c0001t0001g0184 others(124): Show |
130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.2669+2213A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182542634 | |||||||
chr1:182542925 | A | C | 4 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0199 others(1): Show |
4 | HG01069.hp1 HG02922.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2669+2504A>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182542925 | |||||||
chr1:182543000 | G | T | 2 | a0002c0002t0001g0327 a0002c0002t0001g0328 |
2 | HG02145.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.2669+2579G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182543000 | |||||||
chr1:182543065 | T | G | 1 | a0001c0004t0001g0010 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2669+2644T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182543065 | |||||||
chr1:182543136 | A | G | 127 | a0001c0001t0001g0048 a0001c0001t0001g0146 a0001c0001t0001g0184 others(124): Show |
130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.2669+2715A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182543136 | |||||||
chr1:182543179 | C | T | 1 | a0001c0001t0001g0306 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2669+2758C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182543179 | |||||||
chr1:182543192 | C | A | 127 | a0001c0001t0001g0048 a0001c0001t0001g0146 a0001c0001t0001g0184 others(124): Show |
130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.2669+2771C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182543192 | |||||||
chr1:182543363 | G | A | 2 | a0001c0001t0001g0184 a0001c0001t0001g0268 |
2 | HG02109.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2669+2942G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182543363 | |||||||
chr1:182543383 | A | G | 1 | a0001c0001t0001g0088 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2669+2962A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182543383 | |||||||
chr1:182543411 | G | A | 127 | a0001c0001t0001g0048 a0001c0001t0001g0146 a0001c0001t0001g0184 others(124): Show |
130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.2669+2990G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182543411 | |||||||
chr1:182543533 | A | G | 129 | a0001c0001t0001g0048 a0001c0001t0001g0146 a0001c0001t0001g0184 others(126): Show |
132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.2669+3112A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182543533 | |||||||
chr1:182543629 | T | C | 129 | a0001c0001t0001g0048 a0001c0001t0001g0146 a0001c0001t0001g0184 others(126): Show |
132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.2669+3208T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182543629 | |||||||
chr1:182543708 | T | G | 129 | a0001c0001t0001g0048 a0001c0001t0001g0146 a0001c0001t0001g0184 others(126): Show |
132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.2669+3287T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182543708 | |||||||
chr1:182543746 | C | G | 1 | a0001c0001t0001g0184 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2669+3325C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182543746 | |||||||
chr1:182543774 | C | T | 129 | a0001c0001t0001g0048 a0001c0001t0001g0146 a0001c0001t0001g0184 others(126): Show |
132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.2669+3353C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182543774 | |||||||
chr1:182543775 | G | A | 6 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0213 others(3): Show |
6 | HG01884.hp2 HG02451.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.2669+3354G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182543775 | |||||||
chr1:182543851 | A | G | 2 | a0001c0001t0001g0244 a0003c0003t0001g0158 |
2 | NA18963.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.2669+3430A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182543851 | |||||||
chr1:182543952 | A | G | 2 | a0008c0010t0001g0203 a0008c0010t0001g0204 |
2 | HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2669+3531A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182543952 | |||||||
chr1:182544226 | T | A | 13 | a0001c0005t0001g0011 a0001c0005t0001g0108 a0001c0005t0001g0113 others(10): Show |
13 | HG02258.hp2 HG02572.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.2669+3805T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182544226 | |||||||
chr1:182544251 | T | C | 4 | a0002c0002t0001g0081 a0002c0002t0001g0141 a0002c0002t0001g0142 others(1): Show |
4 | NA18978.hp2 NA19011.hp1 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.2669+3830T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182544251 | |||||||
chr1:182544279 | T | G | 138 | a0001c0001t0001g0048 a0001c0001t0001g0146 a0001c0001t0001g0184 others(135): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.2669+3858T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182544279 | |||||||
chr1:182544357 | C | A | 2 | a0001c0001t0001g0146 a0003c0003t0001g0209 |
2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2669+3936C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182544357 | |||||||
chr1:182544558 | A | G | 127 | a0001c0001t0001g0048 a0001c0001t0001g0146 a0001c0001t0001g0184 others(124): Show |
130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.2670-3759A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182544558 | |||||||
chr1:182544575 | A | G | 1 | a0001c0001t0001g0192 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2670-3742A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182544575 | |||||||
chr1:182544598 | A | AT | 129 | a0001c0001t0001g0048 a0001c0001t0001g0146 a0001c0001t0001g0184 others(126): Show |
132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.2670-3717dupT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr1 | 182544598 | ||||||
chr1:182544677 | T | G | 1 | a0003c0024t0001g0105 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2670-3640T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182544677 | |||||||
chr1:182544735 | C | T | 129 | a0001c0001t0001g0048 a0001c0001t0001g0146 a0001c0001t0001g0184 others(126): Show |
132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.2670-3582C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182544735 | |||||||
chr1:182544801 | A | G | 129 | a0001c0001t0001g0048 a0001c0001t0001g0146 a0001c0001t0001g0184 others(126): Show |
132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.2670-3516A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182544801 | |||||||
chr1:182545058 | A | G | 123 | a0001c0001t0001g0048 a0001c0001t0001g0198 a0001c0001t0001g0230 others(120): Show |
126 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.2670-3259A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182545058 | |||||||
chr1:182545243 | T | C | 129 | a0001c0001t0001g0048 a0001c0001t0001g0146 a0001c0001t0001g0184 others(126): Show |
132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.2670-3074T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182545243 | |||||||
chr1:182545246 | A | C | 31 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0053 others(28): Show |
32 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(29): Show |
intron_variant | MODIFIER | c.2670-3071A>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182545246 | |||||||
chr1:182545390 | T | C | 7 | a0003c0003t0001g0047 a0003c0003t0001g0052 a0003c0003t0001g0156 others(4): Show |
7 | HG00280.hp1 NA18947.hp2 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.2670-2927T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182545390 | |||||||
chr1:182545415 | T | C | 19 | a0001c0001t0001g0230 a0001c0001t0001g0238 a0001c0001t0001g0277 others(16): Show |
19 | HG00140.hp1 HG00140.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.2670-2902T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182545415 | |||||||
chr1:182545494 | A | C | 1 | a0002c0002t0001g0171 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.2670-2823A>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182545494 | |||||||
chr1:182545516 | G | C | 2 | a0001c0001t0001g0146 a0003c0003t0001g0209 |
2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2670-2801G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182545516 | |||||||
chr1:182545525 | T | A | 6 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0199 others(3): Show |
6 | HG01069.hp1 HG02280.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2670-2792T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182545525 | |||||||
chr1:182545525 | T | C | 1 | a0001c0001t0001g0091 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2670-2792T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182545525 | |||||||
chr1:182545595 | G | A | 1 | a0001c0004t0001g0129 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2670-2722G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182545595 | |||||||
chr1:182545608 | C | T | 1 | a0002c0002t0001g0109 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2670-2709C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182545608 | |||||||
chr1:182545648 | C | T | 129 | a0001c0001t0001g0048 a0001c0001t0001g0146 a0001c0001t0001g0184 others(126): Show |
132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.2670-2669C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182545648 | |||||||
chr1:182545711 | G | T | 129 | a0001c0001t0001g0048 a0001c0001t0001g0146 a0001c0001t0001g0184 others(126): Show |
132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.2670-2606G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182545711 | |||||||
chr1:182545717 | T | G | 129 | a0001c0001t0001g0048 a0001c0001t0001g0146 a0001c0001t0001g0184 others(126): Show |
132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.2670-2600T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182545717 | |||||||
chr1:182545737 | T | G | 129 | a0001c0001t0001g0048 a0001c0001t0001g0146 a0001c0001t0001g0184 others(126): Show |
132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.2670-2580T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182545737 | |||||||
chr1:182545908 | A | G | 129 | a0001c0001t0001g0048 a0001c0001t0001g0146 a0001c0001t0001g0184 others(126): Show |
132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.2670-2409A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182545908 | |||||||
chr1:182545911 | T | C | 129 | a0001c0001t0001g0048 a0001c0001t0001g0146 a0001c0001t0001g0184 others(126): Show |
132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.2670-2406T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182545911 | |||||||
chr1:182545946 | C | T | 1 | a0013c0015t0001g0050 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2670-2371C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182545946 | |||||||
chr1:182546184 | GTTTGT | G | 7 | a0001c0001t0001g0173 a0001c0001t0001g0175 a0001c0001t0001g0176 others(4): Show |
7 | HG01884.hp2 HG02451.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2670-2128_2670-212 others(9): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr1 | 182546184 | ||||||
chr1:182546332 | T | C | 2 | a0001c0001t0001g0103 a0001c0001t0001g0205 |
2 | HG02965.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2670-1985T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182546332 | |||||||
chr1:182546341 | G | T | 129 | a0001c0001t0001g0048 a0001c0001t0001g0146 a0001c0001t0001g0184 others(126): Show |
132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.2670-1976G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182546341 | |||||||
chr1:182546347 | C | CT | 8 | a0001c0001t0001g0173 a0001c0001t0001g0175 a0001c0001t0001g0176 others(5): Show |
8 | HG01884.hp2 HG02451.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.2670-1958dupT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr1 | 182546347 | ||||||
chr1:182546347 | CT | C | 117 | a0001c0001t0001g0048 a0001c0001t0001g0198 a0001c0001t0001g0238 others(114): Show |
120 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.2670-1958delT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr1 | 182546347 | ||||||
chr1:182546347 | CTT | C | 9 | a0001c0001t0001g0146 a0001c0001t0001g0184 a0001c0001t0001g0230 others(6): Show |
9 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.2670-1959_2670-195 others(6): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr1 | 182546347 | ||||||
chr1:182546403 | T | A | 1 | a0003c0003t0002g0006 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.2670-1914T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182546403 | |||||||
chr1:182546420 | C | T | 5 | a0001c0001t0001g0104 a0001c0001t0001g0185 a0001c0001t0001g0200 others(2): Show |
5 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2670-1897C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182546420 | |||||||
chr1:182546550 | C | T | 1 | a0001c0005t0001g0134 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2670-1767C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182546550 | |||||||
chr1:182546579 | G | A | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2670-1738G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182546579 | |||||||
chr1:182546633 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2670-1684C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182546633 | |||||||
chr1:182546774 | C | G | 1 | a0001c0004t0001g0285 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2670-1543C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182546774 | |||||||
chr1:182546899 | G | A | 129 | a0001c0001t0001g0048 a0001c0001t0001g0146 a0001c0001t0001g0184 others(126): Show |
132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.2670-1418G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182546899 | |||||||
chr1:182547005 | T | G | 1 | a0001c0017t0001g0067 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2670-1312T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182547005 | |||||||
chr1:182547097 | G | T | 1 | a0001c0004t0001g0285 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2670-1220G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182547097 | |||||||
chr1:182547117 | C | T | 129 | a0001c0001t0001g0048 a0001c0001t0001g0146 a0001c0001t0001g0184 others(126): Show |
132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.2670-1200C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182547117 | |||||||
chr1:182547163 | A | G | 3 | a0001c0001t0001g0114 a0001c0001t0001g0182 a0012c0019t0001g0216 |
3 | HG01243.hp2 HG01346.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2670-1154A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182547163 | |||||||
chr1:182547244 | T | C | 129 | a0001c0001t0001g0048 a0001c0001t0001g0146 a0001c0001t0001g0184 others(126): Show |
132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.2670-1073T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182547244 | |||||||
chr1:182547383 | T | TA | 211 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0048 others(208): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.2670-934_2670-933i others(3): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182547383 | |||||||
chr1:182547419 | T | C | 129 | a0001c0001t0001g0048 a0001c0001t0001g0146 a0001c0001t0001g0184 others(126): Show |
132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.2670-898T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182547419 | |||||||
chr1:182547425 | T | C | 1 | a0005c0008t0001g0085 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2670-892T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182547425 | |||||||
chr1:182547536 | T | C | 5 | a0003c0003t0001g0166 a0003c0003t0001g0168 a0003c0003t0002g0002 others(2): Show |
7 | HG02135.hp1 NA18980.hp1 NA19010.hp2 others(4): Show |
intron_variant | MODIFIER | c.2670-781T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182547536 | |||||||
chr1:182547605 | T | C | 1 | a0002c0002t0001g0121 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2670-712T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182547605 | |||||||
chr1:182547689 | G | A | 2 | a0001c0001t0001g0184 a0001c0001t0001g0268 |
2 | HG02109.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2670-628G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182547689 | |||||||
chr1:182547712 | T | A | 129 | a0001c0001t0001g0048 a0001c0001t0001g0146 a0001c0001t0001g0184 others(126): Show |
132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.2670-605T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182547712 | |||||||
chr1:182547758 | G | A | 1 | a0003c0003t0002g0214 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2670-559G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182547758 | |||||||
chr1:182547768 | G | A | 3 | a0001c0001t0001g0114 a0001c0001t0001g0182 a0012c0019t0001g0216 |
3 | HG01243.hp2 HG01346.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2670-549G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182547768 | |||||||
chr1:182547785 | C | T | 1 | a0001c0001t0001g0304 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2670-532C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182547785 | |||||||
chr1:182547816 | A | G | 325 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(322): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.2670-501A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182547816 | |||||||
chr1:182547856 | A | G | 129 | a0001c0001t0001g0048 a0001c0001t0001g0146 a0001c0001t0001g0184 others(126): Show |
132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.2670-461A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182547856 | |||||||
chr1:182547860 | C | CA | 7 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0199 others(4): Show |
7 | HG01069.hp1 HG02280.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.2670-447dupA | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr1 | 182547860 | ||||||
chr1:182547860 | CA | C | 9 | a0001c0004t0001g0178 a0001c0004t0001g0181 a0001c0004t0001g0191 others(6): Show |
9 | HG00099.hp1 HG00642.hp1 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.2670-447delA | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr1 | 182547860 | ||||||
chr1:182548010 | C | T | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2670-307C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182548010 | |||||||
chr1:182548103 | C | A | 129 | a0001c0001t0001g0048 a0001c0001t0001g0146 a0001c0001t0001g0184 others(126): Show |
132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.2670-214C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182548103 | |||||||
chr1:182548222 | G | C | 129 | a0001c0001t0001g0048 a0001c0001t0001g0146 a0001c0001t0001g0184 others(126): Show |
132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.2670-95G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 15/21 | chr1 | 182548222 | |||||||
chr1:182548479 | C | G | 2 | a0003c0003t0002g0029 a0003c0003t0002g0058 |
2 | HG02280.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2808+24C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 16/21 | chr1 | 182548479 | |||||||
chr1:182548507 | C | A | 66 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0053 others(63): Show |
67 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.2808+52C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 16/21 | chr1 | 182548507 | |||||||
chr1:182548916 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2933+92G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182548916 | |||||||
chr1:182549027 | T | C | 22 | a0001c0001t0001g0173 a0001c0001t0001g0175 a0001c0001t0001g0176 others(19): Show |
22 | HG01884.hp2 HG02257.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.2933+203T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182549027 | |||||||
chr1:182549028 | A | G | 2 | a0008c0010t0001g0203 a0008c0010t0001g0204 |
2 | HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2933+204A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182549028 | |||||||
chr1:182549044 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2933+220C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182549044 | |||||||
chr1:182549061 | C | G | 3 | a0001c0001t0001g0114 a0001c0001t0001g0182 a0012c0019t0001g0216 |
3 | HG01243.hp2 HG01346.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2933+237C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182549061 | |||||||
chr1:182549129 | G | C | 128 | a0001c0001t0001g0048 a0001c0001t0001g0146 a0001c0001t0001g0184 others(125): Show |
131 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.2933+305G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182549129 | |||||||
chr1:182549187 | G | A | 5 | a0001c0005t0001g0011 a0001c0005t0001g0108 a0001c0005t0001g0113 others(2): Show |
5 | HG02572.hp2 HG02717.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.2933+363G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182549187 | |||||||
chr1:182549204 | T | C | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2933+380T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182549204 | |||||||
chr1:182549279 | C | T | 128 | a0001c0001t0001g0048 a0001c0001t0001g0057 a0001c0001t0001g0094 others(125): Show |
131 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.2933+455C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182549279 | |||||||
chr1:182549310 | C | T | 2 | a0001c0004t0001g0221 a0001c0004t0001g0222 |
2 | HG01255.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.2933+486C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182549310 | |||||||
chr1:182549347 | T | G | 1 | a0002c0002t0001g0074 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.2933+523T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182549347 | |||||||
chr1:182549356 | T | C | 1 | a0001c0004t0001g0202 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2933+532T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182549356 | |||||||
chr1:182549489 | G | A | 16 | a0001c0004t0001g0178 a0001c0004t0001g0181 a0001c0004t0001g0191 others(13): Show |
16 | HG00099.hp1 HG00642.hp1 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.2933+665G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182549489 | |||||||
chr1:182549507 | T | G | 16 | a0001c0004t0001g0178 a0001c0004t0001g0181 a0001c0004t0001g0191 others(13): Show |
16 | HG00099.hp1 HG00642.hp1 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.2933+683T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182549507 | |||||||
chr1:182549534 | T | C | 1 | a0003c0003t0002g0025 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2933+710T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182549534 | |||||||
chr1:182549585 | G | A | 5 | a0001c0001t0001g0104 a0001c0001t0001g0185 a0001c0001t0001g0200 others(2): Show |
5 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2933+761G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182549585 | |||||||
chr1:182549648 | G | T | 32 | a0001c0001t0001g0244 a0002c0002t0001g0071 a0002c0002t0001g0089 others(29): Show |
32 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.2933+824G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182549648 | |||||||
chr1:182549908 | A | G | 2 | a0001c0001t0001g0182 a0012c0019t0001g0216 |
2 | HG01243.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2933+1084A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182549908 | |||||||
chr1:182549977 | G | C | 1 | a0001c0007t0001g0022 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2934-1123G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182549977 | |||||||
chr1:182550000 | G | A | 3 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0009c0018t0001g0295 |
3 | HG00438.hp2 NA18962.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.2934-1100G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182550000 | |||||||
chr1:182550148 | G | A | 8 | a0001c0001t0001g0184 a0001c0001t0001g0196 a0001c0001t0001g0197 others(5): Show |
8 | HG01069.hp1 HG02109.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.2934-952G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182550148 | |||||||
chr1:182550223 | A | G | 2 | a0001c0001t0001g0184 a0001c0001t0001g0268 |
2 | HG02109.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2934-877A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182550223 | |||||||
chr1:182550227 | A | G | 2 | a0001c0005t0001g0108 a0001c0005t0001g0113 |
2 | HG02572.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2934-873A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182550227 | |||||||
chr1:182550281 | C | A | 2 | a0001c0001t0001g0184 a0001c0001t0001g0268 |
2 | HG02109.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2934-819C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182550281 | |||||||
chr1:182550299 | C | T | 4 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0199 others(1): Show |
4 | HG01069.hp1 HG02922.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2934-801C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182550299 | |||||||
chr1:182550300 | G | A | 2 | a0001c0004t0001g0224 a0001c0004t0001g0275 |
2 | NA18962.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.2934-800G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182550300 | |||||||
chr1:182550330 | A | C | 1 | a0002c0002t0001g0136 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2934-770A>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182550330 | |||||||
chr1:182550431 | G | A | 141 | a0001c0001t0001g0048 a0001c0001t0001g0066 a0001c0001t0001g0173 others(138): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.2934-669G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182550431 | |||||||
chr1:182550436 | A | G | 34 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0015 others(31): Show |
36 | HG00438.hp1 HG00639.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.2934-664A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182550436 | |||||||
chr1:182550679 | AAGT | A | 15 | a0001c0004t0001g0005 a0001c0004t0001g0041 a0001c0004t0001g0093 others(12): Show |
16 | HG01109.hp1 HG02027.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.2934-420_2934-418d others(5): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182550679 | |||||||
chr1:182550682 | T | A | 1 | a0002c0002t0001g0143 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2934-418T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182550682 | |||||||
chr1:182550726 | A | G | 253 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(250): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.2934-374A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182550726 | |||||||
chr1:182550824 | T | C | 91 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(88): Show |
94 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.2934-276T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182550824 | |||||||
chr1:182550862 | A | G | 9 | a0001c0001t0001g0103 a0001c0001t0001g0173 a0001c0001t0001g0175 others(6): Show |
9 | HG01884.hp2 HG02451.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.2934-238A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182550862 | |||||||
chr1:182550885 | T | G | 20 | a0001c0001t0001g0103 a0001c0001t0001g0173 a0001c0001t0001g0175 others(17): Show |
20 | HG01123.hp2 HG01884.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.2934-215T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182550885 | |||||||
chr1:182550894 | C | T | 1 | a0001c0004t0001g0178 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2934-206C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182550894 | |||||||
chr1:182550897 | G | A | 7 | a0001c0001t0001g0173 a0001c0001t0001g0175 a0001c0001t0001g0176 others(4): Show |
7 | HG01884.hp2 HG02451.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2934-203G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182550897 | |||||||
chr1:182550953 | G | A | 1 | a0003c0003t0002g0060 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2934-147G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182550953 | |||||||
chr1:182551071 | C | G | 1 | a0003c0003t0002g0217 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2934-29C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 17/21 | chr1 | 182551071 | |||||||
chr1:182551221 | C | T | 3 | a0001c0001t0001g0114 a0001c0005t0001g0134 a0003c0003t0001g0209 |
3 | HG01346.hp2 HG02258.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.3043+12C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 18/21 | chr1 | 182551221 | |||||||
chr1:182551224 | G | A | 1 | a0003c0024t0001g0105 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3043+15G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 18/21 | chr1 | 182551224 | |||||||
chr1:182551227 | TCA | T | 15 | a0001c0004t0001g0178 a0001c0004t0001g0181 a0001c0004t0001g0191 others(12): Show |
15 | HG00099.hp1 HG00642.hp1 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.3043+21_3043+22del others(2): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr1 | 182551227 | ||||||
chr1:182551292 | C | G | 1 | a0002c0002t0001g0318 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.3043+83C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 18/21 | chr1 | 182551292 | |||||||
chr1:182551477 | A | G | 79 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0015 others(76): Show |
81 | HG00099.hp1 HG00438.hp2 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.3043+268A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 18/21 | chr1 | 182551477 | |||||||
chr1:182551539 | C | G | 2 | a0001c0001t0001g0184 a0001c0001t0001g0268 |
2 | HG02109.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.3043+330C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 18/21 | chr1 | 182551539 | |||||||
chr1:182551569 | G | A | 1 | a0001c0001t0001g0310 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.3043+360G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 18/21 | chr1 | 182551569 | |||||||
chr1:182551592 | G | A | 1 | a0003c0003t0001g0017 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.3043+383G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 18/21 | chr1 | 182551592 | |||||||
chr1:182551737 | CAT | C | 121 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(118): Show |
124 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.3043+540_3043+541d others(4): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr1 | 182551737 | ||||||
chr1:182551931 | G | C | 1 | a0003c0003t0002g0167 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.3043+722G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 18/21 | chr1 | 182551931 | |||||||
chr1:182551990 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3043+781G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 18/21 | chr1 | 182551990 | |||||||
chr1:182552051 | G | A | 6 | a0001c0001t0001g0104 a0001c0001t0001g0185 a0001c0001t0001g0200 others(3): Show |
6 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.3043+842G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 18/21 | chr1 | 182552051 | |||||||
chr1:182552117 | A | AT | 33 | a0001c0001t0001g0007 a0001c0001t0001g0053 a0001c0001t0001g0086 others(30): Show |
34 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(31): Show |
intron_variant | MODIFIER | c.3043+922dupT | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr1 | 182552117 | ||||||
chr1:182552137 | G | A | 34 | a0001c0001t0001g0007 a0001c0001t0001g0053 a0001c0001t0001g0086 others(31): Show |
35 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(32): Show |
intron_variant | MODIFIER | c.3043+928G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 18/21 | chr1 | 182552137 | |||||||
chr1:182552183 | G | A | 15 | a0001c0001t0001g0114 a0001c0001t0001g0146 a0001c0001t0001g0173 others(12): Show |
15 | HG01069.hp1 HG01346.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.3043+974G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 18/21 | chr1 | 182552183 | |||||||
chr1:182552239 | G | A | 1 | a0001c0005t0001g0134 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.3043+1030G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 18/21 | chr1 | 182552239 | |||||||
chr1:182552271 | G | A | 15 | a0001c0004t0001g0178 a0001c0004t0001g0181 a0001c0004t0001g0191 others(12): Show |
15 | HG00099.hp1 HG00642.hp1 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.3043+1062G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 18/21 | chr1 | 182552271 | |||||||
chr1:182552368 | T | C | 244 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(241): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.3044-1087T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 18/21 | chr1 | 182552368 | |||||||
chr1:182552403 | C | T | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3044-1052C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 18/21 | chr1 | 182552403 | |||||||
chr1:182552516 | C | T | 8 | a0001c0001t0001g0114 a0001c0001t0001g0146 a0001c0001t0001g0196 others(5): Show |
8 | HG01069.hp1 HG01346.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.3044-939C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 18/21 | chr1 | 182552516 | |||||||
chr1:182552523 | G | A | 1 | a0002c0002t0001g0032 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3044-932G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 18/21 | chr1 | 182552523 | |||||||
chr1:182552710 | G | A | 2 | a0001c0004t0001g0177 a0001c0004t0001g0269 |
2 | HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.3044-745G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 18/21 | chr1 | 182552710 | |||||||
chr1:182552732 | C | T | 6 | a0001c0001t0001g0104 a0001c0001t0001g0185 a0001c0001t0001g0200 others(3): Show |
6 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.3044-723C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 18/21 | chr1 | 182552732 | |||||||
chr1:182552739 | C | T | 15 | a0001c0004t0001g0178 a0001c0004t0001g0181 a0001c0004t0001g0191 others(12): Show |
15 | HG00099.hp1 HG00642.hp1 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.3044-716C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 18/21 | chr1 | 182552739 | |||||||
chr1:182552740 | T | G | 15 | a0001c0004t0001g0178 a0001c0004t0001g0181 a0001c0004t0001g0191 others(12): Show |
15 | HG00099.hp1 HG00642.hp1 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.3044-715T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 18/21 | chr1 | 182552740 | |||||||
chr1:182552755 | C | T | 4 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0199 others(1): Show |
4 | HG01069.hp1 HG02922.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.3044-700C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 18/21 | chr1 | 182552755 | |||||||
chr1:182553008 | A | G | 59 | a0001c0001t0001g0007 a0001c0001t0001g0053 a0001c0001t0001g0086 others(56): Show |
60 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(57): Show |
intron_variant | MODIFIER | c.3044-447A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 18/21 | chr1 | 182553008 | |||||||
chr1:182553068 | C | CTAATTT | 1 | a0001c0001t0001g0001 | 3 | HG01070.hp1 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.3044-384_3044-379d others(8): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr1 | 182553068 | ||||||
chr1:182553157 | A | G | 123 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(120): Show |
126 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.3044-298A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 18/21 | chr1 | 182553157 | |||||||
chr1:182553397 | T | C | 1 | a0002c0002t0001g0109 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3044-58T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 18/21 | chr1 | 182553397 | |||||||
chr1:182553417 | C | T | 58 | a0001c0001t0001g0007 a0001c0001t0001g0053 a0001c0001t0001g0086 others(55): Show |
59 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(56): Show |
intron_variant | MODIFIER | c.3044-38C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 18/21 | chr1 | 182553417 | |||||||
chr1:182553627 | C | A | 15 | a0001c0004t0001g0178 a0001c0004t0001g0181 a0001c0004t0001g0191 others(12): Show |
15 | HG00099.hp1 HG00642.hp1 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.3130+86C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 19/21 | chr1 | 182553627 | |||||||
chr1:182553789 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.3130+248C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 19/21 | chr1 | 182553789 | |||||||
chr1:182553817 | A | G | 36 | a0001c0001t0001g0007 a0001c0001t0001g0053 a0001c0001t0001g0086 others(33): Show |
37 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.3130+276A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 19/21 | chr1 | 182553817 | |||||||
chr1:182553850 | C | T | 20 | a0001c0001t0001g0103 a0001c0001t0001g0173 a0001c0001t0001g0175 others(17): Show |
20 | HG01123.hp2 HG01884.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.3130+309C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 19/21 | chr1 | 182553850 | |||||||
chr1:182554087 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3131-540C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 19/21 | chr1 | 182554087 | |||||||
chr1:182554349 | T | G | 36 | a0001c0001t0001g0007 a0001c0001t0001g0053 a0001c0001t0001g0086 others(33): Show |
37 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.3131-278T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 19/21 | chr1 | 182554349 | |||||||
chr1:182554368 | A | G | 59 | a0001c0001t0001g0007 a0001c0001t0001g0053 a0001c0001t0001g0086 others(56): Show |
60 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(57): Show |
intron_variant | MODIFIER | c.3131-259A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 19/21 | chr1 | 182554368 | |||||||
chr1:182554369 | A | G | 59 | a0001c0001t0001g0007 a0001c0001t0001g0053 a0001c0001t0001g0086 others(56): Show |
60 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(57): Show |
intron_variant | MODIFIER | c.3131-258A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 19/21 | chr1 | 182554369 | |||||||
chr1:182554397 | G | A | 15 | a0001c0004t0001g0178 a0001c0004t0001g0181 a0001c0004t0001g0191 others(12): Show |
15 | HG00099.hp1 HG00642.hp1 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.3131-230G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 19/21 | chr1 | 182554397 | |||||||
chr1:182554456 | A | C | 125 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(122): Show |
128 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.3131-171A>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 19/21 | chr1 | 182554456 | |||||||
chr1:182554533 | G | A | 1 | a0002c0002t0001g0318 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.3131-94G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 19/21 | chr1 | 182554533 | |||||||
chr1:182554871 | G | A | 1 | a0001c0005t0001g0267 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3197+178G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 20/21 | chr1 | 182554871 | |||||||
chr1:182554947 | A | G | 1 | a0001c0005t0001g0267 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3197+254A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 20/21 | chr1 | 182554947 | |||||||
chr1:182554967 | C | T | 1 | a0003c0003t0001g0168 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.3197+274C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 20/21 | chr1 | 182554967 | |||||||
chr1:182555002 | G | T | 1 | a0001c0004t0002g0124 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.3197+309G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 20/21 | chr1 | 182555002 | |||||||
chr1:182555064 | G | C | 126 | a0001c0001t0001g0048 a0001c0001t0001g0065 a0001c0001t0001g0066 others(123): Show |
129 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.3197+371G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 20/21 | chr1 | 182555064 | |||||||
chr1:182555093 | T | C | 7 | a0001c0001t0001g0173 a0001c0001t0001g0175 a0001c0001t0001g0176 others(4): Show |
7 | HG01884.hp2 HG02451.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.3197+400T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 20/21 | chr1 | 182555093 | |||||||
chr1:182555138 | C | T | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3197+445C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 20/21 | chr1 | 182555138 | |||||||
chr1:182555143 | G | A | 8 | a0001c0001t0001g0114 a0001c0001t0001g0146 a0001c0001t0001g0196 others(5): Show |
8 | HG01069.hp1 HG01346.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.3197+450G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 20/21 | chr1 | 182555143 | |||||||
chr1:182555177 | C | T | 20 | a0001c0001t0001g0103 a0001c0001t0001g0173 a0001c0001t0001g0175 others(17): Show |
20 | HG01123.hp2 HG01884.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.3197+484C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 20/21 | chr1 | 182555177 | |||||||
chr1:182555178 | G | A | 2 | a0001c0004t0001g0284 a0003c0003t0001g0155 |
2 | HG00423.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.3197+485G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 20/21 | chr1 | 182555178 | |||||||
chr1:182555214 | C | T | 1 | a0001c0001t0001g0015 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.3197+521C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 20/21 | chr1 | 182555214 | |||||||
chr1:182555240 | C | G | 123 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(120): Show |
126 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.3197+547C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 20/21 | chr1 | 182555240 | |||||||
chr1:182555283 | A | G | 36 | a0001c0001t0001g0007 a0001c0001t0001g0053 a0001c0001t0001g0086 others(33): Show |
37 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.3197+590A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 20/21 | chr1 | 182555283 | |||||||
chr1:182555379 | A | G | 38 | a0001c0001t0001g0007 a0001c0001t0001g0053 a0001c0001t0001g0086 others(35): Show |
39 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(36): Show |
intron_variant | MODIFIER | c.3198-645A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 20/21 | chr1 | 182555379 | |||||||
chr1:182555556 | T | C | 45 | a0001c0001t0001g0244 a0001c0001t0001g0307 a0001c0004t0002g0019 others(42): Show |
45 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.3198-468T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 20/21 | chr1 | 182555556 | |||||||
chr1:182555676 | G | T | 2 | a0001c0005t0001g0108 a0001c0005t0001g0113 |
2 | HG02572.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.3198-348G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 20/21 | chr1 | 182555676 | |||||||
chr1:182555754 | C | T | 20 | a0001c0001t0001g0103 a0001c0001t0001g0173 a0001c0001t0001g0175 others(17): Show |
20 | HG01123.hp2 HG01884.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.3198-270C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 20/21 | chr1 | 182555754 | |||||||
chr1:182556252 | C | T | 1 | a0001c0005t0001g0134 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.*165+30C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182556252 | |||||||
chr1:182556253 | G | A | 2 | a0001c0001t0001g0182 a0012c0019t0001g0216 |
2 | HG01243.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.*165+31G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182556253 | |||||||
chr1:182556395 | G | A | 1 | a0003c0003t0001g0152 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.*165+173G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182556395 | |||||||
chr1:182556459 | T | C | 1 | a0003c0003t0001g0161 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.*165+237T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182556459 | |||||||
chr1:182556625 | C | T | 8 | a0001c0001t0001g0114 a0001c0001t0001g0146 a0001c0001t0001g0196 others(5): Show |
8 | HG01069.hp1 HG01346.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.*165+403C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182556625 | |||||||
chr1:182556657 | T | C | 2 | a0001c0001t0001g0184 a0001c0001t0001g0268 |
2 | HG02109.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.*165+435T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182556657 | |||||||
chr1:182556669 | C | A | 6 | a0001c0001t0001g0104 a0001c0001t0001g0185 a0001c0001t0001g0200 others(3): Show |
6 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.*165+447C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182556669 | |||||||
chr1:182556710 | C | T | 2 | a0001c0001t0001g0184 a0001c0001t0001g0268 |
2 | HG02109.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.*165+488C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182556710 | |||||||
chr1:182556730 | C | G | 1 | a0017c0023t0001g0139 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.*165+508C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182556730 | |||||||
chr1:182557450 | G | A | 20 | a0001c0001t0001g0103 a0001c0001t0001g0173 a0001c0001t0001g0175 others(17): Show |
20 | HG01123.hp2 HG01884.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.*165+1228G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182557450 | |||||||
chr1:182557530 | A | T | 1 | a0003c0003t0002g0025 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.*165+1308A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182557530 | |||||||
chr1:182557704 | C | A | 126 | a0001c0001t0001g0048 a0001c0001t0001g0065 a0001c0001t0001g0066 others(123): Show |
129 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.*165+1482C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182557704 | |||||||
chr1:182557742 | T | C | 2 | a0001c0005t0001g0326 a0001c0005t0001g0329 |
2 | HG03130.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.*165+1520T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182557742 | |||||||
chr1:182557770 | A | G | 1 | a0001c0001t0001g0304 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.*165+1548A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182557770 | |||||||
chr1:182557945 | G | GGAGTGGT others(9): Show |
1 | a0001c0004t0001g0324 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.*165+1725_*165+174 others(20): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr1 | 182557945 | ||||||
chr1:182558003 | C | T | 1 | a0001c0004t0001g0010 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.*165+1781C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182558003 | |||||||
chr1:182558054 | A | AGAAG | 3 | a0001c0001t0001g0276 a0006c0011t0001g0186 a0006c0011t0001g0187 |
3 | HG01884.hp1 HG01934.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.*165+1855_*165+185 others(8): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr1 | 182558054 | ||||||
chr1:182558054 | A | AGAAGGAA others(1): Show |
34 | a0001c0001t0001g0007 a0001c0001t0001g0053 a0001c0001t0001g0086 others(31): Show |
35 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(32): Show |
intron_variant | MODIFIER | c.*165+1851_*165+185 others(12): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr1 | 182558054 | ||||||
chr1:182558054 | A | AGAAGGAA others(5): Show |
1 | a0001c0001t0001g0277 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.*165+1847_*165+185 others(16): Show |
RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr1 | 182558054 | ||||||
chr1:182558180 | G | A | 1 | a0003c0003t0002g0228 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.*165+1958G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182558180 | |||||||
chr1:182558225 | G | A | 2 | a0001c0004t0001g0177 a0001c0004t0001g0269 |
2 | HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.*165+2003G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182558225 | |||||||
chr1:182558243 | G | C | 1 | a0001c0001t0001g0040 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.*165+2021G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182558243 | |||||||
chr1:182558244 | A | G | 1 | a0001c0001t0001g0235 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.*165+2022A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182558244 | |||||||
chr1:182558274 | G | A | 36 | a0001c0001t0001g0007 a0001c0001t0001g0053 a0001c0001t0001g0086 others(33): Show |
37 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.*166-2005G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182558274 | |||||||
chr1:182558301 | G | A | 1 | a0003c0003t0002g0092 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.*166-1978G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182558301 | |||||||
chr1:182558304 | G | A | 6 | a0001c0001t0001g0104 a0001c0001t0001g0185 a0001c0001t0001g0200 others(3): Show |
6 | HG02145.hp1 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.*166-1975G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182558304 | |||||||
chr1:182558327 | AG | A | 4 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0199 others(1): Show |
4 | HG01069.hp1 HG02922.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.*166-1949delG | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr1 | 182558327 | ||||||
chr1:182558344 | C | G | 4 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0199 others(1): Show |
4 | HG01069.hp1 HG02922.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.*166-1935C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182558344 | |||||||
chr1:182558407 | A | C | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.*166-1872A>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182558407 | |||||||
chr1:182558450 | G | A | 2 | a0002c0002t0001g0096 a0002c0002t0001g0098 |
2 | NA18973.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.*166-1829G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182558450 | |||||||
chr1:182558641 | G | A | 4 | a0001c0001t0001g0114 a0001c0001t0001g0146 a0001c0005t0001g0134 others(1): Show |
4 | HG01346.hp2 HG02055.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.*166-1638G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182558641 | |||||||
chr1:182558670 | C | A | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.*166-1609C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182558670 | |||||||
chr1:182558687 | A | C | 1 | a0001c0017t0001g0067 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.*166-1592A>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182558687 | |||||||
chr1:182558718 | G | C | 3 | a0002c0002t0001g0110 a0002c0002t0001g0150 a0002c0002t0001g0254 |
3 | HG02015.hp1 NA18970.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.*166-1561G>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182558718 | |||||||
chr1:182558823 | T | C | 2 | a0006c0011t0001g0186 a0006c0011t0001g0187 |
2 | HG01884.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.*166-1456T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182558823 | |||||||
chr1:182558896 | C | T | 3 | a0003c0003t0002g0002 a0003c0003t0002g0054 a0003c0003t0002g0167 |
5 | HG02135.hp1 NA18980.hp1 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.*166-1383C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182558896 | |||||||
chr1:182558988 | T | C | 1 | a0001c0007t0001g0193 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.*166-1291T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182558988 | |||||||
chr1:182558994 | C | T | 11 | a0001c0001t0001g0198 a0001c0004t0001g0102 a0001c0004t0001g0106 others(8): Show |
11 | HG01123.hp2 HG01891.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.*166-1285C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182558994 | |||||||
chr1:182559119 | C | T | 1 | a0003c0003t0001g0158 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.*166-1160C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559119 | |||||||
chr1:182559134 | T | C | 254 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(251): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.*166-1145T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559134 | |||||||
chr1:182559169 | A | G | 1 | a0001c0001t0001g0300 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.*166-1110A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559169 | |||||||
chr1:182559292 | T | G | 34 | a0001c0001t0001g0007 a0001c0001t0001g0053 a0001c0001t0001g0086 others(31): Show |
35 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(32): Show |
intron_variant | MODIFIER | c.*166-987T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559292 | |||||||
chr1:182559298 | C | T | 34 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0015 others(31): Show |
36 | HG00438.hp2 HG00639.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.*166-981C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559298 | |||||||
chr1:182559358 | A | T | 2 | a0001c0001t0001g0101 a0001c0001t0001g0239 |
2 | HG02040.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.*166-921A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559358 | |||||||
chr1:182559481 | G | A | 34 | a0001c0001t0001g0007 a0001c0001t0001g0053 a0001c0001t0001g0086 others(31): Show |
35 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(32): Show |
intron_variant | MODIFIER | c.*166-798G>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559481 | |||||||
chr1:182559583 | C | A | 1 | a0001c0004t0001g0324 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.*166-696C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559583 | |||||||
chr1:182559594 | C | T | 20 | a0001c0001t0001g0103 a0001c0001t0001g0173 a0001c0001t0001g0175 others(17): Show |
20 | HG01123.hp2 HG01884.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.*166-685C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559594 | |||||||
chr1:182559614 | T | A | 1 | a0001c0004t0001g0324 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.*166-665T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559614 | |||||||
chr1:182559644 | C | T | 1 | a0001c0004t0001g0324 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.*166-635C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559644 | |||||||
chr1:182559689 | T | A | 1 | a0001c0004t0001g0324 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.*166-590T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559689 | |||||||
chr1:182559690 | T | A | 1 | a0001c0004t0001g0324 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.*166-589T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559690 | |||||||
chr1:182559703 | T | A | 1 | a0001c0004t0001g0324 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.*166-576T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559703 | |||||||
chr1:182559704 | T | G | 1 | a0001c0004t0001g0324 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.*166-575T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559704 | |||||||
chr1:182559708 | C | A | 1 | a0001c0004t0001g0324 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.*166-571C>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559708 | |||||||
chr1:182559711 | T | G | 1 | a0001c0004t0001g0324 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.*166-568T>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559711 | |||||||
chr1:182559712 | T | A | 1 | a0001c0004t0001g0324 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.*166-567T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559712 | |||||||
chr1:182559721 | C | T | 1 | a0001c0004t0001g0324 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.*166-558C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559721 | |||||||
chr1:182559722 | T | A | 1 | a0001c0004t0001g0324 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.*166-557T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559722 | |||||||
chr1:182559725 | C | G | 1 | a0001c0004t0001g0324 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.*166-554C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559725 | |||||||
chr1:182559729 | T | A | 1 | a0001c0004t0001g0324 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.*166-550T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559729 | |||||||
chr1:182559750 | T | C | 5 | a0001c0006t0001g0137 a0001c0006t0001g0138 a0001c0006t0001g0206 others(2): Show |
5 | HG01891.hp1 HG02559.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.*166-529T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559750 | |||||||
chr1:182559757 | T | C | 1 | a0001c0004t0001g0324 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.*166-522T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559757 | |||||||
chr1:182559758 | T | C | 1 | a0001c0004t0001g0324 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.*166-521T>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559758 | |||||||
chr1:182559759 | G | T | 1 | a0001c0004t0001g0324 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.*166-520G>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559759 | |||||||
chr1:182559760 | C | G | 1 | a0001c0004t0001g0324 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.*166-519C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559760 | |||||||
chr1:182559764 | A | C | 1 | a0001c0004t0001g0324 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.*166-515A>C | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559764 | |||||||
chr1:182559775 | C | T | 1 | a0001c0004t0001g0324 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.*166-504C>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559775 | |||||||
chr1:182559781 | T | A | 1 | a0001c0004t0001g0324 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.*166-498T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559781 | |||||||
chr1:182559784 | T | A | 1 | a0001c0004t0001g0324 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.*166-495T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559784 | |||||||
chr1:182559794 | A | T | 1 | a0001c0004t0001g0324 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.*166-485A>T | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559794 | |||||||
chr1:182559839 | T | A | 15 | a0001c0004t0001g0178 a0001c0004t0001g0181 a0001c0004t0001g0191 others(12): Show |
15 | HG00099.hp1 HG00642.hp1 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.*166-440T>A | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559839 | |||||||
chr1:182559998 | A | G | 1 | a0001c0001t0001g0173 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.*166-281A>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182559998 | |||||||
chr1:182560189 | C | G | 1 | a0001c0004t0001g0251 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.*166-90C>G | RGSL1 | ENSG00000121446.20 | transcript | ENST00000294854.13 | protein_coding | 21/21 | chr1 | 182560189 |