Item | Value |
---|---|
geneid | 79745 |
ensemblid | ENSG00000115295.21 |
hgncid | 26108 |
symbol | CLIP4 |
name | CAP-Gly domain containing linker protein family member 4 |
refseq_nuc | NM_024692.6 |
refseq_prot | NP_078968.3 |
ensembl_nuc | ENST00000320081.10 |
ensembl_prot | ENSP00000327009.5 |
mane_status | MANE Select |
chr | chr2 |
start | 29115415 |
end | 29183808 |
strand | + |
ver | v1.2 |
region | chr2:29115415-29183808 |
region5000 | chr2:29110415-29188808 |
regionname0 | CLIP4_chr2_29115415_29183808 |
regionname5000 | CLIP4_chr2_29110415_29188808 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 705 | 270 | 86 | 52 | 91 | 13 | 26 | 74 | CLIP4_chr2_29110415_29188808 | CLIP4 | MTIED others(700): Show |
chr2 | 29110415 | 29188808 |
a0002 | 0/0 | 705 | 8 | 1 | 5 | 0 | 1 | 1 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | MTIED others(700): Show |
chr2 | 29110415 | 29188808 |
a0003 | 0/0 | 705 | 5 | 0 | 0 | 5 | 0 | 0 | 4 | CLIP4_chr2_29110415_29188808 | CLIP4 | MTIED others(700): Show |
chr2 | 29110415 | 29188808 |
a0004 | 0/0 | 705 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | MTIED others(700): Show |
chr2 | 29110415 | 29188808 |
a0005 | 0/0 | 705 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | MTIED others(700): Show |
chr2 | 29110415 | 29188808 |
a0006 | 0/0 | 705 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | MTIED others(700): Show |
chr2 | 29110415 | 29188808 |
a0007 | 0/0 | 705 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | MTIED others(700): Show |
chr2 | 29110415 | 29188808 |
a0008 | 0/0 | 705 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | MTIED others(700): Show |
chr2 | 29110415 | 29188808 |
a0009 | 0/0 | 705 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | MTIED others(700): Show |
chr2 | 29110415 | 29188808 |
a0010 | 0/0 | 705 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | MTIED others(700): Show |
chr2 | 29110415 | 29188808 |
a0011 | 0/0 | 705 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | MTIED others(700): Show |
chr2 | 29110415 | 29188808 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 2115 | 109 | 26 | 23 | 45 | 5 | 9 | CLIP4_chr2_29110415_29188808 | CLIP4 | ATGAC others(2110): Show |
chr2 | 29110415 | 29188808 | ||
a0001c0002 | 0/1 | 2115 | 108 | 43 | 14 | 39 | 3 | 8 | CLIP4_chr2_29110415_29188808 | CLIP4 | ATGAC others(2110): Show |
chr2 | 29110415 | 29188808 | ||
a0001c0003 | 0/0 | 2115 | 24 | 9 | 4 | 3 | 2 | 6 | CLIP4_chr2_29110415_29188808 | CLIP4 | ATGAC others(2110): Show |
chr2 | 29110415 | 29188808 | ||
a0001c0005 | 0/0 | 2115 | 7 | 1 | 5 | 0 | 0 | 1 | CLIP4_chr2_29110415_29188808 | CLIP4 | ATGAC others(2110): Show |
chr2 | 29110415 | 29188808 | ||
a0001c0007 | 0/0 | 2115 | 4 | 0 | 0 | 4 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | ATGAC others(2110): Show |
chr2 | 29110415 | 29188808 | ||
a0001c0008 | 0/0 | 2115 | 4 | 1 | 1 | 0 | 1 | 1 | CLIP4_chr2_29110415_29188808 | CLIP4 | ATGAC others(2110): Show |
chr2 | 29110415 | 29188808 | ||
a0001c0009 | 0/0 | 2115 | 3 | 0 | 2 | 0 | 0 | 1 | CLIP4_chr2_29110415_29188808 | CLIP4 | ATGAC others(2110): Show |
chr2 | 29110415 | 29188808 | ||
a0001c0010 | 0/0 | 2115 | 2 | 2 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | ATGAC others(2110): Show |
chr2 | 29110415 | 29188808 | ||
a0001c0011 | 0/0 | 2115 | 2 | 0 | 0 | 0 | 2 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | ATGAC others(2110): Show |
chr2 | 29110415 | 29188808 | ||
a0001c0013 | 0/0 | 2115 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | ATGAC others(2110): Show |
chr2 | 29110415 | 29188808 | ||
a0001c0016 | 0/0 | 2115 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | ATGAC others(2110): Show |
chr2 | 29110415 | 29188808 | ||
a0001c0018 | 0/0 | 2115 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | ATGAC others(2110): Show |
chr2 | 29110415 | 29188808 | ||
a0001c0020 | 0/0 | 2115 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | ATGAC others(2110): Show |
chr2 | 29110415 | 29188808 | ||
a0001c0021 | 0/0 | 2115 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | ATGAC others(2110): Show |
chr2 | 29110415 | 29188808 | ||
a0001c0023 | 0/0 | 2115 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | ATGAC others(2110): Show |
chr2 | 29110415 | 29188808 | ||
a0001c0026 | 0/0 | 2115 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | ATGAC others(2110): Show |
chr2 | 29110415 | 29188808 | ||
a0002c0004 | 0/0 | 2115 | 7 | 1 | 5 | 0 | 1 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | ATGAC others(2110): Show |
chr2 | 29110415 | 29188808 | ||
a0002c0014 | 0/0 | 2115 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP4_chr2_29110415_29188808 | CLIP4 | ATGAC others(2110): Show |
chr2 | 29110415 | 29188808 | ||
a0003c0006 | 0/0 | 2115 | 5 | 0 | 0 | 5 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | ATGAC others(2110): Show |
chr2 | 29110415 | 29188808 | ||
a0004c0012 | 0/0 | 2115 | 2 | 2 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | ATGAC others(2110): Show |
chr2 | 29110415 | 29188808 | ||
a0005c0019 | 0/0 | 2115 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | ATGAC others(2110): Show |
chr2 | 29110415 | 29188808 | ||
a0006c0022 | 0/0 | 2115 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | ATGAC others(2110): Show |
chr2 | 29110415 | 29188808 | ||
a0007c0027 | 0/0 | 2115 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | ATGAC others(2110): Show |
chr2 | 29110415 | 29188808 | ||
a0008c0017 | 0/0 | 2115 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP4_chr2_29110415_29188808 | CLIP4 | ATGAC others(2110): Show |
chr2 | 29110415 | 29188808 | ||
a0009c0025 | 0/0 | 2115 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | ATGAC others(2110): Show |
chr2 | 29110415 | 29188808 | ||
a0010c0024 | 0/0 | 2115 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP4_chr2_29110415_29188808 | CLIP4 | ATGAC others(2110): Show |
chr2 | 29110415 | 29188808 | ||
a0011c0015 | 0/0 | 2115 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP4_chr2_29110415_29188808 | CLIP4 | ATGAC others(2110): Show |
chr2 | 29110415 | 29188808 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 4299 | 92 | 18 | 18 | 41 | 5 | 9 | CLIP4_chr2_29110415_29188808 | CLIP4 | GTCCC others(4294): Show |
chr2 | 29110415 | 29188808 |
a0001c0001t0002 | 0/0 | 4299 | 2 | 1 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | GTCCC others(4294): Show |
chr2 | 29110415 | 29188808 |
a0001c0001t0003 | 0/0 | 4299 | 3 | 3 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | GTCCC others(4294): Show |
chr2 | 29110415 | 29188808 |
a0001c0001t0004 | 0/0 | 4299 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | GTCCC others(4294): Show |
chr2 | 29110415 | 29188808 |
a0001c0001t0006 | 0/0 | 4299 | 4 | 0 | 4 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | GTCCC others(4294): Show |
chr2 | 29110415 | 29188808 |
a0001c0001t0008 | 0/0 | 4299 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | GTCCC others(4294): Show |
chr2 | 29110415 | 29188808 |
a0001c0001t0009 | 0/0 | 4299 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | GTCCC others(4294): Show |
chr2 | 29110415 | 29188808 |
a0001c0001t0011 | 0/0 | 4299 | 2 | 0 | 0 | 2 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | GTCCC others(4294): Show |
chr2 | 29110415 | 29188808 |
a0001c0001t0012 | 0/0 | 4299 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | GTCCC others(4294): Show |
chr2 | 29110415 | 29188808 |
a0001c0001t0016 | 0/0 | 4299 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | GTCCC others(4294): Show |
chr2 | 29110415 | 29188808 |
a0001c0001t0017 | 0/0 | 4299 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | GTCCC others(4294): Show |
chr2 | 29110415 | 29188808 |
a0001c0002t0001 | 0/1 | 4299 | 72 | 12 | 9 | 39 | 3 | 8 | CLIP4_chr2_29110415_29188808 | CLIP4 | GTCCC others(4294): Show |
chr2 | 29110415 | 29188808 |
a0001c0002t0002 | 0/0 | 4299 | 15 | 14 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | GTCCC others(4294): Show |
chr2 | 29110415 | 29188808 |
a0001c0002t0003 | 0/0 | 4299 | 5 | 2 | 3 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | GTCCC others(4294): Show |
chr2 | 29110415 | 29188808 |
a0001c0002t0004 | 0/0 | 4299 | 2 | 2 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | GTCCC others(4294): Show |
chr2 | 29110415 | 29188808 |
a0001c0002t0005 | 0/0 | 4299 | 6 | 6 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | GTCCC others(4294): Show |
chr2 | 29110415 | 29188808 |
a0001c0002t0007 | 0/0 | 4299 | 3 | 3 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | GTCCC others(4294): Show |
chr2 | 29110415 | 29188808 |
a0001c0002t0009 | 0/0 | 4299 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | GTCCC others(4294): Show |
chr2 | 29110415 | 29188808 |
a0001c0002t0010 | 0/0 | 4299 | 2 | 1 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | GTCCC others(4294): Show |
chr2 | 29110415 | 29188808 |
a0001c0002t0013 | 0/0 | 4299 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | GTCCC others(4294): Show |
chr2 | 29110415 | 29188808 |
a0001c0002t0015 | 0/0 | 4299 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | GTCCC others(4294): Show |
chr2 | 29110415 | 29188808 |
a0001c0003t0001 | 0/0 | 4299 | 20 | 6 | 4 | 3 | 2 | 5 | CLIP4_chr2_29110415_29188808 | CLIP4 | GTCCC others(4294): Show |
chr2 | 29110415 | 29188808 |
a0001c0003t0003 | 0/0 | 4299 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | GTCCC others(4294): Show |
chr2 | 29110415 | 29188808 |
a0001c0003t0004 | 0/0 | 4299 | 2 | 2 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | GTCCC others(4294): Show |
chr2 | 29110415 | 29188808 |
a0001c0003t0014 | 0/0 | 4299 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP4_chr2_29110415_29188808 | CLIP4 | GTCCC others(4294): Show |
chr2 | 29110415 | 29188808 |
a0001c0005t0001 | 0/0 | 4299 | 2 | 1 | 0 | 0 | 0 | 1 | CLIP4_chr2_29110415_29188808 | CLIP4 | GTCCC others(4294): Show |
chr2 | 29110415 | 29188808 |
a0001c0005t0003 | 0/0 | 4299 | 5 | 0 | 5 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | GTCCC others(4294): Show |
chr2 | 29110415 | 29188808 |
a0001c0007t0001 | 0/0 | 4299 | 4 | 0 | 0 | 4 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | GTCCC others(4294): Show |
chr2 | 29110415 | 29188808 |
a0001c0008t0001 | 0/0 | 4299 | 4 | 1 | 1 | 0 | 1 | 1 | CLIP4_chr2_29110415_29188808 | CLIP4 | GTCCC others(4294): Show |
chr2 | 29110415 | 29188808 |
a0001c0009t0001 | 0/0 | 4299 | 3 | 0 | 2 | 0 | 0 | 1 | CLIP4_chr2_29110415_29188808 | CLIP4 | GTCCC others(4294): Show |
chr2 | 29110415 | 29188808 |
a0001c0010t0004 | 0/0 | 4299 | 2 | 2 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | GTCCC others(4294): Show |
chr2 | 29110415 | 29188808 |
a0001c0011t0001 | 0/0 | 4299 | 2 | 0 | 0 | 0 | 2 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | GTCCC others(4294): Show |
chr2 | 29110415 | 29188808 |
a0001c0013t0008 | 0/0 | 4299 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | GTCCC others(4294): Show |
chr2 | 29110415 | 29188808 |
a0001c0016t0001 | 0/0 | 4299 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | GTCCC others(4294): Show |
chr2 | 29110415 | 29188808 |
a0001c0018t0004 | 0/0 | 4299 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | GTCCC others(4294): Show |
chr2 | 29110415 | 29188808 |
a0001c0020t0001 | 0/0 | 4299 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | GTCCC others(4294): Show |
chr2 | 29110415 | 29188808 |
a0001c0021t0001 | 0/0 | 4299 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | GTCCC others(4294): Show |
chr2 | 29110415 | 29188808 |
a0001c0023t0005 | 0/0 | 4299 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | GTCCC others(4294): Show |
chr2 | 29110415 | 29188808 |
a0001c0026t0001 | 0/0 | 4299 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | GTCCC others(4294): Show |
chr2 | 29110415 | 29188808 |
a0002c0004t0001 | 0/0 | 4299 | 7 | 1 | 5 | 0 | 1 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | GTCCC others(4294): Show |
chr2 | 29110415 | 29188808 |
a0002c0014t0001 | 0/0 | 4299 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP4_chr2_29110415_29188808 | CLIP4 | GTCCC others(4294): Show |
chr2 | 29110415 | 29188808 |
a0003c0006t0001 | 0/0 | 4299 | 5 | 0 | 0 | 5 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | GTCCC others(4294): Show |
chr2 | 29110415 | 29188808 |
a0004c0012t0001 | 0/0 | 4299 | 2 | 2 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | GTCCC others(4294): Show |
chr2 | 29110415 | 29188808 |
a0005c0019t0001 | 0/0 | 4299 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | GTCCC others(4294): Show |
chr2 | 29110415 | 29188808 |
a0006c0022t0001 | 0/0 | 4299 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | GTCCC others(4294): Show |
chr2 | 29110415 | 29188808 |
a0007c0027t0001 | 0/0 | 4299 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | GTCCC others(4294): Show |
chr2 | 29110415 | 29188808 |
a0008c0017t0001 | 0/0 | 4299 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP4_chr2_29110415_29188808 | CLIP4 | GTCCC others(4294): Show |
chr2 | 29110415 | 29188808 |
a0009c0025t0003 | 0/0 | 4299 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | GTCCC others(4294): Show |
chr2 | 29110415 | 29188808 |
a0010c0024t0001 | 0/0 | 4299 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP4_chr2_29110415_29188808 | CLIP4 | GTCCC others(4294): Show |
chr2 | 29110415 | 29188808 |
a0011c0015t0001 | 0/0 | 4299 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP4_chr2_29110415_29188808 | CLIP4 | GTCCC others(4294): Show |
chr2 | 29110415 | 29188808 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0082 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0004g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0006g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0006g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0006g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0006g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0008g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0009g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0011g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0011g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0012g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0016g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0001t0017g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0263 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0003g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0003g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0003g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0004g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0004g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0005g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0005g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0005g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0005g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0005g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0005g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0007g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0007g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0007g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0009g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0010g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0010g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0013g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0002t0015g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0003t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0003t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0003t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0003t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0003t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0003t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0003t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0003t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0003t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0003t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0003t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0003t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0003t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0003t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0003t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0003t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0003t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0003t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0003t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0003t0003g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0003t0004g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0003t0004g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0003t0014g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0005t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0005t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0005t0003g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0005t0003g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0005t0003g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0005t0003g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0007t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0007t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0007t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0008t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0008t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0008t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0008t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0009t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0009t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0009t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0010t0004g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0010t0004g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0011t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0011t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0013t0008g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0016t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0018t0004g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0020t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0021t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0023t0005g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0001c0026t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0002c0004t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0002c0004t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0002c0004t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0002c0004t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0002c0004t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0002c0004t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0002c0004t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0002c0014t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0003c0006t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0003c0006t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0003c0006t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0003c0006t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0004c0012t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0004c0012t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0005c0019t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0006c0022t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0007c0027t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0008c0017t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0009c0025t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0010c0024t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
a0011c0015t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0003 | t0001 | g0215 | EUR | GBR | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0182 | EUR | GBR | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG00140 | hp1 | a0001 | c0002 | t0001 | g0243 | EUR | GBR | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG00140 | hp2 | a0001 | c0008 | t0001 | g0184 | EUR | GBR | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0173 | EUR | FIN | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG00280 | hp2 | a0001 | c0003 | t0001 | g0221 | EUR | FIN | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG00558 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG00597 | hp1 | a0003 | c0006 | t0001 | g0007 | EAS | CHS | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG00597 | hp2 | a0001 | c0002 | t0001 | g0094 | EAS | CHS | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG00642 | hp1 | a0001 | c0008 | t0001 | g0185 | AMR | PUR | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG00673 | hp1 | a0001 | c0002 | t0001 | g0017 | EAS | CHS | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG00738 | hp1 | a0001 | c0009 | t0001 | g0226 | AMR | PUR | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG00738 | hp2 | a0001 | c0002 | t0003 | g0009 | AMR | PUR | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG00741 | hp1 | a0002 | c0004 | t0001 | g0276 | AMR | PUR | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG00741 | hp2 | a0001 | c0005 | t0003 | g0116 | AMR | PUR | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG01069 | hp1 | a0001 | c0005 | t0003 | g0005 | AMR | PUR | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG01069 | hp2 | a0002 | c0004 | t0001 | g0274 | AMR | PUR | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG01071 | hp1 | a0001 | c0005 | t0003 | g0005 | AMR | PUR | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG01074 | hp1 | a0001 | c0002 | t0010 | g0233 | AMR | PUR | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG01099 | hp1 | a0002 | c0004 | t0001 | g0270 | AMR | PUR | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG01099 | hp2 | a0001 | c0021 | t0001 | g0018 | AMR | PUR | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG01106 | hp1 | a0001 | c0001 | t0006 | g0200 | AMR | PUR | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG01106 | hp2 | a0001 | c0002 | t0002 | g0128 | AMR | PUR | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG01109 | hp1 | a0001 | c0002 | t0001 | g0044 | AMR | PUR | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG01109 | hp2 | a0001 | c0013 | t0008 | g0051 | AMR | PUR | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG01167 | hp2 | a0001 | c0002 | t0001 | g0113 | AMR | PUR | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG01168 | hp1 | a0001 | c0005 | t0003 | g0111 | AMR | PUR | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG01169 | hp2 | a0001 | c0005 | t0003 | g0109 | AMR | PUR | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG01175 | hp2 | a0001 | c0002 | t0001 | g0283 | AMR | PUR | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG01192 | hp1 | a0001 | c0002 | t0001 | g0284 | AMR | PUR | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG01192 | hp2 | a0005 | c0019 | t0001 | g0191 | AMR | PUR | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG01243 | hp1 | a0001 | c0002 | t0001 | g0236 | AMR | PUR | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG01256 | hp1 | a0002 | c0004 | t0001 | g0269 | AMR | CLM | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG01256 | hp2 | a0001 | c0003 | t0001 | g0089 | AMR | CLM | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG01257 | hp2 | a0001 | c0002 | t0001 | g0271 | AMR | CLM | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG01261 | hp1 | a0001 | c0009 | t0001 | g0211 | AMR | CLM | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0054 | AMR | CLM | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG01433 | hp2 | a0001 | c0003 | t0001 | g0213 | AMR | CLM | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG01496 | hp2 | a0001 | c0002 | t0003 | g0073 | AMR | CLM | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG01515 | hp1 | a0001 | c0011 | t0001 | g0272 | EUR | IBS | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG01515 | hp2 | a0001 | c0002 | t0001 | g0038 | EUR | IBS | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0107 | EUR | IBS | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG01517 | hp2 | a0001 | c0011 | t0001 | g0273 | EUR | IBS | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0197 | AFR | ACB | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG01884 | hp2 | a0001 | c0002 | t0002 | g0086 | AFR | ACB | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG01891 | hp1 | a0001 | c0002 | t0002 | g0266 | AFR | ACB | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG01891 | hp2 | a0001 | c0010 | t0004 | g0257 | AFR | ACB | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PEL | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG01934 | hp2 | a0001 | c0020 | t0001 | g0255 | AMR | PEL | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PEL | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG01978 | hp2 | a0001 | c0001 | t0006 | g0202 | AMR | PEL | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG01981 | hp1 | a0001 | c0002 | t0001 | g0035 | AMR | PEL | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02004 | hp1 | a0001 | c0002 | t0003 | g0110 | AMR | PEL | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02015 | hp1 | a0001 | c0002 | t0001 | g0027 | EAS | KHV | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02040 | hp2 | a0001 | c0003 | t0001 | g0147 | EAS | KHV | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02055 | hp1 | a0001 | c0002 | t0002 | g0250 | AFR | ACB | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02071 | hp2 | a0001 | c0001 | t0011 | g0234 | EAS | KHV | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02080 | hp1 | a0006 | c0022 | t0001 | g0045 | EAS | KHV | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02080 | hp2 | a0001 | c0001 | t0011 | g0235 | EAS | KHV | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02132 | hp2 | a0001 | c0002 | t0001 | g0022 | EAS | KHV | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02135 | hp1 | a0001 | c0002 | t0001 | g0224 | EAS | KHV | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02135 | hp2 | a0007 | c0027 | t0001 | g0026 | EAS | KHV | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02145 | hp1 | a0002 | c0004 | t0001 | g0278 | AFR | ACB | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02145 | hp2 | a0004 | c0012 | t0001 | g0008 | AFR | ACB | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02148 | hp1 | a0001 | c0001 | t0006 | g0203 | AMR | PEL | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02155 | hp1 | a0001 | c0002 | t0001 | g0066 | EAS | CDX | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | CDX | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02257 | hp1 | a0001 | c0001 | t0003 | g0083 | AFR | ACB | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02257 | hp2 | a0001 | c0002 | t0002 | g0085 | AFR | ACB | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02258 | hp1 | a0001 | c0008 | t0001 | g0176 | AFR | ACB | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02258 | hp2 | a0001 | c0002 | t0002 | g0126 | AFR | ACB | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02273 | hp1 | a0001 | c0001 | t0006 | g0210 | AMR | PEL | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02273 | hp2 | a0001 | c0003 | t0001 | g0090 | AMR | PEL | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02300 | hp1 | a0001 | c0003 | t0001 | g0093 | AMR | PEL | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02300 | hp2 | a0002 | c0004 | t0001 | g0275 | AMR | PEL | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02451 | hp1 | a0001 | c0002 | t0015 | g0011 | AFR | ACB | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02451 | hp2 | a0001 | c0002 | t0001 | g0057 | AFR | ACB | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02572 | hp1 | a0001 | c0003 | t0001 | g0248 | AFR | GWD | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02602 | hp2 | a0001 | c0002 | t0001 | g0277 | SAS | PJL | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02615 | hp1 | a0001 | c0002 | t0001 | g0124 | AFR | GWD | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02615 | hp2 | a0001 | c0002 | t0002 | g0252 | AFR | GWD | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02622 | hp1 | a0001 | c0003 | t0004 | g0222 | AFR | GWD | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02622 | hp2 | a0001 | c0002 | t0002 | g0251 | AFR | GWD | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02630 | hp1 | a0001 | c0002 | t0010 | g0232 | AFR | GWD | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02630 | hp2 | a0001 | c0001 | t0003 | g0104 | AFR | GWD | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02647 | hp1 | a0001 | c0003 | t0001 | g0247 | AFR | GWD | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02647 | hp2 | a0001 | c0002 | t0001 | g0267 | AFR | GWD | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02717 | hp1 | a0001 | c0026 | t0001 | g0052 | AFR | GWD | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02717 | hp2 | a0001 | c0002 | t0013 | g0055 | AFR | GWD | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02723 | hp1 | a0001 | c0002 | t0002 | g0127 | AFR | GWD | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02723 | hp2 | a0004 | c0012 | t0001 | g0010 | AFR | GWD | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02735 | hp1 | a0001 | c0002 | t0001 | g0024 | SAS | PJL | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | PJL | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02738 | hp1 | a0008 | c0017 | t0001 | g0150 | SAS | PJL | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02738 | hp2 | a0001 | c0009 | t0001 | g0216 | SAS | PJL | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02809 | hp1 | a0001 | c0002 | t0002 | g0282 | AFR | GWD | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02809 | hp2 | a0001 | c0003 | t0001 | g0212 | AFR | GWD | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02818 | hp1 | a0001 | c0002 | t0002 | g0117 | AFR | GWD | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02818 | hp2 | a0001 | c0003 | t0004 | g0225 | AFR | GWD | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02886 | hp2 | a0001 | c0005 | t0001 | g0231 | AFR | GWD | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02895 | hp1 | a0009 | c0025 | t0003 | g0112 | AFR | GWD | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | GWD | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02897 | hp1 | a0001 | c0003 | t0001 | g0245 | AFR | GWD | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | GWD | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02922 | hp1 | a0001 | c0002 | t0001 | g0056 | AFR | ESN | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02922 | hp2 | a0001 | c0010 | t0004 | g0256 | AFR | ESN | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02965 | hp1 | a0001 | c0002 | t0005 | g0133 | AFR | ESN | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02965 | hp2 | a0001 | c0016 | t0001 | g0075 | AFR | ESN | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | ESN | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02970 | hp2 | a0001 | c0002 | t0001 | g0003 | AFR | ESN | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02976 | hp1 | a0001 | c0002 | t0001 | g0285 | AFR | ESN | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02976 | hp2 | a0001 | c0002 | t0004 | g0125 | AFR | ESN | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG03041 | hp1 | a0001 | c0002 | t0003 | g0121 | AFR | GWD | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG03041 | hp2 | a0001 | c0001 | t0009 | g0149 | AFR | GWD | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG03098 | hp1 | a0001 | c0002 | t0002 | g0123 | AFR | MSL | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG03098 | hp2 | a0001 | c0002 | t0003 | g0070 | AFR | MSL | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ESN | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG03130 | hp2 | a0001 | c0003 | t0001 | g0246 | AFR | ESN | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG03139 | hp1 | a0001 | c0001 | t0004 | g0198 | AFR | ESN | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG03139 | hp2 | a0001 | c0001 | t0017 | g0229 | AFR | ESN | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG03195 | hp1 | a0001 | c0002 | t0005 | g0129 | AFR | ESN | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG03195 | hp2 | a0001 | c0002 | t0001 | g0049 | AFR | ESN | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG03209 | hp1 | a0001 | c0018 | t0004 | g0078 | AFR | MSL | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | MSL | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | MSL | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG03225 | hp2 | a0001 | c0002 | t0005 | g0130 | AFR | MSL | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG03239 | hp2 | a0001 | c0002 | t0001 | g0036 | SAS | PJL | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG03453 | hp1 | a0001 | c0002 | t0005 | g0132 | AFR | MSL | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG03453 | hp2 | a0001 | c0002 | t0007 | g0060 | AFR | MSL | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG03486 | hp1 | a0001 | c0002 | t0007 | g0061 | AFR | MSL | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG03486 | hp2 | a0001 | c0001 | t0008 | g0053 | AFR | MSL | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG03490 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG03490 | hp2 | a0001 | c0003 | t0001 | g0101 | SAS | PJL | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG03492 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | ESN | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG03516 | hp2 | a0001 | c0002 | t0001 | g0003 | AFR | ESN | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG03540 | hp1 | a0001 | c0002 | t0002 | g0118 | AFR | GWD | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG03540 | hp2 | a0001 | c0002 | t0005 | g0254 | AFR | GWD | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | STU | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG03688 | hp2 | a0001 | c0003 | t0001 | g0220 | SAS | STU | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG03831 | hp1 | a0001 | c0003 | t0001 | g0241 | SAS | BEB | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG03831 | hp2 | a0001 | c0002 | t0001 | g0097 | SAS | BEB | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG03834 | hp1 | a0001 | c0003 | t0001 | g0219 | SAS | BEB | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | BEB | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG03927 | hp1 | a0001 | c0002 | t0001 | g0264 | SAS | BEB | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG03927 | hp2 | a0010 | c0024 | t0001 | g0065 | SAS | BEB | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG03942 | hp1 | a0002 | c0014 | t0001 | g0214 | SAS | BEB | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | BEB | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG04184 | hp1 | a0001 | c0003 | t0001 | g0218 | SAS | BEB | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG04184 | hp2 | a0001 | c0002 | t0001 | g0037 | SAS | BEB | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG04199 | hp1 | a0001 | c0008 | t0001 | g0183 | SAS | STU | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG04199 | hp2 | a0001 | c0005 | t0001 | g0114 | SAS | STU | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | STU | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG04228 | hp2 | a0001 | c0003 | t0014 | g0242 | SAS | STU | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA18906 | hp1 | a0001 | c0002 | t0004 | g0119 | AFR | YRI | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA18906 | hp2 | a0001 | c0002 | t0001 | g0238 | AFR | YRI | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA18939 | hp1 | a0001 | c0001 | t0012 | g0154 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA18939 | hp2 | a0003 | c0006 | t0001 | g0007 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA18946 | hp2 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA18947 | hp1 | a0001 | c0002 | t0001 | g0043 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA18948 | hp1 | a0001 | c0007 | t0001 | g0004 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA18949 | hp1 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA18950 | hp1 | a0003 | c0006 | t0001 | g0259 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA18960 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA18961 | hp1 | a0001 | c0002 | t0001 | g0062 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA18961 | hp2 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA18973 | hp1 | a0001 | c0002 | t0001 | g0099 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA18973 | hp2 | a0001 | c0001 | t0016 | g0139 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA18977 | hp1 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA18978 | hp2 | a0001 | c0002 | t0001 | g0047 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA18979 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA18983 | hp1 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA18984 | hp2 | a0001 | c0002 | t0001 | g0064 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA18991 | hp2 | a0001 | c0002 | t0001 | g0279 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA18995 | hp2 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA19004 | hp1 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA19005 | hp1 | a0003 | c0006 | t0001 | g0258 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA19005 | hp2 | a0003 | c0006 | t0001 | g0042 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA19007 | hp2 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA19009 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA19009 | hp2 | a0001 | c0003 | t0001 | g0088 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA19011 | hp2 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA19012 | hp1 | a0001 | c0002 | t0001 | g0041 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA19030 | hp1 | a0001 | c0002 | t0002 | g0120 | AFR | LWK | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | LWK | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA19043 | hp1 | a0001 | c0002 | t0001 | g0108 | AFR | LWK | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | LWK | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA19055 | hp2 | a0001 | c0002 | t0001 | g0067 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA19056 | hp1 | a0001 | c0002 | t0001 | g0046 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA19057 | hp2 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA19059 | hp1 | a0001 | c0007 | t0001 | g0092 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA19059 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA19062 | hp1 | a0001 | c0002 | t0001 | g0068 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA19066 | hp2 | a0001 | c0002 | t0001 | g0063 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA19074 | hp1 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA19077 | hp2 | a0001 | c0003 | t0001 | g0087 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA19084 | hp1 | a0001 | c0007 | t0001 | g0004 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA19085 | hp1 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA19085 | hp2 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA19086 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA19087 | hp1 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA19089 | hp2 | a0001 | c0007 | t0001 | g0091 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA19090 | hp2 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA19091 | hp2 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | YRI | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | YRI | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ASW | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA20129 | hp2 | a0001 | c0023 | t0005 | g0122 | AFR | ASW | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0145 | EUR | TSI | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA20752 | hp2 | a0002 | c0004 | t0001 | g0268 | EUR | TSI | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA20805 | hp1 | a0001 | c0002 | t0001 | g0028 | EUR | TSI | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0177 | EUR | TSI | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | GIH | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA20905 | hp2 | a0011 | c0015 | t0001 | g0217 | SAS | GIH | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG01123 | hp1 | a0001 | c0002 | t0001 | g0050 | AMR | CLM | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG01123 | hp2 | a0001 | c0002 | t0001 | g0039 | AMR | CLM | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02486 | hp1 | a0001 | c0002 | t0002 | g0084 | AFR | ACB | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02559 | hp1 | a0001 | c0003 | t0003 | g0223 | AFR | ACB | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG02559 | hp2 | a0001 | c0002 | t0007 | g0143 | AFR | ACB | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | MSL | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG03471 | hp2 | a0001 | c0002 | t0001 | g0072 | AFR | MSL | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG06807 | hp1 | a0001 | c0002 | t0001 | g0237 | AFR | USA | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
HG06807 | hp2 | a0001 | c0001 | t0003 | g0148 | AFR | USA | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA18955 | hp2 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA20300 | hp1 | a0001 | c0002 | t0005 | g0131 | AFR | USA | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA20300 | hp2 | a0001 | c0002 | t0009 | g0115 | AFR | USA | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA21309 | hp1 | a0001 | c0003 | t0001 | g0249 | AFR | LWK | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | LWK | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0263 | REF | REF | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0082 | REF | REF | CLIP4_chr2_29110415_29188808 | CLIP4 | chr2 | 29110415 | 29188808 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:29143761 | C | T | 1 | a0007 | 1 | HG02135.hp2 | missense_variant | MODERATE | c.701C>T | p.Pro234Leu | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 7/16 | 967/4299 | 701/2118 | 234/705 | chr2 | 29143761 | |||
chr2:29143798 | A | C | 1 | a0010 | 1 | HG03927.hp2 | missense_variant | MODERATE | c.738A>C | p.Glu246Asp | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 7/16 | 1004/4299 | 738/2118 | 246/705 | chr2 | 29143798 | |||
chr2:29157275 | A | G | 1 | a0011 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.1327A>G | p.Lys443Glu | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 11/16 | 1593/4299 | 1327/2118 | 443/705 | chr2 | 29157275 | |||
chr2:29157299 | A | C | 1 | a0005 | 1 | HG01192.hp2 | missense_variant | MODERATE | c.1351A>C | p.Lys451Gln | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 11/16 | 1617/4299 | 1351/2118 | 451/705 | chr2 | 29157299 | |||
chr2:29160390 | G | T | 1 | a0002 | 8 | HG00741.hp1 HG01069.hp2 HG01099.hp1 others(5): Show |
missense_variant | MODERATE | c.1457G>T | p.Arg486Leu | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 12/16 | 1723/4299 | 1457/2118 | 486/705 | chr2 | 29160390 | |||
chr2:29160393 | T | C | 1 | a0008 | 1 | HG02738.hp1 | missense_variant | MODERATE | c.1460T>C | p.Leu487Pro | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 12/16 | 1726/4299 | 1460/2118 | 487/705 | chr2 | 29160393 | |||
chr2:29167520 | A | G | 1 | a0003 | 5 | HG00597.hp1 NA18939.hp2 NA18950.hp1 others(2): Show |
missense_variant | MODERATE | c.1703A>G | p.Lys568Arg | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/16 | 1969/4299 | 1703/2118 | 568/705 | chr2 | 29167520 | |||
chr2:29181589 | G | A | 1 | a0004 | 2 | HG02145.hp2 HG02723.hp2 |
missense_variant | MODERATE | c.1814G>A | p.Arg605His | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 16/16 | 2080/4299 | 1814/2118 | 605/705 | chr2 | 29181589 | |||
chr2:29181648 | G | A | 1 | a0006 | 1 | HG02080.hp1 | missense_variant | MODERATE | c.1873G>A | p.Glu625Lys | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 16/16 | 2139/4299 | 1873/2118 | 625/705 | chr2 | 29181648 | |||
chr2:29181822 | G | C | 1 | a0009 | 1 | HG02895.hp1 | missense_variant | MODERATE | c.2047G>C | p.Val683Leu | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 16/16 | 2313/4299 | 2047/2118 | 683/705 | chr2 | 29181822 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:29131343 | T | C | 1 | a0001c0013 | 1 | HG01109.hp2 | synonymous_variant | LOW | c.219T>C | p.Ile73Ile | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 3/16 | 485/4299 | 219/2118 | 73/705 | chr2 | 29131343 | |||
chr2:29133701 | G | C | 5 | a0001c0003 a0001c0007 a0001c0009 others(2): Show |
33 | HG00099.hp1 HG00280.hp2 HG00738.hp1 others(30): Show |
synonymous_variant | LOW | c.414G>C | p.Leu138Leu | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 5/16 | 680/4299 | 414/2118 | 138/705 | chr2 | 29133701 | |||
chr2:29133803 | A | G | 16 | a0001c0002 a0001c0005 a0001c0010 others(13): Show |
141 | HG00140.hp1 HG00558.hp1 HG00597.hp1 others(138): Show |
synonymous_variant | LOW | c.516A>G | p.Thr172Thr | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 5/16 | 782/4299 | 516/2118 | 172/705 | chr2 | 29133803 | |||
chr2:29135642 | G | A | 2 | a0001c0010 a0001c0020 |
3 | HG01891.hp2 HG01934.hp2 HG02922.hp2 |
synonymous_variant | LOW | c.624G>A | p.Glu208Glu | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/16 | 890/4299 | 624/2118 | 208/705 | chr2 | 29135642 | |||
chr2:29143726 | C | A | 1 | a0001c0016 | 1 | HG02965.hp2 | synonymous_variant | LOW | c.666C>A | p.Ile222Ile | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 7/16 | 932/4299 | 666/2118 | 222/705 | chr2 | 29143726 | |||
chr2:29143777 | C | T | 1 | a0001c0026 | 1 | HG02717.hp1 | synonymous_variant | LOW | c.717C>T | p.Asp239Asp | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 7/16 | 983/4299 | 717/2118 | 239/705 | chr2 | 29143777 | |||
chr2:29143780 | C | T | 2 | a0001c0005 a0009c0025 |
8 | HG00741.hp2 HG01069.hp1 HG01071.hp1 others(5): Show |
synonymous_variant | LOW | c.720C>T | p.Ala240Ala | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 7/16 | 986/4299 | 720/2118 | 240/705 | chr2 | 29143780 | |||
chr2:29143897 | G | A | 1 | a0001c0011 | 2 | HG01515.hp1 HG01517.hp2 |
synonymous_variant | LOW | c.837G>A | p.Thr279Thr | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 7/16 | 1103/4299 | 837/2118 | 279/705 | chr2 | 29143897 | |||
chr2:29167482 | A | G | 2 | a0001c0010 a0001c0018 |
3 | HG01891.hp2 HG02922.hp2 HG03209.hp1 |
synonymous_variant | LOW | c.1665A>G | p.Thr555Thr | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/16 | 1931/4299 | 1665/2118 | 555/705 | chr2 | 29167482 | |||
chr2:29174440 | T | C | 1 | a0001c0026 | 1 | HG02717.hp1 | synonymous_variant | LOW | c.1791T>C | p.Phe597Phe | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/16 | 2057/4299 | 1791/2118 | 597/705 | chr2 | 29174440 | |||
chr2:29181575 | G | A | 3 | a0001c0008 a0001c0009 a0001c0021 |
8 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(5): Show |
synonymous_variant | LOW | c.1800G>A | p.Ser600Ser | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 16/16 | 2066/4299 | 1800/2118 | 600/705 | chr2 | 29181575 | |||
chr2:29181668 | C | T | 1 | a0001c0023 | 1 | NA20129.hp2 | synonymous_variant | LOW | c.1893C>T | p.Leu631Leu | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 16/16 | 2159/4299 | 1893/2118 | 631/705 | chr2 | 29181668 | |||
chr2:29181704 | G | A | 1 | a0001c0007 | 4 | NA18948.hp1 NA19059.hp1 NA19084.hp1 others(1): Show |
synonymous_variant | LOW | c.1929G>A | p.Val643Val | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 16/16 | 2195/4299 | 1929/2118 | 643/705 | chr2 | 29181704 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:29115438 | T | A | 1 | a0001c0001t0006 | 4 | HG01106.hp1 HG01978.hp2 HG02148.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-243T>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 1/16 | 5951 | chr2 | 29115438 | ||||||
chr2:29115504 | C | T | 1 | a0001c0001t0017 | 1 | HG03139.hp2 | 5_prime_UTR_variant | MODIFIER | c.-177C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 1/16 | 5885 | chr2 | 29115504 | ||||||
chr2:29115519 | G | A | 1 | a0001c0001t0012 | 1 | NA18939.hp1 | 5_prime_UTR_variant | MODIFIER | c.-162G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 1/16 | 5870 | chr2 | 29115519 | ||||||
chr2:29181931 | T | C | 1 | a0001c0002t0013 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*38T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 16/16 | 38 | chr2 | 29181931 | ||||||
chr2:29182020 | A | G | 2 | a0001c0002t0005 a0001c0023t0005 |
7 | HG02965.hp1 HG03195.hp1 HG03225.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*127A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 16/16 | 127 | chr2 | 29182020 | ||||||
chr2:29182082 | T | G | 2 | a0001c0001t0008 a0001c0013t0008 |
2 | HG01109.hp2 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*189T>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 16/16 | 189 | chr2 | 29182082 | ||||||
chr2:29182254 | T | G | 3 | a0001c0001t0009 a0001c0001t0017 a0001c0002t0009 |
3 | HG03041.hp2 HG03139.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*361T>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 16/16 | 361 | chr2 | 29182254 | ||||||
chr2:29182267 | G | A | 1 | a0001c0002t0010 | 2 | HG01074.hp1 HG02630.hp1 |
3_prime_UTR_variant | MODIFIER | c.*374G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 16/16 | 374 | chr2 | 29182267 | ||||||
chr2:29182389 | T | A | 1 | a0001c0003t0014 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*496T>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 16/16 | 496 | chr2 | 29182389 | ||||||
chr2:29182524 | C | T | 1 | a0001c0001t0016 | 1 | NA18973.hp2 | 3_prime_UTR_variant | MODIFIER | c.*631C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 16/16 | 631 | chr2 | 29182524 | ||||||
chr2:29182714 | A | G | 1 | a0001c0001t0011 | 2 | HG02071.hp2 HG02080.hp2 |
3_prime_UTR_variant | MODIFIER | c.*821A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 16/16 | 821 | chr2 | 29182714 | ||||||
chr2:29182877 | G | A | 5 | a0001c0001t0003 a0001c0002t0003 a0001c0003t0003 others(2): Show |
15 | HG00738.hp2 HG00741.hp2 HG01069.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*984G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 16/16 | 984 | chr2 | 29182877 | ||||||
chr2:29183125 | A | G | 5 | a0001c0001t0004 a0001c0002t0004 a0001c0003t0004 others(2): Show |
8 | HG01891.hp2 HG02622.hp1 HG02818.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1232A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 16/16 | 1232 | chr2 | 29183125 | ||||||
chr2:29183169 | T | G | 3 | a0001c0001t0002 a0001c0002t0002 a0001c0002t0013 |
18 | HG01106.hp2 HG01346.hp2 HG01884.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1276T>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 16/16 | 1276 | chr2 | 29183169 | ||||||
chr2:29183209 | A | G | 1 | a0001c0002t0007 | 3 | HG02559.hp2 HG03453.hp2 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1316A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 16/16 | 1316 | chr2 | 29183209 | ||||||
chr2:29183409 | G | T | 1 | a0001c0002t0015 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1516G>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 16/16 | 1516 | chr2 | 29183409 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:29115686 | G | C | 2 | a0001c0002t0003g0009 a0004c0012t0001g0008 |
2 | HG00738.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-16+21G>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 1/15 | chr2 | 29115686 | |||||||
chr2:29115718 | G | T | 3 | a0001c0002t0001g0283 a0001c0002t0001g0284 a0001c0002t0001g0285 |
3 | HG01175.hp2 HG01192.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-16+53G>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 1/15 | chr2 | 29115718 | |||||||
chr2:29115758 | G | A | 44 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0002t0001g0001 others(41): Show |
46 | HG00558.hp1 HG00673.hp1 HG01099.hp2 others(43): Show |
intron_variant | MODIFIER | c.-16+93G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 1/15 | chr2 | 29115758 | |||||||
chr2:29115878 | C | G | 3 | a0001c0001t0001g0280 a0001c0001t0001g0281 a0001c0002t0002g0282 |
3 | HG02809.hp1 HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-16+213C>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 1/15 | chr2 | 29115878 | |||||||
chr2:29115972 | T | G | 7 | a0001c0001t0002g0054 a0001c0001t0008g0053 a0001c0002t0001g0049 others(4): Show |
7 | HG01109.hp2 HG01123.hp1 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.-16+307T>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 1/15 | chr2 | 29115972 | |||||||
chr2:29115982 | G | C | 18 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0002t0001g0003 others(15): Show |
19 | HG00738.hp2 HG02145.hp2 HG02155.hp1 others(16): Show |
intron_variant | MODIFIER | c.-16+317G>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 1/15 | chr2 | 29115982 | |||||||
chr2:29116127 | A | T | 16 | a0001c0001t0001g0265 a0001c0002t0001g0264 a0001c0002t0001g0267 others(13): Show |
16 | HG00741.hp1 HG01069.hp2 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.-16+462A>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 1/15 | chr2 | 29116127 | |||||||
chr2:29116364 | A | G | 3 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 |
3 | NA18949.hp2 NA19056.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.-16+699A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 1/15 | chr2 | 29116364 | |||||||
chr2:29116392 | A | C | 3 | a0003c0006t0001g0007 a0003c0006t0001g0258 a0003c0006t0001g0259 |
4 | HG00597.hp1 NA18939.hp2 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16+727A>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 1/15 | chr2 | 29116392 | |||||||
chr2:29116657 | T | C | 1 | a0001c0001t0001g0071 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-16+992T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 1/15 | chr2 | 29116657 | |||||||
chr2:29116697 | C | G | 3 | a0001c0010t0004g0256 a0001c0010t0004g0257 a0001c0020t0001g0255 |
3 | HG01891.hp2 HG01934.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-16+1032C>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 1/15 | chr2 | 29116697 | |||||||
chr2:29116701 | A | T | 1 | a0001c0002t0005g0254 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-16+1036A>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 1/15 | chr2 | 29116701 | |||||||
chr2:29116739 | T | A | 39 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0074 others(36): Show |
40 | HG00738.hp2 HG00741.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.-16+1074T>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 1/15 | chr2 | 29116739 | |||||||
chr2:29116911 | C | T | 242 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(239): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.-16+1246C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 1/15 | chr2 | 29116911 | |||||||
chr2:29117149 | G | T | 3 | a0001c0010t0004g0256 a0001c0010t0004g0257 a0001c0020t0001g0255 |
3 | HG01891.hp2 HG01934.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-16+1484G>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 1/15 | chr2 | 29117149 | |||||||
chr2:29117230 | G | A | 1 | a0001c0001t0001g0260 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-16+1565G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 1/15 | chr2 | 29117230 | |||||||
chr2:29117240 | C | T | 1 | a0001c0002t0001g0048 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-16+1575C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 1/15 | chr2 | 29117240 | |||||||
chr2:29117302 | T | A | 14 | a0001c0001t0001g0265 a0001c0002t0001g0264 a0001c0002t0001g0271 others(11): Show |
14 | HG00741.hp1 HG01069.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.-16+1637T>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 1/15 | chr2 | 29117302 | |||||||
chr2:29117344 | GT | G | 39 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0074 others(36): Show |
40 | HG00738.hp2 HG00741.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.-16+1691delT | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 29117344 | ||||||
chr2:29117503 | C | T | 2 | a0001c0002t0003g0009 a0004c0012t0001g0008 |
2 | HG00738.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-16+1838C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 1/15 | chr2 | 29117503 | |||||||
chr2:29117683 | G | C | 1 | a0001c0002t0003g0070 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-16+2018G>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 1/15 | chr2 | 29117683 | |||||||
chr2:29117839 | G | A | 4 | a0001c0001t0003g0083 a0001c0002t0002g0084 a0001c0002t0002g0085 others(1): Show |
4 | HG01884.hp2 HG02257.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.-16+2174G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 1/15 | chr2 | 29117839 | |||||||
chr2:29118031 | A | G | 1 | a0001c0001t0001g0253 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-16+2366A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 1/15 | chr2 | 29118031 | |||||||
chr2:29118244 | G | T | 9 | a0001c0001t0001g0244 a0001c0002t0002g0250 a0001c0002t0002g0251 others(6): Show |
9 | HG02055.hp1 HG02572.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.-16+2579G>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 1/15 | chr2 | 29118244 | |||||||
chr2:29118282 | A | G | 6 | a0001c0001t0001g0074 a0001c0001t0001g0076 a0001c0002t0003g0009 others(3): Show |
6 | HG00738.hp2 HG02145.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-16+2617A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 1/15 | chr2 | 29118282 | |||||||
chr2:29118346 | G | GA | 8 | a0001c0003t0001g0087 a0001c0003t0001g0088 a0001c0003t0001g0089 others(5): Show |
9 | HG01256.hp2 HG02273.hp2 HG02300.hp1 others(6): Show |
intron_variant | MODIFIER | c.-16+2689dupA | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 29118346 | ||||||
chr2:29118423 | G | T | 1 | a0001c0002t0001g0243 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-16+2758G>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 1/15 | chr2 | 29118423 | |||||||
chr2:29118443 | A | G | 7 | a0001c0001t0002g0054 a0001c0001t0008g0053 a0001c0002t0001g0049 others(4): Show |
7 | HG01109.hp2 HG01123.hp1 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.-16+2778A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 1/15 | chr2 | 29118443 | |||||||
chr2:29118517 | A | AT | 10 | a0001c0001t0001g0074 a0001c0001t0001g0076 a0001c0001t0001g0240 others(7): Show |
10 | HG00738.hp2 HG01496.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.-15-2839dupT | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 29118517 | ||||||
chr2:29118517 | AT | A | 54 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0100 others(51): Show |
56 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.-15-2839delT | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 29118517 | ||||||
chr2:29118595 | C | T | 260 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(257): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.-15-2779C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 1/15 | chr2 | 29118595 | |||||||
chr2:29118778 | C | T | 15 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0002t0001g0003 others(12): Show |
16 | HG02155.hp1 HG02451.hp2 HG02922.hp1 others(13): Show |
intron_variant | MODIFIER | c.-15-2596C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 1/15 | chr2 | 29118778 | |||||||
chr2:29118840 | A | T | 7 | a0001c0001t0002g0054 a0001c0001t0008g0053 a0001c0002t0001g0049 others(4): Show |
7 | HG01109.hp2 HG01123.hp1 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.-15-2534A>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 1/15 | chr2 | 29118840 | |||||||
chr2:29118873 | A | G | 1 | a0001c0002t0013g0055 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-15-2501A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 1/15 | chr2 | 29118873 | |||||||
chr2:29118938 | G | C | 1 | a0001c0001t0001g0103 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-15-2436G>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 1/15 | chr2 | 29118938 | |||||||
chr2:29118995 | G | T | 1 | a0001c0002t0003g0070 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-15-2379G>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 1/15 | chr2 | 29118995 | |||||||
chr2:29119024 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-15-2350A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 1/15 | chr2 | 29119024 | |||||||
chr2:29119110 | G | A | 1 | a0001c0001t0003g0104 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-15-2264G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 1/15 | chr2 | 29119110 | |||||||
chr2:29119218 | T | C | 3 | a0001c0001t0001g0074 a0001c0001t0001g0076 a0001c0016t0001g0075 |
3 | HG02486.hp2 HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-15-2156T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 1/15 | chr2 | 29119218 | |||||||
chr2:29119229 | A | G | 3 | a0001c0001t0001g0006 a0001c0001t0001g0102 a0001c0001t0001g0239 |
4 | HG00558.hp2 NA18950.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15-2145A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 1/15 | chr2 | 29119229 | |||||||
chr2:29119302 | G | T | 3 | a0001c0002t0001g0236 a0001c0002t0001g0237 a0001c0002t0001g0238 |
3 | HG01243.hp1 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-15-2072G>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 1/15 | chr2 | 29119302 | |||||||
chr2:29119331 | G | A | 260 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(257): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.-15-2043G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 1/15 | chr2 | 29119331 | |||||||
chr2:29119364 | A | T | 1 | a0001c0002t0001g0047 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-15-2010A>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 1/15 | chr2 | 29119364 | |||||||
chr2:29119383 | T | A | 15 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0002t0001g0003 others(12): Show |
16 | HG02155.hp1 HG02451.hp2 HG02922.hp1 others(13): Show |
intron_variant | MODIFIER | c.-15-1991T>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 1/15 | chr2 | 29119383 | |||||||
chr2:29119393 | T | A | 257 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(254): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.-15-1981T>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 1/15 | chr2 | 29119393 | |||||||
chr2:29119435 | T | C | 2 | a0001c0002t0015g0011 a0004c0012t0001g0010 |
2 | HG02451.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-15-1939T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 1/15 | chr2 | 29119435 | |||||||
chr2:29119437 | A | G | 1 | a0001c0005t0003g0005 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-15-1937A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 1/15 | chr2 | 29119437 | |||||||
chr2:29119657 | G | C | 3 | a0001c0002t0003g0009 a0001c0002t0003g0070 a0004c0012t0001g0008 |
3 | HG00738.hp2 HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-15-1717G>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 1/15 | chr2 | 29119657 | |||||||
chr2:29119889 | A | G | 2 | a0001c0002t0001g0068 a0001c0002t0001g0069 |
2 | NA19062.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.-15-1485A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 1/15 | chr2 | 29119889 | |||||||
chr2:29119991 | T | C | 2 | a0001c0002t0001g0012 a0001c0002t0001g0013 |
2 | NA18960.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.-15-1383T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 1/15 | chr2 | 29119991 | |||||||
chr2:29120252 | C | T | 2 | a0001c0002t0001g0066 a0001c0002t0001g0067 |
2 | HG02155.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.-15-1122C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 1/15 | chr2 | 29120252 | |||||||
chr2:29120253 | G | A | 3 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 |
3 | HG01175.hp1 HG01517.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.-15-1121G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 1/15 | chr2 | 29120253 | |||||||
chr2:29120276 | T | G | 85 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0244 others(82): Show |
88 | HG00558.hp1 HG00597.hp2 HG00673.hp1 others(85): Show |
intron_variant | MODIFIER | c.-15-1098T>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 1/15 | chr2 | 29120276 | |||||||
chr2:29120402 | A | T | 13 | a0001c0002t0001g0264 a0001c0002t0001g0271 a0001c0002t0001g0277 others(10): Show |
13 | HG00741.hp1 HG01069.hp2 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.-15-972A>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 1/15 | chr2 | 29120402 | |||||||
chr2:29120417 | A | G | 6 | a0001c0001t0001g0074 a0001c0001t0001g0076 a0001c0002t0003g0009 others(3): Show |
6 | HG00738.hp2 HG02145.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-15-957A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 1/15 | chr2 | 29120417 | |||||||
chr2:29120420 | A | G | 2 | a0001c0001t0011g0234 a0001c0001t0011g0235 |
2 | HG02071.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.-15-954A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 1/15 | chr2 | 29120420 | |||||||
chr2:29120762 | G | C | 16 | a0001c0002t0001g0124 a0001c0002t0002g0120 a0001c0002t0002g0123 others(13): Show |
16 | HG01106.hp2 HG02258.hp2 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.-15-612G>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 1/15 | chr2 | 29120762 | |||||||
chr2:29121230 | G | T | 2 | a0001c0002t0003g0009 a0004c0012t0001g0008 |
2 | HG00738.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-15-144G>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 1/15 | chr2 | 29121230 | |||||||
chr2:29121261 | T | G | 17 | a0001c0001t0003g0083 a0001c0002t0001g0056 a0001c0002t0001g0057 others(14): Show |
18 | HG00741.hp2 HG01069.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.-15-113T>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 1/15 | chr2 | 29121261 | |||||||
chr2:29121350 | CT | C | 4 | a0001c0002t0002g0117 a0001c0002t0002g0118 a0001c0010t0004g0256 others(1): Show |
4 | HG01891.hp2 HG02818.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15-15delT | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr2 | 29121350 | ||||||
chr2:29121544 | T | A | 10 | a0001c0002t0001g0108 a0001c0002t0001g0113 a0001c0002t0003g0110 others(7): Show |
11 | HG00741.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.133+23T>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29121544 | |||||||
chr2:29121803 | C | G | 1 | a0001c0002t0010g0233 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.133+282C>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29121803 | |||||||
chr2:29122240 | C | CT | 12 | a0001c0002t0001g0003 a0001c0002t0001g0062 a0001c0002t0001g0063 others(9): Show |
13 | HG02155.hp1 HG02970.hp2 HG03098.hp2 others(10): Show |
intron_variant | MODIFIER | c.133+734dupT | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 29122240 | ||||||
chr2:29122240 | CT | C | 234 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(231): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.133+734delT | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 29122240 | ||||||
chr2:29122314 | T | C | 104 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(101): Show |
105 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.133+793T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29122314 | |||||||
chr2:29122651 | A | T | 1 | a0001c0002t0010g0233 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.133+1130A>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29122651 | |||||||
chr2:29122826 | C | CA | 17 | a0001c0002t0001g0264 a0001c0002t0001g0271 a0001c0002t0002g0084 others(14): Show |
17 | HG01069.hp2 HG01099.hp1 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.133+1329dupA | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 29122826 | ||||||
chr2:29122826 | C | CAAAAAAA others(3): Show |
1 | a0001c0002t0001g0066 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.133+1320_133+1329d others(12): Show |
CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 29122826 | ||||||
chr2:29122826 | CA | C | 179 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(176): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.133+1329delA | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 29122826 | ||||||
chr2:29122826 | CAA | C | 18 | a0001c0001t0001g0209 a0001c0001t0001g0227 a0001c0001t0001g0228 others(15): Show |
18 | HG00738.hp1 HG01243.hp1 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.133+1328_133+1329d others(4): Show |
CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 29122826 | ||||||
chr2:29122826 | CAAAAAAA others(6): Show |
C | 1 | a0001c0003t0001g0249 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.133+1317_133+1329d others(15): Show |
CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 29122826 | ||||||
chr2:29122850 | A | G | 1 | a0001c0002t0001g0285 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.133+1329A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29122850 | |||||||
chr2:29123177 | A | C | 16 | a0001c0002t0001g0003 a0001c0002t0001g0062 a0001c0002t0001g0063 others(13): Show |
17 | HG01074.hp1 HG01243.hp1 HG02155.hp1 others(14): Show |
intron_variant | MODIFIER | c.133+1656A>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29123177 | |||||||
chr2:29123191 | A | G | 1 | a0010c0024t0001g0065 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.133+1670A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29123191 | |||||||
chr2:29123478 | G | T | 1 | a0001c0003t0004g0225 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.133+1957G>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29123478 | |||||||
chr2:29123728 | G | A | 23 | a0001c0002t0001g0124 a0001c0002t0002g0084 a0001c0002t0002g0085 others(20): Show |
23 | HG00738.hp2 HG01106.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.133+2207G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29123728 | |||||||
chr2:29123740 | C | T | 3 | a0001c0002t0001g0236 a0001c0002t0001g0237 a0001c0002t0001g0238 |
3 | HG01243.hp1 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.133+2219C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29123740 | |||||||
chr2:29123841 | G | A | 1 | a0001c0001t0011g0234 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.133+2320G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29123841 | |||||||
chr2:29123968 | A | T | 12 | a0001c0002t0001g0003 a0001c0002t0001g0062 a0001c0002t0001g0063 others(9): Show |
13 | HG02155.hp1 HG02970.hp2 HG03098.hp2 others(10): Show |
intron_variant | MODIFIER | c.133+2447A>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29123968 | |||||||
chr2:29124023 | T | C | 6 | a0001c0003t0001g0212 a0001c0003t0001g0245 a0001c0003t0001g0246 others(3): Show |
6 | HG02572.hp1 HG02647.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.133+2502T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29124023 | |||||||
chr2:29124361 | C | T | 1 | a0001c0001t0001g0208 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.133+2840C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29124361 | |||||||
chr2:29124367 | G | A | 136 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(133): Show |
138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
intron_variant | MODIFIER | c.133+2846G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29124367 | |||||||
chr2:29124439 | G | A | 23 | a0001c0002t0001g0124 a0001c0002t0002g0084 a0001c0002t0002g0085 others(20): Show |
23 | HG00738.hp2 HG01106.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.133+2918G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29124439 | |||||||
chr2:29124528 | A | T | 1 | a0001c0001t0001g0207 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.133+3007A>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29124528 | |||||||
chr2:29124594 | TTGTC | T | 138 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(135): Show |
140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.133+3074_133+3077d others(6): Show |
CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29124594 | |||||||
chr2:29124600 | C | T | 138 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(135): Show |
140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.133+3079C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29124600 | |||||||
chr2:29124603 | AACTCACT others(1): Show |
A | 138 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(135): Show |
140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.133+3084_133+3091d others(10): Show |
CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 29124603 | ||||||
chr2:29124924 | T | C | 13 | a0001c0002t0001g0003 a0001c0002t0001g0062 a0001c0002t0001g0063 others(10): Show |
14 | HG01074.hp1 HG02155.hp1 HG02970.hp2 others(11): Show |
intron_variant | MODIFIER | c.133+3403T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29124924 | |||||||
chr2:29125052 | A | G | 12 | a0001c0002t0001g0003 a0001c0002t0001g0062 a0001c0002t0001g0063 others(9): Show |
13 | HG02155.hp1 HG02970.hp2 HG03098.hp2 others(10): Show |
intron_variant | MODIFIER | c.133+3531A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29125052 | |||||||
chr2:29125143 | A | G | 1 | a0006c0022t0001g0045 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.133+3622A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29125143 | |||||||
chr2:29125193 | G | A | 245 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(242): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.133+3672G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29125193 | |||||||
chr2:29125210 | C | G | 1 | a0001c0001t0001g0206 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.133+3689C>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29125210 | |||||||
chr2:29125222 | G | A | 1 | a0001c0003t0001g0213 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.133+3701G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29125222 | |||||||
chr2:29125237 | G | T | 1 | a0001c0002t0003g0070 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.133+3716G>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29125237 | |||||||
chr2:29125331 | G | C | 2 | a0001c0010t0004g0256 a0001c0010t0004g0257 |
2 | HG01891.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.133+3810G>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29125331 | |||||||
chr2:29125345 | C | G | 52 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0012 others(49): Show |
55 | HG00558.hp1 HG00597.hp1 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.133+3824C>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29125345 | |||||||
chr2:29125377 | T | C | 1 | a0001c0002t0003g0070 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.133+3856T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29125377 | |||||||
chr2:29125466 | G | A | 5 | a0001c0001t0001g0227 a0001c0001t0001g0228 a0001c0001t0002g0054 others(2): Show |
5 | HG01346.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.133+3945G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29125466 | |||||||
chr2:29125472 | A | C | 11 | a0001c0002t0001g0003 a0001c0002t0001g0062 a0001c0002t0001g0063 others(8): Show |
12 | HG02155.hp1 HG02970.hp2 HG03453.hp2 others(9): Show |
intron_variant | MODIFIER | c.133+3951A>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29125472 | |||||||
chr2:29125555 | C | T | 1 | a0001c0002t0001g0267 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.133+4034C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29125555 | |||||||
chr2:29125586 | G | A | 1 | a0001c0002t0001g0017 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.133+4065G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29125586 | |||||||
chr2:29125796 | C | T | 1 | a0001c0002t0010g0233 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.133+4275C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29125796 | |||||||
chr2:29126031 | C | T | 1 | a0001c0002t0003g0070 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.133+4510C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29126031 | |||||||
chr2:29126044 | G | A | 3 | a0001c0002t0002g0250 a0001c0002t0002g0251 a0001c0002t0002g0252 |
3 | HG02055.hp1 HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.133+4523G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29126044 | |||||||
chr2:29126047 | C | T | 2 | a0001c0002t0001g0063 a0001c0002t0001g0064 |
2 | NA18984.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.133+4526C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29126047 | |||||||
chr2:29126360 | T | G | 14 | a0001c0001t0001g0265 a0001c0002t0001g0264 a0001c0002t0001g0271 others(11): Show |
14 | HG00741.hp1 HG01069.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.133+4839T>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29126360 | |||||||
chr2:29126553 | G | A | 1 | a0001c0002t0003g0070 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.134-4705G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29126553 | |||||||
chr2:29126658 | T | C | 5 | a0001c0001t0001g0227 a0001c0001t0001g0228 a0001c0001t0002g0054 others(2): Show |
5 | HG01346.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.134-4600T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29126658 | |||||||
chr2:29126979 | G | A | 139 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(136): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.134-4279G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29126979 | |||||||
chr2:29126995 | A | G | 1 | a0001c0002t0002g0123 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.134-4263A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29126995 | |||||||
chr2:29127145 | T | A | 12 | a0001c0002t0001g0003 a0001c0002t0001g0062 a0001c0002t0001g0063 others(9): Show |
13 | HG02155.hp1 HG02717.hp2 HG02970.hp2 others(10): Show |
intron_variant | MODIFIER | c.134-4113T>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29127145 | |||||||
chr2:29127172 | A | AT | 3 | a0001c0010t0004g0256 a0001c0010t0004g0257 a0001c0020t0001g0255 |
3 | HG01891.hp2 HG01934.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.134-4085dupT | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 29127172 | ||||||
chr2:29127178 | A | G | 1 | a0001c0002t0001g0044 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.134-4080A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29127178 | |||||||
chr2:29127328 | C | T | 3 | a0001c0010t0004g0256 a0001c0010t0004g0257 a0001c0020t0001g0255 |
3 | HG01891.hp2 HG01934.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.134-3930C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29127328 | |||||||
chr2:29127333 | A | G | 3 | a0001c0010t0004g0256 a0001c0010t0004g0257 a0001c0020t0001g0255 |
3 | HG01891.hp2 HG01934.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.134-3925A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29127333 | |||||||
chr2:29127483 | G | A | 1 | a0002c0004t0001g0268 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.134-3775G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29127483 | |||||||
chr2:29127543 | G | A | 1 | a0001c0002t0003g0070 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.134-3715G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29127543 | |||||||
chr2:29127582 | C | G | 1 | a0001c0001t0003g0104 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.134-3676C>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29127582 | |||||||
chr2:29127716 | C | G | 5 | a0001c0001t0001g0227 a0001c0001t0001g0228 a0001c0001t0002g0054 others(2): Show |
5 | HG01346.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.134-3542C>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29127716 | |||||||
chr2:29127830 | G | T | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG03688.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.134-3428G>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29127830 | |||||||
chr2:29127896 | G | T | 6 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0006g0200 others(3): Show |
6 | HG00642.hp2 HG01106.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.134-3362G>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29127896 | |||||||
chr2:29128001 | C | G | 2 | a0001c0001t0002g0197 a0001c0001t0004g0198 |
2 | HG01884.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.134-3257C>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29128001 | |||||||
chr2:29128187 | GT | G | 147 | a0001c0001t0001g0076 a0001c0001t0001g0103 a0001c0001t0001g0144 others(144): Show |
152 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.134-3053delT | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 29128187 | ||||||
chr2:29128187 | GTT | G | 26 | a0001c0001t0001g0227 a0001c0001t0001g0228 a0001c0001t0002g0054 others(23): Show |
27 | HG01123.hp1 HG01169.hp2 HG01346.hp2 others(24): Show |
intron_variant | MODIFIER | c.134-3054_134-3053d others(4): Show |
CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 29128187 | ||||||
chr2:29128272 | G | T | 3 | a0001c0002t0007g0143 a0001c0002t0010g0232 a0001c0005t0001g0231 |
3 | HG02559.hp2 HG02630.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.134-2986G>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29128272 | |||||||
chr2:29128297 | A | G | 1 | a0001c0002t0001g0238 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.134-2961A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29128297 | |||||||
chr2:29128443 | C | A | 5 | a0001c0001t0001g0227 a0001c0001t0001g0228 a0001c0001t0002g0054 others(2): Show |
5 | HG01346.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.134-2815C>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29128443 | |||||||
chr2:29128449 | C | CA | 6 | a0001c0002t0001g0236 a0001c0002t0001g0237 a0001c0002t0001g0238 others(3): Show |
6 | HG01074.hp1 HG01099.hp2 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.134-2800dupA | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | 29128449 | ||||||
chr2:29128501 | A | C | 1 | a0001c0001t0001g0196 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.134-2757A>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29128501 | |||||||
chr2:29128632 | C | T | 3 | a0001c0010t0004g0256 a0001c0010t0004g0257 a0001c0020t0001g0255 |
3 | HG01891.hp2 HG01934.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.134-2626C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29128632 | |||||||
chr2:29128705 | C | T | 3 | a0001c0002t0001g0062 a0001c0002t0001g0068 a0001c0002t0001g0069 |
3 | NA18961.hp1 NA19062.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.134-2553C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29128705 | |||||||
chr2:29129007 | G | T | 1 | a0001c0010t0004g0257 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.134-2251G>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29129007 | |||||||
chr2:29129127 | T | C | 1 | a0001c0002t0013g0055 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.134-2131T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29129127 | |||||||
chr2:29129157 | G | A | 11 | a0001c0002t0001g0003 a0001c0002t0001g0062 a0001c0002t0001g0063 others(8): Show |
12 | HG02155.hp1 HG02970.hp2 HG03453.hp2 others(9): Show |
intron_variant | MODIFIER | c.134-2101G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29129157 | |||||||
chr2:29129229 | G | A | 5 | a0001c0001t0001g0227 a0001c0001t0001g0228 a0001c0001t0002g0054 others(2): Show |
5 | HG01346.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.134-2029G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29129229 | |||||||
chr2:29129247 | G | A | 22 | a0001c0003t0001g0087 a0001c0003t0001g0088 a0001c0003t0001g0089 others(19): Show |
23 | HG00099.hp1 HG00280.hp2 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.134-2011G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29129247 | |||||||
chr2:29129459 | A | G | 11 | a0001c0002t0001g0003 a0001c0002t0001g0062 a0001c0002t0001g0063 others(8): Show |
12 | HG02155.hp1 HG02970.hp2 HG03453.hp2 others(9): Show |
intron_variant | MODIFIER | c.134-1799A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29129459 | |||||||
chr2:29129511 | T | C | 2 | a0001c0002t0001g0049 a0001c0002t0001g0050 |
2 | HG01123.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.134-1747T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29129511 | |||||||
chr2:29129700 | C | A | 12 | a0001c0002t0001g0003 a0001c0002t0001g0062 a0001c0002t0001g0063 others(9): Show |
13 | HG02155.hp1 HG02970.hp2 HG03098.hp2 others(10): Show |
intron_variant | MODIFIER | c.134-1558C>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29129700 | |||||||
chr2:29129814 | C | T | 19 | a0001c0002t0001g0072 a0001c0002t0001g0264 a0001c0002t0001g0271 others(16): Show |
19 | HG00741.hp1 HG01069.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.134-1444C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29129814 | |||||||
chr2:29130004 | G | A | 11 | a0001c0002t0001g0003 a0001c0002t0001g0062 a0001c0002t0001g0063 others(8): Show |
12 | HG02155.hp1 HG02970.hp2 HG03453.hp2 others(9): Show |
intron_variant | MODIFIER | c.134-1254G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29130004 | |||||||
chr2:29130245 | A | G | 11 | a0001c0002t0001g0056 a0001c0002t0001g0057 a0001c0002t0001g0108 others(8): Show |
12 | HG00741.hp2 HG01069.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.134-1013A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29130245 | |||||||
chr2:29130277 | C | G | 11 | a0001c0002t0001g0003 a0001c0002t0001g0062 a0001c0002t0001g0063 others(8): Show |
12 | HG02155.hp1 HG02970.hp2 HG03453.hp2 others(9): Show |
intron_variant | MODIFIER | c.134-981C>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29130277 | |||||||
chr2:29130290 | T | C | 3 | a0001c0010t0004g0256 a0001c0010t0004g0257 a0001c0020t0001g0255 |
3 | HG01891.hp2 HG01934.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.134-968T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29130290 | |||||||
chr2:29130298 | G | A | 11 | a0001c0002t0001g0003 a0001c0002t0001g0062 a0001c0002t0001g0063 others(8): Show |
12 | HG02155.hp1 HG02970.hp2 HG03453.hp2 others(9): Show |
intron_variant | MODIFIER | c.134-960G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29130298 | |||||||
chr2:29130316 | G | A | 1 | a0001c0002t0010g0233 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.134-942G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29130316 | |||||||
chr2:29130318 | A | G | 3 | a0001c0002t0007g0143 a0001c0002t0010g0232 a0001c0005t0001g0231 |
3 | HG02559.hp2 HG02630.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.134-940A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29130318 | |||||||
chr2:29130439 | T | C | 3 | a0001c0002t0007g0143 a0001c0002t0010g0232 a0001c0005t0001g0231 |
3 | HG02559.hp2 HG02630.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.134-819T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29130439 | |||||||
chr2:29130541 | T | C | 3 | a0001c0002t0001g0243 a0001c0002t0001g0283 a0001c0002t0001g0284 |
3 | HG00140.hp1 HG01175.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.134-717T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29130541 | |||||||
chr2:29130627 | C | A | 1 | a0001c0002t0001g0047 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.134-631C>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29130627 | |||||||
chr2:29130673 | T | C | 1 | a0001c0013t0008g0051 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.134-585T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29130673 | |||||||
chr2:29130706 | T | G | 1 | a0001c0002t0001g0003 | 2 | HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.134-552T>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29130706 | |||||||
chr2:29131071 | G | C | 1 | a0001c0002t0003g0073 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.134-187G>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 2/15 | chr2 | 29131071 | |||||||
chr2:29131777 | A | G | 1 | a0001c0001t0003g0083 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.274-375A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 3/15 | chr2 | 29131777 | |||||||
chr2:29131936 | T | C | 24 | a0001c0002t0001g0124 a0001c0002t0002g0084 a0001c0002t0002g0085 others(21): Show |
24 | HG00738.hp2 HG01106.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.274-216T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 3/15 | chr2 | 29131936 | |||||||
chr2:29132328 | TG | T | 8 | a0001c0002t0001g0062 a0001c0002t0001g0063 a0001c0002t0001g0064 others(5): Show |
8 | HG02155.hp1 HG03927.hp2 NA18961.hp1 others(5): Show |
intron_variant | MODIFIER | c.367+88delG | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 29132328 | ||||||
chr2:29132372 | C | T | 1 | a0010c0024t0001g0065 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.367+127C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 4/15 | chr2 | 29132372 | |||||||
chr2:29132437 | C | T | 240 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(237): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.367+192C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 4/15 | chr2 | 29132437 | |||||||
chr2:29132479 | T | C | 240 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(237): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.367+234T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 4/15 | chr2 | 29132479 | |||||||
chr2:29132593 | A | C | 11 | a0001c0002t0001g0003 a0001c0002t0001g0062 a0001c0002t0001g0063 others(8): Show |
12 | HG02155.hp1 HG02970.hp2 HG03453.hp2 others(9): Show |
intron_variant | MODIFIER | c.367+348A>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 4/15 | chr2 | 29132593 | |||||||
chr2:29132751 | G | A | 1 | a0001c0002t0001g0019 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.367+506G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 4/15 | chr2 | 29132751 | |||||||
chr2:29133072 | C | T | 9 | a0001c0002t0001g0003 a0001c0002t0001g0062 a0001c0002t0001g0063 others(6): Show |
10 | HG02155.hp1 HG02970.hp2 HG03516.hp2 others(7): Show |
intron_variant | MODIFIER | c.368-583C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 4/15 | chr2 | 29133072 | |||||||
chr2:29133082 | C | G | 1 | a0001c0001t0001g0059 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.368-573C>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 4/15 | chr2 | 29133082 | |||||||
chr2:29133103 | G | A | 1 | a0001c0002t0001g0020 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.368-552G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 4/15 | chr2 | 29133103 | |||||||
chr2:29133129 | C | T | 2 | a0001c0001t0002g0054 a0001c0001t0008g0053 |
2 | HG01346.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.368-526C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 4/15 | chr2 | 29133129 | |||||||
chr2:29133211 | A | G | 1 | a0001c0005t0001g0114 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.368-444A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 4/15 | chr2 | 29133211 | |||||||
chr2:29133221 | A | G | 2 | a0001c0001t0001g0142 a0001c0001t0001g0195 |
2 | HG03471.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.368-434A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 4/15 | chr2 | 29133221 | |||||||
chr2:29133311 | C | T | 2 | a0001c0002t0001g0068 a0001c0002t0001g0069 |
2 | NA19062.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.368-344C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 4/15 | chr2 | 29133311 | |||||||
chr2:29133431 | A | C | 3 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 |
3 | NA18949.hp2 NA19056.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.368-224A>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 4/15 | chr2 | 29133431 | |||||||
chr2:29133441 | T | A | 3 | a0001c0002t0003g0009 a0001c0002t0013g0055 a0004c0012t0001g0008 |
3 | HG00738.hp2 HG02145.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.368-214T>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 4/15 | chr2 | 29133441 | |||||||
chr2:29133603 | T | TTGGAA | 11 | a0001c0002t0001g0003 a0001c0002t0001g0062 a0001c0002t0001g0063 others(8): Show |
12 | HG02155.hp1 HG02970.hp2 HG03453.hp2 others(9): Show |
intron_variant | MODIFIER | c.368-51_368-47dupTG others(3): Show |
CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | 29133603 | ||||||
chr2:29133862 | T | C | 98 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0012 others(95): Show |
102 | HG00140.hp1 HG00558.hp1 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.529+46T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 5/15 | chr2 | 29133862 | |||||||
chr2:29134023 | A | G | 1 | a0002c0004t0001g0274 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.529+207A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 5/15 | chr2 | 29134023 | |||||||
chr2:29134059 | A | G | 2 | a0001c0013t0008g0051 a0001c0026t0001g0052 |
2 | HG01109.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.529+243A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 5/15 | chr2 | 29134059 | |||||||
chr2:29134080 | G | T | 1 | a0001c0002t0003g0070 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.529+264G>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 5/15 | chr2 | 29134080 | |||||||
chr2:29134171 | G | A | 98 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0012 others(95): Show |
102 | HG00140.hp1 HG00558.hp1 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.529+355G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 5/15 | chr2 | 29134171 | |||||||
chr2:29134234 | G | C | 1 | a0001c0003t0001g0212 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.529+418G>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 5/15 | chr2 | 29134234 | |||||||
chr2:29134265 | G | T | 1 | a0001c0002t0003g0070 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.529+449G>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 5/15 | chr2 | 29134265 | |||||||
chr2:29134347 | G | A | 3 | a0001c0002t0001g0236 a0001c0002t0001g0237 a0001c0002t0001g0238 |
3 | HG01243.hp1 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.529+531G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 5/15 | chr2 | 29134347 | |||||||
chr2:29134537 | C | G | 2 | a0001c0001t0001g0193 a0001c0001t0001g0194 |
2 | NA18978.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.529+721C>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 5/15 | chr2 | 29134537 | |||||||
chr2:29134537 | C | T | 1 | a0001c0002t0003g0070 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.529+721C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 5/15 | chr2 | 29134537 | |||||||
chr2:29134603 | AAG | A | 91 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(88): Show |
92 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.529+792_529+793del others(2): Show |
CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | 29134603 | ||||||
chr2:29134615 | C | T | 19 | a0001c0002t0001g0072 a0001c0002t0001g0264 a0001c0002t0001g0271 others(16): Show |
19 | HG00741.hp1 HG01069.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.529+799C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 5/15 | chr2 | 29134615 | |||||||
chr2:29134765 | G | A | 4 | a0001c0002t0001g0236 a0001c0002t0001g0237 a0001c0002t0001g0238 others(1): Show |
4 | HG01243.hp1 HG02647.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.530-783G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 5/15 | chr2 | 29134765 | |||||||
chr2:29134798 | C | A | 98 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0012 others(95): Show |
102 | HG00140.hp1 HG00558.hp1 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.530-750C>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 5/15 | chr2 | 29134798 | |||||||
chr2:29134992 | A | C | 1 | a0001c0002t0002g0250 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.530-556A>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 5/15 | chr2 | 29134992 | |||||||
chr2:29135333 | A | G | 2 | a0001c0002t0002g0117 a0001c0002t0002g0118 |
2 | HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.530-215A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 5/15 | chr2 | 29135333 | |||||||
chr2:29135906 | G | A | 11 | a0001c0002t0001g0003 a0001c0002t0001g0062 a0001c0002t0001g0063 others(8): Show |
12 | HG02155.hp1 HG02970.hp2 HG03453.hp2 others(9): Show |
intron_variant | MODIFIER | c.648+240G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29135906 | |||||||
chr2:29136069 | G | C | 101 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0012 others(98): Show |
105 | HG00140.hp1 HG00558.hp1 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.648+403G>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29136069 | |||||||
chr2:29136185 | G | GT | 9 | a0001c0002t0001g0108 a0001c0002t0001g0113 a0001c0002t0003g0110 others(6): Show |
10 | HG00741.hp2 HG01069.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.648+521dupT | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 29136185 | ||||||
chr2:29136188 | G | GTT | 11 | a0001c0002t0001g0003 a0001c0002t0001g0062 a0001c0002t0001g0063 others(8): Show |
12 | HG02155.hp1 HG02970.hp2 HG03453.hp2 others(9): Show |
intron_variant | MODIFIER | c.648+532_648+533dup others(2): Show |
CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 29136188 | ||||||
chr2:29136188 | G | T | 96 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0012 others(93): Show |
100 | HG00140.hp1 HG00558.hp1 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.648+522G>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29136188 | |||||||
chr2:29136244 | C | T | 11 | a0001c0002t0001g0003 a0001c0002t0001g0062 a0001c0002t0001g0063 others(8): Show |
12 | HG02155.hp1 HG02970.hp2 HG03453.hp2 others(9): Show |
intron_variant | MODIFIER | c.648+578C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29136244 | |||||||
chr2:29136246 | C | T | 1 | a0001c0002t0015g0011 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.648+580C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29136246 | |||||||
chr2:29136292 | A | T | 1 | a0001c0003t0001g0221 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.648+626A>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29136292 | |||||||
chr2:29136520 | A | G | 2 | a0001c0002t0001g0095 a0001c0002t0001g0099 |
2 | NA18949.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.648+854A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29136520 | |||||||
chr2:29136550 | A | G | 11 | a0001c0002t0001g0056 a0001c0002t0001g0057 a0001c0002t0001g0108 others(8): Show |
12 | HG00741.hp2 HG01069.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.648+884A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29136550 | |||||||
chr2:29136655 | G | A | 3 | a0001c0010t0004g0256 a0001c0010t0004g0257 a0001c0020t0001g0255 |
3 | HG01891.hp2 HG01934.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.648+989G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29136655 | |||||||
chr2:29136695 | C | T | 1 | a0001c0003t0001g0221 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.648+1029C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29136695 | |||||||
chr2:29136739 | G | C | 1 | a0001c0013t0008g0051 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.648+1073G>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29136739 | |||||||
chr2:29136744 | G | C | 1 | a0001c0002t0002g0266 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.648+1078G>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29136744 | |||||||
chr2:29136745 | T | A | 1 | a0001c0013t0008g0051 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.648+1079T>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29136745 | |||||||
chr2:29136920 | A | G | 13 | a0001c0002t0001g0056 a0001c0002t0001g0057 a0001c0002t0001g0108 others(10): Show |
14 | HG00741.hp2 HG01069.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.648+1254A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29136920 | |||||||
chr2:29136954 | TA | T | 13 | a0001c0001t0001g0015 a0001c0001t0001g0141 a0001c0001t0001g0192 others(10): Show |
13 | HG01192.hp2 HG01243.hp2 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.648+1300delA | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 29136954 | ||||||
chr2:29137003 | A | G | 1 | a0001c0002t0007g0061 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.648+1337A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29137003 | |||||||
chr2:29137004 | C | T | 1 | a0001c0001t0001g0190 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.648+1338C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29137004 | |||||||
chr2:29137054 | C | G | 16 | a0001c0002t0001g0072 a0001c0002t0001g0264 a0001c0002t0001g0271 others(13): Show |
16 | HG00741.hp1 HG01069.hp2 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.648+1388C>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29137054 | |||||||
chr2:29137093 | G | A | 9 | a0001c0002t0001g0124 a0001c0002t0002g0123 a0001c0002t0002g0126 others(6): Show |
9 | HG00738.hp2 HG01891.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.648+1427G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29137093 | |||||||
chr2:29137127 | G | A | 82 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0012 others(79): Show |
86 | HG00140.hp1 HG00558.hp1 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.648+1461G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29137127 | |||||||
chr2:29137152 | A | G | 1 | a0001c0002t0009g0115 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.648+1486A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29137152 | |||||||
chr2:29137171 | C | G | 1 | a0001c0013t0008g0051 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.648+1505C>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29137171 | |||||||
chr2:29137185 | C | T | 2 | a0001c0002t0001g0049 a0001c0002t0001g0050 |
2 | HG01123.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.648+1519C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29137185 | |||||||
chr2:29137397 | A | AC | 3 | a0001c0001t0001g0105 a0001c0002t0001g0017 a0002c0004t0001g0276 |
3 | HG00673.hp1 HG00741.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.648+1733dupC | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 29137397 | ||||||
chr2:29137399 | C | T | 3 | a0001c0002t0007g0143 a0001c0002t0010g0232 a0001c0005t0001g0231 |
3 | HG02559.hp2 HG02630.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.648+1733C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29137399 | |||||||
chr2:29137599 | T | G | 1 | a0001c0001t0001g0071 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.648+1933T>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29137599 | |||||||
chr2:29137706 | C | A | 16 | a0001c0002t0001g0072 a0001c0002t0001g0264 a0001c0002t0001g0271 others(13): Show |
16 | HG00741.hp1 HG01069.hp2 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.648+2040C>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29137706 | |||||||
chr2:29137772 | A | G | 1 | a0001c0009t0001g0226 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.648+2106A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29137772 | |||||||
chr2:29138002 | T | C | 2 | a0001c0002t0001g0049 a0001c0002t0001g0050 |
2 | HG01123.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.648+2336T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29138002 | |||||||
chr2:29138079 | C | T | 101 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0012 others(98): Show |
105 | HG00140.hp1 HG00558.hp1 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.648+2413C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29138079 | |||||||
chr2:29138142 | T | C | 1 | a0001c0002t0010g0233 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.648+2476T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29138142 | |||||||
chr2:29138145 | C | T | 1 | a0001c0001t0009g0149 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.648+2479C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29138145 | |||||||
chr2:29138306 | G | A | 2 | a0001c0001t0001g0227 a0001c0001t0001g0228 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.648+2640G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29138306 | |||||||
chr2:29138384 | A | G | 1 | a0001c0002t0003g0070 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.648+2718A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29138384 | |||||||
chr2:29138489 | C | CT | 27 | a0001c0001t0001g0194 a0001c0001t0001g0265 a0001c0002t0001g0049 others(24): Show |
27 | HG00741.hp1 HG01069.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.648+2835dupT | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 29138489 | ||||||
chr2:29138489 | CT | C | 11 | a0001c0002t0001g0003 a0001c0002t0001g0062 a0001c0002t0001g0063 others(8): Show |
12 | HG02155.hp1 HG02970.hp2 HG03453.hp2 others(9): Show |
intron_variant | MODIFIER | c.648+2835delT | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 29138489 | ||||||
chr2:29138718 | G | A | 11 | a0001c0002t0001g0056 a0001c0002t0001g0057 a0001c0002t0001g0108 others(8): Show |
12 | HG00741.hp2 HG01069.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.648+3052G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29138718 | |||||||
chr2:29138737 | A | T | 1 | a0001c0002t0003g0070 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.648+3071A>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29138737 | |||||||
chr2:29138795 | A | T | 1 | a0001c0001t0001g0103 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.648+3129A>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29138795 | |||||||
chr2:29138826 | A | C | 1 | a0001c0002t0001g0048 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.648+3160A>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29138826 | |||||||
chr2:29138914 | A | G | 1 | a0001c0002t0010g0233 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.648+3248A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29138914 | |||||||
chr2:29138973 | C | T | 13 | a0001c0002t0001g0056 a0001c0002t0001g0057 a0001c0002t0001g0108 others(10): Show |
14 | HG00741.hp2 HG01069.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.648+3307C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29138973 | |||||||
chr2:29139055 | A | G | 1 | a0001c0002t0003g0070 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.648+3389A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29139055 | |||||||
chr2:29139195 | G | C | 3 | a0001c0002t0002g0250 a0001c0002t0002g0251 a0001c0002t0002g0252 |
3 | HG02055.hp1 HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.648+3529G>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29139195 | |||||||
chr2:29139196 | G | GT | 23 | a0001c0002t0001g0124 a0001c0002t0002g0084 a0001c0002t0002g0085 others(20): Show |
23 | HG00738.hp2 HG01106.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.648+3542dupT | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 29139196 | ||||||
chr2:29139196 | GT | G | 114 | a0001c0001t0001g0058 a0001c0001t0001g0265 a0001c0002t0001g0001 others(111): Show |
119 | HG00140.hp1 HG00558.hp1 HG00597.hp1 others(116): Show |
intron_variant | MODIFIER | c.648+3542delT | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 29139196 | ||||||
chr2:29139250 | G | A | 21 | a0001c0001t0001g0265 a0001c0002t0001g0072 a0001c0002t0001g0264 others(18): Show |
21 | HG00741.hp1 HG01069.hp2 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.648+3584G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29139250 | |||||||
chr2:29139264 | T | C | 2 | a0001c0002t0001g0049 a0001c0002t0001g0050 |
2 | HG01123.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.648+3598T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29139264 | |||||||
chr2:29139266 | C | A | 33 | a0001c0001t0001g0265 a0001c0002t0001g0003 a0001c0002t0001g0062 others(30): Show |
34 | HG00741.hp1 HG01069.hp2 HG01074.hp1 others(31): Show |
intron_variant | MODIFIER | c.648+3600C>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29139266 | |||||||
chr2:29139300 | C | T | 2 | a0001c0002t0001g0049 a0001c0002t0001g0050 |
2 | HG01123.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.648+3634C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29139300 | |||||||
chr2:29139347 | G | A | 1 | a0001c0002t0001g0108 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.648+3681G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29139347 | |||||||
chr2:29139566 | C | A | 21 | a0001c0001t0001g0265 a0001c0002t0001g0072 a0001c0002t0001g0264 others(18): Show |
21 | HG00741.hp1 HG01069.hp2 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.648+3900C>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29139566 | |||||||
chr2:29139672 | G | A | 137 | a0001c0001t0001g0265 a0001c0002t0001g0001 a0001c0002t0001g0002 others(134): Show |
142 | HG00140.hp1 HG00558.hp1 HG00597.hp1 others(139): Show |
intron_variant | MODIFIER | c.648+4006G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29139672 | |||||||
chr2:29139871 | ATCTT | A | 21 | a0001c0001t0001g0265 a0001c0002t0001g0072 a0001c0002t0001g0264 others(18): Show |
21 | HG00741.hp1 HG01069.hp2 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.649-3832_649-3829d others(6): Show |
CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 29139871 | ||||||
chr2:29139947 | TTGAA | T | 3 | a0001c0001t0001g0244 a0001c0001t0001g0280 a0001c0001t0001g0281 |
3 | HG03225.hp1 NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.649-3759_649-3756d others(6): Show |
CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 29139947 | ||||||
chr2:29140040 | T | C | 1 | a0001c0001t0001g0204 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.649-3669T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29140040 | |||||||
chr2:29140163 | T | C | 262 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(259): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.649-3546T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29140163 | |||||||
chr2:29140326 | G | A | 20 | a0001c0001t0001g0265 a0001c0002t0001g0072 a0001c0002t0001g0264 others(17): Show |
20 | HG00741.hp1 HG01069.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.649-3383G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29140326 | |||||||
chr2:29140348 | C | T | 3 | a0001c0002t0001g0049 a0001c0002t0001g0050 a0001c0026t0001g0052 |
3 | HG01123.hp1 HG02717.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.649-3361C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29140348 | |||||||
chr2:29140446 | G | A | 33 | a0001c0001t0001g0265 a0001c0002t0001g0003 a0001c0002t0001g0062 others(30): Show |
34 | HG00741.hp1 HG01069.hp2 HG01074.hp1 others(31): Show |
intron_variant | MODIFIER | c.649-3263G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29140446 | |||||||
chr2:29140448 | A | T | 1 | a0001c0013t0008g0051 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.649-3261A>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29140448 | |||||||
chr2:29140490 | T | C | 1 | a0008c0017t0001g0150 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.649-3219T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29140490 | |||||||
chr2:29140493 | G | C | 1 | a0001c0002t0003g0070 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.649-3216G>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29140493 | |||||||
chr2:29140528 | T | C | 1 | a0001c0020t0001g0255 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.649-3181T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29140528 | |||||||
chr2:29140541 | T | C | 1 | a0001c0001t0009g0149 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.649-3168T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29140541 | |||||||
chr2:29140542 | G | A | 1 | a0001c0001t0009g0149 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.649-3167G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29140542 | |||||||
chr2:29140596 | T | G | 1 | a0001c0001t0001g0015 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.649-3113T>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29140596 | |||||||
chr2:29140610 | G | A | 104 | a0001c0002t0001g0001 a0001c0002t0001g0002 a0001c0002t0001g0012 others(101): Show |
108 | HG00140.hp1 HG00558.hp1 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.649-3099G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29140610 | |||||||
chr2:29140632 | C | G | 1 | a0001c0003t0001g0213 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.649-3077C>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29140632 | |||||||
chr2:29140715 | G | A | 1 | a0001c0002t0003g0070 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.649-2994G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29140715 | |||||||
chr2:29140721 | C | G | 1 | a0001c0001t0001g0189 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.649-2988C>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29140721 | |||||||
chr2:29140754 | A | T | 33 | a0001c0001t0001g0265 a0001c0002t0001g0003 a0001c0002t0001g0062 others(30): Show |
34 | HG00741.hp1 HG01069.hp2 HG01074.hp1 others(31): Show |
intron_variant | MODIFIER | c.649-2955A>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29140754 | |||||||
chr2:29140766 | G | A | 1 | a0001c0002t0010g0233 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.649-2943G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29140766 | |||||||
chr2:29140825 | A | G | 2 | a0001c0002t0015g0011 a0004c0012t0001g0010 |
2 | HG02451.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.649-2884A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29140825 | |||||||
chr2:29140941 | C | T | 1 | a0001c0001t0006g0210 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.649-2768C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29140941 | |||||||
chr2:29140942 | C | G | 1 | a0001c0001t0006g0210 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.649-2767C>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29140942 | |||||||
chr2:29141049 | G | A | 254 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(251): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.649-2660G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29141049 | |||||||
chr2:29141050 | A | AT | 10 | a0001c0002t0001g0062 a0001c0002t0001g0063 a0001c0002t0001g0064 others(7): Show |
10 | HG02155.hp1 HG03453.hp2 HG03486.hp1 others(7): Show |
intron_variant | MODIFIER | c.649-2651dupT | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 29141050 | ||||||
chr2:29141059 | G | T | 11 | a0001c0002t0001g0003 a0001c0002t0001g0062 a0001c0002t0001g0063 others(8): Show |
12 | HG02155.hp1 HG02970.hp2 HG03453.hp2 others(9): Show |
intron_variant | MODIFIER | c.649-2650G>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29141059 | |||||||
chr2:29141251 | A | C | 1 | a0001c0026t0001g0052 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.649-2458A>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29141251 | |||||||
chr2:29141350 | A | G | 1 | a0001c0002t0013g0055 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.649-2359A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29141350 | |||||||
chr2:29141432 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.649-2277C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29141432 | |||||||
chr2:29141442 | T | C | 3 | a0001c0010t0004g0256 a0001c0010t0004g0257 a0001c0020t0001g0255 |
3 | HG01891.hp2 HG01934.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.649-2267T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29141442 | |||||||
chr2:29141566 | A | G | 25 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(22): Show |
25 | HG00099.hp2 HG00140.hp2 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.649-2143A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29141566 | |||||||
chr2:29141650 | C | T | 21 | a0001c0001t0001g0265 a0001c0002t0001g0072 a0001c0002t0001g0264 others(18): Show |
21 | HG00741.hp1 HG01069.hp2 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.649-2059C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29141650 | |||||||
chr2:29141750 | C | T | 136 | a0001c0001t0001g0265 a0001c0002t0001g0001 a0001c0002t0001g0002 others(133): Show |
141 | HG00140.hp1 HG00558.hp1 HG00597.hp1 others(138): Show |
intron_variant | MODIFIER | c.649-1959C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29141750 | |||||||
chr2:29141774 | C | G | 1 | a0001c0002t0003g0070 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.649-1935C>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29141774 | |||||||
chr2:29142030 | G | A | 1 | a0001c0001t0001g0281 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.649-1679G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29142030 | |||||||
chr2:29142038 | T | G | 1 | a0001c0013t0008g0051 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.649-1671T>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29142038 | |||||||
chr2:29142041 | C | T | 1 | a0001c0002t0003g0070 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.649-1668C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29142041 | |||||||
chr2:29142042 | G | A | 1 | a0001c0002t0001g0021 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.649-1667G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29142042 | |||||||
chr2:29142060 | C | T | 142 | a0001c0001t0001g0227 a0001c0001t0001g0228 a0001c0001t0001g0265 others(139): Show |
147 | HG00140.hp1 HG00558.hp1 HG00597.hp1 others(144): Show |
intron_variant | MODIFIER | c.649-1649C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29142060 | |||||||
chr2:29142174 | G | A | 33 | a0001c0001t0001g0265 a0001c0001t0003g0083 a0001c0002t0001g0003 others(30): Show |
34 | HG00741.hp1 HG01069.hp2 HG01074.hp1 others(31): Show |
intron_variant | MODIFIER | c.649-1535G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29142174 | |||||||
chr2:29142259 | C | G | 137 | a0001c0001t0001g0265 a0001c0002t0001g0001 a0001c0002t0001g0002 others(134): Show |
142 | HG00140.hp1 HG00558.hp1 HG00597.hp1 others(139): Show |
intron_variant | MODIFIER | c.649-1450C>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29142259 | |||||||
chr2:29142282 | A | G | 1 | a0002c0004t0001g0278 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.649-1427A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29142282 | |||||||
chr2:29142288 | T | C | 1 | a0001c0002t0003g0070 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.649-1421T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29142288 | |||||||
chr2:29142308 | GT | G | 6 | a0001c0002t0001g0067 a0001c0002t0003g0070 a0001c0002t0009g0115 others(3): Show |
6 | HG01256.hp1 HG02300.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.649-1389delT | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 29142308 | ||||||
chr2:29142333 | G | A | 2 | a0001c0001t0001g0134 a0001c0001t0001g0135 |
2 | NA19240.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.649-1376G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29142333 | |||||||
chr2:29142443 | G | T | 3 | a0001c0002t0001g0236 a0001c0002t0001g0237 a0001c0002t0001g0238 |
3 | HG01243.hp1 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.649-1266G>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29142443 | |||||||
chr2:29142478 | A | G | 2 | a0001c0001t0001g0188 a0001c0001t0001g0230 |
2 | NA19059.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.649-1231A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29142478 | |||||||
chr2:29142512 | T | C | 3 | a0001c0002t0002g0250 a0001c0002t0002g0251 a0001c0002t0002g0252 |
3 | HG02055.hp1 HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.649-1197T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29142512 | |||||||
chr2:29142513 | A | G | 1 | a0001c0002t0013g0055 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.649-1196A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29142513 | |||||||
chr2:29142596 | A | G | 1 | a0004c0012t0001g0010 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.649-1113A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29142596 | |||||||
chr2:29142663 | C | T | 2 | a0001c0002t0001g0043 a0001c0002t0001g0098 |
2 | NA18947.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.649-1046C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29142663 | |||||||
chr2:29142664 | G | A | 2 | a0001c0002t0001g0049 a0001c0002t0001g0050 |
2 | HG01123.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.649-1045G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29142664 | |||||||
chr2:29142717 | A | G | 142 | a0001c0001t0001g0058 a0001c0001t0001g0173 a0001c0001t0001g0174 others(139): Show |
147 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(144): Show |
intron_variant | MODIFIER | c.649-992A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29142717 | |||||||
chr2:29142811 | A | G | 5 | a0001c0002t0001g0224 a0003c0006t0001g0007 a0003c0006t0001g0042 others(2): Show |
6 | HG00597.hp1 HG02135.hp1 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.649-898A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29142811 | |||||||
chr2:29143207 | C | T | 16 | a0001c0001t0001g0146 a0001c0001t0001g0187 a0001c0001t0003g0083 others(13): Show |
17 | HG01069.hp1 HG01071.hp1 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.649-502C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29143207 | |||||||
chr2:29143211 | T | C | 192 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(189): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.649-498T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29143211 | |||||||
chr2:29143230 | C | G | 2 | a0001c0001t0001g0206 a0001c0002t0001g0022 |
2 | HG02132.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.649-479C>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29143230 | |||||||
chr2:29143295 | ATC | A | 4 | a0001c0001t0001g0103 a0001c0001t0003g0148 a0001c0001t0016g0139 others(1): Show |
4 | HG02486.hp1 HG03130.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.649-410_649-409del others(2): Show |
CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 29143295 | ||||||
chr2:29143299 | CTG | C | 146 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(143): Show |
149 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.649-407_649-406del others(2): Show |
CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 29143299 | ||||||
chr2:29143360 | A | G | 4 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(1): Show |
4 | HG01175.hp1 HG01517.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.649-349A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29143360 | |||||||
chr2:29143363 | A | C | 2 | a0001c0001t0001g0134 a0001c0001t0001g0135 |
2 | NA19240.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.649-346A>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29143363 | |||||||
chr2:29143400 | G | GT | 7 | a0001c0008t0001g0176 a0001c0008t0001g0183 a0001c0008t0001g0184 others(4): Show |
7 | HG00140.hp2 HG00642.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.649-297dupT | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr2 | 29143400 | ||||||
chr2:29143412 | T | C | 1 | a0001c0016t0001g0075 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.649-297T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29143412 | |||||||
chr2:29143412 | T | TTTC | 53 | a0001c0001t0001g0074 a0001c0001t0001g0076 a0001c0001t0001g0105 others(50): Show |
55 | HG00738.hp2 HG00741.hp2 HG01069.hp1 others(52): Show |
intron_variant | MODIFIER | c.649-297_649-296ins others(3): Show |
CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29143412 | |||||||
chr2:29143412 | T | TTTTC | 190 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(187): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.649-297_649-296ins others(4): Show |
CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29143412 | |||||||
chr2:29143578 | C | T | 1 | a0001c0001t0001g0058 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.649-131C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29143578 | |||||||
chr2:29143604 | A | G | 14 | a0001c0001t0002g0197 a0001c0002t0002g0117 a0001c0002t0002g0118 others(11): Show |
14 | HG00738.hp2 HG01884.hp1 HG02809.hp1 others(11): Show |
intron_variant | MODIFIER | c.649-105A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29143604 | |||||||
chr2:29143624 | G | A | 4 | a0001c0002t0001g0236 a0001c0002t0001g0237 a0001c0002t0001g0238 others(1): Show |
4 | HG01243.hp1 HG01891.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.649-85G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29143624 | |||||||
chr2:29143639 | C | T | 2 | a0001c0013t0008g0051 a0001c0016t0001g0075 |
2 | HG01109.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.649-70C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 6/15 | chr2 | 29143639 | |||||||
chr2:29143964 | A | G | 104 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(101): Show |
107 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.885+19A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 7/15 | chr2 | 29143964 | |||||||
chr2:29144009 | C | CACAG | 135 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(132): Show |
138 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.885+65_885+68dupAC others(2): Show |
CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 29144009 | ||||||
chr2:29144088 | T | G | 3 | a0001c0001t0001g0059 a0001c0002t0007g0060 a0001c0002t0007g0061 |
3 | HG03209.hp2 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.885+143T>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 7/15 | chr2 | 29144088 | |||||||
chr2:29144135 | T | A | 2 | a0001c0002t0007g0060 a0001c0002t0007g0061 |
2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.885+190T>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 7/15 | chr2 | 29144135 | |||||||
chr2:29144255 | C | T | 14 | a0001c0001t0003g0104 a0001c0001t0003g0148 a0001c0001t0004g0198 others(11): Show |
15 | HG00741.hp2 HG01069.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.885+310C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 7/15 | chr2 | 29144255 | |||||||
chr2:29144303 | T | A | 4 | a0001c0002t0002g0250 a0001c0002t0002g0251 a0001c0002t0002g0252 others(1): Show |
4 | HG02055.hp1 HG02615.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.885+358T>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 7/15 | chr2 | 29144303 | |||||||
chr2:29144484 | GC | G | 3 | a0001c0001t0001g0103 a0001c0002t0003g0009 a0001c0002t0003g0121 |
3 | HG00738.hp2 HG03041.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.885+541delC | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 29144484 | ||||||
chr2:29144486 | C | G | 3 | a0001c0001t0001g0103 a0001c0002t0003g0009 a0001c0002t0003g0121 |
3 | HG00738.hp2 HG03041.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.885+541C>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 7/15 | chr2 | 29144486 | |||||||
chr2:29144609 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.886-623C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 7/15 | chr2 | 29144609 | |||||||
chr2:29144739 | T | C | 1 | a0001c0002t0001g0023 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.886-493T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 7/15 | chr2 | 29144739 | |||||||
chr2:29144798 | C | CT | 70 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0074 others(67): Show |
73 | HG00099.hp1 HG00280.hp2 HG00738.hp1 others(70): Show |
intron_variant | MODIFIER | c.886-411dupT | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 29144798 | ||||||
chr2:29144798 | C | CTT | 11 | a0001c0001t0001g0228 a0001c0002t0002g0252 a0001c0002t0013g0055 others(8): Show |
11 | HG00140.hp2 HG00642.hp1 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.886-412_886-411dup others(2): Show |
CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 29144798 | ||||||
chr2:29144798 | C | CTTT | 25 | a0001c0001t0001g0103 a0001c0002t0001g0124 a0001c0002t0001g0236 others(22): Show |
25 | HG01106.hp2 HG01109.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.886-413_886-411dup others(3): Show |
CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 29144798 | ||||||
chr2:29144798 | CT | C | 17 | a0001c0001t0001g0265 a0001c0001t0011g0234 a0001c0001t0011g0235 others(14): Show |
17 | HG00741.hp1 HG01069.hp2 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.886-411delT | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 29144798 | ||||||
chr2:29144826 | A | G | 1 | a0001c0003t0001g0219 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.886-406A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 7/15 | chr2 | 29144826 | |||||||
chr2:29144955 | A | C | 3 | a0001c0001t0001g0059 a0001c0002t0007g0060 a0001c0002t0007g0061 |
3 | HG03209.hp2 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.886-277A>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 7/15 | chr2 | 29144955 | |||||||
chr2:29144976 | CT | C | 12 | a0001c0001t0001g0227 a0001c0001t0001g0228 a0001c0001t0002g0054 others(9): Show |
12 | HG01346.hp2 HG01891.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.886-254delT | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr2 | 29144976 | ||||||
chr2:29144980 | T | C | 9 | a0001c0002t0001g0124 a0001c0002t0002g0084 a0001c0002t0002g0085 others(6): Show |
9 | HG01106.hp2 HG01884.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.886-252T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 7/15 | chr2 | 29144980 | |||||||
chr2:29145063 | A | C | 2 | a0001c0002t0001g0020 a0001c0003t0003g0223 |
2 | HG02559.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.886-169A>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 7/15 | chr2 | 29145063 | |||||||
chr2:29145434 | T | G | 13 | a0001c0002t0004g0119 a0001c0002t0004g0125 a0001c0003t0001g0212 others(10): Show |
13 | HG01109.hp2 HG02572.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.1021+67T>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29145434 | |||||||
chr2:29145596 | C | T | 1 | a0001c0002t0001g0267 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1021+229C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29145596 | |||||||
chr2:29145631 | A | T | 211 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(208): Show |
216 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1021+264A>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29145631 | |||||||
chr2:29145718 | G | T | 3 | a0001c0001t0001g0059 a0001c0002t0007g0060 a0001c0002t0007g0061 |
3 | HG03209.hp2 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1021+351G>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29145718 | |||||||
chr2:29145751 | G | A | 100 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(97): Show |
102 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.1021+384G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29145751 | |||||||
chr2:29145838 | T | C | 2 | a0001c0003t0001g0089 a0001c0003t0001g0090 |
2 | HG01256.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.1021+471T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29145838 | |||||||
chr2:29145879 | G | A | 199 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(196): Show |
204 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.1021+512G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29145879 | |||||||
chr2:29145941 | C | T | 7 | a0001c0001t0002g0197 a0001c0002t0001g0003 a0001c0002t0001g0049 others(4): Show |
8 | HG01123.hp1 HG01884.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1021+574C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29145941 | |||||||
chr2:29145945 | G | C | 56 | a0001c0001t0001g0178 a0001c0001t0003g0083 a0001c0001t0003g0104 others(53): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.1021+578G>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29145945 | |||||||
chr2:29146020 | A | T | 3 | a0001c0001t0001g0059 a0001c0002t0007g0060 a0001c0002t0007g0061 |
3 | HG03209.hp2 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1021+653A>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29146020 | |||||||
chr2:29146023 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1021+656G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29146023 | |||||||
chr2:29146152 | T | C | 1 | a0001c0001t0001g0171 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1021+785T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29146152 | |||||||
chr2:29146224 | C | T | 2 | a0001c0002t0001g0034 a0001c0002t0001g0047 |
2 | NA18978.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.1021+857C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29146224 | |||||||
chr2:29146240 | C | T | 1 | a0001c0001t0001g0193 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1021+873C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29146240 | |||||||
chr2:29146266 | A | T | 3 | a0001c0001t0001g0103 a0001c0002t0003g0009 a0001c0002t0003g0121 |
3 | HG00738.hp2 HG03041.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1021+899A>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29146266 | |||||||
chr2:29146387 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1021+1020G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29146387 | |||||||
chr2:29146492 | A | G | 1 | a0001c0013t0008g0051 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1021+1125A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29146492 | |||||||
chr2:29146547 | A | G | 42 | a0001c0001t0001g0175 a0001c0001t0001g0188 a0001c0001t0001g0230 others(39): Show |
44 | HG00558.hp1 HG00597.hp2 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.1021+1180A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29146547 | |||||||
chr2:29146691 | G | A | 1 | a0001c0026t0001g0052 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1021+1324G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29146691 | |||||||
chr2:29146756 | G | A | 53 | a0001c0001t0001g0142 a0001c0001t0001g0175 a0001c0001t0001g0188 others(50): Show |
55 | HG00558.hp1 HG00597.hp2 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.1021+1389G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29146756 | |||||||
chr2:29146798 | G | A | 15 | a0001c0001t0017g0229 a0001c0002t0004g0119 a0001c0002t0004g0125 others(12): Show |
15 | HG01109.hp2 HG02572.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.1021+1431G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29146798 | |||||||
chr2:29146994 | T | G | 53 | a0001c0001t0001g0142 a0001c0001t0001g0175 a0001c0001t0001g0188 others(50): Show |
55 | HG00558.hp1 HG00597.hp2 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.1021+1627T>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29146994 | |||||||
chr2:29147017 | G | C | 193 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(190): Show |
198 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.1021+1650G>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29147017 | |||||||
chr2:29147047 | G | C | 53 | a0001c0001t0001g0142 a0001c0001t0001g0175 a0001c0001t0001g0188 others(50): Show |
55 | HG00558.hp1 HG00597.hp2 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.1021+1680G>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29147047 | |||||||
chr2:29147120 | A | T | 1 | a0001c0001t0001g0014 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1021+1753A>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29147120 | |||||||
chr2:29147147 | T | C | 3 | a0001c0001t0001g0103 a0001c0002t0003g0009 a0001c0002t0003g0121 |
3 | HG00738.hp2 HG03041.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1021+1780T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29147147 | |||||||
chr2:29147225 | AG | A | 3 | a0001c0002t0001g0236 a0001c0002t0001g0237 a0001c0002t0001g0238 |
3 | HG01243.hp1 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1021+1859delG | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29147225 | |||||||
chr2:29147350 | C | G | 1 | a0001c0002t0001g0027 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1021+1983C>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29147350 | |||||||
chr2:29147501 | C | A | 7 | a0001c0001t0002g0197 a0001c0002t0001g0003 a0001c0002t0001g0049 others(4): Show |
8 | HG01123.hp1 HG01884.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1021+2134C>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29147501 | |||||||
chr2:29147734 | A | G | 1 | a0001c0026t0001g0052 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1021+2367A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29147734 | |||||||
chr2:29147768 | C | T | 11 | a0001c0001t0001g0074 a0001c0001t0001g0076 a0001c0001t0001g0140 others(8): Show |
11 | HG02486.hp2 HG03927.hp2 NA18977.hp2 others(8): Show |
intron_variant | MODIFIER | c.1021+2401C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29147768 | |||||||
chr2:29147777 | G | A | 3 | a0001c0001t0001g0227 a0001c0001t0001g0228 a0001c0002t0001g0072 |
3 | HG02895.hp2 HG02897.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1021+2410G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29147777 | |||||||
chr2:29147928 | C | A | 1 | a0001c0002t0001g0267 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1021+2561C>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29147928 | |||||||
chr2:29147973 | A | T | 3 | a0001c0002t0001g0236 a0001c0002t0001g0237 a0001c0002t0001g0238 |
3 | HG01243.hp1 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1021+2606A>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29147973 | |||||||
chr2:29148065 | G | A | 1 | a0001c0013t0008g0051 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1021+2698G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29148065 | |||||||
chr2:29148096 | G | A | 168 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(165): Show |
173 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.1021+2729G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29148096 | |||||||
chr2:29148106 | A | G | 1 | a0001c0016t0001g0075 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1021+2739A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29148106 | |||||||
chr2:29148141 | G | C | 1 | a0002c0004t0001g0270 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1021+2774G>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29148141 | |||||||
chr2:29148180 | C | T | 1 | a0001c0001t0001g0260 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1021+2813C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29148180 | |||||||
chr2:29148298 | C | A | 3 | a0001c0001t0011g0234 a0001c0001t0011g0235 a0001c0002t0001g0277 |
3 | HG02071.hp2 HG02080.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.1021+2931C>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29148298 | |||||||
chr2:29148341 | G | A | 2 | a0001c0001t0001g0074 a0001c0001t0001g0076 |
2 | HG02486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1021+2974G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29148341 | |||||||
chr2:29148363 | T | C | 56 | a0001c0001t0001g0178 a0001c0001t0003g0083 a0001c0001t0003g0104 others(53): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.1021+2996T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29148363 | |||||||
chr2:29148464 | T | C | 1 | a0001c0009t0001g0226 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1021+3097T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29148464 | |||||||
chr2:29148483 | T | TAATAATT others(1328): Show |
1 | a0001c0003t0001g0093 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1021+3132_1021+313 others(1339): Show |
CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 29148483 | ||||||
chr2:29148497 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1021+3130G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29148497 | |||||||
chr2:29148510 | C | T | 1 | a0001c0002t0001g0017 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1021+3143C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29148510 | |||||||
chr2:29148521 | C | A | 226 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(223): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.1021+3154C>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29148521 | |||||||
chr2:29148734 | G | T | 1 | a0001c0001t0001g0138 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1021+3367G>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29148734 | |||||||
chr2:29148753 | A | G | 4 | a0001c0002t0002g0250 a0001c0002t0002g0251 a0001c0002t0002g0252 others(1): Show |
4 | HG02055.hp1 HG02615.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1021+3386A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29148753 | |||||||
chr2:29148903 | A | G | 1 | a0011c0015t0001g0217 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1021+3536A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29148903 | |||||||
chr2:29148968 | A | G | 226 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(223): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.1021+3601A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29148968 | |||||||
chr2:29148981 | TTC | T | 7 | a0001c0002t0002g0250 a0001c0002t0002g0251 a0001c0002t0002g0252 others(4): Show |
7 | HG01891.hp2 HG02055.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1021+3619_1021+362 others(6): Show |
CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 29148981 | ||||||
chr2:29149053 | G | C | 2 | a0001c0001t0001g0261 a0001c0001t0001g0262 |
2 | NA18949.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.1022-3632G>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29149053 | |||||||
chr2:29149072 | C | T | 85 | a0001c0001t0001g0103 a0001c0001t0001g0178 a0001c0001t0001g0227 others(82): Show |
87 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.1022-3613C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29149072 | |||||||
chr2:29149093 | T | C | 23 | a0001c0001t0001g0074 a0001c0001t0001g0076 a0001c0001t0001g0140 others(20): Show |
23 | HG01106.hp2 HG01346.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.1022-3592T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29149093 | |||||||
chr2:29149163 | C | T | 85 | a0001c0001t0001g0103 a0001c0001t0001g0178 a0001c0001t0001g0227 others(82): Show |
87 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.1022-3522C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29149163 | |||||||
chr2:29149171 | C | T | 2 | a0001c0001t0017g0229 a0001c0002t0009g0115 |
2 | HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1022-3514C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29149171 | |||||||
chr2:29149307 | A | G | 7 | a0001c0002t0003g0110 a0001c0005t0001g0114 a0001c0005t0003g0005 others(4): Show |
8 | HG00741.hp2 HG01069.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1022-3378A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29149307 | |||||||
chr2:29149334 | T | C | 1 | a0001c0001t0001g0199 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1022-3351T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29149334 | |||||||
chr2:29149410 | C | CT | 103 | a0001c0001t0001g0074 a0001c0001t0001g0076 a0001c0001t0001g0103 others(100): Show |
105 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.1022-3261dupT | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 29149410 | ||||||
chr2:29149410 | CT | C | 8 | a0001c0001t0001g0058 a0001c0002t0002g0250 a0001c0002t0002g0251 others(5): Show |
8 | HG01891.hp2 HG02055.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1022-3261delT | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 29149410 | ||||||
chr2:29149433 | T | C | 4 | a0002c0004t0001g0269 a0002c0004t0001g0270 a0002c0004t0001g0275 others(1): Show |
4 | HG01099.hp1 HG01256.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.1022-3252T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29149433 | |||||||
chr2:29149475 | G | A | 1 | a0001c0016t0001g0075 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1022-3210G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29149475 | |||||||
chr2:29149503 | A | G | 226 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(223): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.1022-3182A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29149503 | |||||||
chr2:29149619 | A | T | 12 | a0001c0001t0002g0054 a0001c0001t0008g0053 a0001c0002t0001g0124 others(9): Show |
12 | HG01106.hp2 HG01346.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1022-3066A>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29149619 | |||||||
chr2:29149660 | C | T | 1 | a0001c0001t0001g0174 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1022-3025C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29149660 | |||||||
chr2:29149728 | TA | T | 191 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0058 others(188): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.1022-2942delA | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 29149728 | ||||||
chr2:29149728 | TAA | T | 18 | a0001c0001t0001g0015 a0001c0001t0001g0100 a0001c0001t0001g0141 others(15): Show |
18 | HG00741.hp1 HG01069.hp2 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.1022-2943_1022-294 others(6): Show |
CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 29149728 | ||||||
chr2:29149782 | C | T | 3 | a0001c0002t0001g0236 a0001c0002t0001g0237 a0001c0002t0001g0238 |
3 | HG01243.hp1 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1022-2903C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29149782 | |||||||
chr2:29150009 | G | T | 12 | a0001c0002t0004g0119 a0001c0002t0004g0125 a0001c0003t0001g0212 others(9): Show |
12 | HG01109.hp2 HG02572.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1022-2676G>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29150009 | |||||||
chr2:29150030 | G | A | 5 | a0001c0001t0001g0103 a0001c0002t0001g0072 a0001c0002t0003g0009 others(2): Show |
5 | HG00738.hp2 HG02717.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1022-2655G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29150030 | |||||||
chr2:29150063 | A | G | 2 | a0001c0001t0001g0134 a0001c0001t0001g0135 |
2 | NA19240.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1022-2622A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29150063 | |||||||
chr2:29150099 | G | C | 7 | a0001c0001t0002g0197 a0001c0002t0001g0003 a0001c0002t0001g0049 others(4): Show |
8 | HG01123.hp1 HG01884.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1022-2586G>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29150099 | |||||||
chr2:29150488 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1022-2197C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29150488 | |||||||
chr2:29150516 | C | G | 1 | a0001c0001t0017g0229 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1022-2169C>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29150516 | |||||||
chr2:29150519 | T | C | 3 | a0001c0002t0001g0003 a0001c0002t0001g0049 a0001c0002t0001g0050 |
4 | HG01123.hp1 HG02970.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1022-2166T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29150519 | |||||||
chr2:29150643 | C | CT | 11 | a0001c0001t0001g0077 a0001c0001t0001g0195 a0001c0001t0002g0197 others(8): Show |
11 | HG01884.hp1 HG02145.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1022-2017dupT | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 29150643 | ||||||
chr2:29150643 | CT | C | 63 | a0001c0001t0001g0006 a0001c0001t0001g0071 a0001c0001t0001g0100 others(60): Show |
64 | HG00140.hp1 HG00558.hp2 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.1022-2017delT | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 29150643 | ||||||
chr2:29150643 | CTT | C | 88 | a0001c0001t0001g0014 a0001c0001t0001g0136 a0001c0001t0001g0137 others(85): Show |
90 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.1022-2018_1022-201 others(6): Show |
CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 29150643 | ||||||
chr2:29150643 | CTTT | C | 23 | a0001c0001t0001g0193 a0001c0001t0001g0227 a0001c0001t0001g0228 others(20): Show |
24 | HG00741.hp2 HG01069.hp1 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.1022-2019_1022-201 others(7): Show |
CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 29150643 | ||||||
chr2:29150643 | CTTTTTTT others(1): Show |
C | 24 | a0001c0001t0001g0074 a0001c0001t0001g0076 a0001c0001t0001g0140 others(21): Show |
24 | HG00280.hp1 HG01106.hp2 HG01346.hp2 others(21): Show |
intron_variant | MODIFIER | c.1022-2024_1022-201 others(12): Show |
CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 29150643 | ||||||
chr2:29150766 | C | A | 13 | a0001c0001t0011g0234 a0001c0001t0011g0235 a0001c0002t0001g0264 others(10): Show |
13 | HG00741.hp1 HG01069.hp2 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.1022-1919C>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29150766 | |||||||
chr2:29150774 | C | T | 226 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(223): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.1022-1911C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29150774 | |||||||
chr2:29150892 | T | A | 85 | a0001c0001t0001g0103 a0001c0001t0001g0178 a0001c0001t0001g0227 others(82): Show |
87 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.1022-1793T>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29150892 | |||||||
chr2:29150898 | A | G | 111 | a0001c0001t0001g0059 a0001c0001t0001g0074 a0001c0001t0001g0076 others(108): Show |
113 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.1022-1787A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29150898 | |||||||
chr2:29150999 | G | A | 7 | a0001c0002t0003g0110 a0001c0005t0001g0114 a0001c0005t0003g0005 others(4): Show |
8 | HG00741.hp2 HG01069.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1022-1686G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29150999 | |||||||
chr2:29151054 | GAAT | G | 3 | a0001c0002t0002g0250 a0001c0002t0002g0251 a0001c0002t0002g0252 |
3 | HG02055.hp1 HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1022-1626_1022-162 others(7): Show |
CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 29151054 | ||||||
chr2:29151226 | G | A | 1 | a0001c0002t0001g0072 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1022-1459G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29151226 | |||||||
chr2:29151353 | G | A | 3 | a0001c0001t0001g0015 a0001c0001t0001g0141 a0001c0001t0001g0209 |
3 | HG01243.hp2 HG01978.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.1022-1332G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29151353 | |||||||
chr2:29151503 | C | A | 1 | a0001c0016t0001g0075 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1022-1182C>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29151503 | |||||||
chr2:29151530 | T | TA | 112 | a0001c0001t0001g0059 a0001c0001t0001g0074 a0001c0001t0001g0076 others(109): Show |
114 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.1022-1149dupA | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 29151530 | ||||||
chr2:29151644 | A | G | 22 | a0001c0001t0002g0054 a0001c0001t0008g0053 a0001c0001t0017g0229 others(19): Show |
22 | HG01106.hp2 HG01346.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.1022-1041A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29151644 | |||||||
chr2:29151839 | A | G | 25 | a0001c0001t0001g0178 a0001c0002t0001g0113 a0001c0003t0001g0087 others(22): Show |
26 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(23): Show |
intron_variant | MODIFIER | c.1022-846A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29151839 | |||||||
chr2:29151845 | A | G | 2 | a0001c0001t0001g0134 a0001c0001t0001g0135 |
2 | NA19240.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1022-840A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29151845 | |||||||
chr2:29151850 | C | T | 2 | a0001c0001t0011g0235 a0001c0003t0003g0223 |
2 | HG02080.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1022-835C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29151850 | |||||||
chr2:29151863 | G | T | 179 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(176): Show |
184 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.1022-822G>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29151863 | |||||||
chr2:29151939 | A | AC | 7 | a0001c0002t0002g0250 a0001c0002t0002g0251 a0001c0002t0002g0252 others(4): Show |
7 | HG01891.hp2 HG02055.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1022-740dupC | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 29151939 | ||||||
chr2:29151943 | C | G | 1 | a0001c0001t0001g0142 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1022-742C>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29151943 | |||||||
chr2:29151965 | C | T | 1 | a0001c0005t0001g0114 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1022-720C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29151965 | |||||||
chr2:29152213 | G | A | 14 | a0001c0001t0001g0265 a0001c0001t0011g0234 a0001c0001t0011g0235 others(11): Show |
14 | HG00741.hp1 HG01069.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.1022-472G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29152213 | |||||||
chr2:29152254 | A | G | 1 | a0001c0001t0001g0135 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1022-431A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29152254 | |||||||
chr2:29152264 | G | A | 83 | a0001c0001t0001g0059 a0001c0001t0001g0074 a0001c0001t0001g0076 others(80): Show |
85 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.1022-421G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29152264 | |||||||
chr2:29152275 | A | G | 11 | a0001c0002t0004g0119 a0001c0002t0004g0125 a0001c0003t0001g0212 others(8): Show |
11 | HG02572.hp1 HG02622.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.1022-410A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29152275 | |||||||
chr2:29152380 | G | A | 57 | a0001c0001t0001g0178 a0001c0001t0001g0265 a0001c0001t0003g0083 others(54): Show |
59 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.1022-305G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29152380 | |||||||
chr2:29152388 | TA | T | 57 | a0001c0001t0001g0178 a0001c0001t0001g0265 a0001c0001t0003g0083 others(54): Show |
59 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.1022-289delA | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 29152388 | ||||||
chr2:29152476 | C | A | 1 | a0001c0001t0001g0204 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1022-209C>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29152476 | |||||||
chr2:29152529 | A | G | 2 | a0001c0002t0010g0232 a0001c0002t0010g0233 |
2 | HG01074.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1022-156A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29152529 | |||||||
chr2:29152545 | A | AT | 23 | a0001c0001t0001g0074 a0001c0001t0001g0076 a0001c0001t0001g0140 others(20): Show |
23 | HG01106.hp2 HG01346.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.1022-132dupT | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr2 | 29152545 | ||||||
chr2:29152546 | T | C | 1 | a0001c0001t0003g0104 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1022-139T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29152546 | |||||||
chr2:29152562 | C | A | 1 | a0001c0001t0001g0151 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1022-123C>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29152562 | |||||||
chr2:29152584 | A | G | 1 | a0001c0001t0001g0105 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1022-101A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 8/15 | chr2 | 29152584 | |||||||
chr2:29152909 | C | CT | 43 | a0001c0001t0001g0178 a0001c0001t0003g0083 a0001c0001t0003g0104 others(40): Show |
45 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(42): Show |
intron_variant | MODIFIER | c.1165+89dupT | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr2 | 29152909 | ||||||
chr2:29152931 | GAAACCTG others(9): Show |
G | 1 | a0001c0001t0009g0149 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1165+111_1165+126d others(18): Show |
CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr2 | 29152931 | ||||||
chr2:29152962 | T | C | 14 | a0001c0001t0001g0265 a0001c0001t0011g0234 a0001c0001t0011g0235 others(11): Show |
14 | HG00741.hp1 HG01069.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.1165+134T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 9/15 | chr2 | 29152962 | |||||||
chr2:29153036 | T | C | 83 | a0001c0001t0001g0059 a0001c0001t0001g0074 a0001c0001t0001g0076 others(80): Show |
85 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.1165+208T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 9/15 | chr2 | 29153036 | |||||||
chr2:29153072 | A | G | 1 | a0001c0008t0001g0185 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1165+244A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 9/15 | chr2 | 29153072 | |||||||
chr2:29153080 | G | A | 71 | a0001c0001t0001g0059 a0001c0001t0001g0074 a0001c0001t0001g0076 others(68): Show |
73 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.1165+252G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 9/15 | chr2 | 29153080 | |||||||
chr2:29153244 | T | C | 57 | a0001c0001t0001g0178 a0001c0001t0001g0265 a0001c0001t0003g0083 others(54): Show |
59 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.1165+416T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 9/15 | chr2 | 29153244 | |||||||
chr2:29153313 | C | T | 3 | a0001c0001t0001g0059 a0001c0002t0007g0060 a0001c0002t0007g0061 |
3 | HG03209.hp2 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1165+485C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 9/15 | chr2 | 29153313 | |||||||
chr2:29153347 | T | C | 226 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(223): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.1165+519T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 9/15 | chr2 | 29153347 | |||||||
chr2:29153446 | A | C | 1 | a0001c0002t0001g0072 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1165+618A>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 9/15 | chr2 | 29153446 | |||||||
chr2:29153455 | C | G | 1 | a0001c0002t0001g0267 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1165+627C>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 9/15 | chr2 | 29153455 | |||||||
chr2:29153470 | A | G | 3 | a0001c0001t0001g0059 a0001c0002t0007g0060 a0001c0002t0007g0061 |
3 | HG03209.hp2 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1165+642A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 9/15 | chr2 | 29153470 | |||||||
chr2:29153498 | C | CT | 100 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(97): Show |
102 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.1165+677dupT | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr2 | 29153498 | ||||||
chr2:29153586 | G | A | 43 | a0001c0001t0001g0175 a0001c0001t0001g0188 a0001c0001t0001g0230 others(40): Show |
45 | HG00558.hp1 HG00597.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.1165+758G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 9/15 | chr2 | 29153586 | |||||||
chr2:29153656 | A | G | 2 | a0001c0001t0001g0227 a0001c0001t0001g0228 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1165+828A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 9/15 | chr2 | 29153656 | |||||||
chr2:29153719 | G | A | 6 | a0001c0002t0002g0250 a0001c0002t0002g0251 a0001c0002t0002g0252 others(3): Show |
6 | HG01891.hp2 HG02055.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1165+891G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 9/15 | chr2 | 29153719 | |||||||
chr2:29153872 | T | C | 1 | a0001c0001t0009g0149 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1165+1044T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 9/15 | chr2 | 29153872 | |||||||
chr2:29153932 | T | A | 1 | a0010c0024t0001g0065 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1165+1104T>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 9/15 | chr2 | 29153932 | |||||||
chr2:29154178 | C | T | 60 | a0001c0001t0001g0059 a0001c0001t0001g0178 a0001c0001t0001g0265 others(57): Show |
62 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.1165+1350C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 9/15 | chr2 | 29154178 | |||||||
chr2:29154299 | A | G | 80 | a0001c0001t0001g0074 a0001c0001t0001g0076 a0001c0001t0001g0140 others(77): Show |
82 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.1165+1471A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 9/15 | chr2 | 29154299 | |||||||
chr2:29154326 | T | C | 10 | a0001c0001t0017g0229 a0001c0002t0002g0266 a0001c0002t0005g0129 others(7): Show |
10 | HG01891.hp1 HG02965.hp1 HG03139.hp2 others(7): Show |
intron_variant | MODIFIER | c.1165+1498T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 9/15 | chr2 | 29154326 | |||||||
chr2:29154838 | G | A | 3 | a0001c0002t0001g0236 a0001c0002t0001g0237 a0001c0002t0001g0238 |
3 | HG01243.hp1 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1166-1516G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 9/15 | chr2 | 29154838 | |||||||
chr2:29154902 | G | A | 1 | a0001c0001t0001g0193 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1166-1452G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 9/15 | chr2 | 29154902 | |||||||
chr2:29154925 | A | G | 100 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(97): Show |
102 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.1166-1429A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 9/15 | chr2 | 29154925 | |||||||
chr2:29155057 | A | T | 112 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(109): Show |
114 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.1166-1297A>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 9/15 | chr2 | 29155057 | |||||||
chr2:29155151 | A | T | 1 | a0001c0002t0001g0277 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1166-1203A>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 9/15 | chr2 | 29155151 | |||||||
chr2:29155165 | G | A | 2 | a0001c0001t0001g0136 a0001c0001t0001g0152 |
2 | HG01257.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.1166-1189G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 9/15 | chr2 | 29155165 | |||||||
chr2:29155300 | A | G | 42 | a0001c0001t0001g0175 a0001c0001t0001g0188 a0001c0001t0001g0230 others(39): Show |
44 | HG00558.hp1 HG00597.hp2 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.1166-1054A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 9/15 | chr2 | 29155300 | |||||||
chr2:29155405 | T | TAC | 13 | a0001c0001t0002g0054 a0001c0001t0008g0053 a0001c0002t0001g0124 others(10): Show |
13 | HG01106.hp2 HG01346.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.1166-929_1166-928d others(4): Show |
CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr2 | 29155405 | ||||||
chr2:29155405 | TAC | T | 215 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(212): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.1166-929_1166-928d others(4): Show |
CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr2 | 29155405 | ||||||
chr2:29155405 | TACACACA others(1): Show |
T | 14 | a0001c0001t0001g0265 a0001c0001t0011g0234 a0001c0001t0011g0235 others(11): Show |
14 | HG00741.hp1 HG01069.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.1166-935_1166-928d others(10): Show |
CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr2 | 29155405 | ||||||
chr2:29155420 | A | G | 10 | a0001c0001t0017g0229 a0001c0002t0002g0266 a0001c0002t0005g0129 others(7): Show |
10 | HG01891.hp1 HG02965.hp1 HG03139.hp2 others(7): Show |
intron_variant | MODIFIER | c.1166-934A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 9/15 | chr2 | 29155420 | |||||||
chr2:29155427 | A | C | 1 | a0001c0002t0003g0073 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1166-927A>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 9/15 | chr2 | 29155427 | |||||||
chr2:29155732 | A | G | 5 | a0001c0001t0001g0140 a0001c0001t0001g0171 a0001c0001t0001g0172 others(2): Show |
5 | NA18977.hp2 NA19012.hp2 NA19062.hp1 others(2): Show |
intron_variant | MODIFIER | c.1166-622A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 9/15 | chr2 | 29155732 | |||||||
chr2:29155736 | T | A | 2 | a0001c0001t0001g0227 a0001c0001t0001g0228 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1166-618T>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 9/15 | chr2 | 29155736 | |||||||
chr2:29155766 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1166-588C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 9/15 | chr2 | 29155766 | |||||||
chr2:29155773 | C | T | 11 | a0001c0001t0008g0053 a0001c0002t0001g0124 a0001c0002t0002g0084 others(8): Show |
11 | HG01106.hp2 HG01884.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1166-581C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 9/15 | chr2 | 29155773 | |||||||
chr2:29155833 | T | C | 1 | a0001c0001t0001g0153 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1166-521T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 9/15 | chr2 | 29155833 | |||||||
chr2:29156036 | A | G | 106 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(103): Show |
108 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.1166-318A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 9/15 | chr2 | 29156036 | |||||||
chr2:29156244 | T | A | 1 | a0001c0002t0001g0024 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1166-110T>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 9/15 | chr2 | 29156244 | |||||||
chr2:29156304 | A | G | 2 | a0001c0001t0001g0261 a0001c0001t0001g0262 |
2 | NA18949.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.1166-50A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 9/15 | chr2 | 29156304 | |||||||
chr2:29156697 | C | T | 11 | a0001c0001t0001g0074 a0001c0001t0001g0076 a0001c0001t0001g0140 others(8): Show |
11 | HG02486.hp2 HG03927.hp2 NA18977.hp2 others(8): Show |
intron_variant | MODIFIER | c.1255+254C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 10/15 | chr2 | 29156697 | |||||||
chr2:29156875 | A | ATAAG | 263 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(260): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.1256-329_1256-328i others(6): Show |
CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 10/15 | chr2 | 29156875 | |||||||
chr2:29156933 | A | G | 4 | a0001c0002t0002g0250 a0001c0002t0002g0251 a0001c0002t0002g0252 others(1): Show |
4 | HG02055.hp1 HG02615.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1256-271A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 10/15 | chr2 | 29156933 | |||||||
chr2:29156970 | C | T | 234 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(231): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.1256-234C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 10/15 | chr2 | 29156970 | |||||||
chr2:29156990 | G | A | 1 | a0001c0001t0001g0262 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1256-214G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 10/15 | chr2 | 29156990 | |||||||
chr2:29157036 | A | G | 6 | a0001c0001t0001g0103 a0001c0001t0001g0227 a0001c0001t0001g0228 others(3): Show |
6 | HG00738.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1256-168A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 10/15 | chr2 | 29157036 | |||||||
chr2:29157143 | A | G | 4 | a0001c0002t0002g0250 a0001c0002t0002g0251 a0001c0002t0002g0252 others(1): Show |
4 | HG02055.hp1 HG02615.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1256-61A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 10/15 | chr2 | 29157143 | |||||||
chr2:29157185 | C | T | 3 | a0001c0010t0004g0256 a0001c0010t0004g0257 a0001c0018t0004g0078 |
3 | HG01891.hp2 HG02922.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1256-19C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 10/15 | chr2 | 29157185 | |||||||
chr2:29157186 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1256-18G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 10/15 | chr2 | 29157186 | |||||||
chr2:29157189 | C | T | 11 | a0001c0001t0017g0229 a0001c0002t0001g0267 a0001c0002t0002g0266 others(8): Show |
11 | HG01891.hp1 HG02647.hp2 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.1256-15C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 10/15 | chr2 | 29157189 | |||||||
chr2:29157522 | C | T | 4 | a0001c0002t0002g0250 a0001c0002t0002g0251 a0001c0002t0002g0252 others(1): Show |
4 | HG02055.hp1 HG02615.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1399+175C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 11/15 | chr2 | 29157522 | |||||||
chr2:29157527 | C | G | 119 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(116): Show |
122 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.1399+180C>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 11/15 | chr2 | 29157527 | |||||||
chr2:29157577 | T | C | 4 | a0001c0002t0002g0250 a0001c0002t0002g0251 a0001c0002t0002g0252 others(1): Show |
4 | HG02055.hp1 HG02615.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1399+230T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 11/15 | chr2 | 29157577 | |||||||
chr2:29157819 | G | A | 3 | a0001c0010t0004g0256 a0001c0010t0004g0257 a0001c0018t0004g0078 |
3 | HG01891.hp2 HG02922.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1399+472G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 11/15 | chr2 | 29157819 | |||||||
chr2:29157845 | C | T | 234 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(231): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.1399+498C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 11/15 | chr2 | 29157845 | |||||||
chr2:29157945 | G | A | 5 | a0001c0001t0001g0227 a0001c0001t0001g0228 a0001c0002t0001g0072 others(2): Show |
5 | HG00738.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1399+598G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 11/15 | chr2 | 29157945 | |||||||
chr2:29157974 | A | G | 2 | a0001c0002t0002g0117 a0001c0002t0002g0118 |
2 | HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1399+627A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 11/15 | chr2 | 29157974 | |||||||
chr2:29157977 | G | A | 244 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(241): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.1399+630G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 11/15 | chr2 | 29157977 | |||||||
chr2:29158027 | T | C | 1 | a0004c0012t0001g0008 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1399+680T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 11/15 | chr2 | 29158027 | |||||||
chr2:29158056 | A | C | 1 | a0001c0002t0001g0044 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1399+709A>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 11/15 | chr2 | 29158056 | |||||||
chr2:29158235 | G | A | 3 | a0001c0002t0002g0250 a0001c0002t0002g0251 a0001c0002t0002g0252 |
3 | HG02055.hp1 HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1399+888G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 11/15 | chr2 | 29158235 | |||||||
chr2:29158370 | CT | C | 203 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(200): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.1399+1035delT | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr2 | 29158370 | ||||||
chr2:29158422 | A | G | 2 | a0001c0001t0001g0227 a0001c0001t0001g0228 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1399+1075A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 11/15 | chr2 | 29158422 | |||||||
chr2:29158425 | A | G | 120 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(117): Show |
123 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.1399+1078A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 11/15 | chr2 | 29158425 | |||||||
chr2:29158517 | G | T | 4 | a0001c0002t0001g0003 a0001c0002t0001g0049 a0001c0002t0001g0050 others(1): Show |
5 | HG01123.hp1 HG02145.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1399+1170G>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 11/15 | chr2 | 29158517 | |||||||
chr2:29158517 | GGA | G | 3 | a0001c0010t0004g0256 a0001c0010t0004g0257 a0001c0018t0004g0078 |
3 | HG01891.hp2 HG02922.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1399+1173_1399+117 others(6): Show |
CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr2 | 29158517 | ||||||
chr2:29158524 | GGCCGA | G | 3 | a0001c0010t0004g0256 a0001c0010t0004g0257 a0001c0018t0004g0078 |
3 | HG01891.hp2 HG02922.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1399+1179_1399+118 others(9): Show |
CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr2 | 29158524 | ||||||
chr2:29158574 | T | C | 4 | a0001c0002t0002g0250 a0001c0002t0002g0251 a0001c0002t0002g0252 others(1): Show |
4 | HG02055.hp1 HG02615.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1399+1227T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 11/15 | chr2 | 29158574 | |||||||
chr2:29158694 | G | C | 58 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0071 others(55): Show |
60 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.1399+1347G>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 11/15 | chr2 | 29158694 | |||||||
chr2:29158720 | G | A | 4 | a0001c0002t0002g0250 a0001c0002t0002g0251 a0001c0002t0002g0252 others(1): Show |
4 | HG02055.hp1 HG02615.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1399+1373G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 11/15 | chr2 | 29158720 | |||||||
chr2:29158983 | G | A | 125 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(122): Show |
129 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.1400-1350G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 11/15 | chr2 | 29158983 | |||||||
chr2:29159053 | C | A | 124 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(121): Show |
128 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.1400-1280C>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 11/15 | chr2 | 29159053 | |||||||
chr2:29159172 | C | T | 107 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(104): Show |
110 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.1400-1161C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 11/15 | chr2 | 29159172 | |||||||
chr2:29159390 | T | C | 14 | a0001c0001t0001g0167 a0001c0001t0001g0265 a0001c0001t0011g0234 others(11): Show |
14 | HG00741.hp1 HG01069.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.1400-943T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 11/15 | chr2 | 29159390 | |||||||
chr2:29159454 | G | A | 5 | a0001c0002t0001g0108 a0001c0002t0001g0283 a0001c0002t0001g0284 others(2): Show |
5 | HG01175.hp2 HG01192.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1400-879G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 11/15 | chr2 | 29159454 | |||||||
chr2:29159574 | C | T | 1 | a0001c0002t0001g0043 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1400-759C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 11/15 | chr2 | 29159574 | |||||||
chr2:29159683 | T | TA | 129 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(126): Show |
133 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.1400-626dupA | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr2 | 29159683 | ||||||
chr2:29159683 | T | TAA | 38 | a0001c0001t0001g0074 a0001c0001t0001g0076 a0001c0001t0001g0146 others(35): Show |
38 | HG01071.hp2 HG01167.hp1 HG01169.hp1 others(35): Show |
intron_variant | MODIFIER | c.1400-627_1400-626d others(4): Show |
CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr2 | 29159683 | ||||||
chr2:29159683 | TA | T | 6 | a0001c0002t0001g0064 a0001c0002t0015g0011 a0001c0005t0003g0111 others(3): Show |
6 | HG01168.hp1 HG01891.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1400-626delA | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr2 | 29159683 | ||||||
chr2:29159683 | TAAAAAAA others(1): Show |
T | 27 | a0001c0001t0001g0178 a0001c0001t0003g0083 a0001c0002t0001g0001 others(24): Show |
29 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(26): Show |
intron_variant | MODIFIER | c.1400-633_1400-626d others(10): Show |
CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr2 | 29159683 | ||||||
chr2:29159858 | T | G | 1 | a0001c0001t0017g0229 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1400-475T>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 11/15 | chr2 | 29159858 | |||||||
chr2:29159921 | G | A | 1 | a0001c0001t0001g0239 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1400-412G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 11/15 | chr2 | 29159921 | |||||||
chr2:29159924 | G | A | 14 | a0001c0002t0001g0124 a0001c0002t0004g0119 a0001c0002t0004g0125 others(11): Show |
14 | HG01109.hp2 HG02572.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.1400-409G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 11/15 | chr2 | 29159924 | |||||||
chr2:29159981 | C | G | 10 | a0001c0002t0004g0119 a0001c0002t0004g0125 a0001c0003t0001g0212 others(7): Show |
10 | HG02572.hp1 HG02622.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1400-352C>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 11/15 | chr2 | 29159981 | |||||||
chr2:29160112 | ACT | A | 9 | a0001c0001t0001g0140 a0001c0001t0001g0171 a0001c0001t0001g0172 others(6): Show |
9 | HG03927.hp2 NA18977.hp2 NA18984.hp2 others(6): Show |
intron_variant | MODIFIER | c.1400-218_1400-217d others(4): Show |
CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr2 | 29160112 | ||||||
chr2:29160309 | T | C | 1 | a0001c0001t0001g0244 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1400-24T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 11/15 | chr2 | 29160309 | |||||||
chr2:29160475 | A | G | 1 | a0001c0001t0001g0059 | 1 | HG03209.hp2 | splice_region_variant&intron_variant | LOW | c.1534+8A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 12/15 | chr2 | 29160475 | |||||||
chr2:29160508 | G | A | 234 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(231): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.1534+41G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 12/15 | chr2 | 29160508 | |||||||
chr2:29160951 | A | G | 1 | a0001c0002t0001g0066 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1534+484A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 12/15 | chr2 | 29160951 | |||||||
chr2:29160999 | A | C | 6 | a0001c0008t0001g0176 a0001c0008t0001g0183 a0001c0008t0001g0184 others(3): Show |
6 | HG00140.hp2 HG00642.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.1534+532A>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 12/15 | chr2 | 29160999 | |||||||
chr2:29161046 | C | G | 15 | a0001c0001t0001g0059 a0001c0002t0001g0124 a0001c0002t0004g0119 others(12): Show |
15 | HG01109.hp2 HG02572.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.1534+579C>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 12/15 | chr2 | 29161046 | |||||||
chr2:29161078 | G | A | 4 | a0001c0002t0002g0250 a0001c0002t0002g0251 a0001c0002t0002g0252 others(1): Show |
4 | HG02055.hp1 HG02615.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1534+611G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 12/15 | chr2 | 29161078 | |||||||
chr2:29161123 | C | T | 10 | a0001c0002t0004g0119 a0001c0002t0004g0125 a0001c0003t0001g0212 others(7): Show |
10 | HG02572.hp1 HG02622.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1534+656C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 12/15 | chr2 | 29161123 | |||||||
chr2:29161137 | G | A | 1 | a0001c0002t0003g0110 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1534+670G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 12/15 | chr2 | 29161137 | |||||||
chr2:29161174 | A | G | 1 | a0001c0001t0001g0076 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1534+707A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 12/15 | chr2 | 29161174 | |||||||
chr2:29161220 | C | T | 3 | a0001c0010t0004g0256 a0001c0010t0004g0257 a0001c0018t0004g0078 |
3 | HG01891.hp2 HG02922.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1534+753C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 12/15 | chr2 | 29161220 | |||||||
chr2:29161280 | CTTTCT | C | 44 | a0001c0001t0001g0142 a0001c0001t0001g0175 a0001c0001t0001g0188 others(41): Show |
44 | HG00597.hp2 HG00673.hp2 HG01109.hp1 others(41): Show |
intron_variant | MODIFIER | c.1534+817_1534+821d others(7): Show |
CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr2 | 29161280 | ||||||
chr2:29161318 | A | G | 2 | a0001c0001t0001g0173 a0001c0002t0001g0048 |
2 | HG00280.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.1534+851A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 12/15 | chr2 | 29161318 | |||||||
chr2:29161322 | C | T | 16 | a0001c0001t0001g0265 a0001c0001t0011g0234 a0001c0001t0011g0235 others(13): Show |
16 | HG00741.hp1 HG01069.hp2 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.1534+855C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 12/15 | chr2 | 29161322 | |||||||
chr2:29161445 | AT | A | 5 | a0001c0001t0001g0140 a0001c0001t0001g0171 a0001c0001t0001g0172 others(2): Show |
5 | NA18977.hp2 NA19012.hp2 NA19062.hp1 others(2): Show |
intron_variant | MODIFIER | c.1534+981delT | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr2 | 29161445 | ||||||
chr2:29161450 | G | T | 5 | a0001c0001t0001g0140 a0001c0001t0001g0171 a0001c0001t0001g0172 others(2): Show |
5 | NA18977.hp2 NA19012.hp2 NA19062.hp1 others(2): Show |
intron_variant | MODIFIER | c.1534+983G>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 12/15 | chr2 | 29161450 | |||||||
chr2:29161491 | A | G | 1 | a0001c0001t0001g0135 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1534+1024A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 12/15 | chr2 | 29161491 | |||||||
chr2:29161506 | C | T | 11 | a0001c0001t0001g0074 a0001c0001t0001g0076 a0001c0001t0001g0140 others(8): Show |
11 | HG02486.hp2 HG03927.hp2 NA18977.hp2 others(8): Show |
intron_variant | MODIFIER | c.1534+1039C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 12/15 | chr2 | 29161506 | |||||||
chr2:29161712 | G | C | 1 | a0001c0001t0001g0262 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1534+1245G>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 12/15 | chr2 | 29161712 | |||||||
chr2:29161972 | T | C | 1 | a0001c0001t0001g0135 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1534+1505T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 12/15 | chr2 | 29161972 | |||||||
chr2:29161982 | G | C | 6 | a0001c0003t0001g0212 a0001c0003t0001g0245 a0001c0003t0001g0246 others(3): Show |
6 | HG02572.hp1 HG02647.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1534+1515G>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 12/15 | chr2 | 29161982 | |||||||
chr2:29162115 | T | C | 24 | a0001c0001t0001g0074 a0001c0001t0001g0076 a0001c0001t0001g0140 others(21): Show |
24 | HG01106.hp2 HG01346.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.1534+1648T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 12/15 | chr2 | 29162115 | |||||||
chr2:29162142 | A | G | 2 | a0001c0002t0007g0060 a0001c0002t0007g0061 |
2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1534+1675A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 12/15 | chr2 | 29162142 | |||||||
chr2:29162429 | C | T | 13 | a0001c0001t0002g0054 a0001c0001t0002g0197 a0001c0002t0002g0084 others(10): Show |
13 | HG01106.hp2 HG01346.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1535-1402C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 12/15 | chr2 | 29162429 | |||||||
chr2:29162476 | C | G | 1 | a0001c0001t0001g0177 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1535-1355C>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 12/15 | chr2 | 29162476 | |||||||
chr2:29162693 | A | G | 1 | a0001c0002t0001g0097 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1535-1138A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 12/15 | chr2 | 29162693 | |||||||
chr2:29162707 | A | G | 4 | a0001c0001t0001g0227 a0001c0001t0001g0228 a0001c0002t0010g0232 others(1): Show |
4 | HG01074.hp1 HG02630.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1535-1124A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 12/15 | chr2 | 29162707 | |||||||
chr2:29163215 | C | G | 14 | a0001c0002t0001g0124 a0001c0002t0004g0119 a0001c0002t0004g0125 others(11): Show |
14 | HG01109.hp2 HG02572.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.1535-616C>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 12/15 | chr2 | 29163215 | |||||||
chr2:29163249 | C | T | 44 | a0001c0001t0001g0142 a0001c0001t0001g0188 a0001c0001t0001g0195 others(41): Show |
45 | HG00597.hp2 HG01109.hp1 HG01123.hp2 others(42): Show |
intron_variant | MODIFIER | c.1535-582C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 12/15 | chr2 | 29163249 | |||||||
chr2:29163485 | C | G | 4 | a0001c0002t0002g0250 a0001c0002t0002g0251 a0001c0002t0002g0252 others(1): Show |
4 | HG02055.hp1 HG02615.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1535-346C>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 12/15 | chr2 | 29163485 | |||||||
chr2:29163625 | T | C | 2 | a0001c0001t0001g0227 a0001c0001t0001g0228 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1535-206T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 12/15 | chr2 | 29163625 | |||||||
chr2:29163780 | G | C | 195 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(192): Show |
200 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(197): Show |
intron_variant | MODIFIER | c.1535-51G>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 12/15 | chr2 | 29163780 | |||||||
chr2:29164013 | T | C | 1 | a0001c0021t0001g0018 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1658+59T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 13/15 | chr2 | 29164013 | |||||||
chr2:29164162 | T | A | 3 | a0001c0002t0001g0003 a0001c0002t0001g0049 a0001c0002t0001g0050 |
4 | HG01123.hp1 HG02970.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1658+208T>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 13/15 | chr2 | 29164162 | |||||||
chr2:29164188 | T | C | 3 | a0001c0002t0001g0236 a0001c0002t0001g0237 a0001c0002t0001g0238 |
3 | HG01243.hp1 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1658+234T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 13/15 | chr2 | 29164188 | |||||||
chr2:29164210 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1658+256G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 13/15 | chr2 | 29164210 | |||||||
chr2:29164223 | T | A | 4 | a0001c0002t0002g0250 a0001c0002t0002g0251 a0001c0002t0002g0252 others(1): Show |
4 | HG02055.hp1 HG02615.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1658+269T>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 13/15 | chr2 | 29164223 | |||||||
chr2:29164410 | G | T | 5 | a0001c0001t0001g0142 a0001c0001t0001g0195 a0001c0002t0001g0285 others(2): Show |
5 | HG02559.hp2 HG02886.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1658+456G>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 13/15 | chr2 | 29164410 | |||||||
chr2:29164706 | G | A | 45 | a0001c0001t0001g0142 a0001c0001t0001g0175 a0001c0001t0001g0188 others(42): Show |
46 | HG00597.hp2 HG00673.hp2 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.1658+752G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 13/15 | chr2 | 29164706 | |||||||
chr2:29164733 | A | G | 1 | a0001c0001t0001g0244 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1658+779A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 13/15 | chr2 | 29164733 | |||||||
chr2:29164748 | C | G | 1 | a0001c0001t0001g0169 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1658+794C>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 13/15 | chr2 | 29164748 | |||||||
chr2:29164852 | C | T | 1 | a0001c0001t0008g0053 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1658+898C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 13/15 | chr2 | 29164852 | |||||||
chr2:29164892 | T | C | 1 | a0001c0002t0001g0224 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1658+938T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 13/15 | chr2 | 29164892 | |||||||
chr2:29165124 | G | A | 265 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(262): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.1658+1170G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 13/15 | chr2 | 29165124 | |||||||
chr2:29165158 | A | C | 44 | a0001c0001t0001g0074 a0001c0001t0001g0076 a0001c0001t0001g0140 others(41): Show |
45 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(42): Show |
intron_variant | MODIFIER | c.1658+1204A>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 13/15 | chr2 | 29165158 | |||||||
chr2:29165262 | C | CT | 215 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(212): Show |
219 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.1658+1318dupT | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr2 | 29165262 | ||||||
chr2:29165328 | A | T | 1 | a0001c0003t0001g0088 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1658+1374A>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 13/15 | chr2 | 29165328 | |||||||
chr2:29165429 | G | A | 16 | a0001c0001t0001g0227 a0001c0001t0001g0228 a0001c0001t0001g0265 others(13): Show |
16 | HG00741.hp1 HG01069.hp2 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.1658+1475G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 13/15 | chr2 | 29165429 | |||||||
chr2:29165536 | T | C | 2 | a0001c0002t0001g0124 a0001c0016t0001g0075 |
2 | HG02615.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1658+1582T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 13/15 | chr2 | 29165536 | |||||||
chr2:29165764 | C | T | 1 | a0001c0001t0001g0177 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1659-1712C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 13/15 | chr2 | 29165764 | |||||||
chr2:29165813 | A | G | 1 | a0001c0002t0003g0121 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1659-1663A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 13/15 | chr2 | 29165813 | |||||||
chr2:29165833 | T | C | 2 | a0001c0002t0007g0060 a0001c0002t0007g0061 |
2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1659-1643T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 13/15 | chr2 | 29165833 | |||||||
chr2:29165898 | G | A | 16 | a0001c0001t0001g0227 a0001c0001t0001g0228 a0001c0001t0001g0265 others(13): Show |
16 | HG00741.hp1 HG01069.hp2 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.1659-1578G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 13/15 | chr2 | 29165898 | |||||||
chr2:29165941 | A | G | 109 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(106): Show |
112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.1659-1535A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 13/15 | chr2 | 29165941 | |||||||
chr2:29165975 | C | CA | 112 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(109): Show |
115 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.1659-1488dupA | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr2 | 29165975 | ||||||
chr2:29165975 | CA | C | 60 | a0001c0001t0001g0059 a0001c0001t0001g0074 a0001c0001t0001g0076 others(57): Show |
62 | HG00741.hp2 HG01069.hp1 HG01071.hp1 others(59): Show |
intron_variant | MODIFIER | c.1659-1488delA | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr2 | 29165975 | ||||||
chr2:29165976 | A | T | 32 | a0001c0001t0001g0178 a0001c0001t0008g0053 a0001c0002t0001g0113 others(29): Show |
33 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(30): Show |
intron_variant | MODIFIER | c.1659-1500A>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 13/15 | chr2 | 29165976 | |||||||
chr2:29165977 | A | T | 32 | a0001c0001t0001g0178 a0001c0001t0008g0053 a0001c0002t0001g0113 others(29): Show |
33 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(30): Show |
intron_variant | MODIFIER | c.1659-1499A>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 13/15 | chr2 | 29165977 | |||||||
chr2:29165978 | A | C | 32 | a0001c0001t0001g0178 a0001c0001t0008g0053 a0001c0002t0001g0113 others(29): Show |
33 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(30): Show |
intron_variant | MODIFIER | c.1659-1498A>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 13/15 | chr2 | 29165978 | |||||||
chr2:29166015 | T | G | 4 | a0001c0001t0003g0083 a0001c0001t0003g0104 a0001c0001t0003g0148 others(1): Show |
4 | HG02257.hp1 HG02630.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1659-1461T>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 13/15 | chr2 | 29166015 | |||||||
chr2:29166062 | A | G | 3 | a0001c0010t0004g0256 a0001c0010t0004g0257 a0001c0018t0004g0078 |
3 | HG01891.hp2 HG02922.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1659-1414A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 13/15 | chr2 | 29166062 | |||||||
chr2:29166092 | A | G | 2 | a0001c0001t0001g0142 a0001c0001t0001g0195 |
2 | HG03471.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1659-1384A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 13/15 | chr2 | 29166092 | |||||||
chr2:29166162 | T | A | 1 | a0001c0001t0001g0208 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1659-1314T>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 13/15 | chr2 | 29166162 | |||||||
chr2:29166308 | C | T | 1 | a0001c0002t0002g0282 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1659-1168C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 13/15 | chr2 | 29166308 | |||||||
chr2:29166407 | G | A | 2 | a0001c0002t0007g0060 a0001c0002t0007g0061 |
2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1659-1069G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 13/15 | chr2 | 29166407 | |||||||
chr2:29166476 | C | T | 3 | a0001c0001t0001g0074 a0001c0001t0001g0076 a0001c0002t0001g0267 |
3 | HG02486.hp2 HG02647.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1659-1000C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 13/15 | chr2 | 29166476 | |||||||
chr2:29166500 | CACTG | C | 3 | a0001c0001t0001g0074 a0001c0001t0001g0076 a0001c0002t0001g0267 |
3 | HG02486.hp2 HG02647.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1659-972_1659-969d others(6): Show |
CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr2 | 29166500 | ||||||
chr2:29166530 | G | GAC | 39 | a0001c0001t0001g0074 a0001c0001t0001g0076 a0001c0001t0001g0136 others(36): Show |
40 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(37): Show |
intron_variant | MODIFIER | c.1659-915_1659-914d others(4): Show |
CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr2 | 29166530 | ||||||
chr2:29166530 | G | GACAC | 17 | a0001c0001t0001g0100 a0001c0001t0009g0149 a0001c0001t0017g0229 others(14): Show |
17 | HG00738.hp1 HG01891.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.1659-917_1659-914d others(6): Show |
CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr2 | 29166530 | ||||||
chr2:29166530 | GAC | G | 29 | a0001c0001t0001g0102 a0001c0001t0001g0140 a0001c0001t0001g0171 others(26): Show |
30 | HG00280.hp1 HG00558.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.1659-915_1659-914d others(4): Show |
CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr2 | 29166530 | ||||||
chr2:29166530 | GACAC | G | 16 | a0001c0001t0001g0059 a0001c0001t0001g0175 a0001c0001t0001g0227 others(13): Show |
16 | HG00673.hp2 HG01106.hp2 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.1659-917_1659-914d others(6): Show |
CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr2 | 29166530 | ||||||
chr2:29166530 | GACACAC | G | 32 | a0001c0001t0001g0103 a0001c0001t0001g0265 a0001c0001t0011g0234 others(29): Show |
32 | HG00738.hp2 HG00741.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.1659-919_1659-914d others(8): Show |
CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr2 | 29166530 | ||||||
chr2:29166530 | GACACACA others(3): Show |
G | 3 | a0001c0001t0002g0197 a0001c0002t0002g0117 a0001c0002t0002g0118 |
3 | HG01884.hp1 HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1659-923_1659-914d others(12): Show |
CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr2 | 29166530 | ||||||
chr2:29166567 | C | G | 1 | a0001c0002t0015g0011 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1659-909C>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 13/15 | chr2 | 29166567 | |||||||
chr2:29166648 | C | T | 1 | a0001c0026t0001g0052 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1659-828C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 13/15 | chr2 | 29166648 | |||||||
chr2:29166717 | A | G | 2 | a0001c0001t0001g0100 a0001c0001t0001g0144 |
2 | NA18960.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.1659-759A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 13/15 | chr2 | 29166717 | |||||||
chr2:29166843 | T | C | 25 | a0001c0001t0002g0054 a0001c0001t0002g0197 a0001c0002t0001g0124 others(22): Show |
25 | HG01106.hp2 HG01346.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.1659-633T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 13/15 | chr2 | 29166843 | |||||||
chr2:29166888 | C | G | 1 | a0001c0001t0001g0059 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1659-588C>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 13/15 | chr2 | 29166888 | |||||||
chr2:29167379 | T | C | 1 | a0001c0002t0001g0243 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1659-97T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 13/15 | chr2 | 29167379 | |||||||
chr2:29167433 | AG | A | 16 | a0001c0001t0001g0227 a0001c0001t0001g0228 a0001c0001t0001g0265 others(13): Show |
16 | HG00741.hp1 HG01069.hp2 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.1659-42delG | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 13/15 | chr2 | 29167433 | |||||||
chr2:29167435 | A | G | 25 | a0001c0001t0001g0178 a0001c0002t0001g0113 a0001c0003t0001g0087 others(22): Show |
26 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(23): Show |
intron_variant | MODIFIER | c.1659-41A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 13/15 | chr2 | 29167435 | |||||||
chr2:29167461 | T | C | 4 | a0001c0002t0002g0250 a0001c0002t0002g0251 a0001c0002t0002g0252 others(1): Show |
4 | HG02055.hp1 HG02615.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1659-15T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 13/15 | chr2 | 29167461 | |||||||
chr2:29167700 | A | G | 29 | a0001c0001t0001g0103 a0001c0001t0002g0054 a0001c0001t0002g0197 others(26): Show |
30 | HG00738.hp2 HG01074.hp1 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.1723+160A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29167700 | |||||||
chr2:29167720 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1723+180G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29167720 | |||||||
chr2:29167855 | T | G | 2 | a0001c0001t0001g0158 a0001c0001t0001g0170 |
2 | HG02040.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.1723+315T>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29167855 | |||||||
chr2:29168031 | A | T | 14 | a0001c0001t0003g0083 a0001c0001t0003g0104 a0001c0001t0003g0148 others(11): Show |
15 | HG00741.hp2 HG01069.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.1723+491A>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29168031 | |||||||
chr2:29168338 | T | G | 18 | a0001c0001t0001g0059 a0001c0001t0001g0074 a0001c0001t0001g0076 others(15): Show |
18 | HG01891.hp1 HG02055.hp1 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.1723+798T>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29168338 | |||||||
chr2:29168362 | G | A | 1 | a0001c0013t0008g0051 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1723+822G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29168362 | |||||||
chr2:29168376 | T | A | 2 | a0001c0002t0001g0056 a0001c0002t0001g0057 |
2 | HG02451.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1723+836T>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29168376 | |||||||
chr2:29168400 | C | T | 25 | a0001c0001t0001g0178 a0001c0002t0001g0113 a0001c0003t0001g0087 others(22): Show |
26 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(23): Show |
intron_variant | MODIFIER | c.1723+860C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29168400 | |||||||
chr2:29168425 | T | C | 2 | a0001c0001t0001g0146 a0001c0001t0001g0187 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1723+885T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29168425 | |||||||
chr2:29168512 | C | CT | 45 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0077 others(42): Show |
45 | HG00597.hp2 HG00642.hp2 HG00673.hp1 others(42): Show |
intron_variant | MODIFIER | c.1723+1001dupT | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr2 | 29168512 | ||||||
chr2:29168512 | CT | C | 16 | a0001c0001t0002g0054 a0001c0002t0001g0003 a0001c0002t0001g0049 others(13): Show |
17 | HG00140.hp1 HG01346.hp2 HG01934.hp2 others(14): Show |
intron_variant | MODIFIER | c.1723+1001delT | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr2 | 29168512 | ||||||
chr2:29168512 | CTT | C | 58 | a0001c0001t0001g0074 a0001c0001t0001g0076 a0001c0001t0001g0103 others(55): Show |
59 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.1723+1000_1723+100 others(6): Show |
CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr2 | 29168512 | ||||||
chr2:29168512 | CTTT | C | 39 | a0001c0001t0001g0059 a0001c0001t0001g0265 a0001c0001t0003g0083 others(36): Show |
40 | HG00738.hp2 HG00741.hp2 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.1723+999_1723+1001 others(6): Show |
CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr2 | 29168512 | ||||||
chr2:29168512 | CTTTTTTT others(7): Show |
C | 3 | a0001c0010t0004g0256 a0001c0010t0004g0257 a0001c0018t0004g0078 |
3 | HG01891.hp2 HG02922.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1723+988_1723+1001 others(17): Show |
CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr2 | 29168512 | ||||||
chr2:29168512 | CTTTTTTT others(9): Show |
C | 1 | a0002c0004t0001g0270 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1723+986_1723+1001 others(19): Show |
CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr2 | 29168512 | ||||||
chr2:29168585 | C | T | 1 | a0001c0001t0001g0172 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1723+1045C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29168585 | |||||||
chr2:29168600 | G | A | 1 | a0001c0002t0001g0027 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1723+1060G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29168600 | |||||||
chr2:29168603 | A | G | 3 | a0001c0002t0001g0003 a0001c0002t0001g0049 a0001c0002t0001g0050 |
4 | HG01123.hp1 HG02970.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1723+1063A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29168603 | |||||||
chr2:29168679 | C | T | 5 | a0001c0002t0001g0072 a0001c0002t0001g0283 a0001c0002t0001g0284 others(2): Show |
5 | HG00738.hp2 HG01175.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.1723+1139C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29168679 | |||||||
chr2:29168764 | C | T | 14 | a0001c0001t0003g0083 a0001c0001t0003g0104 a0001c0001t0003g0148 others(11): Show |
15 | HG00741.hp2 HG01069.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.1723+1224C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29168764 | |||||||
chr2:29169012 | G | C | 9 | a0001c0001t0001g0140 a0001c0001t0001g0171 a0001c0001t0001g0172 others(6): Show |
9 | HG03927.hp2 NA18977.hp2 NA18984.hp2 others(6): Show |
intron_variant | MODIFIER | c.1723+1472G>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29169012 | |||||||
chr2:29169155 | T | C | 14 | a0001c0001t0001g0265 a0001c0001t0011g0234 a0001c0001t0011g0235 others(11): Show |
14 | HG00741.hp1 HG01069.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.1723+1615T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29169155 | |||||||
chr2:29169214 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1723+1674C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29169214 | |||||||
chr2:29169290 | T | C | 17 | a0001c0001t0002g0054 a0001c0001t0002g0197 a0001c0002t0002g0084 others(14): Show |
17 | HG01074.hp1 HG01106.hp2 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.1723+1750T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29169290 | |||||||
chr2:29169329 | CTG | C | 19 | a0001c0001t0001g0059 a0001c0001t0001g0080 a0001c0001t0008g0053 others(16): Show |
19 | HG00280.hp2 HG00597.hp2 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.1723+1835_1723+183 others(6): Show |
CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr2 | 29169329 | ||||||
chr2:29169329 | CTGTG | C | 52 | a0001c0001t0001g0142 a0001c0001t0001g0175 a0001c0001t0001g0178 others(49): Show |
52 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.1723+1833_1723+183 others(8): Show |
CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr2 | 29169329 | ||||||
chr2:29169329 | CTGTGTG | C | 38 | a0001c0001t0001g0140 a0001c0001t0001g0182 a0001c0001t0001g0201 others(35): Show |
39 | HG00099.hp2 HG01106.hp1 HG01106.hp2 others(36): Show |
intron_variant | MODIFIER | c.1723+1831_1723+183 others(10): Show |
CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr2 | 29169329 | ||||||
chr2:29169329 | CTGTGTGT others(1): Show |
C | 53 | a0001c0001t0001g0015 a0001c0001t0001g0074 a0001c0001t0001g0105 others(50): Show |
54 | HG00597.hp1 HG00738.hp1 HG01167.hp1 others(51): Show |
intron_variant | MODIFIER | c.1723+1829_1723+183 others(12): Show |
CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr2 | 29169329 | ||||||
chr2:29169329 | CTGTGTGT others(3): Show |
C | 78 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0058 others(75): Show |
80 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.1723+1827_1723+183 others(14): Show |
CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr2 | 29169329 | ||||||
chr2:29169329 | CTGTGTGT others(5): Show |
C | 14 | a0001c0001t0001g0152 a0001c0001t0003g0083 a0001c0001t0003g0104 others(11): Show |
15 | HG00741.hp2 HG01069.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.1723+1825_1723+183 others(16): Show |
CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr2 | 29169329 | ||||||
chr2:29169329 | CTGTGTGT others(7): Show |
C | 19 | a0001c0001t0001g0173 a0001c0001t0001g0227 a0001c0001t0001g0228 others(16): Show |
20 | HG00280.hp1 HG00738.hp2 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.1723+1823_1723+183 others(18): Show |
CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr2 | 29169329 | ||||||
chr2:29169329 | CTGTGTGT others(11): Show |
C | 1 | a0001c0001t0006g0202 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1723+1819_1723+183 others(22): Show |
CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr2 | 29169329 | ||||||
chr2:29169334 | T | G | 1 | a0001c0002t0001g0277 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1723+1794T>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29169334 | |||||||
chr2:29169336 | T | G | 9 | a0001c0001t0001g0265 a0001c0002t0001g0271 a0002c0004t0001g0268 others(6): Show |
9 | HG00741.hp1 HG01069.hp2 HG01099.hp1 others(6): Show |
intron_variant | MODIFIER | c.1723+1796T>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29169336 | |||||||
chr2:29169338 | T | G | 3 | a0001c0001t0011g0234 a0001c0001t0011g0235 a0001c0002t0001g0264 |
3 | HG02071.hp2 HG02080.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1723+1798T>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29169338 | |||||||
chr2:29169655 | A | G | 3 | a0001c0001t0001g0103 a0001c0002t0003g0009 a0001c0002t0003g0121 |
3 | HG00738.hp2 HG03041.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1723+2115A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29169655 | |||||||
chr2:29169717 | A | G | 4 | a0001c0001t0008g0053 a0001c0010t0004g0256 a0001c0010t0004g0257 others(1): Show |
4 | HG01891.hp2 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1723+2177A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29169717 | |||||||
chr2:29169719 | C | T | 7 | a0001c0002t0002g0266 a0001c0002t0005g0129 a0001c0002t0005g0130 others(4): Show |
7 | HG01891.hp1 HG03195.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.1723+2179C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29169719 | |||||||
chr2:29169814 | C | T | 30 | a0001c0001t0001g0188 a0001c0001t0001g0230 a0001c0001t0012g0154 others(27): Show |
31 | HG00597.hp2 HG01109.hp1 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.1723+2274C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29169814 | |||||||
chr2:29169823 | C | T | 2 | a0001c0001t0003g0104 a0001c0001t0003g0148 |
2 | HG02630.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1723+2283C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29169823 | |||||||
chr2:29169962 | T | C | 24 | a0001c0001t0001g0178 a0001c0002t0001g0113 a0001c0003t0001g0087 others(21): Show |
25 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(22): Show |
intron_variant | MODIFIER | c.1723+2422T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29169962 | |||||||
chr2:29169984 | T | C | 1 | a0001c0002t0001g0072 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1723+2444T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29169984 | |||||||
chr2:29170365 | A | G | 13 | a0001c0002t0001g0124 a0001c0002t0004g0119 a0001c0002t0004g0125 others(10): Show |
13 | HG02572.hp1 HG02615.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.1723+2825A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29170365 | |||||||
chr2:29170612 | C | T | 1 | a0001c0002t0002g0117 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1723+3072C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29170612 | |||||||
chr2:29170705 | T | G | 2 | a0001c0002t0007g0060 a0001c0002t0007g0061 |
2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1723+3165T>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29170705 | |||||||
chr2:29170788 | C | T | 2 | a0001c0005t0001g0114 a0001c0008t0001g0184 |
2 | HG00140.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1723+3248C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29170788 | |||||||
chr2:29170814 | T | C | 28 | a0001c0001t0001g0103 a0001c0001t0002g0054 a0001c0001t0002g0197 others(25): Show |
29 | HG00738.hp2 HG01074.hp1 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.1723+3274T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29170814 | |||||||
chr2:29171154 | T | C | 1 | a0001c0002t0001g0267 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1724-3219T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29171154 | |||||||
chr2:29171244 | A | G | 1 | a0001c0002t0001g0044 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1724-3129A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29171244 | |||||||
chr2:29171293 | C | T | 3 | a0001c0010t0004g0256 a0001c0010t0004g0257 a0001c0018t0004g0078 |
3 | HG01891.hp2 HG02922.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1724-3080C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29171293 | |||||||
chr2:29171385 | T | C | 12 | a0001c0002t0001g0124 a0001c0002t0004g0119 a0001c0002t0004g0125 others(9): Show |
12 | HG02572.hp1 HG02615.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1724-2988T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29171385 | |||||||
chr2:29171488 | G | T | 25 | a0001c0001t0001g0103 a0001c0001t0002g0054 a0001c0001t0002g0197 others(22): Show |
26 | HG00738.hp2 HG01074.hp1 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.1724-2885G>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29171488 | |||||||
chr2:29171521 | C | CT | 16 | a0001c0001t0001g0103 a0001c0001t0001g0105 a0001c0001t0001g0106 others(13): Show |
16 | HG00741.hp1 HG01069.hp2 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.1724-2837dupT | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr2 | 29171521 | ||||||
chr2:29171521 | CT | C | 26 | a0001c0001t0001g0178 a0001c0002t0001g0113 a0001c0003t0001g0087 others(23): Show |
27 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.1724-2837delT | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr2 | 29171521 | ||||||
chr2:29171557 | C | T | 1 | a0001c0001t0001g0145 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1724-2816C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29171557 | |||||||
chr2:29171581 | C | T | 1 | a0002c0004t0001g0269 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1724-2792C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29171581 | |||||||
chr2:29171611 | C | T | 1 | a0001c0002t0001g0017 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1724-2762C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29171611 | |||||||
chr2:29171679 | C | T | 15 | a0001c0001t0001g0134 a0001c0001t0001g0196 a0001c0001t0002g0054 others(12): Show |
15 | HG01106.hp2 HG01346.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.1724-2694C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29171679 | |||||||
chr2:29171848 | ATCTT | A | 3 | a0001c0001t0009g0149 a0001c0001t0017g0229 a0001c0002t0009g0115 |
3 | HG03041.hp2 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1724-2519_1724-251 others(8): Show |
CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr2 | 29171848 | ||||||
chr2:29171898 | T | C | 6 | a0001c0003t0001g0212 a0001c0003t0001g0245 a0001c0003t0001g0246 others(3): Show |
6 | HG02572.hp1 HG02647.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1724-2475T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29171898 | |||||||
chr2:29172009 | GT | G | 70 | a0001c0001t0001g0140 a0001c0001t0001g0171 a0001c0001t0001g0172 others(67): Show |
71 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.1724-2349delT | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr2 | 29172009 | ||||||
chr2:29172027 | T | C | 44 | a0001c0001t0001g0074 a0001c0001t0001g0076 a0001c0001t0002g0054 others(41): Show |
44 | HG01106.hp2 HG01346.hp2 HG01884.hp1 others(41): Show |
intron_variant | MODIFIER | c.1724-2346T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29172027 | |||||||
chr2:29172128 | G | T | 3 | a0001c0002t0001g0236 a0001c0002t0001g0237 a0001c0002t0001g0238 |
3 | HG01243.hp1 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1724-2245G>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29172128 | |||||||
chr2:29172323 | A | G | 2 | a0001c0002t0010g0232 a0001c0002t0010g0233 |
2 | HG01074.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1724-2050A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29172323 | |||||||
chr2:29172353 | G | T | 1 | a0001c0001t0001g0195 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1724-2020G>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29172353 | |||||||
chr2:29172439 | T | C | 2 | a0001c0001t0001g0074 a0001c0001t0001g0076 |
2 | HG02486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1724-1934T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29172439 | |||||||
chr2:29172450 | G | A | 1 | a0001c0021t0001g0018 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1724-1923G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29172450 | |||||||
chr2:29172461 | T | G | 14 | a0001c0001t0001g0265 a0001c0001t0011g0234 a0001c0001t0011g0235 others(11): Show |
14 | HG00741.hp1 HG01069.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.1724-1912T>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29172461 | |||||||
chr2:29172792 | A | G | 1 | a0001c0002t0015g0011 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1724-1581A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29172792 | |||||||
chr2:29172907 | G | C | 2 | a0001c0002t0007g0060 a0001c0002t0007g0061 |
2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1724-1466G>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29172907 | |||||||
chr2:29172922 | CT | C | 9 | a0001c0001t0001g0140 a0001c0001t0001g0171 a0001c0001t0001g0172 others(6): Show |
9 | HG03927.hp2 NA18977.hp2 NA18984.hp2 others(6): Show |
intron_variant | MODIFIER | c.1724-1448delT | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr2 | 29172922 | ||||||
chr2:29172929 | C | T | 2 | a0001c0001t0001g0074 a0001c0001t0001g0076 |
2 | HG02486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1724-1444C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29172929 | |||||||
chr2:29173061 | G | A | 2 | a0001c0001t0001g0134 a0001c0001t0001g0135 |
2 | NA19240.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1724-1312G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29173061 | |||||||
chr2:29173098 | A | G | 7 | a0001c0001t0001g0175 a0001c0002t0001g0094 a0001c0002t0001g0095 others(4): Show |
7 | HG00597.hp2 HG00673.hp2 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.1724-1275A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29173098 | |||||||
chr2:29173127 | C | T | 13 | a0001c0002t0001g0124 a0001c0002t0004g0119 a0001c0002t0004g0125 others(10): Show |
13 | HG02572.hp1 HG02615.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.1724-1246C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29173127 | |||||||
chr2:29173219 | A | G | 3 | a0001c0002t0001g0236 a0001c0002t0001g0237 a0001c0002t0001g0238 |
3 | HG01243.hp1 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1724-1154A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29173219 | |||||||
chr2:29173221 | A | G | 5 | a0001c0002t0001g0003 a0001c0002t0001g0049 a0001c0002t0001g0050 others(2): Show |
6 | HG01123.hp1 HG02145.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1724-1152A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29173221 | |||||||
chr2:29173334 | T | A | 148 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(145): Show |
152 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.1724-1039T>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29173334 | |||||||
chr2:29173344 | C | T | 24 | a0001c0001t0001g0178 a0001c0002t0001g0113 a0001c0003t0001g0087 others(21): Show |
25 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.1724-1029C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29173344 | |||||||
chr2:29173356 | T | G | 3 | a0001c0002t0001g0003 a0001c0002t0001g0049 a0001c0002t0001g0050 |
4 | HG01123.hp1 HG02970.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1724-1017T>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29173356 | |||||||
chr2:29173404 | G | A | 264 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(261): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1724-969G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29173404 | |||||||
chr2:29173489 | G | T | 14 | a0001c0001t0001g0265 a0001c0001t0011g0234 a0001c0001t0011g0235 others(11): Show |
14 | HG00741.hp1 HG01069.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.1724-884G>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29173489 | |||||||
chr2:29173510 | A | G | 2 | a0001c0001t0001g0227 a0001c0001t0001g0228 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1724-863A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29173510 | |||||||
chr2:29173639 | T | A | 161 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(158): Show |
165 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.1724-734T>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29173639 | |||||||
chr2:29173693 | G | A | 1 | a0001c0002t0005g0131 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1724-680G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29173693 | |||||||
chr2:29173705 | A | G | 26 | a0001c0001t0001g0178 a0001c0001t0008g0053 a0001c0002t0001g0113 others(23): Show |
27 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.1724-668A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29173705 | |||||||
chr2:29173812 | A | G | 1 | a0001c0026t0001g0052 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1724-561A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29173812 | |||||||
chr2:29173868 | C | A | 1 | a0001c0001t0001g0189 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1724-505C>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29173868 | |||||||
chr2:29174020 | A | G | 3 | a0001c0001t0001g0074 a0001c0001t0001g0076 a0001c0002t0001g0267 |
3 | HG02486.hp2 HG02647.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1724-353A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29174020 | |||||||
chr2:29174124 | C | CT | 20 | a0001c0001t0001g0103 a0001c0001t0002g0054 a0001c0001t0002g0197 others(17): Show |
20 | HG00738.hp2 HG01074.hp1 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.1724-240dupT | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr2 | 29174124 | ||||||
chr2:29174149 | C | G | 7 | a0001c0002t0002g0266 a0001c0002t0005g0129 a0001c0002t0005g0130 others(4): Show |
7 | HG01891.hp1 HG03195.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.1724-224C>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29174149 | |||||||
chr2:29174291 | C | T | 1 | a0001c0009t0001g0211 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1724-82C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 14/15 | chr2 | 29174291 | |||||||
chr2:29174894 | T | G | 1 | a0001c0001t0001g0230 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.1796+449T>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29174894 | |||||||
chr2:29174966 | C | G | 1 | a0001c0002t0001g0283 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1796+521C>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29174966 | |||||||
chr2:29174974 | T | C | 3 | a0001c0002t0001g0003 a0001c0002t0001g0049 a0001c0002t0001g0050 |
4 | HG01123.hp1 HG02970.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1796+529T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29174974 | |||||||
chr2:29175101 | G | A | 17 | a0001c0001t0002g0054 a0001c0001t0002g0197 a0001c0002t0002g0084 others(14): Show |
17 | HG01074.hp1 HG01106.hp2 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.1796+656G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29175101 | |||||||
chr2:29175134 | C | T | 1 | a0001c0001t0001g0260 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1796+689C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29175134 | |||||||
chr2:29175323 | C | T | 11 | a0001c0001t0004g0198 a0001c0002t0004g0119 a0001c0002t0004g0125 others(8): Show |
11 | HG02572.hp1 HG02622.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.1796+878C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29175323 | |||||||
chr2:29175516 | G | A | 2 | a0001c0002t0007g0060 a0001c0002t0007g0061 |
2 | HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1796+1071G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29175516 | |||||||
chr2:29175620 | G | T | 3 | a0001c0002t0001g0236 a0001c0002t0001g0237 a0001c0002t0001g0238 |
3 | HG01243.hp1 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1796+1175G>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29175620 | |||||||
chr2:29175623 | C | T | 1 | a0001c0002t0001g0013 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1796+1178C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29175623 | |||||||
chr2:29175830 | C | T | 1 | a0001c0009t0001g0226 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1796+1385C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29175830 | |||||||
chr2:29175853 | C | G | 1 | a0001c0002t0001g0072 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1796+1408C>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29175853 | |||||||
chr2:29175854 | C | T | 1 | a0001c0002t0002g0126 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1796+1409C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29175854 | |||||||
chr2:29175862 | C | T | 4 | a0001c0002t0001g0062 a0001c0002t0001g0236 a0001c0002t0001g0237 others(1): Show |
4 | HG01243.hp1 HG06807.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1796+1417C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29175862 | |||||||
chr2:29175871 | T | C | 1 | a0001c0001t0001g0280 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1796+1426T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29175871 | |||||||
chr2:29175875 | T | C | 1 | a0001c0001t0001g0280 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1796+1430T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29175875 | |||||||
chr2:29175884 | C | T | 1 | a0001c0001t0008g0053 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1796+1439C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29175884 | |||||||
chr2:29175890 | C | T | 2 | a0001c0001t0001g0227 a0001c0001t0001g0228 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1796+1445C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29175890 | |||||||
chr2:29175903 | A | G | 153 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(150): Show |
157 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.1796+1458A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29175903 | |||||||
chr2:29175906 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1796+1461C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29175906 | |||||||
chr2:29175907 | G | GC | 7 | a0001c0001t0001g0180 a0001c0001t0001g0199 a0001c0001t0001g0201 others(4): Show |
7 | HG00642.hp2 HG01106.hp1 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.1796+1465dupC | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 29175907 | ||||||
chr2:29175911 | G | A | 2 | a0001c0001t0001g0182 a0001c0003t0001g0101 |
2 | HG00099.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.1796+1466G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29175911 | |||||||
chr2:29175922 | C | T | 52 | a0001c0001t0001g0059 a0001c0001t0001g0140 a0001c0001t0001g0171 others(49): Show |
53 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.1796+1477C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29175922 | |||||||
chr2:29175994 | A | C | 1 | a0001c0002t0001g0072 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1796+1549A>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29175994 | |||||||
chr2:29175997 | A | G | 1 | a0001c0002t0001g0072 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1796+1552A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29175997 | |||||||
chr2:29176003 | T | C | 1 | a0001c0002t0001g0072 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1796+1558T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29176003 | |||||||
chr2:29176027 | T | C | 1 | a0001c0003t0001g0101 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1796+1582T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29176027 | |||||||
chr2:29176050 | C | A | 8 | a0001c0001t0004g0198 a0001c0002t0004g0119 a0001c0002t0004g0125 others(5): Show |
8 | HG01891.hp2 HG02622.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1796+1605C>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29176050 | |||||||
chr2:29176269 | G | T | 1 | a0001c0002t0003g0073 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1796+1824G>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29176269 | |||||||
chr2:29176445 | G | T | 1 | a0001c0002t0001g0063 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1796+2000G>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29176445 | |||||||
chr2:29176516 | C | T | 1 | a0001c0002t0003g0073 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1796+2071C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29176516 | |||||||
chr2:29176525 | G | A | 1 | a0001c0003t0001g0147 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1796+2080G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29176525 | |||||||
chr2:29176548 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1796+2103G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29176548 | |||||||
chr2:29176561 | A | G | 1 | a0001c0002t0005g0132 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1796+2116A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29176561 | |||||||
chr2:29176654 | C | T | 1 | a0001c0001t0001g0160 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1796+2209C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29176654 | |||||||
chr2:29176666 | C | T | 29 | a0001c0001t0001g0188 a0001c0001t0001g0230 a0001c0001t0012g0154 others(26): Show |
30 | HG00597.hp2 HG01109.hp1 HG01123.hp2 others(27): Show |
intron_variant | MODIFIER | c.1796+2221C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29176666 | |||||||
chr2:29176708 | T | A | 2 | a0001c0005t0003g0109 a0001c0005t0003g0111 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1796+2263T>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29176708 | |||||||
chr2:29176717 | C | T | 3 | a0001c0010t0004g0256 a0001c0010t0004g0257 a0001c0018t0004g0078 |
3 | HG01891.hp2 HG02922.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1796+2272C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29176717 | |||||||
chr2:29176945 | C | T | 12 | a0001c0001t0009g0149 a0001c0001t0017g0229 a0001c0002t0002g0266 others(9): Show |
12 | HG01891.hp1 HG03041.hp2 HG03139.hp2 others(9): Show |
intron_variant | MODIFIER | c.1796+2500C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29176945 | |||||||
chr2:29176992 | T | C | 2 | a0001c0002t0001g0012 a0001c0002t0001g0224 |
2 | HG02135.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.1796+2547T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29176992 | |||||||
chr2:29177407 | C | CA | 128 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(125): Show |
132 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(129): Show |
intron_variant | MODIFIER | c.1796+2978dupA | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 29177407 | ||||||
chr2:29177407 | C | CAA | 7 | a0001c0001t0001g0158 a0001c0001t0001g0164 a0001c0001t0001g0170 others(4): Show |
7 | HG00140.hp1 HG02040.hp1 HG03942.hp2 others(4): Show |
intron_variant | MODIFIER | c.1796+2977_1796+297 others(6): Show |
CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 29177407 | ||||||
chr2:29177407 | CA | C | 84 | a0001c0001t0001g0178 a0001c0001t0001g0227 a0001c0001t0001g0228 others(81): Show |
86 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(83): Show |
intron_variant | MODIFIER | c.1796+2978delA | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 29177407 | ||||||
chr2:29177407 | CAA | C | 20 | a0001c0001t0001g0059 a0001c0001t0001g0074 a0001c0001t0001g0076 others(17): Show |
20 | HG00738.hp2 HG01074.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1796+2977_1796+297 others(6): Show |
CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 29177407 | ||||||
chr2:29177424 | T | C | 21 | a0001c0001t0001g0074 a0001c0001t0001g0076 a0001c0001t0002g0054 others(18): Show |
21 | HG01106.hp2 HG01346.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.1796+2979T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29177424 | |||||||
chr2:29177552 | G | T | 1 | a0001c0002t0015g0011 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1796+3107G>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29177552 | |||||||
chr2:29177617 | G | A | 1 | a0001c0001t0001g0280 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1796+3172G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29177617 | |||||||
chr2:29177788 | A | T | 1 | a0001c0001t0001g0059 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1796+3343A>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29177788 | |||||||
chr2:29177952 | T | C | 7 | a0001c0001t0001g0103 a0001c0002t0001g0072 a0001c0002t0003g0009 others(4): Show |
7 | HG00738.hp2 HG01074.hp1 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.1796+3507T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29177952 | |||||||
chr2:29178085 | C | T | 279 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(276): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.1797-3487C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29178085 | |||||||
chr2:29178146 | C | T | 120 | a0001c0001t0001g0059 a0001c0001t0001g0074 a0001c0001t0001g0076 others(117): Show |
123 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.1797-3426C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29178146 | |||||||
chr2:29178369 | C | T | 29 | a0001c0001t0001g0188 a0001c0001t0001g0230 a0001c0001t0012g0154 others(26): Show |
30 | HG00597.hp2 HG01109.hp1 HG01123.hp2 others(27): Show |
intron_variant | MODIFIER | c.1797-3203C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29178369 | |||||||
chr2:29178473 | G | T | 6 | a0001c0003t0001g0212 a0001c0003t0001g0245 a0001c0003t0001g0246 others(3): Show |
6 | HG02572.hp1 HG02647.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1797-3099G>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29178473 | |||||||
chr2:29178599 | C | G | 13 | a0001c0001t0002g0054 a0001c0001t0002g0197 a0001c0002t0002g0084 others(10): Show |
13 | HG01106.hp2 HG01346.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1797-2973C>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29178599 | |||||||
chr2:29178633 | C | T | 129 | a0001c0001t0001g0059 a0001c0001t0001g0074 a0001c0001t0001g0076 others(126): Show |
132 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.1797-2939C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29178633 | |||||||
chr2:29178678 | T | C | 68 | a0001c0001t0001g0059 a0001c0001t0001g0140 a0001c0001t0001g0171 others(65): Show |
69 | HG00099.hp1 HG00280.hp2 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.1797-2894T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29178678 | |||||||
chr2:29178842 | T | C | 1 | a0001c0002t0001g0037 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1797-2730T>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29178842 | |||||||
chr2:29178967 | G | C | 1 | a0001c0002t0001g0072 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1797-2605G>C | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29178967 | |||||||
chr2:29179026 | C | G | 1 | a0001c0002t0002g0126 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1797-2546C>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29179026 | |||||||
chr2:29179044 | C | T | 1 | a0001c0002t0001g0017 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1797-2528C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29179044 | |||||||
chr2:29179182 | C | T | 158 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(155): Show |
162 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.1797-2390C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29179182 | |||||||
chr2:29179195 | C | T | 9 | a0001c0001t0001g0140 a0001c0001t0001g0171 a0001c0001t0001g0172 others(6): Show |
9 | HG03927.hp2 NA18977.hp2 NA18984.hp2 others(6): Show |
intron_variant | MODIFIER | c.1797-2377C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29179195 | |||||||
chr2:29179271 | CTA | C | 17 | a0001c0001t0002g0054 a0001c0001t0002g0197 a0001c0002t0002g0084 others(14): Show |
17 | HG01106.hp2 HG01346.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.1797-2299_1797-229 others(6): Show |
CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 29179271 | ||||||
chr2:29179302 | A | T | 1 | a0001c0001t0001g0077 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1797-2270A>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29179302 | |||||||
chr2:29179327 | G | A | 1 | a0001c0001t0001g0244 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1797-2245G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29179327 | |||||||
chr2:29179503 | C | T | 5 | a0001c0002t0001g0003 a0001c0002t0001g0049 a0001c0002t0001g0050 others(2): Show |
6 | HG01123.hp1 HG02145.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1797-2069C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29179503 | |||||||
chr2:29179645 | G | A | 1 | a0002c0004t0001g0274 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1797-1927G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29179645 | |||||||
chr2:29179700 | G | T | 1 | a0001c0020t0001g0255 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1797-1872G>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29179700 | |||||||
chr2:29179840 | T | G | 1 | a0001c0001t0002g0054 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1797-1732T>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29179840 | |||||||
chr2:29180049 | AATGAAAT | A | 5 | a0001c0001t0009g0149 a0001c0001t0017g0229 a0001c0002t0007g0060 others(2): Show |
5 | HG03041.hp2 HG03139.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1797-1514_1797-150 others(11): Show |
CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 29180049 | ||||||
chr2:29180070 | G | A | 6 | a0001c0003t0001g0212 a0001c0003t0001g0245 a0001c0003t0001g0246 others(3): Show |
6 | HG02572.hp1 HG02647.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1797-1502G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29180070 | |||||||
chr2:29180275 | T | G | 1 | a0001c0002t0001g0072 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1797-1297T>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29180275 | |||||||
chr2:29180339 | A | G | 9 | a0001c0001t0001g0140 a0001c0001t0001g0171 a0001c0001t0001g0172 others(6): Show |
9 | HG03927.hp2 NA18977.hp2 NA18984.hp2 others(6): Show |
intron_variant | MODIFIER | c.1797-1233A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29180339 | |||||||
chr2:29180486 | C | T | 2 | a0001c0001t0001g0071 a0001c0001t0001g0166 |
2 | NA18955.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.1797-1086C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29180486 | |||||||
chr2:29180535 | C | T | 4 | a0001c0008t0001g0176 a0001c0008t0001g0183 a0001c0008t0001g0184 others(1): Show |
4 | HG00140.hp2 HG00642.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1797-1037C>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29180535 | |||||||
chr2:29180630 | A | G | 4 | a0002c0004t0001g0269 a0002c0004t0001g0270 a0002c0004t0001g0275 others(1): Show |
4 | HG01099.hp1 HG01256.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.1797-942A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29180630 | |||||||
chr2:29180758 | G | T | 129 | a0001c0001t0001g0059 a0001c0001t0001g0074 a0001c0001t0001g0076 others(126): Show |
132 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.1797-814G>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29180758 | |||||||
chr2:29180840 | A | ATG | 5 | a0001c0001t0001g0164 a0001c0001t0001g0205 a0001c0001t0001g0262 others(2): Show |
5 | HG01106.hp1 HG02738.hp1 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.1797-712_1797-711d others(4): Show |
CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 29180840 | ||||||
chr2:29180840 | ATG | A | 105 | a0001c0001t0001g0059 a0001c0001t0001g0074 a0001c0001t0001g0076 others(102): Show |
107 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.1797-712_1797-711d others(4): Show |
CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 29180840 | ||||||
chr2:29180868 | G | GTA | 25 | a0001c0001t0002g0054 a0001c0001t0002g0197 a0001c0002t0001g0003 others(22): Show |
26 | HG01074.hp1 HG01106.hp2 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.1797-690_1797-689d others(4): Show |
CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr2 | 29180868 | ||||||
chr2:29181002 | A | G | 1 | a0001c0002t0001g0033 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1797-570A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29181002 | |||||||
chr2:29181084 | A | G | 21 | a0001c0001t0001g0103 a0001c0002t0002g0266 a0001c0002t0003g0009 others(18): Show |
21 | HG00738.hp2 HG01074.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.1797-488A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29181084 | |||||||
chr2:29181138 | G | A | 1 | a0001c0002t0001g0072 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1797-434G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29181138 | |||||||
chr2:29181186 | A | T | 3 | a0001c0002t0001g0003 a0001c0002t0001g0049 a0001c0002t0001g0050 |
4 | HG01123.hp1 HG02970.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1797-386A>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29181186 | |||||||
chr2:29181248 | A | T | 4 | a0002c0004t0001g0269 a0002c0004t0001g0270 a0002c0004t0001g0275 others(1): Show |
4 | HG01099.hp1 HG01256.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.1797-324A>T | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29181248 | |||||||
chr2:29181385 | G | A | 99 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0058 others(96): Show |
101 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.1797-187G>A | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29181385 | |||||||
chr2:29181404 | A | G | 1 | a0001c0002t0001g0264 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1797-168A>G | CLIP4 | ENSG00000115295.21 | transcript | ENST00000320081.10 | protein_coding | 15/15 | chr2 | 29181404 |