Item | Value |
---|---|
geneid | 51062 |
ensemblid | ENSG00000198513.14 |
hgncid | 11231 |
symbol | ATL1 |
name | atlastin GTPase 1 |
refseq_nuc | NM_015915.5 |
refseq_prot | NP_056999.2 |
ensembl_nuc | ENST00000358385.12 |
ensembl_prot | ENSP00000351155.7 |
mane_status | MANE Select |
chr | chr14 |
start | 50560145 |
end | 50633045 |
strand | + |
ver | v1.2 |
region | chr14:50560145-50633045 |
region5000 | chr14:50555145-50638045 |
regionname0 | ATL1_chr14_50560145_50633045 |
regionname5000 | ATL1_chr14_50555145_50638045 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 558 | 319 | 92 | 66 | 125 | 8 | 26 | 96 | ATL1_chr14_50555145_50638045 | ATL1 | MAKNR others(553): Show |
chr14 | 50555145 | 50638045 |
a0002 | 0/0 | 558 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | MAKNR others(553): Show |
chr14 | 50555145 | 50638045 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1674 | 174 | 47 | 36 | 71 | 5 | 15 | ATL1_chr14_50555145_50638045 | ATL1 | ATGGC others(1669): Show |
chr14 | 50555145 | 50638045 | ||
a0001c0002 | 1/0 | 1674 | 65 | 3 | 15 | 36 | 2 | 8 | ATL1_chr14_50555145_50638045 | ATL1 | ATGGC others(1669): Show |
chr14 | 50555145 | 50638045 | ||
a0001c0003 | 0/1 | 1674 | 58 | 25 | 15 | 14 | 1 | 2 | ATL1_chr14_50555145_50638045 | ATL1 | ATGGC others(1669): Show |
chr14 | 50555145 | 50638045 | ||
a0001c0004 | 0/0 | 1674 | 10 | 10 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | ATGGC others(1669): Show |
chr14 | 50555145 | 50638045 | ||
a0001c0005 | 0/0 | 1674 | 3 | 0 | 0 | 3 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | ATGGC others(1669): Show |
chr14 | 50555145 | 50638045 | ||
a0001c0006 | 0/0 | 1674 | 2 | 2 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | ATGGC others(1669): Show |
chr14 | 50555145 | 50638045 | ||
a0001c0007 | 0/0 | 1674 | 2 | 2 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | ATGGC others(1669): Show |
chr14 | 50555145 | 50638045 | ||
a0001c0008 | 0/0 | 1674 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | ATGGC others(1669): Show |
chr14 | 50555145 | 50638045 | ||
a0001c0009 | 0/0 | 1674 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | ATGGC others(1669): Show |
chr14 | 50555145 | 50638045 | ||
a0001c0010 | 0/0 | 1674 | 1 | 0 | 0 | 0 | 0 | 1 | ATL1_chr14_50555145_50638045 | ATL1 | ATGGC others(1669): Show |
chr14 | 50555145 | 50638045 | ||
a0001c0011 | 0/0 | 1674 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | ATGGC others(1669): Show |
chr14 | 50555145 | 50638045 | ||
a0001c0012 | 0/0 | 1674 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | ATGGC others(1669): Show |
chr14 | 50555145 | 50638045 | ||
a0002c0013 | 0/0 | 1674 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | ATGGC others(1669): Show |
chr14 | 50555145 | 50638045 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2504 | 151 | 47 | 34 | 53 | 5 | 12 | ATL1_chr14_50555145_50638045 | ATL1 | AGAGT others(2499): Show |
chr14 | 50555145 | 50638045 |
a0001c0001t0002 | 0/0 | 2504 | 20 | 0 | 2 | 18 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | AGAGT others(2499): Show |
chr14 | 50555145 | 50638045 |
a0001c0001t0003 | 0/0 | 2504 | 3 | 0 | 0 | 0 | 0 | 3 | ATL1_chr14_50555145_50638045 | ATL1 | AGAGT others(2499): Show |
chr14 | 50555145 | 50638045 |
a0001c0002t0001 | 1/0 | 2504 | 63 | 3 | 15 | 35 | 2 | 7 | ATL1_chr14_50555145_50638045 | ATL1 | AGAGT others(2499): Show |
chr14 | 50555145 | 50638045 |
a0001c0002t0006 | 0/0 | 2504 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | AGAGT others(2499): Show |
chr14 | 50555145 | 50638045 |
a0001c0002t0008 | 0/0 | 2504 | 1 | 0 | 0 | 0 | 0 | 1 | ATL1_chr14_50555145_50638045 | ATL1 | AGAGT others(2499): Show |
chr14 | 50555145 | 50638045 |
a0001c0003t0001 | 0/1 | 2504 | 56 | 23 | 15 | 14 | 1 | 2 | ATL1_chr14_50555145_50638045 | ATL1 | AGAGT others(2499): Show |
chr14 | 50555145 | 50638045 |
a0001c0003t0005 | 0/0 | 2504 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | AGAGT others(2499): Show |
chr14 | 50555145 | 50638045 |
a0001c0003t0007 | 0/0 | 2504 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | AGAGT others(2499): Show |
chr14 | 50555145 | 50638045 |
a0001c0004t0001 | 0/0 | 2504 | 9 | 9 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | AGAGT others(2499): Show |
chr14 | 50555145 | 50638045 |
a0001c0004t0004 | 0/0 | 2504 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | AGAGT others(2499): Show |
chr14 | 50555145 | 50638045 |
a0001c0005t0001 | 0/0 | 2504 | 3 | 0 | 0 | 3 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | AGAGT others(2499): Show |
chr14 | 50555145 | 50638045 |
a0001c0006t0001 | 0/0 | 2504 | 2 | 2 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | AGAGT others(2499): Show |
chr14 | 50555145 | 50638045 |
a0001c0007t0001 | 0/0 | 2504 | 2 | 2 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | AGAGT others(2499): Show |
chr14 | 50555145 | 50638045 |
a0001c0008t0001 | 0/0 | 2504 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | AGAGT others(2499): Show |
chr14 | 50555145 | 50638045 |
a0001c0009t0001 | 0/0 | 2504 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | AGAGT others(2499): Show |
chr14 | 50555145 | 50638045 |
a0001c0010t0001 | 0/0 | 2504 | 1 | 0 | 0 | 0 | 0 | 1 | ATL1_chr14_50555145_50638045 | ATL1 | AGAGT others(2499): Show |
chr14 | 50555145 | 50638045 |
a0001c0011t0001 | 0/0 | 2504 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | AGAGT others(2499): Show |
chr14 | 50555145 | 50638045 |
a0001c0012t0001 | 0/0 | 2504 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | AGAGT others(2499): Show |
chr14 | 50555145 | 50638045 |
a0002c0013t0001 | 0/0 | 2504 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | AGAGT others(2499): Show |
chr14 | 50555145 | 50638045 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0002g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0002t0001g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0002t0001g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0002t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0002t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0002t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0002t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0002t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0002t0001g0023 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0002t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0002t0001g0139 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0002t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0002t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0002t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0002t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0002t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0002t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0002t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0002t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0002t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0002t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0002t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0002t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0002t0006g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0002t0008g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0003t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0003t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0003t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0003t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0003t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0003t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0003t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0003t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0003t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0003t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0003t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0003t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0003t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0003t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0003t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0003t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0003t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0003t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0003t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0003t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0003t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0003t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0003t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0003t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0003t0001g0096 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0003t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0003t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0003t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0003t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0003t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0003t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0003t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0003t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0003t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0003t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0003t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0003t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0003t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0003t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0003t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0003t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0003t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0003t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0003t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0003t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0003t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0003t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0003t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0003t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0003t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0003t0005g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0003t0007g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0004t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0004t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0004t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0004t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0004t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0004t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0004t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0004t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0004t0004g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0005t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0005t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0005t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0006t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0006t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0007t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0007t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0008t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0009t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0010t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0011t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0001c0012t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
a0002c0013t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0104 | EUR | GBR | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG00140 | hp2 | a0001 | c0002 | t0001 | g0266 | EUR | GBR | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG00280 | hp1 | a0001 | c0003 | t0001 | g0285 | EUR | FIN | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0119 | EUR | FIN | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | CHS | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG00408 | hp2 | a0001 | c0003 | t0001 | g0040 | EAS | CHS | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG00423 | hp2 | a0002 | c0013 | t0001 | g0007 | EAS | CHS | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | CHS | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | CHS | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG00639 | hp1 | a0001 | c0003 | t0001 | g0148 | AMR | PUR | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG00639 | hp2 | a0001 | c0002 | t0001 | g0236 | AMR | PUR | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG00642 | hp2 | a0001 | c0003 | t0001 | g0017 | AMR | PUR | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | CHS | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG00733 | hp2 | a0001 | c0003 | t0001 | g0017 | AMR | PUR | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG00735 | hp1 | a0001 | c0002 | t0001 | g0256 | AMR | PUR | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG00735 | hp2 | a0001 | c0003 | t0001 | g0150 | AMR | PUR | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG00738 | hp2 | a0001 | c0002 | t0001 | g0231 | AMR | PUR | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG00741 | hp2 | a0001 | c0002 | t0001 | g0004 | AMR | PUR | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG01069 | hp1 | a0001 | c0003 | t0001 | g0052 | AMR | PUR | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG01069 | hp2 | a0001 | c0003 | t0001 | g0176 | AMR | PUR | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG01071 | hp1 | a0001 | c0003 | t0001 | g0009 | AMR | PUR | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG01109 | hp1 | a0001 | c0003 | t0001 | g0147 | AMR | PUR | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG01167 | hp1 | a0001 | c0003 | t0001 | g0284 | AMR | PUR | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG01192 | hp2 | a0001 | c0003 | t0001 | g0009 | AMR | PUR | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG01243 | hp1 | a0001 | c0002 | t0001 | g0243 | AMR | PUR | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG01255 | hp2 | a0001 | c0002 | t0001 | g0021 | AMR | CLM | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG01256 | hp1 | a0001 | c0002 | t0001 | g0023 | AMR | CLM | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG01261 | hp1 | a0001 | c0003 | t0001 | g0151 | AMR | CLM | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG01261 | hp2 | a0001 | c0003 | t0001 | g0063 | AMR | CLM | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG01346 | hp1 | a0001 | c0003 | t0001 | g0175 | AMR | CLM | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0286 | AMR | CLM | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG01358 | hp1 | a0001 | c0002 | t0001 | g0283 | AMR | CLM | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG01496 | hp1 | a0001 | c0002 | t0001 | g0021 | AMR | CLM | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG01496 | hp2 | a0001 | c0003 | t0001 | g0064 | AMR | CLM | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | IBS | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0118 | EUR | IBS | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG01884 | hp1 | a0001 | c0003 | t0005 | g0225 | AFR | ACB | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | ACB | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PEL | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG01943 | hp2 | a0001 | c0003 | t0001 | g0217 | AMR | PEL | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PEL | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG01952 | hp2 | a0001 | c0002 | t0001 | g0262 | AMR | PEL | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG01975 | hp2 | a0001 | c0002 | t0001 | g0004 | AMR | PEL | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG01978 | hp1 | a0001 | c0002 | t0001 | g0246 | AMR | PEL | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG01981 | hp2 | a0001 | c0002 | t0001 | g0004 | AMR | PEL | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0193 | AMR | PEL | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG01993 | hp2 | a0001 | c0002 | t0001 | g0245 | AMR | PEL | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PEL | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02015 | hp1 | a0001 | c0003 | t0001 | g0047 | EAS | KHV | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | KHV | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02027 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02040 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | KHV | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | KHV | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02055 | hp1 | a0001 | c0004 | t0001 | g0034 | AFR | ACB | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02071 | hp2 | a0001 | c0003 | t0001 | g0046 | EAS | KHV | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | KHV | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02129 | hp1 | a0001 | c0002 | t0001 | g0264 | EAS | KHV | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02135 | hp1 | a0001 | c0002 | t0001 | g0251 | EAS | KHV | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02145 | hp1 | a0001 | c0003 | t0007 | g0094 | AFR | ACB | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CDX | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02165 | hp2 | a0001 | c0002 | t0001 | g0263 | EAS | CDX | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | ACB | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02258 | hp1 | a0001 | c0004 | t0001 | g0032 | AFR | ACB | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02280 | hp2 | a0001 | c0008 | t0001 | g0146 | AFR | ACB | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02293 | hp1 | a0001 | c0002 | t0001 | g0265 | AMR | PEL | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0194 | AMR | PEL | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02523 | hp1 | a0001 | c0002 | t0001 | g0020 | EAS | KHV | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02523 | hp2 | a0001 | c0003 | t0001 | g0051 | EAS | KHV | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02572 | hp2 | a0001 | c0004 | t0001 | g0031 | AFR | GWD | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02615 | hp2 | a0001 | c0003 | t0001 | g0136 | AFR | GWD | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02630 | hp1 | a0001 | c0003 | t0001 | g0043 | AFR | GWD | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02630 | hp2 | a0001 | c0003 | t0001 | g0065 | AFR | GWD | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02647 | hp2 | a0001 | c0006 | t0001 | g0029 | AFR | GWD | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02683 | hp1 | a0001 | c0002 | t0001 | g0274 | SAS | PJL | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02683 | hp2 | a0001 | c0001 | t0003 | g0124 | SAS | PJL | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02717 | hp2 | a0001 | c0003 | t0001 | g0198 | AFR | GWD | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02723 | hp2 | a0001 | c0003 | t0001 | g0173 | AFR | GWD | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02735 | hp1 | a0001 | c0003 | t0001 | g0152 | SAS | PJL | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02735 | hp2 | a0001 | c0002 | t0008 | g0247 | SAS | PJL | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02738 | hp1 | a0001 | c0002 | t0001 | g0235 | SAS | PJL | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02809 | hp1 | a0001 | c0007 | t0001 | g0228 | AFR | GWD | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02818 | hp2 | a0001 | c0003 | t0001 | g0196 | AFR | GWD | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02886 | hp1 | a0001 | c0003 | t0001 | g0158 | AFR | GWD | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02895 | hp1 | a0001 | c0003 | t0001 | g0006 | AFR | GWD | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02896 | hp2 | a0001 | c0004 | t0001 | g0033 | AFR | GWD | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02897 | hp1 | a0001 | c0004 | t0001 | g0030 | AFR | GWD | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02897 | hp2 | a0001 | c0003 | t0001 | g0006 | AFR | GWD | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | ESN | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ESN | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | ESN | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02970 | hp1 | a0001 | c0003 | t0001 | g0157 | AFR | ESN | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ESN | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02976 | hp1 | a0001 | c0012 | t0001 | g0268 | AFR | ESN | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ESN | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG03098 | hp1 | a0001 | c0003 | t0001 | g0045 | AFR | MSL | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG03098 | hp2 | a0001 | c0004 | t0004 | g0141 | AFR | MSL | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG03130 | hp1 | a0001 | c0006 | t0001 | g0028 | AFR | ESN | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG03139 | hp1 | a0001 | c0003 | t0001 | g0038 | AFR | ESN | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG03139 | hp2 | a0001 | c0004 | t0001 | g0005 | AFR | ESN | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ESN | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | ESN | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG03225 | hp2 | a0001 | c0003 | t0001 | g0044 | AFR | MSL | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0276 | SAS | PJL | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG03453 | hp2 | a0001 | c0003 | t0001 | g0159 | AFR | MSL | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | MSL | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG03486 | hp2 | a0001 | c0007 | t0001 | g0070 | AFR | MSL | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG03490 | hp1 | a0001 | c0002 | t0001 | g0019 | SAS | PJL | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG03492 | hp1 | a0001 | c0002 | t0001 | g0019 | SAS | PJL | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG03516 | hp1 | a0001 | c0003 | t0001 | g0105 | AFR | ESN | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ESN | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG03579 | hp1 | a0001 | c0004 | t0001 | g0054 | AFR | MSL | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG03579 | hp2 | a0001 | c0009 | t0001 | g0084 | AFR | MSL | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG03669 | hp1 | a0001 | c0010 | t0001 | g0111 | SAS | PJL | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG03688 | hp1 | a0001 | c0003 | t0001 | g0149 | SAS | STU | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG03688 | hp2 | a0001 | c0001 | t0003 | g0069 | SAS | STU | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG03710 | hp2 | a0001 | c0002 | t0001 | g0252 | SAS | PJL | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | BEB | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG03834 | hp2 | a0001 | c0002 | t0001 | g0267 | SAS | BEB | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG03942 | hp1 | a0001 | c0002 | t0001 | g0233 | SAS | BEB | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | BEB | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG04199 | hp1 | a0001 | c0001 | t0003 | g0068 | SAS | STU | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | STU | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA18522 | hp1 | a0001 | c0004 | t0001 | g0005 | AFR | YRI | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA18522 | hp2 | a0001 | c0004 | t0001 | g0035 | AFR | YRI | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA18906 | hp1 | a0001 | c0003 | t0001 | g0097 | AFR | YRI | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA18906 | hp2 | a0001 | c0003 | t0001 | g0037 | AFR | YRI | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA18939 | hp1 | a0001 | c0002 | t0001 | g0254 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA18940 | hp2 | a0001 | c0003 | t0001 | g0008 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA18944 | hp2 | a0001 | c0005 | t0001 | g0253 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA18945 | hp2 | a0001 | c0002 | t0001 | g0250 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA18950 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA18951 | hp1 | a0001 | c0003 | t0001 | g0048 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA18951 | hp2 | a0001 | c0002 | t0006 | g0249 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA18952 | hp1 | a0001 | c0002 | t0001 | g0024 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA18954 | hp1 | a0001 | c0002 | t0001 | g0234 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA18957 | hp1 | a0001 | c0002 | t0001 | g0232 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA18960 | hp1 | a0001 | c0003 | t0001 | g0039 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA18960 | hp2 | a0001 | c0002 | t0001 | g0024 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA18962 | hp2 | a0001 | c0002 | t0001 | g0230 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA18964 | hp2 | a0001 | c0002 | t0001 | g0255 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA18965 | hp1 | a0001 | c0005 | t0001 | g0244 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA18971 | hp2 | a0001 | c0002 | t0001 | g0260 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA18974 | hp2 | a0001 | c0002 | t0001 | g0270 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA18980 | hp1 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA18981 | hp1 | a0001 | c0003 | t0001 | g0042 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA18983 | hp1 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA18988 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA18989 | hp1 | a0001 | c0002 | t0001 | g0239 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA18999 | hp2 | a0001 | c0002 | t0001 | g0272 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA19001 | hp2 | a0001 | c0002 | t0001 | g0273 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA19003 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA19003 | hp2 | a0001 | c0011 | t0001 | g0109 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA19010 | hp2 | a0001 | c0002 | t0001 | g0271 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA19012 | hp1 | a0001 | c0002 | t0001 | g0257 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | LWK | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA19043 | hp2 | a0001 | c0003 | t0001 | g0204 | AFR | LWK | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA19060 | hp1 | a0001 | c0003 | t0001 | g0008 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA19063 | hp1 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA19065 | hp1 | a0001 | c0003 | t0001 | g0050 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA19068 | hp1 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA19070 | hp1 | a0001 | c0002 | t0001 | g0238 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA19072 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA19077 | hp1 | a0001 | c0005 | t0001 | g0240 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA19077 | hp2 | a0001 | c0003 | t0001 | g0049 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA19078 | hp1 | a0001 | c0002 | t0001 | g0269 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA19079 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA19080 | hp2 | a0001 | c0003 | t0001 | g0041 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA19081 | hp2 | a0001 | c0003 | t0001 | g0007 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA19083 | hp2 | a0001 | c0003 | t0001 | g0053 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA19085 | hp2 | a0001 | c0002 | t0001 | g0248 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA19088 | hp2 | a0001 | c0002 | t0001 | g0258 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA19091 | hp1 | a0001 | c0002 | t0001 | g0259 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | YRI | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | YRI | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA20129 | hp1 | a0001 | c0003 | t0001 | g0218 | AFR | ASW | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | ASW | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0168 | EUR | TSI | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA20752 | hp2 | a0001 | c0002 | t0001 | g0242 | EUR | TSI | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02109 | hp2 | a0001 | c0003 | t0001 | g0098 | AFR | ACB | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02486 | hp1 | a0001 | c0002 | t0001 | g0241 | AFR | ACB | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02486 | hp2 | a0001 | c0003 | t0001 | g0171 | AFR | ACB | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | ACB | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | MSL | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | MSL | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | USA | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | USA | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA20300 | hp1 | a0001 | c0003 | t0001 | g0036 | AFR | USA | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA20300 | hp2 | a0001 | c0002 | t0001 | g0261 | AFR | USA | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA21309 | hp1 | a0001 | c0002 | t0001 | g0237 | AFR | LWK | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
NA21309 | hp2 | a0001 | c0003 | t0001 | g0153 | AFR | LWK | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
homoSapiens | chm13v2 | a0001 | c0003 | t0001 | g0096 | REF | REF | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0139 | REF | REF | ATL1_chr14_50555145_50638045 | ATL1 | chr14 | 50555145 | 50638045 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:50614493 | T | G | 1 | a0002 | 1 | HG00423.hp2 | missense_variant | MODERATE | c.844T>G | p.Phe282Val | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/14 | 965/2504 | 844/1677 | 282/558 | chr14 | 50614493 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:50560295 | T | C | 1 | a0001c0008 | 1 | HG02280.hp2 | synonymous_variant | LOW | c.30T>C | p.Ser10Ser | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/14 | 151/2504 | 30/1677 | 10/558 | chr14 | 50560295 | |||
chr14:50587880 | A | G | 2 | a0001c0003 a0002c0013 |
58 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(55): Show |
synonymous_variant | LOW | c.84A>G | p.Pro28Pro | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 2/14 | 205/2504 | 84/1677 | 28/558 | chr14 | 50587880 | |||
chr14:50591009 | G | A | 10 | a0001c0001 a0001c0003 a0001c0004 others(7): Show |
250 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(247): Show |
synonymous_variant | LOW | c.351G>A | p.Glu117Glu | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 3/14 | 472/2504 | 351/1677 | 117/558 | chr14 | 50591009 | |||
chr14:50591066 | T | C | 1 | a0001c0005 | 3 | NA18944.hp2 NA18965.hp1 NA19077.hp1 |
synonymous_variant | LOW | c.408T>C | p.Asp136Asp | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 3/14 | 529/2504 | 408/1677 | 136/558 | chr14 | 50591066 | |||
chr14:50595623 | G | A | 1 | a0001c0012 | 1 | HG02976.hp1 | synonymous_variant | LOW | c.621G>A | p.Lys207Lys | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/14 | 742/2504 | 621/1677 | 207/558 | chr14 | 50595623 | |||
chr14:50613321 | T | C | 2 | a0001c0006 a0001c0009 |
3 | HG02647.hp2 HG03130.hp1 HG03579.hp2 |
synonymous_variant | LOW | c.693T>C | p.Gly231Gly | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 7/14 | 814/2504 | 693/1677 | 231/558 | chr14 | 50613321 | |||
chr14:50613333 | C | T | 3 | a0001c0004 a0001c0006 a0001c0009 |
13 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(10): Show |
synonymous_variant | LOW | c.705C>T | p.Phe235Phe | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 7/14 | 826/2504 | 705/1677 | 235/558 | chr14 | 50613333 | |||
chr14:50628111 | G | A | 1 | a0001c0006 | 2 | HG02647.hp2 HG03130.hp1 |
synonymous_variant | LOW | c.1200G>A | p.Lys400Lys | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 12/14 | 1321/2504 | 1200/1677 | 400/558 | chr14 | 50628111 | |||
chr14:50628141 | G | A | 1 | a0001c0007 | 2 | HG02809.hp1 HG03486.hp2 |
synonymous_variant | LOW | c.1230G>A | p.Gly410Gly | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 12/14 | 1351/2504 | 1230/1677 | 410/558 | chr14 | 50628141 | |||
chr14:50628222 | T | C | 1 | a0001c0010 | 1 | HG03669.hp1 | synonymous_variant | LOW | c.1311T>C | p.Asp437Asp | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 12/14 | 1432/2504 | 1311/1677 | 437/558 | chr14 | 50628222 | |||
chr14:50628369 | C | T | 1 | a0001c0011 | 1 | NA19003.hp2 | synonymous_variant | LOW | c.1458C>T | p.Ile486Ile | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 12/14 | 1579/2504 | 1458/1677 | 486/558 | chr14 | 50628369 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:50632448 | A | G | 1 | a0001c0002t0008 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*109A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 14/14 | 109 | chr14 | 50632448 | ||||||
chr14:50632551 | T | A | 1 | a0001c0001t0003 | 3 | HG02683.hp2 HG03688.hp2 HG04199.hp1 |
3_prime_UTR_variant | MODIFIER | c.*212T>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 14/14 | 212 | chr14 | 50632551 | ||||||
chr14:50632644 | T | C | 1 | a0001c0001t0002 | 20 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*305T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 14/14 | 305 | chr14 | 50632644 | ||||||
chr14:50632869 | G | A | 1 | a0001c0004t0004 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*530G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 14/14 | 530 | chr14 | 50632869 | ||||||
chr14:50632896 | A | T | 1 | a0001c0003t0007 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*557A>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 14/14 | 557 | chr14 | 50632896 | ||||||
chr14:50632960 | G | A | 1 | a0001c0003t0005 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*621G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 14/14 | 621 | chr14 | 50632960 | ||||||
chr14:50632993 | C | A | 1 | a0001c0002t0006 | 1 | NA18951.hp2 | 3_prime_UTR_variant | MODIFIER | c.*654C>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 14/14 | 654 | chr14 | 50632993 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:50560303 | A | G | 1 | a0001c0001t0001g0286 | 1 | HG01346.hp2 | splice_region_variant&intron_variant | LOW | c.34+4A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50560303 | |||||||
chr14:50560409 | G | C | 35 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0003t0001g0006 others(32): Show |
39 | HG00408.hp2 HG00423.hp2 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.34+110G>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50560409 | |||||||
chr14:50560664 | G | C | 2 | a0001c0001t0001g0010 a0001c0001t0001g0055 |
3 | HG00733.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.34+365G>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50560664 | |||||||
chr14:50560777 | C | G | 2 | a0001c0003t0001g0284 a0001c0003t0001g0285 |
2 | HG00280.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.34+478C>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50560777 | |||||||
chr14:50560797 | C | A | 1 | a0001c0001t0001g0056 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.34+498C>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50560797 | |||||||
chr14:50560800 | G | T | 1 | a0001c0002t0001g0283 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.34+501G>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50560800 | |||||||
chr14:50561270 | T | C | 11 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0057 others(8): Show |
14 | HG01261.hp2 HG01496.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.34+971T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50561270 | |||||||
chr14:50561566 | T | G | 2 | a0001c0001t0002g0066 a0001c0001t0002g0067 |
2 | NA18940.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.34+1267T>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50561566 | |||||||
chr14:50561949 | C | G | 1 | a0001c0004t0001g0054 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.34+1650C>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50561949 | |||||||
chr14:50562027 | G | T | 8 | a0001c0001t0001g0025 a0001c0001t0001g0276 a0001c0001t0001g0277 others(5): Show |
9 | HG01123.hp1 HG02015.hp2 HG03239.hp2 others(6): Show |
intron_variant | MODIFIER | c.34+1728G>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50562027 | |||||||
chr14:50562149 | A | G | 1 | a0001c0001t0001g0275 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.34+1850A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50562149 | |||||||
chr14:50562253 | C | T | 23 | a0001c0003t0001g0006 a0001c0003t0001g0007 a0001c0003t0001g0008 others(20): Show |
26 | HG00408.hp2 HG00423.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.34+1954C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50562253 | |||||||
chr14:50562528 | G | A | 1 | a0001c0002t0001g0012 | 2 | HG02040.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.34+2229G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50562528 | |||||||
chr14:50562600 | C | A | 2 | a0001c0001t0003g0068 a0001c0001t0003g0069 |
2 | HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.34+2301C>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50562600 | |||||||
chr14:50562639 | C | CAACTCAA others(4): Show |
8 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0057 others(5): Show |
11 | HG02257.hp2 HG02280.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.34+2341_34+2351dup others(11): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50562639 | ||||||
chr14:50562995 | A | G | 56 | a0001c0001t0001g0229 a0001c0002t0001g0002 a0001c0002t0001g0004 others(53): Show |
69 | HG00140.hp2 HG00639.hp2 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.34+2696A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50562995 | |||||||
chr14:50563021 | T | A | 1 | a0001c0007t0001g0070 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.34+2722T>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50563021 | |||||||
chr14:50563353 | A | C | 11 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0057 others(8): Show |
14 | HG01261.hp2 HG01496.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.34+3054A>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50563353 | |||||||
chr14:50563483 | T | G | 7 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(4): Show |
7 | HG01361.hp1 HG01433.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.34+3184T>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50563483 | |||||||
chr14:50563728 | C | T | 16 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0018 others(13): Show |
20 | HG01261.hp2 HG01433.hp2 HG01496.hp2 others(17): Show |
intron_variant | MODIFIER | c.34+3429C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50563728 | |||||||
chr14:50563878 | T | C | 1 | a0001c0001t0001g0056 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.34+3579T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50563878 | |||||||
chr14:50564153 | A | G | 10 | a0001c0004t0001g0005 a0001c0004t0001g0030 a0001c0004t0001g0031 others(7): Show |
11 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.34+3854A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50564153 | |||||||
chr14:50564426 | G | C | 1 | a0001c0001t0001g0026 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.34+4127G>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50564426 | |||||||
chr14:50564454 | C | G | 1 | a0001c0003t0005g0225 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.34+4155C>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50564454 | |||||||
chr14:50564465 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.34+4166C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50564465 | |||||||
chr14:50564605 | G | A | 5 | a0001c0001t0001g0013 a0001c0001t0001g0078 a0001c0001t0001g0079 others(2): Show |
6 | HG01123.hp2 HG01943.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.34+4306G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50564605 | |||||||
chr14:50564647 | C | CA | 16 | a0001c0001t0001g0010 a0001c0001t0001g0027 a0001c0001t0001g0073 others(13): Show |
17 | HG00673.hp2 HG01109.hp2 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.34+4378dupA | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50564647 | ||||||
chr14:50564647 | C | CAA | 6 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0077 others(3): Show |
6 | HG01433.hp1 HG01884.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.34+4377_34+4378dup others(2): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50564647 | ||||||
chr14:50564647 | C | CAAA | 8 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0003g0068 others(5): Show |
8 | HG02074.hp1 HG02559.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.34+4376_34+4378dup others(3): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50564647 | ||||||
chr14:50564647 | C | CAAAAAAA others(3): Show |
1 | a0001c0003t0001g0036 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.34+4369_34+4378dup others(10): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50564647 | ||||||
chr14:50564647 | CA | C | 90 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0016 others(87): Show |
98 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.34+4378delA | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50564647 | ||||||
chr14:50564647 | CAA | C | 59 | a0001c0001t0001g0011 a0001c0001t0001g0219 a0001c0001t0001g0220 others(56): Show |
74 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.34+4377_34+4378del others(2): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50564647 | ||||||
chr14:50564647 | CAAAAAAA others(4): Show |
C | 1 | a0001c0003t0001g0039 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.34+4368_34+4378del others(11): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50564647 | ||||||
chr14:50564647 | CAAAAAAA others(5): Show |
C | 18 | a0001c0003t0001g0006 a0001c0003t0001g0007 a0001c0003t0001g0008 others(15): Show |
21 | HG00408.hp2 HG00423.hp2 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.34+4367_34+4378del others(12): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50564647 | ||||||
chr14:50564647 | CAAAAAAA others(6): Show |
C | 1 | a0001c0003t0001g0053 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.34+4366_34+4378del others(13): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50564647 | ||||||
chr14:50564647 | CAAAAAAA others(9): Show |
C | 1 | a0001c0001t0001g0224 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.34+4363_34+4378del others(16): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50564647 | ||||||
chr14:50564678 | G | A | 1 | a0001c0008t0001g0146 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.34+4379G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50564678 | |||||||
chr14:50564751 | C | A | 10 | a0001c0003t0001g0017 a0001c0003t0001g0097 a0001c0003t0001g0098 others(7): Show |
11 | HG00639.hp1 HG00642.hp2 HG00733.hp2 others(8): Show |
intron_variant | MODIFIER | c.34+4452C>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50564751 | |||||||
chr14:50564855 | G | C | 10 | a0001c0004t0001g0005 a0001c0004t0001g0030 a0001c0004t0001g0031 others(7): Show |
11 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.34+4556G>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50564855 | |||||||
chr14:50564981 | A | G | 1 | a0001c0008t0001g0146 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.34+4682A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50564981 | |||||||
chr14:50565014 | C | T | 1 | a0001c0002t0001g0274 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.34+4715C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50565014 | |||||||
chr14:50565238 | C | T | 13 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(10): Show |
13 | HG00597.hp2 HG00673.hp1 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.34+4939C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50565238 | |||||||
chr14:50565450 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.34+5151A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50565450 | |||||||
chr14:50565484 | C | CA | 7 | a0001c0001t0001g0205 a0001c0002t0001g0024 a0001c0002t0001g0235 others(4): Show |
8 | HG02738.hp1 NA18952.hp1 NA18960.hp2 others(5): Show |
intron_variant | MODIFIER | c.34+5198dupA | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50565484 | ||||||
chr14:50565484 | C | CAA | 211 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(208): Show |
233 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.34+5197_34+5198dup others(2): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50565484 | ||||||
chr14:50565531 | T | C | 2 | a0001c0003t0001g0040 a0001c0003t0001g0041 |
2 | HG00408.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.34+5232T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50565531 | |||||||
chr14:50565549 | T | C | 2 | a0001c0001t0001g0010 a0001c0001t0001g0055 |
3 | HG00733.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.34+5250T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50565549 | |||||||
chr14:50565663 | C | A | 1 | a0001c0003t0001g0153 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.34+5364C>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50565663 | |||||||
chr14:50565795 | A | C | 1 | a0001c0004t0004g0141 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.34+5496A>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50565795 | |||||||
chr14:50565988 | T | G | 2 | a0001c0001t0001g0010 a0001c0001t0001g0055 |
3 | HG00733.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.34+5689T>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50565988 | |||||||
chr14:50566074 | T | C | 3 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0076 |
3 | HG01361.hp1 HG02896.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.34+5775T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50566074 | |||||||
chr14:50566084 | G | A | 57 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(54): Show |
66 | HG00408.hp2 HG00423.hp2 HG00733.hp1 others(63): Show |
intron_variant | MODIFIER | c.34+5785G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50566084 | |||||||
chr14:50566251 | GC | G | 230 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(227): Show |
249 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.34+5958delC | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50566251 | ||||||
chr14:50566253 | C | G | 1 | a0001c0001t0001g0138 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.34+5954C>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50566253 | |||||||
chr14:50566455 | G | C | 7 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(4): Show |
7 | HG01361.hp1 HG01433.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.34+6156G>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50566455 | |||||||
chr14:50566792 | C | T | 285 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(282): Show |
317 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.34+6493C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50566792 | |||||||
chr14:50566854 | TTATATTT others(7): Show |
T | 2 | a0001c0007t0001g0070 a0001c0007t0001g0228 |
2 | HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.34+6557_34+6570del others(14): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50566854 | ||||||
chr14:50566897 | G | A | 1 | a0001c0003t0001g0053 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.34+6598G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50566897 | |||||||
chr14:50566904 | A | G | 5 | a0001c0001t0001g0083 a0001c0001t0001g0085 a0001c0001t0001g0086 others(2): Show |
5 | HG01884.hp2 HG02559.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.34+6605A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50566904 | |||||||
chr14:50567017 | C | T | 3 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0009t0001g0084 |
3 | HG02135.hp2 HG03579.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.34+6718C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50567017 | |||||||
chr14:50567550 | A | G | 1 | a0001c0003t0001g0204 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.34+7251A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50567550 | |||||||
chr14:50567620 | A | T | 219 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(216): Show |
242 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.34+7321A>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50567620 | |||||||
chr14:50567643 | A | T | 1 | a0001c0002t0001g0269 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.34+7344A>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50567643 | |||||||
chr14:50567831 | T | C | 1 | a0001c0001t0001g0026 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.34+7532T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50567831 | |||||||
chr14:50567899 | C | A | 54 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0012 others(51): Show |
67 | HG00140.hp2 HG00639.hp2 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.34+7600C>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50567899 | |||||||
chr14:50567947 | T | A | 1 | a0001c0008t0001g0146 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.34+7648T>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50567947 | |||||||
chr14:50567992 | A | T | 3 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 |
3 | HG02257.hp1 HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.34+7693A>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50567992 | |||||||
chr14:50568020 | A | G | 3 | a0001c0001t0001g0018 a0001c0001t0001g0226 a0001c0001t0001g0227 |
4 | HG01433.hp2 HG01891.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.34+7721A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50568020 | |||||||
chr14:50568104 | A | G | 3 | a0001c0001t0001g0018 a0001c0001t0001g0226 a0001c0001t0001g0227 |
4 | HG01433.hp2 HG01891.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.34+7805A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50568104 | |||||||
chr14:50568216 | C | T | 2 | a0001c0001t0003g0068 a0001c0001t0003g0069 |
2 | HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.34+7917C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50568216 | |||||||
chr14:50568282 | G | T | 1 | a0001c0002t0001g0267 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.34+7983G>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50568282 | |||||||
chr14:50568299 | G | A | 1 | a0001c0006t0001g0028 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.34+8000G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50568299 | |||||||
chr14:50568745 | C | T | 2 | a0001c0001t0001g0010 a0001c0001t0001g0055 |
3 | HG00733.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.34+8446C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50568745 | |||||||
chr14:50568976 | C | T | 1 | a0001c0001t0002g0066 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.34+8677C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50568976 | |||||||
chr14:50569010 | T | A | 1 | a0001c0001t0001g0154 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.34+8711T>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50569010 | |||||||
chr14:50569117 | G | A | 1 | a0001c0009t0001g0084 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.34+8818G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50569117 | |||||||
chr14:50569191 | C | CA | 18 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0018 others(15): Show |
22 | HG00639.hp2 HG01261.hp2 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.34+8903dupA | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50569191 | ||||||
chr14:50569268 | T | G | 284 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(281): Show |
316 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.34+8969T>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50569268 | |||||||
chr14:50569418 | C | CAA | 14 | a0001c0002t0001g0022 a0001c0002t0001g0023 a0001c0002t0001g0234 others(11): Show |
16 | HG01256.hp1 HG01358.hp1 HG01952.hp2 others(13): Show |
intron_variant | MODIFIER | c.34+9132_34+9133dup others(2): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50569418 | ||||||
chr14:50569418 | C | CAAA | 39 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0012 others(36): Show |
50 | HG00639.hp2 HG00735.hp1 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.34+9131_34+9133dup others(3): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50569418 | ||||||
chr14:50569533 | A | G | 3 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 |
3 | HG02257.hp1 HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.34+9234A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50569533 | |||||||
chr14:50569795 | T | C | 1 | a0001c0001t0001g0224 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.34+9496T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50569795 | |||||||
chr14:50569902 | T | C | 284 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(281): Show |
316 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.34+9603T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50569902 | |||||||
chr14:50569903 | G | A | 1 | a0001c0001t0001g0099 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.34+9604G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50569903 | |||||||
chr14:50569947 | G | A | 1 | a0001c0001t0001g0155 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.34+9648G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50569947 | |||||||
chr14:50570117 | A | G | 1 | a0001c0001t0001g0200 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.34+9818A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50570117 | |||||||
chr14:50570232 | T | C | 54 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0012 others(51): Show |
67 | HG00140.hp2 HG00639.hp2 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.34+9933T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50570232 | |||||||
chr14:50570234 | A | T | 3 | a0001c0001t0001g0016 a0001c0001t0001g0199 a0001c0001t0001g0286 |
4 | HG01257.hp1 HG01258.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.34+9935A>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50570234 | |||||||
chr14:50570555 | G | C | 1 | a0001c0001t0001g0207 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.34+10256G>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50570555 | |||||||
chr14:50571047 | T | C | 257 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(254): Show |
284 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.34+10748T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50571047 | |||||||
chr14:50571413 | G | A | 2 | a0001c0001t0001g0224 a0001c0003t0001g0063 |
2 | HG01261.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.34+11114G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50571413 | |||||||
chr14:50571721 | T | G | 2 | a0001c0001t0003g0068 a0001c0001t0003g0069 |
2 | HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.34+11422T>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50571721 | |||||||
chr14:50571823 | G | A | 1 | a0001c0001t0001g0100 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.34+11524G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50571823 | |||||||
chr14:50571890 | T | G | 1 | a0001c0001t0001g0079 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.34+11591T>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50571890 | |||||||
chr14:50572138 | C | T | 5 | a0001c0001t0001g0083 a0001c0001t0001g0085 a0001c0001t0001g0086 others(2): Show |
5 | HG01884.hp2 HG02559.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.34+11839C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50572138 | |||||||
chr14:50572223 | G | C | 11 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0057 others(8): Show |
14 | HG01261.hp2 HG01496.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.34+11924G>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50572223 | |||||||
chr14:50572406 | T | G | 1 | a0001c0001t0002g0156 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.34+12107T>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50572406 | |||||||
chr14:50572451 | T | C | 2 | a0001c0001t0001g0010 a0001c0001t0001g0055 |
3 | HG00733.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.34+12152T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50572451 | |||||||
chr14:50572549 | C | G | 3 | a0001c0003t0001g0063 a0001c0003t0001g0064 a0001c0003t0001g0065 |
3 | HG01261.hp2 HG01496.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.34+12250C>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50572549 | |||||||
chr14:50572677 | C | T | 3 | a0001c0003t0001g0063 a0001c0003t0001g0064 a0001c0003t0001g0065 |
3 | HG01261.hp2 HG01496.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.34+12378C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50572677 | |||||||
chr14:50572704 | C | T | 1 | a0001c0001t0001g0216 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.34+12405C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50572704 | |||||||
chr14:50572777 | A | G | 2 | a0001c0003t0001g0136 a0001c0003t0001g0198 |
2 | HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.34+12478A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50572777 | |||||||
chr14:50572901 | G | C | 2 | a0001c0002t0001g0019 a0001c0002t0001g0237 |
3 | HG03490.hp1 HG03492.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.34+12602G>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50572901 | |||||||
chr14:50572996 | G | A | 1 | a0001c0001t0001g0026 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.34+12697G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50572996 | |||||||
chr14:50573144 | G | A | 1 | a0001c0003t0001g0042 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.34+12845G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50573144 | |||||||
chr14:50573219 | C | T | 2 | a0001c0007t0001g0070 a0001c0007t0001g0228 |
2 | HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.34+12920C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50573219 | |||||||
chr14:50573229 | A | G | 1 | a0001c0004t0001g0054 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.34+12930A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50573229 | |||||||
chr14:50573255 | A | G | 2 | a0001c0001t0001g0135 a0001c0001t0001g0197 |
2 | HG02615.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.34+12956A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50573255 | |||||||
chr14:50573332 | T | C | 1 | a0001c0001t0001g0101 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.34+13033T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50573332 | |||||||
chr14:50573480 | A | G | 1 | a0001c0001t0001g0215 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.34+13181A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50573480 | |||||||
chr14:50573606 | AT | A | 3 | a0001c0001t0001g0018 a0001c0001t0001g0226 a0001c0001t0001g0227 |
4 | HG01433.hp2 HG01891.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.34+13312delT | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50573606 | ||||||
chr14:50573617 | G | A | 1 | a0001c0002t0001g0238 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.34+13318G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50573617 | |||||||
chr14:50574001 | G | C | 3 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 |
3 | HG02257.hp1 HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.34+13702G>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50574001 | |||||||
chr14:50574034 | G | A | 2 | a0001c0001t0001g0010 a0001c0001t0001g0055 |
3 | HG00733.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.34+13735G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50574034 | |||||||
chr14:50574120 | A | G | 1 | a0001c0001t0001g0099 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.35-13711A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50574120 | |||||||
chr14:50574135 | G | T | 2 | a0001c0007t0001g0070 a0001c0007t0001g0228 |
2 | HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.35-13696G>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50574135 | |||||||
chr14:50574324 | C | A | 1 | a0001c0003t0001g0037 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.35-13507C>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50574324 | |||||||
chr14:50574326 | A | G | 5 | a0001c0001t0001g0015 a0001c0001t0001g0131 a0001c0001t0001g0132 others(2): Show |
6 | HG01257.hp2 HG01517.hp1 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.35-13505A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50574326 | |||||||
chr14:50574370 | C | T | 2 | a0001c0002t0001g0004 a0001c0002t0001g0265 |
4 | HG00741.hp2 HG01975.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.35-13461C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50574370 | |||||||
chr14:50574843 | C | T | 1 | a0001c0001t0001g0026 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.35-12988C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50574843 | |||||||
chr14:50574908 | A | AGT | 3 | a0001c0002t0001g0012 a0001c0002t0001g0238 a0001c0002t0001g0273 |
4 | HG02040.hp1 NA19001.hp2 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.35-12894_35-12893d others(4): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50574908 | ||||||
chr14:50574908 | AGT | A | 24 | a0001c0001t0001g0003 a0001c0001t0001g0026 a0001c0001t0001g0057 others(21): Show |
26 | HG00597.hp2 HG02015.hp2 HG02257.hp2 others(23): Show |
intron_variant | MODIFIER | c.35-12894_35-12893d others(4): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50574908 | ||||||
chr14:50574908 | AGTGT | A | 18 | a0001c0001t0001g0011 a0001c0001t0001g0125 a0001c0001t0001g0126 others(15): Show |
19 | HG00642.hp1 HG01361.hp2 HG01496.hp2 others(16): Show |
intron_variant | MODIFIER | c.35-12896_35-12893d others(6): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50574908 | ||||||
chr14:50574908 | AGTGTGT | A | 12 | a0001c0001t0001g0025 a0001c0001t0001g0088 a0001c0001t0001g0106 others(9): Show |
13 | HG00597.hp1 HG00738.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.35-12898_35-12893d others(8): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50574908 | ||||||
chr14:50574913 | G | A | 5 | a0001c0001t0001g0071 a0001c0001t0001g0073 a0001c0001t0001g0074 others(2): Show |
5 | HG01361.hp1 HG02145.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.35-12918G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50574913 | |||||||
chr14:50574929 | G | A | 1 | a0001c0012t0001g0268 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.35-12902G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50574929 | |||||||
chr14:50574929 | GTGTGTGT others(3): Show |
G | 1 | a0001c0001t0001g0219 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.35-12900_35-12891d others(12): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50574929 | ||||||
chr14:50574931 | G | A | 3 | a0001c0003t0001g0147 a0001c0003t0001g0218 a0001c0012t0001g0268 |
3 | HG01109.hp1 HG02976.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.35-12900G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50574931 | |||||||
chr14:50574931 | G | GTA | 6 | a0001c0001t0001g0087 a0001c0003t0001g0105 a0001c0003t0001g0157 others(3): Show |
6 | HG00280.hp1 HG01943.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.35-12899_35-12898i others(4): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50574931 | ||||||
chr14:50574931 | G | GTATA | 3 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0003t0001g0150 |
3 | HG00140.hp1 HG00735.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.35-12899_35-12898i others(6): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50574931 | ||||||
chr14:50574931 | G | GTATATAT others(1): Show |
3 | a0001c0003t0001g0148 a0001c0003t0001g0149 a0001c0003t0001g0284 |
3 | HG00639.hp1 HG01167.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.35-12899_35-12898i others(10): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50574931 | ||||||
chr14:50574931 | G | GTATATAT others(3): Show |
1 | a0001c0001t0001g0102 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.35-12899_35-12898i others(12): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50574931 | ||||||
chr14:50574931 | GTGTGTGT others(1): Show |
G | 12 | a0001c0001t0001g0015 a0001c0001t0001g0089 a0001c0001t0001g0101 others(9): Show |
13 | HG01192.hp1 HG01257.hp2 HG01517.hp1 others(10): Show |
intron_variant | MODIFIER | c.35-12898_35-12891d others(10): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50574931 | ||||||
chr14:50574931 | GTGTGTGT others(3): Show |
G | 26 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0090 others(23): Show |
28 | HG00280.hp2 HG00438.hp2 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.35-12898_35-12889d others(12): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50574931 | ||||||
chr14:50574931 | GTGTGTGT others(5): Show |
G | 1 | a0001c0001t0001g0082 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.35-12898_35-12887d others(14): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50574931 | ||||||
chr14:50574931 | GTGTGTGT others(7): Show |
G | 1 | a0001c0001t0003g0124 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.35-12898_35-12885d others(16): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50574931 | ||||||
chr14:50574931 | GTGTGTGT others(15): Show |
G | 2 | a0001c0006t0001g0028 a0001c0006t0001g0029 |
2 | HG02647.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.35-12898_35-12877d others(24): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50574931 | ||||||
chr14:50574933 | G | A | 27 | a0001c0001t0001g0087 a0001c0001t0001g0102 a0001c0001t0001g0103 others(24): Show |
27 | HG00140.hp1 HG00280.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.35-12898G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50574933 | |||||||
chr14:50574933 | G | GTA | 6 | a0001c0001t0001g0083 a0001c0001t0001g0085 a0001c0001t0001g0086 others(3): Show |
7 | HG00642.hp2 HG00733.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.35-12897_35-12896i others(4): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50574933 | ||||||
chr14:50574933 | G | GTATATA | 5 | a0001c0001t0001g0100 a0001c0001t0001g0144 a0001c0003t0001g0038 others(2): Show |
5 | HG00673.hp1 HG01884.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.35-12897_35-12896i others(8): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50574933 | ||||||
chr14:50574933 | GTGTGTA | G | 8 | a0001c0001t0001g0183 a0001c0001t0001g0190 a0001c0001t0001g0210 others(5): Show |
10 | HG00423.hp1 HG01261.hp2 HG03041.hp2 others(7): Show |
intron_variant | MODIFIER | c.35-12896_35-12891d others(8): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50574933 | ||||||
chr14:50574933 | GTGTGTAT others(1): Show |
G | 18 | a0001c0001t0001g0056 a0001c0001t0001g0099 a0001c0001t0001g0145 others(15): Show |
18 | HG00408.hp1 HG01243.hp2 HG01993.hp1 others(15): Show |
intron_variant | MODIFIER | c.35-12896_35-12889d others(10): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50574933 | ||||||
chr14:50574933 | GTGTGTAT others(3): Show |
G | 8 | a0001c0001t0001g0001 a0001c0001t0001g0129 a0001c0001t0001g0130 others(5): Show |
8 | HG00438.hp1 HG01069.hp2 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.35-12896_35-12887d others(12): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50574933 | ||||||
chr14:50574933 | GTGTGTAT others(9): Show |
G | 1 | a0001c0001t0001g0138 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.35-12896_35-12881d others(18): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50574933 | ||||||
chr14:50574935 | G | A | 57 | a0001c0001t0001g0062 a0001c0001t0001g0072 a0001c0001t0001g0083 others(54): Show |
59 | HG00140.hp1 HG00280.hp1 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.35-12896G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50574935 | |||||||
chr14:50574935 | G | GTA | 4 | a0001c0002t0001g0020 a0001c0002t0001g0262 a0001c0003t0001g0046 others(1): Show |
5 | HG01952.hp2 HG02071.hp2 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.35-12895_35-12894i others(4): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50574935 | ||||||
chr14:50574935 | G | GTATA | 9 | a0001c0001t0001g0071 a0001c0001t0001g0074 a0001c0001t0001g0076 others(6): Show |
10 | HG00408.hp2 HG00423.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.35-12895_35-12894i others(6): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50574935 | ||||||
chr14:50574935 | G | GTATATA | 5 | a0001c0002t0001g0283 a0001c0003t0001g0007 a0001c0003t0001g0039 others(2): Show |
5 | HG01358.hp1 HG02818.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.35-12895_35-12894i others(8): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50574935 | ||||||
chr14:50574935 | G | GTATATAT others(3): Show |
2 | a0001c0001t0001g0081 a0001c0003t0001g0048 |
2 | HG02004.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.35-12895_35-12894i others(12): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50574935 | ||||||
chr14:50574935 | G | GTATATAT others(5): Show |
1 | a0001c0003t0001g0006 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.35-12895_35-12894i others(14): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50574935 | ||||||
chr14:50574935 | G | GTATATAT others(7): Show |
1 | a0001c0003t0001g0041 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.35-12895_35-12894i others(16): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50574935 | ||||||
chr14:50574935 | G | GTATATAT others(9): Show |
1 | a0001c0003t0001g0050 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.35-12895_35-12894i others(18): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50574935 | ||||||
chr14:50574935 | G | GTATATAT others(13): Show |
1 | a0001c0003t0001g0047 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.35-12895_35-12894i others(22): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50574935 | ||||||
chr14:50574935 | G | GTATGTAT others(9): Show |
1 | a0001c0003t0001g0051 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.35-12895_35-12894i others(18): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50574935 | ||||||
chr14:50574935 | GTGTA | G | 9 | a0001c0001t0001g0079 a0001c0001t0001g0182 a0001c0002t0001g0022 others(6): Show |
10 | HG01943.hp1 HG01993.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.35-12894_35-12891d others(6): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50574935 | ||||||
chr14:50574935 | GTGTATAT others(1): Show |
G | 4 | a0001c0001t0001g0013 a0001c0001t0001g0078 a0001c0001t0001g0080 others(1): Show |
5 | HG01123.hp2 HG01952.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.35-12894_35-12887d others(10): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50574935 | ||||||
chr14:50574935 | GTGTATAT others(7): Show |
G | 1 | a0001c0009t0001g0084 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.35-12894_35-12881d others(16): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50574935 | ||||||
chr14:50574937 | G | A | 114 | a0001c0001t0001g0003 a0001c0001t0001g0027 a0001c0001t0001g0057 others(111): Show |
121 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.35-12894G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50574937 | |||||||
chr14:50574937 | G | GTA | 9 | a0001c0002t0001g0004 a0001c0002t0001g0019 a0001c0002t0001g0024 others(6): Show |
11 | HG00741.hp2 HG01978.hp1 HG02293.hp1 others(8): Show |
intron_variant | MODIFIER | c.35-12856_35-12855d others(4): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50574937 | ||||||
chr14:50574937 | G | GTATA | 4 | a0001c0002t0001g0021 a0001c0002t0001g0237 a0001c0002t0001g0243 others(1): Show |
5 | HG01243.hp1 HG01255.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.35-12858_35-12855d others(6): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50574937 | ||||||
chr14:50574937 | G | GTATATA | 7 | a0001c0002t0001g0002 a0001c0002t0001g0023 a0001c0002t0001g0256 others(4): Show |
9 | HG00735.hp1 HG02027.hp1 HG02683.hp1 others(6): Show |
intron_variant | MODIFIER | c.35-12860_35-12855d others(8): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50574937 | ||||||
chr14:50574937 | G | GTATATAT others(1): Show |
3 | a0001c0002t0001g0002 a0001c0002t0001g0242 a0001c0004t0004g0141 |
3 | HG03098.hp2 NA18988.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.35-12862_35-12855d others(10): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50574937 | ||||||
chr14:50574937 | G | GTATATAT others(3): Show |
2 | a0001c0002t0001g0251 a0001c0003t0001g0042 |
2 | HG02135.hp1 NA18981.hp1 |
intron_variant | MODIFIER | c.35-12864_35-12855d others(12): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50574937 | ||||||
chr14:50574937 | G | GTATATAT others(5): Show |
1 | a0001c0002t0001g0002 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.35-12866_35-12855d others(14): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50574937 | ||||||
chr14:50574937 | G | GTATATAT others(7): Show |
2 | a0001c0001t0001g0203 a0001c0001t0003g0068 |
2 | HG02922.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.35-12868_35-12855d others(16): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50574937 | ||||||
chr14:50574937 | G | GTATATAT others(9): Show |
1 | a0001c0001t0001g0202 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.35-12870_35-12855d others(18): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50574937 | ||||||
chr14:50574937 | G | GTGTATAT others(5): Show |
3 | a0001c0001t0001g0201 a0001c0004t0001g0030 a0001c0004t0001g0033 |
3 | HG02896.hp2 HG02897.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.35-12893_35-12892i others(14): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50574937 | ||||||
chr14:50574937 | G | GTGTATAT others(11): Show |
2 | a0001c0004t0001g0005 a0001c0004t0001g0035 |
2 | NA18522.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.35-12893_35-12892i others(20): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50574937 | ||||||
chr14:50574937 | G | GTGTATAT others(15): Show |
1 | a0001c0004t0001g0005 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.35-12893_35-12892i others(24): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50574937 | ||||||
chr14:50574937 | G | GTGTGTAT others(3): Show |
1 | a0001c0002t0001g0023 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.35-12893_35-12892i others(12): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50574937 | ||||||
chr14:50574937 | G | GTGTGTAT others(13): Show |
1 | a0001c0004t0001g0034 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.35-12893_35-12892i others(22): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50574937 | ||||||
chr14:50574937 | GTATA | G | 4 | a0001c0002t0001g0235 a0001c0002t0001g0266 a0001c0002t0001g0267 others(1): Show |
4 | HG00140.hp2 HG02280.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.35-12858_35-12855d others(6): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50574937 | ||||||
chr14:50574937 | GTATATAT others(1): Show |
G | 3 | a0001c0001t0001g0018 a0001c0001t0001g0226 a0001c0001t0001g0227 |
4 | HG01433.hp2 HG01891.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.35-12862_35-12855d others(10): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50574937 | ||||||
chr14:50574937 | GTATATAT others(3): Show |
G | 1 | a0001c0001t0001g0075 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.35-12864_35-12855d others(12): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50574937 | ||||||
chr14:50574937 | GTATATAT others(5): Show |
G | 2 | a0001c0001t0001g0010 a0001c0001t0001g0055 |
3 | HG00733.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.35-12866_35-12855d others(14): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50574937 | ||||||
chr14:50574939 | A | G | 1 | a0001c0002t0001g0238 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.35-12892A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50574939 | |||||||
chr14:50574951 | A | G | 2 | a0001c0001t0001g0010 a0001c0001t0001g0055 |
3 | HG00733.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.35-12880A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50574951 | |||||||
chr14:50574955 | A | G | 2 | a0001c0001t0001g0010 a0001c0001t0001g0055 |
3 | HG00733.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.35-12876A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50574955 | |||||||
chr14:50574971 | A | ATATATAT others(11): Show |
1 | a0001c0004t0001g0031 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.35-12855_35-12854i others(20): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50574971 | ||||||
chr14:50574971 | A | ATATATAT others(3): Show |
1 | a0001c0004t0001g0032 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.35-12855_35-12854i others(12): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50574971 | ||||||
chr14:50574971 | A | C | 7 | a0001c0004t0001g0005 a0001c0004t0001g0030 a0001c0004t0001g0033 others(4): Show |
8 | HG02055.hp1 HG02647.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.35-12860A>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50574971 | |||||||
chr14:50574989 | G | A | 3 | a0001c0001t0001g0087 a0001c0001t0001g0102 a0001c0001t0001g0103 |
3 | HG02109.hp1 HG02809.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.35-12842G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50574989 | |||||||
chr14:50575621 | T | A | 3 | a0001c0001t0001g0087 a0001c0001t0001g0102 a0001c0001t0001g0103 |
3 | HG02109.hp1 HG02809.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.35-12210T>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50575621 | |||||||
chr14:50575754 | AT | A | 170 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(167): Show |
181 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.35-12068delT | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50575754 | ||||||
chr14:50576005 | C | T | 1 | a0001c0001t0001g0197 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.35-11826C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50576005 | |||||||
chr14:50576037 | C | A | 2 | a0001c0001t0001g0010 a0001c0001t0001g0055 |
3 | HG00733.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.35-11794C>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50576037 | |||||||
chr14:50576067 | A | G | 1 | a0001c0004t0004g0141 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.35-11764A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50576067 | |||||||
chr14:50576071 | A | G | 171 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(168): Show |
182 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.35-11760A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50576071 | |||||||
chr14:50576188 | T | C | 2 | a0001c0002t0001g0004 a0001c0002t0001g0265 |
4 | HG00741.hp2 HG01975.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.35-11643T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50576188 | |||||||
chr14:50576272 | A | G | 1 | a0001c0003t0001g0196 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.35-11559A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50576272 | |||||||
chr14:50576280 | CATTTTCA others(6): Show |
C | 11 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0057 others(8): Show |
14 | HG01261.hp2 HG01496.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.35-11541_35-11529d others(15): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50576280 | ||||||
chr14:50576438 | C | A | 1 | a0001c0001t0002g0174 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.35-11393C>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50576438 | |||||||
chr14:50576491 | A | C | 2 | a0001c0001t0001g0127 a0001c0001t0001g0128 |
2 | HG01361.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.35-11340A>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50576491 | |||||||
chr14:50576637 | A | G | 1 | a0001c0001t0001g0077 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.35-11194A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50576637 | |||||||
chr14:50576733 | G | A | 2 | a0001c0001t0001g0138 a0001c0009t0001g0084 |
2 | HG03579.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.35-11098G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50576733 | |||||||
chr14:50576945 | CATA | C | 9 | a0001c0003t0001g0043 a0001c0003t0001g0105 a0001c0003t0001g0153 others(6): Show |
9 | HG02145.hp1 HG02630.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.35-10882_35-10880d others(5): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50576945 | ||||||
chr14:50577051 | A | G | 1 | a0001c0001t0001g0138 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.35-10780A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50577051 | |||||||
chr14:50577102 | G | A | 2 | a0001c0004t0004g0141 a0001c0008t0001g0146 |
2 | HG02280.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.35-10729G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50577102 | |||||||
chr14:50577123 | C | T | 1 | a0001c0002t0001g0256 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.35-10708C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50577123 | |||||||
chr14:50577155 | C | T | 2 | a0001c0001t0003g0068 a0001c0001t0003g0069 |
2 | HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.35-10676C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50577155 | |||||||
chr14:50577208 | G | A | 2 | a0001c0007t0001g0070 a0001c0007t0001g0228 |
2 | HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.35-10623G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50577208 | |||||||
chr14:50577264 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.35-10567G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50577264 | |||||||
chr14:50577298 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.35-10533G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50577298 | |||||||
chr14:50577579 | A | G | 2 | a0001c0001t0001g0027 a0001c0001t0001g0140 |
2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.35-10252A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50577579 | |||||||
chr14:50577896 | T | A | 1 | a0001c0001t0001g0161 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.35-9935T>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50577896 | |||||||
chr14:50577911 | C | A | 95 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(92): Show |
105 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.35-9920C>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50577911 | |||||||
chr14:50578056 | C | A | 62 | a0001c0001t0001g0026 a0001c0003t0001g0006 a0001c0003t0001g0007 others(59): Show |
67 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.35-9775C>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50578056 | |||||||
chr14:50578134 | G | C | 62 | a0001c0001t0001g0026 a0001c0003t0001g0006 a0001c0003t0001g0007 others(59): Show |
67 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.35-9697G>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50578134 | |||||||
chr14:50578166 | T | C | 1 | a0001c0001t0001g0276 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.35-9665T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50578166 | |||||||
chr14:50578202 | G | T | 3 | a0001c0001t0001g0018 a0001c0001t0001g0226 a0001c0001t0001g0227 |
4 | HG01433.hp2 HG01891.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.35-9629G>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50578202 | |||||||
chr14:50578324 | C | T | 62 | a0001c0001t0001g0026 a0001c0003t0001g0006 a0001c0003t0001g0007 others(59): Show |
67 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.35-9507C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50578324 | |||||||
chr14:50578632 | C | T | 13 | a0001c0001t0001g0082 a0001c0001t0001g0093 a0001c0001t0001g0112 others(10): Show |
13 | HG00597.hp1 HG01109.hp2 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.35-9199C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50578632 | |||||||
chr14:50578768 | A | G | 1 | a0001c0002t0001g0283 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.35-9063A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50578768 | |||||||
chr14:50578833 | T | C | 2 | a0001c0001t0003g0068 a0001c0001t0003g0069 |
2 | HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.35-8998T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50578833 | |||||||
chr14:50578847 | A | G | 1 | a0001c0001t0001g0026 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.35-8984A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50578847 | |||||||
chr14:50579119 | C | T | 50 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0025 others(47): Show |
53 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.35-8712C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50579119 | |||||||
chr14:50579322 | C | G | 138 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(135): Show |
147 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.35-8509C>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50579322 | |||||||
chr14:50579603 | C | T | 3 | a0001c0002t0001g0232 a0001c0002t0001g0254 a0001c0002t0001g0255 |
3 | NA18939.hp1 NA18957.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.35-8228C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50579603 | |||||||
chr14:50579756 | G | A | 136 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(133): Show |
145 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.35-8075G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50579756 | |||||||
chr14:50579808 | G | C | 136 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(133): Show |
145 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.35-8023G>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50579808 | |||||||
chr14:50580027 | A | C | 3 | a0001c0001t0001g0018 a0001c0001t0001g0226 a0001c0001t0001g0227 |
4 | HG01433.hp2 HG01891.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.35-7804A>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50580027 | |||||||
chr14:50580060 | A | G | 1 | a0001c0002t0001g0230 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.35-7771A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50580060 | |||||||
chr14:50580314 | G | A | 3 | a0001c0003t0001g0036 a0001c0003t0001g0037 a0001c0003t0001g0038 |
3 | HG03139.hp1 NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.35-7517G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50580314 | |||||||
chr14:50580391 | G | A | 1 | a0001c0009t0001g0084 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.35-7440G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50580391 | |||||||
chr14:50580507 | G | A | 3 | a0001c0001t0001g0018 a0001c0001t0001g0226 a0001c0001t0001g0227 |
4 | HG01433.hp2 HG01891.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.35-7324G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50580507 | |||||||
chr14:50580701 | T | A | 2 | a0001c0001t0001g0014 a0001c0001t0001g0090 |
3 | HG01358.hp2 HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.35-7130T>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50580701 | |||||||
chr14:50580758 | T | G | 10 | a0001c0004t0001g0005 a0001c0004t0001g0030 a0001c0004t0001g0031 others(7): Show |
11 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.35-7073T>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50580758 | |||||||
chr14:50580785 | G | A | 2 | a0001c0001t0001g0010 a0001c0001t0001g0055 |
3 | HG00733.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.35-7046G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50580785 | |||||||
chr14:50580876 | TC | T | 3 | a0001c0001t0001g0018 a0001c0001t0001g0226 a0001c0001t0001g0227 |
4 | HG01433.hp2 HG01891.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.35-6954delC | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50580876 | |||||||
chr14:50581009 | A | T | 2 | a0001c0003t0001g0009 a0001c0003t0001g0052 |
3 | HG01069.hp1 HG01071.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.35-6822A>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50581009 | |||||||
chr14:50581219 | A | G | 1 | a0001c0001t0001g0114 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.35-6612A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50581219 | |||||||
chr14:50581346 | C | T | 3 | a0001c0001t0001g0018 a0001c0001t0001g0226 a0001c0001t0001g0227 |
4 | HG01433.hp2 HG01891.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.35-6485C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50581346 | |||||||
chr14:50581355 | T | G | 1 | a0001c0001t0003g0069 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.35-6476T>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50581355 | |||||||
chr14:50581361 | T | G | 1 | a0001c0001t0001g0026 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.35-6470T>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50581361 | |||||||
chr14:50581674 | G | A | 1 | a0001c0005t0001g0240 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.35-6157G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50581674 | |||||||
chr14:50581728 | T | C | 1 | a0001c0001t0001g0027 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.35-6103T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50581728 | |||||||
chr14:50581743 | G | T | 1 | a0001c0003t0001g0105 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.35-6088G>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50581743 | |||||||
chr14:50581902 | T | G | 2 | a0001c0001t0001g0027 a0001c0001t0001g0140 |
2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.35-5929T>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50581902 | |||||||
chr14:50582005 | T | G | 95 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(92): Show |
105 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.35-5826T>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50582005 | |||||||
chr14:50582006 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.35-5825C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50582006 | |||||||
chr14:50582354 | G | C | 13 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0057 others(10): Show |
16 | HG01261.hp2 HG01496.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.35-5477G>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50582354 | |||||||
chr14:50582590 | GT | G | 228 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(225): Show |
246 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.35-5226delT | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 50582590 | ||||||
chr14:50582679 | G | A | 10 | a0001c0001t0001g0016 a0001c0001t0001g0125 a0001c0001t0001g0162 others(7): Show |
11 | HG00741.hp1 HG01071.hp2 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.35-5152G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50582679 | |||||||
chr14:50582686 | A | G | 13 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0057 others(10): Show |
16 | HG01261.hp2 HG01496.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.35-5145A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50582686 | |||||||
chr14:50582825 | T | G | 1 | a0001c0003t0001g0218 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.35-5006T>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50582825 | |||||||
chr14:50582873 | T | C | 9 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(6): Show |
9 | HG01361.hp1 HG01433.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.35-4958T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50582873 | |||||||
chr14:50582892 | G | T | 9 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(6): Show |
9 | HG01361.hp1 HG01433.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.35-4939G>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50582892 | |||||||
chr14:50582930 | C | T | 231 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(228): Show |
250 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.35-4901C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50582930 | |||||||
chr14:50583336 | A | G | 1 | a0001c0003t0001g0051 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.35-4495A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50583336 | |||||||
chr14:50583754 | G | A | 2 | a0001c0003t0001g0009 a0001c0003t0001g0052 |
3 | HG01069.hp1 HG01071.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.35-4077G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50583754 | |||||||
chr14:50583879 | G | A | 7 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(4): Show |
7 | HG01361.hp1 HG01433.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.35-3952G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50583879 | |||||||
chr14:50584064 | A | G | 1 | a0001c0003t0001g0147 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.35-3767A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50584064 | |||||||
chr14:50584104 | G | A | 51 | a0001c0003t0001g0006 a0001c0003t0001g0007 a0001c0003t0001g0008 others(48): Show |
55 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.35-3727G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50584104 | |||||||
chr14:50584114 | C | T | 56 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0025 others(53): Show |
59 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.35-3717C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50584114 | |||||||
chr14:50584147 | C | G | 95 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(92): Show |
105 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.35-3684C>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50584147 | |||||||
chr14:50584270 | C | T | 13 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0057 others(10): Show |
16 | HG01261.hp2 HG01496.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.35-3561C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50584270 | |||||||
chr14:50584342 | C | T | 1 | a0001c0001t0001g0015 | 2 | HG01257.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.35-3489C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50584342 | |||||||
chr14:50584442 | G | A | 1 | a0001c0004t0004g0141 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.35-3389G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50584442 | |||||||
chr14:50584566 | A | G | 1 | a0001c0001t0001g0214 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.35-3265A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50584566 | |||||||
chr14:50584578 | G | A | 1 | a0001c0001t0001g0026 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.35-3253G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50584578 | |||||||
chr14:50584688 | G | A | 1 | a0001c0002t0001g0233 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.35-3143G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50584688 | |||||||
chr14:50584752 | G | A | 2 | a0001c0003t0001g0136 a0001c0003t0001g0198 |
2 | HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.35-3079G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50584752 | |||||||
chr14:50584834 | A | T | 3 | a0001c0001t0001g0087 a0001c0001t0001g0102 a0001c0001t0001g0103 |
3 | HG02109.hp1 HG02809.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.35-2997A>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50584834 | |||||||
chr14:50585096 | A | G | 1 | a0001c0001t0001g0027 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.35-2735A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50585096 | |||||||
chr14:50585350 | T | C | 3 | a0001c0003t0001g0036 a0001c0003t0001g0037 a0001c0003t0001g0038 |
3 | HG03139.hp1 NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.35-2481T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50585350 | |||||||
chr14:50585385 | A | G | 2 | a0001c0001t0001g0027 a0001c0001t0001g0140 |
2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.35-2446A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50585385 | |||||||
chr14:50585400 | T | C | 138 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(135): Show |
147 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.35-2431T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50585400 | |||||||
chr14:50585425 | T | A | 1 | a0001c0002t0001g0256 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.35-2406T>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50585425 | |||||||
chr14:50585795 | G | A | 9 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(6): Show |
9 | HG01361.hp1 HG01433.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.35-2036G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50585795 | |||||||
chr14:50585801 | G | C | 1 | a0001c0002t0001g0235 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.35-2030G>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50585801 | |||||||
chr14:50585857 | C | A | 5 | a0001c0001t0001g0015 a0001c0001t0001g0131 a0001c0001t0001g0132 others(2): Show |
6 | HG01257.hp2 HG01517.hp1 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.35-1974C>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50585857 | |||||||
chr14:50585951 | C | T | 94 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(91): Show |
104 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.35-1880C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50585951 | |||||||
chr14:50585972 | C | T | 9 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(6): Show |
9 | HG01361.hp1 HG01433.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.35-1859C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50585972 | |||||||
chr14:50586250 | G | T | 56 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0025 others(53): Show |
59 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.35-1581G>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50586250 | |||||||
chr14:50586478 | G | A | 2 | a0001c0001t0001g0138 a0001c0009t0001g0084 |
2 | HG03579.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.35-1353G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50586478 | |||||||
chr14:50586507 | T | C | 5 | a0001c0001t0001g0015 a0001c0001t0001g0131 a0001c0001t0001g0132 others(2): Show |
6 | HG01257.hp2 HG01517.hp1 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.35-1324T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50586507 | |||||||
chr14:50586624 | A | C | 2 | a0001c0001t0001g0138 a0001c0009t0001g0084 |
2 | HG03579.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.35-1207A>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50586624 | |||||||
chr14:50586890 | T | C | 3 | a0001c0002t0001g0024 a0001c0002t0001g0270 a0001c0002t0001g0273 |
4 | NA18952.hp1 NA18960.hp2 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.35-941T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50586890 | |||||||
chr14:50587151 | T | C | 7 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(4): Show |
7 | HG01361.hp1 HG01433.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.35-680T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50587151 | |||||||
chr14:50587198 | A | G | 1 | a0001c0001t0003g0124 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.35-633A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50587198 | |||||||
chr14:50587222 | AG | A | 7 | a0001c0001t0001g0088 a0001c0001t0001g0104 a0001c0001t0001g0106 others(4): Show |
7 | HG00140.hp1 HG00738.hp1 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.35-608delG | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50587222 | |||||||
chr14:50587253 | C | A | 1 | a0001c0008t0001g0146 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.35-578C>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50587253 | |||||||
chr14:50587284 | G | A | 5 | a0001c0004t0001g0005 a0001c0004t0001g0030 a0001c0004t0001g0033 others(2): Show |
6 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.35-547G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50587284 | |||||||
chr14:50587444 | T | C | 3 | a0001c0004t0001g0031 a0001c0004t0001g0032 a0001c0004t0001g0035 |
3 | HG02258.hp1 HG02572.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.35-387T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50587444 | |||||||
chr14:50587528 | C | T | 1 | a0001c0003t0001g0050 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.35-303C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50587528 | |||||||
chr14:50587573 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.35-258C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50587573 | |||||||
chr14:50587757 | G | C | 9 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(6): Show |
9 | HG01361.hp1 HG01433.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.35-74G>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50587757 | |||||||
chr14:50587817 | G | A | 4 | a0001c0004t0001g0005 a0001c0004t0001g0030 a0001c0004t0001g0033 others(1): Show |
5 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.35-14G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 1/13 | chr14 | 50587817 | |||||||
chr14:50588337 | T | G | 1 | a0001c0001t0001g0144 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.282+259T>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 2/13 | chr14 | 50588337 | |||||||
chr14:50588601 | A | T | 6 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0211 others(3): Show |
6 | HG00597.hp2 NA18948.hp2 NA18982.hp2 others(3): Show |
intron_variant | MODIFIER | c.282+523A>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 2/13 | chr14 | 50588601 | |||||||
chr14:50588801 | T | C | 1 | a0001c0001t0001g0135 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.282+723T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 2/13 | chr14 | 50588801 | |||||||
chr14:50589051 | C | T | 4 | a0001c0004t0001g0005 a0001c0004t0001g0030 a0001c0004t0001g0033 others(1): Show |
5 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.282+973C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 2/13 | chr14 | 50589051 | |||||||
chr14:50589085 | A | G | 2 | a0001c0001t0001g0014 a0001c0001t0001g0090 |
3 | HG01358.hp2 HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.282+1007A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 2/13 | chr14 | 50589085 | |||||||
chr14:50589155 | C | CT | 80 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0056 others(77): Show |
85 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.282+1098dupT | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr14 | 50589155 | ||||||
chr14:50589155 | CT | C | 8 | a0001c0001t0001g0010 a0001c0001t0001g0055 a0001c0001t0001g0058 others(5): Show |
9 | HG00438.hp2 HG00733.hp1 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.282+1098delT | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr14 | 50589155 | ||||||
chr14:50589185 | G | A | 6 | a0001c0001t0001g0088 a0001c0001t0001g0104 a0001c0001t0001g0106 others(3): Show |
6 | HG00140.hp1 HG00738.hp1 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.282+1107G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 2/13 | chr14 | 50589185 | |||||||
chr14:50589661 | A | G | 1 | a0001c0003t0001g0158 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.283-1280A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 2/13 | chr14 | 50589661 | |||||||
chr14:50589750 | G | C | 1 | a0001c0002t0001g0241 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.283-1191G>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 2/13 | chr14 | 50589750 | |||||||
chr14:50589762 | G | A | 9 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(6): Show |
9 | HG01361.hp1 HG01433.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.283-1179G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 2/13 | chr14 | 50589762 | |||||||
chr14:50589877 | C | T | 1 | a0001c0002t0001g0256 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.283-1064C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 2/13 | chr14 | 50589877 | |||||||
chr14:50589882 | C | T | 136 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(133): Show |
145 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.283-1059C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 2/13 | chr14 | 50589882 | |||||||
chr14:50590182 | T | G | 1 | a0001c0001t0001g0095 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.283-759T>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 2/13 | chr14 | 50590182 | |||||||
chr14:50590320 | G | A | 1 | a0001c0001t0002g0110 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.283-621G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 2/13 | chr14 | 50590320 | |||||||
chr14:50590321 | C | CCTGCAGG others(31): Show |
1 | a0001c0001t0001g0085 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.283-619_283-582dup others(38): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr14 | 50590321 | ||||||
chr14:50590402 | C | G | 5 | a0001c0002t0001g0248 a0001c0002t0001g0250 a0001c0002t0001g0263 others(2): Show |
5 | HG02129.hp1 HG02165.hp2 NA18945.hp2 others(2): Show |
intron_variant | MODIFIER | c.283-539C>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 2/13 | chr14 | 50590402 | |||||||
chr14:50590470 | CTGCT | C | 7 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(4): Show |
7 | HG01361.hp1 HG01433.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.283-467_283-464del others(4): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr14 | 50590470 | ||||||
chr14:50590885 | G | A | 3 | a0001c0003t0001g0036 a0001c0003t0001g0037 a0001c0003t0001g0038 |
3 | HG03139.hp1 NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.283-56G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 2/13 | chr14 | 50590885 | |||||||
chr14:50591078 | A | G | 2 | a0001c0001t0003g0068 a0001c0001t0003g0069 |
2 | HG03688.hp2 HG04199.hp1 |
splice_region_variant&intron_variant | LOW | c.417+3A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 3/13 | chr14 | 50591078 | |||||||
chr14:50591147 | GT | G | 4 | a0001c0002t0001g0022 a0001c0002t0001g0234 a0001c0002t0001g0257 others(1): Show |
5 | NA18954.hp1 NA18983.hp1 NA19012.hp1 others(2): Show |
intron_variant | MODIFIER | c.417+74delT | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr14 | 50591147 | ||||||
chr14:50591182 | A | T | 1 | a0001c0012t0001g0268 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.417+107A>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 3/13 | chr14 | 50591182 | |||||||
chr14:50591257 | A | G | 1 | a0001c0002t0008g0247 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.417+182A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 3/13 | chr14 | 50591257 | |||||||
chr14:50591360 | T | C | 9 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(6): Show |
9 | HG01361.hp1 HG01433.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.418-175T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 3/13 | chr14 | 50591360 | |||||||
chr14:50591509 | C | G | 1 | a0001c0004t0001g0032 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.418-26C>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 3/13 | chr14 | 50591509 | |||||||
chr14:50591516 | G | T | 231 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(228): Show |
250 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.418-19G>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 3/13 | chr14 | 50591516 | |||||||
chr14:50591696 | T | C | 2 | a0001c0004t0004g0141 a0001c0008t0001g0146 |
2 | HG02280.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.522+57T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 4/13 | chr14 | 50591696 | |||||||
chr14:50591793 | G | A | 94 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(91): Show |
104 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.522+154G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 4/13 | chr14 | 50591793 | |||||||
chr14:50592141 | T | A | 1 | a0001c0001t0001g0180 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.522+502T>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 4/13 | chr14 | 50592141 | |||||||
chr14:50592237 | G | A | 9 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(6): Show |
9 | HG01361.hp1 HG01433.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.522+598G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 4/13 | chr14 | 50592237 | |||||||
chr14:50592542 | T | TA | 130 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(127): Show |
139 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.522+913dupA | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 50592542 | ||||||
chr14:50592682 | C | T | 2 | a0001c0001t0001g0010 a0001c0001t0001g0055 |
3 | HG00733.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.522+1043C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 4/13 | chr14 | 50592682 | |||||||
chr14:50592712 | C | T | 1 | a0001c0001t0001g0075 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.522+1073C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 4/13 | chr14 | 50592712 | |||||||
chr14:50592728 | G | A | 46 | a0001c0003t0001g0006 a0001c0003t0001g0007 a0001c0003t0001g0008 others(43): Show |
49 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.522+1089G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 4/13 | chr14 | 50592728 | |||||||
chr14:50592772 | A | G | 95 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(92): Show |
105 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.523-1074A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 4/13 | chr14 | 50592772 | |||||||
chr14:50592804 | G | A | 1 | a0001c0003t0001g0171 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.523-1042G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 4/13 | chr14 | 50592804 | |||||||
chr14:50592827 | C | T | 1 | a0001c0001t0003g0068 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.523-1019C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 4/13 | chr14 | 50592827 | |||||||
chr14:50592853 | C | G | 1 | a0001c0001t0001g0026 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.523-993C>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 4/13 | chr14 | 50592853 | |||||||
chr14:50592861 | C | T | 13 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0057 others(10): Show |
16 | HG01261.hp2 HG01496.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.523-985C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 4/13 | chr14 | 50592861 | |||||||
chr14:50592913 | C | CAA | 11 | a0001c0001t0001g0010 a0001c0001t0001g0055 a0001c0001t0001g0071 others(8): Show |
12 | HG00733.hp1 HG01256.hp2 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.523-917_523-916dup others(2): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 50592913 | ||||||
chr14:50592916 | A | C | 2 | a0001c0001t0001g0161 a0001c0001t0001g0164 |
2 | HG01891.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.523-930A>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 4/13 | chr14 | 50592916 | |||||||
chr14:50592927 | A | AAT | 9 | a0001c0001t0001g0089 a0001c0001t0001g0092 a0001c0001t0001g0104 others(6): Show |
9 | HG00140.hp1 HG00673.hp2 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.523-918_523-917ins others(2): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 50592927 | ||||||
chr14:50592927 | A | T | 2 | a0001c0004t0001g0030 a0001c0004t0001g0033 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.523-919A>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 4/13 | chr14 | 50592927 | |||||||
chr14:50592929 | A | AAAAT | 22 | a0001c0003t0001g0006 a0001c0003t0001g0017 a0001c0003t0001g0043 others(19): Show |
24 | HG00639.hp1 HG00642.hp2 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.523-916_523-915ins others(4): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 50592929 | ||||||
chr14:50592929 | A | AAAT | 11 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(8): Show |
11 | HG01261.hp2 HG01361.hp1 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.523-916_523-915ins others(3): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 50592929 | ||||||
chr14:50592929 | A | AAT | 47 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0025 others(44): Show |
50 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.523-900_523-899dup others(2): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 50592929 | ||||||
chr14:50592929 | A | AATAT | 13 | a0001c0003t0001g0007 a0001c0003t0001g0008 a0001c0003t0001g0009 others(10): Show |
15 | HG00408.hp2 HG00423.hp2 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.523-902_523-899dup others(4): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 50592929 | ||||||
chr14:50592929 | A | AT | 11 | a0001c0001t0001g0081 a0001c0001t0001g0138 a0001c0001t0001g0168 others(8): Show |
12 | HG01243.hp2 HG02004.hp1 HG02683.hp2 others(9): Show |
intron_variant | MODIFIER | c.523-917_523-916ins others(1): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 4/13 | chr14 | 50592929 | |||||||
chr14:50592929 | A | ATAT | 6 | a0001c0001t0001g0085 a0001c0001t0001g0195 a0001c0002t0001g0245 others(3): Show |
6 | HG01884.hp2 HG01952.hp2 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.523-917_523-916ins others(3): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 4/13 | chr14 | 50592929 | |||||||
chr14:50592929 | A | T | 34 | a0001c0001t0001g0003 a0001c0001t0001g0057 a0001c0001t0001g0058 others(31): Show |
36 | HG00140.hp1 HG00642.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.523-917A>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 4/13 | chr14 | 50592929 | |||||||
chr14:50592930 | AT | A | 4 | a0001c0001t0002g0156 a0001c0001t0002g0193 a0001c0004t0001g0032 others(1): Show |
4 | HG01993.hp1 HG02258.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.523-915delT | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 4/13 | chr14 | 50592930 | |||||||
chr14:50592931 | T | A | 20 | a0001c0001t0001g0018 a0001c0001t0001g0167 a0001c0001t0001g0184 others(17): Show |
22 | HG00408.hp1 HG02165.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.523-915T>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 4/13 | chr14 | 50592931 | |||||||
chr14:50592933 | T | A | 5 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(2): Show |
5 | HG02257.hp1 HG02258.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.523-913T>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 4/13 | chr14 | 50592933 | |||||||
chr14:50592946 | A | ATATG | 16 | a0001c0001t0001g0003 a0001c0001t0001g0026 a0001c0001t0001g0057 others(13): Show |
19 | HG02135.hp2 HG02257.hp2 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.523-899_523-898ins others(4): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 50592946 | ||||||
chr14:50592946 | A | ATATGTG | 3 | a0001c0001t0001g0018 a0001c0001t0001g0226 a0001c0001t0001g0227 |
4 | HG01433.hp2 HG01891.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.523-899_523-898ins others(6): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 50592946 | ||||||
chr14:50592946 | A | ATG | 39 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0012 others(36): Show |
50 | HG00140.hp2 HG00639.hp2 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.523-882_523-881dup others(2): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 50592946 | ||||||
chr14:50592946 | A | G | 18 | a0001c0001t0001g0286 a0001c0001t0003g0068 a0001c0001t0003g0069 others(15): Show |
19 | HG00735.hp1 HG01346.hp2 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.523-900A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 4/13 | chr14 | 50592946 | |||||||
chr14:50592948 | G | A | 1 | a0001c0003t0001g0051 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.523-898G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 4/13 | chr14 | 50592948 | |||||||
chr14:50592969 | T | TTA | 93 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(90): Show |
103 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.523-867_523-866dup others(2): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 50592969 | ||||||
chr14:50593006 | T | TAA | 3 | a0001c0001t0001g0155 a0001c0001t0001g0172 a0001c0001t0001g0183 |
3 | NA18948.hp1 NA18992.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.523-839_523-838dup others(2): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 50593006 | ||||||
chr14:50593047 | C | G | 2 | a0001c0001t0001g0161 a0001c0001t0001g0164 |
2 | HG01891.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.523-799C>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 4/13 | chr14 | 50593047 | |||||||
chr14:50593097 | A | T | 19 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(16): Show |
23 | HG00733.hp1 HG01256.hp2 HG01258.hp2 others(20): Show |
intron_variant | MODIFIER | c.523-749A>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 4/13 | chr14 | 50593097 | |||||||
chr14:50593108 | A | G | 3 | a0001c0003t0001g0063 a0001c0003t0001g0064 a0001c0003t0001g0065 |
3 | HG01261.hp2 HG01496.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.523-738A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 4/13 | chr14 | 50593108 | |||||||
chr14:50593134 | C | A | 1 | a0001c0001t0001g0215 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.523-712C>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 4/13 | chr14 | 50593134 | |||||||
chr14:50593205 | T | C | 95 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(92): Show |
105 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.523-641T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 4/13 | chr14 | 50593205 | |||||||
chr14:50593393 | T | A | 11 | a0001c0004t0001g0005 a0001c0004t0001g0030 a0001c0004t0001g0031 others(8): Show |
12 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.523-453T>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 4/13 | chr14 | 50593393 | |||||||
chr14:50593734 | A | G | 231 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(228): Show |
250 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.523-112A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 4/13 | chr14 | 50593734 | |||||||
chr14:50594065 | A | G | 1 | a0001c0001t0001g0179 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.573+169A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 5/13 | chr14 | 50594065 | |||||||
chr14:50594284 | G | T | 1 | a0001c0001t0001g0116 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.573+388G>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 5/13 | chr14 | 50594284 | |||||||
chr14:50594420 | C | T | 1 | a0001c0003t0001g0098 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.573+524C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 5/13 | chr14 | 50594420 | |||||||
chr14:50594489 | A | T | 82 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(79): Show |
91 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.573+593A>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 5/13 | chr14 | 50594489 | |||||||
chr14:50594717 | G | T | 1 | a0001c0001t0001g0123 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.573+821G>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 5/13 | chr14 | 50594717 | |||||||
chr14:50594773 | C | T | 95 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(92): Show |
105 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.574-803C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 5/13 | chr14 | 50594773 | |||||||
chr14:50594802 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.574-774C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 5/13 | chr14 | 50594802 | |||||||
chr14:50594812 | T | C | 2 | a0001c0001t0003g0068 a0001c0001t0003g0069 |
2 | HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.574-764T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 5/13 | chr14 | 50594812 | |||||||
chr14:50594932 | A | G | 12 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0055 others(9): Show |
13 | HG00733.hp1 HG01256.hp2 HG01258.hp2 others(10): Show |
intron_variant | MODIFIER | c.574-644A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 5/13 | chr14 | 50594932 | |||||||
chr14:50594998 | C | CA | 6 | a0001c0001t0001g0083 a0001c0001t0001g0095 a0001c0001t0001g0142 others(3): Show |
6 | HG02559.hp2 HG02738.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.574-564dupA | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr14 | 50594998 | ||||||
chr14:50594998 | CAA | C | 94 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(91): Show |
104 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.574-565_574-564del others(2): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr14 | 50594998 | ||||||
chr14:50595265 | C | T | 1 | a0001c0001t0001g0221 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.574-311C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 5/13 | chr14 | 50595265 | |||||||
chr14:50595402 | C | T | 1 | a0001c0002t0001g0235 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.574-174C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 5/13 | chr14 | 50595402 | |||||||
chr14:50595444 | G | A | 229 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(226): Show |
248 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.574-132G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 5/13 | chr14 | 50595444 | |||||||
chr14:50595518 | TTC | T | 225 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(222): Show |
244 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.574-34_574-33delCT | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr14 | 50595518 | ||||||
chr14:50595530 | C | T | 1 | a0001c0004t0001g0032 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.574-46C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 5/13 | chr14 | 50595530 | |||||||
chr14:50595552 | G | C | 9 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(6): Show |
9 | HG01361.hp1 HG01433.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.574-24G>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 5/13 | chr14 | 50595552 | |||||||
chr14:50595560 | G | C | 1 | a0001c0001t0001g0208 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.574-16G>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 5/13 | chr14 | 50595560 | |||||||
chr14:50595639 | G | A | 48 | a0001c0003t0001g0006 a0001c0003t0001g0007 a0001c0003t0001g0008 others(45): Show |
52 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(49): Show |
splice_region_variant&intron_variant | LOW | c.630+7G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50595639 | |||||||
chr14:50595697 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.630+65T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50595697 | |||||||
chr14:50595706 | G | A | 2 | a0001c0001t0001g0010 a0001c0001t0001g0055 |
3 | HG00733.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.630+74G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50595706 | |||||||
chr14:50595737 | G | A | 137 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(134): Show |
146 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.630+105G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50595737 | |||||||
chr14:50595885 | CT | C | 95 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(92): Show |
105 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.630+264delT | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr14 | 50595885 | ||||||
chr14:50595894 | T | C | 1 | a0001c0010t0001g0111 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.630+262T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50595894 | |||||||
chr14:50595997 | T | C | 2 | a0001c0001t0001g0010 a0001c0001t0001g0055 |
3 | HG00733.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.630+365T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50595997 | |||||||
chr14:50596022 | G | A | 1 | a0001c0004t0004g0141 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.630+390G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50596022 | |||||||
chr14:50596461 | G | A | 1 | a0001c0001t0001g0115 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.630+829G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50596461 | |||||||
chr14:50596467 | T | C | 1 | a0001c0001t0001g0115 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.630+835T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50596467 | |||||||
chr14:50596469 | G | A | 1 | a0001c0001t0001g0115 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.630+837G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50596469 | |||||||
chr14:50596612 | T | C | 6 | a0001c0001t0001g0091 a0001c0001t0001g0101 a0001c0001t0001g0115 others(3): Show |
6 | NA18961.hp1 NA18961.hp2 NA18998.hp1 others(3): Show |
intron_variant | MODIFIER | c.630+980T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50596612 | |||||||
chr14:50596848 | A | T | 11 | a0001c0004t0001g0005 a0001c0004t0001g0030 a0001c0004t0001g0031 others(8): Show |
12 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.630+1216A>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50596848 | |||||||
chr14:50596850 | T | A | 3 | a0001c0001t0001g0018 a0001c0001t0001g0226 a0001c0001t0001g0227 |
4 | HG01433.hp2 HG01891.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.630+1218T>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50596850 | |||||||
chr14:50596947 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.630+1315C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50596947 | |||||||
chr14:50596963 | A | G | 1 | a0001c0002t0001g0261 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.630+1331A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50596963 | |||||||
chr14:50597161 | A | C | 2 | a0001c0001t0001g0027 a0001c0001t0001g0140 |
2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.630+1529A>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50597161 | |||||||
chr14:50597167 | C | A | 3 | a0001c0001t0001g0018 a0001c0001t0001g0226 a0001c0001t0001g0227 |
4 | HG01433.hp2 HG01891.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.630+1535C>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50597167 | |||||||
chr14:50597220 | C | CA | 6 | a0001c0001t0001g0016 a0001c0001t0001g0081 a0001c0001t0001g0162 others(3): Show |
7 | HG01257.hp1 HG01258.hp1 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.630+1601dupA | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr14 | 50597220 | ||||||
chr14:50597220 | C | CAAA | 14 | a0001c0001t0001g0026 a0001c0001t0003g0069 a0001c0003t0001g0159 others(11): Show |
15 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.630+1599_630+1601d others(5): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr14 | 50597220 | ||||||
chr14:50597220 | C | CAAAA | 11 | a0001c0001t0001g0015 a0001c0001t0001g0089 a0001c0001t0001g0131 others(8): Show |
12 | HG01257.hp2 HG01517.hp1 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.630+1598_630+1601d others(6): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr14 | 50597220 | ||||||
chr14:50597220 | C | CAAAAA | 124 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0013 others(121): Show |
132 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.630+1597_630+1601d others(7): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr14 | 50597220 | ||||||
chr14:50597220 | C | CAAAAAA | 8 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(5): Show |
8 | HG00408.hp1 HG00673.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.630+1596_630+1601d others(8): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr14 | 50597220 | ||||||
chr14:50597220 | C | CAAAAAAA others(2): Show |
9 | a0001c0003t0001g0063 a0001c0003t0001g0064 a0001c0003t0001g0136 others(6): Show |
9 | HG00735.hp2 HG01261.hp2 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.630+1593_630+1601d others(11): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr14 | 50597220 | ||||||
chr14:50597220 | C | CAAAAAAA others(3): Show |
44 | a0001c0001t0001g0003 a0001c0001t0001g0057 a0001c0001t0001g0058 others(41): Show |
50 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.630+1592_630+1601d others(12): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr14 | 50597220 | ||||||
chr14:50597220 | C | CAAAAAAA others(4): Show |
7 | a0001c0001t0001g0018 a0001c0001t0001g0227 a0001c0003t0001g0046 others(4): Show |
8 | HG01433.hp2 HG02071.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.630+1591_630+1601d others(13): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr14 | 50597220 | ||||||
chr14:50597220 | C | CAAAAAAA others(3): Show |
1 | a0001c0003t0001g0047 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.630+1596_630+1597i others(12): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr14 | 50597220 | ||||||
chr14:50597278 | A | G | 1 | a0001c0001t0001g0164 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.630+1646A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50597278 | |||||||
chr14:50597391 | T | C | 2 | a0001c0003t0001g0284 a0001c0003t0001g0285 |
2 | HG00280.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.630+1759T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50597391 | |||||||
chr14:50597395 | G | A | 2 | a0001c0001t0001g0027 a0001c0001t0001g0140 |
2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.630+1763G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50597395 | |||||||
chr14:50597613 | C | CAT | 4 | a0001c0001t0001g0027 a0001c0001t0001g0140 a0001c0004t0004g0141 others(1): Show |
4 | HG02280.hp2 HG03098.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.630+1992_630+1993d others(4): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr14 | 50597613 | ||||||
chr14:50597643 | G | C | 1 | a0001c0001t0001g0056 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.630+2011G>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50597643 | |||||||
chr14:50597706 | T | G | 5 | a0001c0001t0001g0015 a0001c0001t0001g0131 a0001c0001t0001g0132 others(2): Show |
6 | HG01257.hp2 HG01517.hp1 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.630+2074T>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50597706 | |||||||
chr14:50597733 | C | T | 1 | a0001c0001t0001g0011 | 2 | HG02723.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.630+2101C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50597733 | |||||||
chr14:50597769 | A | G | 1 | a0001c0002t0001g0264 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.630+2137A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50597769 | |||||||
chr14:50597850 | A | G | 1 | a0001c0003t0001g0105 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.630+2218A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50597850 | |||||||
chr14:50597946 | C | T | 4 | a0001c0001t0001g0083 a0001c0001t0001g0086 a0001c0001t0001g0140 others(1): Show |
4 | HG02559.hp2 HG03195.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.630+2314C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50597946 | |||||||
chr14:50597982 | A | G | 2 | a0001c0001t0003g0068 a0001c0001t0003g0069 |
2 | HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.630+2350A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50597982 | |||||||
chr14:50598063 | A | G | 1 | a0001c0001t0001g0075 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.630+2431A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50598063 | |||||||
chr14:50598274 | C | T | 1 | a0001c0002t0001g0262 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.630+2642C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50598274 | |||||||
chr14:50598280 | G | A | 3 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 |
3 | HG02257.hp1 HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.630+2648G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50598280 | |||||||
chr14:50598364 | A | T | 3 | a0001c0003t0001g0063 a0001c0003t0001g0064 a0001c0003t0001g0065 |
3 | HG01261.hp2 HG01496.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.630+2732A>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50598364 | |||||||
chr14:50598378 | C | T | 1 | a0001c0008t0001g0146 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.630+2746C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50598378 | |||||||
chr14:50598430 | G | A | 1 | a0001c0001t0001g0155 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.630+2798G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50598430 | |||||||
chr14:50598685 | G | A | 1 | a0001c0002t0001g0267 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.630+3053G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50598685 | |||||||
chr14:50598714 | A | G | 1 | a0001c0001t0002g0191 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.630+3082A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50598714 | |||||||
chr14:50598724 | A | G | 1 | a0001c0001t0001g0026 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.630+3092A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50598724 | |||||||
chr14:50598812 | G | A | 12 | a0001c0001t0001g0026 a0001c0004t0001g0005 a0001c0004t0001g0030 others(9): Show |
13 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.630+3180G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50598812 | |||||||
chr14:50598925 | A | ACTGTAAT others(29): Show |
9 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(6): Show |
9 | HG01361.hp1 HG01433.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.630+3294_630+3329d others(38): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr14 | 50598925 | ||||||
chr14:50599088 | TTAC | T | 8 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0057 others(5): Show |
11 | HG02257.hp2 HG02280.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.630+3460_630+3462d others(5): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr14 | 50599088 | ||||||
chr14:50599146 | A | G | 1 | a0001c0001t0001g0138 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.630+3514A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50599146 | |||||||
chr14:50599246 | G | C | 3 | a0001c0003t0001g0063 a0001c0003t0001g0064 a0001c0003t0001g0065 |
3 | HG01261.hp2 HG01496.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.630+3614G>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50599246 | |||||||
chr14:50599437 | G | A | 3 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0134 |
3 | HG02698.hp1 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.630+3805G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50599437 | |||||||
chr14:50599703 | A | G | 3 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 |
3 | HG02257.hp1 HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.630+4071A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50599703 | |||||||
chr14:50599711 | G | A | 29 | a0001c0003t0001g0017 a0001c0003t0001g0044 a0001c0003t0001g0097 others(26): Show |
30 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.630+4079G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50599711 | |||||||
chr14:50599711 | G | C | 2 | a0001c0001t0001g0010 a0001c0001t0001g0055 |
3 | HG00733.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.630+4079G>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50599711 | |||||||
chr14:50599983 | C | CTT | 11 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(8): Show |
11 | HG01361.hp1 HG01433.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.630+4363_630+4364d others(4): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr14 | 50599983 | ||||||
chr14:50599983 | CT | C | 54 | a0001c0001t0001g0018 a0001c0001t0001g0226 a0001c0001t0001g0227 others(51): Show |
59 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.630+4364delT | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr14 | 50599983 | ||||||
chr14:50600269 | A | T | 1 | a0001c0003t0001g0148 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.630+4637A>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50600269 | |||||||
chr14:50600397 | T | C | 3 | a0001c0001t0001g0018 a0001c0001t0001g0226 a0001c0001t0001g0227 |
4 | HG01433.hp2 HG01891.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.630+4765T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50600397 | |||||||
chr14:50600661 | C | T | 48 | a0001c0003t0001g0006 a0001c0003t0001g0007 a0001c0003t0001g0008 others(45): Show |
52 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.630+5029C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50600661 | |||||||
chr14:50600920 | T | C | 7 | a0001c0001t0001g0003 a0001c0001t0001g0057 a0001c0001t0001g0058 others(4): Show |
9 | HG02257.hp2 HG02280.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.630+5288T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50600920 | |||||||
chr14:50600939 | C | T | 1 | a0001c0001t0001g0027 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.630+5307C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50600939 | |||||||
chr14:50601201 | G | A | 1 | a0001c0001t0001g0222 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.630+5569G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50601201 | |||||||
chr14:50601539 | A | G | 1 | a0001c0007t0001g0228 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.630+5907A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50601539 | |||||||
chr14:50601540 | C | T | 1 | a0001c0001t0001g0026 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.630+5908C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50601540 | |||||||
chr14:50601545 | A | G | 3 | a0001c0001t0001g0018 a0001c0001t0001g0226 a0001c0001t0001g0227 |
4 | HG01433.hp2 HG01891.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.630+5913A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50601545 | |||||||
chr14:50601563 | C | A | 1 | a0001c0003t0001g0204 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.630+5931C>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50601563 | |||||||
chr14:50601891 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.630+6259T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50601891 | |||||||
chr14:50602030 | A | G | 1 | a0001c0004t0001g0054 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.630+6398A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50602030 | |||||||
chr14:50602073 | T | A | 1 | a0001c0012t0001g0268 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.630+6441T>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50602073 | |||||||
chr14:50602081 | A | C | 12 | a0001c0001t0001g0018 a0001c0001t0001g0071 a0001c0001t0001g0072 others(9): Show |
13 | HG01361.hp1 HG01433.hp1 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.630+6449A>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50602081 | |||||||
chr14:50602195 | G | A | 2 | a0001c0002t0001g0004 a0001c0002t0001g0265 |
4 | HG00741.hp2 HG01975.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.630+6563G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50602195 | |||||||
chr14:50602484 | A | G | 1 | a0001c0003t0001g0176 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.630+6852A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50602484 | |||||||
chr14:50602626 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.630+6994C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50602626 | |||||||
chr14:50602665 | G | A | 6 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0211 others(3): Show |
6 | HG00597.hp2 NA18948.hp2 NA18982.hp2 others(3): Show |
intron_variant | MODIFIER | c.630+7033G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50602665 | |||||||
chr14:50602882 | A | G | 2 | a0001c0007t0001g0070 a0001c0007t0001g0228 |
2 | HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.630+7250A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50602882 | |||||||
chr14:50603074 | G | T | 1 | a0001c0001t0001g0125 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.630+7442G>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50603074 | |||||||
chr14:50603124 | TA | T | 6 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(3): Show |
6 | HG01361.hp1 HG01433.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.630+7501delA | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr14 | 50603124 | ||||||
chr14:50603285 | C | T | 189 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(186): Show |
204 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.630+7653C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50603285 | |||||||
chr14:50603323 | C | G | 3 | a0001c0001t0001g0018 a0001c0001t0001g0226 a0001c0001t0001g0227 |
4 | HG01433.hp2 HG01891.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.630+7691C>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50603323 | |||||||
chr14:50603427 | A | C | 1 | a0001c0001t0001g0190 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.630+7795A>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50603427 | |||||||
chr14:50603517 | GGAC | G | 11 | a0001c0004t0001g0005 a0001c0004t0001g0030 a0001c0004t0001g0031 others(8): Show |
12 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.630+7886_630+7888d others(5): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50603517 | |||||||
chr14:50603779 | T | A | 1 | a0001c0002t0001g0251 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.630+8147T>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50603779 | |||||||
chr14:50603896 | A | G | 1 | a0001c0001t0003g0069 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.630+8264A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50603896 | |||||||
chr14:50603943 | G | A | 3 | a0001c0003t0001g0159 a0001c0003t0001g0175 a0001c0003t0001g0176 |
3 | HG01069.hp2 HG01346.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.630+8311G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50603943 | |||||||
chr14:50603987 | A | G | 11 | a0001c0004t0001g0005 a0001c0004t0001g0030 a0001c0004t0001g0031 others(8): Show |
12 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.630+8355A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50603987 | |||||||
chr14:50604034 | C | T | 2 | a0001c0001t0001g0010 a0001c0001t0001g0055 |
3 | HG00733.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.630+8402C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50604034 | |||||||
chr14:50604069 | C | T | 2 | a0001c0001t0003g0068 a0001c0001t0003g0069 |
2 | HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.630+8437C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50604069 | |||||||
chr14:50604094 | TA | T | 136 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(133): Show |
145 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.630+8469delA | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr14 | 50604094 | ||||||
chr14:50604129 | C | T | 3 | a0001c0001t0001g0018 a0001c0001t0001g0226 a0001c0001t0001g0227 |
4 | HG01433.hp2 HG01891.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.630+8497C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50604129 | |||||||
chr14:50604130 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.630+8498G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50604130 | |||||||
chr14:50604150 | A | G | 4 | a0001c0001t0001g0083 a0001c0001t0001g0085 a0001c0001t0001g0086 others(1): Show |
4 | HG01884.hp2 HG02559.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.630+8518A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50604150 | |||||||
chr14:50604373 | C | A | 231 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(228): Show |
250 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.630+8741C>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50604373 | |||||||
chr14:50604419 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.630+8787C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50604419 | |||||||
chr14:50604452 | C | T | 1 | a0001c0001t0002g0189 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.631-8807C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50604452 | |||||||
chr14:50604819 | G | A | 1 | a0001c0002t0001g0019 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.631-8440G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50604819 | |||||||
chr14:50604852 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.631-8407T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50604852 | |||||||
chr14:50604867 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.631-8392G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50604867 | |||||||
chr14:50604882 | A | G | 232 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(229): Show |
251 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.631-8377A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50604882 | |||||||
chr14:50604902 | G | A | 2 | a0001c0004t0004g0141 a0001c0008t0001g0146 |
2 | HG02280.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.631-8357G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50604902 | |||||||
chr14:50605122 | C | G | 3 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0076 |
3 | HG01361.hp1 HG02896.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.631-8137C>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50605122 | |||||||
chr14:50605292 | T | TGATTCAT others(2): Show |
11 | a0001c0001t0001g0026 a0001c0004t0001g0005 a0001c0004t0001g0030 others(8): Show |
12 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.631-7966_631-7958d others(11): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr14 | 50605292 | ||||||
chr14:50605371 | A | G | 5 | a0001c0001t0001g0013 a0001c0001t0001g0078 a0001c0001t0001g0079 others(2): Show |
6 | HG01123.hp2 HG01943.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.631-7888A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50605371 | |||||||
chr14:50605404 | A | G | 1 | a0001c0001t0001g0165 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.631-7855A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50605404 | |||||||
chr14:50605492 | A | C | 231 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(228): Show |
250 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.631-7767A>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50605492 | |||||||
chr14:50605879 | C | G | 7 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(4): Show |
7 | HG01361.hp1 HG01433.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.631-7380C>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50605879 | |||||||
chr14:50605995 | C | T | 230 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(227): Show |
249 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.631-7264C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50605995 | |||||||
chr14:50606147 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.631-7112G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50606147 | |||||||
chr14:50606220 | C | T | 1 | a0001c0004t0004g0141 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.631-7039C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50606220 | |||||||
chr14:50606275 | C | T | 1 | a0001c0002t0001g0241 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.631-6984C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50606275 | |||||||
chr14:50606549 | G | A | 1 | a0001c0002t0001g0256 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.631-6710G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50606549 | |||||||
chr14:50606667 | T | C | 2 | a0001c0001t0001g0010 a0001c0001t0001g0055 |
3 | HG00733.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.631-6592T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50606667 | |||||||
chr14:50607288 | A | C | 2 | a0001c0001t0001g0010 a0001c0001t0001g0055 |
3 | HG00733.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.631-5971A>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50607288 | |||||||
chr14:50607290 | C | T | 1 | a0001c0001t0001g0091 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.631-5969C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50607290 | |||||||
chr14:50607476 | A | G | 1 | a0001c0001t0001g0026 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.631-5783A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50607476 | |||||||
chr14:50607482 | G | A | 3 | a0001c0001t0001g0018 a0001c0001t0001g0226 a0001c0001t0001g0227 |
4 | HG01433.hp2 HG01891.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.631-5777G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50607482 | |||||||
chr14:50607537 | C | T | 7 | a0001c0001t0001g0003 a0001c0001t0001g0057 a0001c0001t0001g0058 others(4): Show |
9 | HG02257.hp2 HG02280.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.631-5722C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50607537 | |||||||
chr14:50607664 | C | A | 2 | a0001c0001t0001g0169 a0001c0001t0001g0182 |
2 | HG02886.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.631-5595C>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50607664 | |||||||
chr14:50607743 | A | C | 56 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0025 others(53): Show |
59 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.631-5516A>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50607743 | |||||||
chr14:50607882 | A | G | 1 | a0001c0001t0001g0011 | 2 | HG02723.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.631-5377A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50607882 | |||||||
chr14:50608050 | T | C | 1 | a0001c0001t0001g0092 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.631-5209T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50608050 | |||||||
chr14:50608135 | A | G | 72 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0016 others(69): Show |
78 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.631-5124A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50608135 | |||||||
chr14:50608479 | G | GT | 136 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(133): Show |
145 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.631-4773dupT | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr14 | 50608479 | ||||||
chr14:50608572 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.631-4687G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50608572 | |||||||
chr14:50608643 | T | A | 1 | a0001c0011t0001g0109 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.631-4616T>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50608643 | |||||||
chr14:50608810 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.631-4449T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50608810 | |||||||
chr14:50609268 | G | A | 1 | a0001c0009t0001g0084 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.631-3991G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50609268 | |||||||
chr14:50609312 | G | A | 1 | a0001c0001t0001g0195 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.631-3947G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50609312 | |||||||
chr14:50609507 | A | T | 2 | a0001c0001t0001g0010 a0001c0001t0001g0055 |
3 | HG00733.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.631-3752A>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50609507 | |||||||
chr14:50609551 | A | C | 220 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(217): Show |
238 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.631-3708A>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50609551 | |||||||
chr14:50609554 | A | C | 1 | a0001c0001t0001g0026 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.631-3705A>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50609554 | |||||||
chr14:50609560 | G | C | 1 | a0001c0001t0001g0077 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.631-3699G>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50609560 | |||||||
chr14:50609572 | A | G | 3 | a0001c0001t0001g0018 a0001c0001t0001g0226 a0001c0001t0001g0227 |
4 | HG01433.hp2 HG01891.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.631-3687A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50609572 | |||||||
chr14:50609877 | G | T | 2 | a0001c0001t0001g0010 a0001c0001t0001g0055 |
3 | HG00733.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.631-3382G>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50609877 | |||||||
chr14:50609891 | T | A | 1 | a0001c0001t0001g0117 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.631-3368T>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50609891 | |||||||
chr14:50609999 | G | C | 1 | a0001c0003t0001g0048 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.631-3260G>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50609999 | |||||||
chr14:50610005 | CCTCTGCC others(3): Show |
C | 5 | a0001c0001t0001g0091 a0001c0001t0001g0101 a0001c0001t0001g0115 others(2): Show |
5 | HG00438.hp2 NA18998.hp1 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.631-3242_631-3233d others(12): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr14 | 50610005 | ||||||
chr14:50610406 | T | A | 2 | a0001c0001t0001g0010 a0001c0001t0001g0055 |
3 | HG00733.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.631-2853T>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50610406 | |||||||
chr14:50610743 | G | T | 3 | a0001c0001t0001g0018 a0001c0001t0001g0226 a0001c0001t0001g0227 |
4 | HG01433.hp2 HG01891.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.631-2516G>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50610743 | |||||||
chr14:50610866 | G | A | 2 | a0001c0001t0003g0068 a0001c0001t0003g0069 |
2 | HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.631-2393G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50610866 | |||||||
chr14:50610886 | A | G | 1 | a0001c0001t0001g0138 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.631-2373A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50610886 | |||||||
chr14:50611015 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.631-2244T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50611015 | |||||||
chr14:50611021 | T | G | 1 | a0001c0003t0001g0171 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.631-2238T>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50611021 | |||||||
chr14:50611025 | C | A | 1 | a0001c0001t0001g0131 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.631-2234C>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50611025 | |||||||
chr14:50611027 | C | A | 3 | a0001c0001t0001g0018 a0001c0001t0001g0226 a0001c0001t0001g0227 |
4 | HG01433.hp2 HG01891.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.631-2232C>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50611027 | |||||||
chr14:50611343 | TA | T | 48 | a0001c0003t0001g0006 a0001c0003t0001g0007 a0001c0003t0001g0008 others(45): Show |
52 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.631-1915delA | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50611343 | |||||||
chr14:50611358 | A | C | 230 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(227): Show |
249 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.631-1901A>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50611358 | |||||||
chr14:50611520 | T | C | 56 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0025 others(53): Show |
59 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.631-1739T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50611520 | |||||||
chr14:50611590 | C | T | 1 | a0001c0003t0001g0041 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.631-1669C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50611590 | |||||||
chr14:50611748 | T | C | 1 | a0001c0003t0001g0043 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.631-1511T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50611748 | |||||||
chr14:50611867 | G | A | 137 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(134): Show |
146 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.631-1392G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50611867 | |||||||
chr14:50611969 | T | C | 2 | a0001c0001t0001g0010 a0001c0001t0001g0055 |
3 | HG00733.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.631-1290T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50611969 | |||||||
chr14:50612015 | C | G | 1 | a0001c0001t0002g0110 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.631-1244C>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50612015 | |||||||
chr14:50612182 | C | T | 11 | a0001c0002t0001g0012 a0001c0002t0001g0020 a0001c0002t0001g0022 others(8): Show |
14 | HG02040.hp1 HG02523.hp1 NA18944.hp2 others(11): Show |
intron_variant | MODIFIER | c.631-1077C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50612182 | |||||||
chr14:50612233 | C | T | 1 | a0001c0001t0001g0075 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.631-1026C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50612233 | |||||||
chr14:50612284 | G | A | 1 | a0001c0009t0001g0084 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.631-975G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50612284 | |||||||
chr14:50612338 | T | A | 1 | a0001c0008t0001g0146 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.631-921T>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50612338 | |||||||
chr14:50612522 | C | T | 1 | a0001c0009t0001g0084 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.631-737C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50612522 | |||||||
chr14:50612708 | G | A | 19 | a0001c0001t0001g0082 a0001c0001t0001g0088 a0001c0001t0001g0093 others(16): Show |
19 | HG00140.hp1 HG00597.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.631-551G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50612708 | |||||||
chr14:50612736 | G | A | 2 | a0001c0004t0001g0005 a0001c0004t0001g0034 |
3 | HG02055.hp1 HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.631-523G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50612736 | |||||||
chr14:50613053 | C | A | 3 | a0001c0001t0001g0018 a0001c0001t0001g0226 a0001c0001t0001g0227 |
4 | HG01433.hp2 HG01891.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.631-206C>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50613053 | |||||||
chr14:50613093 | G | A | 2 | a0001c0001t0001g0027 a0001c0001t0001g0140 |
2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.631-166G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50613093 | |||||||
chr14:50613161 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.631-98C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50613161 | |||||||
chr14:50613252 | T | A | 2 | a0001c0006t0001g0028 a0001c0006t0001g0029 |
2 | HG02647.hp2 HG03130.hp1 |
splice_region_variant&intron_variant | LOW | c.631-7T>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 6/13 | chr14 | 50613252 | |||||||
chr14:50613464 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.723+113C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 7/13 | chr14 | 50613464 | |||||||
chr14:50613704 | G | A | 48 | a0001c0003t0001g0006 a0001c0003t0001g0007 a0001c0003t0001g0008 others(45): Show |
52 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.723+353G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 7/13 | chr14 | 50613704 | |||||||
chr14:50613772 | A | G | 1 | a0001c0001t0001g0018 | 2 | HG01433.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.723+421A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 7/13 | chr14 | 50613772 | |||||||
chr14:50613911 | T | A | 2 | a0001c0007t0001g0070 a0001c0007t0001g0228 |
2 | HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.724-462T>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 7/13 | chr14 | 50613911 | |||||||
chr14:50614638 | CAGG | C | 3 | a0001c0003t0001g0063 a0001c0003t0001g0064 a0001c0003t0001g0065 |
3 | HG01261.hp2 HG01496.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.862+130_862+132del others(3): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr14 | 50614638 | ||||||
chr14:50614731 | C | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(131): Show |
143 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.862+220C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50614731 | |||||||
chr14:50614797 | C | T | 147 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(144): Show |
157 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.862+286C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50614797 | |||||||
chr14:50614871 | G | A | 3 | a0001c0005t0001g0240 a0001c0005t0001g0244 a0001c0005t0001g0253 |
3 | NA18944.hp2 NA18965.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.862+360G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50614871 | |||||||
chr14:50614980 | A | C | 7 | a0001c0001t0001g0003 a0001c0001t0001g0057 a0001c0001t0001g0058 others(4): Show |
9 | HG02257.hp2 HG02280.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.862+469A>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50614980 | |||||||
chr14:50615058 | G | C | 1 | a0001c0003t0001g0040 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.862+547G>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50615058 | |||||||
chr14:50615093 | A | T | 1 | a0001c0002t0001g0020 | 2 | HG02523.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.862+582A>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50615093 | |||||||
chr14:50615095 | G | A | 1 | a0001c0002t0001g0020 | 2 | HG02523.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.862+584G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50615095 | |||||||
chr14:50615256 | G | A | 212 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(209): Show |
229 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.862+745G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50615256 | |||||||
chr14:50615259 | G | C | 2 | a0001c0001t0001g0010 a0001c0001t0001g0055 |
3 | HG00733.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.862+748G>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50615259 | |||||||
chr14:50615393 | G | A | 2 | a0001c0003t0001g0009 a0001c0003t0001g0052 |
3 | HG01069.hp1 HG01071.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.862+882G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50615393 | |||||||
chr14:50615465 | C | A | 214 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(211): Show |
232 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(229): Show |
intron_variant | MODIFIER | c.862+954C>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50615465 | |||||||
chr14:50615499 | C | T | 230 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(227): Show |
249 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.862+988C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50615499 | |||||||
chr14:50615553 | A | C | 136 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(133): Show |
145 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.862+1042A>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50615553 | |||||||
chr14:50615868 | T | C | 224 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(221): Show |
242 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.862+1357T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50615868 | |||||||
chr14:50616120 | A | C | 1 | a0001c0001t0001g0026 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.862+1609A>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50616120 | |||||||
chr14:50616373 | T | C | 2 | a0001c0002t0001g0004 a0001c0002t0001g0265 |
4 | HG00741.hp2 HG01975.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.862+1862T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50616373 | |||||||
chr14:50616395 | C | T | 2 | a0001c0007t0001g0070 a0001c0007t0001g0228 |
2 | HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.862+1884C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50616395 | |||||||
chr14:50616452 | C | T | 1 | a0001c0001t0001g0026 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.862+1941C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50616452 | |||||||
chr14:50616455 | G | GTTAT | 5 | a0001c0001t0001g0077 a0001c0001t0001g0085 a0001c0001t0001g0192 others(2): Show |
5 | HG00738.hp2 HG01243.hp2 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.862+1991_862+1994d others(6): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr14 | 50616455 | ||||||
chr14:50616455 | GTTAT | G | 60 | a0001c0001t0001g0014 a0001c0001t0001g0073 a0001c0001t0001g0074 others(57): Show |
67 | HG00140.hp2 HG00280.hp2 HG00673.hp2 others(64): Show |
intron_variant | MODIFIER | c.862+1991_862+1994d others(6): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr14 | 50616455 | ||||||
chr14:50616455 | GTTATTTA others(1): Show |
G | 106 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0015 others(103): Show |
115 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.862+1987_862+1994d others(10): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr14 | 50616455 | ||||||
chr14:50616455 | GTTATTTA others(5): Show |
G | 1 | a0001c0001t0001g0026 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.862+1983_862+1994d others(14): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr14 | 50616455 | ||||||
chr14:50616455 | GTTATTTA others(9): Show |
G | 1 | a0001c0002t0001g0012 | 2 | HG02040.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.862+1979_862+1994d others(18): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr14 | 50616455 | ||||||
chr14:50616455 | GTTATTTA others(13): Show |
G | 66 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(63): Show |
74 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.862+1975_862+1994d others(22): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr14 | 50616455 | ||||||
chr14:50616650 | A | G | 1 | a0001c0001t0001g0056 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.862+2139A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50616650 | |||||||
chr14:50616654 | A | C | 51 | a0001c0003t0001g0006 a0001c0003t0001g0007 a0001c0003t0001g0008 others(48): Show |
55 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.862+2143A>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50616654 | |||||||
chr14:50616763 | T | A | 2 | a0001c0001t0001g0027 a0001c0001t0001g0140 |
2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.862+2252T>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50616763 | |||||||
chr14:50616785 | T | C | 2 | a0001c0001t0001g0027 a0001c0001t0001g0140 |
2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.862+2274T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50616785 | |||||||
chr14:50616876 | T | C | 138 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(135): Show |
147 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.862+2365T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50616876 | |||||||
chr14:50617140 | C | A | 2 | a0001c0001t0001g0010 a0001c0001t0001g0055 |
3 | HG00733.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.862+2629C>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50617140 | |||||||
chr14:50617307 | T | C | 145 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(142): Show |
154 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.862+2796T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50617307 | |||||||
chr14:50617517 | T | C | 51 | a0001c0003t0001g0006 a0001c0003t0001g0007 a0001c0003t0001g0008 others(48): Show |
55 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.862+3006T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50617517 | |||||||
chr14:50617560 | T | C | 1 | a0001c0001t0001g0011 | 2 | HG02723.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.863-3039T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50617560 | |||||||
chr14:50617617 | C | T | 1 | a0001c0001t0001g0075 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.863-2982C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50617617 | |||||||
chr14:50617793 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.863-2806G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50617793 | |||||||
chr14:50617878 | C | T | 15 | a0001c0003t0001g0007 a0001c0003t0001g0008 a0001c0003t0001g0039 others(12): Show |
16 | HG00408.hp2 HG00423.hp2 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.863-2721C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50617878 | |||||||
chr14:50617944 | A | G | 1 | a0001c0001t0001g0095 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.863-2655A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50617944 | |||||||
chr14:50618142 | G | A | 137 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(134): Show |
146 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.863-2457G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50618142 | |||||||
chr14:50618227 | T | C | 7 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(4): Show |
7 | HG01361.hp1 HG01433.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.863-2372T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50618227 | |||||||
chr14:50618236 | G | A | 2 | a0001c0001t0001g0027 a0001c0001t0001g0140 |
2 | HG03453.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.863-2363G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50618236 | |||||||
chr14:50618246 | A | G | 1 | a0001c0001t0001g0100 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.863-2353A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50618246 | |||||||
chr14:50618338 | A | G | 2 | a0001c0001t0001g0092 a0001c0001t0001g0275 |
2 | HG00673.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.863-2261A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50618338 | |||||||
chr14:50618398 | T | C | 68 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(65): Show |
76 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.863-2201T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50618398 | |||||||
chr14:50618483 | T | C | 2 | a0001c0007t0001g0070 a0001c0007t0001g0228 |
2 | HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.863-2116T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50618483 | |||||||
chr14:50618490 | C | T | 232 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(229): Show |
251 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.863-2109C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50618490 | |||||||
chr14:50618711 | C | T | 68 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(65): Show |
76 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.863-1888C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50618711 | |||||||
chr14:50618859 | A | ATG | 127 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(124): Show |
136 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.863-1722_863-1721d others(4): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr14 | 50618859 | ||||||
chr14:50618877 | G | GTGTA | 7 | a0001c0001t0001g0095 a0001c0001t0001g0144 a0001c0001t0001g0201 others(4): Show |
7 | HG00673.hp1 HG02040.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.863-1721_863-1720i others(6): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr14 | 50618877 | ||||||
chr14:50618877 | GTA | G | 3 | a0001c0003t0001g0063 a0001c0003t0001g0064 a0001c0003t0001g0065 |
3 | HG01261.hp2 HG01496.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.863-1708_863-1707d others(4): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr14 | 50618877 | ||||||
chr14:50618879 | A | G | 9 | a0001c0001t0001g0010 a0001c0001t0001g0055 a0001c0001t0001g0207 others(6): Show |
10 | HG00733.hp1 HG01256.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.863-1720A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50618879 | |||||||
chr14:50618889 | A | AT | 5 | a0001c0004t0001g0031 a0001c0004t0001g0032 a0001c0004t0004g0141 others(2): Show |
5 | HG02258.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.863-1709dupT | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr14 | 50618889 | ||||||
chr14:50618890 | TA | T | 53 | a0001c0001t0001g0003 a0001c0001t0001g0057 a0001c0001t0001g0058 others(50): Show |
59 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.863-1708delA | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50618890 | |||||||
chr14:50618891 | A | AT | 11 | a0001c0001t0001g0018 a0001c0001t0001g0226 a0001c0001t0001g0227 others(8): Show |
13 | HG01433.hp2 HG01891.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.863-1699dupT | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr14 | 50618891 | ||||||
chr14:50618891 | A | T | 14 | a0001c0001t0001g0138 a0001c0002t0001g0022 a0001c0002t0001g0234 others(11): Show |
15 | HG01358.hp1 HG02258.hp1 HG02523.hp2 others(12): Show |
intron_variant | MODIFIER | c.863-1708A>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50618891 | |||||||
chr14:50618891 | AT | A | 8 | a0001c0001t0001g0027 a0001c0001t0001g0061 a0001c0001t0001g0062 others(5): Show |
8 | HG01069.hp2 HG01346.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.863-1699delT | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr14 | 50618891 | ||||||
chr14:50618892 | T | TA | 3 | a0001c0003t0001g0036 a0001c0003t0001g0037 a0001c0003t0001g0038 |
3 | HG03139.hp1 NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.863-1707_863-1706i others(3): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50618892 | |||||||
chr14:50618893 | T | A | 144 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0013 others(141): Show |
154 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.863-1706T>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50618893 | |||||||
chr14:50618895 | T | A | 135 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(132): Show |
144 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.863-1704T>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50618895 | |||||||
chr14:50619075 | C | T | 53 | a0001c0001t0001g0027 a0001c0001t0001g0140 a0001c0003t0001g0006 others(50): Show |
57 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.863-1524C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619075 | |||||||
chr14:50619280 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.863-1319C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619280 | |||||||
chr14:50619305 | C | T | 1 | a0001c0001t0001g0200 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.863-1294C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619305 | |||||||
chr14:50619458 | C | T | 51 | a0001c0003t0001g0006 a0001c0003t0001g0007 a0001c0003t0001g0008 others(48): Show |
55 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.863-1141C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619458 | |||||||
chr14:50619669 | A | G | 68 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(65): Show |
76 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.863-930A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619669 | |||||||
chr14:50619674 | A | G | 17 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(14): Show |
21 | HG00733.hp1 HG01256.hp2 HG01258.hp2 others(18): Show |
intron_variant | MODIFIER | c.863-925A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619674 | |||||||
chr14:50619727 | T | A | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-872T>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619727 | |||||||
chr14:50619728 | G | A | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-871G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619728 | |||||||
chr14:50619729 | T | A | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-870T>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619729 | |||||||
chr14:50619730 | G | A | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-869G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619730 | |||||||
chr14:50619732 | T | A | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-867T>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619732 | |||||||
chr14:50619735 | T | A | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-864T>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619735 | |||||||
chr14:50619736 | G | A | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-863G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619736 | |||||||
chr14:50619737 | A | G | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-862A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619737 | |||||||
chr14:50619738 | G | A | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-861G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619738 | |||||||
chr14:50619739 | T | A | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-860T>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619739 | |||||||
chr14:50619740 | T | A | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-859T>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619740 | |||||||
chr14:50619741 | C | A | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-858C>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619741 | |||||||
chr14:50619742 | C | G | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-857C>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619742 | |||||||
chr14:50619743 | A | G | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-856A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619743 | |||||||
chr14:50619748 | T | TTAAGCAG others(3): Show |
1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-851_863-850ins others(10): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619748 | |||||||
chr14:50619757 | C | T | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-842C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619757 | |||||||
chr14:50619760 | C | G | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-839C>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619760 | |||||||
chr14:50619774 | T | G | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-825T>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619774 | |||||||
chr14:50619780 | A | T | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-819A>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619780 | |||||||
chr14:50619781 | C | A | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-818C>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619781 | |||||||
chr14:50619784 | T | A | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-815T>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619784 | |||||||
chr14:50619785 | G | T | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-814G>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619785 | |||||||
chr14:50619788 | G | T | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-811G>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619788 | |||||||
chr14:50619790 | C | A | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-809C>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619790 | |||||||
chr14:50619793 | G | C | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-806G>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619793 | |||||||
chr14:50619807 | C | G | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-792C>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619807 | |||||||
chr14:50619813 | T | A | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-786T>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619813 | |||||||
chr14:50619814 | T | G | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-785T>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619814 | |||||||
chr14:50619815 | T | G | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-784T>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619815 | |||||||
chr14:50619816 | G | T | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-783G>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619816 | |||||||
chr14:50619817 | T | C | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-782T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619817 | |||||||
chr14:50619831 | G | C | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-768G>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619831 | |||||||
chr14:50619832 | G | C | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-767G>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619832 | |||||||
chr14:50619833 | T | A | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-766T>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619833 | |||||||
chr14:50619834 | G | T | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-765G>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619834 | |||||||
chr14:50619835 | G | T | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-764G>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619835 | |||||||
chr14:50619836 | G | A | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-763G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619836 | |||||||
chr14:50619839 | C | G | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-760C>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619839 | |||||||
chr14:50619840 | G | A | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-759G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619840 | |||||||
chr14:50619843 | A | T | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-756A>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619843 | |||||||
chr14:50619844 | T | A | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-755T>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619844 | |||||||
chr14:50619850 | G | A | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-749G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619850 | |||||||
chr14:50619852 | G | A | 1 | a0001c0003t0001g0043 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.863-747G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619852 | |||||||
chr14:50619853 | C | T | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-746C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619853 | |||||||
chr14:50619859 | T | A | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-740T>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619859 | |||||||
chr14:50619861 | G | A | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-738G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619861 | |||||||
chr14:50619864 | T | A | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-735T>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619864 | |||||||
chr14:50619869 | T | G | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-730T>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619869 | |||||||
chr14:50619870 | T | A | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-729T>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619870 | |||||||
chr14:50619873 | T | A | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-726T>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619873 | |||||||
chr14:50619874 | G | C | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-725G>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619874 | |||||||
chr14:50619878 | G | A | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-721G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619878 | |||||||
chr14:50619884 | C | T | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-715C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619884 | |||||||
chr14:50619885 | A | C | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-714A>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619885 | |||||||
chr14:50619888 | A | T | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-711A>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619888 | |||||||
chr14:50619889 | T | G | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-710T>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619889 | |||||||
chr14:50619892 | T | C | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-707T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619892 | |||||||
chr14:50619894 | A | T | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-705A>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619894 | |||||||
chr14:50619895 | G | T | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-704G>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619895 | |||||||
chr14:50619900 | T | G | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-699T>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619900 | |||||||
chr14:50619901 | A | G | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-698A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619901 | |||||||
chr14:50619903 | A | C | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-696A>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619903 | |||||||
chr14:50619906 | T | C | 1 | a0001c0001t0001g0026 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.863-693T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619906 | |||||||
chr14:50619929 | G | A | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-670G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619929 | |||||||
chr14:50619930 | C | T | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-669C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619930 | |||||||
chr14:50619933 | A | G | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-666A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619933 | |||||||
chr14:50619935 | A | T | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-664A>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619935 | |||||||
chr14:50619936 | T | C | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-663T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619936 | |||||||
chr14:50619939 | A | T | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-660A>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619939 | |||||||
chr14:50619941 | A | T | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-658A>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619941 | |||||||
chr14:50619947 | A | C | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-652A>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619947 | |||||||
chr14:50619953 | A | T | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-646A>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619953 | |||||||
chr14:50619955 | G | T | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-644G>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619955 | |||||||
chr14:50619959 | T | G | 1 | a0001c0002t0001g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.863-640T>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50619959 | |||||||
chr14:50620114 | T | C | 1 | a0001c0002t0001g0243 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.863-485T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50620114 | |||||||
chr14:50620195 | T | G | 3 | a0001c0001t0001g0155 a0001c0001t0001g0172 a0001c0001t0001g0183 |
3 | NA18948.hp1 NA18992.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.863-404T>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50620195 | |||||||
chr14:50620215 | A | G | 1 | a0001c0003t0001g0149 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.863-384A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50620215 | |||||||
chr14:50620545 | A | G | 129 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(126): Show |
138 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.863-54A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 8/13 | chr14 | 50620545 | |||||||
chr14:50620806 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.990+80G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 9/13 | chr14 | 50620806 | |||||||
chr14:50620971 | G | A | 203 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(200): Show |
220 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.990+245G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 9/13 | chr14 | 50620971 | |||||||
chr14:50621013 | T | C | 1 | a0001c0003t0001g0171 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.990+287T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 9/13 | chr14 | 50621013 | |||||||
chr14:50621030 | T | C | 2 | a0001c0001t0001g0010 a0001c0001t0001g0055 |
3 | HG00733.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.990+304T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 9/13 | chr14 | 50621030 | |||||||
chr14:50621046 | C | T | 1 | a0001c0002t0001g0254 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.990+320C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 9/13 | chr14 | 50621046 | |||||||
chr14:50621223 | A | G | 1 | a0001c0003t0001g0043 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.990+497A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 9/13 | chr14 | 50621223 | |||||||
chr14:50621234 | C | G | 1 | a0001c0001t0001g0138 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.990+508C>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 9/13 | chr14 | 50621234 | |||||||
chr14:50621837 | T | G | 1 | a0001c0001t0001g0116 | 1 | HG00438.hp2 | splice_region_variant&intron_variant | LOW | c.991-6T>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 9/13 | chr14 | 50621837 | |||||||
chr14:50621937 | A | C | 1 | a0001c0001t0001g0131 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1047+38A>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 10/13 | chr14 | 50621937 | |||||||
chr14:50622393 | C | T | 2 | a0001c0001t0003g0068 a0001c0001t0003g0069 |
2 | HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1047+494C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 10/13 | chr14 | 50622393 | |||||||
chr14:50622407 | C | T | 2 | a0001c0002t0001g0021 a0001c0002t0001g0246 |
3 | HG01255.hp2 HG01496.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.1047+508C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 10/13 | chr14 | 50622407 | |||||||
chr14:50622414 | T | A | 1 | a0001c0001t0001g0016 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1047+515T>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 10/13 | chr14 | 50622414 | |||||||
chr14:50622453 | G | C | 7 | a0001c0001t0001g0003 a0001c0001t0001g0057 a0001c0001t0001g0058 others(4): Show |
9 | HG02257.hp2 HG02280.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1047+554G>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 10/13 | chr14 | 50622453 | |||||||
chr14:50622477 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1047+578C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 10/13 | chr14 | 50622477 | |||||||
chr14:50622495 | G | C | 4 | a0001c0004t0001g0005 a0001c0004t0001g0030 a0001c0004t0001g0033 others(1): Show |
5 | HG02055.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1047+596G>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 10/13 | chr14 | 50622495 | |||||||
chr14:50622526 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1047+627C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 10/13 | chr14 | 50622526 | |||||||
chr14:50622684 | A | T | 5 | a0001c0001t0001g0082 a0001c0001t0001g0113 a0001c0001t0001g0122 others(2): Show |
5 | HG02074.hp1 HG02129.hp2 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.1048-493A>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 10/13 | chr14 | 50622684 | |||||||
chr14:50622952 | C | T | 2 | a0001c0001t0001g0010 a0001c0001t0001g0055 |
3 | HG00733.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1048-225C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 10/13 | chr14 | 50622952 | |||||||
chr14:50622971 | A | G | 1 | a0001c0008t0001g0146 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1048-206A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 10/13 | chr14 | 50622971 | |||||||
chr14:50623009 | G | T | 185 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(182): Show |
198 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.1048-168G>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 10/13 | chr14 | 50623009 | |||||||
chr14:50623119 | G | A | 26 | a0001c0001t0001g0018 a0001c0001t0001g0071 a0001c0001t0001g0072 others(23): Show |
28 | HG01361.hp1 HG01433.hp1 HG01433.hp2 others(25): Show |
intron_variant | MODIFIER | c.1048-58G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 10/13 | chr14 | 50623119 | |||||||
chr14:50623384 | C | CAT | 138 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(135): Show |
147 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.1119+136_1119+137i others(4): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 11/13 | chr14 | 50623384 | |||||||
chr14:50623397 | T | G | 138 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(135): Show |
147 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.1119+149T>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 11/13 | chr14 | 50623397 | |||||||
chr14:50623398 | A | G | 11 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0057 others(8): Show |
14 | HG01261.hp2 HG01496.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1119+150A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 11/13 | chr14 | 50623398 | |||||||
chr14:50623435 | T | C | 14 | a0001c0003t0001g0007 a0001c0003t0001g0008 a0001c0003t0001g0039 others(11): Show |
15 | HG00408.hp2 HG00423.hp2 HG02015.hp1 others(12): Show |
intron_variant | MODIFIER | c.1119+187T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 11/13 | chr14 | 50623435 | |||||||
chr14:50623494 | G | C | 3 | a0001c0002t0001g0024 a0001c0002t0001g0270 a0001c0002t0001g0273 |
4 | NA18952.hp1 NA18960.hp2 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.1119+246G>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 11/13 | chr14 | 50623494 | |||||||
chr14:50623559 | G | A | 1 | a0001c0012t0001g0268 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1119+311G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 11/13 | chr14 | 50623559 | |||||||
chr14:50623577 | A | G | 138 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(135): Show |
147 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.1119+329A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 11/13 | chr14 | 50623577 | |||||||
chr14:50623618 | AG | A | 6 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(3): Show |
6 | HG01361.hp1 HG01433.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1119+372delG | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr14 | 50623618 | ||||||
chr14:50623630 | A | T | 4 | a0001c0001t0001g0083 a0001c0001t0001g0085 a0001c0001t0001g0086 others(1): Show |
4 | HG01884.hp2 HG02559.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1119+382A>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 11/13 | chr14 | 50623630 | |||||||
chr14:50623861 | G | A | 2 | a0001c0003t0001g0175 a0001c0003t0001g0176 |
2 | HG01069.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.1119+613G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 11/13 | chr14 | 50623861 | |||||||
chr14:50623896 | C | CA | 33 | a0001c0001t0001g0015 a0001c0001t0001g0025 a0001c0001t0001g0089 others(30): Show |
35 | HG00280.hp2 HG00438.hp2 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.1119+657dupA | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr14 | 50623896 | ||||||
chr14:50623971 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1119+723C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 11/13 | chr14 | 50623971 | |||||||
chr14:50624013 | CCACTGCA others(1013): Show |
C | 1 | a0001c0002t0001g0283 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1119+785_1119+1804 others(3): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr14 | 50624013 | ||||||
chr14:50624059 | A | C | 2 | a0001c0001t0001g0010 a0001c0001t0001g0055 |
3 | HG00733.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1119+811A>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 11/13 | chr14 | 50624059 | |||||||
chr14:50624163 | G | A | 54 | a0001c0003t0001g0006 a0001c0003t0001g0007 a0001c0003t0001g0008 others(51): Show |
58 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.1119+915G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 11/13 | chr14 | 50624163 | |||||||
chr14:50624191 | G | A | 1 | a0001c0001t0001g0013 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1119+943G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 11/13 | chr14 | 50624191 | |||||||
chr14:50624216 | G | A | 8 | a0001c0001t0001g0013 a0001c0001t0001g0078 a0001c0001t0001g0079 others(5): Show |
9 | HG01123.hp2 HG01943.hp1 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.1119+968G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 11/13 | chr14 | 50624216 | |||||||
chr14:50624461 | T | A | 2 | a0001c0003t0001g0009 a0001c0003t0001g0052 |
3 | HG01069.hp1 HG01071.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.1119+1213T>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 11/13 | chr14 | 50624461 | |||||||
chr14:50624549 | C | T | 138 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(135): Show |
147 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.1119+1301C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 11/13 | chr14 | 50624549 | |||||||
chr14:50624561 | C | A | 3 | a0001c0001t0001g0018 a0001c0001t0001g0226 a0001c0001t0001g0227 |
4 | HG01433.hp2 HG01891.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1119+1313C>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 11/13 | chr14 | 50624561 | |||||||
chr14:50624600 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1119+1352C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 11/13 | chr14 | 50624600 | |||||||
chr14:50624689 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1119+1441G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 11/13 | chr14 | 50624689 | |||||||
chr14:50624695 | A | G | 1 | a0001c0008t0001g0146 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1119+1447A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 11/13 | chr14 | 50624695 | |||||||
chr14:50624699 | G | A | 1 | a0001c0003t0001g0147 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1119+1451G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 11/13 | chr14 | 50624699 | |||||||
chr14:50624724 | T | A | 197 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(194): Show |
210 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.1119+1476T>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 11/13 | chr14 | 50624724 | |||||||
chr14:50624725 | T | C | 141 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(138): Show |
150 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.1119+1477T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 11/13 | chr14 | 50624725 | |||||||
chr14:50624757 | G | C | 54 | a0001c0003t0001g0006 a0001c0003t0001g0007 a0001c0003t0001g0008 others(51): Show |
58 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.1119+1509G>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 11/13 | chr14 | 50624757 | |||||||
chr14:50624781 | A | T | 232 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(229): Show |
251 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.1119+1533A>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 11/13 | chr14 | 50624781 | |||||||
chr14:50624936 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1119+1688G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 11/13 | chr14 | 50624936 | |||||||
chr14:50624950 | G | T | 2 | a0001c0001t0003g0068 a0001c0001t0003g0069 |
2 | HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1119+1702G>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 11/13 | chr14 | 50624950 | |||||||
chr14:50624985 | G | A | 2 | a0001c0001t0001g0010 a0001c0001t0001g0055 |
3 | HG00733.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1119+1737G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 11/13 | chr14 | 50624985 | |||||||
chr14:50625072 | C | G | 1 | a0001c0001t0001g0138 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1119+1824C>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 11/13 | chr14 | 50625072 | |||||||
chr14:50625085 | G | GA | 209 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(206): Show |
226 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.1119+1844dupA | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr14 | 50625085 | ||||||
chr14:50625209 | A | G | 1 | a0001c0001t0001g0227 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1119+1961A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 11/13 | chr14 | 50625209 | |||||||
chr14:50625416 | A | G | 2 | a0001c0001t0001g0010 a0001c0001t0001g0055 |
3 | HG00733.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1119+2168A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 11/13 | chr14 | 50625416 | |||||||
chr14:50625433 | C | T | 1 | a0001c0003t0001g0038 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1119+2185C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 11/13 | chr14 | 50625433 | |||||||
chr14:50625602 | T | C | 48 | a0001c0003t0001g0006 a0001c0003t0001g0007 a0001c0003t0001g0008 others(45): Show |
52 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.1119+2354T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 11/13 | chr14 | 50625602 | |||||||
chr14:50625640 | G | A | 9 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0210 others(6): Show |
9 | HG00597.hp2 HG02040.hp2 NA18948.hp2 others(6): Show |
intron_variant | MODIFIER | c.1120-2391G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 11/13 | chr14 | 50625640 | |||||||
chr14:50625653 | C | G | 24 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(21): Show |
28 | HG00733.hp1 HG01256.hp2 HG01258.hp2 others(25): Show |
intron_variant | MODIFIER | c.1120-2378C>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 11/13 | chr14 | 50625653 | |||||||
chr14:50625691 | C | A | 1 | a0001c0012t0001g0268 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1120-2340C>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 11/13 | chr14 | 50625691 | |||||||
chr14:50625695 | G | A | 1 | a0001c0001t0001g0213 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1120-2336G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 11/13 | chr14 | 50625695 | |||||||
chr14:50625702 | G | A | 1 | a0001c0003t0001g0043 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1120-2329G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 11/13 | chr14 | 50625702 | |||||||
chr14:50625771 | G | A | 1 | a0001c0003t0001g0038 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1120-2260G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 11/13 | chr14 | 50625771 | |||||||
chr14:50625788 | T | A | 2 | a0001c0001t0001g0278 a0001c0001t0001g0281 |
2 | NA18992.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.1120-2243T>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 11/13 | chr14 | 50625788 | |||||||
chr14:50625806 | A | G | 2 | a0001c0001t0003g0068 a0001c0001t0003g0069 |
2 | HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1120-2225A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 11/13 | chr14 | 50625806 | |||||||
chr14:50625836 | A | G | 138 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(135): Show |
147 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.1120-2195A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 11/13 | chr14 | 50625836 | |||||||
chr14:50625844 | A | G | 138 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(135): Show |
147 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.1120-2187A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 11/13 | chr14 | 50625844 | |||||||
chr14:50625901 | C | CA | 136 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(133): Show |
145 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.1120-2118dupA | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr14 | 50625901 | ||||||
chr14:50625914 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1120-2117G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 11/13 | chr14 | 50625914 | |||||||
chr14:50625915 | A | G | 1 | a0001c0001t0001g0180 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1120-2116A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 11/13 | chr14 | 50625915 | |||||||
chr14:50625968 | A | G | 55 | a0001c0001t0001g0026 a0001c0003t0001g0006 a0001c0003t0001g0007 others(52): Show |
59 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.1120-2063A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 11/13 | chr14 | 50625968 | |||||||
chr14:50625969 | A | C | 55 | a0001c0001t0001g0026 a0001c0003t0001g0006 a0001c0003t0001g0007 others(52): Show |
59 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.1120-2062A>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 11/13 | chr14 | 50625969 | |||||||
chr14:50626203 | A | G | 3 | a0001c0006t0001g0028 a0001c0006t0001g0029 a0001c0009t0001g0084 |
3 | HG02647.hp2 HG03130.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1120-1828A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 11/13 | chr14 | 50626203 | |||||||
chr14:50626219 | GT | G | 5 | a0001c0002t0001g0022 a0001c0002t0001g0234 a0001c0002t0001g0257 others(2): Show |
6 | NA18954.hp1 NA18983.hp1 NA19012.hp1 others(3): Show |
intron_variant | MODIFIER | c.1120-1811delT | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 11/13 | chr14 | 50626219 | |||||||
chr14:50626424 | G | A | 136 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(133): Show |
145 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.1120-1607G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 11/13 | chr14 | 50626424 | |||||||
chr14:50626498 | T | A | 136 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(133): Show |
145 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.1120-1533T>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 11/13 | chr14 | 50626498 | |||||||
chr14:50626557 | A | G | 1 | a0001c0001t0001g0192 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1120-1474A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 11/13 | chr14 | 50626557 | |||||||
chr14:50626732 | T | C | 3 | a0001c0003t0001g0063 a0001c0003t0001g0064 a0001c0003t0001g0065 |
3 | HG01261.hp2 HG01496.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1120-1299T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 11/13 | chr14 | 50626732 | |||||||
chr14:50626815 | T | C | 13 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0057 others(10): Show |
16 | HG01261.hp2 HG01496.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1120-1216T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 11/13 | chr14 | 50626815 | |||||||
chr14:50626924 | C | G | 1 | a0001c0002t0001g0243 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1120-1107C>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 11/13 | chr14 | 50626924 | |||||||
chr14:50627027 | T | C | 231 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(228): Show |
250 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.1120-1004T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 11/13 | chr14 | 50627027 | |||||||
chr14:50627090 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1120-941T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 11/13 | chr14 | 50627090 | |||||||
chr14:50627264 | C | T | 2 | a0001c0001t0001g0101 a0001c0001t0001g0115 |
2 | NA18998.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1120-767C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 11/13 | chr14 | 50627264 | |||||||
chr14:50627329 | T | C | 54 | a0001c0001t0001g0155 a0001c0001t0001g0172 a0001c0001t0001g0183 others(51): Show |
58 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.1120-702T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 11/13 | chr14 | 50627329 | |||||||
chr14:50627630 | C | T | 6 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(3): Show |
6 | HG01361.hp1 HG01433.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1120-401C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 11/13 | chr14 | 50627630 | |||||||
chr14:50627683 | C | T | 54 | a0001c0001t0001g0155 a0001c0001t0001g0172 a0001c0001t0001g0183 others(51): Show |
58 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.1120-348C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 11/13 | chr14 | 50627683 | |||||||
chr14:50627984 | A | C | 5 | a0001c0001t0001g0083 a0001c0001t0001g0085 a0001c0001t0001g0086 others(2): Show |
5 | HG01884.hp2 HG02559.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1120-47A>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 11/13 | chr14 | 50627984 | |||||||
chr14:50628570 | C | A | 1 | a0001c0001t0001g0075 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1551+108C>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 12/13 | chr14 | 50628570 | |||||||
chr14:50628620 | T | C | 4 | a0001c0003t0001g0063 a0001c0003t0001g0064 a0001c0003t0001g0065 others(1): Show |
4 | HG01261.hp2 HG01496.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1551+158T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 12/13 | chr14 | 50628620 | |||||||
chr14:50628702 | T | G | 1 | a0001c0001t0001g0166 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1551+240T>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 12/13 | chr14 | 50628702 | |||||||
chr14:50628711 | T | C | 2 | a0001c0001t0001g0167 a0001c0001t0001g0170 |
2 | HG00642.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.1551+249T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 12/13 | chr14 | 50628711 | |||||||
chr14:50629018 | T | C | 2 | a0001c0007t0001g0070 a0001c0007t0001g0228 |
2 | HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1551+556T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 12/13 | chr14 | 50629018 | |||||||
chr14:50629062 | C | A | 70 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0027 others(67): Show |
77 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.1551+600C>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 12/13 | chr14 | 50629062 | |||||||
chr14:50629299 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1552-696T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 12/13 | chr14 | 50629299 | |||||||
chr14:50629464 | C | G | 1 | a0001c0003t0001g0049 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1552-531C>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 12/13 | chr14 | 50629464 | |||||||
chr14:50629512 | C | T | 10 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0165 others(7): Show |
11 | HG01433.hp2 HG01891.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1552-483C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 12/13 | chr14 | 50629512 | |||||||
chr14:50629529 | C | T | 2 | a0001c0001t0003g0068 a0001c0001t0003g0069 |
2 | HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1552-466C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 12/13 | chr14 | 50629529 | |||||||
chr14:50629582 | C | CA | 59 | a0001c0001t0001g0003 a0001c0001t0001g0057 a0001c0001t0001g0058 others(56): Show |
65 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.1552-413_1552-412i others(3): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 12/13 | chr14 | 50629582 | |||||||
chr14:50629582 | C | CAA | 3 | a0001c0003t0001g0149 a0001c0003t0001g0284 a0001c0004t0001g0032 |
3 | HG01167.hp1 HG02258.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1552-413_1552-412i others(4): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 12/13 | chr14 | 50629582 | |||||||
chr14:50629583 | C | A | 81 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0027 others(78): Show |
88 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.1552-412C>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 12/13 | chr14 | 50629583 | |||||||
chr14:50629583 | C | CA | 31 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0089 others(28): Show |
32 | HG00597.hp1 HG00733.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.1552-395dupA | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr14 | 50629583 | ||||||
chr14:50629584 | A | C | 6 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0073 others(3): Show |
6 | HG01361.hp1 HG01433.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1552-411A>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 12/13 | chr14 | 50629584 | |||||||
chr14:50629601 | C | A | 2 | a0001c0001t0003g0068 a0001c0001t0003g0069 |
2 | HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1552-394C>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 12/13 | chr14 | 50629601 | |||||||
chr14:50629819 | C | T | 10 | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0165 others(7): Show |
11 | HG01433.hp2 HG01891.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1552-176C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 12/13 | chr14 | 50629819 | |||||||
chr14:50629892 | G | GTTCTT | 232 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0010 others(229): Show |
251 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.1552-103_1552-102i others(7): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 12/13 | chr14 | 50629892 | |||||||
chr14:50629926 | G | GAAT | 81 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0027 others(78): Show |
88 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.1552-68_1552-67ins others(3): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr14 | 50629926 | ||||||
chr14:50629926 | G | T | 1 | a0001c0001t0001g0223 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1552-69G>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 12/13 | chr14 | 50629926 | |||||||
chr14:50629934 | T | A | 2 | a0001c0001t0003g0068 a0001c0001t0003g0069 |
2 | HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1552-61T>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 12/13 | chr14 | 50629934 | |||||||
chr14:50629966 | TTTTTC | T | 5 | a0001c0001t0001g0015 a0001c0001t0001g0131 a0001c0001t0001g0132 others(2): Show |
6 | HG01257.hp2 HG01517.hp1 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.1552-24_1552-20del others(5): Show |
ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr14 | 50629966 | ||||||
chr14:50630288 | T | A | 3 | a0001c0002t0001g0232 a0001c0002t0001g0254 a0001c0002t0001g0255 |
3 | NA18939.hp1 NA18957.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.1566+279T>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 13/13 | chr14 | 50630288 | |||||||
chr14:50630709 | T | C | 10 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0057 others(7): Show |
13 | HG02257.hp1 HG02257.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.1566+700T>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 13/13 | chr14 | 50630709 | |||||||
chr14:50630864 | A | C | 4 | a0001c0003t0001g0063 a0001c0003t0001g0064 a0001c0003t0001g0065 others(1): Show |
4 | HG01261.hp2 HG01496.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1566+855A>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 13/13 | chr14 | 50630864 | |||||||
chr14:50630996 | C | T | 1 | a0001c0001t0001g0286 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1566+987C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 13/13 | chr14 | 50630996 | |||||||
chr14:50631097 | A | G | 7 | a0001c0001t0003g0068 a0001c0001t0003g0069 a0001c0001t0003g0124 others(4): Show |
7 | HG01261.hp2 HG01496.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1566+1088A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 13/13 | chr14 | 50631097 | |||||||
chr14:50631100 | A | C | 1 | a0001c0001t0001g0144 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1566+1091A>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 13/13 | chr14 | 50631100 | |||||||
chr14:50631147 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1567-1082C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 13/13 | chr14 | 50631147 | |||||||
chr14:50631190 | G | C | 1 | a0001c0001t0001g0162 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1567-1039G>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 13/13 | chr14 | 50631190 | |||||||
chr14:50631194 | T | G | 1 | a0001c0003t0001g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1567-1035T>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 13/13 | chr14 | 50631194 | |||||||
chr14:50631211 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1567-1018C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 13/13 | chr14 | 50631211 | |||||||
chr14:50631212 | G | A | 1 | a0001c0002t0001g0245 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1567-1017G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 13/13 | chr14 | 50631212 | |||||||
chr14:50631257 | C | T | 3 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 |
3 | HG02257.hp1 HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1567-972C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 13/13 | chr14 | 50631257 | |||||||
chr14:50631266 | TA | T | 4 | a0001c0001t0001g0027 a0001c0001t0001g0140 a0001c0003t0001g0284 others(1): Show |
4 | HG00280.hp1 HG01167.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1567-957delA | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr14 | 50631266 | ||||||
chr14:50631272 | A | C | 1 | a0001c0001t0001g0138 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1567-957A>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 13/13 | chr14 | 50631272 | |||||||
chr14:50631272 | AC | A | 53 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0057 others(50): Show |
59 | HG00423.hp2 HG00639.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.1567-956delC | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 13/13 | chr14 | 50631272 | |||||||
chr14:50631273 | C | A | 167 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(164): Show |
179 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.1567-956C>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 13/13 | chr14 | 50631273 | |||||||
chr14:50631278 | A | C | 1 | a0001c0001t0001g0117 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1567-951A>C | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 13/13 | chr14 | 50631278 | |||||||
chr14:50631279 | C | A | 1 | a0001c0001t0001g0091 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1567-950C>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 13/13 | chr14 | 50631279 | |||||||
chr14:50631415 | C | G | 3 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 |
3 | HG02257.hp1 HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1567-814C>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 13/13 | chr14 | 50631415 | |||||||
chr14:50631505 | C | G | 1 | a0001c0001t0001g0088 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1567-724C>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 13/13 | chr14 | 50631505 | |||||||
chr14:50631696 | G | A | 4 | a0001c0003t0001g0063 a0001c0003t0001g0064 a0001c0003t0001g0065 others(1): Show |
4 | HG01261.hp2 HG01496.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1567-533G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 13/13 | chr14 | 50631696 | |||||||
chr14:50631713 | G | A | 2 | a0001c0001t0003g0068 a0001c0001t0003g0069 |
2 | HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1567-516G>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 13/13 | chr14 | 50631713 | |||||||
chr14:50631894 | C | T | 1 | a0001c0001t0002g0188 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1567-335C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 13/13 | chr14 | 50631894 | |||||||
chr14:50632033 | A | AC | 3 | a0001c0006t0001g0028 a0001c0006t0001g0029 a0001c0009t0001g0084 |
3 | HG02647.hp2 HG03130.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1567-195dupC | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr14 | 50632033 | ||||||
chr14:50632151 | A | G | 8 | a0001c0001t0001g0010 a0001c0001t0001g0055 a0001c0001t0001g0059 others(5): Show |
10 | HG00733.hp1 HG01256.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1567-78A>G | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 13/13 | chr14 | 50632151 | |||||||
chr14:50632152 | C | A | 5 | a0001c0003t0001g0105 a0001c0003t0001g0157 a0001c0003t0001g0158 others(2): Show |
5 | HG02145.hp1 HG02818.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1567-77C>A | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 13/13 | chr14 | 50632152 | |||||||
chr14:50632152 | C | T | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | HG00438.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.1567-77C>T | ATL1 | ENSG00000198513.14 | transcript | ENST00000358385.12 | protein_coding | 13/13 | chr14 | 50632152 |