Item | Value |
---|---|
geneid | 957 |
ensemblid | ENSG00000187097.13 |
hgncid | 3367 |
symbol | ENTPD5 |
name | ectonucleoside triphosphate diphosphohydrolase 5 (inactive) |
refseq_nuc | NM_001249.5 |
refseq_prot | NP_001240.1 |
ensembl_nuc | ENST00000334696.11 |
ensembl_prot | ENSP00000335246.6 |
mane_status | MANE Select |
chr | chr14 |
start | 73963230 |
end | 74019288 |
strand | - |
ver | v1.2 |
region | chr14:73963230-74019288 |
region5000 | chr14:73958230-74024288 |
regionname0 | ENTPD5_chr14_73963230_74019288 |
regionname5000 | ENTPD5_chr14_73958230_74024288 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 428 | 371 | 83 | 68 | 154 | 16 | 48 | 120 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | MATSW others(423): Show |
chr14 | 73958230 | 74024288 |
a0002 | 0/0 | 428 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | MATSW others(423): Show |
chr14 | 73958230 | 74024288 |
a0003 | 0/0 | 428 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | MATSW others(423): Show |
chr14 | 73958230 | 74024288 |
a0004 | 0/0 | 428 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | MATSW others(423): Show |
chr14 | 73958230 | 74024288 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1284 | 199 | 51 | 24 | 95 | 7 | 20 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | ATGGC others(1279): Show |
chr14 | 73958230 | 74024288 | ||
a0001c0002 | 0/0 | 1284 | 168 | 31 | 44 | 57 | 9 | 27 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | ATGGC others(1279): Show |
chr14 | 73958230 | 74024288 | ||
a0001c0005 | 0/0 | 1284 | 2 | 0 | 0 | 2 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | ATGGC others(1279): Show |
chr14 | 73958230 | 74024288 | ||
a0001c0007 | 0/0 | 1284 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | ATGGC others(1279): Show |
chr14 | 73958230 | 74024288 | ||
a0001c0008 | 0/0 | 1284 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | ATGGC others(1279): Show |
chr14 | 73958230 | 74024288 | ||
a0002c0003 | 0/0 | 1284 | 5 | 5 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | ATGGC others(1279): Show |
chr14 | 73958230 | 74024288 | ||
a0003c0004 | 0/0 | 1284 | 2 | 2 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | ATGGC others(1279): Show |
chr14 | 73958230 | 74024288 | ||
a0004c0006 | 0/0 | 1284 | 2 | 2 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | ATGGC others(1279): Show |
chr14 | 73958230 | 74024288 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 5262 | 62 | 1 | 9 | 43 | 2 | 6 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | GAGGG others(5257): Show |
chr14 | 73958230 | 74024288 |
a0001c0001t0004 | 0/0 | 5261 | 37 | 17 | 1 | 9 | 0 | 10 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | GAGGG others(5256): Show |
chr14 | 73958230 | 74024288 |
a0001c0001t0005 | 0/0 | 5262 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | GAGGG others(5257): Show |
chr14 | 73958230 | 74024288 |
a0001c0001t0006 | 1/0 | 5261 | 30 | 7 | 5 | 11 | 4 | 2 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | GAGGG others(5256): Show |
chr14 | 73958230 | 74024288 |
a0001c0001t0007 | 0/0 | 5261 | 24 | 0 | 0 | 24 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | GAGGG others(5256): Show |
chr14 | 73958230 | 74024288 |
a0001c0001t0011 | 0/0 | 5251 | 6 | 6 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | GAGGG others(5246): Show |
chr14 | 73958230 | 74024288 |
a0001c0001t0012 | 0/0 | 5260 | 5 | 4 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | GAGGG others(5255): Show |
chr14 | 73958230 | 74024288 |
a0001c0001t0013 | 0/0 | 5261 | 4 | 0 | 0 | 4 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | GAGGG others(5256): Show |
chr14 | 73958230 | 74024288 |
a0001c0001t0014 | 0/0 | 5261 | 4 | 0 | 3 | 0 | 1 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | GAGGG others(5256): Show |
chr14 | 73958230 | 74024288 |
a0001c0001t0015 | 0/0 | 5261 | 4 | 1 | 3 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | GAGGG others(5256): Show |
chr14 | 73958230 | 74024288 |
a0001c0001t0016 | 0/0 | 5260 | 4 | 3 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | GAGGG others(5255): Show |
chr14 | 73958230 | 74024288 |
a0001c0001t0018 | 0/0 | 5261 | 3 | 3 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | GAGGG others(5256): Show |
chr14 | 73958230 | 74024288 |
a0001c0001t0019 | 0/0 | 5261 | 3 | 2 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | GAGGG others(5256): Show |
chr14 | 73958230 | 74024288 |
a0001c0001t0022 | 0/0 | 5251 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | GAGGG others(5246): Show |
chr14 | 73958230 | 74024288 |
a0001c0001t0023 | 0/0 | 5261 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | GAGGG others(5256): Show |
chr14 | 73958230 | 74024288 |
a0001c0001t0024 | 0/0 | 5261 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | GAGGG others(5256): Show |
chr14 | 73958230 | 74024288 |
a0001c0001t0025 | 0/0 | 5261 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | GAGGG others(5256): Show |
chr14 | 73958230 | 74024288 |
a0001c0001t0026 | 0/0 | 5260 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | GAGGG others(5255): Show |
chr14 | 73958230 | 74024288 |
a0001c0001t0028 | 0/0 | 5261 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | GAGGG others(5256): Show |
chr14 | 73958230 | 74024288 |
a0001c0001t0030 | 0/0 | 5261 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | GAGGG others(5256): Show |
chr14 | 73958230 | 74024288 |
a0001c0001t0031 | 0/0 | 5261 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | GAGGG others(5256): Show |
chr14 | 73958230 | 74024288 |
a0001c0001t0032 | 0/0 | 5261 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | GAGGG others(5256): Show |
chr14 | 73958230 | 74024288 |
a0001c0001t0033 | 0/0 | 5261 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | GAGGG others(5256): Show |
chr14 | 73958230 | 74024288 |
a0001c0001t0034 | 0/0 | 5262 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | GAGGG others(5257): Show |
chr14 | 73958230 | 74024288 |
a0001c0001t0035 | 0/0 | 5261 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | GAGGG others(5256): Show |
chr14 | 73958230 | 74024288 |
a0001c0002t0002 | 0/0 | 5262 | 54 | 2 | 9 | 30 | 2 | 11 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | GAGGG others(5257): Show |
chr14 | 73958230 | 74024288 |
a0001c0002t0003 | 0/0 | 5261 | 44 | 10 | 6 | 15 | 4 | 9 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | GAGGG others(5256): Show |
chr14 | 73958230 | 74024288 |
a0001c0002t0005 | 0/0 | 5262 | 35 | 0 | 18 | 9 | 2 | 6 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | GAGGG others(5257): Show |
chr14 | 73958230 | 74024288 |
a0001c0002t0008 | 0/0 | 5261 | 12 | 9 | 3 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | GAGGG others(5256): Show |
chr14 | 73958230 | 74024288 |
a0001c0002t0009 | 0/0 | 5258 | 4 | 3 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | GAGGG others(5253): Show |
chr14 | 73958230 | 74024288 |
a0001c0002t0010 | 0/0 | 5261 | 7 | 6 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | GAGGG others(5256): Show |
chr14 | 73958230 | 74024288 |
a0001c0002t0017 | 0/0 | 5261 | 4 | 0 | 3 | 0 | 1 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | GAGGG others(5256): Show |
chr14 | 73958230 | 74024288 |
a0001c0002t0020 | 0/0 | 5262 | 2 | 0 | 0 | 2 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | GAGGG others(5257): Show |
chr14 | 73958230 | 74024288 |
a0001c0002t0021 | 0/0 | 5261 | 2 | 1 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | GAGGG others(5256): Show |
chr14 | 73958230 | 74024288 |
a0001c0002t0027 | 0/0 | 5261 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | GAGGG others(5256): Show |
chr14 | 73958230 | 74024288 |
a0001c0002t0029 | 0/0 | 5262 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | GAGGG others(5257): Show |
chr14 | 73958230 | 74024288 |
a0001c0002t0036 | 0/0 | 5261 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | GAGGG others(5256): Show |
chr14 | 73958230 | 74024288 |
a0001c0002t0037 | 0/0 | 5261 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | GAGGG others(5256): Show |
chr14 | 73958230 | 74024288 |
a0001c0005t0002 | 0/0 | 5262 | 2 | 0 | 0 | 2 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | GAGGG others(5257): Show |
chr14 | 73958230 | 74024288 |
a0001c0007t0009 | 0/0 | 5258 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | GAGGG others(5253): Show |
chr14 | 73958230 | 74024288 |
a0001c0008t0002 | 0/0 | 5262 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | GAGGG others(5257): Show |
chr14 | 73958230 | 74024288 |
a0002c0003t0009 | 0/0 | 5258 | 5 | 5 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | GAGGG others(5253): Show |
chr14 | 73958230 | 74024288 |
a0003c0004t0006 | 0/0 | 5261 | 2 | 2 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | GAGGG others(5256): Show |
chr14 | 73958230 | 74024288 |
a0004c0006t0004 | 0/0 | 5261 | 2 | 2 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | GAGGG others(5256): Show |
chr14 | 73958230 | 74024288 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 13 | 0 | 0 | 10 | 1 | 2 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0186 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0004g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0005g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0006g0011 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0006g0025 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0006g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0006g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0006g0068 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0006g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0006g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0006g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0006g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0006g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0006g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0006g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0006g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0006g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0006g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0006g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0006g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0006g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0006g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0006g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0006g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0006g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0006g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0006g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0006g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0006g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0006g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0007g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0007g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0007g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0007g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0007g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0007g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0007g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0007g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0007g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0007g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0007g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0007g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0007g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0007g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0007g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0007g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0007g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0007g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0007g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0011g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0011g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0011g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0011g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0011g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0011g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0012g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0012g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0012g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0012g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0012g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0013g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0013g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0013g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0013g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0014g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0014g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0014g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0014g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0015g0017 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0015g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0015g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0016g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0016g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0016g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0016g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0018g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0018g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0019g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0019g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0022g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0023g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0024g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0025g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0026g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0028g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0030g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0031g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0032g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0033g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0034g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0001t0035g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0006 | 0/0 | 4 | 0 | 0 | 1 | 2 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0027 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0028 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0002g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0005 | 0/0 | 4 | 2 | 1 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0009 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0015 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0003g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0005g0002 | 0/0 | 5 | 0 | 3 | 1 | 1 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0005g0004 | 0/0 | 4 | 0 | 0 | 1 | 0 | 3 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0005g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0005g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0005g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0005g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0005g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0005g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0005g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0005g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0005g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0005g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0005g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0005g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0005g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0005g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0005g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0005g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0005g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0005g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0005g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0005g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0005g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0005g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0005g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0005g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0005g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0005g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0008g0032 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0008g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0008g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0008g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0008g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0008g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0008g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0008g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0008g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0008g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0008g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0009g0010 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0009g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0010g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0010g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0010g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0010g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0010g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0010g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0017g0014 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0017g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0017g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0020g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0020g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0021g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0021g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0027g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0029g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0036g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0002t0037g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0005t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0005t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0007t0009g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0001c0008t0002g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0002c0003t0009g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0002c0003t0009g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0002c0003t0009g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0003c0004t0006g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0003c0004t0006g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
a0004c0006t0004g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0014 | g0237 | EUR | GBR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG00099 | hp2 | a0001 | c0002 | t0003 | g0092 | EUR | GBR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG00280 | hp1 | a0001 | c0002 | t0017 | g0014 | EUR | FIN | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG00280 | hp2 | a0001 | c0002 | t0005 | g0002 | EUR | FIN | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG00323 | hp1 | a0001 | c0002 | t0005 | g0046 | EUR | FIN | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0194 | EUR | FIN | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG00408 | hp1 | a0001 | c0002 | t0002 | g0030 | EAS | CHS | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG00408 | hp2 | a0001 | c0001 | t0004 | g0235 | EAS | CHS | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | CHS | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG00423 | hp2 | a0001 | c0002 | t0002 | g0285 | EAS | CHS | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG00438 | hp1 | a0001 | c0001 | t0013 | g0229 | EAS | CHS | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG00438 | hp2 | a0001 | c0001 | t0007 | g0157 | EAS | CHS | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG00558 | hp2 | a0001 | c0002 | t0003 | g0005 | EAS | CHS | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG00639 | hp1 | a0001 | c0002 | t0003 | g0122 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG00639 | hp2 | a0001 | c0002 | t0005 | g0002 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG00642 | hp1 | a0001 | c0002 | t0003 | g0096 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG00642 | hp2 | a0001 | c0002 | t0002 | g0299 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG00673 | hp1 | a0001 | c0002 | t0002 | g0027 | EAS | CHS | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG00735 | hp1 | a0001 | c0001 | t0006 | g0079 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG00735 | hp2 | a0001 | c0002 | t0002 | g0298 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG00738 | hp1 | a0001 | c0002 | t0003 | g0083 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG00738 | hp2 | a0001 | c0001 | t0014 | g0239 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG00741 | hp1 | a0001 | c0002 | t0005 | g0056 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG00741 | hp2 | a0001 | c0001 | t0014 | g0238 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01069 | hp2 | a0001 | c0002 | t0002 | g0292 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01070 | hp1 | a0001 | c0002 | t0005 | g0034 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01070 | hp2 | a0001 | c0001 | t0006 | g0025 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01071 | hp2 | a0001 | c0002 | t0005 | g0002 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01074 | hp1 | a0001 | c0001 | t0015 | g0017 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01074 | hp2 | a0001 | c0001 | t0004 | g0219 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01081 | hp1 | a0001 | c0001 | t0019 | g0115 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01099 | hp1 | a0001 | c0001 | t0015 | g0125 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01099 | hp2 | a0001 | c0002 | t0005 | g0040 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01106 | hp1 | a0001 | c0002 | t0005 | g0047 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01106 | hp2 | a0001 | c0001 | t0006 | g0070 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01109 | hp1 | a0001 | c0002 | t0008 | g0032 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01109 | hp2 | a0001 | c0002 | t0009 | g0010 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01167 | hp1 | a0001 | c0002 | t0005 | g0039 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01167 | hp2 | a0001 | c0002 | t0002 | g0276 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01168 | hp1 | a0001 | c0002 | t0002 | g0269 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01168 | hp2 | a0001 | c0002 | t0005 | g0051 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01169 | hp1 | a0001 | c0002 | t0005 | g0052 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01169 | hp2 | a0001 | c0002 | t0002 | g0278 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01175 | hp1 | a0001 | c0001 | t0014 | g0247 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01175 | hp2 | a0001 | c0001 | t0015 | g0124 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01192 | hp1 | a0001 | c0001 | t0006 | g0026 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01243 | hp1 | a0001 | c0002 | t0008 | g0065 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01243 | hp2 | a0001 | c0002 | t0010 | g0202 | AMR | PUR | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01255 | hp1 | a0001 | c0001 | t0006 | g0069 | AMR | CLM | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01255 | hp2 | a0001 | c0002 | t0017 | g0014 | AMR | CLM | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01256 | hp1 | a0001 | c0002 | t0029 | g0043 | AMR | CLM | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01258 | hp1 | a0001 | c0002 | t0017 | g0090 | AMR | CLM | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01261 | hp1 | a0001 | c0002 | t0005 | g0050 | AMR | CLM | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01261 | hp2 | a0001 | c0002 | t0003 | g0207 | AMR | CLM | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01346 | hp1 | a0001 | c0002 | t0002 | g0272 | AMR | CLM | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01346 | hp2 | a0001 | c0002 | t0005 | g0048 | AMR | CLM | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01358 | hp1 | a0001 | c0002 | t0002 | g0027 | AMR | CLM | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01358 | hp2 | a0001 | c0002 | t0003 | g0100 | AMR | CLM | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01433 | hp1 | a0001 | c0001 | t0035 | g0041 | AMR | CLM | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01433 | hp2 | a0001 | c0002 | t0037 | g0091 | AMR | CLM | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01496 | hp2 | a0001 | c0002 | t0008 | g0302 | AMR | CLM | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01515 | hp1 | a0001 | c0001 | t0006 | g0104 | EUR | IBS | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01515 | hp2 | a0001 | c0001 | t0006 | g0011 | EUR | IBS | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01516 | hp1 | a0001 | c0002 | t0003 | g0015 | EUR | IBS | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01516 | hp2 | a0001 | c0002 | t0002 | g0006 | EUR | IBS | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01517 | hp1 | a0001 | c0002 | t0003 | g0105 | EUR | IBS | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01517 | hp2 | a0001 | c0001 | t0006 | g0011 | EUR | IBS | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01884 | hp1 | a0001 | c0001 | t0006 | g0199 | AFR | ACB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01884 | hp2 | a0001 | c0001 | t0006 | g0116 | AFR | ACB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01891 | hp1 | a0003 | c0004 | t0006 | g0111 | AFR | ACB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01891 | hp2 | a0004 | c0006 | t0004 | g0013 | AFR | ACB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PEL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01928 | hp2 | a0001 | c0002 | t0005 | g0042 | AMR | PEL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01934 | hp1 | a0001 | c0002 | t0005 | g0044 | AMR | PEL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01934 | hp2 | a0001 | c0002 | t0003 | g0005 | AMR | PEL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01943 | hp2 | a0001 | c0002 | t0005 | g0062 | AMR | PEL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01978 | hp1 | a0001 | c0002 | t0005 | g0057 | AMR | PEL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01978 | hp2 | a0001 | c0002 | t0021 | g0081 | AMR | PEL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01981 | hp1 | a0001 | c0002 | t0005 | g0045 | AMR | PEL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01981 | hp2 | a0001 | c0002 | t0002 | g0315 | AMR | PEL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02040 | hp1 | a0001 | c0002 | t0003 | g0088 | EAS | KHV | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02040 | hp2 | a0001 | c0002 | t0005 | g0002 | EAS | KHV | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02055 | hp1 | a0001 | c0002 | t0002 | g0086 | AFR | ACB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02055 | hp2 | a0002 | c0003 | t0009 | g0074 | AFR | ACB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02071 | hp1 | a0001 | c0001 | t0007 | g0063 | EAS | KHV | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | KHV | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02080 | hp1 | a0001 | c0001 | t0007 | g0003 | EAS | KHV | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02083 | hp2 | a0001 | c0002 | t0002 | g0279 | EAS | KHV | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02129 | hp1 | a0001 | c0002 | t0005 | g0004 | EAS | KHV | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02132 | hp1 | a0001 | c0001 | t0004 | g0226 | EAS | KHV | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02132 | hp2 | a0001 | c0002 | t0003 | g0089 | EAS | KHV | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02135 | hp2 | a0001 | c0002 | t0002 | g0297 | EAS | KHV | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02145 | hp1 | a0001 | c0002 | t0008 | g0304 | AFR | ACB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02145 | hp2 | a0001 | c0002 | t0003 | g0317 | AFR | ACB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02148 | hp1 | a0001 | c0002 | t0005 | g0002 | AMR | PEL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02148 | hp2 | a0001 | c0002 | t0017 | g0077 | AMR | PEL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02155 | hp1 | a0001 | c0001 | t0006 | g0255 | EAS | CDX | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02155 | hp2 | a0001 | c0001 | t0004 | g0240 | EAS | CDX | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02165 | hp1 | a0001 | c0002 | t0005 | g0054 | EAS | CDX | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02257 | hp1 | a0002 | c0003 | t0009 | g0007 | AFR | ACB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02257 | hp2 | a0001 | c0002 | t0003 | g0084 | AFR | ACB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02258 | hp1 | a0001 | c0001 | t0011 | g0137 | AFR | ACB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02258 | hp2 | a0001 | c0001 | t0004 | g0075 | AFR | ACB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02280 | hp1 | a0001 | c0001 | t0011 | g0139 | AFR | ACB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02280 | hp2 | a0001 | c0002 | t0003 | g0102 | AFR | ACB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02451 | hp1 | a0001 | c0002 | t0003 | g0005 | AFR | ACB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02451 | hp2 | a0001 | c0001 | t0004 | g0023 | AFR | ACB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02523 | hp1 | a0001 | c0001 | t0007 | g0283 | EAS | KHV | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02572 | hp1 | a0001 | c0001 | t0006 | g0109 | AFR | GWD | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02572 | hp2 | a0001 | c0001 | t0012 | g0131 | AFR | GWD | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02602 | hp1 | a0001 | c0002 | t0005 | g0004 | SAS | PJL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02602 | hp2 | a0001 | c0001 | t0004 | g0246 | SAS | PJL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02622 | hp1 | a0001 | c0001 | t0022 | g0140 | AFR | GWD | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02622 | hp2 | a0001 | c0001 | t0012 | g0320 | AFR | GWD | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02630 | hp1 | a0001 | c0001 | t0006 | g0123 | AFR | GWD | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02630 | hp2 | a0001 | c0002 | t0008 | g0301 | AFR | GWD | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02647 | hp1 | a0001 | c0001 | t0012 | g0130 | AFR | GWD | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02647 | hp2 | a0001 | c0001 | t0015 | g0017 | AFR | GWD | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02683 | hp2 | a0001 | c0002 | t0003 | g0085 | SAS | PJL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02698 | hp1 | a0001 | c0001 | t0004 | g0222 | SAS | PJL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02717 | hp1 | a0001 | c0001 | t0004 | g0210 | AFR | GWD | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02717 | hp2 | a0001 | c0001 | t0012 | g0319 | AFR | GWD | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02723 | hp1 | a0002 | c0003 | t0009 | g0007 | AFR | GWD | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02723 | hp2 | a0001 | c0002 | t0008 | g0066 | AFR | GWD | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02735 | hp1 | a0001 | c0002 | t0005 | g0055 | SAS | PJL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02735 | hp2 | a0001 | c0001 | t0030 | g0120 | SAS | PJL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02738 | hp1 | a0001 | c0002 | t0002 | g0293 | SAS | PJL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02738 | hp2 | a0001 | c0002 | t0005 | g0060 | SAS | PJL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02809 | hp1 | a0001 | c0002 | t0003 | g0197 | AFR | GWD | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02809 | hp2 | a0001 | c0001 | t0004 | g0201 | AFR | GWD | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02818 | hp1 | a0001 | c0001 | t0026 | g0033 | AFR | GWD | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02818 | hp2 | a0001 | c0001 | t0025 | g0133 | AFR | GWD | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02886 | hp1 | a0002 | c0003 | t0009 | g0073 | AFR | GWD | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02886 | hp2 | a0001 | c0001 | t0004 | g0216 | AFR | GWD | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02895 | hp1 | a0001 | c0002 | t0003 | g0005 | AFR | GWD | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02895 | hp2 | a0001 | c0002 | t0010 | g0206 | AFR | GWD | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02897 | hp1 | a0001 | c0002 | t0010 | g0204 | AFR | GWD | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02897 | hp2 | a0001 | c0002 | t0003 | g0087 | AFR | GWD | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02922 | hp1 | a0001 | c0001 | t0011 | g0135 | AFR | ESN | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02922 | hp2 | a0001 | c0001 | t0018 | g0249 | AFR | ESN | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02965 | hp1 | a0001 | c0001 | t0011 | g0134 | AFR | ESN | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02965 | hp2 | a0001 | c0001 | t0023 | g0132 | AFR | ESN | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02970 | hp1 | a0001 | c0001 | t0016 | g0113 | AFR | ESN | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02970 | hp2 | a0001 | c0001 | t0004 | g0209 | AFR | ESN | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02976 | hp1 | a0001 | c0001 | t0018 | g0012 | AFR | ESN | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02976 | hp2 | a0001 | c0002 | t0008 | g0300 | AFR | ESN | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03017 | hp2 | a0001 | c0002 | t0003 | g0245 | SAS | PJL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03041 | hp1 | a0001 | c0002 | t0008 | g0064 | AFR | GWD | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03041 | hp2 | a0001 | c0001 | t0004 | g0196 | AFR | GWD | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03098 | hp1 | a0001 | c0001 | t0004 | g0129 | AFR | MSL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03098 | hp2 | a0001 | c0001 | t0006 | g0127 | AFR | MSL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03130 | hp1 | a0001 | c0001 | t0004 | g0195 | AFR | ESN | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03130 | hp2 | a0001 | c0001 | t0004 | g0076 | AFR | ESN | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03139 | hp1 | a0001 | c0001 | t0028 | g0200 | AFR | ESN | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03139 | hp2 | a0004 | c0006 | t0004 | g0013 | AFR | ESN | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03195 | hp1 | a0001 | c0001 | t0004 | g0215 | AFR | ESN | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03195 | hp2 | a0001 | c0002 | t0009 | g0010 | AFR | ESN | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03209 | hp1 | a0001 | c0001 | t0004 | g0023 | AFR | MSL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03209 | hp2 | a0001 | c0002 | t0008 | g0303 | AFR | MSL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03239 | hp1 | a0001 | c0002 | t0002 | g0277 | SAS | PJL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03239 | hp2 | a0001 | c0002 | t0003 | g0093 | SAS | PJL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03453 | hp1 | a0001 | c0001 | t0011 | g0138 | AFR | MSL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03453 | hp2 | a0001 | c0002 | t0009 | g0010 | AFR | MSL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03486 | hp1 | a0001 | c0001 | t0004 | g0128 | AFR | MSL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03486 | hp2 | a0001 | c0002 | t0010 | g0205 | AFR | MSL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03490 | hp1 | a0001 | c0002 | t0003 | g0009 | SAS | PJL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03490 | hp2 | a0001 | c0002 | t0002 | g0112 | SAS | PJL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03491 | hp1 | a0001 | c0002 | t0002 | g0270 | SAS | PJL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03491 | hp2 | a0001 | c0002 | t0005 | g0004 | SAS | PJL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03492 | hp1 | a0001 | c0002 | t0005 | g0004 | SAS | PJL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03492 | hp2 | a0001 | c0002 | t0003 | g0009 | SAS | PJL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03540 | hp1 | a0001 | c0001 | t0019 | g0016 | AFR | GWD | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03540 | hp2 | a0001 | c0002 | t0010 | g0022 | AFR | GWD | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03579 | hp1 | a0001 | c0002 | t0008 | g0250 | AFR | MSL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03579 | hp2 | a0001 | c0001 | t0024 | g0260 | AFR | MSL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03654 | hp1 | a0001 | c0002 | t0003 | g0080 | SAS | PJL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03654 | hp2 | a0001 | c0002 | t0003 | g0078 | SAS | PJL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03669 | hp1 | a0001 | c0002 | t0003 | g0009 | SAS | PJL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03669 | hp2 | a0001 | c0001 | t0004 | g0234 | SAS | PJL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03688 | hp1 | a0001 | c0002 | t0002 | g0290 | SAS | STU | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03688 | hp2 | a0001 | c0001 | t0004 | g0243 | SAS | STU | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03704 | hp1 | a0001 | c0002 | t0003 | g0244 | SAS | PJL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03704 | hp2 | a0001 | c0008 | t0002 | g0287 | SAS | PJL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | BEB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03831 | hp2 | a0001 | c0001 | t0004 | g0241 | SAS | BEB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03834 | hp1 | a0001 | c0002 | t0002 | g0028 | SAS | BEB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03834 | hp2 | a0001 | c0002 | t0002 | g0223 | SAS | BEB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03927 | hp1 | a0001 | c0002 | t0036 | g0049 | SAS | BEB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03927 | hp2 | a0001 | c0002 | t0002 | g0263 | SAS | BEB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03942 | hp1 | a0001 | c0002 | t0005 | g0059 | SAS | BEB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03942 | hp2 | a0001 | c0001 | t0004 | g0242 | SAS | BEB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG04115 | hp1 | a0001 | c0002 | t0002 | g0295 | SAS | STU | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG04115 | hp2 | a0001 | c0001 | t0004 | g0225 | SAS | STU | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG04184 | hp1 | a0001 | c0001 | t0012 | g0141 | SAS | BEB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG04184 | hp2 | a0001 | c0001 | t0006 | g0067 | SAS | BEB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG04199 | hp1 | a0001 | c0002 | t0002 | g0006 | SAS | STU | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG04199 | hp2 | a0001 | c0001 | t0004 | g0224 | SAS | STU | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG04204 | hp1 | a0001 | c0001 | t0004 | g0230 | SAS | STU | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG04204 | hp2 | a0001 | c0002 | t0002 | g0294 | SAS | STU | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG04228 | hp1 | a0001 | c0001 | t0006 | g0071 | SAS | STU | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG04228 | hp2 | a0001 | c0001 | t0004 | g0232 | SAS | STU | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18522 | hp1 | a0001 | c0001 | t0004 | g0218 | AFR | YRI | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18522 | hp2 | a0001 | c0001 | t0006 | g0117 | AFR | YRI | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18612 | hp1 | a0001 | c0001 | t0006 | g0254 | EAS | CHB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | CHB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18906 | hp1 | a0001 | c0002 | t0010 | g0022 | AFR | YRI | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18906 | hp2 | a0001 | c0002 | t0009 | g0208 | AFR | YRI | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18941 | hp2 | a0001 | c0002 | t0002 | g0262 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18944 | hp1 | a0001 | c0001 | t0006 | g0257 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18944 | hp2 | a0001 | c0002 | t0002 | g0311 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18946 | hp1 | a0001 | c0002 | t0002 | g0261 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18946 | hp2 | a0001 | c0001 | t0007 | g0198 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18947 | hp1 | a0001 | c0002 | t0003 | g0118 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18947 | hp2 | a0001 | c0002 | t0002 | g0312 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18948 | hp1 | a0001 | c0002 | t0002 | g0286 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18948 | hp2 | a0001 | c0001 | t0007 | g0003 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18950 | hp1 | a0001 | c0002 | t0002 | g0031 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18952 | hp1 | a0001 | c0002 | t0003 | g0101 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18952 | hp2 | a0001 | c0001 | t0006 | g0253 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18953 | hp1 | a0001 | c0005 | t0002 | g0306 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18953 | hp2 | a0001 | c0001 | t0007 | g0164 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18954 | hp1 | a0001 | c0002 | t0002 | g0030 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18956 | hp2 | a0001 | c0002 | t0002 | g0028 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18957 | hp1 | a0001 | c0002 | t0002 | g0275 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18957 | hp2 | a0001 | c0002 | t0005 | g0144 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18959 | hp1 | a0001 | c0001 | t0007 | g0145 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18959 | hp2 | a0001 | c0002 | t0002 | g0271 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18960 | hp1 | a0001 | c0005 | t0002 | g0305 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18960 | hp2 | a0001 | c0001 | t0007 | g0187 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18961 | hp1 | a0001 | c0001 | t0005 | g0058 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18961 | hp2 | a0001 | c0001 | t0007 | g0146 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18962 | hp1 | a0001 | c0002 | t0003 | g0103 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18964 | hp1 | a0001 | c0001 | t0004 | g0313 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18967 | hp2 | a0001 | c0002 | t0005 | g0035 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18969 | hp2 | a0001 | c0001 | t0007 | g0189 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18971 | hp1 | a0001 | c0001 | t0004 | g0233 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18971 | hp2 | a0001 | c0002 | t0020 | g0264 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18974 | hp1 | a0001 | c0001 | t0032 | g0163 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18974 | hp2 | a0001 | c0001 | t0013 | g0248 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18975 | hp1 | a0001 | c0001 | t0007 | g0280 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18981 | hp1 | a0001 | c0001 | t0013 | g0221 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18981 | hp2 | a0001 | c0002 | t0002 | g0291 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18982 | hp2 | a0001 | c0001 | t0007 | g0003 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18983 | hp2 | a0001 | c0002 | t0002 | g0310 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18984 | hp1 | a0001 | c0002 | t0003 | g0097 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18984 | hp2 | a0001 | c0001 | t0007 | g0019 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18985 | hp2 | a0001 | c0002 | t0002 | g0289 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18986 | hp2 | a0001 | c0001 | t0004 | g0308 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18988 | hp1 | a0001 | c0002 | t0003 | g0119 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18990 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18994 | hp1 | a0001 | c0002 | t0005 | g0061 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18994 | hp2 | a0001 | c0002 | t0027 | g0281 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19001 | hp1 | a0001 | c0001 | t0006 | g0258 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19002 | hp1 | a0001 | c0002 | t0002 | g0282 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19002 | hp2 | a0001 | c0001 | t0007 | g0185 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19004 | hp1 | a0001 | c0002 | t0003 | g0099 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19004 | hp2 | a0001 | c0002 | t0002 | g0029 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19007 | hp1 | a0001 | c0002 | t0020 | g0265 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19007 | hp2 | a0001 | c0002 | t0003 | g0008 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19009 | hp2 | a0001 | c0001 | t0004 | g0024 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19010 | hp1 | a0001 | c0002 | t0005 | g0037 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19010 | hp2 | a0001 | c0001 | t0006 | g0252 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19012 | hp2 | a0001 | c0002 | t0002 | g0309 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19030 | hp1 | a0001 | c0001 | t0016 | g0114 | AFR | LWK | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19030 | hp2 | a0001 | c0002 | t0008 | g0321 | AFR | LWK | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19043 | hp1 | a0001 | c0001 | t0016 | g0121 | AFR | LWK | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19043 | hp2 | a0001 | c0002 | t0003 | g0318 | AFR | LWK | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19054 | hp1 | a0001 | c0001 | t0007 | g0188 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19056 | hp1 | a0001 | c0002 | t0002 | g0314 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19056 | hp2 | a0001 | c0002 | t0003 | g0098 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19057 | hp2 | a0001 | c0001 | t0006 | g0025 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19058 | hp1 | a0001 | c0002 | t0002 | g0267 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19058 | hp2 | a0001 | c0001 | t0006 | g0256 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19063 | hp1 | a0001 | c0001 | t0031 | g0227 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19063 | hp2 | a0001 | c0001 | t0007 | g0150 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19065 | hp1 | a0001 | c0001 | t0007 | g0003 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19065 | hp2 | a0001 | c0002 | t0002 | g0029 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19067 | hp1 | a0001 | c0001 | t0006 | g0026 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19067 | hp2 | a0001 | c0001 | t0004 | g0024 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19070 | hp1 | a0001 | c0002 | t0005 | g0036 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19070 | hp2 | a0001 | c0001 | t0007 | g0149 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19074 | hp1 | a0001 | c0001 | t0006 | g0251 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19074 | hp2 | a0001 | c0002 | t0003 | g0008 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19075 | hp2 | a0001 | c0002 | t0002 | g0307 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19077 | hp1 | a0001 | c0001 | t0006 | g0259 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19077 | hp2 | a0001 | c0001 | t0013 | g0228 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19078 | hp1 | a0001 | c0002 | t0002 | g0288 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19078 | hp2 | a0001 | c0001 | t0007 | g0162 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19079 | hp1 | a0001 | c0002 | t0003 | g0126 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19079 | hp2 | a0001 | c0001 | t0004 | g0231 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19080 | hp1 | a0001 | c0002 | t0002 | g0031 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19080 | hp2 | a0001 | c0001 | t0007 | g0178 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19081 | hp1 | a0001 | c0001 | t0034 | g0211 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19082 | hp2 | a0001 | c0002 | t0005 | g0038 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19084 | hp1 | a0001 | c0002 | t0003 | g0008 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19084 | hp2 | a0001 | c0001 | t0007 | g0003 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19085 | hp2 | a0001 | c0002 | t0003 | g0082 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19088 | hp1 | a0001 | c0001 | t0007 | g0266 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19090 | hp2 | a0001 | c0002 | t0002 | g0268 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19091 | hp1 | a0001 | c0001 | t0007 | g0019 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19091 | hp2 | a0001 | c0002 | t0002 | g0274 | EAS | JPT | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19240 | hp1 | a0001 | c0001 | t0033 | g0106 | AFR | YRI | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA19240 | hp2 | a0001 | c0002 | t0008 | g0032 | AFR | YRI | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA20129 | hp1 | a0002 | c0003 | t0009 | g0007 | AFR | ASW | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA20129 | hp2 | a0001 | c0002 | t0003 | g0015 | AFR | ASW | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA20752 | hp2 | a0001 | c0001 | t0006 | g0151 | EUR | TSI | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA20805 | hp1 | a0001 | c0002 | t0002 | g0006 | EUR | TSI | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA20805 | hp2 | a0001 | c0002 | t0003 | g0094 | EUR | TSI | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01123 | hp1 | a0001 | c0001 | t0016 | g0110 | AMR | CLM | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG01123 | hp2 | a0001 | c0002 | t0005 | g0053 | AMR | CLM | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02109 | hp1 | a0001 | c0001 | t0004 | g0217 | AFR | ACB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02109 | hp2 | a0001 | c0001 | t0004 | g0214 | AFR | ACB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02486 | hp1 | a0001 | c0002 | t0010 | g0203 | AFR | ACB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02486 | hp2 | a0001 | c0007 | t0009 | g0072 | AFR | ACB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02559 | hp1 | a0001 | c0001 | t0004 | g0220 | AFR | ACB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG02559 | hp2 | a0001 | c0001 | t0018 | g0012 | AFR | ACB | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03471 | hp1 | a0001 | c0001 | t0019 | g0016 | AFR | MSL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | MSL | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG06807 | hp1 | a0001 | c0002 | t0003 | g0316 | AFR | USA | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
HG06807 | hp2 | a0001 | c0001 | t0011 | g0136 | AFR | USA | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA20300 | hp1 | a0001 | c0002 | t0021 | g0095 | AFR | USA | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA20300 | hp2 | a0001 | c0001 | t0006 | g0108 | AFR | USA | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA21309 | hp1 | a0003 | c0004 | t0006 | g0107 | AFR | LWK | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
NA21309 | hp2 | a0001 | c0002 | t0002 | g0273 | AFR | LWK | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0186 | REF | REF | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
homoSapiens | grch38p0 | a0001 | c0001 | t0006 | g0068 | REF | REF | ENTPD5_chr14_73958230_74024288 | ENTPD5 | chr14 | 73958230 | 74024288 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:73972970 | T | C | 1 | a0002 | 5 | HG02055.hp2 HG02257.hp1 HG02723.hp1 others(2): Show |
missense_variant | MODERATE | c.941A>G | p.Lys314Arg | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 13/16 | 1217/5261 | 941/1287 | 314/428 | chr14 | 73972970 | |||
chr14:73987972 | C | G | 1 | a0003 | 2 | HG01891.hp1 NA21309.hp1 |
missense_variant | MODERATE | c.131G>C | p.Ser44Thr | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 4/16 | 407/5261 | 131/1287 | 44/428 | chr14 | 73987972 | |||
chr14:73987978 | T | C | 1 | a0004 | 2 | HG01891.hp2 HG03139.hp2 |
missense_variant | MODERATE | c.125A>G | p.Asn42Ser | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 4/16 | 401/5261 | 125/1287 | 42/428 | chr14 | 73987978 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:73972936 | G | A | 1 | a0001c0008 | 1 | HG03704.hp2 | synonymous_variant | LOW | c.975C>T | p.Ser325Ser | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 13/16 | 1251/5261 | 975/1287 | 325/428 | chr14 | 73972936 | |||
chr14:73972990 | C | G | 2 | a0001c0007 a0002c0003 |
6 | HG02055.hp2 HG02257.hp1 HG02486.hp2 others(3): Show |
synonymous_variant | LOW | c.921G>C | p.Val307Val | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 13/16 | 1197/5261 | 921/1287 | 307/428 | chr14 | 73972990 | |||
chr14:73974981 | G | A | 5 | a0001c0002 a0001c0005 a0001c0007 others(2): Show |
177 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(174): Show |
synonymous_variant | LOW | c.727C>T | p.Leu243Leu | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 11/16 | 1003/5261 | 727/1287 | 243/428 | chr14 | 73974981 | |||
chr14:73983150 | G | A | 1 | a0001c0005 | 2 | NA18953.hp1 NA18960.hp1 |
synonymous_variant | LOW | c.309C>T | p.Thr103Thr | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/16 | 585/5261 | 309/1287 | 103/428 | chr14 | 73983150 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:73963280 | C | T | 1 | a0001c0002t0010 | 7 | HG01243.hp2 HG02486.hp1 HG02895.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3648G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 3648 | chr14 | 73963280 | ||||||
chr14:73963436 | G | A | 1 | a0001c0001t0033 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3492C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 3492 | chr14 | 73963436 | ||||||
chr14:73963583 | C | T | 1 | a0001c0001t0015 | 4 | HG01074.hp1 HG01099.hp1 HG01175.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3345G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 3345 | chr14 | 73963583 | ||||||
chr14:73963744 | C | T | 11 | a0001c0002t0002 a0001c0002t0003 a0001c0002t0008 others(8): Show |
124 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*3184G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 3184 | chr14 | 73963744 | ||||||
chr14:73964185 | T | C | 1 | a0001c0001t0031 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2743A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 2743 | chr14 | 73964185 | ||||||
chr14:73964214 | CAAT | C | 2 | a0001c0001t0011 a0001c0001t0022 |
7 | HG02258.hp1 HG02280.hp1 HG02622.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2711_*2713delATT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 2711 | chr14 | 73964214 | ||||||
chr14:73964250 | A | G | 2 | a0001c0001t0013 a0001c0001t0031 |
5 | HG00438.hp1 NA18974.hp2 NA18981.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2678T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 2678 | chr14 | 73964250 | ||||||
chr14:73964297 | T | G | 1 | a0001c0002t0017 | 4 | HG00280.hp1 HG01255.hp2 HG01258.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2631A>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 2631 | chr14 | 73964297 | ||||||
chr14:73964299 | T | G | 1 | a0001c0001t0032 | 1 | NA18974.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2629A>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 2629 | chr14 | 73964299 | ||||||
chr14:73964488 | A | G | 18 | a0001c0001t0005 a0001c0002t0002 a0001c0002t0003 others(15): Show |
178 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(175): Show |
3_prime_UTR_variant | MODIFIER | c.*2440T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 2440 | chr14 | 73964488 | ||||||
chr14:73964725 | G | A | 2 | a0001c0001t0007 a0001c0001t0032 |
25 | HG00438.hp2 HG02071.hp1 HG02080.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*2203C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 2203 | chr14 | 73964725 | ||||||
chr14:73964788 | ATTT | A | 3 | a0001c0002t0009 a0001c0007t0009 a0002c0003t0009 |
10 | HG01109.hp2 HG02055.hp2 HG02257.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2137_*2139delAAA | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 2137 | chr14 | 73964788 | ||||||
chr14:73964860 | A | AT | 3 | a0001c0001t0001 a0001c0001t0034 a0001c0001t0035 |
63 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*2067dupA | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 2067 | chr14 | 73964860 | ||||||
chr14:73964905 | A | G | 2 | a0001c0002t0036 a0001c0002t0037 |
2 | HG01433.hp2 HG03927.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2023T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 2023 | chr14 | 73964905 | ||||||
chr14:73965192 | C | T | 1 | a0001c0001t0030 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1736G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 1736 | chr14 | 73965192 | ||||||
chr14:73965268 | AGAGGATG | A | 2 | a0001c0001t0011 a0001c0001t0022 |
7 | HG02258.hp1 HG02280.hp1 HG02622.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1653_*1659delCATC others(3): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 1653 | chr14 | 73965268 | ||||||
chr14:73965363 | C | T | 1 | a0001c0001t0023 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1565G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 1565 | chr14 | 73965363 | ||||||
chr14:73965415 | G | A | 1 | a0001c0001t0012 | 5 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1513C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 1513 | chr14 | 73965415 | ||||||
chr14:73965415 | G | C | 1 | a0001c0001t0014 | 4 | HG00099.hp1 HG00738.hp2 HG00741.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1513C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 1513 | chr14 | 73965415 | ||||||
chr14:73965455 | G | A | 5 | a0001c0002t0002 a0001c0002t0020 a0001c0002t0027 others(2): Show |
60 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*1473C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 1473 | chr14 | 73965455 | ||||||
chr14:73965459 | T | C | 10 | a0001c0002t0002 a0001c0002t0003 a0001c0002t0017 others(7): Show |
112 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*1469A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 1469 | chr14 | 73965459 | ||||||
chr14:73965505 | T | C | 1 | a0001c0002t0037 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1423A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 1423 | chr14 | 73965505 | ||||||
chr14:73965527 | A | G | 1 | a0001c0001t0034 | 1 | NA19081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1401T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 1401 | chr14 | 73965527 | ||||||
chr14:73965562 | C | A | 11 | a0001c0002t0002 a0001c0002t0003 a0001c0002t0008 others(8): Show |
124 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*1366G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 1366 | chr14 | 73965562 | ||||||
chr14:73965720 | C | CA | 4 | a0001c0002t0002 a0001c0002t0020 a0001c0005t0002 others(1): Show |
59 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*1207dupT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 1207 | chr14 | 73965720 | ||||||
chr14:73965727 | A | G | 5 | a0001c0002t0003 a0001c0002t0017 a0001c0002t0021 others(2): Show |
52 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*1201T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 1201 | chr14 | 73965727 | ||||||
chr14:73965892 | G | A | 1 | a0001c0002t0029 | 1 | HG01256.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1036C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 1036 | chr14 | 73965892 | ||||||
chr14:73966282 | C | G | 2 | a0001c0001t0023 a0001c0001t0024 |
2 | HG02965.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*646G>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 646 | chr14 | 73966282 | ||||||
chr14:73966299 | T | G | 1 | a0001c0001t0019 | 3 | HG01081.hp1 HG03471.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*629A>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 629 | chr14 | 73966299 | ||||||
chr14:73966300 | T | C | 1 | a0001c0001t0019 | 3 | HG01081.hp1 HG03471.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*628A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 628 | chr14 | 73966300 | ||||||
chr14:73966409 | A | G | 1 | a0001c0002t0020 | 2 | NA18971.hp2 NA19007.hp1 |
3_prime_UTR_variant | MODIFIER | c.*519T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 519 | chr14 | 73966409 | ||||||
chr14:73966422 | T | C | 1 | a0001c0002t0021 | 2 | HG01978.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*506A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 506 | chr14 | 73966422 | ||||||
chr14:73966426 | C | A | 3 | a0001c0001t0001 a0001c0001t0034 a0001c0001t0035 |
63 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*502G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 502 | chr14 | 73966426 | ||||||
chr14:73966435 | C | T | 26 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0007 others(23): Show |
252 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(249): Show |
3_prime_UTR_variant | MODIFIER | c.*493G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 493 | chr14 | 73966435 | ||||||
chr14:73966438 | T | C | 7 | a0001c0001t0005 a0001c0002t0005 a0001c0002t0009 others(4): Show |
54 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*490A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 490 | chr14 | 73966438 | ||||||
chr14:73966468 | G | GT | 3 | a0001c0001t0005 a0001c0002t0005 a0001c0002t0029 |
37 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*459dupA | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 459 | chr14 | 73966468 | ||||||
chr14:73966468 | GT | G | 4 | a0001c0001t0012 a0001c0001t0016 a0001c0001t0026 others(1): Show |
11 | HG01123.hp1 HG01433.hp1 HG02572.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*459delA | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 459 | chr14 | 73966468 | ||||||
chr14:73966646 | C | T | 1 | a0001c0001t0028 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*282G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 282 | chr14 | 73966646 | ||||||
chr14:73966849 | A | T | 11 | a0001c0002t0002 a0001c0002t0003 a0001c0002t0008 others(8): Show |
124 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*79T>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 79 | chr14 | 73966849 | ||||||
chr14:73966861 | A | G | 1 | a0001c0001t0012 | 5 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*67T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 67 | chr14 | 73966861 | ||||||
chr14:73966881 | C | T | 1 | a0001c0001t0022 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*47G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 47 | chr14 | 73966881 | ||||||
chr14:73966903 | C | G | 1 | a0001c0001t0026 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*25G>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 25 | chr14 | 73966903 | ||||||
chr14:73966908 | C | T | 3 | a0001c0001t0023 a0001c0001t0024 a0001c0001t0025 |
3 | HG02818.hp2 HG02965.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*20G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 16/16 | 20 | chr14 | 73966908 | ||||||
chr14:73988110 | C | A | 3 | a0001c0001t0001 a0001c0001t0034 a0001c0001t0035 |
63 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(60): Show |
5_prime_UTR_variant | MODIFIER | c.-8G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 4/16 | 8 | chr14 | 73988110 | ||||||
chr14:73988116 | T | A | 5 | a0001c0002t0003 a0001c0002t0017 a0001c0002t0021 others(2): Show |
52 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(49): Show |
5_prime_UTR_variant | MODIFIER | c.-14A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 4/16 | 14 | chr14 | 73988116 | ||||||
chr14:74015893 | A | C | 1 | a0001c0001t0018 | 3 | HG02559.hp2 HG02922.hp2 HG02976.hp1 |
5_prime_UTR_variant | MODIFIER | c.-200T>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/16 | 27791 | chr14 | 74015893 | ||||||
chr14:74015895 | A | G | 2 | a0001c0001t0011 a0001c0001t0022 |
7 | HG02258.hp1 HG02280.hp1 HG02622.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-202T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/16 | 27793 | chr14 | 74015895 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:73967156 | T | C | 106 | a0001c0002t0002g0006 a0001c0002t0002g0027 a0001c0002t0002g0028 others(103): Show |
124 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.1201-142A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73967156 | |||||||
chr14:73967183 | C | T | 2 | a0001c0002t0008g0064 a0001c0002t0008g0065 |
2 | HG01243.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1201-169G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73967183 | |||||||
chr14:73967760 | A | C | 1 | a0001c0001t0001g0172 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1201-746T>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73967760 | |||||||
chr14:73967799 | CA | C | 197 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0020 others(194): Show |
235 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.1201-786delT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73967799 | |||||||
chr14:73967799 | CAA | C | 44 | a0001c0001t0007g0189 a0001c0002t0003g0005 a0001c0002t0003g0008 others(41): Show |
53 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.1201-787_1201-786d others(4): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73967799 | |||||||
chr14:73967799 | CAAAAAAA others(3): Show |
C | 2 | a0001c0002t0002g0031 a0001c0002t0002g0262 |
3 | NA18941.hp2 NA18950.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.1201-795_1201-786d others(12): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73967799 | |||||||
chr14:73967813 | A | G | 1 | a0001c0002t0002g0293 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1201-799T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73967813 | |||||||
chr14:73967817 | A | G | 11 | a0001c0002t0008g0032 a0001c0002t0008g0064 a0001c0002t0008g0065 others(8): Show |
12 | HG01109.hp1 HG01243.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1201-803T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73967817 | |||||||
chr14:73967818 | G | A | 11 | a0001c0002t0008g0032 a0001c0002t0008g0064 a0001c0002t0008g0065 others(8): Show |
12 | HG01109.hp1 HG01243.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1201-804C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73967818 | |||||||
chr14:73967832 | C | T | 11 | a0001c0002t0008g0032 a0001c0002t0008g0064 a0001c0002t0008g0065 others(8): Show |
12 | HG01109.hp1 HG01243.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1201-818G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73967832 | |||||||
chr14:73967911 | G | A | 1 | a0001c0001t0011g0136 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1201-897C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73967911 | |||||||
chr14:73967920 | T | A | 106 | a0001c0002t0002g0006 a0001c0002t0002g0027 a0001c0002t0002g0028 others(103): Show |
124 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.1201-906A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73967920 | |||||||
chr14:73968325 | G | A | 42 | a0001c0001t0005g0058 a0001c0002t0005g0002 a0001c0002t0005g0004 others(39): Show |
54 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.1201-1311C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73968325 | |||||||
chr14:73968425 | CT | C | 171 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0020 others(168): Show |
206 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.1201-1412delA | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73968425 | |||||||
chr14:73968425 | CTT | C | 102 | a0001c0001t0001g0161 a0001c0002t0002g0006 a0001c0002t0002g0027 others(99): Show |
120 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.1201-1413_1201-141 others(6): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73968425 | |||||||
chr14:73968667 | C | T | 30 | a0001c0001t0005g0058 a0001c0002t0005g0002 a0001c0002t0005g0004 others(27): Show |
37 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.1200+1343G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73968667 | |||||||
chr14:73968674 | C | G | 2 | a0001c0001t0004g0128 a0001c0001t0004g0129 |
2 | HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1200+1336G>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73968674 | |||||||
chr14:73968705 | C | T | 1 | a0001c0001t0011g0135 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1200+1305G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73968705 | |||||||
chr14:73968765 | A | G | 1 | a0001c0001t0006g0254 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1200+1245T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73968765 | |||||||
chr14:73968780 | A | G | 30 | a0001c0001t0005g0058 a0001c0002t0005g0002 a0001c0002t0005g0004 others(27): Show |
37 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.1200+1230T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73968780 | |||||||
chr14:73968816 | C | T | 1 | a0001c0001t0030g0120 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1200+1194G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73968816 | |||||||
chr14:73968820 | A | C | 1 | a0001c0001t0028g0200 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1200+1190T>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73968820 | |||||||
chr14:73968912 | G | C | 63 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0075 others(60): Show |
71 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.1200+1098C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73968912 | |||||||
chr14:73969156 | T | C | 23 | a0001c0001t0006g0025 a0001c0001t0006g0026 a0001c0001t0006g0104 others(20): Show |
27 | HG01070.hp2 HG01074.hp1 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.1200+854A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73969156 | |||||||
chr14:73969211 | C | T | 6 | a0001c0002t0010g0022 a0001c0002t0010g0202 a0001c0002t0010g0203 others(3): Show |
7 | HG01243.hp2 HG02486.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1200+799G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73969211 | |||||||
chr14:73969255 | G | C | 5 | a0001c0001t0012g0130 a0001c0001t0012g0131 a0001c0001t0012g0141 others(2): Show |
5 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1200+755C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73969255 | |||||||
chr14:73969261 | C | A | 5 | a0001c0001t0012g0130 a0001c0001t0012g0131 a0001c0001t0012g0141 others(2): Show |
5 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1200+749G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73969261 | |||||||
chr14:73969332 | G | A | 7 | a0001c0001t0011g0134 a0001c0001t0011g0135 a0001c0001t0011g0136 others(4): Show |
7 | HG02258.hp1 HG02280.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1200+678C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73969332 | |||||||
chr14:73969440 | C | G | 2 | a0001c0001t0004g0023 a0001c0001t0004g0209 |
3 | HG02451.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1200+570G>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73969440 | |||||||
chr14:73969528 | C | A | 7 | a0001c0001t0011g0134 a0001c0001t0011g0135 a0001c0001t0011g0136 others(4): Show |
7 | HG02258.hp1 HG02280.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1200+482G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73969528 | |||||||
chr14:73969532 | T | C | 7 | a0001c0002t0008g0032 a0001c0002t0008g0066 a0001c0002t0008g0300 others(4): Show |
8 | HG01109.hp1 HG01496.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1200+478A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73969532 | |||||||
chr14:73969654 | A | G | 8 | a0001c0002t0003g0008 a0001c0002t0003g0097 a0001c0002t0003g0098 others(5): Show |
10 | NA18947.hp1 NA18962.hp1 NA18984.hp1 others(7): Show |
intron_variant | MODIFIER | c.1200+356T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73969654 | |||||||
chr14:73969712 | T | A | 2 | a0001c0002t0009g0010 a0001c0002t0009g0208 |
4 | HG01109.hp2 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1200+298A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73969712 | |||||||
chr14:73969715 | T | TAATA | 42 | a0001c0001t0005g0058 a0001c0002t0005g0002 a0001c0002t0005g0004 others(39): Show |
54 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.1200+291_1200+294d others(6): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73969715 | |||||||
chr14:73969715 | T | TAATAAAT others(1): Show |
103 | a0001c0002t0002g0006 a0001c0002t0002g0027 a0001c0002t0002g0028 others(100): Show |
121 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.1200+287_1200+294d others(10): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73969715 | |||||||
chr14:73969715 | T | TAATAAAT others(5): Show |
3 | a0001c0002t0002g0277 a0001c0002t0003g0317 a0001c0002t0008g0321 |
3 | HG02145.hp2 HG03239.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1200+283_1200+294d others(14): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73969715 | |||||||
chr14:73969718 | T | A | 8 | a0001c0001t0001g0143 a0001c0001t0001g0182 a0001c0001t0001g0184 others(5): Show |
8 | HG02015.hp2 HG02572.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1200+292A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73969718 | |||||||
chr14:73969799 | G | A | 169 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0075 others(166): Show |
195 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.1200+211C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73969799 | |||||||
chr14:73969996 | G | A | 6 | a0001c0002t0009g0010 a0001c0002t0009g0208 a0001c0007t0009g0072 others(3): Show |
10 | HG01109.hp2 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1200+14C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 15/15 | chr14 | 73969996 | |||||||
chr14:73970366 | G | A | 49 | a0001c0001t0004g0024 a0001c0001t0004g0222 a0001c0001t0004g0224 others(46): Show |
55 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.1085-241C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 14/15 | chr14 | 73970366 | |||||||
chr14:73970429 | T | C | 11 | a0001c0002t0008g0032 a0001c0002t0008g0064 a0001c0002t0008g0065 others(8): Show |
12 | HG01109.hp1 HG01243.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1085-304A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 14/15 | chr14 | 73970429 | |||||||
chr14:73970510 | G | A | 8 | a0001c0002t0008g0032 a0001c0002t0008g0066 a0001c0002t0008g0250 others(5): Show |
9 | HG01109.hp1 HG01496.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1085-385C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 14/15 | chr14 | 73970510 | |||||||
chr14:73970541 | C | T | 1 | a0001c0002t0003g0080 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1085-416G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 14/15 | chr14 | 73970541 | |||||||
chr14:73970545 | G | T | 3 | a0001c0001t0004g0224 a0001c0001t0004g0225 a0001c0001t0004g0232 |
3 | HG04115.hp2 HG04199.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1085-420C>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 14/15 | chr14 | 73970545 | |||||||
chr14:73970742 | A | G | 1 | a0001c0002t0010g0202 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1085-617T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 14/15 | chr14 | 73970742 | |||||||
chr14:73970842 | T | C | 5 | a0001c0002t0010g0022 a0001c0002t0010g0202 a0001c0002t0010g0204 others(2): Show |
6 | HG01243.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1085-717A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 14/15 | chr14 | 73970842 | |||||||
chr14:73970928 | C | A | 11 | a0001c0002t0008g0032 a0001c0002t0008g0064 a0001c0002t0008g0065 others(8): Show |
12 | HG01109.hp1 HG01243.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1085-803G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 14/15 | chr14 | 73970928 | |||||||
chr14:73970947 | TC | T | 2 | a0001c0002t0009g0010 a0001c0002t0009g0208 |
4 | HG01109.hp2 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1085-823delG | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 14/15 | chr14 | 73970947 | |||||||
chr14:73970975 | C | A | 1 | a0001c0001t0006g0199 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1085-850G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 14/15 | chr14 | 73970975 | |||||||
chr14:73970990 | C | A | 4 | a0001c0002t0008g0066 a0001c0002t0008g0302 a0001c0002t0008g0303 others(1): Show |
4 | HG01496.hp2 HG02145.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1084+862G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 14/15 | chr14 | 73970990 | |||||||
chr14:73971131 | C | T | 106 | a0001c0002t0002g0006 a0001c0002t0002g0027 a0001c0002t0002g0028 others(103): Show |
124 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.1084+721G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 14/15 | chr14 | 73971131 | |||||||
chr14:73971136 | T | G | 1 | a0001c0002t0005g0062 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1084+716A>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 14/15 | chr14 | 73971136 | |||||||
chr14:73971162 | GT | G | 104 | a0001c0002t0002g0006 a0001c0002t0002g0027 a0001c0002t0002g0028 others(101): Show |
122 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.1084+689delA | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 14/15 | chr14 | 73971162 | |||||||
chr14:73971253 | G | A | 63 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0075 others(60): Show |
71 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.1084+599C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 14/15 | chr14 | 73971253 | |||||||
chr14:73971261 | G | A | 63 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0075 others(60): Show |
71 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.1084+591C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 14/15 | chr14 | 73971261 | |||||||
chr14:73971270 | A | G | 2 | a0001c0001t0012g0319 a0001c0001t0012g0320 |
2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1084+582T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 14/15 | chr14 | 73971270 | |||||||
chr14:73971304 | C | T | 1 | a0001c0002t0017g0077 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1084+548G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 14/15 | chr14 | 73971304 | |||||||
chr14:73971364 | G | A | 2 | a0001c0002t0002g0276 a0001c0002t0002g0278 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1084+488C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 14/15 | chr14 | 73971364 | |||||||
chr14:73971447 | G | A | 5 | a0001c0001t0006g0116 a0001c0001t0006g0117 a0001c0001t0006g0123 others(2): Show |
6 | HG01081.hp1 HG01884.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1084+405C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 14/15 | chr14 | 73971447 | |||||||
chr14:73971564 | C | T | 3 | a0001c0002t0010g0022 a0001c0002t0010g0205 a0001c0002t0010g0206 |
4 | HG02895.hp2 HG03486.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1084+288G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 14/15 | chr14 | 73971564 | |||||||
chr14:73971774 | GCTTTAGG others(3): Show |
G | 7 | a0001c0001t0011g0134 a0001c0001t0011g0135 a0001c0001t0011g0136 others(4): Show |
7 | HG02258.hp1 HG02280.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1084+68_1084+77del others(10): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 14/15 | chr14 | 73971774 | |||||||
chr14:73971789 | A | G | 1 | a0001c0001t0007g0266 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1084+63T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 14/15 | chr14 | 73971789 | |||||||
chr14:73972101 | G | A | 1 | a0001c0002t0002g0261 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1028-193C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 13/15 | chr14 | 73972101 | |||||||
chr14:73972142 | GC | G | 11 | a0001c0002t0008g0032 a0001c0002t0008g0064 a0001c0002t0008g0065 others(8): Show |
12 | HG01109.hp1 HG01243.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1028-235delG | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 13/15 | chr14 | 73972142 | |||||||
chr14:73972144 | C | T | 1 | a0001c0001t0004g0219 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1028-236G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 13/15 | chr14 | 73972144 | |||||||
chr14:73972160 | C | T | 1 | a0001c0001t0001g0184 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1028-252G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 13/15 | chr14 | 73972160 | |||||||
chr14:73972260 | G | T | 1 | a0001c0002t0003g0082 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1028-352C>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 13/15 | chr14 | 73972260 | |||||||
chr14:73972679 | TA | T | 221 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0075 others(218): Show |
259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.1027+204delT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 13/15 | chr14 | 73972679 | |||||||
chr14:73972792 | G | A | 169 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0075 others(166): Show |
195 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.1027+92C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 13/15 | chr14 | 73972792 | |||||||
chr14:73973168 | G | A | 1 | a0001c0002t0005g0039 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.887-144C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 12/15 | chr14 | 73973168 | |||||||
chr14:73973177 | A | C | 2 | a0001c0001t0004g0023 a0001c0001t0004g0209 |
3 | HG02451.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.887-153T>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 12/15 | chr14 | 73973177 | |||||||
chr14:73973192 | C | T | 52 | a0001c0002t0002g0006 a0001c0002t0002g0027 a0001c0002t0002g0028 others(49): Show |
60 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.887-168G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 12/15 | chr14 | 73973192 | |||||||
chr14:73973248 | C | T | 5 | a0001c0001t0012g0130 a0001c0001t0012g0131 a0001c0001t0012g0141 others(2): Show |
5 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.887-224G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 12/15 | chr14 | 73973248 | |||||||
chr14:73973299 | T | C | 6 | a0001c0002t0009g0010 a0001c0002t0009g0208 a0001c0007t0009g0072 others(3): Show |
10 | HG01109.hp2 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.887-275A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 12/15 | chr14 | 73973299 | |||||||
chr14:73973416 | A | G | 52 | a0001c0002t0002g0006 a0001c0002t0002g0027 a0001c0002t0002g0028 others(49): Show |
60 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.887-392T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 12/15 | chr14 | 73973416 | |||||||
chr14:73973427 | A | G | 1 | a0001c0002t0008g0250 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.887-403T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 12/15 | chr14 | 73973427 | |||||||
chr14:73973458 | C | G | 106 | a0001c0002t0002g0006 a0001c0002t0002g0027 a0001c0002t0002g0028 others(103): Show |
124 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.886+419G>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 12/15 | chr14 | 73973458 | |||||||
chr14:73973655 | A | C | 1 | a0001c0001t0006g0259 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.886+222T>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 12/15 | chr14 | 73973655 | |||||||
chr14:73973738 | T | C | 4 | a0001c0002t0003g0015 a0001c0002t0003g0105 a0001c0002t0003g0122 others(1): Show |
5 | HG00639.hp1 HG01261.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.886+139A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 12/15 | chr14 | 73973738 | |||||||
chr14:73973762 | A | G | 2 | a0001c0001t0004g0023 a0001c0001t0004g0209 |
3 | HG02451.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.886+115T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 12/15 | chr14 | 73973762 | |||||||
chr14:73974017 | T | G | 5 | a0001c0002t0010g0022 a0001c0002t0010g0202 a0001c0002t0010g0204 others(2): Show |
6 | HG01243.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.785-39A>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 11/15 | chr14 | 73974017 | |||||||
chr14:73974150 | A | G | 6 | a0001c0002t0009g0010 a0001c0002t0009g0208 a0001c0007t0009g0072 others(3): Show |
10 | HG01109.hp2 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.785-172T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 11/15 | chr14 | 73974150 | |||||||
chr14:73974256 | A | T | 9 | a0001c0002t0008g0032 a0001c0002t0008g0066 a0001c0002t0008g0250 others(6): Show |
10 | HG01109.hp1 HG01496.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.785-278T>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 11/15 | chr14 | 73974256 | |||||||
chr14:73974286 | C | T | 1 | a0001c0002t0003g0080 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.785-308G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 11/15 | chr14 | 73974286 | |||||||
chr14:73974338 | A | G | 1 | a0001c0001t0011g0138 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.785-360T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 11/15 | chr14 | 73974338 | |||||||
chr14:73974473 | T | C | 45 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0020 others(42): Show |
60 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.784+451A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 11/15 | chr14 | 73974473 | |||||||
chr14:73974541 | T | C | 11 | a0001c0002t0008g0032 a0001c0002t0008g0064 a0001c0002t0008g0065 others(8): Show |
12 | HG01109.hp1 HG01243.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.784+383A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 11/15 | chr14 | 73974541 | |||||||
chr14:73974590 | G | A | 1 | a0001c0001t0004g0219 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.784+334C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 11/15 | chr14 | 73974590 | |||||||
chr14:73974642 | G | T | 147 | a0001c0002t0002g0006 a0001c0002t0002g0027 a0001c0002t0002g0028 others(144): Show |
177 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.784+282C>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 11/15 | chr14 | 73974642 | |||||||
chr14:73974834 | T | C | 225 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0075 others(222): Show |
263 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.784+90A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 11/15 | chr14 | 73974834 | |||||||
chr14:73975050 | T | C | 1 | a0001c0001t0035g0041 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.723-65A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 10/15 | chr14 | 73975050 | |||||||
chr14:73975403 | CT | C | 186 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0020 others(183): Show |
219 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(216): Show |
intron_variant | MODIFIER | c.723-419delA | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 10/15 | chr14 | 73975403 | |||||||
chr14:73975403 | CTT | C | 90 | a0001c0001t0004g0201 a0001c0001t0006g0258 a0001c0001t0015g0125 others(87): Show |
107 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.723-420_723-419del others(2): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 10/15 | chr14 | 73975403 | |||||||
chr14:73975448 | C | T | 106 | a0001c0002t0002g0006 a0001c0002t0002g0027 a0001c0002t0002g0028 others(103): Show |
124 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.723-463G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 10/15 | chr14 | 73975448 | |||||||
chr14:73975483 | C | A | 1 | a0001c0001t0023g0132 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.722+453G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 10/15 | chr14 | 73975483 | |||||||
chr14:73975507 | T | C | 1 | a0001c0002t0008g0250 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.722+429A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 10/15 | chr14 | 73975507 | |||||||
chr14:73975549 | T | A | 43 | a0001c0002t0003g0005 a0001c0002t0003g0008 a0001c0002t0003g0009 others(40): Show |
52 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.722+387A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 10/15 | chr14 | 73975549 | |||||||
chr14:73975554 | G | A | 1 | a0001c0002t0003g0083 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.722+382C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 10/15 | chr14 | 73975554 | |||||||
chr14:73975663 | C | G | 1 | a0001c0002t0008g0250 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.722+273G>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 10/15 | chr14 | 73975663 | |||||||
chr14:73975797 | G | C | 6 | a0001c0002t0010g0022 a0001c0002t0010g0202 a0001c0002t0010g0203 others(3): Show |
7 | HG01243.hp2 HG02486.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.722+139C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 10/15 | chr14 | 73975797 | |||||||
chr14:73975896 | TACA | T | 5 | a0001c0002t0005g0040 a0001c0002t0005g0042 a0001c0002t0005g0045 others(2): Show |
5 | HG01099.hp2 HG01168.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.722+37_722+39delTG others(1): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 10/15 | chr14 | 73975896 | |||||||
chr14:73975928 | G | A | 5 | a0001c0001t0012g0130 a0001c0001t0012g0131 a0001c0001t0012g0141 others(2): Show |
5 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.722+8C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 10/15 | chr14 | 73975928 | |||||||
chr14:73976018 | G | A | 1 | a0001c0002t0002g0112 | 1 | HG03490.hp2 | splice_region_variant&intron_variant | LOW | c.643-3C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 9/15 | chr14 | 73976018 | |||||||
chr14:73976022 | A | G | 2 | a0001c0002t0002g0291 a0001c0002t0027g0281 |
2 | NA18981.hp2 NA18994.hp2 |
splice_region_variant&intron_variant | LOW | c.643-7T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 9/15 | chr14 | 73976022 | |||||||
chr14:73976154 | G | A | 29 | a0001c0002t0005g0002 a0001c0002t0005g0004 a0001c0002t0005g0034 others(26): Show |
36 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.643-139C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 9/15 | chr14 | 73976154 | |||||||
chr14:73976225 | C | T | 1 | a0001c0002t0003g0318 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.642+99G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 9/15 | chr14 | 73976225 | |||||||
chr14:73976444 | C | T | 1 | a0001c0002t0008g0032 | 2 | HG01109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.554-32G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 8/15 | chr14 | 73976444 | |||||||
chr14:73976447 | C | T | 5 | a0001c0001t0012g0130 a0001c0001t0012g0131 a0001c0001t0012g0141 others(2): Show |
5 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.554-35G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 8/15 | chr14 | 73976447 | |||||||
chr14:73976523 | C | T | 1 | a0001c0002t0003g0101 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.554-111G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 8/15 | chr14 | 73976523 | |||||||
chr14:73976595 | G | GT | 28 | a0001c0001t0001g0160 a0001c0001t0001g0167 a0001c0001t0001g0168 others(25): Show |
28 | HG01175.hp1 HG01433.hp1 HG01928.hp1 others(25): Show |
intron_variant | MODIFIER | c.554-184dupA | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 8/15 | chr14 | 73976595 | |||||||
chr14:73976596 | T | C | 1 | a0001c0001t0005g0058 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.554-184A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 8/15 | chr14 | 73976596 | |||||||
chr14:73976651 | C | G | 106 | a0001c0002t0002g0006 a0001c0002t0002g0027 a0001c0002t0002g0028 others(103): Show |
124 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.554-239G>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 8/15 | chr14 | 73976651 | |||||||
chr14:73976795 | G | A | 42 | a0001c0001t0005g0058 a0001c0002t0005g0002 a0001c0002t0005g0004 others(39): Show |
54 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.553+229C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 8/15 | chr14 | 73976795 | |||||||
chr14:73976926 | A | C | 1 | a0001c0002t0008g0065 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.553+98T>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 8/15 | chr14 | 73976926 | |||||||
chr14:73976996 | T | G | 2 | a0001c0001t0012g0130 a0001c0001t0012g0131 |
2 | HG02572.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.553+28A>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 8/15 | chr14 | 73976996 | |||||||
chr14:73977095 | G | T | 1 | a0001c0001t0001g0152 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.518-36C>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 7/15 | chr14 | 73977095 | |||||||
chr14:73977137 | T | C | 9 | a0001c0001t0006g0108 a0001c0001t0006g0127 a0001c0001t0015g0017 others(6): Show |
11 | HG01074.hp1 HG01099.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.518-78A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 7/15 | chr14 | 73977137 | |||||||
chr14:73977380 | G | T | 11 | a0001c0002t0008g0032 a0001c0002t0008g0064 a0001c0002t0008g0065 others(8): Show |
12 | HG01109.hp1 HG01243.hp1 HG01496.hp2 others(9): Show |
splice_region_variant&intron_variant | LOW | c.442-6C>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73977380 | |||||||
chr14:73977387 | G | GA | 55 | a0001c0001t0001g0159 a0001c0001t0001g0193 a0001c0001t0004g0201 others(52): Show |
64 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.442-14dupT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73977387 | |||||||
chr14:73977535 | C | T | 11 | a0001c0002t0008g0032 a0001c0002t0008g0064 a0001c0002t0008g0065 others(8): Show |
12 | HG01109.hp1 HG01243.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.442-161G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73977535 | |||||||
chr14:73977736 | G | C | 1 | a0001c0002t0003g0092 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.442-362C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73977736 | |||||||
chr14:73977922 | C | A | 223 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0075 others(220): Show |
261 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.442-548G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73977922 | |||||||
chr14:73977951 | T | C | 1 | a0001c0001t0032g0163 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.442-577A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73977951 | |||||||
chr14:73978026 | A | G | 4 | a0001c0001t0001g0170 a0001c0001t0001g0175 a0001c0001t0001g0191 others(1): Show |
4 | HG00323.hp2 HG01256.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-652T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73978026 | |||||||
chr14:73978075 | G | T | 43 | a0001c0002t0003g0005 a0001c0002t0003g0008 a0001c0002t0003g0009 others(40): Show |
52 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.442-701C>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73978075 | |||||||
chr14:73978270 | T | TAAAAATG others(309): Show |
5 | a0001c0001t0011g0134 a0001c0001t0011g0135 a0001c0001t0011g0136 others(2): Show |
5 | HG02258.hp1 HG02622.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.442-897_442-896ins others(316): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73978270 | |||||||
chr14:73978270 | T | TAAAAATG others(310): Show |
2 | a0001c0001t0011g0138 a0001c0001t0011g0139 |
2 | HG02280.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.442-897_442-896ins others(317): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73978270 | |||||||
chr14:73978283 | C | A | 1 | a0001c0002t0005g0055 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.442-909G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73978283 | |||||||
chr14:73978285 | A | G | 3 | a0001c0001t0023g0132 a0001c0001t0024g0260 a0001c0001t0025g0133 |
3 | HG02818.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.442-911T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73978285 | |||||||
chr14:73978336 | G | C | 6 | a0001c0002t0009g0010 a0001c0002t0009g0208 a0001c0007t0009g0072 others(3): Show |
10 | HG01109.hp2 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.442-962C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73978336 | |||||||
chr14:73978369 | C | T | 1 | a0001c0001t0025g0133 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.442-995G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73978369 | |||||||
chr14:73978429 | C | T | 1 | a0001c0002t0002g0274 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.442-1055G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73978429 | |||||||
chr14:73978468 | G | A | 1 | a0001c0001t0004g0216 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.442-1094C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73978468 | |||||||
chr14:73978549 | C | T | 1 | a0001c0002t0005g0040 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.442-1175G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73978549 | |||||||
chr14:73978558 | G | A | 5 | a0001c0001t0006g0116 a0001c0001t0006g0117 a0001c0001t0006g0123 others(2): Show |
6 | HG01081.hp1 HG01884.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.442-1184C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73978558 | |||||||
chr14:73978601 | C | CAAACA | 108 | a0001c0001t0004g0023 a0001c0001t0004g0209 a0001c0002t0002g0006 others(105): Show |
127 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.442-1232_442-1228d others(7): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73978601 | |||||||
chr14:73978687 | G | C | 43 | a0001c0002t0003g0005 a0001c0002t0003g0008 a0001c0002t0003g0009 others(40): Show |
52 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.442-1313C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73978687 | |||||||
chr14:73978766 | C | G | 3 | a0002c0003t0009g0007 a0002c0003t0009g0073 a0002c0003t0009g0074 |
5 | HG02055.hp2 HG02257.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.442-1392G>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73978766 | |||||||
chr14:73978915 | AG | A | 4 | a0001c0001t0007g0185 a0001c0002t0003g0098 a0001c0002t0005g0051 others(1): Show |
4 | HG01168.hp2 NA18957.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-1542delC | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73978915 | |||||||
chr14:73978916 | G | A | 207 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0075 others(204): Show |
245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.442-1542C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73978916 | |||||||
chr14:73979027 | C | T | 7 | a0001c0001t0011g0134 a0001c0001t0011g0135 a0001c0001t0011g0136 others(4): Show |
7 | HG02258.hp1 HG02280.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.442-1653G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73979027 | |||||||
chr14:73979149 | C | T | 7 | a0001c0002t0008g0032 a0001c0002t0008g0066 a0001c0002t0008g0300 others(4): Show |
8 | HG01109.hp1 HG01496.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.442-1775G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73979149 | |||||||
chr14:73979173 | C | T | 5 | a0001c0001t0012g0130 a0001c0001t0012g0131 a0001c0001t0012g0141 others(2): Show |
5 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.442-1799G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73979173 | |||||||
chr14:73979179 | G | A | 43 | a0001c0002t0003g0005 a0001c0002t0003g0008 a0001c0002t0003g0009 others(40): Show |
52 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.442-1805C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73979179 | |||||||
chr14:73979200 | T | C | 1 | a0001c0002t0008g0321 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.442-1826A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73979200 | |||||||
chr14:73979271 | C | T | 3 | a0001c0001t0001g0020 a0001c0001t0001g0155 a0001c0001t0001g0193 |
4 | HG02080.hp2 HG02129.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-1897G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73979271 | |||||||
chr14:73979288 | T | A | 1 | a0001c0002t0003g0096 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.442-1914A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73979288 | |||||||
chr14:73979472 | C | CT | 62 | a0001c0001t0001g0155 a0001c0001t0001g0184 a0001c0001t0004g0209 others(59): Show |
72 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.442-2099dupA | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73979472 | |||||||
chr14:73979499 | T | C | 1 | a0001c0002t0008g0065 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.442-2125A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73979499 | |||||||
chr14:73979572 | C | T | 6 | a0001c0002t0009g0010 a0001c0002t0009g0208 a0001c0007t0009g0072 others(3): Show |
10 | HG01109.hp2 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.442-2198G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73979572 | |||||||
chr14:73979596 | C | T | 1 | a0001c0002t0008g0321 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.442-2222G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73979596 | |||||||
chr14:73979621 | A | G | 214 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0075 others(211): Show |
252 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.442-2247T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73979621 | |||||||
chr14:73979773 | G | C | 1 | a0001c0001t0001g0236 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.442-2399C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73979773 | |||||||
chr14:73979934 | T | G | 1 | a0001c0002t0002g0223 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.442-2560A>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73979934 | |||||||
chr14:73979943 | A | AT | 69 | a0001c0001t0001g0172 a0001c0001t0004g0024 a0001c0001t0004g0075 others(66): Show |
77 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.442-2570dupA | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73979943 | |||||||
chr14:73979943 | A | ATT | 57 | a0001c0001t0004g0215 a0001c0001t0004g0216 a0001c0001t0004g0224 others(54): Show |
65 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.442-2571_442-2570d others(4): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73979943 | |||||||
chr14:73979943 | A | ATTT | 8 | a0001c0002t0002g0268 a0001c0002t0002g0272 a0001c0002t0002g0288 others(5): Show |
8 | HG00735.hp2 HG01346.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.442-2572_442-2570d others(5): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73979943 | |||||||
chr14:73979943 | AT | A | 13 | a0001c0001t0001g0169 a0001c0001t0001g0191 a0001c0001t0012g0130 others(10): Show |
15 | HG00099.hp2 HG01243.hp1 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.442-2570delA | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73979943 | |||||||
chr14:73979943 | ATT | A | 9 | a0001c0002t0008g0032 a0001c0002t0008g0066 a0001c0002t0008g0250 others(6): Show |
10 | HG01109.hp1 HG01496.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.442-2571_442-2570d others(4): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73979943 | |||||||
chr14:73980105 | C | T | 1 | a0001c0001t0026g0033 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.442-2731G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73980105 | |||||||
chr14:73980136 | A | T | 1 | a0001c0001t0013g0228 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.442-2762T>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73980136 | |||||||
chr14:73980194 | G | A | 1 | a0001c0002t0005g0053 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.442-2820C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73980194 | |||||||
chr14:73980200 | G | A | 1 | a0001c0002t0002g0271 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.441+2818C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73980200 | |||||||
chr14:73980269 | C | CT | 14 | a0001c0002t0003g0098 a0001c0002t0008g0032 a0001c0002t0008g0066 others(11): Show |
16 | HG01109.hp1 HG01243.hp2 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.441+2748dupA | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73980269 | |||||||
chr14:73980333 | C | T | 1 | a0001c0001t0001g0190 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.441+2685G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73980333 | |||||||
chr14:73980343 | C | T | 2 | a0001c0001t0006g0199 a0001c0001t0028g0200 |
2 | HG01884.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.441+2675G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73980343 | |||||||
chr14:73980366 | G | C | 1 | a0001c0001t0006g0199 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.441+2652C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73980366 | |||||||
chr14:73980369 | A | G | 2 | a0001c0001t0006g0252 a0001c0001t0006g0253 |
2 | NA18952.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.441+2649T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73980369 | |||||||
chr14:73980409 | G | A | 43 | a0001c0002t0003g0005 a0001c0002t0003g0008 a0001c0002t0003g0009 others(40): Show |
52 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.441+2609C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73980409 | |||||||
chr14:73980479 | G | T | 1 | a0001c0002t0003g0082 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.441+2539C>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73980479 | |||||||
chr14:73980495 | C | T | 6 | a0001c0002t0009g0010 a0001c0002t0009g0208 a0001c0007t0009g0072 others(3): Show |
10 | HG01109.hp2 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.441+2523G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73980495 | |||||||
chr14:73980554 | A | G | 106 | a0001c0002t0002g0006 a0001c0002t0002g0027 a0001c0002t0002g0028 others(103): Show |
124 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.441+2464T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73980554 | |||||||
chr14:73980680 | G | C | 52 | a0001c0002t0002g0006 a0001c0002t0002g0027 a0001c0002t0002g0028 others(49): Show |
60 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.441+2338C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73980680 | |||||||
chr14:73980690 | C | T | 106 | a0001c0002t0002g0006 a0001c0002t0002g0027 a0001c0002t0002g0028 others(103): Show |
124 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.441+2328G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73980690 | |||||||
chr14:73980704 | T | C | 6 | a0001c0002t0010g0022 a0001c0002t0010g0202 a0001c0002t0010g0203 others(3): Show |
7 | HG01243.hp2 HG02486.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.441+2314A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73980704 | |||||||
chr14:73981082 | G | C | 52 | a0001c0002t0002g0006 a0001c0002t0002g0027 a0001c0002t0002g0028 others(49): Show |
60 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.441+1936C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73981082 | |||||||
chr14:73981103 | A | AAAAT | 3 | a0001c0001t0001g0182 a0001c0001t0004g0195 a0001c0001t0004g0196 |
3 | HG02015.hp2 HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.441+1911_441+1914d others(6): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73981103 | |||||||
chr14:73981266 | C | T | 5 | a0001c0001t0013g0221 a0001c0001t0013g0228 a0001c0001t0013g0229 others(2): Show |
5 | HG00438.hp1 NA18974.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.441+1752G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73981266 | |||||||
chr14:73981267 | G | A | 2 | a0001c0002t0005g0054 a0001c0002t0005g0144 |
2 | HG02165.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.441+1751C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73981267 | |||||||
chr14:73981285 | G | A | 4 | a0001c0001t0006g0067 a0001c0001t0006g0070 a0001c0001t0006g0071 others(1): Show |
4 | HG00735.hp1 HG01106.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+1733C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73981285 | |||||||
chr14:73981494 | G | GTA | 63 | a0001c0001t0004g0024 a0001c0001t0004g0075 a0001c0001t0004g0076 others(60): Show |
70 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.441+1522_441+1523d others(4): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73981494 | |||||||
chr14:73981507 | T | C | 1 | a0001c0002t0003g0093 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.441+1511A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73981507 | |||||||
chr14:73981807 | C | CA | 8 | a0001c0001t0001g0172 a0001c0001t0004g0235 a0001c0001t0004g0246 others(5): Show |
8 | HG00408.hp2 HG02602.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.441+1210dupT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73981807 | |||||||
chr14:73981807 | CA | C | 110 | a0001c0001t0001g0155 a0001c0001t0006g0116 a0001c0001t0007g0146 others(107): Show |
130 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.441+1210delT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73981807 | |||||||
chr14:73981807 | CAA | C | 36 | a0001c0001t0005g0058 a0001c0002t0005g0002 a0001c0002t0005g0004 others(33): Show |
46 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.441+1209_441+1210d others(4): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73981807 | |||||||
chr14:73981869 | G | A | 6 | a0001c0002t0009g0010 a0001c0002t0009g0208 a0001c0007t0009g0072 others(3): Show |
10 | HG01109.hp2 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.441+1149C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73981869 | |||||||
chr14:73981922 | T | C | 106 | a0001c0002t0002g0006 a0001c0002t0002g0027 a0001c0002t0002g0028 others(103): Show |
124 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.441+1096A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73981922 | |||||||
chr14:73981948 | T | C | 1 | a0001c0001t0001g0296 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.441+1070A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73981948 | |||||||
chr14:73982213 | T | C | 1 | a0001c0001t0012g0141 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.441+805A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73982213 | |||||||
chr14:73982224 | G | A | 1 | a0001c0001t0006g0079 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.441+794C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73982224 | |||||||
chr14:73982385 | A | G | 11 | a0001c0002t0008g0032 a0001c0002t0008g0064 a0001c0002t0008g0065 others(8): Show |
12 | HG01109.hp1 HG01243.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.441+633T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73982385 | |||||||
chr14:73982416 | A | C | 11 | a0001c0002t0008g0032 a0001c0002t0008g0064 a0001c0002t0008g0065 others(8): Show |
12 | HG01109.hp1 HG01243.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.441+602T>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73982416 | |||||||
chr14:73982430 | C | T | 1 | a0001c0002t0008g0321 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.441+588G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73982430 | |||||||
chr14:73982538 | C | T | 2 | a0001c0001t0004g0023 a0001c0001t0004g0209 |
3 | HG02451.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.441+480G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73982538 | |||||||
chr14:73982781 | A | G | 3 | a0001c0001t0023g0132 a0001c0001t0024g0260 a0001c0001t0025g0133 |
3 | HG02818.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.441+237T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73982781 | |||||||
chr14:73982826 | A | G | 1 | a0001c0001t0006g0109 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.441+192T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73982826 | |||||||
chr14:73982961 | A | G | 43 | a0001c0002t0003g0005 a0001c0002t0003g0008 a0001c0002t0003g0009 others(40): Show |
52 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.441+57T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 6/15 | chr14 | 73982961 | |||||||
chr14:73983437 | A | G | 3 | a0002c0003t0009g0007 a0002c0003t0009g0073 a0002c0003t0009g0074 |
5 | HG02055.hp2 HG02257.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.298-276T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73983437 | |||||||
chr14:73983605 | C | T | 2 | a0001c0001t0004g0308 a0001c0001t0004g0313 |
2 | NA18964.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.298-444G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73983605 | |||||||
chr14:73983619 | A | G | 211 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0075 others(208): Show |
249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.298-458T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73983619 | |||||||
chr14:73983623 | C | CA | 145 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0020 others(142): Show |
169 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.298-463dupT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73983623 | |||||||
chr14:73983623 | C | CAA | 53 | a0001c0001t0013g0221 a0001c0002t0002g0006 a0001c0002t0002g0027 others(50): Show |
61 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.298-464_298-463dup others(2): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73983623 | |||||||
chr14:73983623 | CA | C | 6 | a0001c0002t0009g0010 a0001c0002t0009g0208 a0001c0007t0009g0072 others(3): Show |
10 | HG01109.hp2 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.298-463delT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73983623 | |||||||
chr14:73983675 | AATTATT | A | 2 | a0001c0001t0004g0023 a0001c0001t0004g0209 |
3 | HG02451.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.298-520_298-515del others(6): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73983675 | |||||||
chr14:73983689 | TTA | T | 51 | a0001c0002t0002g0006 a0001c0002t0002g0027 a0001c0002t0002g0028 others(48): Show |
59 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.298-530_298-529del others(2): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73983689 | |||||||
chr14:73983690 | TA | T | 54 | a0001c0002t0003g0005 a0001c0002t0003g0008 a0001c0002t0003g0009 others(51): Show |
62 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.298-530delT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73983690 | |||||||
chr14:73983691 | ATTATTT | A | 61 | a0001c0001t0004g0024 a0001c0001t0004g0075 a0001c0001t0004g0076 others(58): Show |
68 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.298-536_298-531del others(6): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73983691 | |||||||
chr14:73983694 | A | T | 107 | a0001c0001t0001g0155 a0001c0001t0004g0201 a0001c0002t0002g0006 others(104): Show |
123 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.298-533T>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73983694 | |||||||
chr14:73983697 | T | A | 7 | a0001c0001t0011g0134 a0001c0001t0011g0135 a0001c0001t0011g0136 others(4): Show |
7 | HG02258.hp1 HG02280.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.298-536A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73983697 | |||||||
chr14:73983702 | T | G | 31 | a0001c0001t0001g0173 a0001c0001t0005g0058 a0001c0002t0005g0002 others(28): Show |
38 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.298-541A>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73983702 | |||||||
chr14:73983704 | G | A | 106 | a0001c0002t0002g0006 a0001c0002t0002g0027 a0001c0002t0002g0028 others(103): Show |
124 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.298-543C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73983704 | |||||||
chr14:73983752 | G | C | 1 | a0001c0001t0001g0167 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.298-591C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73983752 | |||||||
chr14:73983778 | C | T | 1 | a0001c0002t0003g0089 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.298-617G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73983778 | |||||||
chr14:73983910 | C | T | 7 | a0001c0001t0011g0134 a0001c0001t0011g0135 a0001c0001t0011g0136 others(4): Show |
7 | HG02258.hp1 HG02280.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.298-749G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73983910 | |||||||
chr14:73984030 | C | A | 6 | a0001c0002t0009g0010 a0001c0002t0009g0208 a0001c0007t0009g0072 others(3): Show |
10 | HG01109.hp2 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.298-869G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984030 | |||||||
chr14:73984049 | C | T | 30 | a0001c0001t0005g0058 a0001c0002t0005g0002 a0001c0002t0005g0004 others(27): Show |
37 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.298-888G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984049 | |||||||
chr14:73984061 | CTT | C | 52 | a0001c0002t0002g0006 a0001c0002t0002g0027 a0001c0002t0002g0028 others(49): Show |
60 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.298-902_298-901del others(2): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984061 | |||||||
chr14:73984260 | G | C | 2 | a0001c0001t0012g0130 a0001c0001t0012g0131 |
2 | HG02572.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.298-1099C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984260 | |||||||
chr14:73984329 | T | G | 1 | a0001c0001t0001g0183 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.298-1168A>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984329 | |||||||
chr14:73984451 | A | G | 1 | a0001c0001t0004g0230 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.298-1290T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984451 | |||||||
chr14:73984468 | T | C | 276 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0020 others(273): Show |
329 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.298-1307A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984468 | |||||||
chr14:73984523 | A | G | 1 | a0001c0002t0003g0317 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.298-1362T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984523 | |||||||
chr14:73984601 | C | T | 1 | a0001c0001t0006g0255 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.298-1440G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984601 | |||||||
chr14:73984612 | C | T | 42 | a0001c0001t0005g0058 a0001c0002t0005g0002 a0001c0002t0005g0004 others(39): Show |
54 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.298-1451G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984612 | |||||||
chr14:73984684 | TTTAA | T | 3 | a0001c0001t0006g0116 a0001c0001t0006g0117 a0001c0001t0006g0123 |
3 | HG01884.hp2 HG02630.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.298-1527_298-1524d others(6): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984684 | |||||||
chr14:73984831 | G | A | 1 | a0001c0002t0036g0049 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.298-1670C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984831 | |||||||
chr14:73984896 | T | C | 148 | a0001c0001t0005g0058 a0001c0002t0002g0006 a0001c0002t0002g0027 others(145): Show |
178 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.298-1735A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984896 | |||||||
chr14:73984912 | C | T | 11 | a0001c0002t0008g0032 a0001c0002t0008g0064 a0001c0002t0008g0065 others(8): Show |
12 | HG01109.hp1 HG01243.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.298-1751G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984912 | |||||||
chr14:73984918 | G | C | 1 | a0001c0002t0020g0265 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.298-1757C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984918 | |||||||
chr14:73984919 | C | CACCTCAT others(9): Show |
1 | a0001c0002t0020g0265 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.298-1759_298-1758i others(18): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984919 | |||||||
chr14:73984923 | G | A | 1 | a0001c0002t0020g0265 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.298-1762C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984923 | |||||||
chr14:73984924 | G | C | 1 | a0001c0002t0020g0265 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.298-1763C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984924 | |||||||
chr14:73984926 | G | A | 1 | a0001c0002t0020g0265 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.298-1765C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984926 | |||||||
chr14:73984934 | T | A | 1 | a0001c0002t0020g0265 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.298-1773A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984934 | |||||||
chr14:73984935 | T | A | 1 | a0001c0002t0020g0265 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.298-1774A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984935 | |||||||
chr14:73984939 | C | A | 1 | a0001c0002t0020g0265 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.298-1778G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984939 | |||||||
chr14:73984940 | A | T | 1 | a0001c0002t0020g0265 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.298-1779T>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984940 | |||||||
chr14:73984963 | T | C | 1 | a0001c0002t0020g0265 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.298-1802A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984963 | |||||||
chr14:73984964 | C | A | 1 | a0001c0002t0020g0265 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.298-1803G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984964 | |||||||
chr14:73984979 | G | T | 1 | a0001c0002t0020g0265 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.298-1818C>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984979 | |||||||
chr14:73984984 | T | A | 1 | a0001c0002t0020g0265 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.298-1823A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984984 | |||||||
chr14:73984985 | G | C | 1 | a0001c0002t0020g0265 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.298-1824C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984985 | |||||||
chr14:73984987 | G | C | 1 | a0001c0002t0020g0265 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.298-1826C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984987 | |||||||
chr14:73984988 | G | C | 1 | a0001c0002t0020g0265 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.297+1826C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984988 | |||||||
chr14:73984990 | G | T | 1 | a0001c0002t0020g0265 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.297+1824C>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984990 | |||||||
chr14:73984991 | T | C | 1 | a0001c0002t0020g0265 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.297+1823A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984991 | |||||||
chr14:73984992 | T | A | 1 | a0001c0002t0020g0265 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.297+1822A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984992 | |||||||
chr14:73984994 | G | C | 1 | a0001c0002t0020g0265 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.297+1820C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984994 | |||||||
chr14:73984996 | T | A | 1 | a0001c0002t0020g0265 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.297+1818A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984996 | |||||||
chr14:73984997 | T | C | 1 | a0001c0002t0020g0265 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.297+1817A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73984997 | |||||||
chr14:73985000 | C | G | 1 | a0001c0002t0020g0265 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.297+1814G>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985000 | |||||||
chr14:73985001 | T | A | 1 | a0001c0002t0020g0265 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.297+1813A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985001 | |||||||
chr14:73985002 | G | T | 1 | a0001c0002t0020g0265 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.297+1812C>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985002 | |||||||
chr14:73985003 | T | A | 1 | a0001c0002t0020g0265 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.297+1811A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985003 | |||||||
chr14:73985004 | T | A | 1 | a0001c0002t0020g0265 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.297+1810A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985004 | |||||||
chr14:73985006 | T | A | 1 | a0001c0002t0020g0265 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.297+1808A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985006 | |||||||
chr14:73985009 | C | G | 1 | a0001c0002t0002g0285 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.297+1805G>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985009 | |||||||
chr14:73985010 | G | A | 2 | a0001c0001t0006g0199 a0001c0001t0028g0200 |
2 | HG01884.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.297+1804C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985010 | |||||||
chr14:73985011 | A | T | 1 | a0001c0002t0020g0265 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.297+1803T>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985011 | |||||||
chr14:73985023 | G | T | 1 | a0001c0002t0020g0265 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.297+1791C>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985023 | |||||||
chr14:73985024 | A | T | 1 | a0001c0002t0020g0265 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.297+1790T>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985024 | |||||||
chr14:73985027 | G | A | 1 | a0001c0002t0020g0265 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.297+1787C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985027 | |||||||
chr14:73985031 | G | T | 1 | a0001c0002t0020g0265 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.297+1783C>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985031 | |||||||
chr14:73985034 | T | C | 1 | a0001c0002t0020g0265 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.297+1780A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985034 | |||||||
chr14:73985036 | C | A | 1 | a0001c0002t0020g0265 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.297+1778G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985036 | |||||||
chr14:73985040 | T | G | 1 | a0001c0002t0020g0265 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.297+1774A>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985040 | |||||||
chr14:73985041 | T | A | 1 | a0001c0002t0020g0265 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.297+1773A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985041 | |||||||
chr14:73985049 | G | T | 1 | a0001c0002t0020g0265 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.297+1765C>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985049 | |||||||
chr14:73985060 | G | C | 1 | a0001c0002t0020g0265 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.297+1754C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985060 | |||||||
chr14:73985061 | G | T | 1 | a0001c0002t0020g0265 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.297+1753C>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985061 | |||||||
chr14:73985160 | G | A | 1 | a0001c0002t0003g0094 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.297+1654C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985160 | |||||||
chr14:73985235 | A | G | 52 | a0001c0002t0002g0006 a0001c0002t0002g0027 a0001c0002t0002g0028 others(49): Show |
60 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.297+1579T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985235 | |||||||
chr14:73985249 | A | G | 1 | a0001c0001t0001g0168 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.297+1565T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985249 | |||||||
chr14:73985252 | T | A | 1 | a0001c0002t0020g0265 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.297+1562A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985252 | |||||||
chr14:73985256 | G | C | 1 | a0001c0002t0027g0281 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.297+1558C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985256 | |||||||
chr14:73985258 | G | A | 2 | a0001c0002t0009g0010 a0001c0002t0009g0208 |
4 | HG01109.hp2 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.297+1556C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985258 | |||||||
chr14:73985258 | G | C | 1 | a0001c0002t0020g0265 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.297+1556C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985258 | |||||||
chr14:73985259 | T | C | 1 | a0001c0002t0020g0265 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.297+1555A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985259 | |||||||
chr14:73985273 | G | GAACCCAA others(4): Show |
1 | a0001c0002t0020g0265 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.297+1540_297+1541i others(13): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985273 | |||||||
chr14:73985274 | G | C | 1 | a0001c0002t0020g0265 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.297+1540C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985274 | |||||||
chr14:73985302 | T | C | 1 | a0001c0002t0008g0304 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.297+1512A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985302 | |||||||
chr14:73985350 | T | C | 1 | a0001c0001t0004g0201 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.297+1464A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985350 | |||||||
chr14:73985488 | G | A | 1 | a0001c0002t0008g0064 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.297+1326C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985488 | |||||||
chr14:73985491 | A | G | 1 | a0001c0001t0006g0079 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.297+1323T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985491 | |||||||
chr14:73985497 | G | C | 1 | a0001c0002t0008g0064 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.297+1317C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985497 | |||||||
chr14:73985631 | C | A | 1 | a0001c0001t0006g0011 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.297+1183G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985631 | |||||||
chr14:73985726 | G | A | 2 | a0001c0002t0005g0004 a0001c0002t0005g0055 |
5 | HG02129.hp1 HG02602.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.297+1088C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985726 | |||||||
chr14:73985762 | C | T | 43 | a0001c0002t0003g0005 a0001c0002t0003g0008 a0001c0002t0003g0009 others(40): Show |
52 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.297+1052G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985762 | |||||||
chr14:73985792 | G | C | 52 | a0001c0002t0002g0006 a0001c0002t0002g0027 a0001c0002t0002g0028 others(49): Show |
60 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.297+1022C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985792 | |||||||
chr14:73985996 | C | T | 1 | a0001c0001t0001g0167 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.297+818G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985996 | |||||||
chr14:73985998 | C | T | 1 | a0001c0001t0006g0109 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.297+816G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73985998 | |||||||
chr14:73986069 | C | CA | 54 | a0001c0002t0002g0006 a0001c0002t0002g0027 a0001c0002t0002g0028 others(51): Show |
62 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.297+744dupT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73986069 | |||||||
chr14:73986069 | CA | C | 64 | a0001c0001t0001g0166 a0001c0001t0004g0023 a0001c0001t0004g0024 others(61): Show |
72 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.297+744delT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73986069 | |||||||
chr14:73986081 | A | G | 6 | a0001c0002t0009g0010 a0001c0002t0009g0208 a0001c0007t0009g0072 others(3): Show |
10 | HG01109.hp2 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.297+733T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73986081 | |||||||
chr14:73986505 | G | A | 11 | a0001c0002t0008g0032 a0001c0002t0008g0064 a0001c0002t0008g0065 others(8): Show |
12 | HG01109.hp1 HG01243.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.297+309C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73986505 | |||||||
chr14:73986510 | C | T | 2 | a0001c0002t0008g0064 a0001c0002t0008g0065 |
2 | HG01243.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.297+304G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73986510 | |||||||
chr14:73986562 | A | G | 1 | a0001c0002t0002g0293 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.297+252T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73986562 | |||||||
chr14:73986644 | G | A | 1 | a0001c0001t0026g0033 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.297+170C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 5/15 | chr14 | 73986644 | |||||||
chr14:73987003 | AT | A | 48 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0020 others(45): Show |
63 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.218-111delA | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 4/15 | chr14 | 73987003 | |||||||
chr14:73987008 | A | C | 48 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0020 others(45): Show |
63 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.218-115T>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 4/15 | chr14 | 73987008 | |||||||
chr14:73987014 | T | A | 2 | a0001c0001t0004g0195 a0001c0001t0004g0196 |
2 | HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.218-121A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 4/15 | chr14 | 73987014 | |||||||
chr14:73987114 | T | C | 3 | a0001c0001t0004g0195 a0001c0001t0004g0196 a0001c0001t0004g0201 |
3 | HG02809.hp2 HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.218-221A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 4/15 | chr14 | 73987114 | |||||||
chr14:73987162 | G | A | 4 | a0001c0001t0004g0217 a0001c0001t0004g0218 a0001c0001t0004g0219 others(1): Show |
4 | HG01074.hp2 HG02109.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.218-269C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 4/15 | chr14 | 73987162 | |||||||
chr14:73987260 | T | A | 1 | a0001c0001t0004g0220 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.218-367A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 4/15 | chr14 | 73987260 | |||||||
chr14:73987284 | G | A | 5 | a0001c0001t0012g0130 a0001c0001t0012g0131 a0001c0001t0012g0141 others(2): Show |
5 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.218-391C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 4/15 | chr14 | 73987284 | |||||||
chr14:73987398 | T | G | 1 | a0001c0002t0008g0065 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.217+488A>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 4/15 | chr14 | 73987398 | |||||||
chr14:73987404 | G | C | 2 | a0001c0002t0009g0010 a0001c0002t0009g0208 |
4 | HG01109.hp2 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.217+482C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 4/15 | chr14 | 73987404 | |||||||
chr14:73987492 | C | T | 44 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0020 others(41): Show |
59 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.217+394G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 4/15 | chr14 | 73987492 | |||||||
chr14:73987815 | A | G | 1 | a0001c0002t0003g0245 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.217+71T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 4/15 | chr14 | 73987815 | |||||||
chr14:73987847 | G | T | 8 | a0001c0002t0002g0029 a0001c0002t0002g0031 a0001c0002t0002g0262 others(5): Show |
10 | NA18941.hp2 NA18950.hp1 NA18959.hp2 others(7): Show |
intron_variant | MODIFIER | c.217+39C>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 4/15 | chr14 | 73987847 | |||||||
chr14:73988493 | T | G | 7 | a0001c0002t0008g0032 a0001c0002t0008g0066 a0001c0002t0008g0300 others(4): Show |
8 | HG01109.hp1 HG01496.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.-70-321A>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73988493 | |||||||
chr14:73988516 | G | C | 52 | a0001c0002t0002g0006 a0001c0002t0002g0027 a0001c0002t0002g0028 others(49): Show |
60 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.-70-344C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73988516 | |||||||
chr14:73988651 | A | G | 1 | a0001c0001t0004g0231 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-70-479T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73988651 | |||||||
chr14:73988686 | C | T | 106 | a0001c0002t0002g0006 a0001c0002t0002g0027 a0001c0002t0002g0028 others(103): Show |
124 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.-70-514G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73988686 | |||||||
chr14:73988769 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-70-597C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73988769 | |||||||
chr14:73988791 | C | T | 1 | a0001c0002t0003g0101 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-70-619G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73988791 | |||||||
chr14:73989008 | C | G | 275 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0020 others(272): Show |
328 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.-70-836G>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73989008 | |||||||
chr14:73989069 | G | A | 52 | a0001c0002t0002g0006 a0001c0002t0002g0027 a0001c0002t0002g0028 others(49): Show |
60 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.-70-897C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73989069 | |||||||
chr14:73989113 | C | T | 5 | a0001c0001t0012g0130 a0001c0001t0012g0131 a0001c0001t0012g0141 others(2): Show |
5 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-70-941G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73989113 | |||||||
chr14:73989114 | G | T | 1 | a0001c0001t0006g0199 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-70-942C>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73989114 | |||||||
chr14:73989237 | T | G | 1 | a0001c0001t0023g0132 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-70-1065A>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73989237 | |||||||
chr14:73989276 | C | T | 48 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0020 others(45): Show |
63 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.-70-1104G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73989276 | |||||||
chr14:73989344 | GTGAGGTC others(129): Show |
G | 2 | a0001c0002t0003g0009 a0001c0002t0003g0080 |
4 | HG03490.hp1 HG03492.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.-70-1308_-70-1173d others(2): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73989344 | |||||||
chr14:73989388 | C | G | 1 | a0001c0001t0013g0248 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-70-1216G>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73989388 | |||||||
chr14:73989423 | C | T | 66 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0075 others(63): Show |
74 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.-70-1251G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73989423 | |||||||
chr14:73989425 | C | T | 48 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0020 others(45): Show |
63 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.-70-1253G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73989425 | |||||||
chr14:73989469 | G | A | 37 | a0001c0002t0003g0005 a0001c0002t0003g0008 a0001c0002t0003g0015 others(34): Show |
44 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.-70-1297C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73989469 | |||||||
chr14:73989563 | G | T | 52 | a0001c0002t0002g0006 a0001c0002t0002g0027 a0001c0002t0002g0028 others(49): Show |
60 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.-70-1391C>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73989563 | |||||||
chr14:73989609 | G | A | 44 | a0001c0001t0012g0130 a0001c0001t0012g0131 a0001c0001t0012g0141 others(41): Show |
53 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.-70-1437C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73989609 | |||||||
chr14:73989631 | C | T | 1 | a0001c0001t0028g0200 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-70-1459G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73989631 | |||||||
chr14:73989632 | A | G | 1 | a0001c0001t0028g0200 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-70-1460T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73989632 | |||||||
chr14:73989777 | G | A | 2 | a0001c0002t0017g0014 a0001c0002t0017g0077 |
3 | HG00280.hp1 HG01255.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.-70-1605C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73989777 | |||||||
chr14:73989782 | G | A | 5 | a0001c0002t0002g0029 a0001c0002t0002g0031 a0001c0002t0002g0262 others(2): Show |
7 | NA18941.hp2 NA18950.hp1 NA18971.hp2 others(4): Show |
intron_variant | MODIFIER | c.-70-1610C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73989782 | |||||||
chr14:73989832 | C | CA | 12 | a0001c0001t0001g0165 a0001c0001t0004g0023 a0001c0001t0004g0209 others(9): Show |
14 | HG01175.hp2 HG02055.hp1 HG02083.hp2 others(11): Show |
intron_variant | MODIFIER | c.-70-1661dupT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73989832 | |||||||
chr14:73989832 | C | CAA | 103 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0020 others(100): Show |
123 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.-70-1662_-70-1661d others(4): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73989832 | |||||||
chr14:73989832 | C | CAAA | 43 | a0001c0001t0001g0142 a0001c0001t0001g0179 a0001c0001t0001g0180 others(40): Show |
51 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.-70-1663_-70-1661d others(5): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73989832 | |||||||
chr14:73989832 | C | CAAAA | 9 | a0001c0001t0012g0131 a0001c0001t0012g0141 a0001c0002t0005g0037 others(6): Show |
11 | HG01099.hp2 HG01109.hp2 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.-70-1664_-70-1661d others(6): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73989832 | |||||||
chr14:73989832 | C | CAAAAA | 5 | a0001c0002t0009g0208 a0001c0002t0010g0203 a0001c0002t0010g0204 others(2): Show |
7 | HG02257.hp1 HG02486.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-70-1665_-70-1661d others(7): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73989832 | |||||||
chr14:73989832 | CA | C | 45 | a0001c0001t0006g0067 a0001c0002t0002g0006 a0001c0002t0002g0027 others(42): Show |
53 | HG00423.hp2 HG00642.hp2 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.-70-1661delT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73989832 | |||||||
chr14:73989970 | A | G | 1 | a0001c0002t0005g0050 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-70-1798T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73989970 | |||||||
chr14:73990176 | C | T | 11 | a0001c0002t0008g0032 a0001c0002t0008g0064 a0001c0002t0008g0065 others(8): Show |
12 | HG01109.hp1 HG01243.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.-70-2004G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73990176 | |||||||
chr14:73990293 | C | G | 52 | a0001c0002t0002g0006 a0001c0002t0002g0027 a0001c0002t0002g0028 others(49): Show |
60 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.-70-2121G>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73990293 | |||||||
chr14:73990313 | C | T | 1 | a0001c0001t0004g0240 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-70-2141G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73990313 | |||||||
chr14:73990381 | C | CTGGAG | 43 | a0001c0002t0003g0005 a0001c0002t0003g0008 a0001c0002t0003g0009 others(40): Show |
52 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.-70-2214_-70-2210d others(7): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73990381 | |||||||
chr14:73990390 | A | G | 36 | a0001c0001t0005g0058 a0001c0002t0005g0002 a0001c0002t0005g0004 others(33): Show |
44 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.-70-2218T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73990390 | |||||||
chr14:73990418 | A | G | 30 | a0001c0001t0005g0058 a0001c0002t0005g0002 a0001c0002t0005g0004 others(27): Show |
37 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.-70-2246T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73990418 | |||||||
chr14:73990459 | C | T | 78 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0020 others(75): Show |
100 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.-70-2287G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73990459 | |||||||
chr14:73990489 | C | T | 3 | a0001c0001t0023g0132 a0001c0001t0024g0260 a0001c0001t0025g0133 |
3 | HG02818.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-70-2317G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73990489 | |||||||
chr14:73990511 | T | C | 52 | a0001c0002t0002g0006 a0001c0002t0002g0027 a0001c0002t0002g0028 others(49): Show |
60 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.-70-2339A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73990511 | |||||||
chr14:73990525 | G | C | 63 | a0001c0001t0004g0023 a0001c0001t0004g0024 a0001c0001t0004g0075 others(60): Show |
71 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.-70-2353C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73990525 | |||||||
chr14:73990775 | T | G | 30 | a0001c0001t0005g0058 a0001c0002t0005g0002 a0001c0002t0005g0004 others(27): Show |
37 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.-70-2603A>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73990775 | |||||||
chr14:73991026 | C | T | 3 | a0001c0001t0004g0075 a0001c0001t0004g0076 a0004c0006t0004g0013 |
4 | HG01891.hp2 HG02258.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-70-2854G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73991026 | |||||||
chr14:73991241 | C | T | 95 | a0001c0002t0002g0006 a0001c0002t0002g0027 a0001c0002t0002g0028 others(92): Show |
112 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.-70-3069G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73991241 | |||||||
chr14:73991288 | G | A | 7 | a0001c0001t0011g0134 a0001c0001t0011g0135 a0001c0001t0011g0136 others(4): Show |
7 | HG02258.hp1 HG02280.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-70-3116C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73991288 | |||||||
chr14:73991293 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-70-3121C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73991293 | |||||||
chr14:73991363 | G | A | 1 | a0001c0002t0008g0304 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-70-3191C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73991363 | |||||||
chr14:73991376 | T | G | 4 | a0001c0001t0004g0023 a0001c0001t0004g0209 a0001c0002t0008g0064 others(1): Show |
5 | HG01243.hp1 HG02451.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-70-3204A>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73991376 | |||||||
chr14:73991587 | T | TA | 51 | a0001c0002t0002g0006 a0001c0002t0002g0027 a0001c0002t0002g0028 others(48): Show |
59 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.-70-3416dupT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73991587 | |||||||
chr14:73991587 | TA | T | 31 | a0001c0001t0005g0058 a0001c0001t0006g0251 a0001c0002t0005g0002 others(28): Show |
38 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.-70-3416delT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73991587 | |||||||
chr14:73991601 | C | A | 1 | a0001c0001t0006g0117 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-70-3429G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73991601 | |||||||
chr14:73991608 | C | CA | 16 | a0001c0001t0005g0058 a0001c0001t0007g0146 a0001c0001t0011g0135 others(13): Show |
17 | HG00438.hp1 HG01243.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.-70-3437dupT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73991608 | |||||||
chr14:73991608 | CA | C | 48 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0020 others(45): Show |
63 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.-70-3437delT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73991608 | |||||||
chr14:73991620 | A | C | 3 | a0001c0001t0023g0132 a0001c0001t0024g0260 a0001c0001t0025g0133 |
3 | HG02818.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-70-3448T>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73991620 | |||||||
chr14:73991625 | A | AAAAAG | 33 | a0001c0002t0003g0005 a0001c0002t0003g0008 a0001c0002t0003g0015 others(30): Show |
40 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.-70-3454_-70-3453i others(7): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73991625 | |||||||
chr14:73991625 | A | AAAAG | 63 | a0001c0002t0002g0006 a0001c0002t0002g0028 a0001c0002t0002g0029 others(60): Show |
73 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.-70-3454_-70-3453i others(6): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73991625 | |||||||
chr14:73991625 | A | AAAG | 8 | a0001c0001t0004g0023 a0001c0001t0004g0209 a0001c0002t0002g0027 others(5): Show |
10 | HG00673.hp1 HG01243.hp1 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.-70-3454_-70-3453i others(5): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73991625 | |||||||
chr14:73991705 | T | G | 1 | a0001c0002t0002g0312 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-70-3533A>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73991705 | |||||||
chr14:73991858 | T | A | 106 | a0001c0002t0002g0006 a0001c0002t0002g0027 a0001c0002t0002g0028 others(103): Show |
124 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.-70-3686A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73991858 | |||||||
chr14:73991915 | C | G | 2 | a0001c0001t0012g0319 a0001c0001t0012g0320 |
2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-70-3743G>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73991915 | |||||||
chr14:73991960 | T | C | 48 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0020 others(45): Show |
63 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.-70-3788A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73991960 | |||||||
chr14:73992011 | G | GTA | 53 | a0001c0001t0001g0296 a0001c0002t0002g0006 a0001c0002t0002g0027 others(50): Show |
61 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.-70-3841_-70-3840d others(4): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73992011 | |||||||
chr14:73992026 | A | T | 52 | a0001c0002t0002g0006 a0001c0002t0002g0027 a0001c0002t0002g0028 others(49): Show |
60 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.-70-3854T>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73992026 | |||||||
chr14:73992058 | G | A | 1 | a0001c0002t0003g0101 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-70-3886C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73992058 | |||||||
chr14:73992551 | G | T | 6 | a0001c0002t0010g0022 a0001c0002t0010g0202 a0001c0002t0010g0203 others(3): Show |
7 | HG01243.hp2 HG02486.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-70-4379C>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73992551 | |||||||
chr14:73992674 | A | C | 1 | a0001c0002t0008g0066 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-70-4502T>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73992674 | |||||||
chr14:73992683 | C | CA | 23 | a0001c0001t0001g0155 a0001c0001t0001g0175 a0001c0001t0001g0176 others(20): Show |
25 | HG00423.hp1 HG00438.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.-70-4512dupT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73992683 | |||||||
chr14:73992683 | CAAAAAAA others(1): Show |
C | 50 | a0001c0002t0002g0006 a0001c0002t0002g0027 a0001c0002t0002g0028 others(47): Show |
58 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.-70-4519_-70-4512d others(10): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73992683 | |||||||
chr14:73992737 | G | A | 8 | a0001c0002t0008g0032 a0001c0002t0008g0066 a0001c0002t0008g0250 others(5): Show |
9 | HG01109.hp1 HG01496.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.-70-4565C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73992737 | |||||||
chr14:73992833 | T | C | 1 | a0001c0001t0004g0214 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-70-4661A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73992833 | |||||||
chr14:73992914 | A | C | 2 | a0001c0002t0009g0010 a0001c0002t0009g0208 |
4 | HG01109.hp2 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-70-4742T>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73992914 | |||||||
chr14:73992917 | C | T | 30 | a0001c0001t0005g0058 a0001c0002t0005g0002 a0001c0002t0005g0004 others(27): Show |
37 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.-70-4745G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73992917 | |||||||
chr14:73992976 | A | G | 108 | a0001c0001t0004g0023 a0001c0001t0004g0209 a0001c0002t0002g0006 others(105): Show |
127 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.-70-4804T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73992976 | |||||||
chr14:73992986 | G | C | 10 | a0001c0002t0003g0008 a0001c0002t0003g0097 a0001c0002t0003g0098 others(7): Show |
12 | HG01358.hp2 NA18947.hp1 NA18952.hp1 others(9): Show |
intron_variant | MODIFIER | c.-70-4814C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73992986 | |||||||
chr14:73993012 | A | C | 1 | a0001c0001t0004g0230 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-70-4840T>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73993012 | |||||||
chr14:73993392 | C | T | 106 | a0001c0002t0002g0006 a0001c0002t0002g0027 a0001c0002t0002g0028 others(103): Show |
124 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.-70-5220G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73993392 | |||||||
chr14:73993423 | C | T | 148 | a0001c0001t0005g0058 a0001c0002t0002g0006 a0001c0002t0002g0027 others(145): Show |
178 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.-70-5251G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73993423 | |||||||
chr14:73993590 | C | T | 7 | a0001c0002t0008g0032 a0001c0002t0008g0066 a0001c0002t0008g0300 others(4): Show |
8 | HG01109.hp1 HG01496.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.-70-5418G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73993590 | |||||||
chr14:73993608 | T | A | 1 | a0001c0001t0001g0182 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-70-5436A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73993608 | |||||||
chr14:73993735 | CAGCAGCT others(8807): Show |
C | 1 | a0004c0006t0004g0013 | 2 | HG01891.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-71+8542_-70-5564d others(2): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73993735 | |||||||
chr14:73993785 | A | T | 106 | a0001c0002t0002g0006 a0001c0002t0002g0027 a0001c0002t0002g0028 others(103): Show |
124 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.-70-5613T>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73993785 | |||||||
chr14:73993921 | C | CA | 4 | a0001c0001t0001g0173 a0001c0001t0012g0319 a0001c0001t0012g0320 others(1): Show |
4 | HG02083.hp1 HG02622.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-70-5750dupT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73993921 | |||||||
chr14:73993921 | C | CAA | 7 | a0001c0001t0011g0134 a0001c0001t0011g0135 a0001c0001t0011g0136 others(4): Show |
7 | HG02258.hp1 HG02280.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-70-5751_-70-5750d others(4): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73993921 | |||||||
chr14:73993921 | CA | C | 59 | a0001c0001t0004g0024 a0001c0001t0004g0075 a0001c0001t0004g0076 others(56): Show |
65 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.-70-5750delT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73993921 | |||||||
chr14:73993924 | AC | A | 44 | a0001c0001t0004g0195 a0001c0001t0004g0196 a0001c0001t0004g0201 others(41): Show |
55 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.-70-5753delG | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73993924 | |||||||
chr14:73993925 | C | A | 65 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0020 others(62): Show |
75 | HG00323.hp2 HG00558.hp1 HG00673.hp2 others(72): Show |
intron_variant | MODIFIER | c.-70-5753G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73993925 | |||||||
chr14:73993928 | A | C | 1 | a0001c0001t0012g0141 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-70-5756T>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73993928 | |||||||
chr14:73993929 | A | C | 4 | a0001c0001t0006g0071 a0001c0002t0005g0048 a0001c0002t0005g0059 others(1): Show |
4 | HG01346.hp2 HG02738.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.-70-5757T>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73993929 | |||||||
chr14:73993933 | AAC | A | 94 | a0001c0002t0002g0006 a0001c0002t0002g0027 a0001c0002t0002g0028 others(91): Show |
111 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.-70-5763_-70-5762d others(4): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73993933 | |||||||
chr14:73993934 | AC | A | 5 | a0001c0001t0004g0023 a0001c0001t0004g0209 a0001c0002t0008g0064 others(2): Show |
6 | HG01243.hp1 HG02451.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-70-5763delG | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73993934 | |||||||
chr14:73993935 | C | A | 9 | a0001c0002t0008g0032 a0001c0002t0008g0066 a0001c0002t0008g0250 others(6): Show |
10 | HG01109.hp1 HG01496.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.-70-5763G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73993935 | |||||||
chr14:73993938 | A | C | 43 | a0001c0002t0003g0005 a0001c0002t0003g0008 a0001c0002t0003g0009 others(40): Show |
52 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.-70-5766T>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73993938 | |||||||
chr14:73993971 | A | C | 1 | a0001c0002t0009g0010 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-70-5799T>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73993971 | |||||||
chr14:73993988 | T | C | 2 | a0001c0001t0004g0195 a0001c0001t0004g0196 |
2 | HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-70-5816A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73993988 | |||||||
chr14:73994271 | G | A | 1 | a0001c0002t0003g0317 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-70-6099C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73994271 | |||||||
chr14:73994414 | T | A | 63 | a0001c0002t0002g0006 a0001c0002t0002g0027 a0001c0002t0002g0028 others(60): Show |
72 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.-70-6242A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73994414 | |||||||
chr14:73994418 | C | T | 63 | a0001c0002t0002g0006 a0001c0002t0002g0027 a0001c0002t0002g0028 others(60): Show |
72 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.-70-6246G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73994418 | |||||||
chr14:73994500 | C | T | 1 | a0001c0002t0002g0027 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-70-6328G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73994500 | |||||||
chr14:73994607 | C | T | 1 | a0001c0002t0003g0100 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-70-6435G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73994607 | |||||||
chr14:73994710 | G | A | 1 | a0001c0002t0002g0031 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-70-6538C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73994710 | |||||||
chr14:73994730 | C | CA | 43 | a0001c0002t0003g0005 a0001c0002t0003g0008 a0001c0002t0003g0009 others(40): Show |
52 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.-70-6559dupT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73994730 | |||||||
chr14:73994768 | T | A | 11 | a0001c0001t0007g0280 a0001c0001t0007g0283 a0001c0002t0002g0030 others(8): Show |
12 | HG00408.hp1 HG02083.hp2 HG02523.hp1 others(9): Show |
intron_variant | MODIFIER | c.-70-6596A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73994768 | |||||||
chr14:73994879 | T | A | 1 | a0001c0001t0031g0227 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-70-6707A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73994879 | |||||||
chr14:73994895 | C | G | 3 | a0001c0001t0004g0128 a0001c0001t0004g0129 a0001c0002t0008g0064 |
3 | HG03041.hp1 HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-70-6723G>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73994895 | |||||||
chr14:73994927 | T | C | 41 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0154 others(38): Show |
50 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(47): Show |
intron_variant | MODIFIER | c.-70-6755A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73994927 | |||||||
chr14:73995048 | A | AT | 38 | a0001c0002t0002g0086 a0001c0002t0003g0005 a0001c0002t0003g0008 others(35): Show |
47 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.-70-6877dupA | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73995048 | |||||||
chr14:73995048 | AT | A | 88 | a0001c0001t0001g0152 a0001c0001t0001g0166 a0001c0001t0001g0236 others(85): Show |
99 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.-70-6877delA | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73995048 | |||||||
chr14:73995048 | ATT | A | 40 | a0001c0001t0001g0183 a0001c0001t0004g0023 a0001c0001t0004g0209 others(37): Show |
48 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.-70-6878_-70-6877d others(4): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73995048 | |||||||
chr14:73995066 | A | T | 1 | a0001c0002t0008g0250 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-70-6894T>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73995066 | |||||||
chr14:73995079 | T | C | 1 | a0001c0001t0007g0178 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-70-6907A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73995079 | |||||||
chr14:73995359 | A | G | 1 | a0001c0001t0013g0248 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-70-7187T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73995359 | |||||||
chr14:73995406 | G | T | 1 | a0001c0001t0013g0248 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-70-7234C>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73995406 | |||||||
chr14:73995501 | T | C | 65 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0020 others(62): Show |
85 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.-70-7329A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73995501 | |||||||
chr14:73995510 | A | G | 276 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0020 others(273): Show |
328 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.-70-7338T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73995510 | |||||||
chr14:73995513 | G | A | 1 | a0001c0002t0008g0250 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-70-7341C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73995513 | |||||||
chr14:73995585 | A | AAAT | 43 | a0001c0001t0001g0020 a0001c0001t0001g0193 a0001c0001t0004g0024 others(40): Show |
45 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.-70-7416_-70-7414d others(5): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73995585 | |||||||
chr14:73995585 | A | AAATAAT | 42 | a0001c0001t0001g0155 a0001c0001t0001g0236 a0001c0001t0004g0075 others(39): Show |
47 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.-70-7419_-70-7414d others(8): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73995585 | |||||||
chr14:73995585 | A | AAATAATA others(2): Show |
16 | a0001c0001t0004g0195 a0001c0001t0004g0196 a0001c0001t0004g0214 others(13): Show |
19 | HG01069.hp2 HG01168.hp1 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.-70-7422_-70-7414d others(11): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73995585 | |||||||
chr14:73995585 | A | AAATAATA others(5): Show |
50 | a0001c0001t0007g0280 a0001c0001t0011g0134 a0001c0001t0011g0135 others(47): Show |
57 | HG00423.hp2 HG00642.hp2 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.-70-7425_-70-7414d others(14): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73995585 | |||||||
chr14:73995585 | A | AAATAATA others(8): Show |
9 | a0001c0002t0002g0031 a0001c0002t0002g0223 a0001c0002t0002g0262 others(6): Show |
9 | HG02486.hp2 HG03239.hp1 HG03834.hp2 others(6): Show |
intron_variant | MODIFIER | c.-70-7428_-70-7414d others(17): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73995585 | |||||||
chr14:73995585 | A | AAATAATA others(11): Show |
1 | a0001c0002t0002g0030 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-70-7431_-70-7414d others(20): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73995585 | |||||||
chr14:73995585 | A | T | 1 | a0001c0001t0001g0020 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-70-7413T>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73995585 | |||||||
chr14:73995585 | AAAT | A | 108 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0021 others(105): Show |
133 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.-70-7416_-70-7414d others(5): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73995585 | |||||||
chr14:73995729 | T | C | 1 | a0001c0001t0001g0192 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-70-7557A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73995729 | |||||||
chr14:73995769 | G | A | 1 | a0001c0001t0006g0067 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-70-7597C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73995769 | |||||||
chr14:73995861 | T | A | 1 | a0001c0002t0005g0004 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-70-7689A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73995861 | |||||||
chr14:73995898 | T | A | 1 | a0001c0002t0017g0077 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-70-7726A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73995898 | |||||||
chr14:73995987 | G | C | 210 | a0001c0001t0001g0236 a0001c0001t0004g0023 a0001c0001t0004g0024 others(207): Show |
242 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.-70-7815C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73995987 | |||||||
chr14:73996007 | A | G | 1 | a0001c0001t0006g0255 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-70-7835T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73996007 | |||||||
chr14:73996020 | C | T | 1 | a0001c0002t0002g0270 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-70-7848G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73996020 | |||||||
chr14:73996056 | A | C | 5 | a0001c0001t0006g0199 a0001c0001t0023g0132 a0001c0001t0024g0260 others(2): Show |
5 | HG01884.hp1 HG02818.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-70-7884T>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73996056 | |||||||
chr14:73996165 | C | T | 64 | a0001c0001t0004g0308 a0001c0001t0004g0313 a0001c0001t0007g0280 others(61): Show |
73 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.-70-7993G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73996165 | |||||||
chr14:73996186 | T | C | 2 | a0001c0001t0018g0012 a0001c0001t0018g0249 |
3 | HG02559.hp2 HG02922.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-70-8014A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73996186 | |||||||
chr14:73996231 | T | C | 1 | a0001c0002t0003g0244 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-70-8059A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73996231 | |||||||
chr14:73996369 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-70-8197G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73996369 | |||||||
chr14:73996504 | T | TA | 33 | a0001c0001t0004g0231 a0001c0001t0005g0058 a0001c0001t0006g0116 others(30): Show |
38 | HG00280.hp2 HG00639.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.-70-8333dupT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73996504 | |||||||
chr14:73996504 | TA | T | 71 | a0001c0001t0001g0001 a0001c0001t0001g0165 a0001c0001t0004g0308 others(68): Show |
78 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.-70-8333delT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73996504 | |||||||
chr14:73996857 | C | T | 64 | a0001c0001t0004g0308 a0001c0001t0004g0313 a0001c0001t0007g0280 others(61): Show |
73 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.-70-8685G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73996857 | |||||||
chr14:73996979 | C | A | 11 | a0001c0001t0004g0128 a0001c0001t0004g0129 a0001c0001t0006g0108 others(8): Show |
13 | HG01074.hp1 HG01099.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.-70-8807G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73996979 | |||||||
chr14:73997020 | C | T | 1 | a0001c0001t0007g0162 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-70-8848G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73997020 | |||||||
chr14:73997147 | C | A | 8 | a0001c0002t0003g0008 a0001c0002t0003g0097 a0001c0002t0003g0098 others(5): Show |
9 | NA18947.hp1 NA18962.hp1 NA18984.hp1 others(6): Show |
intron_variant | MODIFIER | c.-70-8975G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73997147 | |||||||
chr14:73997283 | G | A | 1 | a0001c0001t0001g0236 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-70-9111C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73997283 | |||||||
chr14:73997305 | T | C | 3 | a0001c0001t0023g0132 a0001c0001t0024g0260 a0001c0001t0025g0133 |
3 | HG02818.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-70-9133A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73997305 | |||||||
chr14:73997368 | T | C | 5 | a0001c0002t0005g0035 a0001c0002t0005g0036 a0001c0002t0005g0037 others(2): Show |
5 | NA18967.hp2 NA18994.hp1 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.-70-9196A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73997368 | |||||||
chr14:73997632 | C | T | 1 | a0001c0002t0002g0028 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-70-9460G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73997632 | |||||||
chr14:73997862 | C | T | 1 | a0001c0001t0028g0200 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-70-9690G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73997862 | |||||||
chr14:73998197 | G | A | 2 | a0001c0002t0003g0244 a0001c0002t0003g0245 |
2 | HG03017.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.-70-10025C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73998197 | |||||||
chr14:73998288 | C | G | 5 | a0001c0001t0012g0130 a0001c0001t0012g0131 a0001c0001t0012g0141 others(2): Show |
5 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-70-10116G>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73998288 | |||||||
chr14:73998405 | C | G | 1 | a0001c0002t0003g0101 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-70-10233G>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73998405 | |||||||
chr14:73998412 | TTTTGTC | T | 9 | a0001c0001t0004g0128 a0001c0001t0004g0129 a0001c0001t0006g0108 others(6): Show |
10 | HG01074.hp1 HG01099.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.-70-10246_-70-1024 others(10): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73998412 | |||||||
chr14:73998582 | GA | G | 51 | a0001c0001t0005g0058 a0001c0001t0007g0063 a0001c0001t0011g0134 others(48): Show |
63 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.-70-10411delT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73998582 | |||||||
chr14:73998587 | A | G | 64 | a0001c0001t0004g0308 a0001c0001t0004g0313 a0001c0001t0007g0280 others(61): Show |
73 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.-70-10415T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73998587 | |||||||
chr14:73998702 | G | A | 1 | a0001c0001t0004g0210 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-70-10530C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73998702 | |||||||
chr14:73998742 | A | G | 6 | a0001c0002t0009g0010 a0001c0002t0009g0208 a0001c0007t0009g0072 others(3): Show |
10 | HG01109.hp2 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-70-10570T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73998742 | |||||||
chr14:73998908 | G | C | 1 | a0001c0002t0003g0005 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-70-10736C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73998908 | |||||||
chr14:73998959 | T | C | 45 | a0001c0001t0030g0120 a0001c0002t0002g0086 a0001c0002t0003g0005 others(42): Show |
54 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.-70-10787A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73998959 | |||||||
chr14:73999038 | A | T | 96 | a0001c0001t0001g0236 a0001c0001t0004g0023 a0001c0001t0004g0024 others(93): Show |
107 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.-70-10866T>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73999038 | |||||||
chr14:73999053 | T | A | 64 | a0001c0001t0004g0308 a0001c0001t0004g0313 a0001c0001t0007g0280 others(61): Show |
73 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.-70-10881A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73999053 | |||||||
chr14:73999122 | T | TTCA | 40 | a0001c0001t0001g0236 a0001c0001t0004g0024 a0001c0001t0004g0075 others(37): Show |
41 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.-70-10953_-70-1095 others(7): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73999122 | |||||||
chr14:73999256 | A | G | 211 | a0001c0001t0001g0236 a0001c0001t0004g0023 a0001c0001t0004g0024 others(208): Show |
243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.-70-11084T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73999256 | |||||||
chr14:73999275 | G | C | 1 | a0001c0001t0007g0003 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-70-11103C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73999275 | |||||||
chr14:73999360 | C | T | 7 | a0001c0001t0011g0134 a0001c0001t0011g0135 a0001c0001t0011g0136 others(4): Show |
7 | HG02258.hp1 HG02280.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-70-11188G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73999360 | |||||||
chr14:73999460 | C | A | 1 | a0001c0002t0008g0065 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-70-11288G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73999460 | |||||||
chr14:73999496 | C | A | 1 | a0001c0002t0008g0064 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-70-11324G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73999496 | |||||||
chr14:73999496 | C | CA | 37 | a0001c0001t0001g0236 a0001c0001t0004g0024 a0001c0001t0004g0075 others(34): Show |
38 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.-70-11325_-70-1132 others(5): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73999496 | |||||||
chr14:73999497 | C | A | 140 | a0001c0001t0001g0236 a0001c0001t0004g0023 a0001c0001t0004g0024 others(137): Show |
163 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.-70-11325G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73999497 | |||||||
chr14:73999524 | G | A | 1 | a0001c0002t0008g0321 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-70-11352C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73999524 | |||||||
chr14:73999550 | C | T | 2 | a0001c0001t0004g0023 a0001c0001t0004g0209 |
3 | HG02451.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-70-11378G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73999550 | |||||||
chr14:73999591 | T | C | 203 | a0001c0001t0001g0236 a0001c0001t0004g0023 a0001c0001t0004g0024 others(200): Show |
233 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.-70-11419A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73999591 | |||||||
chr14:73999591 | T | G | 3 | a0002c0003t0009g0007 a0002c0003t0009g0073 a0002c0003t0009g0074 |
5 | HG02055.hp2 HG02257.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-70-11419A>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73999591 | |||||||
chr14:73999653 | G | A | 7 | a0001c0001t0012g0130 a0001c0001t0012g0131 a0001c0001t0012g0141 others(4): Show |
9 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.-71+11438C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73999653 | |||||||
chr14:73999653 | GC | G | 3 | a0001c0001t0023g0132 a0001c0001t0024g0260 a0001c0001t0025g0133 |
3 | HG02818.hp2 HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-71+11437delG | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73999653 | |||||||
chr14:73999660 | C | T | 1 | a0001c0001t0001g0001 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-71+11431G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73999660 | |||||||
chr14:73999791 | C | CA | 5 | a0001c0001t0006g0116 a0001c0001t0006g0117 a0001c0001t0006g0123 others(2): Show |
6 | HG01081.hp1 HG01884.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-71+11299dupT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73999791 | |||||||
chr14:73999812 | G | A | 5 | a0001c0001t0007g0280 a0001c0002t0002g0030 a0001c0002t0002g0279 others(2): Show |
5 | HG00408.hp1 HG02083.hp2 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.-71+11279C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73999812 | |||||||
chr14:73999860 | C | T | 1 | a0001c0008t0002g0287 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-71+11231G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73999860 | |||||||
chr14:73999948 | C | T | 7 | a0001c0002t0005g0002 a0001c0002t0005g0040 a0001c0002t0005g0042 others(4): Show |
7 | HG01099.hp2 HG01168.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.-71+11143G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 73999948 | |||||||
chr14:74000087 | C | CA | 13 | a0001c0001t0011g0134 a0001c0001t0011g0135 a0001c0001t0011g0136 others(10): Show |
14 | HG01243.hp2 HG02258.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.-71+11003dupT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74000087 | |||||||
chr14:74000087 | CA | C | 36 | a0001c0001t0001g0191 a0001c0001t0001g0212 a0001c0001t0004g0201 others(33): Show |
43 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.-71+11003delT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74000087 | |||||||
chr14:74000195 | G | A | 1 | a0001c0001t0001g0001 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-71+10896C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74000195 | |||||||
chr14:74000235 | T | C | 63 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0020 others(60): Show |
83 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.-71+10856A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74000235 | |||||||
chr14:74000255 | G | A | 7 | a0001c0001t0011g0134 a0001c0001t0011g0135 a0001c0001t0011g0136 others(4): Show |
7 | HG02258.hp1 HG02280.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-71+10836C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74000255 | |||||||
chr14:74000378 | G | A | 5 | a0001c0001t0001g0021 a0001c0001t0001g0148 a0001c0001t0001g0156 others(2): Show |
6 | HG02015.hp1 NA18956.hp1 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.-71+10713C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74000378 | |||||||
chr14:74000378 | G | C | 1 | a0001c0002t0003g0009 | 3 | HG03490.hp1 HG03492.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.-71+10713C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74000378 | |||||||
chr14:74000469 | A | T | 5 | a0001c0001t0012g0130 a0001c0001t0012g0131 a0001c0001t0012g0141 others(2): Show |
5 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-71+10622T>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74000469 | |||||||
chr14:74000519 | G | A | 54 | a0001c0001t0004g0308 a0001c0001t0004g0313 a0001c0001t0007g0280 others(51): Show |
62 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.-71+10572C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74000519 | |||||||
chr14:74000547 | G | A | 64 | a0001c0001t0004g0308 a0001c0001t0004g0313 a0001c0001t0007g0280 others(61): Show |
73 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.-71+10544C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74000547 | |||||||
chr14:74000651 | T | A | 6 | a0001c0002t0010g0022 a0001c0002t0010g0202 a0001c0002t0010g0203 others(3): Show |
7 | HG01243.hp2 HG02486.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-71+10440A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74000651 | |||||||
chr14:74000698 | G | A | 1 | a0001c0001t0004g0214 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-71+10393C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74000698 | |||||||
chr14:74000746 | C | A | 64 | a0001c0001t0004g0308 a0001c0001t0004g0313 a0001c0001t0007g0280 others(61): Show |
73 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.-71+10345G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74000746 | |||||||
chr14:74000769 | A | C | 211 | a0001c0001t0001g0236 a0001c0001t0004g0023 a0001c0001t0004g0024 others(208): Show |
243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.-71+10322T>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74000769 | |||||||
chr14:74000828 | G | A | 64 | a0001c0001t0004g0308 a0001c0001t0004g0313 a0001c0001t0007g0280 others(61): Show |
73 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.-71+10263C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74000828 | |||||||
chr14:74000943 | A | G | 3 | a0001c0002t0008g0064 a0001c0002t0008g0065 a0001c0002t0008g0066 |
3 | HG01243.hp1 HG02723.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-71+10148T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74000943 | |||||||
chr14:74001054 | G | A | 64 | a0001c0001t0004g0308 a0001c0001t0004g0313 a0001c0001t0007g0280 others(61): Show |
73 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.-71+10037C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001054 | |||||||
chr14:74001112 | C | T | 3 | a0001c0001t0015g0017 a0001c0001t0015g0124 a0001c0001t0015g0125 |
4 | HG01074.hp1 HG01099.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.-71+9979G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001112 | |||||||
chr14:74001136 | T | C | 64 | a0001c0001t0004g0308 a0001c0001t0004g0313 a0001c0001t0007g0280 others(61): Show |
73 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.-71+9955A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001136 | |||||||
chr14:74001176 | A | G | 211 | a0001c0001t0001g0236 a0001c0001t0004g0023 a0001c0001t0004g0024 others(208): Show |
243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.-71+9915T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001176 | |||||||
chr14:74001284 | C | T | 40 | a0001c0001t0001g0236 a0001c0001t0004g0024 a0001c0001t0004g0075 others(37): Show |
41 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.-71+9807G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001284 | |||||||
chr14:74001362 | T | A | 2 | a0001c0001t0004g0023 a0001c0001t0004g0209 |
3 | HG02451.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-71+9729A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001362 | |||||||
chr14:74001371 | G | C | 6 | a0001c0002t0008g0032 a0001c0002t0008g0300 a0001c0002t0008g0301 others(3): Show |
7 | HG01109.hp1 HG01496.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.-71+9720C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001371 | |||||||
chr14:74001415 | T | C | 1 | a0001c0002t0008g0032 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-71+9676A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001415 | |||||||
chr14:74001427 | G | A | 1 | a0001c0002t0003g0005 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-71+9664C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001427 | |||||||
chr14:74001432 | G | A | 1 | a0001c0002t0003g0317 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-71+9659C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001432 | |||||||
chr14:74001450 | C | T | 2 | a0001c0001t0006g0199 a0001c0001t0028g0200 |
2 | HG01884.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-71+9641G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001450 | |||||||
chr14:74001496 | C | T | 1 | a0001c0002t0002g0297 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-71+9595G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001496 | |||||||
chr14:74001502 | A | C | 6 | a0001c0001t0001g0184 a0001c0001t0006g0116 a0001c0001t0006g0117 others(3): Show |
7 | HG01081.hp1 HG01884.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-71+9589T>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001502 | |||||||
chr14:74001526 | G | C | 2 | a0001c0001t0006g0199 a0001c0001t0028g0200 |
2 | HG01884.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-71+9565C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001526 | |||||||
chr14:74001536 | C | T | 1 | a0001c0001t0006g0199 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-71+9555G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001536 | |||||||
chr14:74001542 | C | T | 7 | a0001c0001t0011g0134 a0001c0001t0011g0135 a0001c0001t0011g0136 others(4): Show |
7 | HG02258.hp1 HG02280.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-71+9549G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001542 | |||||||
chr14:74001552 | G | A | 2 | a0001c0001t0001g0152 a0001c0001t0001g0153 |
2 | NA18954.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.-71+9539C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001552 | |||||||
chr14:74001632 | C | T | 40 | a0001c0001t0001g0236 a0001c0001t0004g0024 a0001c0001t0004g0075 others(37): Show |
41 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.-71+9459G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001632 | |||||||
chr14:74001666 | C | CA | 10 | a0001c0001t0006g0026 a0001c0001t0006g0070 a0001c0001t0006g0108 others(7): Show |
10 | HG01106.hp2 HG01123.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.-71+9424dupT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001666 | |||||||
chr14:74001666 | C | CAAAAA | 28 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0021 others(25): Show |
35 | HG00323.hp2 HG01256.hp2 HG01258.hp2 others(32): Show |
intron_variant | MODIFIER | c.-71+9420_-71+9424d others(7): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001666 | |||||||
chr14:74001666 | C | CAAAAAA | 16 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0142 others(13): Show |
17 | HG00438.hp2 HG00673.hp2 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.-71+9419_-71+9424d others(8): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001666 | |||||||
chr14:74001666 | C | CAAAAAAA | 13 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0152 others(10): Show |
16 | HG00423.hp1 HG01069.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.-71+9418_-71+9424d others(9): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001666 | |||||||
chr14:74001666 | C | CAAAAAAA others(3): Show |
1 | a0001c0001t0001g0147 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-71+9415_-71+9424d others(12): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001666 | |||||||
chr14:74001666 | C | CAAAAAAA others(4): Show |
1 | a0001c0001t0001g0001 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-71+9414_-71+9424d others(13): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001666 | |||||||
chr14:74001666 | CAAAAAAA others(1): Show |
C | 7 | a0001c0001t0011g0134 a0001c0001t0011g0135 a0001c0001t0011g0136 others(4): Show |
7 | HG02258.hp1 HG02280.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-71+9417_-71+9424d others(10): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001666 | |||||||
chr14:74001666 | CAAAAAAA others(2): Show |
C | 7 | a0001c0002t0005g0002 a0001c0002t0005g0037 a0001c0002t0005g0038 others(4): Show |
8 | HG00639.hp2 HG00741.hp1 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.-71+9416_-71+9424d others(11): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001666 | |||||||
chr14:74001666 | CAAAAAAA others(3): Show |
C | 40 | a0001c0001t0001g0001 a0001c0001t0005g0058 a0001c0001t0007g0063 others(37): Show |
49 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(46): Show |
intron_variant | MODIFIER | c.-71+9415_-71+9424d others(12): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001666 | |||||||
chr14:74001666 | CAAAAAAA others(4): Show |
C | 71 | a0001c0001t0004g0024 a0001c0001t0004g0222 a0001c0001t0004g0230 others(68): Show |
78 | HG00408.hp1 HG00642.hp2 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.-71+9414_-71+9424d others(13): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001666 | |||||||
chr14:74001666 | CAAAAAAA others(5): Show |
C | 87 | a0001c0001t0001g0236 a0001c0001t0004g0023 a0001c0001t0004g0024 others(84): Show |
94 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.-71+9413_-71+9424d others(14): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001666 | |||||||
chr14:74001666 | CAAAAAAA others(6): Show |
C | 8 | a0001c0001t0023g0132 a0001c0001t0024g0260 a0001c0001t0025g0133 others(5): Show |
8 | HG01517.hp1 HG02818.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.-71+9412_-71+9424d others(15): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001666 | |||||||
chr14:74001666 | CAAAAAAA others(9): Show |
C | 5 | a0001c0001t0001g0143 a0001c0001t0001g0182 a0001c0001t0001g0184 others(2): Show |
5 | HG01070.hp2 HG01192.hp1 HG02015.hp2 others(2): Show |
intron_variant | MODIFIER | c.-71+9409_-71+9424d others(18): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001666 | |||||||
chr14:74001745 | G | C | 1 | a0001c0001t0006g0254 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-71+9346C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001745 | |||||||
chr14:74001829 | T | G | 211 | a0001c0001t0001g0236 a0001c0001t0004g0023 a0001c0001t0004g0024 others(208): Show |
243 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.-71+9262A>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001829 | |||||||
chr14:74001910 | C | T | 147 | a0001c0001t0001g0236 a0001c0001t0004g0023 a0001c0001t0004g0024 others(144): Show |
170 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.-71+9181G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001910 | |||||||
chr14:74001940 | T | C | 64 | a0001c0001t0004g0308 a0001c0001t0004g0313 a0001c0001t0007g0280 others(61): Show |
73 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.-71+9151A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74001940 | |||||||
chr14:74002034 | G | A | 1 | a0001c0002t0002g0027 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-71+9057C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74002034 | |||||||
chr14:74002194 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-71+8897G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74002194 | |||||||
chr14:74002195 | G | A | 44 | a0001c0001t0030g0120 a0001c0002t0002g0086 a0001c0002t0003g0005 others(41): Show |
53 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.-71+8896C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74002195 | |||||||
chr14:74002263 | T | C | 1 | a0003c0004t0006g0107 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-71+8828A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74002263 | |||||||
chr14:74002485 | T | C | 32 | a0001c0001t0005g0058 a0001c0001t0007g0063 a0001c0002t0005g0002 others(29): Show |
39 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.-71+8606A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74002485 | |||||||
chr14:74002513 | A | G | 1 | a0001c0002t0008g0250 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-71+8578T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74002513 | |||||||
chr14:74002567 | A | G | 1 | a0001c0001t0001g0148 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-71+8524T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74002567 | |||||||
chr14:74002744 | TCTCCTTT others(5): Show |
T | 1 | a0001c0002t0003g0105 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.-71+8335_-71+8346d others(14): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74002744 | |||||||
chr14:74002777 | A | T | 64 | a0001c0001t0004g0308 a0001c0001t0004g0313 a0001c0001t0007g0280 others(61): Show |
73 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.-71+8314T>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74002777 | |||||||
chr14:74002824 | C | T | 5 | a0001c0001t0013g0221 a0001c0001t0013g0228 a0001c0001t0013g0229 others(2): Show |
5 | HG00438.hp1 NA18974.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.-71+8267G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74002824 | |||||||
chr14:74002856 | T | C | 44 | a0001c0001t0030g0120 a0001c0002t0002g0086 a0001c0002t0003g0005 others(41): Show |
53 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.-71+8235A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74002856 | |||||||
chr14:74002924 | C | G | 26 | a0001c0001t0004g0128 a0001c0001t0004g0129 a0001c0001t0006g0025 others(23): Show |
30 | HG00735.hp1 HG01070.hp2 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.-71+8167G>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74002924 | |||||||
chr14:74002950 | C | T | 2 | a0001c0001t0001g0160 a0001c0001t0001g0161 |
2 | NA18990.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.-71+8141G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74002950 | |||||||
chr14:74003212 | G | T | 212 | a0001c0001t0001g0236 a0001c0001t0004g0023 a0001c0001t0004g0024 others(209): Show |
245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.-71+7879C>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74003212 | |||||||
chr14:74003238 | T | C | 6 | a0001c0002t0009g0010 a0001c0002t0009g0208 a0001c0007t0009g0072 others(3): Show |
10 | HG01109.hp2 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-71+7853A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74003238 | |||||||
chr14:74003305 | C | A | 2 | a0001c0001t0004g0023 a0001c0001t0004g0209 |
3 | HG02451.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-71+7786G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74003305 | |||||||
chr14:74003305 | C | T | 3 | a0002c0003t0009g0007 a0002c0003t0009g0073 a0002c0003t0009g0074 |
5 | HG02055.hp2 HG02257.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-71+7786G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74003305 | |||||||
chr14:74003360 | C | T | 63 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0020 others(60): Show |
83 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.-71+7731G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74003360 | |||||||
chr14:74003361 | A | G | 276 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0020 others(273): Show |
329 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.-71+7730T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74003361 | |||||||
chr14:74003597 | A | G | 2 | a0001c0001t0001g0152 a0001c0001t0001g0153 |
2 | NA18954.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.-71+7494T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74003597 | |||||||
chr14:74003617 | T | G | 1 | a0001c0002t0005g0144 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-71+7474A>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74003617 | |||||||
chr14:74003789 | A | G | 3 | a0001c0001t0006g0104 a0001c0001t0006g0151 a0001c0001t0026g0033 |
3 | HG01515.hp1 HG02818.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-71+7302T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74003789 | |||||||
chr14:74003840 | T | C | 5 | a0001c0001t0001g0021 a0001c0001t0001g0148 a0001c0001t0001g0156 others(2): Show |
6 | HG02015.hp1 NA18956.hp1 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.-71+7251A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74003840 | |||||||
chr14:74003870 | GAGGATCA others(136): Show |
G | 2 | a0001c0001t0012g0319 a0001c0001t0012g0320 |
2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-71+7078_-71+7220d others(2): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74003870 | |||||||
chr14:74003929 | A | T | 3 | a0001c0001t0012g0130 a0001c0001t0012g0131 a0001c0001t0012g0141 |
3 | HG02572.hp2 HG02647.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.-71+7162T>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74003929 | |||||||
chr14:74003936 | A | T | 5 | a0001c0001t0006g0104 a0001c0001t0006g0151 a0001c0001t0018g0012 others(2): Show |
6 | HG01515.hp1 HG02559.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.-71+7155T>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74003936 | |||||||
chr14:74003960 | C | A | 1 | a0001c0001t0007g0266 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-71+7131G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74003960 | |||||||
chr14:74003963 | G | A | 7 | a0001c0001t0011g0134 a0001c0001t0011g0135 a0001c0001t0011g0136 others(4): Show |
7 | HG02258.hp1 HG02280.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-71+7128C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74003963 | |||||||
chr14:74004078 | A | C | 212 | a0001c0001t0001g0236 a0001c0001t0004g0023 a0001c0001t0004g0024 others(209): Show |
245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.-71+7013T>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74004078 | |||||||
chr14:74004119 | T | A | 1 | a0001c0002t0003g0207 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-71+6972A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74004119 | |||||||
chr14:74004119 | T | G | 55 | a0001c0001t0004g0023 a0001c0001t0004g0209 a0001c0001t0006g0199 others(52): Show |
65 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.-71+6972A>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74004119 | |||||||
chr14:74004178 | A | T | 1 | a0001c0001t0016g0110 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-71+6913T>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74004178 | |||||||
chr14:74004190 | CAG | C | 41 | a0001c0001t0001g0236 a0001c0001t0004g0024 a0001c0001t0004g0075 others(38): Show |
43 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.-71+6899_-71+6900d others(4): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74004190 | |||||||
chr14:74004204 | A | G | 212 | a0001c0001t0001g0236 a0001c0001t0004g0023 a0001c0001t0004g0024 others(209): Show |
245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.-71+6887T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74004204 | |||||||
chr14:74004313 | A | G | 64 | a0001c0001t0004g0308 a0001c0001t0004g0313 a0001c0001t0007g0280 others(61): Show |
73 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.-71+6778T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74004313 | |||||||
chr14:74004356 | C | A | 2 | a0001c0001t0004g0023 a0001c0001t0004g0209 |
3 | HG02451.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-71+6735G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74004356 | |||||||
chr14:74004371 | T | C | 1 | a0001c0002t0003g0102 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-71+6720A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74004371 | |||||||
chr14:74004376 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-71+6715G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74004376 | |||||||
chr14:74004500 | G | T | 1 | a0001c0001t0004g0195 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-71+6591C>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74004500 | |||||||
chr14:74004513 | G | A | 1 | a0001c0001t0028g0200 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-71+6578C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74004513 | |||||||
chr14:74004559 | G | A | 6 | a0001c0002t0009g0010 a0001c0002t0009g0208 a0001c0007t0009g0072 others(3): Show |
10 | HG01109.hp2 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-71+6532C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74004559 | |||||||
chr14:74004564 | T | C | 64 | a0001c0001t0004g0308 a0001c0001t0004g0313 a0001c0001t0007g0280 others(61): Show |
73 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.-71+6527A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74004564 | |||||||
chr14:74004674 | C | T | 64 | a0001c0001t0004g0308 a0001c0001t0004g0313 a0001c0001t0007g0280 others(61): Show |
73 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.-71+6417G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74004674 | |||||||
chr14:74004689 | T | C | 51 | a0001c0001t0005g0058 a0001c0001t0007g0063 a0001c0001t0011g0134 others(48): Show |
63 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.-71+6402A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74004689 | |||||||
chr14:74004969 | T | G | 6 | a0001c0002t0010g0022 a0001c0002t0010g0202 a0001c0002t0010g0203 others(3): Show |
7 | HG01243.hp2 HG02486.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-71+6122A>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74004969 | |||||||
chr14:74005068 | G | C | 1 | a0001c0002t0005g0144 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-71+6023C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74005068 | |||||||
chr14:74005134 | G | A | 3 | a0001c0002t0010g0022 a0001c0002t0010g0205 a0001c0002t0010g0206 |
4 | HG02895.hp2 HG03486.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-71+5957C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74005134 | |||||||
chr14:74005159 | G | A | 5 | a0001c0001t0012g0130 a0001c0001t0012g0131 a0001c0001t0012g0141 others(2): Show |
5 | HG02572.hp2 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-71+5932C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74005159 | |||||||
chr14:74005161 | G | A | 7 | a0001c0002t0008g0032 a0001c0002t0008g0300 a0001c0002t0008g0301 others(4): Show |
8 | HG01109.hp1 HG01496.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.-71+5930C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74005161 | |||||||
chr14:74005192 | G | A | 6 | a0001c0002t0010g0022 a0001c0002t0010g0202 a0001c0002t0010g0203 others(3): Show |
7 | HG01243.hp2 HG02486.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-71+5899C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74005192 | |||||||
chr14:74005234 | C | A | 3 | a0001c0002t0005g0048 a0001c0002t0005g0059 a0001c0002t0005g0060 |
3 | HG01346.hp2 HG02738.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.-71+5857G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74005234 | |||||||
chr14:74005265 | C | CA | 36 | a0001c0001t0001g0181 a0001c0001t0001g0191 a0001c0001t0001g0296 others(33): Show |
43 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.-71+5825dupT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74005265 | |||||||
chr14:74005272 | AAAAAAAA others(11): Show |
A | 1 | a0001c0002t0002g0307 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-71+5801_-71+5818d others(20): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74005272 | |||||||
chr14:74005273 | AAAAAAAA others(10): Show |
A | 58 | a0001c0001t0004g0308 a0001c0001t0004g0313 a0001c0001t0007g0280 others(55): Show |
67 | HG00408.hp1 HG00642.hp2 HG00673.hp1 others(64): Show |
intron_variant | MODIFIER | c.-71+5801_-71+5817d others(19): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74005273 | |||||||
chr14:74005274 | AAAAAAAA others(1): Show |
A | 7 | a0001c0001t0023g0132 a0001c0002t0010g0022 a0001c0002t0010g0202 others(4): Show |
8 | HG01243.hp2 HG02486.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.-71+5809_-71+5816d others(10): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74005274 | |||||||
chr14:74005274 | AAAAAAAA others(9): Show |
A | 3 | a0001c0001t0016g0110 a0001c0002t0002g0285 a0001c0002t0008g0321 |
3 | HG00423.hp2 HG01123.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-71+5801_-71+5816d others(18): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74005274 | |||||||
chr14:74005290 | G | A | 2 | a0001c0001t0023g0132 a0001c0001t0024g0260 |
2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-71+5801C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74005290 | |||||||
chr14:74005320 | G | GT | 32 | a0001c0001t0005g0058 a0001c0001t0007g0063 a0001c0002t0005g0002 others(29): Show |
39 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.-71+5770dupA | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74005320 | |||||||
chr14:74005350 | G | A | 1 | a0001c0002t0008g0250 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-71+5741C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74005350 | |||||||
chr14:74005364 | C | CAAAA | 54 | a0001c0001t0004g0023 a0001c0001t0004g0209 a0001c0001t0006g0199 others(51): Show |
64 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.-71+5723_-71+5726d others(6): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74005364 | |||||||
chr14:74005364 | C | CAAAAAAA others(6): Show |
2 | a0001c0001t0011g0135 a0001c0002t0005g0046 |
2 | HG00323.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-71+5726_-71+5727i others(15): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74005364 | |||||||
chr14:74005364 | C | CAAAAAAA others(7): Show |
48 | a0001c0001t0001g0148 a0001c0001t0001g0190 a0001c0001t0001g0192 others(45): Show |
59 | HG00280.hp2 HG00639.hp2 HG00741.hp1 others(56): Show |
intron_variant | MODIFIER | c.-71+5726_-71+5727i others(16): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74005364 | |||||||
chr14:74005364 | C | CAAAAAAA others(8): Show |
148 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0020 others(145): Show |
179 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(176): Show |
intron_variant | MODIFIER | c.-71+5726_-71+5727i others(17): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74005364 | |||||||
chr14:74005364 | C | CAAAAAAA others(9): Show |
14 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(11): Show |
14 | HG00099.hp1 HG00423.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.-71+5726_-71+5727i others(18): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74005364 | |||||||
chr14:74005364 | C | CAAAAAAA others(10): Show |
1 | a0001c0001t0014g0239 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-71+5726_-71+5727i others(19): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74005364 | |||||||
chr14:74005364 | C | CAAAAAAA others(11): Show |
1 | a0001c0001t0004g0240 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-71+5726_-71+5727i others(20): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74005364 | |||||||
chr14:74005369 | A | AAAAAAAA others(7): Show |
6 | a0001c0002t0010g0022 a0001c0002t0010g0202 a0001c0002t0010g0203 others(3): Show |
7 | HG01243.hp2 HG02486.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-71+5721_-71+5722i others(16): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74005369 | |||||||
chr14:74005403 | G | GT | 7 | a0001c0001t0011g0134 a0001c0001t0011g0135 a0001c0001t0011g0136 others(4): Show |
7 | HG02258.hp1 HG02280.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-71+5687dupA | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74005403 | |||||||
chr14:74005460 | A | G | 1 | a0001c0001t0035g0041 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-71+5631T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74005460 | |||||||
chr14:74005494 | C | A | 64 | a0001c0001t0004g0308 a0001c0001t0004g0313 a0001c0001t0007g0280 others(61): Show |
73 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.-71+5597G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74005494 | |||||||
chr14:74005497 | C | T | 1 | a0001c0002t0002g0269 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-71+5594G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74005497 | |||||||
chr14:74005523 | A | G | 56 | a0001c0001t0004g0023 a0001c0001t0004g0209 a0001c0001t0006g0199 others(53): Show |
66 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.-71+5568T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74005523 | |||||||
chr14:74005529 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-71+5562G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74005529 | |||||||
chr14:74005611 | C | G | 1 | a0001c0001t0001g0158 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-71+5480G>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74005611 | |||||||
chr14:74005615 | C | G | 1 | a0001c0002t0005g0042 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-71+5476G>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74005615 | |||||||
chr14:74005827 | A | C | 1 | a0001c0001t0007g0157 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-71+5264T>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74005827 | |||||||
chr14:74006145 | A | C | 212 | a0001c0001t0001g0236 a0001c0001t0004g0023 a0001c0001t0004g0024 others(209): Show |
245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.-71+4946T>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74006145 | |||||||
chr14:74006146 | G | A | 1 | a0001c0005t0002g0306 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-71+4945C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74006146 | |||||||
chr14:74006178 | A | G | 312 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0020 others(309): Show |
370 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(367): Show |
intron_variant | MODIFIER | c.-71+4913T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74006178 | |||||||
chr14:74006225 | T | A | 2 | a0001c0002t0009g0010 a0001c0002t0009g0208 |
4 | HG01109.hp2 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-71+4866A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74006225 | |||||||
chr14:74006276 | C | T | 64 | a0001c0001t0004g0308 a0001c0001t0004g0313 a0001c0001t0007g0280 others(61): Show |
73 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.-71+4815G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74006276 | |||||||
chr14:74006284 | C | CT | 72 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(69): Show |
80 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.-71+4806dupA | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74006284 | |||||||
chr14:74006298 | T | TC | 1 | a0001c0002t0003g0009 | 3 | HG03490.hp1 HG03492.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.-71+4792_-71+4793i others(3): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74006298 | |||||||
chr14:74006314 | C | T | 40 | a0001c0001t0030g0120 a0001c0002t0002g0086 a0001c0002t0003g0005 others(37): Show |
49 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(46): Show |
intron_variant | MODIFIER | c.-71+4777G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74006314 | |||||||
chr14:74006352 | C | T | 32 | a0001c0001t0005g0058 a0001c0001t0007g0063 a0001c0002t0005g0002 others(29): Show |
39 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.-71+4739G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74006352 | |||||||
chr14:74006369 | C | T | 5 | a0001c0001t0006g0116 a0001c0001t0006g0117 a0001c0001t0006g0123 others(2): Show |
6 | HG01081.hp1 HG01884.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-71+4722G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74006369 | |||||||
chr14:74006427 | G | C | 41 | a0001c0001t0001g0236 a0001c0001t0004g0024 a0001c0001t0004g0075 others(38): Show |
43 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.-71+4664C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74006427 | |||||||
chr14:74006432 | C | T | 2 | a0001c0001t0001g0152 a0001c0001t0001g0153 |
2 | NA18954.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.-71+4659G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74006432 | |||||||
chr14:74006436 | G | T | 46 | a0001c0001t0004g0023 a0001c0001t0004g0209 a0001c0001t0030g0120 others(43): Show |
56 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.-71+4655C>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74006436 | |||||||
chr14:74006467 | C | T | 64 | a0001c0001t0004g0308 a0001c0001t0004g0313 a0001c0001t0007g0280 others(61): Show |
73 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.-71+4624G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74006467 | |||||||
chr14:74006534 | C | T | 1 | a0001c0001t0033g0106 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-71+4557G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74006534 | |||||||
chr14:74006589 | T | C | 1 | a0001c0002t0008g0250 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-71+4502A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74006589 | |||||||
chr14:74006600 | A | T | 6 | a0001c0002t0010g0022 a0001c0002t0010g0202 a0001c0002t0010g0203 others(3): Show |
7 | HG01243.hp2 HG02486.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-71+4491T>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74006600 | |||||||
chr14:74006650 | G | A | 207 | a0001c0001t0001g0236 a0001c0001t0004g0023 a0001c0001t0004g0024 others(204): Show |
238 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.-71+4441C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74006650 | |||||||
chr14:74006692 | C | T | 41 | a0001c0001t0001g0236 a0001c0001t0004g0024 a0001c0001t0004g0075 others(38): Show |
43 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.-71+4399G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74006692 | |||||||
chr14:74006710 | T | C | 64 | a0001c0001t0004g0308 a0001c0001t0004g0313 a0001c0001t0007g0280 others(61): Show |
73 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.-71+4381A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74006710 | |||||||
chr14:74006722 | C | T | 4 | a0001c0001t0007g0146 a0001c0001t0007g0187 a0001c0001t0007g0188 others(1): Show |
4 | NA18960.hp2 NA18961.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.-71+4369G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74006722 | |||||||
chr14:74006731 | T | C | 46 | a0001c0001t0004g0023 a0001c0001t0004g0209 a0001c0001t0030g0120 others(43): Show |
56 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.-71+4360A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74006731 | |||||||
chr14:74006759 | A | AT | 40 | a0001c0001t0030g0120 a0001c0002t0002g0086 a0001c0002t0003g0005 others(37): Show |
49 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(46): Show |
intron_variant | MODIFIER | c.-71+4331dupA | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74006759 | |||||||
chr14:74006844 | C | T | 2 | a0001c0002t0008g0300 a0001c0002t0008g0301 |
2 | HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-71+4247G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74006844 | |||||||
chr14:74006875 | C | A | 63 | a0001c0001t0004g0308 a0001c0001t0004g0313 a0001c0001t0007g0280 others(60): Show |
71 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.-71+4216G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74006875 | |||||||
chr14:74006892 | AAAAGTCA others(3): Show |
A | 1 | a0001c0001t0004g0217 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-71+4189_-71+4198d others(12): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74006892 | |||||||
chr14:74006904 | T | C | 38 | a0001c0001t0005g0058 a0001c0001t0007g0063 a0001c0002t0005g0002 others(35): Show |
46 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.-71+4187A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74006904 | |||||||
chr14:74006961 | A | G | 1 | a0001c0002t0008g0065 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-71+4130T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74006961 | |||||||
chr14:74007122 | G | A | 63 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0021 others(60): Show |
82 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.-71+3969C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74007122 | |||||||
chr14:74007184 | C | G | 28 | a0001c0001t0001g0236 a0001c0001t0004g0024 a0001c0001t0004g0214 others(25): Show |
29 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(26): Show |
intron_variant | MODIFIER | c.-71+3907G>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74007184 | |||||||
chr14:74007238 | A | G | 35 | a0001c0001t0005g0058 a0001c0001t0007g0063 a0001c0002t0002g0292 others(32): Show |
42 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.-71+3853T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74007238 | |||||||
chr14:74007249 | C | T | 1 | a0001c0002t0003g0082 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-71+3842G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74007249 | |||||||
chr14:74007314 | A | G | 1 | a0001c0002t0008g0321 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-71+3777T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74007314 | |||||||
chr14:74007318 | A | G | 1 | a0001c0002t0008g0321 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-71+3773T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74007318 | |||||||
chr14:74007329 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-71+3762C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74007329 | |||||||
chr14:74007332 | T | C | 2 | a0001c0002t0008g0065 a0001c0002t0008g0066 |
2 | HG01243.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-71+3759A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74007332 | |||||||
chr14:74007333 | A | G | 12 | a0001c0001t0004g0075 a0001c0001t0004g0076 a0001c0001t0013g0221 others(9): Show |
14 | HG01496.hp2 HG01891.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.-71+3758T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74007333 | |||||||
chr14:74007338 | G | A | 1 | a0001c0001t0013g0221 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-71+3753C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74007338 | |||||||
chr14:74007365 | T | C | 1 | a0001c0001t0001g0142 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-71+3726A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74007365 | |||||||
chr14:74007365 | T | TA | 33 | a0001c0001t0001g0183 a0001c0001t0005g0058 a0001c0001t0007g0063 others(30): Show |
40 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.-71+3725dupT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74007365 | |||||||
chr14:74007377 | T | C | 1 | a0001c0002t0010g0202 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-71+3714A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74007377 | |||||||
chr14:74007382 | A | G | 2 | a0001c0001t0024g0260 a0001c0002t0010g0202 |
2 | HG01243.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-71+3709T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74007382 | |||||||
chr14:74007479 | G | A | 2 | a0001c0001t0001g0143 a0001c0001t0001g0184 |
2 | NA18966.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.-71+3612C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74007479 | |||||||
chr14:74007693 | T | C | 57 | a0001c0001t0001g0284 a0001c0001t0001g0296 a0001c0001t0004g0308 others(54): Show |
65 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.-71+3398A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74007693 | |||||||
chr14:74007733 | A | T | 8 | a0001c0001t0024g0260 a0001c0002t0008g0032 a0001c0002t0008g0300 others(5): Show |
9 | HG01109.hp1 HG01496.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.-71+3358T>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74007733 | |||||||
chr14:74007831 | AAT | A | 40 | a0001c0001t0001g0236 a0001c0001t0004g0024 a0001c0001t0004g0195 others(37): Show |
41 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.-71+3258_-71+3259d others(4): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74007831 | |||||||
chr14:74007832 | AT | A | 9 | a0001c0001t0001g0156 a0001c0001t0001g0167 a0001c0001t0006g0104 others(6): Show |
10 | HG01168.hp2 HG01515.hp1 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.-71+3258delA | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74007832 | |||||||
chr14:74007834 | T | A | 1 | a0001c0002t0003g0105 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.-71+3257A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74007834 | |||||||
chr14:74007853 | T | TG | 5 | a0001c0001t0012g0319 a0001c0001t0012g0320 a0001c0002t0003g0316 others(2): Show |
5 | HG02145.hp2 HG02622.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-71+3237dupC | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74007853 | |||||||
chr14:74007873 | G | C | 1 | a0001c0002t0002g0285 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-71+3218C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74007873 | |||||||
chr14:74007967 | A | AT | 5 | a0001c0001t0012g0319 a0001c0001t0012g0320 a0001c0002t0003g0316 others(2): Show |
5 | HG02145.hp2 HG02622.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-71+3123dupA | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74007967 | |||||||
chr14:74007993 | G | C | 64 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0020 others(61): Show |
84 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.-71+3098C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74007993 | |||||||
chr14:74008147 | A | T | 181 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0020 others(178): Show |
220 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(217): Show |
intron_variant | MODIFIER | c.-71+2944T>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74008147 | |||||||
chr14:74008153 | T | A | 64 | a0001c0001t0001g0284 a0001c0001t0001g0296 a0001c0001t0004g0308 others(61): Show |
73 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.-71+2938A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74008153 | |||||||
chr14:74008339 | C | T | 1 | a0001c0001t0006g0256 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-71+2752G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74008339 | |||||||
chr14:74008340 | G | A | 5 | a0001c0001t0004g0075 a0001c0001t0004g0076 a0001c0001t0004g0210 others(2): Show |
6 | HG01891.hp2 HG02258.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-71+2751C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74008340 | |||||||
chr14:74008379 | A | C | 1 | a0001c0002t0008g0300 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-71+2712T>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74008379 | |||||||
chr14:74008394 | T | C | 1 | a0001c0001t0001g0191 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-71+2697A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74008394 | |||||||
chr14:74008439 | A | G | 48 | a0001c0001t0005g0058 a0001c0001t0007g0063 a0001c0001t0011g0134 others(45): Show |
58 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.-71+2652T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74008439 | |||||||
chr14:74008439 | A | T | 5 | a0001c0001t0012g0319 a0001c0001t0012g0320 a0001c0002t0003g0316 others(2): Show |
5 | HG02145.hp2 HG02622.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-71+2652T>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74008439 | |||||||
chr14:74008464 | C | T | 1 | a0001c0002t0008g0321 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-71+2627G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74008464 | |||||||
chr14:74008481 | C | T | 1 | a0001c0001t0007g0150 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-71+2610G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74008481 | |||||||
chr14:74008510 | CA | C | 5 | a0001c0001t0006g0116 a0001c0001t0006g0117 a0001c0001t0006g0123 others(2): Show |
6 | HG01081.hp1 HG01884.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-71+2580delT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74008510 | |||||||
chr14:74008540 | C | T | 1 | a0001c0002t0005g0040 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-71+2551G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74008540 | |||||||
chr14:74008586 | G | A | 5 | a0001c0001t0006g0116 a0001c0001t0006g0117 a0001c0001t0006g0123 others(2): Show |
6 | HG01081.hp1 HG01884.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-71+2505C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74008586 | |||||||
chr14:74008617 | G | A | 2 | a0001c0002t0008g0065 a0001c0002t0008g0066 |
2 | HG01243.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-71+2474C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74008617 | |||||||
chr14:74008739 | C | A | 1 | a0001c0002t0003g0118 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-71+2352G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74008739 | |||||||
chr14:74008740 | A | G | 1 | a0001c0002t0003g0118 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-71+2351T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74008740 | |||||||
chr14:74008866 | T | C | 7 | a0001c0001t0011g0134 a0001c0001t0011g0135 a0001c0001t0011g0136 others(4): Show |
7 | HG02258.hp1 HG02280.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-71+2225A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74008866 | |||||||
chr14:74009093 | T | C | 234 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0020 others(231): Show |
277 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(274): Show |
intron_variant | MODIFIER | c.-71+1998A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74009093 | |||||||
chr14:74009125 | C | G | 1 | a0001c0002t0021g0081 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-71+1966G>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74009125 | |||||||
chr14:74009153 | CAGA | C | 64 | a0001c0001t0001g0284 a0001c0001t0001g0296 a0001c0001t0004g0308 others(61): Show |
73 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.-71+1935_-71+1937d others(5): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74009153 | |||||||
chr14:74009243 | T | C | 5 | a0001c0001t0012g0319 a0001c0001t0012g0320 a0001c0002t0003g0316 others(2): Show |
5 | HG02145.hp2 HG02622.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-71+1848A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74009243 | |||||||
chr14:74009321 | A | T | 36 | a0001c0001t0001g0236 a0001c0001t0004g0024 a0001c0001t0004g0214 others(33): Show |
37 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(34): Show |
intron_variant | MODIFIER | c.-71+1770T>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74009321 | |||||||
chr14:74009464 | G | A | 1 | a0001c0002t0003g0080 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-71+1627C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74009464 | |||||||
chr14:74009556 | G | A | 2 | a0001c0002t0009g0010 a0001c0002t0009g0208 |
4 | HG01109.hp2 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-71+1535C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74009556 | |||||||
chr14:74009591 | TCCTTCTA others(4): Show |
T | 2 | a0001c0001t0023g0132 a0001c0001t0025g0133 |
2 | HG02818.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-71+1489_-71+1499d others(13): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74009591 | |||||||
chr14:74009595 | T | C | 1 | a0001c0002t0003g0082 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-71+1496A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74009595 | |||||||
chr14:74009696 | C | T | 64 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0020 others(61): Show |
84 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.-71+1395G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74009696 | |||||||
chr14:74009697 | G | C | 5 | a0001c0001t0012g0319 a0001c0001t0012g0320 a0001c0002t0003g0316 others(2): Show |
5 | HG02145.hp2 HG02622.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-71+1394C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74009697 | |||||||
chr14:74009791 | C | CG | 3 | a0001c0001t0006g0079 a0001c0002t0003g0078 a0001c0002t0003g0080 |
3 | HG00735.hp1 HG03654.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.-71+1299dupC | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74009791 | |||||||
chr14:74009792 | G | T | 1 | a0001c0001t0016g0121 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-71+1299C>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74009792 | |||||||
chr14:74009793 | A | AT | 48 | a0001c0001t0005g0058 a0001c0001t0007g0063 a0001c0001t0007g0149 others(45): Show |
58 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.-71+1297dupA | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74009793 | |||||||
chr14:74009793 | A | G | 37 | a0001c0001t0006g0104 a0001c0001t0030g0120 a0001c0002t0002g0086 others(34): Show |
46 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.-71+1298T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74009793 | |||||||
chr14:74009793 | A | T | 3 | a0001c0001t0006g0079 a0001c0002t0003g0078 a0001c0002t0003g0080 |
3 | HG00735.hp1 HG03654.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.-71+1298T>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74009793 | |||||||
chr14:74009831 | A | G | 10 | a0001c0001t0004g0023 a0001c0001t0004g0209 a0001c0001t0006g0199 others(7): Show |
13 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.-71+1260T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74009831 | |||||||
chr14:74009849 | T | C | 61 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0020 others(58): Show |
81 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.-71+1242A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74009849 | |||||||
chr14:74009860 | C | T | 2 | a0001c0002t0017g0014 a0001c0002t0017g0077 |
3 | HG00280.hp1 HG01255.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.-71+1231G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74009860 | |||||||
chr14:74009920 | T | C | 56 | a0001c0001t0001g0284 a0001c0001t0001g0296 a0001c0001t0004g0308 others(53): Show |
64 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.-71+1171A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74009920 | |||||||
chr14:74009924 | A | G | 2 | a0001c0001t0006g0199 a0001c0001t0028g0200 |
2 | HG01884.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-71+1167T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74009924 | |||||||
chr14:74010041 | C | T | 2 | a0001c0001t0006g0199 a0001c0001t0028g0200 |
2 | HG01884.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-71+1050G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74010041 | |||||||
chr14:74010163 | A | G | 69 | a0001c0001t0001g0284 a0001c0001t0001g0296 a0001c0001t0004g0308 others(66): Show |
78 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.-71+928T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74010163 | |||||||
chr14:74010231 | C | G | 61 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0020 others(58): Show |
81 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.-71+860G>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74010231 | |||||||
chr14:74010292 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-71+799G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74010292 | |||||||
chr14:74010469 | G | A | 1 | a0001c0002t0008g0321 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-71+622C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74010469 | |||||||
chr14:74010497 | T | G | 40 | a0001c0001t0001g0236 a0001c0001t0004g0024 a0001c0001t0004g0195 others(37): Show |
41 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.-71+594A>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74010497 | |||||||
chr14:74010503 | G | A | 48 | a0001c0001t0005g0058 a0001c0001t0007g0063 a0001c0001t0011g0134 others(45): Show |
58 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.-71+588C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74010503 | |||||||
chr14:74010554 | C | CA | 42 | a0001c0001t0001g0236 a0001c0001t0004g0024 a0001c0001t0004g0195 others(39): Show |
43 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.-71+536dupT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74010554 | |||||||
chr14:74010567 | T | A | 1 | a0001c0002t0002g0263 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-71+524A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74010567 | |||||||
chr14:74010581 | A | G | 64 | a0001c0001t0001g0284 a0001c0001t0001g0296 a0001c0001t0004g0308 others(61): Show |
73 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.-71+510T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74010581 | |||||||
chr14:74010611 | A | T | 234 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0020 others(231): Show |
277 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(274): Show |
intron_variant | MODIFIER | c.-71+480T>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74010611 | |||||||
chr14:74010633 | A | G | 181 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0020 others(178): Show |
220 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(217): Show |
intron_variant | MODIFIER | c.-71+458T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74010633 | |||||||
chr14:74010705 | C | T | 6 | a0001c0002t0010g0022 a0001c0002t0010g0202 a0001c0002t0010g0203 others(3): Show |
7 | HG01243.hp2 HG02486.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-71+386G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74010705 | |||||||
chr14:74010785 | A | C | 133 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0020 others(130): Show |
162 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.-71+306T>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74010785 | |||||||
chr14:74010804 | C | T | 5 | a0001c0001t0012g0319 a0001c0001t0012g0320 a0001c0002t0003g0316 others(2): Show |
5 | HG02145.hp2 HG02622.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-71+287G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74010804 | |||||||
chr14:74010870 | A | G | 1 | a0001c0001t0001g0143 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-71+221T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74010870 | |||||||
chr14:74010944 | T | C | 5 | a0001c0001t0004g0075 a0001c0001t0004g0076 a0001c0001t0004g0210 others(2): Show |
6 | HG01891.hp2 HG02258.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-71+147A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74010944 | |||||||
chr14:74010979 | C | A | 3 | a0001c0002t0008g0064 a0001c0002t0008g0065 a0001c0002t0008g0066 |
3 | HG01243.hp1 HG02723.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-71+112G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 3/15 | chr14 | 74010979 | |||||||
chr14:74011167 | T | G | 2 | a0001c0002t0008g0300 a0001c0002t0008g0301 |
2 | HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-130-17A>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74011167 | |||||||
chr14:74011200 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-130-50G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74011200 | |||||||
chr14:74011735 | T | C | 61 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0020 others(58): Show |
81 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.-130-585A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74011735 | |||||||
chr14:74011779 | T | C | 69 | a0001c0001t0001g0284 a0001c0001t0001g0296 a0001c0001t0004g0308 others(66): Show |
78 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.-130-629A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74011779 | |||||||
chr14:74011881 | T | C | 69 | a0001c0001t0001g0284 a0001c0001t0001g0296 a0001c0001t0004g0308 others(66): Show |
78 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.-130-731A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74011881 | |||||||
chr14:74011958 | T | C | 5 | a0001c0001t0004g0075 a0001c0001t0004g0076 a0001c0001t0004g0210 others(2): Show |
6 | HG01891.hp2 HG02258.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-130-808A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74011958 | |||||||
chr14:74012133 | C | T | 1 | a0001c0002t0002g0223 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-130-983G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74012133 | |||||||
chr14:74012156 | G | C | 1 | a0001c0001t0004g0201 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-130-1006C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74012156 | |||||||
chr14:74012290 | GA | G | 4 | a0001c0001t0004g0195 a0001c0001t0004g0196 a0001c0002t0003g0197 others(1): Show |
4 | HG02486.hp2 HG02809.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-130-1141delT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74012290 | |||||||
chr14:74012291 | A | G | 1 | a0001c0001t0016g0113 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-130-1141T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74012291 | |||||||
chr14:74012291 | AG | A | 64 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0020 others(61): Show |
84 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.-130-1142delC | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74012291 | |||||||
chr14:74012291 | AGG | A | 69 | a0001c0001t0001g0284 a0001c0001t0001g0296 a0001c0001t0004g0308 others(66): Show |
78 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.-130-1143_-130-114 others(6): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74012291 | |||||||
chr14:74012292 | G | A | 1 | a0001c0001t0006g0255 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-130-1142C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74012292 | |||||||
chr14:74012294 | G | C | 8 | a0001c0002t0009g0010 a0001c0002t0009g0208 a0001c0002t0010g0022 others(5): Show |
11 | HG01109.hp2 HG01243.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.-130-1144C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74012294 | |||||||
chr14:74012362 | C | A | 1 | a0001c0001t0030g0120 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-130-1212G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74012362 | |||||||
chr14:74012487 | A | G | 2 | a0001c0001t0004g0128 a0001c0001t0004g0129 |
2 | HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-130-1337T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74012487 | |||||||
chr14:74012514 | C | T | 64 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0020 others(61): Show |
84 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.-130-1364G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74012514 | |||||||
chr14:74012583 | C | A | 1 | a0001c0001t0016g0121 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-130-1433G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74012583 | |||||||
chr14:74012660 | G | T | 7 | a0001c0001t0011g0134 a0001c0001t0011g0135 a0001c0001t0011g0136 others(4): Show |
7 | HG02258.hp1 HG02280.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-130-1510C>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74012660 | |||||||
chr14:74012668 | C | T | 1 | a0001c0002t0005g0039 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-130-1518G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74012668 | |||||||
chr14:74012718 | G | GGAAT | 40 | a0001c0001t0001g0236 a0001c0001t0004g0024 a0001c0001t0004g0195 others(37): Show |
41 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.-130-1572_-130-156 others(8): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74012718 | |||||||
chr14:74013043 | T | G | 8 | a0001c0002t0009g0010 a0001c0002t0009g0208 a0001c0002t0010g0022 others(5): Show |
11 | HG01109.hp2 HG01243.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.-130-1893A>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74013043 | |||||||
chr14:74013059 | C | T | 1 | a0001c0002t0008g0321 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-130-1909G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74013059 | |||||||
chr14:74013114 | G | C | 4 | a0001c0001t0004g0241 a0001c0001t0004g0242 a0001c0001t0004g0243 others(1): Show |
4 | HG02602.hp2 HG03688.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.-130-1964C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74013114 | |||||||
chr14:74013181 | T | C | 1 | a0001c0001t0023g0132 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-130-2031A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74013181 | |||||||
chr14:74013329 | C | T | 4 | a0001c0002t0005g0035 a0001c0002t0005g0036 a0001c0002t0005g0037 others(1): Show |
4 | NA18967.hp2 NA19010.hp1 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.-130-2179G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74013329 | |||||||
chr14:74013367 | C | A | 56 | a0001c0001t0001g0284 a0001c0001t0001g0296 a0001c0001t0004g0308 others(53): Show |
64 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.-130-2217G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74013367 | |||||||
chr14:74013381 | G | A | 2 | a0001c0001t0023g0132 a0001c0001t0025g0133 |
2 | HG02818.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-130-2231C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74013381 | |||||||
chr14:74013418 | T | C | 3 | a0001c0001t0006g0256 a0001c0001t0006g0257 a0001c0001t0006g0259 |
3 | NA18944.hp1 NA19058.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.-130-2268A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74013418 | |||||||
chr14:74013431 | G | A | 2 | a0001c0001t0006g0199 a0001c0001t0028g0200 |
2 | HG01884.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-130-2281C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74013431 | |||||||
chr14:74013433 | T | C | 133 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0020 others(130): Show |
162 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.-130-2283A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74013433 | |||||||
chr14:74013497 | AT | A | 9 | a0001c0002t0005g0062 a0001c0002t0009g0010 a0001c0002t0009g0208 others(6): Show |
12 | HG01109.hp2 HG01243.hp2 HG01943.hp2 others(9): Show |
intron_variant | MODIFIER | c.-131+2326delA | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74013497 | |||||||
chr14:74013577 | T | C | 1 | a0001c0002t0003g0122 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-131+2247A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74013577 | |||||||
chr14:74013601 | A | G | 181 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0020 others(178): Show |
220 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(217): Show |
intron_variant | MODIFIER | c.-131+2223T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74013601 | |||||||
chr14:74013816 | T | C | 1 | a0001c0001t0006g0123 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-131+2008A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74013816 | |||||||
chr14:74013910 | T | C | 3 | a0001c0001t0012g0130 a0001c0001t0012g0131 a0001c0001t0012g0141 |
3 | HG02572.hp2 HG02647.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.-131+1914A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74013910 | |||||||
chr14:74013956 | C | G | 8 | a0001c0002t0009g0010 a0001c0002t0009g0208 a0001c0002t0010g0022 others(5): Show |
11 | HG01109.hp2 HG01243.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.-131+1868G>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74013956 | |||||||
chr14:74014091 | G | C | 33 | a0001c0001t0005g0058 a0001c0001t0007g0063 a0001c0001t0035g0041 others(30): Show |
40 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.-131+1733C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74014091 | |||||||
chr14:74014099 | A | G | 64 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0020 others(61): Show |
84 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.-131+1725T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74014099 | |||||||
chr14:74014121 | T | A | 64 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0020 others(61): Show |
84 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.-131+1703A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74014121 | |||||||
chr14:74014171 | C | T | 30 | a0001c0001t0001g0236 a0001c0001t0004g0024 a0001c0001t0004g0214 others(27): Show |
31 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(28): Show |
intron_variant | MODIFIER | c.-131+1653G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74014171 | |||||||
chr14:74014234 | G | A | 4 | a0001c0007t0009g0072 a0002c0003t0009g0007 a0002c0003t0009g0073 others(1): Show |
6 | HG02055.hp2 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-131+1590C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74014234 | |||||||
chr14:74014365 | A | G | 64 | a0001c0001t0001g0284 a0001c0001t0001g0296 a0001c0001t0004g0308 others(61): Show |
73 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.-131+1459T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74014365 | |||||||
chr14:74014368 | T | A | 2 | a0001c0002t0003g0244 a0001c0002t0003g0245 |
2 | HG03017.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.-131+1456A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74014368 | |||||||
chr14:74014380 | TCC | T | 61 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0020 others(58): Show |
81 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.-131+1442_-131+144 others(6): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74014380 | |||||||
chr14:74014385 | C | A | 2 | a0001c0002t0002g0031 a0001c0002t0002g0262 |
3 | NA18941.hp2 NA18950.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.-131+1439G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74014385 | |||||||
chr14:74014385 | C | T | 1 | a0001c0002t0003g0317 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-131+1439G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74014385 | |||||||
chr14:74014386 | C | G | 5 | a0001c0001t0012g0319 a0001c0001t0012g0320 a0001c0002t0003g0316 others(2): Show |
5 | HG02145.hp2 HG02622.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-131+1438G>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74014386 | |||||||
chr14:74014387 | C | CA | 7 | a0001c0001t0011g0134 a0001c0001t0011g0135 a0001c0001t0011g0136 others(4): Show |
7 | HG02258.hp1 HG02280.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-131+1436_-131+143 others(5): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74014387 | |||||||
chr14:74014387 | C | G | 6 | a0001c0001t0004g0075 a0001c0001t0004g0076 a0001c0001t0004g0210 others(3): Show |
7 | HG01891.hp2 HG02135.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-131+1437G>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74014387 | |||||||
chr14:74014388 | C | A | 3 | a0001c0001t0015g0017 a0001c0001t0015g0124 a0001c0001t0015g0125 |
4 | HG01074.hp1 HG01099.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.-131+1436G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74014388 | |||||||
chr14:74014389 | C | G | 2 | a0001c0002t0009g0010 a0001c0002t0009g0208 |
4 | HG01109.hp2 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-131+1435G>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74014389 | |||||||
chr14:74014390 | CA | C | 65 | a0001c0001t0001g0284 a0001c0001t0001g0296 a0001c0001t0004g0308 others(62): Show |
74 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.-131+1433delT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74014390 | |||||||
chr14:74014391 | A | C | 3 | a0001c0002t0002g0289 a0001c0002t0002g0290 a0001c0002t0002g0291 |
3 | HG03688.hp1 NA18981.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.-131+1433T>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74014391 | |||||||
chr14:74014537 | T | G | 2 | a0001c0001t0012g0130 a0001c0001t0012g0131 |
2 | HG02572.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-131+1287A>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74014537 | |||||||
chr14:74014566 | T | C | 4 | a0001c0001t0004g0195 a0001c0001t0004g0196 a0001c0001t0004g0201 others(1): Show |
4 | HG02809.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-131+1258A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74014566 | |||||||
chr14:74014650 | T | A | 4 | a0001c0001t0007g0146 a0001c0001t0007g0187 a0001c0001t0007g0188 others(1): Show |
4 | NA18960.hp2 NA18961.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.-131+1174A>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74014650 | |||||||
chr14:74014781 | G | A | 2 | a0001c0001t0004g0023 a0001c0001t0004g0209 |
3 | HG02451.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-131+1043C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74014781 | |||||||
chr14:74014834 | C | T | 1 | a0001c0001t0011g0134 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-131+990G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74014834 | |||||||
chr14:74014953 | G | T | 2 | a0001c0002t0020g0264 a0001c0002t0020g0265 |
2 | NA18971.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.-131+871C>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74014953 | |||||||
chr14:74014975 | G | A | 1 | a0001c0001t0006g0259 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-131+849C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74014975 | |||||||
chr14:74015080 | CA | C | 160 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0020 others(157): Show |
193 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.-131+743delT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74015080 | |||||||
chr14:74015080 | CAA | C | 67 | a0001c0001t0001g0284 a0001c0001t0001g0296 a0001c0001t0004g0308 others(64): Show |
76 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.-131+742_-131+743d others(4): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74015080 | |||||||
chr14:74015214 | T | C | 3 | a0001c0001t0004g0195 a0001c0001t0004g0196 a0001c0002t0003g0197 |
3 | HG02809.hp1 HG03041.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-131+610A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74015214 | |||||||
chr14:74015250 | G | A | 69 | a0001c0001t0001g0284 a0001c0001t0001g0296 a0001c0001t0004g0308 others(66): Show |
78 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.-131+574C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74015250 | |||||||
chr14:74015260 | C | T | 2 | a0001c0001t0004g0023 a0001c0001t0004g0209 |
3 | HG02451.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-131+564G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74015260 | |||||||
chr14:74015276 | G | A | 64 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0020 others(61): Show |
84 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.-131+548C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74015276 | |||||||
chr14:74015336 | A | G | 69 | a0001c0001t0001g0284 a0001c0001t0001g0296 a0001c0001t0004g0308 others(66): Show |
78 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.-131+488T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74015336 | |||||||
chr14:74015359 | G | C | 2 | a0001c0002t0002g0297 a0001c0002t0002g0307 |
2 | HG02135.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.-131+465C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74015359 | |||||||
chr14:74015359 | G | GC | 21 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0296 others(18): Show |
21 | HG00642.hp2 HG01069.hp2 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.-131+464dupG | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74015359 | |||||||
chr14:74015360 | C | T | 1 | a0001c0001t0023g0132 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-131+464G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74015360 | |||||||
chr14:74015504 | C | T | 1 | a0001c0001t0006g0067 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-131+320G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74015504 | |||||||
chr14:74015534 | G | A | 1 | a0001c0002t0008g0064 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-131+290C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74015534 | |||||||
chr14:74015596 | G | A | 3 | a0001c0001t0012g0130 a0001c0001t0012g0131 a0001c0001t0012g0141 |
3 | HG02572.hp2 HG02647.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.-131+228C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74015596 | |||||||
chr14:74015608 | C | T | 3 | a0001c0001t0012g0130 a0001c0001t0012g0131 a0001c0001t0012g0141 |
3 | HG02572.hp2 HG02647.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.-131+216G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74015608 | |||||||
chr14:74015699 | T | C | 1 | a0001c0001t0001g0192 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-131+125A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74015699 | |||||||
chr14:74015717 | T | C | 1 | a0001c0002t0008g0066 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-131+107A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74015717 | |||||||
chr14:74015747 | A | C | 2 | a0001c0002t0008g0300 a0001c0002t0008g0301 |
2 | HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-131+77T>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 2/15 | chr14 | 74015747 | |||||||
chr14:74015931 | C | T | 1 | a0001c0001t0001g0143 | 1 | NA18966.hp1 | splice_acceptor_variant&intron_variant | HIGH | c.-237-1G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74015931 | |||||||
chr14:74015932 | T | C | 2 | a0001c0002t0002g0298 a0001c0002t0002g0299 |
2 | HG00642.hp2 HG00735.hp2 |
splice_acceptor_variant&intron_variant | HIGH | c.-237-2A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74015932 | |||||||
chr14:74016066 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-237-136C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74016066 | |||||||
chr14:74016222 | T | G | 2 | a0001c0001t0012g0319 a0001c0001t0012g0320 |
2 | HG02622.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-237-292A>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74016222 | |||||||
chr14:74016245 | A | G | 56 | a0001c0001t0001g0284 a0001c0001t0001g0296 a0001c0001t0004g0308 others(53): Show |
64 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.-237-315T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74016245 | |||||||
chr14:74016281 | C | T | 4 | a0001c0007t0009g0072 a0002c0003t0009g0007 a0002c0003t0009g0073 others(1): Show |
6 | HG02055.hp2 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-237-351G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74016281 | |||||||
chr14:74016468 | C | G | 6 | a0001c0002t0010g0022 a0001c0002t0010g0202 a0001c0002t0010g0203 others(3): Show |
7 | HG01243.hp2 HG02486.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-237-538G>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74016468 | |||||||
chr14:74016489 | A | T | 2 | a0001c0002t0009g0010 a0001c0002t0009g0208 |
4 | HG01109.hp2 HG03195.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-237-559T>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74016489 | |||||||
chr14:74016495 | G | A | 2 | a0001c0005t0002g0305 a0001c0005t0002g0306 |
2 | NA18953.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.-237-565C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74016495 | |||||||
chr14:74016640 | A | G | 1 | a0001c0002t0002g0263 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-237-710T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74016640 | |||||||
chr14:74016641 | C | A | 36 | a0001c0001t0001g0236 a0001c0001t0004g0024 a0001c0001t0004g0214 others(33): Show |
37 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(34): Show |
intron_variant | MODIFIER | c.-237-711G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74016641 | |||||||
chr14:74016700 | C | T | 2 | a0001c0001t0001g0142 a0001c0001t0004g0214 |
2 | HG00673.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.-237-770G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74016700 | |||||||
chr14:74016745 | C | A | 181 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0020 others(178): Show |
220 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(217): Show |
intron_variant | MODIFIER | c.-237-815G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74016745 | |||||||
chr14:74016839 | C | A | 1 | a0001c0001t0012g0141 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-237-909G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74016839 | |||||||
chr14:74016865 | T | C | 62 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0020 others(59): Show |
82 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.-237-935A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74016865 | |||||||
chr14:74016912 | C | T | 64 | a0001c0001t0001g0284 a0001c0001t0001g0296 a0001c0001t0004g0308 others(61): Show |
73 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.-237-982G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74016912 | |||||||
chr14:74017045 | G | A | 4 | a0001c0001t0004g0128 a0001c0001t0004g0129 a0001c0002t0009g0010 others(1): Show |
6 | HG01109.hp2 HG03098.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.-237-1115C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74017045 | |||||||
chr14:74017102 | T | C | 1 | a0001c0001t0001g0194 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-237-1172A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74017102 | |||||||
chr14:74017116 | C | T | 1 | a0001c0001t0004g0222 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-237-1186G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74017116 | |||||||
chr14:74017185 | G | A | 4 | a0001c0007t0009g0072 a0002c0003t0009g0007 a0002c0003t0009g0073 others(1): Show |
6 | HG02055.hp2 HG02257.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-237-1255C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74017185 | |||||||
chr14:74017211 | G | A | 1 | a0001c0001t0004g0210 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-237-1281C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74017211 | |||||||
chr14:74017242 | T | C | 69 | a0001c0001t0001g0284 a0001c0001t0001g0296 a0001c0001t0004g0308 others(66): Show |
78 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.-237-1312A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74017242 | |||||||
chr14:74017258 | C | T | 69 | a0001c0001t0001g0284 a0001c0001t0001g0296 a0001c0001t0004g0308 others(66): Show |
78 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.-237-1328G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74017258 | |||||||
chr14:74017272 | C | T | 64 | a0001c0001t0001g0284 a0001c0001t0001g0296 a0001c0001t0004g0308 others(61): Show |
73 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.-237-1342G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74017272 | |||||||
chr14:74017326 | AAG | A | 233 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0020 others(230): Show |
276 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.-237-1398_-237-139 others(6): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74017326 | |||||||
chr14:74017327 | AG | A | 10 | a0001c0001t0004g0075 a0001c0001t0004g0076 a0001c0001t0004g0210 others(7): Show |
12 | HG01081.hp1 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.-237-1398delC | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74017327 | |||||||
chr14:74017328 | G | A | 1 | a0001c0002t0002g0307 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-237-1398C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74017328 | |||||||
chr14:74017408 | T | C | 32 | a0001c0001t0005g0058 a0001c0001t0007g0063 a0001c0001t0035g0041 others(29): Show |
39 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.-237-1478A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74017408 | |||||||
chr14:74017450 | G | C | 11 | a0001c0001t0006g0025 a0001c0001t0006g0026 a0001c0001t0006g0251 others(8): Show |
13 | HG01070.hp2 HG01192.hp1 HG02155.hp1 others(10): Show |
intron_variant | MODIFIER | c.-237-1520C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74017450 | |||||||
chr14:74017569 | ACT | A | 64 | a0001c0001t0001g0284 a0001c0001t0001g0296 a0001c0001t0004g0308 others(61): Show |
73 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.-237-1641_-237-164 others(6): Show |
ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74017569 | |||||||
chr14:74017578 | CA | C | 12 | a0001c0001t0004g0210 a0001c0001t0004g0308 a0001c0001t0006g0025 others(9): Show |
15 | HG01070.hp2 HG02055.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-237-1649delT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74017578 | |||||||
chr14:74017607 | G | A | 40 | a0001c0001t0001g0236 a0001c0001t0004g0024 a0001c0001t0004g0195 others(37): Show |
41 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.-238+1643C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74017607 | |||||||
chr14:74017613 | G | A | 9 | a0001c0001t0004g0308 a0001c0001t0004g0313 a0001c0001t0007g0198 others(6): Show |
9 | NA18944.hp2 NA18946.hp2 NA18947.hp2 others(6): Show |
intron_variant | MODIFIER | c.-238+1637C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74017613 | |||||||
chr14:74017657 | G | A | 2 | a0001c0001t0006g0199 a0001c0001t0028g0200 |
2 | HG01884.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-238+1593C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74017657 | |||||||
chr14:74017698 | T | C | 314 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0020 others(311): Show |
372 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(369): Show |
intron_variant | MODIFIER | c.-238+1552A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74017698 | |||||||
chr14:74017806 | C | T | 3 | a0001c0002t0008g0064 a0001c0002t0008g0065 a0001c0002t0008g0066 |
3 | HG01243.hp1 HG02723.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-238+1444G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74017806 | |||||||
chr14:74017905 | G | A | 1 | a0001c0001t0004g0201 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-238+1345C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74017905 | |||||||
chr14:74017967 | A | G | 64 | a0001c0001t0001g0284 a0001c0001t0001g0296 a0001c0001t0004g0308 others(61): Show |
73 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.-238+1283T>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74017967 | |||||||
chr14:74018096 | C | G | 1 | a0001c0001t0024g0260 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-238+1154G>C | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74018096 | |||||||
chr14:74018146 | A | T | 6 | a0001c0002t0010g0022 a0001c0002t0010g0202 a0001c0002t0010g0203 others(3): Show |
7 | HG01243.hp2 HG02486.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-238+1104T>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74018146 | |||||||
chr14:74018179 | G | GA | 72 | a0001c0001t0001g0236 a0001c0001t0004g0023 a0001c0001t0004g0024 others(69): Show |
84 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.-238+1070dupT | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74018179 | |||||||
chr14:74018240 | G | A | 2 | a0001c0001t0004g0023 a0001c0001t0004g0209 |
3 | HG02451.hp2 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-238+1010C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74018240 | |||||||
chr14:74018356 | T | C | 1 | a0001c0001t0004g0210 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-238+894A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74018356 | |||||||
chr14:74018430 | C | T | 32 | a0001c0001t0005g0058 a0001c0001t0007g0063 a0001c0001t0035g0041 others(29): Show |
39 | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.-238+820G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74018430 | |||||||
chr14:74018436 | G | C | 3 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0034g0211 |
3 | NA19057.hp1 NA19081.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.-238+814C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74018436 | |||||||
chr14:74018544 | G | T | 1 | a0001c0001t0026g0033 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-238+706C>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74018544 | |||||||
chr14:74018661 | G | A | 11 | a0001c0001t0006g0025 a0001c0001t0006g0026 a0001c0001t0006g0251 others(8): Show |
13 | HG01070.hp2 HG01192.hp1 HG02155.hp1 others(10): Show |
intron_variant | MODIFIER | c.-238+589C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74018661 | |||||||
chr14:74018679 | C | T | 64 | a0001c0001t0001g0284 a0001c0001t0001g0296 a0001c0001t0004g0308 others(61): Show |
73 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.-238+571G>A | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74018679 | |||||||
chr14:74018820 | G | A | 69 | a0001c0001t0001g0284 a0001c0001t0001g0296 a0001c0001t0004g0308 others(66): Show |
78 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.-238+430C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74018820 | |||||||
chr14:74018889 | G | A | 36 | a0001c0001t0001g0236 a0001c0001t0004g0024 a0001c0001t0004g0214 others(33): Show |
37 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(34): Show |
intron_variant | MODIFIER | c.-238+361C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74018889 | |||||||
chr14:74018959 | G | C | 1 | a0001c0001t0018g0249 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-238+291C>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74018959 | |||||||
chr14:74019030 | G | A | 1 | a0001c0002t0008g0321 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-238+220C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74019030 | |||||||
chr14:74019078 | T | C | 69 | a0001c0001t0001g0284 a0001c0001t0001g0296 a0001c0001t0004g0308 others(66): Show |
78 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.-238+172A>G | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74019078 | |||||||
chr14:74019158 | G | A | 1 | a0001c0002t0008g0250 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-238+92C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74019158 | |||||||
chr14:74019171 | G | A | 11 | a0001c0001t0006g0025 a0001c0001t0006g0026 a0001c0001t0006g0251 others(8): Show |
13 | HG01070.hp2 HG01192.hp1 HG02155.hp1 others(10): Show |
intron_variant | MODIFIER | c.-238+79C>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74019171 | |||||||
chr14:74019223 | C | A | 69 | a0001c0001t0001g0284 a0001c0001t0001g0296 a0001c0001t0004g0308 others(66): Show |
78 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.-238+27G>T | ENTPD5 | ENSG00000187097.13 | transcript | ENST00000334696.11 | protein_coding | 1/15 | chr14 | 74019223 |