Item | Value |
---|---|
geneid | 51099 |
ensemblid | ENSG00000011198.10 |
hgncid | 21396 |
symbol | ABHD5 |
name | abhydrolase domain containing 5, lysophosphatidic acid acyltransferase |
refseq_nuc | NM_016006.6 |
refseq_prot | NP_057090.2 |
ensembl_nuc | ENST00000644371.2 |
ensembl_prot | ENSP00000495778.1 |
mane_status | MANE Select |
chr | chr3 |
start | 43690938 |
end | 43722725 |
strand | + |
ver | v1.2 |
region | chr3:43690938-43722725 |
region5000 | chr3:43685938-43727725 |
regionname0 | ABHD5_chr3_43690938_43722725 |
regionname5000 | ABHD5_chr3_43685938_43727725 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 349 | 275 | 77 | 49 | 109 | 6 | 32 | ABHD5_chr3_43685938_43727725 | ABHD5 | MAAEE others(344): Show |
chr3 | 43685938 | 43727725 |
a0002 | 0/0 | 349 | 3 | 2 | 1 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | MAAAE others(344): Show |
chr3 | 43685938 | 43727725 |
a0003 | 0/0 | 349 | 2 | 2 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | MAAEE others(344): Show |
chr3 | 43685938 | 43727725 |
a0004 | 0/0 | 349 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | MAAEE others(344): Show |
chr3 | 43685938 | 43727725 |
a0005 | 0/0 | 349 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | MAAEE others(344): Show |
chr3 | 43685938 | 43727725 |
a0006 | 0/0 | 349 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | MAAEE others(344): Show |
chr3 | 43685938 | 43727725 |
a0007 | 0/0 | 349 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | MAAEE others(344): Show |
chr3 | 43685938 | 43727725 |
a0008 | 0/0 | 349 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | MAAEE others(344): Show |
chr3 | 43685938 | 43727725 |
a0009 | 0/0 | 349 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | MAAEE others(344): Show |
chr3 | 43685938 | 43727725 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1047 | 260 | 74 | 45 | 105 | 6 | 28 | ABHD5_chr3_43685938_43727725 | ABHD5 | ATGGC others(1042): Show |
chr3 | 43685938 | 43727725 | ||
a0001c0002 | 0/0 | 1047 | 14 | 3 | 4 | 4 | 0 | 3 | ABHD5_chr3_43685938_43727725 | ABHD5 | ATGGC others(1042): Show |
chr3 | 43685938 | 43727725 | ||
a0001c0011 | 0/0 | 1047 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD5_chr3_43685938_43727725 | ABHD5 | ATGGC others(1042): Show |
chr3 | 43685938 | 43727725 | ||
a0002c0003 | 0/0 | 1047 | 3 | 2 | 1 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | ATGGC others(1042): Show |
chr3 | 43685938 | 43727725 | ||
a0003c0004 | 0/0 | 1047 | 2 | 2 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | ATGGC others(1042): Show |
chr3 | 43685938 | 43727725 | ||
a0004c0009 | 0/0 | 1047 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | ATGGC others(1042): Show |
chr3 | 43685938 | 43727725 | ||
a0005c0008 | 0/0 | 1047 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | ATGGC others(1042): Show |
chr3 | 43685938 | 43727725 | ||
a0006c0005 | 0/0 | 1047 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | ATGGC others(1042): Show |
chr3 | 43685938 | 43727725 | ||
a0007c0007 | 0/0 | 1047 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | ATGGC others(1042): Show |
chr3 | 43685938 | 43727725 | ||
a0008c0006 | 0/0 | 1047 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | ATGGC others(1042): Show |
chr3 | 43685938 | 43727725 | ||
a0009c0010 | 0/0 | 1047 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | ATGGC others(1042): Show |
chr3 | 43685938 | 43727725 |
acthapid | grch38/chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 5298 | 93 | 13 | 20 | 43 | 4 | 12 | ABHD5_chr3_43685938_43727725 | ABHD5 | AGTCG others(5293): Show |
chr3 | 43685938 | 43727725 |
a0001c0001t0002 | 1/0 | 5298 | 54 | 22 | 8 | 15 | 1 | 7 | ABHD5_chr3_43685938_43727725 | ABHD5 | AGTCG others(5293): Show |
chr3 | 43685938 | 43727725 |
a0001c0001t0003 | 0/0 | 5298 | 44 | 5 | 6 | 27 | 0 | 6 | ABHD5_chr3_43685938_43727725 | ABHD5 | AGTCG others(5293): Show |
chr3 | 43685938 | 43727725 |
a0001c0001t0004 | 0/0 | 5295 | 19 | 14 | 4 | 0 | 0 | 1 | ABHD5_chr3_43685938_43727725 | ABHD5 | AGTCG others(5290): Show |
chr3 | 43685938 | 43727725 |
a0001c0001t0006 | 0/0 | 5296 | 5 | 5 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | AGTCG others(5291): Show |
chr3 | 43685938 | 43727725 |
a0001c0001t0007 | 0/0 | 5295 | 5 | 5 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | AGTCG others(5290): Show |
chr3 | 43685938 | 43727725 |
a0001c0001t0008 | 0/0 | 5298 | 4 | 0 | 4 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | AGTCG others(5293): Show |
chr3 | 43685938 | 43727725 |
a0001c0001t0009 | 0/0 | 5299 | 4 | 0 | 1 | 2 | 0 | 1 | ABHD5_chr3_43685938_43727725 | ABHD5 | AGTCG others(5294): Show |
chr3 | 43685938 | 43727725 |
a0001c0001t0010 | 0/0 | 5299 | 4 | 0 | 0 | 4 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | AGTCG others(5294): Show |
chr3 | 43685938 | 43727725 |
a0001c0001t0011 | 0/0 | 5298 | 3 | 3 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | AGTCG others(5293): Show |
chr3 | 43685938 | 43727725 |
a0001c0001t0013 | 0/0 | 5298 | 3 | 0 | 0 | 3 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | AGTCG others(5293): Show |
chr3 | 43685938 | 43727725 |
a0001c0001t0014 | 0/0 | 5298 | 2 | 2 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | AGTCG others(5293): Show |
chr3 | 43685938 | 43727725 |
a0001c0001t0016 | 0/0 | 5297 | 2 | 0 | 1 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | AGTCG others(5292): Show |
chr3 | 43685938 | 43727725 |
a0001c0001t0017 | 0/0 | 5296 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | AGTCG others(5291): Show |
chr3 | 43685938 | 43727725 |
a0001c0001t0019 | 0/0 | 5298 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | AGTCG others(5293): Show |
chr3 | 43685938 | 43727725 |
a0001c0001t0020 | 0/0 | 5297 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | AGTCG others(5292): Show |
chr3 | 43685938 | 43727725 |
a0001c0001t0021 | 0/0 | 5299 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | AGTCG others(5294): Show |
chr3 | 43685938 | 43727725 |
a0001c0001t0022 | 0/0 | 5298 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | AGTCG others(5293): Show |
chr3 | 43685938 | 43727725 |
a0001c0001t0023 | 0/0 | 5297 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | AGTCG others(5292): Show |
chr3 | 43685938 | 43727725 |
a0001c0001t0024 | 0/0 | 5299 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | AGTCG others(5294): Show |
chr3 | 43685938 | 43727725 |
a0001c0001t0025 | 0/0 | 5298 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | AGTCG others(5293): Show |
chr3 | 43685938 | 43727725 |
a0001c0001t0026 | 0/0 | 5298 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | AGTCG others(5293): Show |
chr3 | 43685938 | 43727725 |
a0001c0001t0029 | 0/0 | 5298 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | AGTCG others(5293): Show |
chr3 | 43685938 | 43727725 |
a0001c0001t0030 | 0/0 | 5296 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | AGTCG others(5291): Show |
chr3 | 43685938 | 43727725 |
a0001c0001t0031 | 0/0 | 5298 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | AGTCG others(5293): Show |
chr3 | 43685938 | 43727725 |
a0001c0001t0032 | 0/0 | 5298 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | AGTCG others(5293): Show |
chr3 | 43685938 | 43727725 |
a0001c0001t0033 | 0/0 | 5298 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | AGTCG others(5293): Show |
chr3 | 43685938 | 43727725 |
a0001c0001t0034 | 0/0 | 5298 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | AGTCG others(5293): Show |
chr3 | 43685938 | 43727725 |
a0001c0001t0035 | 0/0 | 5298 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | AGTCG others(5293): Show |
chr3 | 43685938 | 43727725 |
a0001c0001t0036 | 0/0 | 5298 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD5_chr3_43685938_43727725 | ABHD5 | AGTCG others(5293): Show |
chr3 | 43685938 | 43727725 |
a0001c0001t0037 | 0/0 | 5294 | 1 | 0 | 0 | 0 | 1 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | AGTCG others(5289): Show |
chr3 | 43685938 | 43727725 |
a0001c0002t0005 | 0/0 | 5297 | 9 | 0 | 4 | 3 | 0 | 2 | ABHD5_chr3_43685938_43727725 | ABHD5 | AGTCG others(5292): Show |
chr3 | 43685938 | 43727725 |
a0001c0002t0018 | 0/0 | 5298 | 2 | 1 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | AGTCG others(5293): Show |
chr3 | 43685938 | 43727725 |
a0001c0002t0027 | 0/0 | 5297 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | AGTCG others(5292): Show |
chr3 | 43685938 | 43727725 |
a0001c0002t0028 | 0/0 | 5297 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | AGTCG others(5292): Show |
chr3 | 43685938 | 43727725 |
a0001c0002t0038 | 0/0 | 5297 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD5_chr3_43685938_43727725 | ABHD5 | AGTCG others(5292): Show |
chr3 | 43685938 | 43727725 |
a0001c0011t0001 | 0/0 | 5298 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD5_chr3_43685938_43727725 | ABHD5 | AGTCG others(5293): Show |
chr3 | 43685938 | 43727725 |
a0002c0003t0012 | 0/0 | 5295 | 3 | 2 | 1 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | AGTCG others(5290): Show |
chr3 | 43685938 | 43727725 |
a0003c0004t0015 | 0/0 | 5298 | 2 | 2 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | AGTCG others(5293): Show |
chr3 | 43685938 | 43727725 |
a0004c0009t0001 | 0/0 | 5298 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | AGTCG others(5293): Show |
chr3 | 43685938 | 43727725 |
a0005c0008t0017 | 0/0 | 5296 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | AGTCG others(5291): Show |
chr3 | 43685938 | 43727725 |
a0006c0005t0002 | 0/0 | 5298 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | AGTCG others(5293): Show |
chr3 | 43685938 | 43727725 |
a0007c0007t0001 | 0/0 | 5298 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | AGTCG others(5293): Show |
chr3 | 43685938 | 43727725 |
a0008c0006t0001 | 0/0 | 5298 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | AGTCG others(5293): Show |
chr3 | 43685938 | 43727725 |
a0009c0010t0001 | 0/0 | 5298 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | AGTCG others(5293): Show |
chr3 | 43685938 | 43727725 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 9 | 1 | 3 | 5 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0001g0003 | 0/0 | 10 | 0 | 1 | 6 | 0 | 3 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0001g0006 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0001g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0001g0021 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0002g0004 | 0/0 | 7 | 1 | 2 | 1 | 1 | 2 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0002g0007 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0002g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0002g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0002g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0002g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0002g0027 | 1/0 | 2 | 0 | 0 | 0 | 0 | 1 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0003g0001 | 0/0 | 8 | 0 | 1 | 6 | 0 | 1 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0003g0005 | 0/0 | 7 | 0 | 3 | 4 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0003g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0003g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0003g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0003g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0003g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0004g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0004g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0004g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0004g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0004g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0004g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0004g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0004g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0004g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0004g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0004g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0004g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0006g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0006g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0006g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0006g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0007g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0007g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0008g0001 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0009g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0009g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0009g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0009g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0010g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0010g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0010g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0011g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0011g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0011g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0013g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0013g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0013g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0014g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0014g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0016g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0016g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0017g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0019g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0020g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0021g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0022g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0023g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0024g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0025g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0026g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0029g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0030g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0031g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0032g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0033g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0034g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0035g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0036g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0001t0037g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0002t0005g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0002t0005g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0002t0005g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0002t0005g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0002t0005g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0002t0005g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0002t0005g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0002t0005g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0002t0018g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0002t0018g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0002t0027g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0002t0028g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0002t0038g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0001c0011t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0002c0003t0012g0018 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0003c0004t0015g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0003c0004t0015g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0004c0009t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0005c0008t0017g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0006c0005t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0007c0007t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0008c0006t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
a0009c0010t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00408 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | CHS | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG00544 | hp1 | a0004 | c0009 | t0001 | g0003 | EAS | CHS | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | CHS | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG00738 | hp1 | a0001 | c0001 | t0004 | g0133 | AMR | PUR | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG00738 | hp2 | a0001 | c0001 | t0003 | g0174 | AMR | PUR | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG01070 | hp2 | a0001 | c0001 | t0008 | g0001 | AMR | PUR | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG01071 | hp2 | a0001 | c0001 | t0008 | g0001 | AMR | PUR | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG01074 | hp1 | a0001 | c0001 | t0008 | g0001 | AMR | PUR | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0024 | AMR | PUR | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG01081 | hp1 | a0001 | c0002 | t0005 | g0149 | AMR | PUR | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG01081 | hp2 | a0001 | c0001 | t0016 | g0082 | AMR | PUR | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0121 | AMR | PUR | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG01099 | hp2 | a0001 | c0001 | t0008 | g0001 | AMR | PUR | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0119 | AMR | PUR | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG01109 | hp2 | a0002 | c0003 | t0012 | g0018 | AMR | PUR | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG01167 | hp1 | a0001 | c0001 | t0004 | g0025 | AMR | PUR | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG01168 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG01169 | hp1 | a0001 | c0001 | t0004 | g0025 | AMR | PUR | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG01169 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | PUR | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0041 | AMR | PUR | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG01192 | hp2 | a0001 | c0001 | t0004 | g0132 | AMR | PUR | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG01255 | hp2 | a0001 | c0002 | t0005 | g0031 | AMR | CLM | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | CLM | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0111 | AMR | CLM | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG01496 | hp2 | a0001 | c0001 | t0003 | g0169 | AMR | CLM | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0054 | EUR | IBS | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG01515 | hp2 | a0001 | c0001 | t0037 | g0131 | EUR | IBS | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0099 | EUR | IBS | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0055 | EUR | IBS | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG01884 | hp1 | a0001 | c0001 | t0004 | g0017 | AFR | ACB | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | ACB | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG01934 | hp1 | a0001 | c0001 | t0019 | g0170 | AMR | PEL | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0142 | AMR | PEL | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG01952 | hp1 | a0001 | c0002 | t0005 | g0152 | AMR | PEL | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG01952 | hp2 | a0001 | c0001 | t0009 | g0024 | AMR | PEL | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG01978 | hp1 | a0001 | c0002 | t0005 | g0031 | AMR | PEL | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02004 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | PEL | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02055 | hp1 | a0001 | c0002 | t0018 | g0156 | AFR | ACB | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | ACB | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02056 | hp1 | a0001 | c0001 | t0003 | g0160 | EAS | KHV | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02056 | hp2 | a0001 | c0001 | t0031 | g0096 | EAS | KHV | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02071 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | KHV | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02071 | hp2 | a0001 | c0001 | t0009 | g0128 | EAS | KHV | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02074 | hp1 | a0001 | c0001 | t0003 | g0166 | EAS | KHV | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02080 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02129 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | KHV | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02155 | hp2 | a0001 | c0001 | t0003 | g0177 | EAS | CDX | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02258 | hp1 | a0001 | c0001 | t0004 | g0028 | AFR | ACB | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02258 | hp2 | a0001 | c0001 | t0006 | g0145 | AFR | ACB | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02293 | hp2 | a0001 | c0001 | t0003 | g0005 | AMR | PEL | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02451 | hp2 | a0001 | c0002 | t0027 | g0032 | AFR | ACB | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02523 | hp1 | a0001 | c0001 | t0010 | g0002 | EAS | KHV | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | KHV | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02572 | hp2 | a0001 | c0001 | t0007 | g0135 | AFR | GWD | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0115 | AFR | GWD | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02622 | hp1 | a0001 | c0001 | t0004 | g0190 | AFR | GWD | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02622 | hp2 | a0002 | c0003 | t0012 | g0018 | AFR | GWD | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02630 | hp1 | a0001 | c0001 | t0004 | g0026 | AFR | GWD | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0123 | AFR | GWD | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02683 | hp2 | a0001 | c0002 | t0005 | g0158 | SAS | PJL | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02717 | hp1 | a0001 | c0001 | t0006 | g0146 | AFR | GWD | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02723 | hp1 | a0001 | c0001 | t0003 | g0167 | AFR | GWD | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0042 | AFR | GWD | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02735 | hp1 | a0001 | c0001 | t0003 | g0173 | SAS | PJL | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0027 | SAS | PJL | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02738 | hp1 | a0001 | c0001 | t0036 | g0021 | SAS | PJL | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02738 | hp2 | a0001 | c0001 | t0003 | g0162 | SAS | PJL | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02809 | hp1 | a0001 | c0001 | t0003 | g0033 | AFR | GWD | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02818 | hp1 | a0001 | c0001 | t0007 | g0011 | AFR | GWD | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02818 | hp2 | a0001 | c0001 | t0017 | g0136 | AFR | GWD | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0120 | AFR | GWD | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | GWD | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02896 | hp2 | a0001 | c0001 | t0006 | g0030 | AFR | GWD | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02897 | hp2 | a0001 | c0001 | t0006 | g0030 | AFR | GWD | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02922 | hp1 | a0001 | c0001 | t0014 | g0186 | AFR | ESN | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02922 | hp2 | a0001 | c0001 | t0004 | g0029 | AFR | ESN | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02965 | hp1 | a0003 | c0004 | t0015 | g0184 | AFR | ESN | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02970 | hp1 | a0001 | c0001 | t0006 | g0147 | AFR | ESN | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02970 | hp2 | a0001 | c0001 | t0004 | g0017 | AFR | ESN | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02976 | hp2 | a0001 | c0001 | t0004 | g0137 | AFR | ESN | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0113 | SAS | PJL | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG03017 | hp2 | a0001 | c0001 | t0003 | g0189 | SAS | PJL | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG03041 | hp1 | a0002 | c0003 | t0012 | g0018 | AFR | GWD | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG03041 | hp2 | a0001 | c0001 | t0003 | g0180 | AFR | GWD | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0124 | AFR | MSL | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ESN | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG03130 | hp2 | a0001 | c0001 | t0014 | g0187 | AFR | ESN | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0037 | AFR | ESN | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG03139 | hp2 | a0001 | c0001 | t0003 | g0033 | AFR | ESN | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG03195 | hp1 | a0001 | c0001 | t0003 | g0179 | AFR | ESN | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0116 | AFR | ESN | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG03239 | hp2 | a0001 | c0011 | t0001 | g0002 | SAS | PJL | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0023 | AFR | MSL | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG03486 | hp2 | a0001 | c0001 | t0026 | g0034 | AFR | MSL | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG03490 | hp1 | a0001 | c0002 | t0038 | g0155 | SAS | PJL | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG03516 | hp1 | a0005 | c0008 | t0017 | g0110 | AFR | ESN | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG03516 | hp2 | a0001 | c0001 | t0022 | g0182 | AFR | ESN | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG03540 | hp1 | a0001 | c0001 | t0004 | g0058 | AFR | GWD | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0035 | AFR | GWD | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | MSL | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG03579 | hp2 | a0001 | c0001 | t0007 | g0011 | AFR | MSL | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0114 | SAS | PJL | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG03654 | hp2 | a0001 | c0001 | t0004 | g0134 | SAS | PJL | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG03669 | hp1 | a0001 | c0001 | t0003 | g0046 | SAS | PJL | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | STU | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | STU | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG03710 | hp2 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG03927 | hp1 | a0001 | c0002 | t0005 | g0150 | SAS | BEB | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | BEB | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG03942 | hp2 | a0001 | c0001 | t0009 | g0057 | SAS | BEB | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0051 | SAS | BEB | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | BEB | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | STU | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG04199 | hp2 | a0001 | c0001 | t0003 | g0164 | SAS | STU | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | STU | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0127 | SAS | STU | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0039 | AFR | YRI | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA18522 | hp2 | a0006 | c0005 | t0002 | g0122 | AFR | YRI | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | CHB | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | CHB | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA18906 | hp1 | a0003 | c0004 | t0015 | g0185 | AFR | YRI | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA18906 | hp2 | a0001 | c0001 | t0004 | g0017 | AFR | YRI | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA18942 | hp1 | a0001 | c0002 | t0005 | g0157 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA18943 | hp2 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA18946 | hp1 | a0007 | c0007 | t0001 | g0060 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA18951 | hp2 | a0001 | c0001 | t0032 | g0108 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA18956 | hp2 | a0001 | c0001 | t0003 | g0176 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA18957 | hp1 | a0001 | c0001 | t0013 | g0014 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA18961 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA18962 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA18962 | hp2 | a0001 | c0001 | t0035 | g0010 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA18963 | hp1 | a0001 | c0001 | t0010 | g0016 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA18963 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA18964 | hp1 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA18967 | hp1 | a0001 | c0001 | t0010 | g0062 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA18967 | hp2 | a0001 | c0002 | t0018 | g0154 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA18968 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA18974 | hp2 | a0001 | c0001 | t0024 | g0159 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA18979 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA18982 | hp1 | a0001 | c0002 | t0005 | g0153 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA18990 | hp2 | a0001 | c0001 | t0003 | g0168 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA18993 | hp1 | a0001 | c0001 | t0020 | g0175 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA18994 | hp1 | a0001 | c0001 | t0034 | g0063 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA18994 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA18995 | hp1 | a0001 | c0001 | t0003 | g0171 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA18998 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA18999 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA19002 | hp1 | a0008 | c0006 | t0001 | g0095 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA19003 | hp1 | a0001 | c0002 | t0005 | g0151 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA19009 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA19011 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA19012 | hp1 | a0001 | c0001 | t0009 | g0049 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA19012 | hp2 | a0001 | c0001 | t0016 | g0098 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA19030 | hp1 | a0009 | c0010 | t0001 | g0015 | AFR | LWK | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | LWK | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | LWK | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA19043 | hp2 | a0001 | c0001 | t0011 | g0181 | AFR | LWK | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA19060 | hp1 | a0001 | c0001 | t0013 | g0045 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA19063 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA19064 | hp1 | a0001 | c0001 | t0029 | g0004 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA19065 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA19067 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA19068 | hp1 | a0001 | c0001 | t0023 | g0001 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA19076 | hp2 | a0001 | c0001 | t0021 | g0012 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA19081 | hp2 | a0001 | c0001 | t0033 | g0141 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA19084 | hp1 | a0001 | c0001 | t0003 | g0172 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA19089 | hp1 | a0001 | c0001 | t0003 | g0183 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA19089 | hp2 | a0001 | c0001 | t0010 | g0002 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA19090 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA19240 | hp1 | a0001 | c0001 | t0004 | g0029 | AFR | YRI | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | YRI | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0129 | AFR | ASW | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA20129 | hp2 | a0001 | c0002 | t0028 | g0032 | AFR | ASW | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0004 | EUR | TSI | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0104 | EUR | TSI | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02109 | hp1 | a0001 | c0001 | t0004 | g0028 | AFR | ACB | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02486 | hp1 | a0001 | c0001 | t0004 | g0056 | AFR | ACB | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02559 | hp1 | a0001 | c0001 | t0007 | g0011 | AFR | ACB | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG02559 | hp2 | a0001 | c0001 | t0030 | g0148 | AFR | ACB | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG03471 | hp2 | a0001 | c0001 | t0011 | g0165 | AFR | MSL | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG06807 | hp1 | a0001 | c0001 | t0025 | g0188 | AFR | USA | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
HG06807 | hp2 | a0001 | c0001 | t0011 | g0178 | AFR | USA | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA18955 | hp1 | a0001 | c0001 | t0013 | g0043 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA20300 | hp1 | a0001 | c0001 | t0007 | g0011 | AFR | USA | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA20300 | hp2 | a0001 | c0001 | t0004 | g0026 | AFR | USA | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA21309 | hp1 | a0001 | c0001 | t0004 | g0117 | AFR | LWK | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | LWK | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0021 | REF | REF | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0027 | REF | REF | ABHD5_chr3_43685938_43727725 | ABHD5 | chr3 | 43685938 | 43727725 |
view | chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:43691003 | A | C | 1 | a0002 | 3 | HG01109.hp2 HG02622.hp2 HG03041.hp1 |
missense_variant | MODERATE | c.11A>C | p.Glu4Ala | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/7 | 66/5298 | 11/1050 | 4/349 | chr3 | 43691003 | |||
chr3:43691011 | G | A | 1 | a0003 | 2 | HG02965.hp1 NA18906.hp1 |
missense_variant | MODERATE | c.19G>A | p.Glu7Lys | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/7 | 74/5298 | 19/1050 | 7/349 | chr3 | 43691011 | |||
chr3:43702283 | T | C | 1 | a0006 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.202T>C | p.Phe68Leu | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/7 | 257/5298 | 202/1050 | 68/349 | chr3 | 43702283 | |||
chr3:43702296 | T | C | 1 | a0008 | 1 | NA19002.hp1 | missense_variant | MODERATE | c.215T>C | p.Ile72Thr | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/7 | 270/5298 | 215/1050 | 72/349 | chr3 | 43702296 | |||
chr3:43702371 | A | C | 1 | a0009 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.290A>C | p.Asp97Ala | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/7 | 345/5298 | 290/1050 | 97/349 | chr3 | 43702371 | |||
chr3:43711753 | G | A | 1 | a0007 | 1 | NA18946.hp1 | missense_variant | MODERATE | c.551G>A | p.Arg184Gln | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 4/7 | 606/5298 | 551/1050 | 184/349 | chr3 | 43711753 | |||
chr3:43711830 | C | G | 1 | a0004 | 1 | HG00544.hp1 | missense_variant | MODERATE | c.628C>G | p.Pro210Ala | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 4/7 | 683/5298 | 628/1050 | 210/349 | chr3 | 43711830 | |||
chr3:43717717 | A | G | 1 | a0005 | 1 | HG03516.hp1 | missense_variant | MODERATE | c.820A>G | p.Lys274Glu | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 6/7 | 875/5298 | 820/1050 | 274/349 | chr3 | 43717717 | |||
chr3:43722725 | A | G | 1 | a0001 | 1 | NA18951.hp2 | splice_region_variant | LOW | c.*4193A>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 7/7 | chr3 | 43722725 |
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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:43691004 | G | A | 1 | a0001c0002 | 14 | HG01081.hp1 HG01255.hp2 HG01952.hp1 others(11): Show |
synonymous_variant | LOW | c.12G>A | p.Glu4Glu | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/7 | 67/5298 | 12/1050 | 4/349 | chr3 | 43691004 | |||
chr3:43691031 | C | T | 1 | a0001c0011 | 1 | HG03239.hp2 | synonymous_variant | LOW | c.39C>T | p.Thr13Thr | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/7 | 94/5298 | 39/1050 | 13/349 | chr3 | 43691031 |
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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:43690974 | C | T | 3 | a0001c0002t0005a0001c0002t0018a0001c0002t0038 | 12 | HG01081.hp1 HG01255.hp2 HG01952.hp1 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-19C>T | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/7 | 19 | chr3 | 43690974 | ||||||
chr3:43718570 | T | G | 13 | a0001c0001t0003a0001c0001t0008a0001c0001t0011others(10): Show | 63 | HG00408.hp1 HG00738.hp2 HG01070.hp2 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*38T>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 7/7 | 38 | chr3 | 43718570 | ||||||
chr3:43718813 | C | A | 9 | a0001c0001t0003a0001c0001t0008a0001c0001t0011others(6): Show | 57 | HG00408.hp1 HG00738.hp2 HG01070.hp2 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*281C>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 7/7 | 281 | chr3 | 43718813 | ||||||
chr3:43718924 | T | G | 1 | a0002c0003t0012 | 3 | HG01109.hp2 HG02622.hp2 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*392T>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 7/7 | 392 | chr3 | 43718924 | ||||||
chr3:43719297 | C | T | 1 | a0001c0001t0026 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*765C>T | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 7/7 | 765 | chr3 | 43719297 | ||||||
chr3:43719642 | G | C | 18 | a0001c0001t0003a0001c0001t0008a0001c0001t0011others(15): Show | 77 | HG00408.hp1 HG00738.hp2 HG01070.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*1110G>C | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 7/7 | 1110 | chr3 | 43719642 | ||||||
chr3:43719863 | T | C | 1 | a0001c0001t0026 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1331T>C | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 7/7 | 1331 | chr3 | 43719863 | ||||||
chr3:43719876 | ATAG | A | 6 | a0001c0001t0004a0001c0001t0007a0001c0001t0017others(3): Show | 30 | HG00738.hp1 HG01109.hp2 HG01167.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*1346_*1348delAGT | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 7/7 | 1346 | INFO_REALIGN_3_PRIME | chr3 | 43719876 | |||||
chr3:43719949 | A | G | 15 | a0001c0001t0001a0001c0001t0010a0001c0001t0013others(12): Show | 112 | HG00544.hp1 HG00544.hp2 HG00621.hp1 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*1417A>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 7/7 | 1417 | chr3 | 43719949 | ||||||
chr3:43720017 | A | T | 1 | a0001c0001t0036 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1485A>T | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 7/7 | 1485 | chr3 | 43720017 | ||||||
chr3:43720052 | A | G | 1 | a0001c0001t0024 | 1 | NA18974.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1520A>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 7/7 | 1520 | chr3 | 43720052 | ||||||
chr3:43720145 | T | C | 18 | a0001c0001t0003a0001c0001t0008a0001c0001t0011others(15): Show | 77 | HG00408.hp1 HG00738.hp2 HG01070.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*1613T>C | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 7/7 | 1613 | chr3 | 43720145 | ||||||
chr3:43720194 | A | G | 3 | a0001c0002t0005a0001c0002t0018a0001c0002t0038 | 12 | HG01081.hp1 HG01255.hp2 HG01952.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1662A>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 7/7 | 1662 | chr3 | 43720194 | ||||||
chr3:43720261 | T | G | 2 | a0001c0002t0027a0001c0002t0028 | 2 | HG02451.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1729T>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 7/7 | 1729 | chr3 | 43720261 | ||||||
chr3:43720283 | T | C | 1 | a0001c0001t0019 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1751T>C | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 7/7 | 1751 | chr3 | 43720283 | ||||||
chr3:43720284 | G | A | 1 | a0001c0001t0019 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1752G>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 7/7 | 1752 | chr3 | 43720284 | ||||||
chr3:43720285 | G | C | 1 | a0001c0001t0019 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1753G>C | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 7/7 | 1753 | chr3 | 43720285 | ||||||
chr3:43720286 | G | A | 1 | a0001c0001t0020 | 1 | NA18993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1754G>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 7/7 | 1754 | chr3 | 43720286 | ||||||
chr3:43720287 | A | T | 1 | a0001c0001t0020 | 1 | NA18993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1755A>T | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 7/7 | 1755 | chr3 | 43720287 | ||||||
chr3:43720288 | G | A | 1 | a0001c0001t0020 | 1 | NA18993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1756G>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 7/7 | 1756 | chr3 | 43720288 | ||||||
chr3:43720288 | G | C | 1 | a0001c0001t0019 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1756G>C | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 7/7 | 1756 | chr3 | 43720288 | ||||||
chr3:43720288 | G | T | 7 | a0001c0001t0003a0001c0001t0008a0001c0001t0011others(4): Show | 55 | HG00408.hp1 HG00738.hp2 HG01070.hp2 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*1756G>T | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 7/7 | 1756 | chr3 | 43720288 | ||||||
chr3:43720289 | A | G | 2 | a0001c0001t0006a0001c0001t0030 | 6 | HG02258.hp2 HG02559.hp2 HG02717.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1757A>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 7/7 | 1757 | chr3 | 43720289 | ||||||
chr3:43720290 | A | AG | 7 | a0001c0001t0003a0001c0001t0008a0001c0001t0011others(4): Show | 55 | HG00408.hp1 HG00738.hp2 HG01070.hp2 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*1758_*1759insG | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 7/7 | 1759 | chr3 | 43720290 | ||||||
chr3:43720290 | A | G | 1 | a0001c0001t0020 | 1 | NA18993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1758A>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 7/7 | 1758 | chr3 | 43720290 | ||||||
chr3:43720291 | T | C | 1 | a0001c0001t0019 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1759T>C | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 7/7 | 1759 | chr3 | 43720291 | ||||||
chr3:43720295 | A | T | 1 | a0001c0001t0019 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1763A>T | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 7/7 | 1763 | chr3 | 43720295 | ||||||
chr3:43720297 | G | T | 1 | a0001c0001t0019 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1765G>T | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 7/7 | 1765 | chr3 | 43720297 | ||||||
chr3:43720366 | C | G | 18 | a0001c0001t0003a0001c0001t0008a0001c0001t0011others(15): Show | 77 | HG00408.hp1 HG00738.hp2 HG01070.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*1834C>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 7/7 | 1834 | chr3 | 43720366 | ||||||
chr3:43720395 | G | A | 18 | a0001c0001t0003a0001c0001t0008a0001c0001t0011others(15): Show | 77 | HG00408.hp1 HG00738.hp2 HG01070.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*1863G>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 7/7 | 1863 | chr3 | 43720395 | ||||||
chr3:43720475 | A | G | 1 | a0003c0004t0015 | 2 | HG02965.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1943A>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 7/7 | 1943 | chr3 | 43720475 | ||||||
chr3:43720489 | G | T | 1 | a0001c0001t0013 | 3 | NA18955.hp1 NA18957.hp1 NA19060.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1957G>T | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 7/7 | 1957 | chr3 | 43720489 | ||||||
chr3:43720596 | G | C | 2 | a0001c0002t0027a0001c0002t0028 | 2 | HG02451.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2064G>C | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 7/7 | 2064 | chr3 | 43720596 | ||||||
chr3:43720641 | T | C | 1 | a0001c0001t0031 | 1 | HG02056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2109T>C | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 7/7 | 2109 | chr3 | 43720641 | ||||||
chr3:43720669 | A | G | 1 | a0001c0001t0030 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2137A>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 7/7 | 2137 | chr3 | 43720669 | ||||||
chr3:43720856 | G | T | 18 | a0001c0001t0003a0001c0001t0008a0001c0001t0011others(15): Show | 77 | HG00408.hp1 HG00738.hp2 HG01070.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*2324G>T | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 7/7 | 2324 | chr3 | 43720856 | ||||||
chr3:43720977 | T | G | 1 | a0002c0003t0012 | 3 | HG01109.hp2 HG02622.hp2 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2445T>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 7/7 | 2445 | chr3 | 43720977 | ||||||
chr3:43720995 | A | G | 1 | a0001c0001t0007 | 5 | HG02559.hp1 HG02572.hp2 HG02818.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2463A>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 7/7 | 2463 | chr3 | 43720995 | ||||||
chr3:43720995 | A | T | 1 | a0001c0001t0035 | 1 | NA18962.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2463A>T | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 7/7 | 2463 | chr3 | 43720995 | ||||||
chr3:43721040 | A | G | 1 | a0001c0001t0011 | 3 | HG03471.hp2 HG06807.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2508A>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 7/7 | 2508 | chr3 | 43721040 | ||||||
chr3:43721401 | A | G | 1 | a0001c0002t0038 | 1 | HG03490.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2869A>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 7/7 | 2869 | chr3 | 43721401 | ||||||
chr3:43721431 | A | G | 1 | a0001c0001t0029 | 1 | NA19064.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2899A>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 7/7 | 2899 | chr3 | 43721431 | ||||||
chr3:43721467 | C | A | 9 | a0001c0001t0003a0001c0001t0008a0001c0001t0011others(6): Show | 57 | HG00408.hp1 HG00738.hp2 HG01070.hp2 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*2935C>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 7/7 | 2935 | chr3 | 43721467 | ||||||
chr3:43721562 | C | CA | 4 | a0001c0001t0009a0001c0001t0010a0001c0001t0017others(1): Show | 10 | HG01952.hp2 HG02071.hp2 HG02523.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3051dupA | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 7/7 | 3052 | INFO_REALIGN_3_PRIME | chr3 | 43721562 | |||||
chr3:43721562 | CA | C | 11 | a0001c0001t0003a0001c0001t0008a0001c0001t0011others(8): Show | 68 | HG00408.hp1 HG00738.hp2 HG01070.hp2 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*3051delA | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 7/7 | 3051 | INFO_REALIGN_3_PRIME | chr3 | 43721562 | |||||
chr3:43721562 | CAA | C | 3 | a0001c0001t0006a0001c0001t0023a0001c0001t0030 | 7 | HG02258.hp2 HG02559.hp2 HG02717.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3050_*3051delAA | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 7/7 | 3050 | INFO_REALIGN_3_PRIME | chr3 | 43721562 | |||||
chr3:43721785 | A | T | 18 | a0001c0001t0003a0001c0001t0008a0001c0001t0011others(15): Show | 77 | HG00408.hp1 HG00738.hp2 HG01070.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*3253A>T | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 7/7 | 3253 | chr3 | 43721785 | ||||||
chr3:43721866 | C | G | 1 | a0001c0001t0008 | 4 | HG01070.hp2 HG01071.hp2 HG01074.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3334C>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 7/7 | 3334 | chr3 | 43721866 | ||||||
chr3:43721879 | A | G | 1 | a0001c0001t0034 | 1 | NA18994.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3347A>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 7/7 | 3347 | chr3 | 43721879 | ||||||
chr3:43722049 | T | C | 1 | a0001c0001t0022 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3517T>C | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 7/7 | 3517 | chr3 | 43722049 | ||||||
chr3:43722212 | A | C | 1 | a0001c0001t0033 | 1 | NA19081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3680A>C | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 7/7 | 3680 | chr3 | 43722212 | ||||||
chr3:43722287 | G | A | 1 | a0001c0002t0027 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3755G>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 7/7 | 3755 | chr3 | 43722287 | ||||||
chr3:43722484 | T | C | 9 | a0001c0001t0003a0001c0001t0008a0001c0001t0011others(6): Show | 57 | HG00408.hp1 HG00738.hp2 HG01070.hp2 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*3952T>C | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 7/7 | 3952 | chr3 | 43722484 | ||||||
chr3:43722487 | C | A | 1 | a0001c0001t0014 | 2 | HG02922.hp1 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3955C>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 7/7 | 3955 | chr3 | 43722487 | ||||||
chr3:43722679 | G | T | 13 | a0001c0001t0003a0001c0001t0008a0001c0001t0011others(10): Show | 63 | HG00408.hp1 HG00738.hp2 HG01070.hp2 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*4147G>T | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 7/7 | 4147 | chr3 | 43722679 |
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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:43691052 | G | A | 1 | a0001c0001t0026g0034 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.47+13G>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43691052 | |||||||
chr3:43691098 | G | A | 9 | a0001c0001t0002g0007a0001c0001t0002g0035a0001c0001t0002g0036others(6): Show | 12 | HG01192.hp1 HG02055.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.47+59G>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43691098 | |||||||
chr3:43691101 | T | A | 5 | a0001c0001t0001g0014a0001c0001t0001g0044a0001c0001t0013g0014others(2): Show | 6 | NA18953.hp1 NA18955.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.47+62T>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43691101 | |||||||
chr3:43691126 | G | A | 1 | a0001c0001t0003g0046 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.47+87G>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43691126 | |||||||
chr3:43691147 | C | T | 1 | a0001c0001t0002g0042 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.47+108C>T | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43691147 | |||||||
chr3:43691148 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.47+109G>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43691148 | |||||||
chr3:43691234 | C | T | 1 | a0001c0001t0026g0034 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.47+195C>T | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43691234 | |||||||
chr3:43691286 | G | A | 1 | a0001c0001t0001g0048 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.47+247G>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43691286 | |||||||
chr3:43691390 | C | G | 1 | a0001c0001t0004g0190 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.47+351C>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43691390 | |||||||
chr3:43691432 | C | G | 41 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0012others(38): Show | 63 | HG00408.hp1 HG00738.hp2 HG01070.hp2 others(60): Show |
intron_variant | MODIFIER | c.47+393C>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43691432 | |||||||
chr3:43691580 | T | C | 6 | a0001c0001t0002g0008a0001c0001t0002g0019a0001c0001t0002g0050others(3): Show | 10 | HG00408.hp2 HG02135.hp1 HG04184.hp1 others(7): Show |
intron_variant | MODIFIER | c.47+541T>C | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43691580 | |||||||
chr3:43691615 | C | G | 1 | a0001c0001t0003g0189 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.47+576C>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43691615 | |||||||
chr3:43691616 | G | A | 1 | a0001c0001t0003g0189 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.47+577G>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43691616 | |||||||
chr3:43691621 | G | GGCTGGCG others(15): Show |
1 | a0001c0001t0003g0189 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.47+582_47+583insGC others(20): Show |
ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43691621 | |||||||
chr3:43691625 | C | A | 1 | a0001c0001t0003g0189 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.47+586C>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43691625 | |||||||
chr3:43691630 | G | T | 1 | a0001c0001t0003g0189 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.47+591G>T | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43691630 | |||||||
chr3:43691637 | G | A | 1 | a0001c0001t0003g0189 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.47+598G>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43691637 | |||||||
chr3:43691640 | G | A | 1 | a0001c0001t0003g0189 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.47+601G>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43691640 | |||||||
chr3:43691641 | C | A | 1 | a0001c0001t0003g0189 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.47+602C>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43691641 | |||||||
chr3:43691645 | G | C | 1 | a0001c0001t0001g0053 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.47+606G>C | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43691645 | |||||||
chr3:43691651 | G | T | 1 | a0001c0001t0003g0189 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.47+612G>T | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43691651 | |||||||
chr3:43691656 | G | A | 1 | a0001c0001t0003g0189 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.47+617G>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43691656 | |||||||
chr3:43691692 | A | G | 59 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0012others(56): Show | 83 | HG00408.hp1 HG00738.hp2 HG01070.hp2 others(80): Show |
intron_variant | MODIFIER | c.47+653A>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43691692 | |||||||
chr3:43691890 | G | T | 1 | a0001c0001t0001g0144 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.47+851G>T | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43691890 | |||||||
chr3:43691908 | A | G | 1 | a0001c0001t0026g0034 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.47+869A>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43691908 | |||||||
chr3:43692110 | T | C | 2 | a0001c0001t0001g0054a0001c0001t0001g0055 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.47+1071T>C | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43692110 | |||||||
chr3:43692153 | C | G | 1 | a0001c0001t0025g0188 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.47+1114C>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43692153 | |||||||
chr3:43692408 | C | T | 5 | a0001c0001t0014g0186a0001c0001t0014g0187a0001c0001t0025g0188others(2): Show | 5 | HG02922.hp1 HG02965.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.47+1369C>T | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43692408 | |||||||
chr3:43692543 | G | A | 1 | a0001c0001t0004g0056 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.47+1504G>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43692543 | |||||||
chr3:43692546 | C | G | 1 | a0001c0001t0001g0143 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.47+1507C>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43692546 | |||||||
chr3:43692570 | G | A | 2 | a0003c0004t0015g0184a0003c0004t0015g0185 | 2 | HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.47+1531G>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43692570 | |||||||
chr3:43692704 | G | A | 1 | a0001c0001t0009g0049 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.47+1665G>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43692704 | |||||||
chr3:43692718 | C | T | 1 | a0001c0001t0002g0142 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.47+1679C>T | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43692718 | |||||||
chr3:43692840 | G | A | 41 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0012others(38): Show | 63 | HG00408.hp1 HG00738.hp2 HG01070.hp2 others(60): Show |
intron_variant | MODIFIER | c.47+1801G>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43692840 | |||||||
chr3:43692898 | A | C | 41 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0012others(38): Show | 63 | HG00408.hp1 HG00738.hp2 HG01070.hp2 others(60): Show |
intron_variant | MODIFIER | c.47+1859A>C | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43692898 | |||||||
chr3:43693304 | A | G | 2 | a0001c0002t0027g0032a0001c0002t0028g0032 | 2 | HG02451.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.47+2265A>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43693304 | |||||||
chr3:43693472 | T | C | 5 | a0001c0001t0014g0186a0001c0001t0014g0187a0001c0001t0025g0188others(2): Show | 5 | HG02922.hp1 HG02965.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.47+2433T>C | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43693472 | |||||||
chr3:43693507 | C | T | 2 | a0001c0001t0004g0028a0001c0001t0004g0029 | 4 | HG02109.hp1 HG02258.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.47+2468C>T | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43693507 | |||||||
chr3:43693671 | T | A | 1 | a0001c0001t0009g0057 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.47+2632T>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43693671 | |||||||
chr3:43693750 | C | CT | 13 | a0001c0001t0002g0007a0001c0001t0002g0036a0001c0001t0002g0037others(10): Show | 18 | HG01192.hp1 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.47+2725dupT | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 43693750 | ||||||
chr3:43693750 | CT | C | 122 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(119): Show | 176 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(173): Show |
intron_variant | MODIFIER | c.47+2725delT | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 43693750 | ||||||
chr3:43694066 | G | GGGAGGCC others(41): Show |
59 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0012others(56): Show | 83 | HG00408.hp1 HG00738.hp2 HG01070.hp2 others(80): Show |
intron_variant | MODIFIER | c.47+3029_47+3030ins others(48): Show |
ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 43694066 | ||||||
chr3:43694069 | G | C | 59 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0012others(56): Show | 83 | HG00408.hp1 HG00738.hp2 HG01070.hp2 others(80): Show |
intron_variant | MODIFIER | c.47+3030G>C | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43694069 | |||||||
chr3:43694125 | TGGC | T | 13 | a0001c0002t0005g0031a0001c0002t0005g0149a0001c0002t0005g0150others(10): Show | 14 | HG01081.hp1 HG01255.hp2 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.47+3091_47+3093del others(3): Show |
ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 43694125 | ||||||
chr3:43694217 | C | T | 80 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(77): Show | 111 | HG00544.hp1 HG00544.hp2 HG00621.hp1 others(108): Show |
intron_variant | MODIFIER | c.47+3178C>T | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43694217 | |||||||
chr3:43694258 | C | CA | 25 | a0001c0001t0001g0059a0001c0001t0001g0061a0001c0001t0001g0064others(22): Show | 26 | HG01255.hp2 HG01346.hp2 HG01952.hp1 others(23): Show |
intron_variant | MODIFIER | c.47+3240dupA | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 43694258 | ||||||
chr3:43694258 | C | CAA | 28 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0012others(25): Show | 50 | HG00408.hp1 HG00738.hp2 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.47+3239_47+3240dup others(2): Show |
ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 43694258 | ||||||
chr3:43694258 | C | CAAA | 9 | a0001c0001t0003g0046a0001c0001t0003g0160a0001c0001t0003g0161others(6): Show | 9 | HG02056.hp1 HG02074.hp1 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.47+3238_47+3240dup others(3): Show |
ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 43694258 | ||||||
chr3:43694258 | CA | C | 6 | a0001c0001t0001g0010a0001c0001t0001g0107a0001c0001t0004g0137others(3): Show | 8 | HG02976.hp2 HG03130.hp2 NA18951.hp1 others(5): Show |
intron_variant | MODIFIER | c.47+3240delA | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 43694258 | ||||||
chr3:43694590 | C | G | 54 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0012others(51): Show | 77 | HG00408.hp1 HG00738.hp2 HG01070.hp2 others(74): Show |
intron_variant | MODIFIER | c.47+3551C>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43694590 | |||||||
chr3:43694659 | T | C | 5 | a0001c0001t0006g0030a0001c0001t0006g0145a0001c0001t0006g0146others(2): Show | 6 | HG02258.hp2 HG02559.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.47+3620T>C | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43694659 | |||||||
chr3:43694679 | T | C | 5 | a0001c0001t0006g0030a0001c0001t0006g0145a0001c0001t0006g0146others(2): Show | 6 | HG02258.hp2 HG02559.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.47+3640T>C | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43694679 | |||||||
chr3:43694714 | G | C | 9 | a0001c0001t0002g0007a0001c0001t0002g0035a0001c0001t0002g0036others(6): Show | 12 | HG01192.hp1 HG02055.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.47+3675G>C | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43694714 | |||||||
chr3:43694737 | G | A | 1 | a0001c0001t0014g0187 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.47+3698G>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43694737 | |||||||
chr3:43694838 | G | A | 80 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(77): Show | 111 | HG00544.hp1 HG00544.hp2 HG00621.hp1 others(108): Show |
intron_variant | MODIFIER | c.47+3799G>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43694838 | |||||||
chr3:43694886 | T | G | 15 | a0001c0001t0001g0067a0001c0001t0002g0112a0001c0002t0005g0031others(12): Show | 16 | HG01081.hp1 HG01255.hp2 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.47+3847T>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43694886 | |||||||
chr3:43695036 | C | A | 2 | a0001c0002t0027g0032a0001c0002t0028g0032 | 2 | HG02451.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.47+3997C>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43695036 | |||||||
chr3:43695208 | A | G | 35 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0012others(32): Show | 57 | HG00408.hp1 HG00738.hp2 HG01070.hp2 others(54): Show |
intron_variant | MODIFIER | c.48-4068A>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43695208 | |||||||
chr3:43695259 | T | A | 59 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0012others(56): Show | 83 | HG00408.hp1 HG00738.hp2 HG01070.hp2 others(80): Show |
intron_variant | MODIFIER | c.48-4017T>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43695259 | |||||||
chr3:43695352 | T | G | 1 | a0001c0001t0001g0068 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.48-3924T>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43695352 | |||||||
chr3:43695398 | G | A | 54 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0012others(51): Show | 77 | HG00408.hp1 HG00738.hp2 HG01070.hp2 others(74): Show |
intron_variant | MODIFIER | c.48-3878G>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43695398 | |||||||
chr3:43695399 | A | T | 54 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0012others(51): Show | 77 | HG00408.hp1 HG00738.hp2 HG01070.hp2 others(74): Show |
intron_variant | MODIFIER | c.48-3877A>T | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43695399 | |||||||
chr3:43695400 | G | A | 54 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0012others(51): Show | 77 | HG00408.hp1 HG00738.hp2 HG01070.hp2 others(74): Show |
intron_variant | MODIFIER | c.48-3876G>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43695400 | |||||||
chr3:43695597 | G | A | 2 | a0001c0001t0003g0183a0001c0001t0024g0159 | 2 | NA18974.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.48-3679G>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43695597 | |||||||
chr3:43695617 | A | G | 1 | a0001c0001t0017g0136 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.48-3659A>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43695617 | |||||||
chr3:43695632 | T | G | 11 | a0001c0002t0005g0031a0001c0002t0005g0149a0001c0002t0005g0150others(8): Show | 12 | HG01081.hp1 HG01255.hp2 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.48-3644T>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43695632 | |||||||
chr3:43695743 | A | G | 1 | a0001c0001t0014g0187 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.48-3533A>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43695743 | |||||||
chr3:43695761 | C | T | 2 | a0001c0002t0027g0032a0001c0002t0028g0032 | 2 | HG02451.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.48-3515C>T | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43695761 | |||||||
chr3:43695762 | G | A | 2 | a0001c0001t0001g0015a0009c0010t0001g0015 | 3 | HG00733.hp2 HG03239.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.48-3514G>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43695762 | |||||||
chr3:43695967 | G | A | 54 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0012others(51): Show | 77 | HG00408.hp1 HG00738.hp2 HG01070.hp2 others(74): Show |
intron_variant | MODIFIER | c.48-3309G>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43695967 | |||||||
chr3:43696034 | TTGCCTTG others(13): Show |
T | 1 | a0001c0001t0003g0167 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.48-3237_48-3218del others(20): Show |
ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 43696034 | ||||||
chr3:43696320 | A | G | 1 | a0001c0001t0026g0034 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.48-2956A>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43696320 | |||||||
chr3:43696517 | A | C | 2 | a0001c0001t0007g0011a0001c0001t0007g0135 | 5 | HG02559.hp1 HG02572.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.48-2759A>C | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43696517 | |||||||
chr3:43696536 | C | T | 2 | a0001c0002t0027g0032a0001c0002t0028g0032 | 2 | HG02451.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.48-2740C>T | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43696536 | |||||||
chr3:43696537 | G | A | 1 | a0001c0001t0002g0035 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.48-2739G>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43696537 | |||||||
chr3:43696627 | GA | G | 6 | a0001c0001t0004g0058a0001c0001t0004g0132a0001c0001t0004g0133others(3): Show | 6 | HG00738.hp1 HG01192.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.48-2647delA | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 43696627 | ||||||
chr3:43696639 | G | A | 11 | a0001c0002t0005g0031a0001c0002t0005g0149a0001c0002t0005g0150others(8): Show | 12 | HG01081.hp1 HG01255.hp2 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.48-2637G>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43696639 | |||||||
chr3:43696833 | A | G | 1 | a0001c0001t0001g0106 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.48-2443A>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43696833 | |||||||
chr3:43696859 | C | G | 40 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0012others(37): Show | 62 | HG00408.hp1 HG00738.hp2 HG01070.hp2 others(59): Show |
intron_variant | MODIFIER | c.48-2417C>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43696859 | |||||||
chr3:43696892 | A | G | 4 | a0001c0001t0014g0186a0001c0001t0014g0187a0003c0004t0015g0184others(1): Show | 4 | HG02922.hp1 HG02965.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.48-2384A>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43696892 | |||||||
chr3:43696906 | T | TA | 11 | a0001c0002t0005g0031a0001c0002t0005g0149a0001c0002t0005g0150others(8): Show | 12 | HG01081.hp1 HG01255.hp2 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.48-2364dupA | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr3 | 43696906 | ||||||
chr3:43697066 | C | T | 54 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0012others(51): Show | 77 | HG00408.hp1 HG00738.hp2 HG01070.hp2 others(74): Show |
intron_variant | MODIFIER | c.48-2210C>T | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43697066 | |||||||
chr3:43697258 | A | G | 1 | a0001c0001t0030g0148 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.48-2018A>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43697258 | |||||||
chr3:43697292 | G | T | 11 | a0001c0002t0005g0031a0001c0002t0005g0149a0001c0002t0005g0150others(8): Show | 12 | HG01081.hp1 HG01255.hp2 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.48-1984G>T | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43697292 | |||||||
chr3:43697522 | A | C | 1 | a0001c0001t0003g0166 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.48-1754A>C | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43697522 | |||||||
chr3:43697792 | G | A | 1 | a0001c0001t0006g0145 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.48-1484G>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43697792 | |||||||
chr3:43698060 | T | C | 1 | a0001c0001t0033g0141 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.48-1216T>C | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43698060 | |||||||
chr3:43698166 | G | A | 1 | a0001c0001t0002g0113 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.48-1110G>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43698166 | |||||||
chr3:43698195 | C | A | 1 | a0001c0001t0002g0114 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.48-1081C>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43698195 | |||||||
chr3:43698218 | C | G | 1 | a0001c0001t0026g0034 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.48-1058C>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43698218 | |||||||
chr3:43698425 | G | T | 1 | a0001c0001t0001g0006 | 5 | HG00735.hp2 HG01496.hp1 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.48-851G>T | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43698425 | |||||||
chr3:43698539 | G | C | 7 | a0001c0001t0001g0109a0001c0001t0002g0022a0001c0001t0002g0023others(4): Show | 9 | HG01074.hp2 HG01884.hp2 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.48-737G>C | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43698539 | |||||||
chr3:43698560 | A | G | 1 | a0001c0001t0022g0182 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.48-716A>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43698560 | |||||||
chr3:43698650 | G | A | 2 | a0001c0001t0001g0020a0001c0001t0001g0069 | 3 | HG02486.hp2 HG03471.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.48-626G>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43698650 | |||||||
chr3:43698809 | A | C | 1 | a0001c0001t0032g0108 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.48-467A>C | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43698809 | |||||||
chr3:43699073 | T | C | 2 | a0001c0001t0001g0070a0001c0001t0001g0071 | 2 | HG00642.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.48-203T>C | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 1/6 | chr3 | 43699073 | |||||||
chr3:43699693 | C | A | 5 | a0001c0001t0006g0030a0001c0001t0006g0145a0001c0001t0006g0146others(2): Show | 6 | HG02258.hp2 HG02559.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.133+332C>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 2/6 | chr3 | 43699693 | |||||||
chr3:43699741 | G | A | 2 | a0001c0001t0014g0186a0001c0001t0014g0187 | 2 | HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.133+380G>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 2/6 | chr3 | 43699741 | |||||||
chr3:43699820 | G | A | 2 | a0001c0001t0002g0036a0001c0001t0002g0037 | 2 | HG02055.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.133+459G>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 2/6 | chr3 | 43699820 | |||||||
chr3:43699845 | A | T | 1 | a0001c0001t0017g0136 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.133+484A>T | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 2/6 | chr3 | 43699845 | |||||||
chr3:43699850 | T | C | 1 | a0001c0001t0003g0168 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.133+489T>C | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 2/6 | chr3 | 43699850 | |||||||
chr3:43699919 | C | G | 8 | a0001c0001t0003g0033a0001c0001t0003g0167a0001c0001t0003g0179others(5): Show | 9 | HG02723.hp1 HG02809.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.133+558C>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 2/6 | chr3 | 43699919 | |||||||
chr3:43699963 | G | A | 59 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0012others(56): Show | 83 | HG00408.hp1 HG00738.hp2 HG01070.hp2 others(80): Show |
intron_variant | MODIFIER | c.133+602G>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 2/6 | chr3 | 43699963 | |||||||
chr3:43700020 | T | C | 2 | a0001c0002t0005g0150a0001c0002t0005g0158 | 2 | HG02683.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.133+659T>C | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 2/6 | chr3 | 43700020 | |||||||
chr3:43700133 | C | T | 1 | a0001c0001t0001g0105 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.133+772C>T | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 2/6 | chr3 | 43700133 | |||||||
chr3:43700168 | G | GGGGTAGG others(9): Show |
1 | a0001c0001t0026g0034 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.133+808_133+823dup others(16): Show |
ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 43700168 | ||||||
chr3:43700184 | A | G | 5 | a0001c0001t0006g0030a0001c0001t0006g0145a0001c0001t0006g0146others(2): Show | 6 | HG02258.hp2 HG02559.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.133+823A>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 2/6 | chr3 | 43700184 | |||||||
chr3:43700363 | A | G | 2 | a0001c0001t0014g0186a0001c0001t0014g0187 | 2 | HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.133+1002A>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 2/6 | chr3 | 43700363 | |||||||
chr3:43700576 | AT | A | 59 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0012others(56): Show | 83 | HG00408.hp1 HG00738.hp2 HG01070.hp2 others(80): Show |
intron_variant | MODIFIER | c.133+1230delT | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 43700576 | ||||||
chr3:43700592 | G | A | 1 | a0001c0001t0003g0177 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.133+1231G>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 2/6 | chr3 | 43700592 | |||||||
chr3:43700732 | C | CCCAGCTA others(93): Show |
5 | a0001c0002t0005g0031a0001c0002t0005g0149a0001c0002t0005g0151others(2): Show | 6 | HG01081.hp1 HG01255.hp2 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.133+1384_133+1385i others(102): Show |
ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 43700732 | ||||||
chr3:43700732 | C | CCCAGCTA others(94): Show |
4 | a0001c0002t0005g0150a0001c0002t0005g0153a0001c0002t0018g0154others(1): Show | 4 | HG03490.hp1 HG03927.hp1 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.133+1384_133+1385i others(103): Show |
ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 43700732 | ||||||
chr3:43700732 | C | CCCAGCTA others(95): Show |
2 | a0001c0002t0005g0158a0001c0002t0018g0156 | 2 | HG02055.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.133+1384_133+1385i others(104): Show |
ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr3 | 43700732 | ||||||
chr3:43701107 | T | G | 2 | a0001c0001t0002g0022a0001c0001t0002g0115 | 3 | HG01884.hp2 HG02615.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.134-1108T>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 2/6 | chr3 | 43701107 | |||||||
chr3:43701128 | G | A | 1 | a0001c0001t0025g0188 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.134-1087G>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 2/6 | chr3 | 43701128 | |||||||
chr3:43701242 | T | C | 13 | a0001c0002t0005g0031a0001c0002t0005g0149a0001c0002t0005g0150others(10): Show | 14 | HG01081.hp1 HG01255.hp2 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.134-973T>C | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 2/6 | chr3 | 43701242 | |||||||
chr3:43701375 | A | G | 1 | a0001c0001t0002g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.134-840A>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 2/6 | chr3 | 43701375 | |||||||
chr3:43701412 | A | G | 1 | a0001c0001t0001g0104 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.134-803A>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 2/6 | chr3 | 43701412 | |||||||
chr3:43701596 | A | G | 1 | a0001c0001t0017g0136 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.134-619A>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 2/6 | chr3 | 43701596 | |||||||
chr3:43701715 | A | G | 5 | a0001c0001t0006g0030a0001c0001t0006g0145a0001c0001t0006g0146others(2): Show | 6 | HG02258.hp2 HG02559.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.134-500A>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 2/6 | chr3 | 43701715 | |||||||
chr3:43701722 | A | G | 1 | a0001c0001t0001g0066 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.134-493A>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 2/6 | chr3 | 43701722 | |||||||
chr3:43701827 | C | T | 2 | a0001c0001t0003g0013a0001c0001t0003g0176 | 5 | NA18956.hp2 NA18961.hp2 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.134-388C>T | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 2/6 | chr3 | 43701827 | |||||||
chr3:43702018 | C | A | 13 | a0001c0001t0004g0017a0001c0001t0004g0025a0001c0001t0004g0026others(10): Show | 24 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.134-197C>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 2/6 | chr3 | 43702018 | |||||||
chr3:43702682 | A | G | 2 | a0001c0001t0002g0035a0001c0001t0002g0041 | 2 | HG01192.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.506+95A>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43702682 | |||||||
chr3:43702756 | T | C | 2 | a0001c0001t0011g0165a0001c0001t0011g0178 | 2 | HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.506+169T>C | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43702756 | |||||||
chr3:43702777 | G | A | 1 | a0001c0001t0002g0130 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.506+190G>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43702777 | |||||||
chr3:43702875 | TTTATTA | T | 54 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0012others(51): Show | 77 | HG00408.hp1 HG00738.hp2 HG01070.hp2 others(74): Show |
intron_variant | MODIFIER | c.506+296_506+301del others(6): Show |
ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 43702875 | ||||||
chr3:43702916 | C | T | 54 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0012others(51): Show | 77 | HG00408.hp1 HG00738.hp2 HG01070.hp2 others(74): Show |
intron_variant | MODIFIER | c.506+329C>T | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43702916 | |||||||
chr3:43703062 | A | G | 1 | a0001c0001t0001g0009 | 4 | HG02895.hp1 HG02896.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.506+475A>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43703062 | |||||||
chr3:43703182 | C | CT | 166 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(163): Show | 235 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(232): Show |
intron_variant | MODIFIER | c.506+608dupT | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 43703182 | ||||||
chr3:43703202 | T | G | 1 | a0001c0001t0002g0142 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.506+615T>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43703202 | |||||||
chr3:43703248 | C | T | 1 | a0001c0001t0006g0030 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.506+661C>T | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43703248 | |||||||
chr3:43703284 | ATTC | A | 9 | a0001c0001t0002g0007a0001c0001t0002g0035a0001c0001t0002g0036others(6): Show | 12 | HG01192.hp1 HG02055.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.506+702_506+704del others(3): Show |
ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 43703284 | ||||||
chr3:43703404 | C | T | 1 | a0001c0001t0004g0026 | 2 | HG02630.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.506+817C>T | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43703404 | |||||||
chr3:43703431 | G | A | 2 | a0001c0001t0003g0012a0001c0001t0021g0012 | 4 | NA18968.hp2 NA19011.hp2 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.506+844G>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43703431 | |||||||
chr3:43703516 | A | G | 1 | a0001c0001t0004g0134 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.506+929A>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43703516 | |||||||
chr3:43703744 | TATGTACC others(6): Show |
T | 54 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0012others(51): Show | 77 | HG00408.hp1 HG00738.hp2 HG01070.hp2 others(74): Show |
intron_variant | MODIFIER | c.506+1160_506+1172d others(15): Show |
ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 43703744 | ||||||
chr3:43703921 | G | C | 1 | a0001c0001t0002g0118 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.506+1334G>C | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43703921 | |||||||
chr3:43704028 | A | T | 2 | a0001c0001t0001g0073a0001c0001t0001g0103 | 2 | HG01168.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.506+1441A>T | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43704028 | |||||||
chr3:43704033 | C | CT | 8 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0003g0163others(5): Show | 8 | HG01346.hp1 HG02922.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.506+1468dupT | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 43704033 | ||||||
chr3:43704033 | CT | C | 112 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(109): Show | 159 | HG00408.hp2 HG00544.hp2 HG00621.hp1 others(156): Show |
intron_variant | MODIFIER | c.506+1468delT | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 43704033 | ||||||
chr3:43704033 | CTTTTTTT others(3): Show |
C | 13 | a0001c0002t0005g0031a0001c0002t0005g0149a0001c0002t0005g0150others(10): Show | 14 | HG01081.hp1 HG01255.hp2 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.506+1459_506+1468d others(12): Show |
ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 43704033 | ||||||
chr3:43704037 | T | C | 1 | a0001c0001t0026g0034 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.506+1450T>C | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43704037 | |||||||
chr3:43704038 | T | C | 8 | a0001c0001t0003g0033a0001c0001t0003g0167a0001c0001t0003g0179others(5): Show | 9 | HG02723.hp1 HG02809.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.506+1451T>C | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43704038 | |||||||
chr3:43704139 | A | G | 1 | a0001c0001t0003g0164 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.506+1552A>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43704139 | |||||||
chr3:43704278 | A | T | 5 | a0001c0001t0006g0030a0001c0001t0006g0145a0001c0001t0006g0146others(2): Show | 6 | HG02258.hp2 HG02559.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.506+1691A>T | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43704278 | |||||||
chr3:43704281 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.506+1694C>T | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43704281 | |||||||
chr3:43704335 | G | T | 41 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0012others(38): Show | 63 | HG00408.hp1 HG00738.hp2 HG01070.hp2 others(60): Show |
intron_variant | MODIFIER | c.506+1748G>T | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43704335 | |||||||
chr3:43704483 | T | C | 35 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0012others(32): Show | 57 | HG00408.hp1 HG00738.hp2 HG01070.hp2 others(54): Show |
intron_variant | MODIFIER | c.506+1896T>C | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43704483 | |||||||
chr3:43704520 | C | T | 2 | a0001c0001t0014g0186a0001c0001t0014g0187 | 2 | HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.506+1933C>T | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43704520 | |||||||
chr3:43704565 | T | G | 1 | a0001c0001t0001g0090 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.506+1978T>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43704565 | |||||||
chr3:43704580 | A | G | 1 | a0001c0001t0001g0090 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.506+1993A>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43704580 | |||||||
chr3:43704591 | C | T | 1 | a0001c0001t0025g0188 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.506+2004C>T | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43704591 | |||||||
chr3:43704612 | A | G | 1 | a0002c0003t0012g0018 | 3 | HG01109.hp2 HG02622.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.506+2025A>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43704612 | |||||||
chr3:43704678 | A | G | 1 | a0001c0001t0003g0174 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.506+2091A>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43704678 | |||||||
chr3:43704883 | C | T | 1 | a0001c0001t0004g0117 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.506+2296C>T | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43704883 | |||||||
chr3:43705278 | A | G | 1 | a0001c0001t0004g0025 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.506+2691A>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43705278 | |||||||
chr3:43705283 | T | G | 3 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0010g0062 | 3 | NA18947.hp1 NA18957.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.506+2696T>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43705283 | |||||||
chr3:43705373 | C | A | 9 | a0001c0001t0002g0007a0001c0001t0002g0035a0001c0001t0002g0036others(6): Show | 12 | HG01192.hp1 HG02055.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.506+2786C>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43705373 | |||||||
chr3:43705466 | C | T | 13 | a0001c0001t0004g0017a0001c0001t0004g0025a0001c0001t0004g0026others(10): Show | 24 | HG01109.hp2 HG01167.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.506+2879C>T | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43705466 | |||||||
chr3:43705505 | G | A | 54 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0012others(51): Show | 77 | HG00408.hp1 HG00738.hp2 HG01070.hp2 others(74): Show |
intron_variant | MODIFIER | c.506+2918G>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43705505 | |||||||
chr3:43705860 | C | T | 168 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(165): Show | 237 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(234): Show |
intron_variant | MODIFIER | c.506+3273C>T | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43705860 | |||||||
chr3:43706329 | C | A | 1 | a0001c0001t0017g0136 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.506+3742C>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43706329 | |||||||
chr3:43706341 | G | A | 1 | a0001c0001t0003g0183 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.506+3754G>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43706341 | |||||||
chr3:43706514 | T | C | 54 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0012others(51): Show | 77 | HG00408.hp1 HG00738.hp2 HG01070.hp2 others(74): Show |
intron_variant | MODIFIER | c.506+3927T>C | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43706514 | |||||||
chr3:43706528 | C | T | 27 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0012others(24): Show | 48 | HG00408.hp1 HG00738.hp2 HG01070.hp2 others(45): Show |
intron_variant | MODIFIER | c.506+3941C>T | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43706528 | |||||||
chr3:43706576 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.506+3989C>T | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43706576 | |||||||
chr3:43706578 | C | T | 35 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0012others(32): Show | 57 | HG00408.hp1 HG00738.hp2 HG01070.hp2 others(54): Show |
intron_variant | MODIFIER | c.506+3991C>T | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43706578 | |||||||
chr3:43706728 | A | G | 2 | a0001c0001t0001g0087a0001c0001t0001g0088 | 2 | NA18955.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.506+4141A>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43706728 | |||||||
chr3:43706758 | T | C | 1 | a0001c0001t0002g0041 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.506+4171T>C | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43706758 | |||||||
chr3:43707172 | A | G | 5 | a0001c0001t0006g0030a0001c0001t0006g0145a0001c0001t0006g0146others(2): Show | 6 | HG02258.hp2 HG02559.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.507-4537A>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43707172 | |||||||
chr3:43707263 | A | G | 54 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0012others(51): Show | 77 | HG00408.hp1 HG00738.hp2 HG01070.hp2 others(74): Show |
intron_variant | MODIFIER | c.507-4446A>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43707263 | |||||||
chr3:43707434 | A | G | 1 | a0001c0001t0003g0168 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.507-4275A>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43707434 | |||||||
chr3:43707450 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.507-4259A>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43707450 | |||||||
chr3:43707491 | A | C | 4 | a0001c0001t0004g0132a0001c0001t0004g0133a0001c0001t0004g0134others(1): Show | 4 | HG00738.hp1 HG01192.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.507-4218A>C | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43707491 | |||||||
chr3:43707723 | G | T | 1 | a0001c0001t0004g0056 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.507-3986G>T | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43707723 | |||||||
chr3:43707881 | T | C | 59 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0012others(56): Show | 83 | HG00408.hp1 HG00738.hp2 HG01070.hp2 others(80): Show |
intron_variant | MODIFIER | c.507-3828T>C | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43707881 | |||||||
chr3:43708003 | C | G | 6 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0084others(3): Show | 6 | HG00544.hp2 NA18947.hp1 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.507-3706C>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43708003 | |||||||
chr3:43708361 | A | C | 4 | a0001c0001t0002g0008a0001c0001t0002g0050a0001c0001t0002g0052others(1): Show | 7 | HG00408.hp2 HG02135.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.507-3348A>C | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43708361 | |||||||
chr3:43708510 | A | T | 1 | a0001c0001t0030g0148 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.507-3199A>T | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43708510 | |||||||
chr3:43708528 | A | C | 1 | a0001c0001t0001g0068 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.507-3181A>C | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43708528 | |||||||
chr3:43708557 | A | G | 1 | a0001c0001t0002g0051 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.507-3152A>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43708557 | |||||||
chr3:43708616 | G | A | 168 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(165): Show | 237 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(234): Show |
intron_variant | MODIFIER | c.507-3093G>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43708616 | |||||||
chr3:43708678 | G | T | 2 | a0001c0002t0027g0032a0001c0002t0028g0032 | 2 | HG02451.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.507-3031G>T | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43708678 | |||||||
chr3:43708863 | C | T | 1 | a0001c0001t0026g0034 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.507-2846C>T | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43708863 | |||||||
chr3:43708878 | A | G | 1 | a0001c0001t0003g0168 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.507-2831A>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43708878 | |||||||
chr3:43708982 | A | G | 2 | a0001c0001t0002g0127a0001c0001t0009g0057 | 2 | HG03942.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.507-2727A>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43708982 | |||||||
chr3:43709179 | T | C | 1 | a0001c0001t0001g0090 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.507-2530T>C | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43709179 | |||||||
chr3:43709210 | ATAGAATT others(18): Show |
A | 3 | a0001c0001t0003g0167a0001c0001t0003g0179a0001c0001t0003g0180 | 3 | HG02723.hp1 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.507-2453_507-2429d others(27): Show |
ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 43709210 | ||||||
chr3:43709435 | A | G | 1 | a0001c0001t0003g0173 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.507-2274A>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43709435 | |||||||
chr3:43709512 | A | AGAGCAGA others(2): Show |
54 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0012others(51): Show | 77 | HG00408.hp1 HG00738.hp2 HG01070.hp2 others(74): Show |
intron_variant | MODIFIER | c.507-2192_507-2191i others(11): Show |
ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 43709512 | ||||||
chr3:43709532 | A | G | 2 | a0001c0002t0027g0032a0001c0002t0028g0032 | 2 | HG02451.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.507-2177A>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43709532 | |||||||
chr3:43709582 | A | G | 1 | a0001c0001t0001g0100 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.507-2127A>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43709582 | |||||||
chr3:43709657 | T | G | 1 | a0001c0001t0025g0188 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.507-2052T>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43709657 | |||||||
chr3:43709818 | G | T | 1 | a0001c0001t0001g0099 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.507-1891G>T | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43709818 | |||||||
chr3:43709959 | C | G | 2 | a0001c0002t0027g0032a0001c0002t0028g0032 | 2 | HG02451.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.507-1750C>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43709959 | |||||||
chr3:43709973 | G | A | 27 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0012others(24): Show | 48 | HG00408.hp1 HG00738.hp2 HG01070.hp2 others(45): Show |
intron_variant | MODIFIER | c.507-1736G>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43709973 | |||||||
chr3:43709995 | A | G | 2 | a0001c0002t0027g0032a0001c0002t0028g0032 | 2 | HG02451.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.507-1714A>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43709995 | |||||||
chr3:43710047 | CAAATAA | C | 9 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0059others(6): Show | 11 | HG00621.hp1 HG02074.hp2 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.507-1652_507-1647d others(8): Show |
ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr3 | 43710047 | ||||||
chr3:43710351 | C | A | 59 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0012others(56): Show | 83 | HG00408.hp1 HG00738.hp2 HG01070.hp2 others(80): Show |
intron_variant | MODIFIER | c.507-1358C>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43710351 | |||||||
chr3:43710398 | A | G | 1 | a0001c0001t0030g0148 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.507-1311A>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43710398 | |||||||
chr3:43710408 | G | A | 1 | a0001c0001t0001g0077 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.507-1301G>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43710408 | |||||||
chr3:43710493 | T | C | 4 | a0001c0001t0001g0066a0001c0001t0001g0090a0001c0001t0001g0091others(1): Show | 4 | HG02109.hp2 HG02615.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.507-1216T>C | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43710493 | |||||||
chr3:43710695 | T | G | 13 | a0001c0002t0005g0031a0001c0002t0005g0149a0001c0002t0005g0150others(10): Show | 14 | HG01081.hp1 HG01255.hp2 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.507-1014T>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43710695 | |||||||
chr3:43710726 | A | T | 1 | a0001c0002t0018g0156 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.507-983A>T | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43710726 | |||||||
chr3:43710761 | A | T | 1 | a0001c0001t0025g0188 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.507-948A>T | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43710761 | |||||||
chr3:43710819 | T | G | 1 | a0001c0001t0025g0188 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.507-890T>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43710819 | |||||||
chr3:43710856 | C | A | 2 | a0001c0001t0001g0067a0001c0001t0001g0106 | 2 | HG02451.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.507-853C>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43710856 | |||||||
chr3:43711167 | A | G | 1 | a0001c0001t0003g0180 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.507-542A>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43711167 | |||||||
chr3:43711173 | A | G | 2 | a0001c0001t0007g0011a0001c0001t0007g0135 | 5 | HG02559.hp1 HG02572.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.507-536A>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43711173 | |||||||
chr3:43711470 | A | T | 3 | a0001c0001t0001g0066a0001c0001t0001g0091a0001c0001t0001g0092 | 3 | HG02109.hp2 HG02615.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.507-239A>T | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43711470 | |||||||
chr3:43711575 | A | G | 2 | a0001c0002t0027g0032a0001c0002t0028g0032 | 2 | HG02451.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.507-134A>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43711575 | |||||||
chr3:43711580 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.507-129G>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43711580 | |||||||
chr3:43711586 | A | G | 54 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0012others(51): Show | 77 | HG00408.hp1 HG00738.hp2 HG01070.hp2 others(74): Show |
intron_variant | MODIFIER | c.507-123A>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 3/6 | chr3 | 43711586 | |||||||
chr3:43712019 | C | T | 1 | a0001c0001t0002g0040 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.661+156C>T | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 4/6 | chr3 | 43712019 | |||||||
chr3:43712457 | T | C | 1 | a0001c0001t0004g0028 | 2 | HG02109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.661+594T>C | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 4/6 | chr3 | 43712457 | |||||||
chr3:43712701 | G | A | 5 | a0001c0001t0014g0186a0001c0001t0014g0187a0001c0001t0025g0188others(2): Show | 5 | HG02922.hp1 HG02965.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.661+838G>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 4/6 | chr3 | 43712701 | |||||||
chr3:43712737 | T | G | 1 | a0001c0001t0002g0129 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.661+874T>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 4/6 | chr3 | 43712737 | |||||||
chr3:43713030 | G | A | 2 | a0001c0001t0001g0015a0009c0010t0001g0015 | 3 | HG00733.hp2 HG03239.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.661+1167G>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 4/6 | chr3 | 43713030 | |||||||
chr3:43713059 | G | T | 1 | a0001c0001t0016g0098 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.661+1196G>T | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 4/6 | chr3 | 43713059 | |||||||
chr3:43713125 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.661+1262G>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 4/6 | chr3 | 43713125 | |||||||
chr3:43713141 | C | T | 11 | a0001c0002t0005g0031a0001c0002t0005g0149a0001c0002t0005g0150others(8): Show | 12 | HG01081.hp1 HG01255.hp2 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.661+1278C>T | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 4/6 | chr3 | 43713141 | |||||||
chr3:43713322 | C | CA | 16 | a0001c0001t0001g0020a0001c0001t0001g0069a0001c0001t0001g0079others(13): Show | 17 | HG00408.hp2 HG01109.hp1 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.661+1479dupA | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 43713322 | ||||||
chr3:43713322 | CA | C | 13 | a0001c0001t0001g0071a0001c0001t0002g0126a0001c0001t0003g0046others(10): Show | 14 | HG01070.hp1 HG01081.hp1 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.661+1479delA | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 43713322 | ||||||
chr3:43713356 | A | G | 1 | a0001c0001t0026g0034 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.661+1493A>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 4/6 | chr3 | 43713356 | |||||||
chr3:43713437 | C | T | 4 | a0001c0001t0014g0186a0001c0001t0014g0187a0003c0004t0015g0184others(1): Show | 4 | HG02922.hp1 HG02965.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.662-1510C>T | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 4/6 | chr3 | 43713437 | |||||||
chr3:43713463 | C | T | 2 | a0001c0001t0002g0022a0001c0001t0002g0115 | 3 | HG01884.hp2 HG02615.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.662-1484C>T | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 4/6 | chr3 | 43713463 | |||||||
chr3:43713555 | A | G | 4 | a0001c0001t0002g0008a0001c0001t0002g0050a0001c0001t0002g0052others(1): Show | 7 | HG00408.hp2 HG02135.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.662-1392A>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 4/6 | chr3 | 43713555 | |||||||
chr3:43713622 | A | C | 1 | a0001c0002t0005g0150 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.662-1325A>C | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 4/6 | chr3 | 43713622 | |||||||
chr3:43713649 | C | G | 59 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0012others(56): Show | 83 | HG00408.hp1 HG00738.hp2 HG01070.hp2 others(80): Show |
intron_variant | MODIFIER | c.662-1298C>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 4/6 | chr3 | 43713649 | |||||||
chr3:43713981 | C | T | 41 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0012others(38): Show | 63 | HG00408.hp1 HG00738.hp2 HG01070.hp2 others(60): Show |
intron_variant | MODIFIER | c.662-966C>T | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 4/6 | chr3 | 43713981 | |||||||
chr3:43714133 | T | C | 2 | a0001c0001t0014g0186a0001c0001t0014g0187 | 2 | HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.662-814T>C | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 4/6 | chr3 | 43714133 | |||||||
chr3:43714137 | C | CT | 10 | a0001c0001t0001g0079a0001c0001t0002g0125a0001c0001t0004g0017others(7): Show | 17 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.662-795dupT | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 43714137 | ||||||
chr3:43714137 | CT | C | 46 | a0001c0001t0001g0073a0001c0001t0001g0080a0001c0001t0002g0130others(43): Show | 58 | HG00408.hp1 HG00738.hp2 HG01070.hp2 others(55): Show |
intron_variant | MODIFIER | c.662-795delT | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 43714137 | ||||||
chr3:43714137 | CTT | C | 12 | a0001c0001t0003g0005a0001c0001t0003g0012a0001c0001t0003g0013others(9): Show | 23 | HG01169.hp2 HG01934.hp1 HG02004.hp1 others(20): Show |
intron_variant | MODIFIER | c.662-796_662-795del others(2): Show |
ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 43714137 | ||||||
chr3:43714140 | T | A | 2 | a0001c0001t0001g0064a0001c0001t0001g0094 | 2 | NA18968.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.662-807T>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 4/6 | chr3 | 43714140 | |||||||
chr3:43714174 | G | A | 1 | a0008c0006t0001g0095 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.662-773G>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 4/6 | chr3 | 43714174 | |||||||
chr3:43714335 | G | A | 41 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0012others(38): Show | 63 | HG00408.hp1 HG00738.hp2 HG01070.hp2 others(60): Show |
intron_variant | MODIFIER | c.662-612G>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 4/6 | chr3 | 43714335 | |||||||
chr3:43714365 | C | T | 1 | a0001c0001t0002g0114 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.662-582C>T | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 4/6 | chr3 | 43714365 | |||||||
chr3:43714580 | G | GT | 8 | a0001c0001t0002g0007a0001c0001t0002g0035a0001c0001t0002g0036others(5): Show | 11 | HG01192.hp1 HG02055.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.662-365dupT | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr3 | 43714580 | ||||||
chr3:43715083 | C | CCCTGTGT others(13): Show |
1 | a0001c0001t0026g0034 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.773+25_773+26insCC others(18): Show |
ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 5/6 | chr3 | 43715083 | |||||||
chr3:43715085 | C | CTG | 63 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(60): Show | 99 | HG00544.hp1 HG00544.hp2 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.773+61_773+62dupGT | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 43715085 | ||||||
chr3:43715085 | C | CTGTG | 25 | a0001c0001t0001g0053a0001c0001t0001g0066a0001c0001t0001g0081others(22): Show | 31 | HG00735.hp1 HG00738.hp1 HG01515.hp2 others(28): Show |
intron_variant | MODIFIER | c.773+59_773+62dupGT others(2): Show |
ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 43715085 | ||||||
chr3:43715085 | C | CTGTGTG | 13 | a0001c0001t0001g0105a0001c0001t0002g0041a0001c0001t0002g0119others(10): Show | 13 | HG01099.hp1 HG01109.hp1 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.773+57_773+62dupGT others(4): Show |
ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 43715085 | ||||||
chr3:43715085 | C | CTGTGTGT others(1): Show |
22 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0012others(19): Show | 43 | HG00408.hp1 HG00738.hp2 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.773+55_773+62dupGT others(6): Show |
ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 43715085 | ||||||
chr3:43715085 | C | CTGTGTGT others(3): Show |
14 | a0001c0001t0003g0167a0001c0001t0003g0171a0001c0001t0003g0172others(11): Show | 15 | HG01192.hp2 HG01255.hp2 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.773+53_773+62dupGT others(8): Show |
ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 43715085 | ||||||
chr3:43715085 | C | CTGTGTGT others(5): Show |
7 | a0001c0001t0003g0033a0001c0001t0003g0173a0001c0001t0011g0165others(4): Show | 8 | HG02055.hp1 HG02735.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.773+51_773+62dupGT others(10): Show |
ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 43715085 | ||||||
chr3:43715085 | C | CTGTGTGT others(9): Show |
1 | a0001c0001t0003g0179 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.773+47_773+62dupGT others(14): Show |
ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 43715085 | ||||||
chr3:43715085 | C | G | 1 | a0001c0001t0026g0034 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.773+27C>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 5/6 | chr3 | 43715085 | |||||||
chr3:43715085 | CTG | C | 5 | a0001c0001t0001g0076a0001c0001t0001g0101a0001c0001t0002g0023others(2): Show | 6 | HG02886.hp1 HG03486.hp1 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.773+61_773+62delGT | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 43715085 | ||||||
chr3:43715085 | CTGTG | C | 14 | a0001c0001t0001g0006a0001c0001t0001g0047a0001c0001t0001g0080others(11): Show | 19 | HG00735.hp2 HG01074.hp2 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.773+59_773+62delGT others(2): Show |
ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 43715085 | ||||||
chr3:43715085 | CTGTGTGT others(3): Show |
C | 2 | a0001c0001t0014g0186a0001c0001t0014g0187 | 2 | HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.773+53_773+62delGT others(8): Show |
ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 43715085 | ||||||
chr3:43715120 | T | TGTGTGTG others(4): Show |
1 | a0001c0002t0005g0150 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.773+62_773+63insGT others(9): Show |
ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 5/6 | chr3 | 43715120 | |||||||
chr3:43715121 | T | G | 1 | a0001c0001t0001g0107 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.773+63T>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 5/6 | chr3 | 43715121 | |||||||
chr3:43715131 | T | G | 1 | a0001c0001t0001g0107 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.773+73T>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 5/6 | chr3 | 43715131 | |||||||
chr3:43715139 | A | T | 1 | a0001c0001t0009g0057 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.773+81A>T | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 5/6 | chr3 | 43715139 | |||||||
chr3:43715152 | CTATT | C | 5 | a0001c0001t0006g0030a0001c0001t0006g0145a0001c0001t0006g0146others(2): Show | 6 | HG02258.hp2 HG02559.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.773+111_773+114del others(4): Show |
ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 43715152 | ||||||
chr3:43715246 | C | T | 1 | a0001c0001t0001g0075 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.773+188C>T | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 5/6 | chr3 | 43715246 | |||||||
chr3:43715369 | G | C | 1 | a0001c0001t0026g0034 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.773+311G>C | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 5/6 | chr3 | 43715369 | |||||||
chr3:43715452 | C | T | 1 | a0001c0001t0025g0188 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.773+394C>T | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 5/6 | chr3 | 43715452 | |||||||
chr3:43715453 | G | A | 1 | a0001c0001t0002g0123 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.773+395G>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 5/6 | chr3 | 43715453 | |||||||
chr3:43715527 | G | T | 1 | a0001c0001t0026g0034 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.773+469G>T | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 5/6 | chr3 | 43715527 | |||||||
chr3:43715625 | A | G | 3 | a0001c0002t0005g0031a0001c0002t0005g0149a0001c0002t0018g0154 | 4 | HG01081.hp1 HG01255.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.773+567A>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 5/6 | chr3 | 43715625 | |||||||
chr3:43715895 | A | G | 13 | a0001c0002t0005g0031a0001c0002t0005g0149a0001c0002t0005g0150others(10): Show | 14 | HG01081.hp1 HG01255.hp2 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.773+837A>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 5/6 | chr3 | 43715895 | |||||||
chr3:43715987 | A | G | 2 | a0001c0001t0004g0058a0001c0001t0004g0190 | 2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.773+929A>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 5/6 | chr3 | 43715987 | |||||||
chr3:43716154 | A | C | 1 | a0001c0001t0003g0179 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.773+1096A>C | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 5/6 | chr3 | 43716154 | |||||||
chr3:43716158 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.773+1100C>T | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 5/6 | chr3 | 43716158 | |||||||
chr3:43716499 | G | T | 1 | a0002c0003t0012g0018 | 3 | HG01109.hp2 HG02622.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.774-1172G>T | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 5/6 | chr3 | 43716499 | |||||||
chr3:43716795 | G | A | 4 | a0001c0001t0001g0066a0001c0001t0001g0090a0001c0001t0001g0091others(1): Show | 4 | HG02109.hp2 HG02615.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.774-876G>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 5/6 | chr3 | 43716795 | |||||||
chr3:43716801 | T | A | 1 | a0002c0003t0012g0018 | 3 | HG01109.hp2 HG02622.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.774-870T>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 5/6 | chr3 | 43716801 | |||||||
chr3:43716900 | G | A | 5 | a0001c0001t0006g0030a0001c0001t0006g0145a0001c0001t0006g0146others(2): Show | 6 | HG02258.hp2 HG02559.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.774-771G>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 5/6 | chr3 | 43716900 | |||||||
chr3:43716909 | A | G | 1 | a0006c0005t0002g0122 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.774-762A>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 5/6 | chr3 | 43716909 | |||||||
chr3:43717096 | G | A | 1 | a0001c0001t0014g0186 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.774-575G>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 5/6 | chr3 | 43717096 | |||||||
chr3:43717183 | CAAAAAAA others(11): Show |
C | 41 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0012others(38): Show | 63 | HG00408.hp1 HG00738.hp2 HG01070.hp2 others(60): Show |
intron_variant | MODIFIER | c.774-484_774-467del others(18): Show |
ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 43717183 | ||||||
chr3:43717192 | CA | C | 5 | a0001c0001t0006g0030a0001c0001t0006g0145a0001c0001t0006g0146others(2): Show | 6 | HG02258.hp2 HG02559.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.774-467delA | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr3 | 43717192 | ||||||
chr3:43717195 | A | C | 2 | a0001c0001t0001g0002a0001c0001t0001g0010 | 2 | NA18999.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.774-476A>C | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 5/6 | chr3 | 43717195 | |||||||
chr3:43717196 | A | C | 2 | a0001c0001t0001g0002a0001c0001t0002g0004 | 2 | HG00642.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.774-475A>C | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 5/6 | chr3 | 43717196 | |||||||
chr3:43717197 | A | C | 1 | a0001c0001t0001g0084 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.774-474A>C | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 5/6 | chr3 | 43717197 | |||||||
chr3:43717201 | A | C | 13 | a0001c0002t0005g0031a0001c0002t0005g0149a0001c0002t0005g0150others(10): Show | 13 | HG01081.hp1 HG01952.hp1 HG01978.hp1 others(10): Show |
intron_variant | MODIFIER | c.774-470A>C | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 5/6 | chr3 | 43717201 | |||||||
chr3:43717312 | G | A | 1 | a0001c0001t0002g0113 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.774-359G>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 5/6 | chr3 | 43717312 | |||||||
chr3:43717375 | A | G | 11 | a0001c0002t0005g0031a0001c0002t0005g0149a0001c0002t0005g0150others(8): Show | 12 | HG01081.hp1 HG01255.hp2 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.774-296A>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 5/6 | chr3 | 43717375 | |||||||
chr3:43717456 | T | A | 1 | a0001c0001t0017g0136 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.774-215T>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 5/6 | chr3 | 43717456 | |||||||
chr3:43717565 | T | C | 2 | a0001c0001t0004g0058a0001c0001t0004g0190 | 2 | HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.774-106T>C | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 5/6 | chr3 | 43717565 | |||||||
chr3:43717923 | A | G | 1 | a0001c0001t0026g0034 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.960+66A>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 6/6 | chr3 | 43717923 | |||||||
chr3:43717949 | C | T | 2 | a0001c0002t0027g0032a0001c0002t0028g0032 | 2 | HG02451.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.960+92C>T | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 6/6 | chr3 | 43717949 | |||||||
chr3:43718023 | G | A | 1 | a0001c0001t0017g0136 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.960+166G>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 6/6 | chr3 | 43718023 | |||||||
chr3:43718029 | A | G | 1 | a0001c0001t0026g0034 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.960+172A>G | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 6/6 | chr3 | 43718029 | |||||||
chr3:43718046 | G | A | 5 | a0001c0001t0014g0186a0001c0001t0014g0187a0001c0001t0025g0188others(2): Show | 5 | HG02922.hp1 HG02965.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.960+189G>A | ABHD5 | ENSG00000011198.10 | transcript | ENST00000644371.2 | protein_coding | 6/6 | chr3 | 43718046 |