Item | Value |
---|---|
geneid | 641371 |
ensemblid | ENSG00000184227.8 |
hgncid | 33128 |
symbol | ACOT1 |
name | acyl-CoA thioesterase 1 |
refseq_nuc | NM_001037161.2 |
refseq_prot | NP_001032238.1 |
ensembl_nuc | ENST00000311148.9 |
ensembl_prot | ENSP00000311224.4 |
mane_status | MANE Select |
chr | chr14 |
start | 73537143 |
end | 73543796 |
strand | + |
ver | v1.2 |
region | chr14:73537143-73543796 |
region5000 | chr14:73532143-73548796 |
regionname0 | ACOT1_chr14_73537143_73543796 |
regionname5000 | ACOT1_chr14_73532143_73548796 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1263 | 115 | 55 | 27 | 7 | 5 | 19 | ACOT1_chr14_73532143_73548796 | ACOT1 | ATGGC others(1258): Show |
chr14 | 73532143 | 73548796 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 1686 | 115 | 55 | 27 | 7 | 5 | 19 | ACOT1_chr14_73532143_73548796 | ACOT1 | ATTCC others(1681): Show |
chr14 | 73532143 | 73548796 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 1/1 | 115 | 55 | 27 | 7 | 5 | 19 | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0001 | REF | REF | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | ACOT1_chr14_73532143_73548796 | ACOT1 | chr14 | 73532143 | 73548796 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:73537426 | C | G | 1 | a0001 | 1 | NA20905.hp1 | missense_variant | MODERATE | c.5C>G | p.Ala2Gly | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 1/3 | 284/1686 | 5/1266 | 2/421 | chr14 | 73537426 | |||
chr14:73537797 | G | C | 1 | a0001 | 1 | NA19079.hp2 | missense_variant | MODERATE | c.376G>C | p.Glu126Gln | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 1/3 | 655/1686 | 376/1266 | 126/421 | chr14 | 73537797 | |||
chr14:73537813 | C | T | 1 | a0001 | 6 | HG01496.hp1 HG01884.hp2 HG02976.hp1 others(3): Show |
missense_variant | MODERATE | c.392C>T | p.Pro131Leu | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 1/3 | 671/1686 | 392/1266 | 131/421 | chr14 | 73537813 | |||
chr14:73537843 | C | T | 1 | a0001 | 2 | HG02818.hp1 HG03540.hp1 |
missense_variant | MODERATE | c.422C>T | p.Ala141Val | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 1/3 | 701/1686 | 422/1266 | 141/421 | chr14 | 73537843 | |||
chr14:73541600 | G | A | 1 | a0001 | 5 | HG01243.hp2 HG01891.hp1 HG02895.hp2 others(2): Show |
missense_variant | MODERATE | c.565G>A | p.Ala189Thr | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/3 | 844/1686 | 565/1266 | 189/421 | chr14 | 73541600 | |||
chr14:73541669 | G | A | 1 | a0001 | 10 | HG02698.hp2 HG02717.hp1 HG02895.hp1 others(7): Show |
missense_variant | MODERATE | c.634G>A | p.Val212Met | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/3 | 913/1686 | 634/1266 | 212/421 | chr14 | 73541669 | |||
chr14:73541675 | T | A | 1 | a0001 | 1 | HG02897.hp1 | missense_variant | MODERATE | c.640T>A | p.Tyr214Asn | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/3 | 919/1686 | 640/1266 | 214/421 | chr14 | 73541675 | |||
chr14:73543186 | G | A | 1 | a0001 | 1 | HG03579.hp2 | missense_variant | MODERATE | c.797G>A | p.Arg266His | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 3/3 | 1076/1686 | 797/1266 | 266/421 | chr14 | 73543186 | |||
chr14:73543442 | G | C | 1 | a0001 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.1053G>C | p.Gln351His | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 3/3 | 1332/1686 | 1053/1266 | 351/421 | chr14 | 73543442 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:73537589 | C | T | 1 | a0001c0001 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.168C>T | p.Thr56Thr | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 1/3 | 447/1686 | 168/1266 | 56/421 | chr14 | 73537589 | |||
chr14:73541512 | C | G | 1 | a0001c0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
synonymous_variant | LOW | c.477C>G | p.Gly159Gly | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/3 | 756/1686 | 477/1266 | 159/421 | chr14 | 73541512 | |||
chr14:73541605 | C | T | 1 | a0001c0001 | 20 | HG01109.hp1 HG01243.hp1 HG02055.hp2 others(17): Show |
synonymous_variant | LOW | c.570C>T | p.Tyr190Tyr | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/3 | 849/1686 | 570/1266 | 190/421 | chr14 | 73541605 | |||
chr14:73541668 | T | C | 1 | a0001c0001 | 10 | HG02698.hp2 HG02717.hp1 HG02895.hp1 others(7): Show |
synonymous_variant | LOW | c.633T>C | p.Ala211Ala | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/3 | 912/1686 | 633/1266 | 211/421 | chr14 | 73541668 | |||
chr14:73541692 | T | C | 1 | a0001c0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
synonymous_variant | LOW | c.657T>C | p.Pro219Pro | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/3 | 936/1686 | 657/1266 | 219/421 | chr14 | 73541692 | |||
chr14:73543625 | C | G | 1 | a0001c0001 | 10 | HG01109.hp1 HG01243.hp1 HG02055.hp2 others(7): Show |
synonymous_variant | LOW | c.1236C>G | p.Gly412Gly | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 3/3 | 1515/1686 | 1236/1266 | 412/421 | chr14 | 73543625 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:73537401 | A | T | 1 | a0001c0001t0001 | 8 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-21A>T | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 1/3 | 21 | chr14 | 73537401 | ||||||
chr14:73537408 | G | C | 1 | a0001c0001t0001 | 9 | HG02572.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-14G>C | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 1/3 | 14 | chr14 | 73537408 | ||||||
chr14:73543682 | G | C | 1 | a0001c0001t0001 | 6 | HG01496.hp1 HG01884.hp2 HG02976.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*27G>C | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 3/3 | 27 | chr14 | 73543682 | ||||||
chr14:73543739 | C | CTTTTG | 1 | a0001c0001t0001 | 27 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*87_*88insTGTTT | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 3/3 | 88 | INFO_REALIGN_3_PRIME | chr14 | 73543739 | |||||
chr14:73543743 | C | T | 1 | a0001c0001t0001 | 27 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*88C>T | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 3/3 | 88 | chr14 | 73543743 | ||||||
chr14:73543745 | C | A | 1 | a0001c0001t0001 | 27 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*90C>A | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 3/3 | 90 | chr14 | 73543745 | ||||||
chr14:73543750 | CTTCT | C | 1 | a0001c0001t0001 | 27 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*97_*100delTCTT | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 3/3 | 97 | INFO_REALIGN_3_PRIME | chr14 | 73543750 | |||||
chr14:73543763 | C | T | 1 | a0001c0001t0001 | 27 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*108C>T | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 3/3 | 108 | chr14 | 73543763 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:73537891 | C | T | 1 | a0001c0001t0001g0001 | 60 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.457+13C>T | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 1/2 | chr14 | 73537891 | |||||||
chr14:73537935 | C | CTG | 1 | a0001c0001t0001g0001 | 6 | HG01081.hp1 HG02258.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.457+73_457+74dupGT | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr14 | 73537935 | ||||||
chr14:73537935 | C | CTGTGTG | 1 | a0001c0001t0001g0001 | 2 | HG02109.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.457+69_457+74dupGT others(4): Show |
ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr14 | 73537935 | ||||||
chr14:73538056 | G | T | 1 | a0001c0001t0001g0001 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.457+178G>T | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 1/2 | chr14 | 73538056 | |||||||
chr14:73538462 | A | G | 1 | a0001c0001t0001g0001 | 9 | HG02572.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.457+584A>G | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 1/2 | chr14 | 73538462 | |||||||
chr14:73538611 | C | CA | 1 | a0001c0001t0001g0001 | 18 | HG00741.hp1 HG01109.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.457+752dupA | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr14 | 73538611 | ||||||
chr14:73538611 | CA | C | 1 | a0001c0001t0001g0001 | 13 | HG01169.hp1 HG02165.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.457+752delA | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr14 | 73538611 | ||||||
chr14:73538632 | G | A | 1 | a0001c0001t0001g0001 | 10 | HG00639.hp2 HG00733.hp2 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.457+754G>A | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 1/2 | chr14 | 73538632 | |||||||
chr14:73538784 | A | G | 1 | a0001c0001t0001g0001 | 9 | HG02572.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.457+906A>G | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 1/2 | chr14 | 73538784 | |||||||
chr14:73538979 | A | T | 1 | a0001c0001t0001g0001 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.457+1101A>T | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 1/2 | chr14 | 73538979 | |||||||
chr14:73539069 | T | A | 1 | a0001c0001t0001g0001 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.457+1191T>A | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 1/2 | chr14 | 73539069 | |||||||
chr14:73539090 | G | T | 1 | a0001c0001t0001g0001 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.457+1212G>T | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 1/2 | chr14 | 73539090 | |||||||
chr14:73539224 | C | G | 1 | a0001c0001t0001g0001 | 26 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.457+1346C>G | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 1/2 | chr14 | 73539224 | |||||||
chr14:73539300 | C | T | 1 | a0001c0001t0001g0001 | 6 | HG01081.hp1 HG02109.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.457+1422C>T | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 1/2 | chr14 | 73539300 | |||||||
chr14:73539340 | C | A | 1 | a0001c0001t0001g0001 | 9 | HG02572.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.457+1462C>A | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 1/2 | chr14 | 73539340 | |||||||
chr14:73539437 | G | A | 1 | a0001c0001t0001g0001 | 7 | HG02572.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.457+1559G>A | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 1/2 | chr14 | 73539437 | |||||||
chr14:73539452 | G | A | 1 | a0001c0001t0001g0001 | 5 | HG01109.hp1 HG02055.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.457+1574G>A | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 1/2 | chr14 | 73539452 | |||||||
chr14:73539698 | C | G | 1 | a0001c0001t0001g0001 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.458-1795C>G | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 1/2 | chr14 | 73539698 | |||||||
chr14:73539699 | G | A | 1 | a0001c0001t0001g0001 | 5 | HG01109.hp1 HG02055.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.458-1794G>A | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 1/2 | chr14 | 73539699 | |||||||
chr14:73539726 | C | G | 1 | a0001c0001t0001g0001 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.458-1767C>G | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 1/2 | chr14 | 73539726 | |||||||
chr14:73539789 | C | T | 1 | a0001c0001t0001g0001 | 76 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.458-1704C>T | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 1/2 | chr14 | 73539789 | |||||||
chr14:73539807 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.458-1686C>T | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 1/2 | chr14 | 73539807 | |||||||
chr14:73539808 | G | A | 1 | a0001c0001t0001g0001 | 7 | HG02165.hp2 HG02602.hp2 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.458-1685G>A | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 1/2 | chr14 | 73539808 | |||||||
chr14:73540105 | A | G | 1 | a0001c0001t0001g0001 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.458-1388A>G | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 1/2 | chr14 | 73540105 | |||||||
chr14:73540179 | A | AATTTGTC others(18): Show |
1 | a0001c0001t0001g0001 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.458-1304_458-1303i others(27): Show |
ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr14 | 73540179 | ||||||
chr14:73540399 | G | C | 1 | a0001c0001t0001g0001 | 14 | HG02109.hp1 HG02258.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.458-1094G>C | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 1/2 | chr14 | 73540399 | |||||||
chr14:73540438 | AAAAAT | A | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.458-1050_458-1046d others(7): Show |
ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr14 | 73540438 | ||||||
chr14:73540500 | A | C | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.458-993A>C | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 1/2 | chr14 | 73540500 | |||||||
chr14:73540524 | T | A | 1 | a0001c0001t0001g0001 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.458-969T>A | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 1/2 | chr14 | 73540524 | |||||||
chr14:73540539 | G | A | 1 | a0001c0001t0001g0001 | 5 | HG01081.hp1 HG02109.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.458-954G>A | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 1/2 | chr14 | 73540539 | |||||||
chr14:73540548 | A | C | 1 | a0001c0001t0001g0001 | 15 | HG01081.hp1 HG02109.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.458-945A>C | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 1/2 | chr14 | 73540548 | |||||||
chr14:73540564 | ATTGT | A | 1 | a0001c0001t0001g0001 | 15 | HG01081.hp1 HG02109.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.458-926_458-923del others(4): Show |
ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr14 | 73540564 | ||||||
chr14:73540742 | C | CT | 1 | a0001c0001t0001g0001 | 15 | HG01109.hp1 HG01243.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.458-732dupT | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr14 | 73540742 | ||||||
chr14:73540742 | CT | C | 1 | a0001c0001t0001g0001 | 10 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(7): Show |
intron_variant | MODIFIER | c.458-732delT | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr14 | 73540742 | ||||||
chr14:73540742 | CTTTTT | C | 1 | a0001c0001t0001g0001 | 9 | HG02572.hp2 HG02717.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.458-736_458-732del others(5): Show |
ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr14 | 73540742 | ||||||
chr14:73540783 | G | A | 1 | a0001c0001t0001g0001 | 2 | HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.458-710G>A | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 1/2 | chr14 | 73540783 | |||||||
chr14:73540829 | A | C | 1 | a0001c0001t0001g0001 | 18 | HG01081.hp1 HG02109.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.458-664A>C | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 1/2 | chr14 | 73540829 | |||||||
chr14:73541032 | A | G | 1 | a0001c0001t0001g0001 | 21 | HG01496.hp1 HG01884.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.458-461A>G | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 1/2 | chr14 | 73541032 | |||||||
chr14:73541052 | T | C | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.458-441T>C | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 1/2 | chr14 | 73541052 | |||||||
chr14:73541054 | C | A | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.458-439C>A | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 1/2 | chr14 | 73541054 | |||||||
chr14:73541102 | AT | A | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.458-389delT | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr14 | 73541102 | ||||||
chr14:73541152 | A | G | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.458-341A>G | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 1/2 | chr14 | 73541152 | |||||||
chr14:73541157 | A | G | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.458-336A>G | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 1/2 | chr14 | 73541157 | |||||||
chr14:73541303 | T | C | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.458-190T>C | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 1/2 | chr14 | 73541303 | |||||||
chr14:73541306 | A | G | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.458-187A>G | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 1/2 | chr14 | 73541306 | |||||||
chr14:73541333 | A | G | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.458-160A>G | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 1/2 | chr14 | 73541333 | |||||||
chr14:73541345 | AAC | A | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.458-144_458-143del others(2): Show |
ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr14 | 73541345 | ||||||
chr14:73541346 | A | C | 1 | a0001c0001t0001g0001 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.458-147A>C | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 1/2 | chr14 | 73541346 | |||||||
chr14:73541367 | G | A | 1 | a0001c0001t0001g0001 | 26 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.458-126G>A | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 1/2 | chr14 | 73541367 | |||||||
chr14:73541426 | TGGTAAG | T | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.458-66_458-61delGG others(4): Show |
ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 1/2 | chr14 | 73541426 | |||||||
chr14:73541698 | G | T | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
splice_region_variant&intron_variant | LOW | c.660+3G>T | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73541698 | |||||||
chr14:73541708 | C | T | 1 | a0001c0001t0001g0001 | 11 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(8): Show |
intron_variant | MODIFIER | c.660+13C>T | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73541708 | |||||||
chr14:73541742 | T | C | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.660+47T>C | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73541742 | |||||||
chr14:73541798 | C | A | 1 | a0001c0001t0001g0001 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.660+103C>A | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73541798 | |||||||
chr14:73541839 | GTTTCTTT others(17): Show |
G | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.660+152_660+175del others(24): Show |
ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr14 | 73541839 | ||||||
chr14:73541919 | G | A | 1 | a0001c0001t0001g0001 | 12 | HG02109.hp1 HG02165.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.660+224G>A | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73541919 | |||||||
chr14:73541974 | G | C | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.660+279G>C | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73541974 | |||||||
chr14:73541981 | A | G | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.660+286A>G | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73541981 | |||||||
chr14:73542009 | A | C | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.660+314A>C | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73542009 | |||||||
chr14:73542015 | C | T | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.660+320C>T | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73542015 | |||||||
chr14:73542019 | A | C | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.660+324A>C | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73542019 | |||||||
chr14:73542035 | C | T | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.660+340C>T | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73542035 | |||||||
chr14:73542039 | A | G | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.660+344A>G | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73542039 | |||||||
chr14:73542043 | A | G | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.660+348A>G | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73542043 | |||||||
chr14:73542061 | T | G | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.660+366T>G | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73542061 | |||||||
chr14:73542079 | T | C | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.660+384T>C | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73542079 | |||||||
chr14:73542105 | C | T | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.660+410C>T | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73542105 | |||||||
chr14:73542109 | G | A | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.660+414G>A | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73542109 | |||||||
chr14:73542113 | C | A | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.660+418C>A | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73542113 | |||||||
chr14:73542118 | G | A | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.660+423G>A | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73542118 | |||||||
chr14:73542150 | T | C | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.660+455T>C | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73542150 | |||||||
chr14:73542159 | T | A | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.660+464T>A | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73542159 | |||||||
chr14:73542165 | AT | A | 1 | a0001c0001t0001g0001 | 27 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.660+482delT | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr14 | 73542165 | ||||||
chr14:73542177 | T | TA | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.660+483dupA | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr14 | 73542177 | ||||||
chr14:73542196 | C | T | 1 | a0001c0001t0001g0001 | 10 | HG01243.hp2 HG01891.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.660+501C>T | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73542196 | |||||||
chr14:73542249 | C | T | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.660+554C>T | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73542249 | |||||||
chr14:73542353 | T | G | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.660+658T>G | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73542353 | |||||||
chr14:73542357 | T | C | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.660+662T>C | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73542357 | |||||||
chr14:73542365 | G | T | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.660+670G>T | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73542365 | |||||||
chr14:73542367 | A | G | 1 | a0001c0001t0001g0001 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.660+672A>G | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73542367 | |||||||
chr14:73542390 | A | G | 1 | a0001c0001t0001g0001 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.661-660A>G | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73542390 | |||||||
chr14:73542390 | ATGTTTTT others(7): Show |
A | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.661-658_661-645del others(14): Show |
ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr14 | 73542390 | ||||||
chr14:73542400 | T | C | 1 | a0001c0001t0001g0001 | 3 | HG02818.hp1 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.661-650T>C | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73542400 | |||||||
chr14:73542403 | C | CT | 1 | a0001c0001t0001g0001 | 5 | HG02109.hp1 HG02258.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.661-628dupT | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr14 | 73542403 | ||||||
chr14:73542403 | CT | C | 1 | a0001c0001t0001g0001 | 9 | HG00099.hp2 HG02165.hp2 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.661-628delT | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr14 | 73542403 | ||||||
chr14:73542423 | A | G | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.661-627A>G | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73542423 | |||||||
chr14:73542427 | C | T | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.661-623C>T | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73542427 | |||||||
chr14:73542438 | C | T | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.661-612C>T | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73542438 | |||||||
chr14:73542439 | G | A | 1 | a0001c0001t0001g0001 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.661-611G>A | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73542439 | |||||||
chr14:73542445 | A | C | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.661-605A>C | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73542445 | |||||||
chr14:73542447 | G | C | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.661-603G>C | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73542447 | |||||||
chr14:73542461 | G | A | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.661-589G>A | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73542461 | |||||||
chr14:73542473 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.661-577C>T | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73542473 | |||||||
chr14:73542478 | T | C | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.661-572T>C | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73542478 | |||||||
chr14:73542486 | C | A | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.661-564C>A | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73542486 | |||||||
chr14:73542506 | G | T | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.661-544G>T | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73542506 | |||||||
chr14:73542507 | C | T | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.661-543C>T | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73542507 | |||||||
chr14:73542514 | C | T | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.661-536C>T | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73542514 | |||||||
chr14:73542522 | G | A | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.661-528G>A | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73542522 | |||||||
chr14:73542529 | T | C | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.661-521T>C | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73542529 | |||||||
chr14:73542530 | G | A | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.661-520G>A | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73542530 | |||||||
chr14:73542531 | A | C | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.661-519A>C | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73542531 | |||||||
chr14:73542539 | G | T | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.661-511G>T | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73542539 | |||||||
chr14:73542550 | G | A | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.661-500G>A | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73542550 | |||||||
chr14:73542552 | A | G | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.661-498A>G | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73542552 | |||||||
chr14:73542560 | T | A | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.661-490T>A | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73542560 | |||||||
chr14:73542566 | T | C | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.661-484T>C | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73542566 | |||||||
chr14:73542575 | T | C | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.661-475T>C | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73542575 | |||||||
chr14:73542575 | T | G | 1 | a0001c0001t0001g0001 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.661-475T>G | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73542575 | |||||||
chr14:73542593 | ACAG | A | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.661-456_661-454del others(3): Show |
ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73542593 | |||||||
chr14:73542597 | G | T | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.661-453G>T | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73542597 | |||||||
chr14:73542608 | A | G | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.661-442A>G | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73542608 | |||||||
chr14:73542617 | G | A | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.661-433G>A | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73542617 | |||||||
chr14:73542621 | G | A | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.661-429G>A | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73542621 | |||||||
chr14:73542626 | G | A | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.661-424G>A | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73542626 | |||||||
chr14:73542682 | A | T | 1 | a0001c0001t0001g0001 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.661-368A>T | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73542682 | |||||||
chr14:73542698 | G | T | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.661-352G>T | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73542698 | |||||||
chr14:73542715 | C | T | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.661-335C>T | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73542715 | |||||||
chr14:73542730 | C | T | 1 | a0001c0001t0001g0001 | 35 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.661-320C>T | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73542730 | |||||||
chr14:73542798 | TA | T | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.661-250delA | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr14 | 73542798 | ||||||
chr14:73542801 | T | C | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.661-249T>C | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73542801 | |||||||
chr14:73542827 | G | GAA | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.661-223_661-222ins others(2): Show |
ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73542827 | |||||||
chr14:73542861 | G | T | 1 | a0001c0001t0001g0001 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.661-189G>T | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73542861 | |||||||
chr14:73542913 | C | T | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.661-137C>T | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73542913 | |||||||
chr14:73542919 | C | T | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.661-131C>T | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73542919 | |||||||
chr14:73542938 | G | C | 1 | a0001c0001t0001g0001 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.661-112G>C | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73542938 | |||||||
chr14:73542946 | C | T | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.661-104C>T | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73542946 | |||||||
chr14:73542983 | G | A | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.661-67G>A | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73542983 | |||||||
chr14:73543012 | G | A | 1 | a0001c0001t0001g0001 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.661-38G>A | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73543012 | |||||||
chr14:73543014 | G | A | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.661-36G>A | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73543014 | |||||||
chr14:73543015 | C | T | 1 | a0001c0001t0001g0001 | 9 | HG02717.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.661-35C>T | ACOT1 | ENSG00000184227.8 | transcript | ENST00000311148.9 | protein_coding | 2/2 | chr14 | 73543015 |