Item | Value |
---|---|
geneid | 643847 |
ensemblid | ENSG00000229183.10 |
hgncid | 8886 |
symbol | PGA4 |
name | pepsinogen A4 |
refseq_nuc | NM_001079808.6 |
refseq_prot | NP_001073276.1 |
ensembl_nuc | ENST00000378149.9 |
ensembl_prot | ENSP00000367391.3 |
mane_status | MANE Select |
chr | chr11 |
start | 61222347 |
end | 61231694 |
strand | + |
ver | v1.2 |
region | chr11:61222347-61231694 |
region5000 | chr11:61217347-61236694 |
regionname0 | PGA4_chr11_61222347_61231694 |
regionname5000 | PGA4_chr11_61217347_61236694 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1164 | 302 | 84 | 53 | 120 | 8 | 37 | PGA4_chr11_61217347_61236694 | PGA4 | ATGAA others(1159): Show |
chr11 | 61217347 | 61236694 | ||
a0002c0000 | 0/0 | 0 | 2 | 0 | 1 | 0 | 0 | 1 | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 1384 | 302 | 84 | 53 | 120 | 8 | 37 | PGA4_chr11_61217347_61236694 | PGA4 | CTGCA others(1379): Show |
chr11 | 61217347 | 61236694 |
a0002c0000t0000 | 0/0 | 0 | 2 | 0 | 1 | 0 | 0 | 1 | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 302 | 84 | 53 | 120 | 8 | 37 | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
a0002c0000t0000g0000 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG01978 | hp1 | a0002 | c0000 | t0000 | g0000 | AMR | PEL | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG03492 | hp1 | a0002 | c0000 | t0000 | g0000 | SAS | PJL | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | PGA4_chr11_61217347_61236694 | PGA4 | chr11 | 61217347 | 61236694 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:61223058 | G | A | 1 | a0001 | 1 | HG03834.hp2 | missense_variant | MODERATE | c.172G>A | p.Glu58Lys | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/9 | 226/1384 | 172/1167 | 58/388 | chr11 | 61223058 | |||
chr11:61223086 | C | T | 1 | a0001 | 1 | HG00639.hp2 | missense_variant | MODERATE | c.200C>T | p.Pro67Leu | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/9 | 254/1384 | 200/1167 | 67/388 | chr11 | 61223086 | |||
chr11:61223849 | GGGCACAA others(12838): Show |
G | 1 | a0001 | 1 | HG02630.hp1 | exon_loss_variant | HIGH | c.219+745_*5163del | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 3/9 | chr11 | 61223849 | |||||||
chr11:61225360 | G | A | 1 | a0001 | 9 | NA18941.hp2 NA18961.hp1 NA18973.hp2 others(6): Show |
missense_variant | MODERATE | c.241G>A | p.Gly81Ser | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 3/9 | 295/1384 | 241/1167 | 81/388 | chr11 | 61225360 | |||
chr11:61225393 | G | C | 1 | a0001 | 6 | HG01071.hp1 HG01891.hp1 HG03834.hp2 others(3): Show |
missense_variant | MODERATE | c.274G>C | p.Val92Leu | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 3/9 | 328/1384 | 274/1167 | 92/388 | chr11 | 61225393 | |||
chr11:61226513 | A | ATGAGTCT others(18727): Show |
1 | a0001 | 1 | HG01255.hp2 | frameshift_variant&stop_gained | HIGH | c.741_742insATCGAGGG others(18726): Show |
p.Val248fs | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 6/9 | 796/1384 | 742/1167 | 248/388 | INFO_REALIGN_3_PRIME | chr11 | 61226513 | ||
chr11:61227153 | G | A | 1 | a0001 | 1 | NA18981.hp2 | missense_variant | MODERATE | c.490G>A | p.Gly164Ser | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/9 | 544/1384 | 490/1167 | 164/388 | chr11 | 61227153 | |||
chr11:61227162 | G | A | 1 | a0001 | 1 | HG01361.hp1 | missense_variant | MODERATE | c.499G>A | p.Glu167Lys | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/9 | 553/1384 | 499/1167 | 167/388 | chr11 | 61227162 | |||
chr11:61228678 | C | A | 1 | a0001 | 3 | NA18966.hp1 NA18986.hp1 NA21309.hp2 |
missense_variant | MODERATE | c.664C>A | p.Gln222Lys | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 6/9 | 718/1384 | 664/1167 | 222/388 | chr11 | 61228678 | |||
chr11:61229938 | G | A | 1 | a0001 | 2 | NA18966.hp1 NA18986.hp1 |
missense_variant | MODERATE | c.793G>A | p.Ala265Thr | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 7/9 | 847/1384 | 793/1167 | 265/388 | chr11 | 61229938 | |||
chr11:61229947 | T | G | 1 | a0001 | 1 | HG03516.hp2 | missense_variant | MODERATE | c.802T>G | p.Cys268Gly | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 7/9 | 856/1384 | 802/1167 | 268/388 | chr11 | 61229947 | |||
chr11:61230850 | CTCAACAA others(5837): Show |
C | 1 | a0001 | 1 | NA21309.hp1 | exon_loss_variant&splice_acceptor_variant&3_prime_UTR_truncation&exon_loss_variant&splice_region_variant&intron_variant | HIGH | c.1018-531_*5163del | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 9/9 | chr11 | 61230850 | |||||||
chr11:61231421 | C | G | 1 | a0001 | 4 | HG01884.hp2 HG02258.hp2 HG02486.hp2 others(1): Show |
missense_variant | MODERATE | c.1057C>G | p.Leu353Val | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 9/9 | 1111/1384 | 1057/1167 | 353/388 | chr11 | 61231421 | |||
chr11:61231506 | A | T | 1 | a0001 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.1142A>T | p.Gln381Leu | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 9/9 | 1196/1384 | 1142/1167 | 381/388 | chr11 | 61231506 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:61222433 | G | A | 1 | a0001c0001 | 9 | HG01168.hp2 HG02109.hp1 HG02723.hp2 others(6): Show |
synonymous_variant | LOW | c.33G>A | p.Ala11Ala | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 1/9 | 87/1384 | 33/1167 | 11/388 | chr11 | 61222433 | |||
chr11:61223087 | C | A | 1 | a0001c0001 | 1 | HG02630.hp1 | synonymous_variant | LOW | c.201C>A | p.Pro67Pro | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/9 | 255/1384 | 201/1167 | 67/388 | chr11 | 61223087 | |||
chr11:61225389 | C | T | 1 | a0001c0001 | 10 | HG01891.hp1 HG02145.hp2 HG02559.hp2 others(7): Show |
synonymous_variant | LOW | c.270C>T | p.Thr90Thr | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 3/9 | 324/1384 | 270/1167 | 90/388 | chr11 | 61225389 | |||
chr11:61227212 | G | A | 1 | a0001c0001 | 1 | NA18950.hp1 | synonymous_variant | LOW | c.549G>A | p.Leu183Leu | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/9 | 603/1384 | 549/1167 | 183/388 | chr11 | 61227212 | |||
chr11:61227216 | C | T | 1 | a0001c0001 | 3 | HG02015.hp2 NA18966.hp1 NA18986.hp1 |
synonymous_variant | LOW | c.553C>T | p.Leu185Leu | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/9 | 607/1384 | 553/1167 | 185/388 | chr11 | 61227216 | |||
chr11:61229949 | C | T | 1 | a0001c0001 | 2 | NA18966.hp1 NA18986.hp1 |
synonymous_variant | LOW | c.804C>T | p.Cys268Cys | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 7/9 | 858/1384 | 804/1167 | 268/388 | chr11 | 61229949 | |||
chr11:61231384 | C | T | 1 | a0001c0001 | 1 | HG03209.hp2 | splice_region_variant&synonymous_variant | LOW | c.1020C>T | p.Ser340Ser | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 9/9 | 1074/1384 | 1020/1167 | 340/388 | chr11 | 61231384 | |||
chr11:61231522 | C | T | 1 | a0001c0001 | 1 | HG02818.hp1 | synonymous_variant | LOW | c.1158C>T | p.Pro386Pro | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 9/9 | 1212/1384 | 1158/1167 | 386/388 | chr11 | 61231522 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:61222362 | A | G | 1 | a0001c0001t0001 | 267 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(264): Show |
5_prime_UTR_variant | MODIFIER | c.-39A>G | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 1/9 | 39 | chr11 | 61222362 | ||||||
chr11:61222391 | G | A | 1 | a0001c0001t0001 | 5 | HG02615.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-10G>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 1/9 | 10 | chr11 | 61222391 | ||||||
chr11:61222397 | A | T | 1 | a0001c0001t0001 | 2 | NA18969.hp2 NA18977.hp2 |
5_prime_UTR_variant | MODIFIER | c.-4A>T | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 1/9 | 4 | chr11 | 61222397 | ||||||
chr11:61231568 | G | A | 1 | a0001c0001t0001 | 6 | HG00621.hp2 HG00673.hp1 HG02132.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*37G>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 9/9 | 37 | chr11 | 61231568 | ||||||
chr11:61231583 | C | T | 1 | a0001c0001t0001 | 1 | NA18955.hp1 | 3_prime_UTR_variant | MODIFIER | c.*52C>T | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 9/9 | 52 | chr11 | 61231583 | ||||||
chr11:61231626 | G | C | 1 | a0001c0001t0001 | 1 | NA19000.hp2 | 3_prime_UTR_variant | MODIFIER | c.*95G>C | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 9/9 | 95 | chr11 | 61231626 | ||||||
chr11:61231642 | G | C | 1 | a0001c0001t0001 | 5 | HG02615.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*111G>C | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 9/9 | 111 | chr11 | 61231642 | ||||||
chr11:61231644 | C | T | 1 | a0001c0001t0001 | 2 | HG02015.hp1 NA18960.hp2 |
3_prime_UTR_variant | MODIFIER | c.*113C>T | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 9/9 | 113 | chr11 | 61231644 | ||||||
chr11:61231688 | A | G | 1 | a0001c0001t0001 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*157A>G | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 9/9 | 157 | chr11 | 61231688 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:61222516 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.56+60C>T | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 1/8 | chr11 | 61222516 | |||||||
chr11:61222540 | T | C | 1 | a0001c0001t0001g0001 | 4 | HG02109.hp2 HG02148.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.56+84T>C | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 1/8 | chr11 | 61222540 | |||||||
chr11:61222543 | T | C | 1 | a0001c0001t0001g0001 | 4 | HG02109.hp2 HG02148.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.56+87T>C | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 1/8 | chr11 | 61222543 | |||||||
chr11:61222550 | C | A | 1 | a0001c0001t0001g0001 | 6 | HG02109.hp2 HG02148.hp2 HG03834.hp2 others(3): Show |
intron_variant | MODIFIER | c.56+94C>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 1/8 | chr11 | 61222550 | |||||||
chr11:61222576 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.56+120C>T | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 1/8 | chr11 | 61222576 | |||||||
chr11:61222577 | G | A | 1 | a0001c0001t0001g0001 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.56+121G>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 1/8 | chr11 | 61222577 | |||||||
chr11:61223116 | G | A | 1 | a0001c0001t0001g0001 | 4 | HG00280.hp1 HG01346.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.219+11G>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | chr11 | 61223116 | |||||||
chr11:61223338 | A | G | 1 | a0001c0001t0001g0001 | 6 | HG02622.hp2 HG03139.hp2 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.219+233A>G | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | chr11 | 61223338 | |||||||
chr11:61223429 | C | G | 1 | a0001c0001t0001g0001 | 255 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.219+324C>G | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | chr11 | 61223429 | |||||||
chr11:61223438 | A | G | 1 | a0001c0001t0001g0001 | 267 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.219+333A>G | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | chr11 | 61223438 | |||||||
chr11:61223533 | A | G | 1 | a0001c0001t0001g0001 | 10 | HG01109.hp2 HG02109.hp2 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.219+428A>G | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | chr11 | 61223533 | |||||||
chr11:61223535 | G | C | 1 | a0001c0001t0001g0001 | 10 | HG01109.hp2 HG02109.hp2 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.219+430G>C | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | chr11 | 61223535 | |||||||
chr11:61223547 | G | C | 1 | a0001c0001t0001g0001 | 10 | HG01109.hp2 HG02109.hp2 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.219+442G>C | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | chr11 | 61223547 | |||||||
chr11:61223559 | A | G | 1 | a0001c0001t0001g0001 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.219+454A>G | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | chr11 | 61223559 | |||||||
chr11:61223666 | C | T | 1 | a0001c0001t0001g0001 | 97 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.219+561C>T | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | chr11 | 61223666 | |||||||
chr11:61223672 | A | G | 1 | a0001c0001t0001g0001 | 165 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(162): Show |
intron_variant | MODIFIER | c.219+567A>G | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | chr11 | 61223672 | |||||||
chr11:61223674 | T | C | 1 | a0001c0001t0001g0001 | 165 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(162): Show |
intron_variant | MODIFIER | c.219+569T>C | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | chr11 | 61223674 | |||||||
chr11:61223733 | G | T | 1 | a0001c0001t0001g0001 | 160 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(157): Show |
intron_variant | MODIFIER | c.219+628G>T | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | chr11 | 61223733 | |||||||
chr11:61223734 | A | G | 1 | a0001c0001t0001g0001 | 160 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(157): Show |
intron_variant | MODIFIER | c.219+629A>G | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | chr11 | 61223734 | |||||||
chr11:61223778 | G | A | 1 | a0001c0001t0001g0001 | 161 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(158): Show |
intron_variant | MODIFIER | c.219+673G>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | chr11 | 61223778 | |||||||
chr11:61223789 | C | T | 1 | a0001c0001t0001g0001 | 161 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(158): Show |
intron_variant | MODIFIER | c.219+684C>T | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | chr11 | 61223789 | |||||||
chr11:61223842 | T | TGGCACAG | 1 | a0001c0001t0001g0001 | 160 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(157): Show |
intron_variant | MODIFIER | c.219+744_219+750dup others(7): Show |
PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 61223842 | ||||||
chr11:61223867 | C | G | 1 | a0001c0001t0001g0001 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.219+762C>G | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | chr11 | 61223867 | |||||||
chr11:61223869 | T | C | 1 | a0001c0001t0001g0001 | 8 | HG02109.hp2 HG02148.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.219+764T>C | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | chr11 | 61223869 | |||||||
chr11:61224042 | C | A | 1 | a0001c0001t0001g0001 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.219+937C>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | chr11 | 61224042 | |||||||
chr11:61224230 | A | G | 1 | a0001c0001t0001g0001 | 161 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(158): Show |
intron_variant | MODIFIER | c.220-1109A>G | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | chr11 | 61224230 | |||||||
chr11:61224253 | T | G | 1 | a0001c0001t0001g0001 | 161 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(158): Show |
intron_variant | MODIFIER | c.220-1086T>G | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | chr11 | 61224253 | |||||||
chr11:61224262 | G | A | 1 | a0001c0001t0001g0001 | 161 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(158): Show |
intron_variant | MODIFIER | c.220-1077G>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | chr11 | 61224262 | |||||||
chr11:61224270 | A | G | 1 | a0001c0001t0001g0001 | 161 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(158): Show |
intron_variant | MODIFIER | c.220-1069A>G | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | chr11 | 61224270 | |||||||
chr11:61224274 | G | A | 1 | a0001c0001t0001g0001 | 161 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(158): Show |
intron_variant | MODIFIER | c.220-1065G>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | chr11 | 61224274 | |||||||
chr11:61224277 | T | A | 1 | a0001c0001t0001g0001 | 161 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(158): Show |
intron_variant | MODIFIER | c.220-1062T>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | chr11 | 61224277 | |||||||
chr11:61224280 | G | A | 1 | a0001c0001t0001g0001 | 161 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(158): Show |
intron_variant | MODIFIER | c.220-1059G>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | chr11 | 61224280 | |||||||
chr11:61224294 | G | T | 1 | a0001c0001t0001g0001 | 161 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(158): Show |
intron_variant | MODIFIER | c.220-1045G>T | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | chr11 | 61224294 | |||||||
chr11:61224298 | G | C | 1 | a0001c0001t0001g0001 | 161 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(158): Show |
intron_variant | MODIFIER | c.220-1041G>C | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | chr11 | 61224298 | |||||||
chr11:61224299 | C | T | 1 | a0001c0001t0001g0001 | 161 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(158): Show |
intron_variant | MODIFIER | c.220-1040C>T | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | chr11 | 61224299 | |||||||
chr11:61224311 | G | A | 1 | a0001c0001t0001g0001 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.220-1028G>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | chr11 | 61224311 | |||||||
chr11:61224350 | G | A | 1 | a0001c0001t0001g0001 | 3 | HG02809.hp2 NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.220-989G>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | chr11 | 61224350 | |||||||
chr11:61224354 | G | T | 1 | a0001c0001t0001g0001 | 3 | HG02809.hp2 NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.220-985G>T | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | chr11 | 61224354 | |||||||
chr11:61224415 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.220-924C>T | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | chr11 | 61224415 | |||||||
chr11:61224416 | A | G | 1 | a0001c0001t0001g0001 | 174 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(171): Show |
intron_variant | MODIFIER | c.220-923A>G | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | chr11 | 61224416 | |||||||
chr11:61224441 | AT | A | 1 | a0001c0001t0001g0001 | 172 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(169): Show |
intron_variant | MODIFIER | c.220-894delT | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 61224441 | ||||||
chr11:61224592 | G | T | 1 | a0001c0001t0001g0001 | 26 | HG00642.hp1 HG00738.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.220-747G>T | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | chr11 | 61224592 | |||||||
chr11:61224625 | G | A | 1 | a0001c0001t0001g0001 | 178 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(175): Show |
intron_variant | MODIFIER | c.220-714G>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | chr11 | 61224625 | |||||||
chr11:61224632 | G | T | 1 | a0001c0001t0001g0001 | 178 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(175): Show |
intron_variant | MODIFIER | c.220-707G>T | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | chr11 | 61224632 | |||||||
chr11:61224635 | C | T | 1 | a0001c0001t0001g0001 | 178 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(175): Show |
intron_variant | MODIFIER | c.220-704C>T | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | chr11 | 61224635 | |||||||
chr11:61224642 | ATGG | A | 1 | a0001c0001t0001g0001 | 178 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(175): Show |
intron_variant | MODIFIER | c.220-694_220-692del others(3): Show |
PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 61224642 | ||||||
chr11:61224668 | A | C | 1 | a0001c0001t0001g0001 | 152 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(149): Show |
intron_variant | MODIFIER | c.220-671A>C | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | chr11 | 61224668 | |||||||
chr11:61224679 | T | A | 1 | a0001c0001t0001g0001 | 181 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(178): Show |
intron_variant | MODIFIER | c.220-660T>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | chr11 | 61224679 | |||||||
chr11:61224681 | C | A | 1 | a0001c0001t0001g0001 | 181 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(178): Show |
intron_variant | MODIFIER | c.220-658C>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | chr11 | 61224681 | |||||||
chr11:61224687 | A | G | 1 | a0001c0001t0001g0001 | 46 | HG00642.hp1 HG00738.hp2 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.220-652A>G | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | chr11 | 61224687 | |||||||
chr11:61224700 | C | G | 1 | a0001c0001t0001g0001 | 41 | HG00642.hp1 HG00738.hp2 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.220-639C>G | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | chr11 | 61224700 | |||||||
chr11:61224725 | T | C | 1 | a0001c0001t0001g0001 | 181 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(178): Show |
intron_variant | MODIFIER | c.220-614T>C | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | chr11 | 61224725 | |||||||
chr11:61224733 | G | A | 1 | a0001c0001t0001g0001 | 181 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(178): Show |
intron_variant | MODIFIER | c.220-606G>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | chr11 | 61224733 | |||||||
chr11:61224761 | G | A | 1 | a0001c0001t0001g0001 | 161 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(158): Show |
intron_variant | MODIFIER | c.220-578G>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | chr11 | 61224761 | |||||||
chr11:61224821 | T | C | 1 | a0001c0001t0001g0001 | 153 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(150): Show |
intron_variant | MODIFIER | c.220-518T>C | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | chr11 | 61224821 | |||||||
chr11:61224823 | T | TTAAAAA | 1 | a0001c0001t0001g0001 | 5 | HG01243.hp2 HG03041.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.220-516_220-515ins others(6): Show |
PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | chr11 | 61224823 | |||||||
chr11:61224823 | T | TTAAAAAA | 1 | a0001c0001t0001g0001 | 148 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(145): Show |
intron_variant | MODIFIER | c.220-516_220-515ins others(7): Show |
PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | chr11 | 61224823 | |||||||
chr11:61224824 | C | A | 1 | a0001c0001t0001g0001 | 153 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(150): Show |
intron_variant | MODIFIER | c.220-515C>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | chr11 | 61224824 | |||||||
chr11:61224824 | C | CAAAAAAA others(18727): Show |
1 | a0001c0001t0001g0001 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.220-496_220-495ins others(18734): Show |
PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 61224824 | ||||||
chr11:61224824 | C | CAAAAAAA others(18727): Show |
1 | a0001c0001t0001g0001 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.220-496_220-495ins others(18734): Show |
PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 61224824 | ||||||
chr11:61224824 | C | CAAAAAAA others(18727): Show |
1 | a0001c0001t0001g0001 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.220-496_220-495ins others(18734): Show |
PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 61224824 | ||||||
chr11:61224824 | C | CAAAAAAA others(75126): Show |
1 | a0001c0001t0001g0001 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.220-496_220-495ins others(75133): Show |
PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 61224824 | ||||||
chr11:61224824 | C | CAAAAAAA others(18727): Show |
1 | a0001c0001t0001g0001 | 2 | HG00408.hp1 HG00642.hp2 |
intron_variant | MODIFIER | c.220-496_220-495ins others(18734): Show |
PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 61224824 | ||||||
chr11:61224824 | C | CAAAAAAA others(18727): Show |
1 | a0001c0001t0001g0001 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.220-496_220-495ins others(18734): Show |
PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 61224824 | ||||||
chr11:61224844 | A | T | 1 | a0001c0001t0001g0001 | 240 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.220-495A>T | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | chr11 | 61224844 | |||||||
chr11:61224848 | T | G | 1 | a0001c0001t0001g0001 | 240 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.220-491T>G | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | chr11 | 61224848 | |||||||
chr11:61224862 | T | C | 1 | a0001c0001t0001g0001 | 240 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.220-477T>C | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | chr11 | 61224862 | |||||||
chr11:61224863 | G | A | 1 | a0001c0001t0001g0001 | 240 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.220-476G>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | chr11 | 61224863 | |||||||
chr11:61224864 | C | A | 1 | a0001c0001t0001g0001 | 240 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.220-475C>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | chr11 | 61224864 | |||||||
chr11:61224873 | A | G | 1 | a0001c0001t0001g0001 | 241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.220-466A>G | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | chr11 | 61224873 | |||||||
chr11:61224886 | T | C | 1 | a0001c0001t0001g0001 | 257 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.220-453T>C | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | chr11 | 61224886 | |||||||
chr11:61224984 | C | T | 1 | a0001c0001t0001g0001 | 5 | HG01071.hp1 HG02896.hp1 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.220-355C>T | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | chr11 | 61224984 | |||||||
chr11:61225063 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.220-276C>T | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | chr11 | 61225063 | |||||||
chr11:61225164 | G | A | 1 | a0001c0001t0001g0001 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.220-175G>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | chr11 | 61225164 | |||||||
chr11:61225309 | C | A | 1 | a0001c0001t0001g0001 | 20 | HG00408.hp2 HG00544.hp2 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.220-30C>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 2/8 | chr11 | 61225309 | |||||||
chr11:61225510 | T | TG | 1 | a0001c0001t0001g0001 | 6 | HG00280.hp1 HG01346.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.337+58dupG | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 61225510 | ||||||
chr11:61225660 | G | A | 1 | a0001c0001t0001g0001 | 2 | HG02145.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.337+204G>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 3/8 | chr11 | 61225660 | |||||||
chr11:61225689 | G | A | 1 | a0001c0001t0001g0001 | 4 | HG01884.hp2 HG02257.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.337+233G>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 3/8 | chr11 | 61225689 | |||||||
chr11:61225719 | G | GAGAGGAA others(18727): Show |
1 | a0001c0001t0001g0001 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.338-115_338-114ins others(18734): Show |
PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 61225719 | ||||||
chr11:61225853 | T | TA | 1 | a0001c0001t0001g0001 | 11 | HG01071.hp1 HG01256.hp1 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.337+410dupA | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 61225853 | ||||||
chr11:61225853 | TA | T | 1 | a0001c0001t0001g0001 | 13 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.337+410delA | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 61225853 | ||||||
chr11:61225854 | A | T | 1 | a0001c0001t0001g0001 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.337+398A>T | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 3/8 | chr11 | 61225854 | |||||||
chr11:61225981 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.338-345C>T | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 3/8 | chr11 | 61225981 | |||||||
chr11:61226168 | G | A | 1 | a0001c0001t0001g0001 | 5 | HG01071.hp1 HG02896.hp1 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.338-158G>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 3/8 | chr11 | 61226168 | |||||||
chr11:61226203 | C | G | 1 | a0001c0001t0001g0001 | 6 | HG01071.hp1 HG02896.hp1 HG03834.hp2 others(3): Show |
intron_variant | MODIFIER | c.338-123C>G | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 3/8 | chr11 | 61226203 | |||||||
chr11:61226212 | G | A | 1 | a0001c0001t0001g0001 | 245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.338-114G>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 3/8 | chr11 | 61226212 | |||||||
chr11:61226252 | C | A | 1 | a0001c0001t0001g0001 | 5 | HG01071.hp1 HG02027.hp1 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.338-74C>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 3/8 | chr11 | 61226252 | |||||||
chr11:61226611 | G | C | 1 | a0001c0001t0001g0001 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.456+167G>C | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 4/8 | chr11 | 61226611 | |||||||
chr11:61226698 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.456+254C>T | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 4/8 | chr11 | 61226698 | |||||||
chr11:61226879 | T | C | 1 | a0001c0001t0001g0001 | 6 | HG03139.hp2 HG06807.hp2 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.457-241T>C | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 4/8 | chr11 | 61226879 | |||||||
chr11:61226954 | G | A | 1 | a0001c0001t0001g0001 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.457-166G>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 4/8 | chr11 | 61226954 | |||||||
chr11:61227456 | G | T | 1 | a0001c0001t0001g0001 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.656+137G>T | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61227456 | |||||||
chr11:61227534 | C | G | 1 | a0001c0001t0001g0001 | 3 | HG02572.hp1 HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.656+215C>G | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61227534 | |||||||
chr11:61227585 | C | G | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.656+266C>G | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61227585 | |||||||
chr11:61227591 | C | T | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.656+272C>T | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61227591 | |||||||
chr11:61227595 | A | G | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.656+276A>G | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61227595 | |||||||
chr11:61227608 | T | A | 1 | a0001c0001t0001g0001 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.656+289T>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61227608 | |||||||
chr11:61227608 | T | C | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.656+289T>C | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61227608 | |||||||
chr11:61227618 | G | C | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.656+299G>C | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61227618 | |||||||
chr11:61227626 | G | A | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.656+307G>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61227626 | |||||||
chr11:61227645 | C | G | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.656+326C>G | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61227645 | |||||||
chr11:61227648 | G | A | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.656+329G>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61227648 | |||||||
chr11:61227655 | T | C | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.656+336T>C | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61227655 | |||||||
chr11:61227656 | G | A | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.656+337G>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61227656 | |||||||
chr11:61227662 | G | T | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.656+343G>T | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61227662 | |||||||
chr11:61227685 | T | G | 1 | a0001c0001t0001g0001 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.656+366T>G | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61227685 | |||||||
chr11:61227692 | G | T | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.656+373G>T | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61227692 | |||||||
chr11:61227701 | A | G | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.656+382A>G | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61227701 | |||||||
chr11:61227703 | C | G | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.656+384C>G | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61227703 | |||||||
chr11:61227724 | A | G | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.656+405A>G | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61227724 | |||||||
chr11:61227732 | C | CCAGCCTG others(889): Show |
1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.656+413_656+414ins others(896): Show |
PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61227732 | |||||||
chr11:61227733 | T | G | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.656+414T>G | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61227733 | |||||||
chr11:61227742 | T | C | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.656+423T>C | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61227742 | |||||||
chr11:61227743 | G | C | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.656+424G>C | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61227743 | |||||||
chr11:61227744 | G | C | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.656+425G>C | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61227744 | |||||||
chr11:61227747 | A | T | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.656+428A>T | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61227747 | |||||||
chr11:61227764 | G | C | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.656+445G>C | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61227764 | |||||||
chr11:61227768 | A | T | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.656+449A>T | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61227768 | |||||||
chr11:61227773 | A | ACCTCGTG others(6): Show |
1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.656+455_656+456ins others(13): Show |
PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr11 | 61227773 | ||||||
chr11:61227780 | C | T | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.656+461C>T | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61227780 | |||||||
chr11:61227781 | A | G | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.656+462A>G | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61227781 | |||||||
chr11:61227787 | C | A | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.656+468C>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61227787 | |||||||
chr11:61227809 | G | A | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.656+490G>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61227809 | |||||||
chr11:61227819 | G | A | 1 | a0001c0001t0001g0001 | 8 | HG02622.hp2 HG03139.hp2 HG06807.hp2 others(5): Show |
intron_variant | MODIFIER | c.656+500G>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61227819 | |||||||
chr11:61227820 | T | C | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.656+501T>C | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61227820 | |||||||
chr11:61227824 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.656+505C>T | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61227824 | |||||||
chr11:61227825 | G | A | 1 | a0001c0001t0001g0001 | 3 | NA18522.hp2 NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.656+506G>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61227825 | |||||||
chr11:61227830 | T | C | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.656+511T>C | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61227830 | |||||||
chr11:61227835 | G | A | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.656+516G>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61227835 | |||||||
chr11:61227837 | C | T | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.656+518C>T | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61227837 | |||||||
chr11:61227847 | C | A | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.656+528C>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61227847 | |||||||
chr11:61227852 | T | C | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.656+533T>C | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61227852 | |||||||
chr11:61227863 | G | C | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.656+544G>C | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61227863 | |||||||
chr11:61227869 | T | A | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.656+550T>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61227869 | |||||||
chr11:61227891 | A | G | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.656+572A>G | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61227891 | |||||||
chr11:61227900 | C | A | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.656+581C>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61227900 | |||||||
chr11:61227937 | C | A | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.656+618C>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61227937 | |||||||
chr11:61228046 | C | T | 1 | a0001c0001t0001g0001 | 3 | NA18522.hp2 NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.657-625C>T | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61228046 | |||||||
chr11:61228086 | A | G | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.657-585A>G | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61228086 | |||||||
chr11:61228109 | G | T | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.657-562G>T | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61228109 | |||||||
chr11:61228110 | A | T | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.657-561A>T | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61228110 | |||||||
chr11:61228111 | G | C | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.657-560G>C | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61228111 | |||||||
chr11:61228122 | G | A | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.657-549G>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61228122 | |||||||
chr11:61228198 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.657-473C>T | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61228198 | |||||||
chr11:61228238 | T | G | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.657-433T>G | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61228238 | |||||||
chr11:61228361 | C | G | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.657-310C>G | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61228361 | |||||||
chr11:61228362 | A | G | 1 | a0001c0001t0001g0001 | 3 | HG02258.hp1 NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.657-309A>G | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61228362 | |||||||
chr11:61228374 | G | C | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.657-297G>C | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61228374 | |||||||
chr11:61228376 | C | T | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.657-295C>T | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61228376 | |||||||
chr11:61228381 | C | A | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.657-290C>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61228381 | |||||||
chr11:61228385 | A | T | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.657-286A>T | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61228385 | |||||||
chr11:61228397 | T | C | 1 | a0001c0001t0001g0001 | 9 | HG00738.hp2 HG01071.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.657-274T>C | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61228397 | |||||||
chr11:61228431 | A | G | 1 | a0001c0001t0001g0001 | 24 | HG00642.hp1 HG00738.hp2 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.657-240A>G | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61228431 | |||||||
chr11:61228491 | T | C | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.657-180T>C | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61228491 | |||||||
chr11:61228499 | A | G | 1 | a0001c0001t0001g0001 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.657-172A>G | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61228499 | |||||||
chr11:61228501 | A | G | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.657-170A>G | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61228501 | |||||||
chr11:61228515 | A | G | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.657-156A>G | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61228515 | |||||||
chr11:61228519 | A | C | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.657-152A>C | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61228519 | |||||||
chr11:61228522 | G | A | 1 | a0001c0001t0001g0001 | 9 | HG02145.hp2 HG02257.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.657-149G>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61228522 | |||||||
chr11:61228548 | A | G | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.657-123A>G | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61228548 | |||||||
chr11:61228557 | G | A | 1 | a0001c0001t0001g0001 | 9 | HG02559.hp2 HG02615.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.657-114G>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61228557 | |||||||
chr11:61228557 | G | C | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.657-114G>C | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61228557 | |||||||
chr11:61228570 | A | G | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.657-101A>G | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61228570 | |||||||
chr11:61228587 | G | C | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.657-84G>C | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61228587 | |||||||
chr11:61228591 | A | C | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.657-80A>C | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61228591 | |||||||
chr11:61228594 | C | T | 1 | a0001c0001t0001g0001 | 3 | HG03834.hp2 NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.657-77C>T | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 5/8 | chr11 | 61228594 | |||||||
chr11:61228794 | C | T | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
splice_region_variant&intron_variant | LOW | c.773+7C>T | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 6/8 | chr11 | 61228794 | |||||||
chr11:61228798 | C | A | 1 | a0001c0001t0001g0001 | 4 | HG02630.hp2 HG02809.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.773+11C>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 6/8 | chr11 | 61228798 | |||||||
chr11:61228882 | G | A | 1 | a0001c0001t0001g0001 | 3 | HG02559.hp2 HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.773+95G>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 6/8 | chr11 | 61228882 | |||||||
chr11:61228987 | A | G | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.773+200A>G | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 6/8 | chr11 | 61228987 | |||||||
chr11:61228994 | C | T | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.773+207C>T | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 6/8 | chr11 | 61228994 | |||||||
chr11:61228995 | A | G | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.773+208A>G | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 6/8 | chr11 | 61228995 | |||||||
chr11:61229016 | A | G | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.773+229A>G | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 6/8 | chr11 | 61229016 | |||||||
chr11:61229100 | G | C | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.773+313G>C | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 6/8 | chr11 | 61229100 | |||||||
chr11:61229114 | C | G | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.773+327C>G | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 6/8 | chr11 | 61229114 | |||||||
chr11:61229116 | G | T | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.773+329G>T | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 6/8 | chr11 | 61229116 | |||||||
chr11:61229123 | C | A | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.773+336C>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 6/8 | chr11 | 61229123 | |||||||
chr11:61229164 | G | A | 1 | a0001c0001t0001g0001 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.773+377G>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 6/8 | chr11 | 61229164 | |||||||
chr11:61229203 | G | A | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.773+416G>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 6/8 | chr11 | 61229203 | |||||||
chr11:61229228 | A | G | 1 | a0001c0001t0001g0001 | 4 | HG00621.hp2 HG00673.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.773+441A>G | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 6/8 | chr11 | 61229228 | |||||||
chr11:61229239 | G | GGTCTCCC others(18727): Show |
1 | a0001c0001t0001g0001 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1017+100_1017+101i others(18736): Show |
PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr11 | 61229239 | ||||||
chr11:61229239 | G | T | 1 | a0001c0001t0001g0001 | 5 | HG00621.hp2 HG00673.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.773+452G>T | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 6/8 | chr11 | 61229239 | |||||||
chr11:61229248 | T | G | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.773+461T>G | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 6/8 | chr11 | 61229248 | |||||||
chr11:61229262 | C | T | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.773+475C>T | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 6/8 | chr11 | 61229262 | |||||||
chr11:61229268 | C | G | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.773+481C>G | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 6/8 | chr11 | 61229268 | |||||||
chr11:61229293 | G | A | 1 | a0001c0001t0001g0001 | 3 | HG02559.hp2 HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.773+506G>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 6/8 | chr11 | 61229293 | |||||||
chr11:61229402 | T | C | 1 | a0001c0001t0001g0001 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.774-517T>C | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 6/8 | chr11 | 61229402 | |||||||
chr11:61229425 | T | G | 1 | a0001c0001t0001g0001 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.774-494T>G | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 6/8 | chr11 | 61229425 | |||||||
chr11:61229530 | A | T | 1 | a0001c0001t0001g0001 | 3 | HG03239.hp1 NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.774-389A>T | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 6/8 | chr11 | 61229530 | |||||||
chr11:61229554 | C | G | 1 | a0001c0001t0001g0001 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.774-365C>G | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 6/8 | chr11 | 61229554 | |||||||
chr11:61229578 | A | G | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.774-341A>G | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 6/8 | chr11 | 61229578 | |||||||
chr11:61229657 | A | C | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.774-262A>C | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 6/8 | chr11 | 61229657 | |||||||
chr11:61229663 | C | G | 1 | a0001c0001t0001g0001 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.774-256C>G | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 6/8 | chr11 | 61229663 | |||||||
chr11:61229700 | A | G | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.774-219A>G | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 6/8 | chr11 | 61229700 | |||||||
chr11:61229707 | A | G | 1 | a0001c0001t0001g0001 | 10 | HG02015.hp2 HG02074.hp1 HG02165.hp2 others(7): Show |
intron_variant | MODIFIER | c.774-212A>G | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 6/8 | chr11 | 61229707 | |||||||
chr11:61229727 | A | G | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.774-192A>G | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 6/8 | chr11 | 61229727 | |||||||
chr11:61229749 | G | A | 1 | a0001c0001t0001g0001 | 6 | HG02145.hp2 HG02257.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.774-170G>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 6/8 | chr11 | 61229749 | |||||||
chr11:61229751 | T | A | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.774-168T>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 6/8 | chr11 | 61229751 | |||||||
chr11:61229755 | C | T | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.774-164C>T | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 6/8 | chr11 | 61229755 | |||||||
chr11:61229765 | C | T | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.774-154C>T | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 6/8 | chr11 | 61229765 | |||||||
chr11:61229770 | C | T | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.774-149C>T | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 6/8 | chr11 | 61229770 | |||||||
chr11:61229781 | G | T | 1 | a0001c0001t0001g0001 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.774-138G>T | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 6/8 | chr11 | 61229781 | |||||||
chr11:61229834 | A | G | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.774-85A>G | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 6/8 | chr11 | 61229834 | |||||||
chr11:61229855 | A | G | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.774-64A>G | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 6/8 | chr11 | 61229855 | |||||||
chr11:61229873 | A | T | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.774-46A>T | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 6/8 | chr11 | 61229873 | |||||||
chr11:61229875 | T | A | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.774-44T>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 6/8 | chr11 | 61229875 | |||||||
chr11:61229885 | A | G | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.774-34A>G | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 6/8 | chr11 | 61229885 | |||||||
chr11:61229911 | G | A | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
splice_region_variant&intron_variant | LOW | c.774-8G>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 6/8 | chr11 | 61229911 | |||||||
chr11:61230084 | T | C | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.918+21T>C | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 7/8 | chr11 | 61230084 | |||||||
chr11:61230106 | G | A | 1 | a0001c0001t0001g0001 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.918+43G>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 7/8 | chr11 | 61230106 | |||||||
chr11:61230123 | G | C | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.919-43G>C | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 7/8 | chr11 | 61230123 | |||||||
chr11:61230124 | G | T | 1 | a0001c0001t0001g0001 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.919-42G>T | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 7/8 | chr11 | 61230124 | |||||||
chr11:61230127 | A | G | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.919-39A>G | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 7/8 | chr11 | 61230127 | |||||||
chr11:61230128 | G | A | 1 | a0001c0001t0001g0001 | 2 | NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.919-38G>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 7/8 | chr11 | 61230128 | |||||||
chr11:61230294 | G | A | 1 | a0001c0001t0001g0001 | 5 | HG02615.hp2 HG02630.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1017+30G>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 8/8 | chr11 | 61230294 | |||||||
chr11:61230322 | T | C | 1 | a0001c0001t0001g0001 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1017+58T>C | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 8/8 | chr11 | 61230322 | |||||||
chr11:61230326 | C | T | 1 | a0001c0001t0001g0001 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1017+62C>T | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 8/8 | chr11 | 61230326 | |||||||
chr11:61230365 | G | A | 1 | a0001c0001t0001g0001 | 261 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.1017+101G>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 8/8 | chr11 | 61230365 | |||||||
chr11:61230366 | C | G | 1 | a0001c0001t0001g0001 | 261 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.1017+102C>G | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 8/8 | chr11 | 61230366 | |||||||
chr11:61230440 | T | A | 1 | a0001c0001t0001g0001 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1017+176T>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 8/8 | chr11 | 61230440 | |||||||
chr11:61230477 | A | T | 1 | a0001c0001t0001g0001 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1017+213A>T | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 8/8 | chr11 | 61230477 | |||||||
chr11:61230483 | G | A | 1 | a0001c0001t0001g0001 | 45 | HG00738.hp2 HG01071.hp2 HG01169.hp1 others(42): Show |
intron_variant | MODIFIER | c.1017+219G>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 8/8 | chr11 | 61230483 | |||||||
chr11:61230484 | G | A | 1 | a0001c0001t0001g0001 | 45 | HG00738.hp2 HG01071.hp2 HG01169.hp1 others(42): Show |
intron_variant | MODIFIER | c.1017+220G>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 8/8 | chr11 | 61230484 | |||||||
chr11:61230564 | G | A | 1 | a0001c0001t0001g0001 | 150 | HG00558.hp1 HG00639.hp1 HG00738.hp2 others(147): Show |
intron_variant | MODIFIER | c.1017+300G>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 8/8 | chr11 | 61230564 | |||||||
chr11:61230568 | G | A | 1 | a0001c0001t0001g0001 | 149 | HG00558.hp1 HG00639.hp1 HG00738.hp2 others(146): Show |
intron_variant | MODIFIER | c.1017+304G>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 8/8 | chr11 | 61230568 | |||||||
chr11:61230569 | C | A | 1 | a0001c0001t0001g0001 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1017+305C>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 8/8 | chr11 | 61230569 | |||||||
chr11:61230569 | C | T | 1 | a0001c0001t0001g0001 | 149 | HG00558.hp1 HG00639.hp1 HG00738.hp2 others(146): Show |
intron_variant | MODIFIER | c.1017+305C>T | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 8/8 | chr11 | 61230569 | |||||||
chr11:61230574 | G | A | 1 | a0001c0001t0001g0001 | 150 | HG00558.hp1 HG00639.hp1 HG00738.hp2 others(147): Show |
intron_variant | MODIFIER | c.1017+310G>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 8/8 | chr11 | 61230574 | |||||||
chr11:61230649 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1017+385C>T | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 8/8 | chr11 | 61230649 | |||||||
chr11:61230713 | A | G | 1 | a0001c0001t0001g0001 | 179 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(176): Show |
intron_variant | MODIFIER | c.1017+449A>G | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 8/8 | chr11 | 61230713 | |||||||
chr11:61230728 | T | C | 1 | a0001c0001t0001g0001 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1017+464T>C | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 8/8 | chr11 | 61230728 | |||||||
chr11:61230801 | T | C | 1 | a0001c0001t0001g0001 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1017+537T>C | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 8/8 | chr11 | 61230801 | |||||||
chr11:61230805 | C | T | 1 | a0001c0001t0001g0001 | 5 | HG02622.hp2 HG03139.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1017+541C>T | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 8/8 | chr11 | 61230805 | |||||||
chr11:61230845 | T | A | 1 | a0001c0001t0001g0001 | 9 | HG02622.hp2 HG03139.hp2 HG06807.hp2 others(6): Show |
intron_variant | MODIFIER | c.1018-537T>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 8/8 | chr11 | 61230845 | |||||||
chr11:61230850 | C | T | 1 | a0001c0001t0001g0001 | 9 | HG02622.hp2 HG03139.hp2 HG06807.hp2 others(6): Show |
intron_variant | MODIFIER | c.1018-532C>T | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 8/8 | chr11 | 61230850 | |||||||
chr11:61230860 | A | G | 1 | a0001c0001t0001g0001 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1018-522A>G | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 8/8 | chr11 | 61230860 | |||||||
chr11:61230938 | G | A | 1 | a0001c0001t0001g0001 | 17 | HG02145.hp2 HG02451.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.1018-444G>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 8/8 | chr11 | 61230938 | |||||||
chr11:61230962 | T | C | 1 | a0001c0001t0001g0001 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1018-420T>C | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 8/8 | chr11 | 61230962 | |||||||
chr11:61231027 | C | T | 1 | a0001c0001t0001g0001 | 2 | HG02698.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1018-355C>T | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 8/8 | chr11 | 61231027 | |||||||
chr11:61231029 | T | C | 1 | a0001c0001t0001g0001 | 2 | HG02698.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1018-353T>C | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 8/8 | chr11 | 61231029 | |||||||
chr11:61231034 | C | T | 1 | a0001c0001t0001g0001 | 2 | HG02698.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1018-348C>T | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 8/8 | chr11 | 61231034 | |||||||
chr11:61231035 | C | G | 1 | a0001c0001t0001g0001 | 2 | HG02698.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1018-347C>G | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 8/8 | chr11 | 61231035 | |||||||
chr11:61231036 | G | A | 1 | a0001c0001t0001g0001 | 2 | HG02698.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1018-346G>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 8/8 | chr11 | 61231036 | |||||||
chr11:61231040 | C | A | 1 | a0001c0001t0001g0001 | 2 | HG02698.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1018-342C>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 8/8 | chr11 | 61231040 | |||||||
chr11:61231061 | C | A | 1 | a0001c0001t0001g0001 | 2 | HG02698.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1018-321C>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 8/8 | chr11 | 61231061 | |||||||
chr11:61231063 | A | G | 1 | a0001c0001t0001g0001 | 2 | HG02698.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1018-319A>G | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 8/8 | chr11 | 61231063 | |||||||
chr11:61231065 | G | A | 1 | a0001c0001t0001g0001 | 2 | HG02698.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1018-317G>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 8/8 | chr11 | 61231065 | |||||||
chr11:61231067 | C | T | 1 | a0001c0001t0001g0001 | 2 | HG02698.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1018-315C>T | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 8/8 | chr11 | 61231067 | |||||||
chr11:61231079 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1018-303C>T | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 8/8 | chr11 | 61231079 | |||||||
chr11:61231106 | C | A | 1 | a0001c0001t0001g0001 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1018-276C>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 8/8 | chr11 | 61231106 | |||||||
chr11:61231183 | G | A | 1 | a0001c0001t0001g0001 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1018-199G>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 8/8 | chr11 | 61231183 | |||||||
chr11:61231220 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1018-162C>T | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 8/8 | chr11 | 61231220 | |||||||
chr11:61231221 | G | A | 1 | a0001c0001t0001g0001 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1018-161G>A | PGA4 | ENSG00000229183.10 | transcript | ENST00000378149.9 | protein_coding | 8/8 | chr11 | 61231221 |