Item | Value |
---|---|
geneid | 55023 |
ensemblid | ENSG00000146247.15 |
hgncid | 15673 |
symbol | PHIP |
name | pleckstrin homology domain interacting protein |
refseq_nuc | NM_017934.7 |
refseq_prot | NP_060404.4 |
ensembl_nuc | ENST00000275034.5 |
ensembl_prot | ENSP00000275034.3 |
mane_status | MANE Select |
chr | chr6 |
start | 78934419 |
end | 79078254 |
strand | - |
ver | v1.2 |
region | chr6:78934419-79078254 |
region5000 | chr6:78929419-79083254 |
regionname0 | PHIP_chr6_78934419_79078254 |
regionname5000 | PHIP_chr6_78929419_79083254 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 1821 | 178 | 72 | 24 | 62 | 2 | 17 | 52 | PHIP_chr6_78929419_79083254 | PHIP | MSCER others(1816): Show |
chr6 | 78929419 | 79083254 |
a0002 | 0/0 | 1821 | 85 | 14 | 16 | 39 | 6 | 10 | 32 | PHIP_chr6_78929419_79083254 | PHIP | MSCER others(1816): Show |
chr6 | 78929419 | 79083254 |
a0003 | 0/0 | 1821 | 33 | 2 | 5 | 19 | 4 | 3 | 13 | PHIP_chr6_78929419_79083254 | PHIP | MSCER others(1816): Show |
chr6 | 78929419 | 79083254 |
a0004 | 1/0 | 1821 | 18 | 5 | 9 | 0 | 0 | 3 | 0 | PHIP_chr6_78929419_79083254 | PHIP | MSCER others(1816): Show |
chr6 | 78929419 | 79083254 |
a0005 | 0/0 | 1821 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | MSCER others(1816): Show |
chr6 | 78929419 | 79083254 |
a0006 | 0/0 | 1821 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PHIP_chr6_78929419_79083254 | PHIP | MSCER others(1816): Show |
chr6 | 78929419 | 79083254 |
a0007 | 0/0 | 1821 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | MSCER others(1816): Show |
chr6 | 78929419 | 79083254 |
a0008 | 0/0 | 1821 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | MSCER others(1816): Show |
chr6 | 78929419 | 79083254 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 5463 | 123 | 30 | 21 | 52 | 2 | 17 | PHIP_chr6_78929419_79083254 | PHIP | ATGTC others(5458): Show |
chr6 | 78929419 | 79083254 | ||
a0001c0005 | 0/0 | 5463 | 17 | 16 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | ATGTC others(5458): Show |
chr6 | 78929419 | 79083254 | ||
a0001c0006 | 0/0 | 5463 | 17 | 9 | 1 | 7 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | ATGTC others(5458): Show |
chr6 | 78929419 | 79083254 | ||
a0001c0007 | 0/0 | 5463 | 7 | 7 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | ATGTC others(5458): Show |
chr6 | 78929419 | 79083254 | ||
a0001c0008 | 0/0 | 5463 | 4 | 4 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | ATGTC others(5458): Show |
chr6 | 78929419 | 79083254 | ||
a0001c0010 | 0/0 | 5463 | 3 | 2 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | ATGTC others(5458): Show |
chr6 | 78929419 | 79083254 | ||
a0001c0011 | 0/0 | 5463 | 3 | 0 | 0 | 3 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | ATGTC others(5458): Show |
chr6 | 78929419 | 79083254 | ||
a0001c0012 | 0/0 | 5463 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | ATGTC others(5458): Show |
chr6 | 78929419 | 79083254 | ||
a0001c0013 | 0/0 | 5463 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | ATGTC others(5458): Show |
chr6 | 78929419 | 79083254 | ||
a0001c0015 | 0/0 | 5463 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | ATGTC others(5458): Show |
chr6 | 78929419 | 79083254 | ||
a0001c0021 | 0/0 | 5463 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | ATGTC others(5458): Show |
chr6 | 78929419 | 79083254 | ||
a0002c0002 | 0/0 | 5463 | 79 | 14 | 11 | 38 | 6 | 10 | PHIP_chr6_78929419_79083254 | PHIP | ATGTC others(5458): Show |
chr6 | 78929419 | 79083254 | ||
a0002c0009 | 0/0 | 5463 | 4 | 0 | 4 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | ATGTC others(5458): Show |
chr6 | 78929419 | 79083254 | ||
a0002c0014 | 0/0 | 5463 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | ATGTC others(5458): Show |
chr6 | 78929419 | 79083254 | ||
a0002c0020 | 0/0 | 5463 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | ATGTC others(5458): Show |
chr6 | 78929419 | 79083254 | ||
a0003c0003 | 0/0 | 5463 | 33 | 2 | 5 | 19 | 4 | 3 | PHIP_chr6_78929419_79083254 | PHIP | ATGTC others(5458): Show |
chr6 | 78929419 | 79083254 | ||
a0004c0004 | 1/0 | 5463 | 18 | 5 | 9 | 0 | 0 | 3 | PHIP_chr6_78929419_79083254 | PHIP | ATGTC others(5458): Show |
chr6 | 78929419 | 79083254 | ||
a0005c0016 | 0/0 | 5463 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | ATGTC others(5458): Show |
chr6 | 78929419 | 79083254 | ||
a0006c0018 | 0/0 | 5463 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | ATGTC others(5458): Show |
chr6 | 78929419 | 79083254 | ||
a0007c0017 | 0/0 | 5463 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | ATGTC others(5458): Show |
chr6 | 78929419 | 79083254 | ||
a0008c0019 | 0/0 | 5463 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | ATGTC others(5458): Show |
chr6 | 78929419 | 79083254 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 11927 | 59 | 5 | 12 | 31 | 1 | 9 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11922): Show |
chr6 | 78929419 | 79083254 |
a0001c0001t0005 | 0/0 | 11928 | 22 | 2 | 3 | 13 | 0 | 4 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11923): Show |
chr6 | 78929419 | 79083254 |
a0001c0001t0011 | 0/0 | 11928 | 6 | 6 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11923): Show |
chr6 | 78929419 | 79083254 |
a0001c0001t0014 | 0/0 | 11930 | 4 | 1 | 1 | 0 | 0 | 2 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11925): Show |
chr6 | 78929419 | 79083254 |
a0001c0001t0015 | 0/0 | 11929 | 4 | 1 | 1 | 0 | 0 | 2 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11924): Show |
chr6 | 78929419 | 79083254 |
a0001c0001t0017 | 0/0 | 11929 | 3 | 3 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11924): Show |
chr6 | 78929419 | 79083254 |
a0001c0001t0018 | 0/0 | 11929 | 3 | 3 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11924): Show |
chr6 | 78929419 | 79083254 |
a0001c0001t0021 | 0/0 | 11928 | 3 | 3 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11923): Show |
chr6 | 78929419 | 79083254 |
a0001c0001t0025 | 0/0 | 11928 | 2 | 2 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11923): Show |
chr6 | 78929419 | 79083254 |
a0001c0001t0026 | 0/0 | 11928 | 2 | 2 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11923): Show |
chr6 | 78929419 | 79083254 |
a0001c0001t0032 | 0/0 | 11929 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11924): Show |
chr6 | 78929419 | 79083254 |
a0001c0001t0033 | 0/0 | 11929 | 1 | 0 | 0 | 0 | 1 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11924): Show |
chr6 | 78929419 | 79083254 |
a0001c0001t0034 | 0/0 | 11928 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11923): Show |
chr6 | 78929419 | 79083254 |
a0001c0001t0035 | 0/0 | 11928 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11923): Show |
chr6 | 78929419 | 79083254 |
a0001c0001t0037 | 0/0 | 11927 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11922): Show |
chr6 | 78929419 | 79083254 |
a0001c0001t0039 | 0/0 | 11927 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11922): Show |
chr6 | 78929419 | 79083254 |
a0001c0001t0040 | 0/0 | 11927 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11922): Show |
chr6 | 78929419 | 79083254 |
a0001c0001t0041 | 0/0 | 11927 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11922): Show |
chr6 | 78929419 | 79083254 |
a0001c0001t0042 | 0/0 | 11927 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11922): Show |
chr6 | 78929419 | 79083254 |
a0001c0001t0043 | 0/0 | 11923 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11918): Show |
chr6 | 78929419 | 79083254 |
a0001c0001t0044 | 0/0 | 11926 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11921): Show |
chr6 | 78929419 | 79083254 |
a0001c0001t0050 | 0/0 | 11928 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11923): Show |
chr6 | 78929419 | 79083254 |
a0001c0001t0059 | 0/0 | 11924 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11919): Show |
chr6 | 78929419 | 79083254 |
a0001c0001t0067 | 0/0 | 11923 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11918): Show |
chr6 | 78929419 | 79083254 |
a0001c0001t0069 | 0/0 | 11913 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11908): Show |
chr6 | 78929419 | 79083254 |
a0001c0005t0003 | 0/0 | 11928 | 3 | 3 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11923): Show |
chr6 | 78929419 | 79083254 |
a0001c0005t0019 | 0/0 | 11928 | 3 | 3 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11923): Show |
chr6 | 78929419 | 79083254 |
a0001c0005t0023 | 0/0 | 11930 | 2 | 2 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11925): Show |
chr6 | 78929419 | 79083254 |
a0001c0005t0027 | 0/0 | 11930 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11925): Show |
chr6 | 78929419 | 79083254 |
a0001c0005t0030 | 0/0 | 11924 | 2 | 2 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11919): Show |
chr6 | 78929419 | 79083254 |
a0001c0005t0038 | 0/0 | 11928 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11923): Show |
chr6 | 78929419 | 79083254 |
a0001c0005t0045 | 0/0 | 11927 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11922): Show |
chr6 | 78929419 | 79083254 |
a0001c0005t0046 | 0/0 | 11929 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11924): Show |
chr6 | 78929419 | 79083254 |
a0001c0005t0049 | 0/0 | 11929 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11924): Show |
chr6 | 78929419 | 79083254 |
a0001c0005t0054 | 0/0 | 11928 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11923): Show |
chr6 | 78929419 | 79083254 |
a0001c0005t0055 | 0/0 | 11928 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11923): Show |
chr6 | 78929419 | 79083254 |
a0001c0006t0002 | 0/0 | 11924 | 11 | 6 | 1 | 4 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11919): Show |
chr6 | 78929419 | 79083254 |
a0001c0006t0008 | 0/0 | 11929 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11924): Show |
chr6 | 78929419 | 79083254 |
a0001c0006t0009 | 0/0 | 11925 | 2 | 2 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11920): Show |
chr6 | 78929419 | 79083254 |
a0001c0006t0020 | 0/0 | 11927 | 3 | 0 | 0 | 3 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11922): Show |
chr6 | 78929419 | 79083254 |
a0001c0007t0012 | 0/0 | 11928 | 6 | 6 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11923): Show |
chr6 | 78929419 | 79083254 |
a0001c0007t0047 | 0/0 | 11929 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11924): Show |
chr6 | 78929419 | 79083254 |
a0001c0008t0003 | 0/0 | 11928 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11923): Show |
chr6 | 78929419 | 79083254 |
a0001c0008t0007 | 0/0 | 11927 | 3 | 3 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11922): Show |
chr6 | 78929419 | 79083254 |
a0001c0010t0029 | 0/0 | 11928 | 2 | 2 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11923): Show |
chr6 | 78929419 | 79083254 |
a0001c0010t0057 | 0/0 | 11927 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11922): Show |
chr6 | 78929419 | 79083254 |
a0001c0011t0016 | 0/0 | 11937 | 3 | 0 | 0 | 3 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGCCG others(11932): Show |
chr6 | 78929419 | 79083254 |
a0001c0012t0024 | 0/0 | 11931 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11926): Show |
chr6 | 78929419 | 79083254 |
a0001c0013t0007 | 0/0 | 11927 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11922): Show |
chr6 | 78929419 | 79083254 |
a0001c0015t0024 | 0/0 | 11931 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11926): Show |
chr6 | 78929419 | 79083254 |
a0001c0021t0036 | 0/0 | 11928 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11923): Show |
chr6 | 78929419 | 79083254 |
a0002c0002t0003 | 0/0 | 11928 | 25 | 4 | 4 | 12 | 1 | 4 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11923): Show |
chr6 | 78929419 | 79083254 |
a0002c0002t0004 | 0/0 | 11924 | 18 | 1 | 1 | 10 | 2 | 4 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11919): Show |
chr6 | 78929419 | 79083254 |
a0002c0002t0007 | 0/0 | 11927 | 7 | 1 | 3 | 0 | 3 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11922): Show |
chr6 | 78929419 | 79083254 |
a0002c0002t0008 | 0/0 | 11929 | 8 | 3 | 0 | 4 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11924): Show |
chr6 | 78929419 | 79083254 |
a0002c0002t0010 | 0/0 | 11925 | 7 | 0 | 0 | 6 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11920): Show |
chr6 | 78929419 | 79083254 |
a0002c0002t0022 | 0/0 | 11924 | 2 | 0 | 0 | 2 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11919): Show |
chr6 | 78929419 | 79083254 |
a0002c0002t0027 | 0/0 | 11930 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11925): Show |
chr6 | 78929419 | 79083254 |
a0002c0002t0028 | 0/0 | 11928 | 2 | 0 | 2 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11923): Show |
chr6 | 78929419 | 79083254 |
a0002c0002t0048 | 0/0 | 11929 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11924): Show |
chr6 | 78929419 | 79083254 |
a0002c0002t0051 | 0/0 | 11929 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11924): Show |
chr6 | 78929419 | 79083254 |
a0002c0002t0053 | 0/0 | 11928 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11923): Show |
chr6 | 78929419 | 79083254 |
a0002c0002t0056 | 0/0 | 11930 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11925): Show |
chr6 | 78929419 | 79083254 |
a0002c0002t0058 | 0/0 | 11929 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11924): Show |
chr6 | 78929419 | 79083254 |
a0002c0002t0062 | 0/0 | 11926 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11921): Show |
chr6 | 78929419 | 79083254 |
a0002c0002t0063 | 0/0 | 11926 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11921): Show |
chr6 | 78929419 | 79083254 |
a0002c0002t0066 | 0/0 | 11924 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11919): Show |
chr6 | 78929419 | 79083254 |
a0002c0002t0068 | 0/0 | 11924 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11919): Show |
chr6 | 78929419 | 79083254 |
a0002c0009t0004 | 0/0 | 11924 | 4 | 0 | 4 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11919): Show |
chr6 | 78929419 | 79083254 |
a0002c0014t0003 | 0/0 | 11928 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11923): Show |
chr6 | 78929419 | 79083254 |
a0002c0020t0022 | 0/0 | 11924 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11919): Show |
chr6 | 78929419 | 79083254 |
a0003c0003t0002 | 0/0 | 11924 | 23 | 2 | 3 | 14 | 3 | 1 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11919): Show |
chr6 | 78929419 | 79083254 |
a0003c0003t0009 | 0/0 | 11925 | 5 | 0 | 0 | 3 | 1 | 1 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11920): Show |
chr6 | 78929419 | 79083254 |
a0003c0003t0031 | 0/0 | 11923 | 2 | 0 | 1 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11918): Show |
chr6 | 78929419 | 79083254 |
a0003c0003t0052 | 0/0 | 11926 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11921): Show |
chr6 | 78929419 | 79083254 |
a0003c0003t0060 | 0/0 | 11924 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11919): Show |
chr6 | 78929419 | 79083254 |
a0003c0003t0061 | 0/0 | 11924 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11919): Show |
chr6 | 78929419 | 79083254 |
a0004c0004t0006 | 0/0 | 11926 | 12 | 0 | 9 | 0 | 0 | 3 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11921): Show |
chr6 | 78929419 | 79083254 |
a0004c0004t0013 | 0/0 | 11926 | 4 | 4 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11921): Show |
chr6 | 78929419 | 79083254 |
a0004c0004t0064 | 1/0 | 11926 | 1 | 0 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11921): Show |
chr6 | 78929419 | 79083254 |
a0004c0004t0065 | 0/0 | 11925 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11920): Show |
chr6 | 78929419 | 79083254 |
a0005c0016t0001 | 0/0 | 11927 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11922): Show |
chr6 | 78929419 | 79083254 |
a0006c0018t0001 | 0/0 | 11927 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11922): Show |
chr6 | 78929419 | 79083254 |
a0007c0017t0004 | 0/0 | 11924 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11919): Show |
chr6 | 78929419 | 79083254 |
a0008c0019t0013 | 0/0 | 11926 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | AGTCG others(11921): Show |
chr6 | 78929419 | 79083254 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0001g0144 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0005g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0005g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0005g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0005g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0005g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0005g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0005g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0005g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0005g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0005g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0005g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0005g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0005g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0005g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0005g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0005g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0005g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0005g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0005g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0005g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0005g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0005g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0011g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0011g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0011g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0011g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0011g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0011g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0014g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0014g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0014g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0014g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0015g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0015g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0015g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0015g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0017g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0017g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0017g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0018g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0018g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0018g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0021g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0021g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0021g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0025g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0025g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0026g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0026g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0032g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0033g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0034g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0035g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0037g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0039g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0040g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0041g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0042g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0043g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0044g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0050g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0059g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0067g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0001t0069g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0005t0003g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0005t0019g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0005t0019g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0005t0023g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0005t0023g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0005t0027g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0005t0030g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0005t0030g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0005t0038g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0005t0045g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0005t0046g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0005t0049g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0005t0054g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0005t0055g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0006t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0006t0002g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0006t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0006t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0006t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0006t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0006t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0006t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0006t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0006t0008g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0006t0009g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0006t0009g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0006t0020g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0006t0020g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0007t0012g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0007t0012g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0007t0012g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0007t0012g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0007t0012g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0007t0012g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0007t0047g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0008t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0008t0007g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0008t0007g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0008t0007g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0010t0029g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0010t0029g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0010t0057g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0011t0016g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0011t0016g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0011t0016g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0012t0024g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0013t0007g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0015t0024g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0001c0021t0036g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0003g0010 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0003g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0003g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0003g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0003g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0003g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0003g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0003g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0003g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0003g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0004g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0004g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0004g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0004g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0004g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0004g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0004g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0004g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0004g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0004g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0004g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0004g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0004g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0004g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0004g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0004g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0004g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0004g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0007g0003 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0007g0004 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0007g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0007g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0007g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0008g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0008g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0008g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0008g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0008g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0008g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0008g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0008g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0010g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0010g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0010g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0010g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0010g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0010g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0010g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0022g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0022g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0027g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0028g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0028g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0048g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0051g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0053g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0056g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0058g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0062g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0063g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0066g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0002t0068g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0009t0004g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0009t0004g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0009t0004g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0014t0003g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0002c0020t0022g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0003c0003t0002g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0003c0003t0002g0015 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0003c0003t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0003c0003t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0003c0003t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0003c0003t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0003c0003t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0003c0003t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0003c0003t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0003c0003t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0003c0003t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0003c0003t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0003c0003t0002g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0003c0003t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0003c0003t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0003c0003t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0003c0003t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0003c0003t0002g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0003c0003t0002g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0003c0003t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0003c0003t0009g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0003c0003t0009g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0003c0003t0009g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0003c0003t0009g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0003c0003t0031g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0003c0003t0031g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0003c0003t0052g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0003c0003t0060g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0003c0003t0061g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0004c0004t0006g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0004c0004t0006g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0004c0004t0006g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0004c0004t0006g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0004c0004t0006g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0004c0004t0006g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0004c0004t0006g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0004c0004t0006g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0004c0004t0006g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0004c0004t0006g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0004c0004t0013g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0004c0004t0013g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0004c0004t0013g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0004c0004t0013g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0004c0004t0064g0177 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0004c0004t0065g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0005c0016t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0006c0018t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0007c0017t0004g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
a0008c0019t0013g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0007 | g0004 | EUR | GBR | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG00099 | hp2 | a0003 | c0003 | t0002 | g0286 | EUR | GBR | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0121 | EUR | GBR | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG00140 | hp2 | a0002 | c0002 | t0007 | g0004 | EUR | GBR | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG00280 | hp1 | a0002 | c0002 | t0007 | g0003 | EUR | FIN | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG00280 | hp2 | a0001 | c0001 | t0033 | g0021 | EUR | FIN | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG00438 | hp2 | a0003 | c0003 | t0052 | g0298 | EAS | CHS | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG00558 | hp1 | a0002 | c0002 | t0010 | g0224 | EAS | CHS | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG00558 | hp2 | a0005 | c0016 | t0001 | g0126 | EAS | CHS | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG00621 | hp1 | a0002 | c0002 | t0004 | g0198 | EAS | CHS | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG00621 | hp2 | a0001 | c0001 | t0005 | g0299 | EAS | CHS | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG00639 | hp1 | a0001 | c0001 | t0015 | g0159 | AMR | PUR | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG00639 | hp2 | a0001 | c0001 | t0037 | g0055 | AMR | PUR | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG00642 | hp1 | a0001 | c0001 | t0040 | g0080 | AMR | PUR | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG00642 | hp2 | a0002 | c0014 | t0003 | g0210 | AMR | PUR | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG00673 | hp2 | a0002 | c0002 | t0008 | g0240 | EAS | CHS | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG00733 | hp1 | a0002 | c0002 | t0004 | g0216 | AMR | PUR | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG00735 | hp1 | a0003 | c0003 | t0002 | g0279 | AMR | PUR | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG00735 | hp2 | a0004 | c0004 | t0006 | g0008 | AMR | PUR | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG00738 | hp1 | a0002 | c0009 | t0004 | g0259 | AMR | PUR | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG00738 | hp2 | a0001 | c0001 | t0005 | g0071 | AMR | PUR | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG01069 | hp1 | a0002 | c0002 | t0007 | g0039 | AMR | PUR | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG01070 | hp1 | a0003 | c0003 | t0031 | g0273 | AMR | PUR | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG01071 | hp1 | a0002 | c0002 | t0007 | g0003 | AMR | PUR | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG01071 | hp2 | a0001 | c0001 | t0005 | g0059 | AMR | PUR | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG01074 | hp2 | a0002 | c0002 | t0003 | g0010 | AMR | PUR | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG01106 | hp1 | a0002 | c0009 | t0004 | g0214 | AMR | PUR | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG01106 | hp2 | a0004 | c0004 | t0006 | g0008 | AMR | PUR | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG01109 | hp1 | a0002 | c0002 | t0003 | g0193 | AMR | PUR | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG01109 | hp2 | a0001 | c0005 | t0027 | g0033 | AMR | PUR | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG01175 | hp1 | a0001 | c0001 | t0014 | g0160 | AMR | PUR | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG01255 | hp1 | a0003 | c0003 | t0002 | g0288 | AMR | CLM | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG01255 | hp2 | a0004 | c0004 | t0006 | g0184 | AMR | CLM | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG01257 | hp2 | a0002 | c0009 | t0004 | g0009 | AMR | CLM | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG01258 | hp1 | a0001 | c0001 | t0044 | g0056 | AMR | CLM | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG01258 | hp2 | a0002 | c0009 | t0004 | g0009 | AMR | CLM | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG01261 | hp1 | a0002 | c0002 | t0007 | g0040 | AMR | CLM | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG01261 | hp2 | a0003 | c0003 | t0060 | g0280 | AMR | CLM | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG01346 | hp2 | a0003 | c0003 | t0002 | g0274 | AMR | CLM | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG01358 | hp1 | a0001 | c0010 | t0057 | g0163 | AMR | CLM | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG01358 | hp2 | a0004 | c0004 | t0006 | g0186 | AMR | CLM | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG01496 | hp1 | a0001 | c0001 | t0041 | g0129 | AMR | CLM | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG01496 | hp2 | a0004 | c0004 | t0006 | g0179 | AMR | CLM | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG01516 | hp1 | a0003 | c0003 | t0002 | g0015 | EUR | IBS | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG01516 | hp2 | a0002 | c0002 | t0004 | g0232 | EUR | IBS | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG01517 | hp1 | a0002 | c0002 | t0004 | g0215 | EUR | IBS | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG01517 | hp2 | a0003 | c0003 | t0002 | g0015 | EUR | IBS | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG01884 | hp1 | a0004 | c0004 | t0013 | g0178 | AFR | ACB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG01884 | hp2 | a0001 | c0005 | t0030 | g0048 | AFR | ACB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG01891 | hp1 | a0001 | c0001 | t0017 | g0031 | AFR | ACB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG01891 | hp2 | a0001 | c0006 | t0009 | g0266 | AFR | ACB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG01934 | hp1 | a0004 | c0004 | t0006 | g0007 | AMR | PEL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0300 | AMR | PEL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG01952 | hp2 | a0004 | c0004 | t0006 | g0007 | AMR | PEL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG01975 | hp1 | a0004 | c0004 | t0006 | g0180 | AMR | PEL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG01975 | hp2 | a0002 | c0002 | t0003 | g0249 | AMR | PEL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG01978 | hp2 | a0004 | c0004 | t0006 | g0189 | AMR | PEL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG01981 | hp2 | a0002 | c0002 | t0028 | g0261 | AMR | PEL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02004 | hp1 | a0002 | c0002 | t0028 | g0260 | AMR | PEL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02027 | hp1 | a0001 | c0001 | t0035 | g0067 | EAS | KHV | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02027 | hp2 | a0003 | c0003 | t0002 | g0287 | EAS | KHV | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02055 | hp1 | a0001 | c0001 | t0018 | g0152 | AFR | ACB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02055 | hp2 | a0002 | c0002 | t0008 | g0246 | AFR | ACB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02074 | hp1 | a0003 | c0003 | t0002 | g0281 | EAS | KHV | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02080 | hp1 | a0001 | c0001 | t0005 | g0116 | EAS | KHV | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02080 | hp2 | a0002 | c0002 | t0010 | g0206 | EAS | KHV | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02145 | hp1 | a0001 | c0001 | t0014 | g0162 | AFR | ACB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02145 | hp2 | a0001 | c0001 | t0034 | g0132 | AFR | ACB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02148 | hp1 | a0002 | c0002 | t0051 | g0248 | AMR | PEL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02148 | hp2 | a0001 | c0001 | t0005 | g0109 | AMR | PEL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | CDX | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02155 | hp2 | a0003 | c0003 | t0002 | g0292 | EAS | CDX | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02165 | hp1 | a0001 | c0001 | t0032 | g0093 | EAS | CDX | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02165 | hp2 | a0003 | c0003 | t0002 | g0290 | EAS | CDX | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02257 | hp1 | a0004 | c0004 | t0013 | g0188 | AFR | ACB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02257 | hp2 | a0001 | c0001 | t0005 | g0139 | AFR | ACB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02258 | hp1 | a0001 | c0006 | t0002 | g0014 | AFR | ACB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02258 | hp2 | a0001 | c0001 | t0011 | g0255 | AFR | ACB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02280 | hp1 | a0001 | c0005 | t0003 | g0001 | AFR | ACB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02280 | hp2 | a0001 | c0008 | t0007 | g0165 | AFR | ACB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02451 | hp2 | a0002 | c0002 | t0003 | g0041 | AFR | ACB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02523 | hp1 | a0003 | c0003 | t0002 | g0296 | EAS | KHV | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02523 | hp2 | a0002 | c0002 | t0004 | g0221 | EAS | KHV | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02572 | hp1 | a0001 | c0006 | t0008 | g0037 | AFR | GWD | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02572 | hp2 | a0002 | c0002 | t0048 | g0020 | AFR | GWD | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02602 | hp2 | a0002 | c0002 | t0003 | g0205 | SAS | PJL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02622 | hp1 | a0001 | c0008 | t0007 | g0164 | AFR | GWD | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02622 | hp2 | a0001 | c0007 | t0012 | g0174 | AFR | GWD | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02683 | hp1 | a0003 | c0003 | t0002 | g0294 | SAS | PJL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02683 | hp2 | a0002 | c0002 | t0010 | g0222 | SAS | PJL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02698 | hp1 | a0002 | c0002 | t0004 | g0211 | SAS | PJL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02717 | hp1 | a0002 | c0002 | t0008 | g0192 | AFR | GWD | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02723 | hp1 | a0001 | c0005 | t0054 | g0038 | AFR | GWD | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02723 | hp2 | a0001 | c0006 | t0002 | g0265 | AFR | GWD | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02735 | hp1 | a0002 | c0002 | t0003 | g0245 | SAS | PJL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02809 | hp1 | a0001 | c0007 | t0047 | g0175 | AFR | GWD | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02809 | hp2 | a0001 | c0001 | t0011 | g0151 | AFR | GWD | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02818 | hp1 | a0001 | c0005 | t0038 | g0047 | AFR | GWD | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02818 | hp2 | a0002 | c0002 | t0063 | g0176 | AFR | GWD | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02886 | hp1 | a0001 | c0006 | t0009 | g0297 | AFR | GWD | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02886 | hp2 | a0001 | c0005 | t0045 | g0046 | AFR | GWD | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02895 | hp1 | a0004 | c0004 | t0065 | g0182 | AFR | GWD | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02895 | hp2 | a0001 | c0006 | t0002 | g0267 | AFR | GWD | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02896 | hp1 | a0001 | c0001 | t0011 | g0256 | AFR | GWD | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02896 | hp2 | a0001 | c0007 | t0012 | g0172 | AFR | GWD | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02897 | hp1 | a0004 | c0004 | t0013 | g0181 | AFR | GWD | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02897 | hp2 | a0001 | c0007 | t0012 | g0171 | AFR | GWD | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02922 | hp1 | a0001 | c0007 | t0012 | g0169 | AFR | ESN | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02922 | hp2 | a0001 | c0001 | t0021 | g0028 | AFR | ESN | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02965 | hp1 | a0001 | c0005 | t0003 | g0001 | AFR | ESN | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02965 | hp2 | a0001 | c0010 | t0029 | g0054 | AFR | ESN | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02970 | hp1 | a0002 | c0002 | t0008 | g0197 | AFR | ESN | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02970 | hp2 | a0001 | c0001 | t0018 | g0258 | AFR | ESN | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02976 | hp1 | a0001 | c0005 | t0023 | g0049 | AFR | ESN | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02976 | hp2 | a0001 | c0001 | t0026 | g0149 | AFR | ESN | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG03017 | hp1 | a0004 | c0004 | t0006 | g0185 | SAS | PJL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG03041 | hp1 | a0001 | c0005 | t0019 | g0012 | AFR | GWD | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG03041 | hp2 | a0001 | c0013 | t0007 | g0166 | AFR | GWD | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG03098 | hp1 | a0001 | c0001 | t0017 | g0026 | AFR | MSL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG03098 | hp2 | a0002 | c0002 | t0003 | g0042 | AFR | MSL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG03130 | hp1 | a0001 | c0005 | t0019 | g0012 | AFR | ESN | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG03130 | hp2 | a0001 | c0001 | t0011 | g0029 | AFR | ESN | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG03139 | hp1 | a0001 | c0001 | t0017 | g0023 | AFR | ESN | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG03139 | hp2 | a0002 | c0002 | t0053 | g0194 | AFR | ESN | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG03195 | hp1 | a0002 | c0002 | t0058 | g0043 | AFR | ESN | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG03195 | hp2 | a0001 | c0006 | t0002 | g0269 | AFR | ESN | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG03209 | hp1 | a0001 | c0006 | t0002 | g0270 | AFR | MSL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG03209 | hp2 | a0001 | c0015 | t0024 | g0035 | AFR | MSL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG03225 | hp1 | a0001 | c0005 | t0055 | g0045 | AFR | MSL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG03225 | hp2 | a0002 | c0002 | t0056 | g0196 | AFR | MSL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG03239 | hp1 | a0002 | c0002 | t0004 | g0233 | SAS | PJL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG03453 | hp1 | a0002 | c0002 | t0003 | g0254 | AFR | MSL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG03453 | hp2 | a0001 | c0001 | t0005 | g0141 | AFR | MSL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG03486 | hp1 | a0001 | c0001 | t0018 | g0257 | AFR | MSL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG03492 | hp1 | a0001 | c0001 | t0015 | g0156 | SAS | PJL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG03516 | hp1 | a0001 | c0005 | t0046 | g0263 | AFR | ESN | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ESN | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG03540 | hp1 | a0001 | c0007 | t0012 | g0173 | AFR | GWD | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG03540 | hp2 | a0003 | c0003 | t0002 | g0295 | AFR | GWD | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG03579 | hp1 | a0001 | c0010 | t0029 | g0053 | AFR | MSL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG03579 | hp2 | a0001 | c0001 | t0026 | g0154 | AFR | MSL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG03654 | hp1 | a0004 | c0004 | t0006 | g0191 | SAS | PJL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG03654 | hp2 | a0001 | c0001 | t0014 | g0161 | SAS | PJL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG03669 | hp1 | a0002 | c0002 | t0008 | g0209 | SAS | PJL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG03669 | hp2 | a0001 | c0001 | t0005 | g0099 | SAS | PJL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG03831 | hp1 | a0002 | c0002 | t0004 | g0208 | SAS | BEB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG03831 | hp2 | a0001 | c0001 | t0005 | g0094 | SAS | BEB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG03834 | hp1 | a0004 | c0004 | t0006 | g0187 | SAS | BEB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | BEB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG03942 | hp1 | a0001 | c0001 | t0005 | g0065 | SAS | BEB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG03942 | hp2 | a0001 | c0001 | t0015 | g0155 | SAS | BEB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | STU | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG04115 | hp2 | a0001 | c0001 | t0014 | g0158 | SAS | STU | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG04184 | hp1 | a0002 | c0002 | t0003 | g0244 | SAS | BEB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG04184 | hp2 | a0001 | c0001 | t0005 | g0052 | SAS | BEB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG04199 | hp1 | a0002 | c0002 | t0003 | g0010 | SAS | STU | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG04199 | hp2 | a0003 | c0003 | t0009 | g0272 | SAS | STU | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | STU | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG04204 | hp2 | a0002 | c0002 | t0004 | g0207 | SAS | STU | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG04228 | hp1 | a0006 | c0018 | t0001 | g0087 | SAS | STU | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG04228 | hp2 | a0003 | c0003 | t0061 | g0283 | SAS | STU | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA18522 | hp1 | a0001 | c0001 | t0011 | g0153 | AFR | YRI | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA18522 | hp2 | a0001 | c0005 | t0023 | g0051 | AFR | YRI | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | CHB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA18612 | hp2 | a0002 | c0002 | t0004 | g0229 | EAS | CHB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | CHB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA18747 | hp2 | a0002 | c0002 | t0004 | g0213 | EAS | CHB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA18906 | hp1 | a0001 | c0001 | t0021 | g0030 | AFR | YRI | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA18906 | hp2 | a0001 | c0005 | t0030 | g0050 | AFR | YRI | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA18941 | hp2 | a0002 | c0002 | t0004 | g0227 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA18943 | hp1 | a0003 | c0003 | t0002 | g0282 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA18944 | hp1 | a0001 | c0006 | t0020 | g0006 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA18944 | hp2 | a0001 | c0001 | t0043 | g0085 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA18945 | hp1 | a0001 | c0001 | t0042 | g0090 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA18945 | hp2 | a0002 | c0002 | t0003 | g0203 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA18950 | hp2 | a0003 | c0003 | t0009 | g0277 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA18959 | hp1 | a0001 | c0001 | t0005 | g0106 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA18959 | hp2 | a0002 | c0002 | t0004 | g0236 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA18960 | hp2 | a0003 | c0003 | t0002 | g0002 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA18962 | hp1 | a0002 | c0002 | t0003 | g0243 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA18964 | hp2 | a0003 | c0003 | t0002 | g0289 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA18965 | hp1 | a0002 | c0002 | t0004 | g0223 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA18965 | hp2 | a0001 | c0006 | t0020 | g0148 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA18974 | hp1 | a0002 | c0002 | t0003 | g0202 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA18974 | hp2 | a0001 | c0001 | t0005 | g0102 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA18975 | hp1 | a0003 | c0003 | t0002 | g0002 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA18975 | hp2 | a0001 | c0001 | t0005 | g0114 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA18977 | hp1 | a0001 | c0001 | t0005 | g0082 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA18977 | hp2 | a0003 | c0003 | t0002 | g0284 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA18978 | hp2 | a0002 | c0002 | t0008 | g0204 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA18980 | hp2 | a0002 | c0002 | t0003 | g0201 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA18982 | hp2 | a0002 | c0002 | t0022 | g0225 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA18984 | hp1 | a0003 | c0003 | t0002 | g0002 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA18984 | hp2 | a0001 | c0001 | t0050 | g0061 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA18985 | hp2 | a0002 | c0002 | t0010 | g0234 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA18986 | hp1 | a0003 | c0003 | t0002 | g0278 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA18986 | hp2 | a0001 | c0001 | t0005 | g0078 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA18987 | hp1 | a0002 | c0002 | t0003 | g0242 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA18988 | hp1 | a0002 | c0002 | t0022 | g0235 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA18988 | hp2 | a0001 | c0001 | t0005 | g0145 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA18989 | hp1 | a0002 | c0002 | t0010 | g0228 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA18989 | hp2 | a0003 | c0003 | t0031 | g0293 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA18991 | hp2 | a0002 | c0002 | t0003 | g0262 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA18995 | hp1 | a0001 | c0001 | t0067 | g0063 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA18995 | hp2 | a0007 | c0017 | t0004 | g0226 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA18998 | hp1 | a0001 | c0006 | t0020 | g0006 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA18998 | hp2 | a0002 | c0002 | t0003 | g0011 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA18999 | hp2 | a0002 | c0002 | t0008 | g0247 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA19000 | hp1 | a0002 | c0002 | t0008 | g0200 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA19000 | hp2 | a0001 | c0001 | t0005 | g0062 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA19002 | hp1 | a0003 | c0003 | t0009 | g0016 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA19002 | hp2 | a0002 | c0002 | t0010 | g0218 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA19003 | hp1 | a0001 | c0011 | t0016 | g0017 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA19003 | hp2 | a0001 | c0001 | t0005 | g0076 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA19007 | hp1 | a0002 | c0002 | t0010 | g0212 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA19009 | hp1 | a0002 | c0002 | t0003 | g0237 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA19009 | hp2 | a0001 | c0001 | t0005 | g0103 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA19011 | hp1 | a0001 | c0006 | t0002 | g0013 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA19012 | hp1 | a0002 | c0002 | t0003 | g0252 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA19012 | hp2 | a0001 | c0001 | t0069 | g0117 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA19030 | hp1 | a0001 | c0008 | t0003 | g0167 | AFR | LWK | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA19030 | hp2 | a0001 | c0005 | t0049 | g0036 | AFR | LWK | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA19043 | hp1 | a0001 | c0005 | t0019 | g0264 | AFR | LWK | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA19043 | hp2 | a0001 | c0005 | t0003 | g0001 | AFR | LWK | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA19056 | hp2 | a0002 | c0002 | t0068 | g0220 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA19057 | hp1 | a0001 | c0006 | t0002 | g0268 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA19058 | hp1 | a0002 | c0002 | t0066 | g0230 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA19060 | hp1 | a0003 | c0003 | t0002 | g0285 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA19064 | hp2 | a0002 | c0002 | t0027 | g0239 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA19065 | hp1 | a0001 | c0001 | t0039 | g0084 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA19065 | hp2 | a0001 | c0011 | t0016 | g0018 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA19068 | hp1 | a0002 | c0002 | t0004 | g0022 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA19070 | hp1 | a0001 | c0006 | t0002 | g0275 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA19070 | hp2 | a0001 | c0001 | t0005 | g0125 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA19079 | hp1 | a0002 | c0002 | t0004 | g0219 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA19081 | hp1 | a0002 | c0020 | t0022 | g0253 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA19081 | hp2 | a0001 | c0006 | t0002 | g0013 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA19084 | hp2 | a0002 | c0002 | t0003 | g0238 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA19085 | hp1 | a0002 | c0002 | t0003 | g0011 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA19089 | hp2 | a0002 | c0002 | t0062 | g0199 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA19090 | hp1 | a0003 | c0003 | t0002 | g0032 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA19090 | hp2 | a0002 | c0002 | t0003 | g0241 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA19091 | hp1 | a0002 | c0002 | t0004 | g0231 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA19091 | hp2 | a0001 | c0011 | t0016 | g0019 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA19240 | hp1 | a0001 | c0006 | t0002 | g0014 | AFR | YRI | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA19240 | hp2 | a0001 | c0008 | t0007 | g0168 | AFR | YRI | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA20129 | hp1 | a0001 | c0001 | t0025 | g0024 | AFR | ASW | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA20129 | hp2 | a0001 | c0001 | t0021 | g0027 | AFR | ASW | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA20752 | hp1 | a0003 | c0003 | t0009 | g0276 | EUR | TSI | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA20752 | hp2 | a0002 | c0002 | t0003 | g0251 | EUR | TSI | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG01123 | hp1 | a0001 | c0006 | t0002 | g0271 | AMR | CLM | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG01123 | hp2 | a0002 | c0002 | t0003 | g0250 | AMR | CLM | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02109 | hp1 | a0001 | c0001 | t0025 | g0025 | AFR | ACB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02109 | hp2 | a0002 | c0002 | t0007 | g0044 | AFR | ACB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02486 | hp1 | a0003 | c0003 | t0002 | g0291 | AFR | ACB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02486 | hp2 | a0002 | c0002 | t0003 | g0195 | AFR | ACB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02559 | hp1 | a0001 | c0001 | t0059 | g0118 | AFR | ACB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG02559 | hp2 | a0001 | c0007 | t0012 | g0170 | AFR | ACB | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG03471 | hp1 | a0001 | c0001 | t0015 | g0157 | AFR | MSL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG03471 | hp2 | a0001 | c0012 | t0024 | g0034 | AFR | MSL | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG06807 | hp1 | a0004 | c0004 | t0013 | g0183 | AFR | USA | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
HG06807 | hp2 | a0002 | c0002 | t0004 | g0217 | AFR | USA | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA18955 | hp1 | a0003 | c0003 | t0009 | g0016 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA18955 | hp2 | a0001 | c0001 | t0005 | g0064 | EAS | JPT | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA20300 | hp1 | a0001 | c0021 | t0036 | g0070 | AFR | USA | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | USA | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA21309 | hp1 | a0001 | c0001 | t0011 | g0150 | AFR | LWK | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
NA21309 | hp2 | a0008 | c0019 | t0013 | g0190 | AFR | LWK | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0144 | REF | REF | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
homoSapiens | grch38p0 | a0004 | c0004 | t0064 | g0177 | REF | REF | PHIP_chr6_78929419_79083254 | PHIP | chr6 | 78929419 | 79083254 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:78946145 | C | T | 1 | a0007 | 1 | NA18995.hp2 | missense_variant | MODERATE | c.4486G>A | p.Gly1496Ser | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 38/40 | 4672/11926 | 4486/5466 | 1496/1821 | chr6 | 78946145 | |||
chr6:78963145 | C | T | 1 | a0005 | 1 | HG00558.hp2 | missense_variant | MODERATE | c.3487G>A | p.Glu1163Lys | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 30/40 | 3673/11926 | 3487/5466 | 1163/1821 | chr6 | 78963145 | |||
chr6:78965984 | A | G | 2 | a0002 a0007 |
86 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(83): Show |
missense_variant | MODERATE | c.3278T>C | p.Leu1093Pro | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 28/40 | 3464/11926 | 3278/5466 | 1093/1821 | chr6 | 78965984 | |||
chr6:78983034 | G | A | 1 | a0003 | 33 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(30): Show |
missense_variant | MODERATE | c.2621C>T | p.Thr874Ile | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/40 | 2807/11926 | 2621/5466 | 874/1821 | chr6 | 78983034 | |||
chr6:78997475 | G | A | 1 | a0006 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.2140C>T | p.Arg714Trp | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/40 | 2326/11926 | 2140/5466 | 714/1821 | chr6 | 78997475 | |||
chr6:78998283 | A | C | 6 | a0001 a0002 a0003 others(3): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
missense_variant | MODERATE | c.1988T>G | p.Val663Gly | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 18/40 | 2174/11926 | 1988/5466 | 663/1821 | chr6 | 78998283 | |||
chr6:79015709 | T | C | 1 | a0008 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.1310A>G | p.Asn437Ser | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 14/40 | 1496/11926 | 1310/5466 | 437/1821 | chr6 | 79015709 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:78946760 | T | G | 1 | a0001c0011 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
synonymous_variant | LOW | c.4321A>C | p.Arg1441Arg | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 37/40 | 4507/11926 | 4321/5466 | 1441/1821 | chr6 | 78946760 | |||
chr6:78946800 | A | G | 1 | a0001c0013 | 1 | HG03041.hp2 | synonymous_variant | LOW | c.4281T>C | p.Ser1427Ser | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 37/40 | 4467/11926 | 4281/5466 | 1427/1821 | chr6 | 78946800 | |||
chr6:78946845 | A | T | 7 | a0001c0008 a0001c0013 a0002c0002 others(4): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(88): Show |
synonymous_variant | LOW | c.4236T>A | p.Ala1412Ala | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 37/40 | 4422/11926 | 4236/5466 | 1412/1821 | chr6 | 78946845 | |||
chr6:78946853 | G | A | 9 | a0001c0007 a0001c0008 a0001c0010 others(6): Show |
101 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(98): Show |
synonymous_variant | LOW | c.4228C>T | p.Leu1410Leu | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 37/40 | 4414/11926 | 4228/5466 | 1410/1821 | chr6 | 78946853 | |||
chr6:78947674 | G | A | 4 | a0001c0001 a0001c0021 a0005c0016 others(1): Show |
125 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(122): Show |
synonymous_variant | LOW | c.4155C>T | p.Val1385Val | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 36/40 | 4341/11926 | 4155/5466 | 1385/1821 | chr6 | 78947674 | |||
chr6:78969860 | A | G | 8 | a0001c0001 a0001c0005 a0001c0011 others(5): Show |
147 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(144): Show |
synonymous_variant | LOW | c.3180T>C | p.Asp1060Asp | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/40 | 3366/11926 | 3180/5466 | 1060/1821 | chr6 | 78969860 | |||
chr6:78978649 | T | C | 1 | a0002c0009 | 4 | HG00738.hp1 HG01106.hp1 HG01257.hp2 others(1): Show |
synonymous_variant | LOW | c.2832A>G | p.Thr944Thr | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/40 | 3018/11926 | 2832/5466 | 944/1821 | chr6 | 78978649 | |||
chr6:78990931 | C | T | 2 | a0001c0012 a0001c0015 |
2 | HG03209.hp2 HG03471.hp2 |
synonymous_variant | LOW | c.2256G>A | p.Arg752Arg | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 20/40 | 2442/11926 | 2256/5466 | 752/1821 | chr6 | 78990931 | |||
chr6:78997467 | C | A | 1 | a0001c0011 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
synonymous_variant | LOW | c.2148G>T | p.Leu716Leu | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/40 | 2334/11926 | 2148/5466 | 716/1821 | chr6 | 78997467 | |||
chr6:79017564 | C | T | 1 | a0001c0007 | 7 | HG02559.hp2 HG02622.hp2 HG02809.hp1 others(4): Show |
synonymous_variant | LOW | c.1014G>A | p.Thr338Thr | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 11/40 | 1200/11926 | 1014/5466 | 338/1821 | chr6 | 79017564 | |||
chr6:79019114 | T | C | 1 | a0002c0020 | 1 | NA19081.hp1 | synonymous_variant | LOW | c.969A>G | p.Gln323Gln | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 10/40 | 1155/11926 | 969/5466 | 323/1821 | chr6 | 79019114 | |||
chr6:79026042 | T | C | 1 | a0001c0021 | 1 | NA20300.hp1 | synonymous_variant | LOW | c.723A>G | p.Ala241Ala | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 8/40 | 909/11926 | 723/5466 | 241/1821 | chr6 | 79026042 | |||
chr6:79026162 | A | G | 1 | a0002c0014 | 1 | HG00642.hp2 | splice_region_variant&synonymous_variant | LOW | c.603T>C | p.Gly201Gly | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 8/40 | 789/11926 | 603/5466 | 201/1821 | chr6 | 79026162 | |||
chr6:79042879 | A | G | 2 | a0001c0008 a0001c0013 |
5 | HG02280.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
synonymous_variant | LOW | c.564T>C | p.Cys188Cys | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/40 | 750/11926 | 564/5466 | 188/1821 | chr6 | 79042879 | |||
chr6:79042993 | C | G | 1 | a0001c0012 | 1 | HG03471.hp2 | synonymous_variant | LOW | c.450G>C | p.Leu150Leu | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/40 | 636/11926 | 450/5466 | 150/1821 | chr6 | 79042993 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:78934770 | C | G | 1 | a0001c0001t0059 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5923G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 5923 | chr6 | 78934770 | ||||||
chr6:78935410 | ATT | A | 1 | a0001c0011t0016 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5281_*5282delAA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 5281 | chr6 | 78935410 | ||||||
chr6:78935440 | C | CCCTTT | 1 | a0001c0011t0016 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5252_*5253insAAAG others(1): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 5252 | chr6 | 78935440 | ||||||
chr6:78935449 | CTTT | C | 1 | a0001c0011t0016 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5241_*5243delAAA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 5241 | chr6 | 78935449 | ||||||
chr6:78935505 | G | A | 1 | a0001c0001t0035 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5188C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 5188 | chr6 | 78935505 | ||||||
chr6:78936028 | G | A | 1 | a0001c0001t0026 | 2 | HG02976.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4665C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 4665 | chr6 | 78936028 | ||||||
chr6:78936060 | C | T | 1 | a0001c0011t0016 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4633G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 4633 | chr6 | 78936060 | ||||||
chr6:78936203 | A | C | 2 | a0001c0001t0037 a0001c0001t0044 |
2 | HG00639.hp2 HG01258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4490T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 4490 | chr6 | 78936203 | ||||||
chr6:78936330 | A | G | 2 | a0002c0002t0022 a0002c0020t0022 |
3 | NA18982.hp2 NA18988.hp1 NA19081.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4363T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 4363 | chr6 | 78936330 | ||||||
chr6:78936406 | A | C | 3 | a0001c0001t0059 a0001c0005t0023 a0001c0005t0030 |
5 | HG01884.hp2 HG02559.hp1 HG02976.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4287T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 4287 | chr6 | 78936406 | ||||||
chr6:78936437 | T | C | 1 | a0002c0002t0028 | 2 | HG01981.hp2 HG02004.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4256A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 4256 | chr6 | 78936437 | ||||||
chr6:78936723 | T | C | 1 | a0001c0005t0049 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3970A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 3970 | chr6 | 78936723 | ||||||
chr6:78936816 | A | G | 1 | a0001c0001t0034 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3877T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 3877 | chr6 | 78936816 | ||||||
chr6:78936846 | G | T | 1 | a0001c0001t0033 | 1 | HG00280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3847C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 3847 | chr6 | 78936846 | ||||||
chr6:78936858 | A | G | 30 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0011 others(27): Show |
129 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*3835T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 3835 | chr6 | 78936858 | ||||||
chr6:78937114 | C | T | 1 | a0001c0021t0036 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3579G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 3579 | chr6 | 78937114 | ||||||
chr6:78937256 | T | C | 1 | a0001c0011t0016 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3437A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 3437 | chr6 | 78937256 | ||||||
chr6:78937530 | A | G | 1 | a0001c0021t0036 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3163T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 3163 | chr6 | 78937530 | ||||||
chr6:78937646 | G | A | 3 | a0001c0001t0014 a0001c0001t0015 a0001c0001t0033 |
9 | HG00280.hp2 HG00639.hp1 HG01175.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3047C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 3047 | chr6 | 78937646 | ||||||
chr6:78937678 | G | A | 1 | a0001c0010t0029 | 2 | HG02965.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3015C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 3015 | chr6 | 78937678 | ||||||
chr6:78937690 | GT | G | 17 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0032 others(14): Show |
95 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*3002delA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 3002 | chr6 | 78937690 | ||||||
chr6:78937695 | T | C | 1 | a0004c0004t0006 | 12 | HG00735.hp2 HG01106.hp2 HG01255.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2998A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 2998 | chr6 | 78937695 | ||||||
chr6:78937727 | T | C | 2 | a0001c0005t0038 a0001c0005t0045 |
2 | HG02818.hp1 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2966A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 2966 | chr6 | 78937727 | ||||||
chr6:78937732 | G | C | 1 | a0001c0001t0039 | 1 | NA19065.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2961C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 2961 | chr6 | 78937732 | ||||||
chr6:78937869 | G | A | 2 | a0001c0005t0054 a0001c0005t0055 |
2 | HG02723.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2824C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 2824 | chr6 | 78937869 | ||||||
chr6:78937959 | G | A | 1 | a0001c0011t0016 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2734C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 2734 | chr6 | 78937959 | ||||||
chr6:78937994 | A | G | 1 | a0003c0003t0061 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2699T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 2699 | chr6 | 78937994 | ||||||
chr6:78938311 | A | G | 2 | a0001c0001t0017 a0001c0001t0025 |
5 | HG01891.hp1 HG02109.hp1 HG03098.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2382T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 2382 | chr6 | 78938311 | ||||||
chr6:78938315 | G | A | 1 | a0001c0005t0055 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2378C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 2378 | chr6 | 78938315 | ||||||
chr6:78938333 | A | G | 1 | a0001c0010t0057 | 1 | HG01358.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2360T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 2360 | chr6 | 78938333 | ||||||
chr6:78938547 | A | G | 2 | a0001c0007t0012 a0001c0007t0047 |
7 | HG02559.hp2 HG02622.hp2 HG02809.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2146T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 2146 | chr6 | 78938547 | ||||||
chr6:78938667 | T | G | 1 | a0002c0002t0053 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2026A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 2026 | chr6 | 78938667 | ||||||
chr6:78938953 | T | G | 1 | a0001c0001t0040 | 1 | HG00642.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1740A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 1740 | chr6 | 78938953 | ||||||
chr6:78938975 | T | C | 1 | a0002c0002t0051 | 1 | HG02148.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1718A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 1718 | chr6 | 78938975 | ||||||
chr6:78939079 | A | T | 4 | a0004c0004t0006 a0004c0004t0013 a0004c0004t0065 others(1): Show |
18 | HG00735.hp2 HG01106.hp2 HG01255.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1614T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 1614 | chr6 | 78939079 | ||||||
chr6:78939085 | A | T | 2 | a0002c0002t0048 a0002c0002t0053 |
2 | HG02572.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1608T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 1608 | chr6 | 78939085 | ||||||
chr6:78939361 | G | A | 1 | a0001c0006t0020 | 3 | NA18944.hp1 NA18965.hp2 NA18998.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1332C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 1332 | chr6 | 78939361 | ||||||
chr6:78939524 | A | T | 1 | a0002c0002t0066 | 1 | NA19058.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1169T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 1169 | chr6 | 78939524 | ||||||
chr6:78939595 | A | G | 1 | a0003c0003t0060 | 1 | HG01261.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1098T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 1098 | chr6 | 78939595 | ||||||
chr6:78939894 | C | A | 1 | a0002c0002t0063 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*799G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 799 | chr6 | 78939894 | ||||||
chr6:78939908 | A | C | 2 | a0001c0007t0012 a0001c0007t0047 |
7 | HG02559.hp2 HG02622.hp2 HG02809.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*785T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 785 | chr6 | 78939908 | ||||||
chr6:78939994 | T | C | 1 | a0001c0001t0041 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*699A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 699 | chr6 | 78939994 | ||||||
chr6:78939996 | T | C | 1 | a0002c0002t0068 | 1 | NA19056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*697A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 697 | chr6 | 78939996 | ||||||
chr6:78940076 | T | TAA | 76 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0011 others(73): Show |
270 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(267): Show |
3_prime_UTR_variant | MODIFIER | c.*616_*617insTT | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 616 | chr6 | 78940076 | ||||||
chr6:78940120 | T | C | 1 | a0001c0001t0042 | 1 | NA18945.hp1 | 3_prime_UTR_variant | MODIFIER | c.*573A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 573 | chr6 | 78940120 | ||||||
chr6:78940165 | C | T | 2 | a0001c0005t0019 a0001c0005t0046 |
4 | HG03041.hp1 HG03130.hp1 HG03516.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*528G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 528 | chr6 | 78940165 | ||||||
chr6:78940496 | TTA | T | 51 | a0001c0001t0050 a0001c0001t0067 a0001c0005t0003 others(48): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(179): Show |
3_prime_UTR_variant | MODIFIER | c.*195_*196delTA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 195 | chr6 | 78940496 | ||||||
chr6:78940496 | TTATA | T | 31 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0011 others(28): Show |
132 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(129): Show |
3_prime_UTR_variant | MODIFIER | c.*193_*196delTATA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 193 | chr6 | 78940496 | ||||||
chr6:78940543 | A | AGTTT | 1 | a0001c0001t0021 | 3 | HG02922.hp2 NA18906.hp1 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*146_*149dupAAAC | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 149 | chr6 | 78940543 | ||||||
chr6:78940548 | G | GT | 8 | a0001c0006t0009 a0001c0006t0020 a0001c0008t0007 others(5): Show |
23 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*144dupA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 144 | chr6 | 78940548 | ||||||
chr6:78940548 | G | GTT | 13 | a0001c0005t0003 a0001c0005t0019 a0001c0005t0054 others(10): Show |
48 | HG00438.hp2 HG00642.hp2 HG01074.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*143_*144dupAA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 144 | chr6 | 78940548 | ||||||
chr6:78940548 | G | GTTT | 10 | a0001c0001t0044 a0001c0001t0050 a0001c0005t0045 others(7): Show |
17 | HG00673.hp2 HG01258.hp1 HG02055.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*142_*144dupAAA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 144 | chr6 | 78940548 | ||||||
chr6:78940548 | G | GTTTT | 15 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0025 others(12): Show |
79 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*141_*144dupAAAA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 144 | chr6 | 78940548 | ||||||
chr6:78940548 | G | GTTTTT | 9 | a0001c0001t0005 a0001c0001t0015 a0001c0001t0017 others(6): Show |
37 | HG00280.hp2 HG00621.hp2 HG00639.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*140_*144dupAAAAA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 144 | chr6 | 78940548 | ||||||
chr6:78940548 | G | GTTTTTT | 3 | a0001c0001t0014 a0001c0001t0032 a0001c0005t0023 |
7 | HG01175.hp1 HG02145.hp1 HG02165.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*139_*144dupAAAAAA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 144 | chr6 | 78940548 | ||||||
chr6:78940548 | G | T | 1 | a0001c0001t0043 | 1 | NA18944.hp2 | 3_prime_UTR_variant | MODIFIER | c.*145C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 145 | chr6 | 78940548 | ||||||
chr6:78940548 | GT | G | 3 | a0002c0002t0010 a0003c0003t0031 a0004c0004t0065 |
10 | HG00558.hp1 HG01070.hp1 HG02080.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*144delA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 144 | chr6 | 78940548 | ||||||
chr6:78940548 | GTT | G | 8 | a0001c0001t0067 a0002c0002t0004 a0002c0002t0022 others(5): Show |
29 | HG00621.hp1 HG00733.hp1 HG00738.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*143_*144delAA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 143 | chr6 | 78940548 | ||||||
chr6:78940548 | GTTTTTTT others(3): Show |
G | 1 | a0001c0001t0069 | 1 | NA19012.hp2 | 3_prime_UTR_variant | MODIFIER | c.*135_*144delAAAAAA others(4): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 135 | chr6 | 78940548 | ||||||
chr6:78940551 | T | G | 1 | a0001c0011t0016 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
3_prime_UTR_variant | MODIFIER | c.*142A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 142 | chr6 | 78940551 | ||||||
chr6:78940558 | T | TTTTGTTT others(6): Show |
1 | a0001c0011t0016 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
3_prime_UTR_variant | MODIFIER | c.*134_*135insCAAAAC others(7): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 40/40 | 134 | chr6 | 78940558 | ||||||
chr6:79078252 | A | G | 1 | a0001c0011t0016 | 3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
5_prime_UTR_variant | MODIFIER | c.-184T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 1/40 | 184 | chr6 | 79078252 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:78941559 | T | C | 6 | a0001c0005t0023g0049 a0001c0005t0023g0051 a0001c0005t0030g0048 others(3): Show |
6 | HG01884.hp2 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.4829-229A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78941559 | |||||||
chr6:78941599 | G | T | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.4829-269C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78941599 | |||||||
chr6:78941685 | T | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.4829-355A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78941685 | |||||||
chr6:78941727 | T | C | 4 | a0001c0001t0011g0150 a0001c0001t0011g0151 a0001c0001t0011g0153 others(1): Show |
4 | HG02055.hp1 HG02809.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.4829-397A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78941727 | |||||||
chr6:78941760 | G | A | 2 | a0001c0012t0024g0034 a0001c0015t0024g0035 |
2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.4829-430C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78941760 | |||||||
chr6:78941955 | T | C | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.4829-625A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78941955 | |||||||
chr6:78942016 | C | CAGT | 10 | a0004c0004t0006g0007 a0004c0004t0006g0008 a0004c0004t0006g0179 others(7): Show |
12 | HG00735.hp2 HG01106.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.4829-689_4829-687d others(5): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78942016 | |||||||
chr6:78942202 | G | T | 1 | a0001c0001t0001g0100 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.4829-872C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78942202 | |||||||
chr6:78942258 | G | A | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.4829-928C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78942258 | |||||||
chr6:78942311 | C | T | 8 | a0001c0005t0003g0001 a0001c0005t0019g0012 a0001c0005t0019g0264 others(5): Show |
11 | HG01109.hp2 HG02280.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.4829-981G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78942311 | |||||||
chr6:78942313 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.4829-983A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78942313 | |||||||
chr6:78942616 | T | C | 10 | a0001c0005t0003g0001 a0001c0005t0019g0012 a0001c0005t0019g0264 others(7): Show |
13 | HG01109.hp2 HG02280.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.4829-1286A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78942616 | |||||||
chr6:78942665 | G | C | 1 | a0001c0001t0005g0099 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.4829-1335C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78942665 | |||||||
chr6:78942678 | T | G | 1 | a0001c0001t0001g0101 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.4829-1348A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78942678 | |||||||
chr6:78942751 | A | C | 1 | a0001c0001t0017g0023 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.4829-1421T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78942751 | |||||||
chr6:78942946 | A | G | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.4829-1616T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78942946 | |||||||
chr6:78943061 | C | T | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.4829-1731G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78943061 | |||||||
chr6:78943126 | T | C | 1 | a0004c0004t0013g0178 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4829-1796A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78943126 | |||||||
chr6:78943159 | G | A | 4 | a0001c0006t0002g0265 a0001c0006t0002g0267 a0001c0006t0009g0266 others(1): Show |
4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.4829-1829C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78943159 | |||||||
chr6:78943171 | A | C | 2 | a0001c0006t0020g0006 a0001c0006t0020g0148 |
3 | NA18944.hp1 NA18965.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.4829-1841T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78943171 | |||||||
chr6:78943182 | C | T | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.4829-1852G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78943182 | |||||||
chr6:78943481 | G | A | 2 | a0001c0006t0020g0006 a0001c0006t0020g0148 |
3 | NA18944.hp1 NA18965.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.4828+1819C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78943481 | |||||||
chr6:78943490 | C | T | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.4828+1810G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78943490 | |||||||
chr6:78943752 | C | T | 2 | a0001c0006t0020g0006 a0001c0006t0020g0148 |
3 | NA18944.hp1 NA18965.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.4828+1548G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78943752 | |||||||
chr6:78943823 | T | C | 2 | a0004c0004t0006g0186 a0004c0004t0006g0187 |
2 | HG01358.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.4828+1477A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78943823 | |||||||
chr6:78943889 | G | A | 1 | a0001c0005t0003g0001 | 3 | HG02280.hp1 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.4828+1411C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78943889 | |||||||
chr6:78943962 | G | A | 2 | a0001c0010t0029g0053 a0001c0010t0029g0054 |
2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.4828+1338C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78943962 | |||||||
chr6:78943983 | C | CT | 6 | a0001c0005t0049g0036 a0001c0005t0055g0045 a0001c0006t0002g0265 others(3): Show |
6 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.4828+1316dupA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78943983 | |||||||
chr6:78943988 | T | TA | 94 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(91): Show |
95 | HG00140.hp1 HG00280.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.4828+1311_4828+131 others(5): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78943988 | |||||||
chr6:78943988 | T | TAA | 13 | a0001c0001t0001g0060 a0001c0001t0001g0069 a0001c0001t0001g0091 others(10): Show |
13 | HG01070.hp2 HG01071.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.4828+1311_4828+131 others(6): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78943988 | |||||||
chr6:78943988 | T | TAAA | 3 | a0001c0001t0011g0255 a0001c0001t0037g0055 a0001c0001t0044g0056 |
3 | HG00639.hp2 HG01258.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.4828+1311_4828+131 others(7): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78943988 | |||||||
chr6:78943989 | T | A | 126 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(123): Show |
127 | HG00140.hp1 HG00280.hp2 HG00558.hp2 others(124): Show |
intron_variant | MODIFIER | c.4828+1311A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78943989 | |||||||
chr6:78943989 | T | TA | 83 | a0001c0001t0001g0092 a0001c0007t0012g0170 a0001c0007t0012g0171 others(80): Show |
87 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.4828+1310_4828+131 others(5): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78943989 | |||||||
chr6:78943989 | T | TAA | 4 | a0001c0010t0057g0163 a0002c0002t0003g0262 a0002c0002t0008g0246 others(1): Show |
4 | HG01358.hp1 HG02055.hp2 HG02080.hp2 others(1): Show |
intron_variant | MODIFIER | c.4828+1310_4828+131 others(6): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78943989 | |||||||
chr6:78943990 | T | A | 221 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(218): Show |
226 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.4828+1310A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78943990 | |||||||
chr6:78943990 | T | TA | 38 | a0001c0006t0002g0013 a0001c0006t0002g0268 a0001c0006t0002g0269 others(35): Show |
44 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(41): Show |
intron_variant | MODIFIER | c.4828+1309dupT | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78943990 | |||||||
chr6:78943990 | T | TAA | 6 | a0001c0005t0019g0012 a0001c0005t0019g0264 a0001c0005t0046g0263 others(3): Show |
8 | HG02258.hp1 HG03041.hp1 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.4828+1308_4828+130 others(6): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78943990 | |||||||
chr6:78943990 | T | TTA | 2 | a0001c0005t0003g0001 a0001c0005t0054g0038 |
4 | HG02280.hp1 HG02723.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.4828+1309_4828+131 others(6): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78943990 | |||||||
chr6:78944014 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.4828+1286C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78944014 | |||||||
chr6:78944043 | A | C | 4 | a0001c0001t0011g0255 a0001c0001t0011g0256 a0001c0001t0018g0257 others(1): Show |
4 | HG02258.hp2 HG02896.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.4828+1257T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78944043 | |||||||
chr6:78944084 | G | A | 2 | a0001c0006t0002g0265 a0001c0006t0009g0266 |
2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.4828+1216C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78944084 | |||||||
chr6:78944437 | A | T | 96 | a0001c0007t0012g0169 a0001c0007t0012g0170 a0001c0007t0012g0171 others(93): Show |
101 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.4828+863T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78944437 | |||||||
chr6:78944447 | G | C | 4 | a0001c0005t0027g0033 a0001c0006t0008g0037 a0001c0012t0024g0034 others(1): Show |
4 | HG01109.hp2 HG02572.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.4828+853C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78944447 | |||||||
chr6:78944852 | T | G | 3 | a0001c0005t0027g0033 a0001c0012t0024g0034 a0001c0015t0024g0035 |
3 | HG01109.hp2 HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.4828+448A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78944852 | |||||||
chr6:78944938 | A | G | 28 | a0001c0001t0011g0029 a0001c0001t0011g0150 a0001c0001t0011g0151 others(25): Show |
28 | HG00280.hp2 HG00639.hp1 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.4828+362T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78944938 | |||||||
chr6:78944939 | T | C | 1 | a0004c0004t0006g0179 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.4828+361A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78944939 | |||||||
chr6:78944968 | G | GA | 94 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(91): Show |
95 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.4828+331dupT | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78944968 | |||||||
chr6:78945082 | CT | C | 8 | a0001c0005t0003g0001 a0001c0005t0019g0012 a0001c0005t0019g0264 others(5): Show |
11 | HG01109.hp2 HG02280.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.4828+217delA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78945082 | |||||||
chr6:78945166 | A | G | 1 | a0002c0002t0003g0254 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4828+134T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 39/39 | chr6 | 78945166 | |||||||
chr6:78945760 | G | A | 124 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(121): Show |
125 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.4630+241C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 38/39 | chr6 | 78945760 | |||||||
chr6:78946308 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.4371-48G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 37/39 | chr6 | 78946308 | |||||||
chr6:78946926 | T | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.4207-52A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 36/39 | chr6 | 78946926 | |||||||
chr6:78947163 | C | G | 1 | a0001c0001t0001g0107 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.4207-289G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 36/39 | chr6 | 78947163 | |||||||
chr6:78947230 | C | T | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.4207-356G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 36/39 | chr6 | 78947230 | |||||||
chr6:78947231 | G | A | 1 | a0001c0001t0033g0021 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.4207-357C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 36/39 | chr6 | 78947231 | |||||||
chr6:78947247 | C | G | 3 | a0001c0001t0001g0083 a0001c0001t0005g0102 a0001c0001t0039g0084 |
3 | NA18974.hp2 NA19065.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.4207-373G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 36/39 | chr6 | 78947247 | |||||||
chr6:78947311 | G | A | 2 | a0001c0001t0001g0108 a0001c0001t0001g0119 |
2 | HG02735.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.4206+312C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 36/39 | chr6 | 78947311 | |||||||
chr6:78947325 | C | T | 72 | a0002c0002t0003g0010 a0002c0002t0003g0011 a0002c0002t0003g0193 others(69): Show |
75 | HG00558.hp1 HG00621.hp1 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.4206+298G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 36/39 | chr6 | 78947325 | |||||||
chr6:78947602 | G | A | 1 | a0001c0006t0008g0037 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.4206+21C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 36/39 | chr6 | 78947602 | |||||||
chr6:78947614 | ATTAT | A | 10 | a0001c0005t0003g0001 a0001c0005t0019g0012 a0001c0005t0019g0264 others(7): Show |
13 | HG01109.hp2 HG02280.hp1 HG02572.hp1 others(10): Show |
splice_region_variant&intron_variant | LOW | c.4206+5_4206+8delAT others(2): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 36/39 | chr6 | 78947614 | |||||||
chr6:78947935 | C | T | 2 | a0001c0005t0038g0047 a0001c0005t0045g0046 |
2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.4054-160G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78947935 | |||||||
chr6:78947951 | T | TC | 99 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(96): Show |
100 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.4054-177dupG | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78947951 | |||||||
chr6:78948352 | T | C | 1 | a0003c0003t0002g0284 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.4054-577A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78948352 | |||||||
chr6:78948398 | C | G | 40 | a0001c0006t0002g0013 a0001c0006t0002g0014 a0001c0006t0002g0265 others(37): Show |
46 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.4054-623G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78948398 | |||||||
chr6:78948412 | A | C | 4 | a0001c0005t0003g0001 a0001c0005t0019g0012 a0001c0005t0019g0264 others(1): Show |
7 | HG02280.hp1 HG02965.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.4054-637T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78948412 | |||||||
chr6:78948505 | C | A | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.4054-730G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78948505 | |||||||
chr6:78948588 | A | G | 5 | a0001c0001t0017g0023 a0001c0001t0017g0026 a0001c0001t0017g0031 others(2): Show |
5 | HG01891.hp1 HG02109.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.4054-813T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78948588 | |||||||
chr6:78948767 | T | C | 1 | a0001c0005t0038g0047 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4054-992A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78948767 | |||||||
chr6:78948811 | C | T | 6 | a0004c0004t0006g0007 a0004c0004t0006g0008 a0004c0004t0006g0179 others(3): Show |
8 | HG00735.hp2 HG01106.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.4054-1036G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78948811 | |||||||
chr6:78948818 | T | C | 94 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(91): Show |
95 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.4054-1043A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78948818 | |||||||
chr6:78948841 | G | GT | 5 | a0001c0001t0059g0118 a0001c0005t0023g0049 a0001c0005t0023g0051 others(2): Show |
5 | HG01884.hp2 HG02559.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.4054-1067dupA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78948841 | |||||||
chr6:78948887 | C | T | 9 | a0001c0001t0011g0029 a0001c0001t0017g0023 a0001c0001t0017g0026 others(6): Show |
9 | HG01891.hp1 HG02109.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.4054-1112G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78948887 | |||||||
chr6:78948937 | A | T | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.4054-1162T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78948937 | |||||||
chr6:78949116 | G | A | 1 | a0002c0002t0008g0240 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.4054-1341C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78949116 | |||||||
chr6:78949168 | G | A | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.4054-1393C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78949168 | |||||||
chr6:78949174 | G | A | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.4054-1399C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78949174 | |||||||
chr6:78949200 | T | C | 1 | a0001c0001t0011g0150 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.4054-1425A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78949200 | |||||||
chr6:78949315 | G | A | 4 | a0001c0001t0001g0101 a0001c0001t0001g0110 a0001c0001t0005g0099 others(1): Show |
4 | HG00642.hp1 HG02698.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.4054-1540C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78949315 | |||||||
chr6:78949325 | G | A | 1 | a0002c0002t0008g0200 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.4054-1550C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78949325 | |||||||
chr6:78949367 | A | G | 1 | a0001c0001t0005g0052 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.4054-1592T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78949367 | |||||||
chr6:78949453 | A | G | 133 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(130): Show |
134 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.4054-1678T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78949453 | |||||||
chr6:78949488 | G | A | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.4054-1713C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78949488 | |||||||
chr6:78949662 | C | T | 1 | a0001c0001t0015g0156 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.4054-1887G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78949662 | |||||||
chr6:78949696 | T | G | 86 | a0001c0001t0001g0121 a0001c0001t0001g0131 a0001c0010t0057g0163 others(83): Show |
91 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(88): Show |
intron_variant | MODIFIER | c.4054-1921A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78949696 | |||||||
chr6:78949696 | T | TG | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.4054-1922_4054-192 others(5): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78949696 | |||||||
chr6:78949737 | A | G | 1 | a0001c0010t0029g0054 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.4054-1962T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78949737 | |||||||
chr6:78949950 | A | G | 1 | a0001c0001t0005g0109 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.4054-2175T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78949950 | |||||||
chr6:78950174 | A | T | 1 | a0001c0001t0005g0078 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.4054-2399T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78950174 | |||||||
chr6:78950455 | A | G | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.4054-2680T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78950455 | |||||||
chr6:78950688 | ATGC | A | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.4054-2916_4054-291 others(7): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78950688 | |||||||
chr6:78950759 | C | G | 1 | a0001c0001t0005g0082 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.4054-2984G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78950759 | |||||||
chr6:78950818 | ATTG | A | 28 | a0001c0001t0011g0029 a0001c0001t0011g0150 a0001c0001t0011g0151 others(25): Show |
28 | HG00280.hp2 HG00639.hp1 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.4054-3046_4054-304 others(7): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78950818 | |||||||
chr6:78950882 | T | C | 1 | a0002c0002t0003g0243 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.4054-3107A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78950882 | |||||||
chr6:78950930 | C | G | 2 | a0001c0001t0001g0097 a0001c0001t0001g0098 |
2 | NA18941.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.4054-3155G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78950930 | |||||||
chr6:78951018 | C | T | 1 | a0001c0006t0008g0037 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.4054-3243G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78951018 | |||||||
chr6:78951195 | G | T | 19 | a0001c0001t0011g0150 a0001c0001t0011g0151 a0001c0001t0011g0153 others(16): Show |
19 | HG00280.hp2 HG00639.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.4054-3420C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78951195 | |||||||
chr6:78951219 | T | G | 1 | a0002c0002t0004g0213 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.4054-3444A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78951219 | |||||||
chr6:78951235 | T | A | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.4054-3460A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78951235 | |||||||
chr6:78951336 | A | T | 2 | a0001c0008t0003g0167 a0001c0008t0007g0165 |
2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4053+3478T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78951336 | |||||||
chr6:78951341 | C | T | 1 | a0002c0002t0004g0223 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.4053+3473G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78951341 | |||||||
chr6:78951408 | T | C | 128 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(125): Show |
129 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.4053+3406A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78951408 | |||||||
chr6:78951434 | T | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.4053+3380A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78951434 | |||||||
chr6:78951464 | G | A | 6 | a0002c0002t0004g0219 a0002c0002t0004g0223 a0002c0002t0004g0227 others(3): Show |
6 | NA18941.hp2 NA18959.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.4053+3350C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78951464 | |||||||
chr6:78951535 | G | A | 7 | a0001c0005t0003g0001 a0001c0005t0019g0012 a0001c0005t0019g0264 others(4): Show |
10 | HG02280.hp1 HG02723.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.4053+3279C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78951535 | |||||||
chr6:78951580 | A | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.4053+3234T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78951580 | |||||||
chr6:78951739 | T | C | 1 | a0001c0005t0030g0048 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.4053+3075A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78951739 | |||||||
chr6:78951913 | T | C | 2 | a0002c0002t0004g0208 a0002c0002t0008g0209 |
2 | HG03669.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.4053+2901A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78951913 | |||||||
chr6:78951925 | T | C | 4 | a0001c0001t0011g0255 a0001c0001t0011g0256 a0001c0001t0018g0257 others(1): Show |
4 | HG02258.hp2 HG02896.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.4053+2889A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78951925 | |||||||
chr6:78951948 | G | C | 5 | a0001c0001t0059g0118 a0001c0005t0023g0049 a0001c0005t0023g0051 others(2): Show |
5 | HG01884.hp2 HG02559.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.4053+2866C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78951948 | |||||||
chr6:78951979 | C | G | 7 | a0001c0007t0012g0169 a0001c0007t0012g0170 a0001c0007t0012g0171 others(4): Show |
7 | HG02559.hp2 HG02622.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.4053+2835G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78951979 | |||||||
chr6:78952009 | A | G | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.4053+2805T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78952009 | |||||||
chr6:78952053 | A | G | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.4053+2761T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78952053 | |||||||
chr6:78952060 | G | T | 72 | a0002c0002t0003g0010 a0002c0002t0003g0011 a0002c0002t0003g0193 others(69): Show |
75 | HG00558.hp1 HG00621.hp1 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.4053+2754C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78952060 | |||||||
chr6:78952176 | T | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.4053+2638A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78952176 | |||||||
chr6:78952213 | G | A | 6 | a0001c0001t0011g0150 a0001c0001t0011g0151 a0001c0001t0011g0153 others(3): Show |
6 | HG02055.hp1 HG02809.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.4053+2601C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78952213 | |||||||
chr6:78952312 | G | A | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.4053+2502C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78952312 | |||||||
chr6:78952417 | CAAAAAAA others(6): Show |
C | 11 | a0001c0001t0014g0160 a0001c0001t0015g0156 a0001c0001t0015g0159 others(8): Show |
11 | HG00099.hp2 HG00639.hp1 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.4053+2384_4053+239 others(17): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78952417 | |||||||
chr6:78952426 | A | G | 1 | a0001c0005t0027g0033 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.4053+2388T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78952426 | |||||||
chr6:78952428 | G | A | 4 | a0001c0005t0003g0001 a0001c0005t0019g0012 a0001c0005t0019g0264 others(1): Show |
7 | HG02280.hp1 HG02965.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.4053+2386C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78952428 | |||||||
chr6:78952429 | A | G | 4 | a0001c0005t0003g0001 a0001c0005t0019g0012 a0001c0005t0019g0264 others(1): Show |
7 | HG02280.hp1 HG02965.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.4053+2385T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78952429 | |||||||
chr6:78952611 | A | G | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.4053+2203T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78952611 | |||||||
chr6:78952667 | G | A | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.4053+2147C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78952667 | |||||||
chr6:78952776 | A | G | 1 | a0001c0005t0003g0001 | 3 | HG02280.hp1 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.4053+2038T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78952776 | |||||||
chr6:78952827 | ACTAT | A | 3 | a0004c0004t0013g0181 a0004c0004t0013g0183 a0004c0004t0065g0182 |
3 | HG02895.hp1 HG02897.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.4053+1983_4053+198 others(8): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78952827 | |||||||
chr6:78953057 | C | T | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.4053+1757G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78953057 | |||||||
chr6:78953246 | G | A | 6 | a0001c0005t0023g0049 a0001c0005t0023g0051 a0001c0005t0030g0048 others(3): Show |
6 | HG01884.hp2 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.4053+1568C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78953246 | |||||||
chr6:78953344 | T | C | 2 | a0001c0012t0024g0034 a0001c0015t0024g0035 |
2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.4053+1470A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78953344 | |||||||
chr6:78953352 | C | A | 96 | a0001c0007t0012g0169 a0001c0007t0012g0170 a0001c0007t0012g0171 others(93): Show |
101 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.4053+1462G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78953352 | |||||||
chr6:78953391 | T | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.4053+1423A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78953391 | |||||||
chr6:78953488 | C | A | 14 | a0002c0002t0003g0201 a0002c0002t0003g0202 a0002c0002t0003g0203 others(11): Show |
14 | HG00642.hp2 HG01123.hp2 HG01975.hp2 others(11): Show |
intron_variant | MODIFIER | c.4053+1326G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78953488 | |||||||
chr6:78953707 | C | T | 36 | a0001c0006t0002g0013 a0001c0006t0002g0014 a0001c0006t0002g0268 others(33): Show |
42 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.4053+1107G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78953707 | |||||||
chr6:78953923 | T | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.4053+891A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78953923 | |||||||
chr6:78954016 | T | A | 1 | a0001c0006t0002g0269 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.4053+798A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78954016 | |||||||
chr6:78954033 | T | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.4053+781A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78954033 | |||||||
chr6:78954157 | G | A | 2 | a0001c0005t0038g0047 a0001c0005t0045g0046 |
2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.4053+657C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78954157 | |||||||
chr6:78954195 | G | A | 2 | a0001c0001t0026g0149 a0001c0001t0026g0154 |
2 | HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.4053+619C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78954195 | |||||||
chr6:78954268 | A | AT | 90 | a0001c0007t0012g0169 a0001c0007t0012g0170 a0001c0007t0012g0171 others(87): Show |
95 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.4053+545dupA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78954268 | |||||||
chr6:78954308 | G | A | 2 | a0001c0005t0038g0047 a0001c0005t0045g0046 |
2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.4053+506C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78954308 | |||||||
chr6:78954366 | A | G | 2 | a0001c0010t0029g0053 a0001c0010t0029g0054 |
2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.4053+448T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78954366 | |||||||
chr6:78954401 | C | T | 19 | a0001c0001t0011g0150 a0001c0001t0011g0151 a0001c0001t0011g0153 others(16): Show |
19 | HG00280.hp2 HG00639.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.4053+413G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78954401 | |||||||
chr6:78954446 | C | T | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.4053+368G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78954446 | |||||||
chr6:78954462 | C | T | 4 | a0001c0005t0027g0033 a0001c0006t0008g0037 a0001c0012t0024g0034 others(1): Show |
4 | HG01109.hp2 HG02572.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.4053+352G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78954462 | |||||||
chr6:78954723 | T | C | 128 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(125): Show |
129 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.4053+91A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78954723 | |||||||
chr6:78954727 | CATAAAAA others(52): Show |
C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.4053+28_4053+86del others(59): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 35/39 | chr6 | 78954727 | |||||||
chr6:78954977 | G | T | 9 | a0001c0007t0012g0169 a0001c0007t0012g0170 a0001c0007t0012g0171 others(6): Show |
9 | HG02559.hp2 HG02622.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.3904-14C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 34/39 | chr6 | 78954977 | |||||||
chr6:78955031 | T | C | 133 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(130): Show |
134 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.3904-68A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 34/39 | chr6 | 78955031 | |||||||
chr6:78955124 | T | A | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3903+108A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 34/39 | chr6 | 78955124 | |||||||
chr6:78955350 | C | T | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3853-68G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 33/39 | chr6 | 78955350 | |||||||
chr6:78955402 | C | A | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3853-120G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 33/39 | chr6 | 78955402 | |||||||
chr6:78955402 | C | G | 2 | a0001c0005t0038g0047 a0001c0005t0045g0046 |
2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.3853-120G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 33/39 | chr6 | 78955402 | |||||||
chr6:78955442 | A | T | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3853-160T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 33/39 | chr6 | 78955442 | |||||||
chr6:78955481 | GT | G | 9 | a0001c0006t0008g0037 a0002c0002t0003g0041 a0002c0002t0003g0042 others(6): Show |
11 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(8): Show |
intron_variant | MODIFIER | c.3852+131delA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 33/39 | chr6 | 78955481 | |||||||
chr6:78955491 | T | C | 1 | a0001c0021t0036g0070 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3852+122A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 33/39 | chr6 | 78955491 | |||||||
chr6:78955493 | T | A | 132 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(129): Show |
133 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.3852+120A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 33/39 | chr6 | 78955493 | |||||||
chr6:78955496 | A | G | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3852+117T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 33/39 | chr6 | 78955496 | |||||||
chr6:78955513 | A | G | 1 | a0001c0001t0001g0128 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.3852+100T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 33/39 | chr6 | 78955513 | |||||||
chr6:78955571 | T | C | 1 | a0001c0005t0054g0038 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3852+42A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 33/39 | chr6 | 78955571 | |||||||
chr6:78955724 | GATA | G | 5 | a0001c0008t0003g0167 a0001c0008t0007g0164 a0001c0008t0007g0165 others(2): Show |
5 | HG02280.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.3783-45_3783-43del others(3): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 32/39 | chr6 | 78955724 | |||||||
chr6:78955860 | A | G | 9 | a0001c0001t0011g0029 a0001c0001t0017g0023 a0001c0001t0017g0026 others(6): Show |
9 | HG01891.hp1 HG02109.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.3783-178T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 32/39 | chr6 | 78955860 | |||||||
chr6:78956030 | T | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3783-348A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 32/39 | chr6 | 78956030 | |||||||
chr6:78956076 | T | C | 1 | a0003c0003t0002g0291 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3783-394A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 32/39 | chr6 | 78956076 | |||||||
chr6:78956148 | C | T | 1 | a0001c0005t0027g0033 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3783-466G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 32/39 | chr6 | 78956148 | |||||||
chr6:78956166 | G | A | 2 | a0001c0005t0054g0038 a0001c0005t0055g0045 |
2 | HG02723.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.3783-484C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 32/39 | chr6 | 78956166 | |||||||
chr6:78956170 | A | G | 1 | a0001c0021t0036g0070 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3783-488T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 32/39 | chr6 | 78956170 | |||||||
chr6:78956210 | C | G | 1 | a0003c0003t0060g0280 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.3783-528G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 32/39 | chr6 | 78956210 | |||||||
chr6:78956408 | A | G | 7 | a0002c0002t0004g0022 a0002c0002t0004g0221 a0002c0002t0004g0229 others(4): Show |
7 | HG02080.hp2 HG02523.hp2 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.3783-726T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 32/39 | chr6 | 78956408 | |||||||
chr6:78956492 | T | G | 2 | a0001c0001t0014g0161 a0001c0001t0014g0162 |
2 | HG02145.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.3783-810A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 32/39 | chr6 | 78956492 | |||||||
chr6:78956605 | T | C | 2 | a0002c0002t0048g0020 a0002c0002t0053g0194 |
2 | HG02572.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.3783-923A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 32/39 | chr6 | 78956605 | |||||||
chr6:78956639 | A | T | 1 | a0001c0001t0001g0107 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.3783-957T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 32/39 | chr6 | 78956639 | |||||||
chr6:78956735 | C | T | 4 | a0001c0005t0003g0001 a0001c0005t0019g0012 a0001c0005t0019g0264 others(1): Show |
7 | HG02280.hp1 HG02965.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.3783-1053G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 32/39 | chr6 | 78956735 | |||||||
chr6:78956778 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3783-1096G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 32/39 | chr6 | 78956778 | |||||||
chr6:78956944 | T | C | 2 | a0001c0007t0012g0171 a0001c0007t0012g0172 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.3783-1262A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 32/39 | chr6 | 78956944 | |||||||
chr6:78956963 | A | G | 1 | a0002c0002t0056g0196 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3783-1281T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 32/39 | chr6 | 78956963 | |||||||
chr6:78957159 | T | C | 9 | a0001c0001t0011g0029 a0001c0001t0017g0023 a0001c0001t0017g0026 others(6): Show |
9 | HG01891.hp1 HG02109.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.3782+1316A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 32/39 | chr6 | 78957159 | |||||||
chr6:78957579 | T | TA | 5 | a0001c0001t0001g0134 a0001c0005t0019g0012 a0001c0005t0019g0264 others(2): Show |
6 | HG02723.hp1 HG03041.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.3782+895dupT | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 32/39 | chr6 | 78957579 | |||||||
chr6:78957642 | C | T | 1 | a0001c0001t0015g0157 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3782+833G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 32/39 | chr6 | 78957642 | |||||||
chr6:78957645 | C | T | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3782+830G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 32/39 | chr6 | 78957645 | |||||||
chr6:78957996 | T | C | 4 | a0001c0005t0023g0049 a0001c0005t0023g0051 a0001c0005t0030g0048 others(1): Show |
4 | HG01884.hp2 HG02976.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.3782+479A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 32/39 | chr6 | 78957996 | |||||||
chr6:78958020 | T | C | 2 | a0001c0012t0024g0034 a0001c0015t0024g0035 |
2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.3782+455A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 32/39 | chr6 | 78958020 | |||||||
chr6:78958032 | C | G | 7 | a0001c0007t0012g0169 a0001c0007t0012g0170 a0001c0007t0012g0171 others(4): Show |
7 | HG02559.hp2 HG02622.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.3782+443G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 32/39 | chr6 | 78958032 | |||||||
chr6:78958248 | C | T | 1 | a0002c0002t0004g0215 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.3782+227G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 32/39 | chr6 | 78958248 | |||||||
chr6:78959086 | A | C | 5 | a0001c0001t0017g0023 a0001c0001t0017g0026 a0001c0001t0017g0031 others(2): Show |
5 | HG01891.hp1 HG02109.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.3657-486T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 31/39 | chr6 | 78959086 | |||||||
chr6:78959180 | A | G | 9 | a0001c0007t0012g0169 a0001c0007t0012g0170 a0001c0007t0012g0171 others(6): Show |
9 | HG02559.hp2 HG02622.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.3657-580T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 31/39 | chr6 | 78959180 | |||||||
chr6:78959194 | G | T | 1 | a0002c0002t0004g0198 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.3657-594C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 31/39 | chr6 | 78959194 | |||||||
chr6:78959211 | C | T | 2 | a0001c0001t0001g0081 a0001c0001t0001g0105 |
2 | HG01978.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.3657-611G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 31/39 | chr6 | 78959211 | |||||||
chr6:78959419 | C | T | 1 | a0006c0018t0001g0087 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3657-819G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 31/39 | chr6 | 78959419 | |||||||
chr6:78959496 | TA | T | 3 | a0001c0005t0019g0012 a0001c0005t0019g0264 a0001c0005t0046g0263 |
4 | HG03041.hp1 HG03130.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.3657-897delT | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 31/39 | chr6 | 78959496 | |||||||
chr6:78959523 | C | T | 4 | a0002c0002t0003g0010 a0002c0002t0003g0244 a0002c0002t0003g0245 others(1): Show |
5 | HG01074.hp2 HG02055.hp2 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.3657-923G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 31/39 | chr6 | 78959523 | |||||||
chr6:78959597 | T | C | 1 | a0001c0005t0003g0001 | 3 | HG02280.hp1 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3657-997A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 31/39 | chr6 | 78959597 | |||||||
chr6:78959818 | T | G | 11 | a0001c0005t0003g0001 a0001c0005t0019g0012 a0001c0005t0019g0264 others(8): Show |
14 | HG01109.hp2 HG02280.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.3657-1218A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 31/39 | chr6 | 78959818 | |||||||
chr6:78959842 | T | C | 1 | a0001c0001t0001g0135 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.3657-1242A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 31/39 | chr6 | 78959842 | |||||||
chr6:78960078 | T | A | 1 | a0002c0002t0008g0240 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.3657-1478A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 31/39 | chr6 | 78960078 | |||||||
chr6:78960450 | C | CT | 8 | a0001c0005t0023g0049 a0001c0005t0023g0051 a0001c0005t0030g0048 others(5): Show |
8 | HG01884.hp2 HG02976.hp1 NA18522.hp2 others(5): Show |
intron_variant | MODIFIER | c.3656+1239dupA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 31/39 | chr6 | 78960450 | |||||||
chr6:78960450 | CT | C | 10 | a0001c0007t0012g0169 a0001c0007t0012g0170 a0001c0007t0012g0171 others(7): Show |
10 | HG02559.hp2 HG02622.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.3656+1239delA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 31/39 | chr6 | 78960450 | |||||||
chr6:78960465 | T | C | 1 | a0006c0018t0001g0087 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3656+1225A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 31/39 | chr6 | 78960465 | |||||||
chr6:78960484 | C | A | 2 | a0001c0005t0054g0038 a0001c0005t0055g0045 |
2 | HG02723.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.3656+1206G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 31/39 | chr6 | 78960484 | |||||||
chr6:78960507 | G | A | 2 | a0001c0005t0054g0038 a0001c0005t0055g0045 |
2 | HG02723.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.3656+1183C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 31/39 | chr6 | 78960507 | |||||||
chr6:78960642 | G | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3656+1048C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 31/39 | chr6 | 78960642 | |||||||
chr6:78960895 | T | C | 1 | a0001c0001t0001g0300 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.3656+795A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 31/39 | chr6 | 78960895 | |||||||
chr6:78960914 | G | A | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3656+776C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 31/39 | chr6 | 78960914 | |||||||
chr6:78960948 | A | G | 1 | a0001c0005t0019g0264 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3656+742T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 31/39 | chr6 | 78960948 | |||||||
chr6:78961242 | T | C | 1 | a0002c0009t0004g0214 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.3656+448A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 31/39 | chr6 | 78961242 | |||||||
chr6:78961256 | C | T | 283 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(280): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.3656+434G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 31/39 | chr6 | 78961256 | |||||||
chr6:78961285 | C | T | 1 | a0002c0002t0063g0176 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3656+405G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 31/39 | chr6 | 78961285 | |||||||
chr6:78961366 | C | T | 2 | a0002c0002t0003g0201 a0002c0002t0003g0202 |
2 | NA18974.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.3656+324G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 31/39 | chr6 | 78961366 | |||||||
chr6:78961383 | A | C | 1 | a0001c0005t0003g0001 | 3 | HG02280.hp1 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3656+307T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 31/39 | chr6 | 78961383 | |||||||
chr6:78961428 | G | A | 7 | a0004c0004t0006g0007 a0004c0004t0006g0008 a0004c0004t0006g0179 others(4): Show |
9 | HG00735.hp2 HG01106.hp2 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.3656+262C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 31/39 | chr6 | 78961428 | |||||||
chr6:78961635 | G | C | 15 | a0002c0002t0003g0201 a0002c0002t0003g0202 a0002c0002t0003g0203 others(12): Show |
15 | HG00642.hp2 HG01123.hp2 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.3656+55C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 31/39 | chr6 | 78961635 | |||||||
chr6:78961914 | C | G | 1 | a0001c0005t0003g0001 | 3 | HG02280.hp1 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3536-104G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 30/39 | chr6 | 78961914 | |||||||
chr6:78962016 | T | C | 40 | a0001c0006t0002g0013 a0001c0006t0002g0014 a0001c0006t0002g0265 others(37): Show |
46 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.3536-206A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 30/39 | chr6 | 78962016 | |||||||
chr6:78962028 | T | C | 4 | a0001c0005t0027g0033 a0001c0006t0008g0037 a0001c0012t0024g0034 others(1): Show |
4 | HG01109.hp2 HG02572.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.3536-218A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 30/39 | chr6 | 78962028 | |||||||
chr6:78962196 | C | G | 11 | a0001c0005t0003g0001 a0001c0005t0019g0012 a0001c0005t0019g0264 others(8): Show |
14 | HG01109.hp2 HG02280.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.3536-386G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 30/39 | chr6 | 78962196 | |||||||
chr6:78962416 | G | T | 124 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(121): Show |
125 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.3536-606C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 30/39 | chr6 | 78962416 | |||||||
chr6:78962502 | CTCT | C | 5 | a0001c0008t0003g0167 a0001c0008t0007g0164 a0001c0008t0007g0165 others(2): Show |
5 | HG02280.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.3535+592_3535+594d others(5): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 30/39 | chr6 | 78962502 | |||||||
chr6:78962578 | C | T | 1 | a0001c0005t0049g0036 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3535+519G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 30/39 | chr6 | 78962578 | |||||||
chr6:78962586 | A | C | 1 | a0001c0001t0005g0052 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.3535+511T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 30/39 | chr6 | 78962586 | |||||||
chr6:78962630 | G | T | 3 | a0001c0005t0019g0012 a0001c0005t0019g0264 a0001c0005t0046g0263 |
4 | HG03041.hp1 HG03130.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.3535+467C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 30/39 | chr6 | 78962630 | |||||||
chr6:78962721 | T | C | 96 | a0001c0007t0012g0169 a0001c0007t0012g0170 a0001c0007t0012g0171 others(93): Show |
101 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.3535+376A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 30/39 | chr6 | 78962721 | |||||||
chr6:78962805 | A | G | 128 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(125): Show |
129 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.3535+292T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 30/39 | chr6 | 78962805 | |||||||
chr6:78962928 | T | C | 1 | a0001c0001t0001g0086 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.3535+169A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 30/39 | chr6 | 78962928 | |||||||
chr6:78963064 | G | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3535+33C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 30/39 | chr6 | 78963064 | |||||||
chr6:78963287 | G | A | 1 | a0001c0001t0005g0106 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.3380-35C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 29/39 | chr6 | 78963287 | |||||||
chr6:78963576 | C | T | 1 | a0002c0002t0004g0022 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.3380-324G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 29/39 | chr6 | 78963576 | |||||||
chr6:78963796 | G | A | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3380-544C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 29/39 | chr6 | 78963796 | |||||||
chr6:78963816 | C | A | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3380-564G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 29/39 | chr6 | 78963816 | |||||||
chr6:78963954 | GAAC | G | 11 | a0001c0001t0017g0023 a0001c0001t0017g0026 a0001c0001t0017g0031 others(8): Show |
12 | HG00738.hp1 HG01106.hp1 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.3380-705_3380-703d others(5): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 29/39 | chr6 | 78963954 | |||||||
chr6:78963973 | C | T | 1 | a0003c0003t0002g0279 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.3380-721G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 29/39 | chr6 | 78963973 | |||||||
chr6:78964024 | C | A | 1 | a0002c0002t0066g0230 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.3380-772G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 29/39 | chr6 | 78964024 | |||||||
chr6:78964070 | C | T | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3380-818G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 29/39 | chr6 | 78964070 | |||||||
chr6:78964148 | A | G | 40 | a0001c0006t0002g0013 a0001c0006t0002g0014 a0001c0006t0002g0265 others(37): Show |
46 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.3380-896T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 29/39 | chr6 | 78964148 | |||||||
chr6:78964171 | A | G | 1 | a0001c0001t0025g0024 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3380-919T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 29/39 | chr6 | 78964171 | |||||||
chr6:78964176 | A | C | 9 | a0001c0007t0012g0169 a0001c0007t0012g0170 a0001c0007t0012g0171 others(6): Show |
9 | HG02559.hp2 HG02622.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.3380-924T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 29/39 | chr6 | 78964176 | |||||||
chr6:78964225 | A | T | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3380-973T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 29/39 | chr6 | 78964225 | |||||||
chr6:78964355 | T | C | 1 | a0002c0002t0004g0211 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.3380-1103A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 29/39 | chr6 | 78964355 | |||||||
chr6:78964459 | G | A | 94 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(91): Show |
95 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.3380-1207C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 29/39 | chr6 | 78964459 | |||||||
chr6:78964545 | C | T | 128 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(125): Show |
129 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.3379+1158G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 29/39 | chr6 | 78964545 | |||||||
chr6:78964692 | C | T | 1 | a0001c0005t0027g0033 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.3379+1011G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 29/39 | chr6 | 78964692 | |||||||
chr6:78964700 | T | C | 2 | a0001c0012t0024g0034 a0001c0015t0024g0035 |
2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.3379+1003A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 29/39 | chr6 | 78964700 | |||||||
chr6:78964706 | T | A | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.3379+997A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 29/39 | chr6 | 78964706 | |||||||
chr6:78964716 | C | T | 1 | a0008c0019t0013g0190 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3379+987G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 29/39 | chr6 | 78964716 | |||||||
chr6:78964721 | G | A | 7 | a0004c0004t0006g0007 a0004c0004t0006g0008 a0004c0004t0006g0179 others(4): Show |
9 | HG00735.hp2 HG01106.hp2 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.3379+982C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 29/39 | chr6 | 78964721 | |||||||
chr6:78964808 | T | C | 1 | a0001c0001t0026g0149 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3379+895A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 29/39 | chr6 | 78964808 | |||||||
chr6:78964916 | T | A | 1 | a0001c0006t0009g0266 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3379+787A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 29/39 | chr6 | 78964916 | |||||||
chr6:78964993 | T | C | 1 | a0001c0006t0008g0037 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3379+710A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 29/39 | chr6 | 78964993 | |||||||
chr6:78965103 | GAC | G | 4 | a0001c0005t0027g0033 a0001c0006t0008g0037 a0001c0012t0024g0034 others(1): Show |
4 | HG01109.hp2 HG02572.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.3379+598_3379+599d others(4): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 29/39 | chr6 | 78965103 | |||||||
chr6:78965139 | T | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3379+564A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 29/39 | chr6 | 78965139 | |||||||
chr6:78965212 | T | C | 99 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(96): Show |
100 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.3379+491A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 29/39 | chr6 | 78965212 | |||||||
chr6:78965552 | ACTT | A | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3379+148_3379+150d others(5): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 29/39 | chr6 | 78965552 | |||||||
chr6:78965558 | A | G | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3379+145T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 29/39 | chr6 | 78965558 | |||||||
chr6:78965910 | C | T | 1 | a0001c0001t0001g0096 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.3317+35G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 28/39 | chr6 | 78965910 | |||||||
chr6:78966228 | A | G | 1 | a0001c0005t0054g0038 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3206-172T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78966228 | |||||||
chr6:78966230 | G | A | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3206-174C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78966230 | |||||||
chr6:78966231 | A | T | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3206-175T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78966231 | |||||||
chr6:78966322 | G | A | 1 | a0001c0005t0003g0001 | 3 | HG02280.hp1 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3206-266C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78966322 | |||||||
chr6:78966345 | G | A | 96 | a0001c0007t0012g0169 a0001c0007t0012g0170 a0001c0007t0012g0171 others(93): Show |
101 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.3206-289C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78966345 | |||||||
chr6:78966539 | A | G | 1 | a0001c0005t0055g0045 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3206-483T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78966539 | |||||||
chr6:78966611 | A | T | 124 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(121): Show |
125 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.3206-555T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78966611 | |||||||
chr6:78966711 | A | G | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3206-655T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78966711 | |||||||
chr6:78966728 | T | C | 1 | a0001c0001t0001g0079 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3206-672A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78966728 | |||||||
chr6:78966741 | A | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3206-685T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78966741 | |||||||
chr6:78966862 | C | T | 279 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(276): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.3206-806G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78966862 | |||||||
chr6:78966895 | A | G | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3206-839T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78966895 | |||||||
chr6:78966996 | A | G | 1 | a0001c0006t0002g0267 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.3206-940T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78966996 | |||||||
chr6:78967328 | AC | A | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3206-1273delG | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78967328 | |||||||
chr6:78967483 | C | T | 2 | a0001c0001t0014g0161 a0001c0001t0014g0162 |
2 | HG02145.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.3206-1427G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78967483 | |||||||
chr6:78967533 | C | T | 2 | a0001c0001t0005g0102 a0001c0001t0033g0021 |
2 | HG00280.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.3206-1477G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78967533 | |||||||
chr6:78967534 | G | A | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3206-1478C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78967534 | |||||||
chr6:78967653 | T | C | 1 | a0001c0001t0040g0080 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.3206-1597A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78967653 | |||||||
chr6:78967927 | G | A | 5 | a0001c0005t0023g0049 a0001c0005t0023g0051 a0001c0005t0030g0050 others(2): Show |
5 | HG02818.hp1 HG02886.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.3206-1871C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78967927 | |||||||
chr6:78967963 | T | C | 5 | a0001c0001t0017g0023 a0001c0001t0017g0026 a0001c0001t0017g0031 others(2): Show |
5 | HG01891.hp1 HG02109.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.3205+1872A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78967963 | |||||||
chr6:78967969 | C | A | 1 | a0001c0005t0055g0045 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3205+1866G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78967969 | |||||||
chr6:78968072 | T | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3205+1763A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78968072 | |||||||
chr6:78968122 | G | A | 1 | a0003c0003t0002g0032 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.3205+1713C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78968122 | |||||||
chr6:78968214 | T | C | 2 | a0001c0001t0026g0149 a0001c0001t0026g0154 |
2 | HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.3205+1621A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78968214 | |||||||
chr6:78968239 | C | T | 2 | a0004c0004t0013g0181 a0004c0004t0065g0182 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.3205+1596G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78968239 | |||||||
chr6:78968254 | CT | C | 9 | a0001c0001t0011g0029 a0001c0001t0017g0023 a0001c0001t0017g0026 others(6): Show |
9 | HG01891.hp1 HG02109.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.3205+1580delA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78968254 | |||||||
chr6:78968379 | T | C | 3 | a0001c0005t0019g0012 a0001c0005t0019g0264 a0001c0005t0046g0263 |
4 | HG03041.hp1 HG03130.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.3205+1456A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78968379 | |||||||
chr6:78968405 | G | C | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.3205+1430C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78968405 | |||||||
chr6:78968446 | G | A | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3205+1389C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78968446 | |||||||
chr6:78968494 | G | A | 124 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(121): Show |
125 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.3205+1341C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78968494 | |||||||
chr6:78968550 | G | A | 1 | a0001c0001t0005g0106 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.3205+1285C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78968550 | |||||||
chr6:78968610 | A | G | 40 | a0001c0006t0002g0013 a0001c0006t0002g0014 a0001c0006t0002g0265 others(37): Show |
46 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.3205+1225T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78968610 | |||||||
chr6:78968613 | A | G | 1 | a0003c0003t0002g0295 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3205+1222T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78968613 | |||||||
chr6:78968667 | A | C | 5 | a0002c0002t0003g0201 a0002c0002t0003g0202 a0002c0002t0003g0203 others(2): Show |
5 | NA18945.hp2 NA18974.hp1 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.3205+1168T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78968667 | |||||||
chr6:78968731 | AAATT | A | 124 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(121): Show |
125 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.3205+1100_3205+110 others(8): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78968731 | |||||||
chr6:78968952 | T | C | 6 | a0001c0005t0023g0049 a0001c0005t0023g0051 a0001c0005t0030g0048 others(3): Show |
6 | HG01884.hp2 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.3205+883A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78968952 | |||||||
chr6:78968960 | A | G | 1 | a0001c0001t0021g0028 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3205+875T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78968960 | |||||||
chr6:78969089 | T | C | 4 | a0001c0005t0027g0033 a0001c0006t0008g0037 a0001c0012t0024g0034 others(1): Show |
4 | HG01109.hp2 HG02572.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.3205+746A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78969089 | |||||||
chr6:78969242 | C | T | 1 | a0001c0006t0008g0037 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3205+593G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78969242 | |||||||
chr6:78969282 | C | T | 5 | a0001c0008t0003g0167 a0001c0008t0007g0164 a0001c0008t0007g0165 others(2): Show |
5 | HG02280.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.3205+553G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78969282 | |||||||
chr6:78969376 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3205+459A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78969376 | |||||||
chr6:78969403 | C | A | 1 | a0001c0001t0001g0122 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.3205+432G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78969403 | |||||||
chr6:78969404 | A | T | 2 | a0001c0010t0029g0053 a0001c0010t0029g0054 |
2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.3205+431T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78969404 | |||||||
chr6:78969406 | A | C | 1 | a0003c0003t0002g0296 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.3205+429T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78969406 | |||||||
chr6:78969646 | G | A | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3205+189C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78969646 | |||||||
chr6:78969810 | G | T | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3205+25C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 27/39 | chr6 | 78969810 | |||||||
chr6:78970043 | C | T | 7 | a0001c0007t0012g0169 a0001c0007t0012g0170 a0001c0007t0012g0171 others(4): Show |
7 | HG02559.hp2 HG02622.hp2 HG02809.hp1 others(4): Show |
splice_region_variant&intron_variant | LOW | c.3122+6G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 26/39 | chr6 | 78970043 | |||||||
chr6:78970287 | G | T | 1 | a0001c0001t0034g0132 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2998-114C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 25/39 | chr6 | 78970287 | |||||||
chr6:78970346 | T | C | 28 | a0001c0001t0011g0029 a0001c0001t0011g0150 a0001c0001t0011g0151 others(25): Show |
28 | HG00280.hp2 HG00639.hp1 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.2998-173A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 25/39 | chr6 | 78970346 | |||||||
chr6:78970352 | T | C | 1 | a0001c0005t0049g0036 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2998-179A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 25/39 | chr6 | 78970352 | |||||||
chr6:78970506 | G | A | 3 | a0001c0005t0019g0012 a0001c0005t0019g0264 a0001c0005t0046g0263 |
4 | HG03041.hp1 HG03130.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2997+275C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 25/39 | chr6 | 78970506 | |||||||
chr6:78970581 | T | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2997+200A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 25/39 | chr6 | 78970581 | |||||||
chr6:78970703 | T | C | 9 | a0001c0007t0012g0169 a0001c0007t0012g0170 a0001c0007t0012g0171 others(6): Show |
9 | HG02559.hp2 HG02622.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.2997+78A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 25/39 | chr6 | 78970703 | |||||||
chr6:78970989 | C | G | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2890-101G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78970989 | |||||||
chr6:78971040 | C | G | 3 | a0003c0003t0002g0292 a0003c0003t0009g0016 a0003c0003t0052g0298 |
4 | HG00438.hp2 HG02155.hp2 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.2890-152G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78971040 | |||||||
chr6:78971047 | T | C | 1 | a0001c0021t0036g0070 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2890-159A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78971047 | |||||||
chr6:78971134 | C | A | 1 | a0001c0006t0002g0269 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2890-246G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78971134 | |||||||
chr6:78971274 | C | A | 1 | a0001c0011t0016g0018 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.2890-386G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78971274 | |||||||
chr6:78971475 | C | T | 2 | a0002c0002t0004g0208 a0002c0002t0008g0209 |
2 | HG03669.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.2890-587G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78971475 | |||||||
chr6:78971516 | G | A | 1 | a0001c0005t0038g0047 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2890-628C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78971516 | |||||||
chr6:78971652 | C | T | 96 | a0001c0007t0012g0169 a0001c0007t0012g0170 a0001c0007t0012g0171 others(93): Show |
101 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.2890-764G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78971652 | |||||||
chr6:78971658 | T | A | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2890-770A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78971658 | |||||||
chr6:78971663 | G | A | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2890-775C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78971663 | |||||||
chr6:78971668 | C | A | 1 | a0001c0006t0008g0037 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2890-780G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78971668 | |||||||
chr6:78971670 | C | T | 2 | a0001c0001t0001g0128 a0001c0006t0008g0037 |
2 | HG01069.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.2890-782G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78971670 | |||||||
chr6:78971671 | G | A | 96 | a0001c0007t0012g0169 a0001c0007t0012g0170 a0001c0007t0012g0171 others(93): Show |
101 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.2890-783C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78971671 | |||||||
chr6:78971678 | G | T | 1 | a0001c0001t0001g0101 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2890-790C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78971678 | |||||||
chr6:78971679 | T | C | 1 | a0001c0001t0001g0101 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2890-791A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78971679 | |||||||
chr6:78971682 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2890-794C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78971682 | |||||||
chr6:78971766 | C | T | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2890-878G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78971766 | |||||||
chr6:78971809 | C | T | 1 | a0003c0003t0002g0274 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2890-921G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78971809 | |||||||
chr6:78971833 | C | A | 1 | a0004c0004t0006g0187 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2890-945G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78971833 | |||||||
chr6:78971843 | C | T | 3 | a0001c0006t0002g0265 a0001c0006t0009g0266 a0001c0006t0009g0297 |
3 | HG01891.hp2 HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.2890-955G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78971843 | |||||||
chr6:78971844 | G | A | 2 | a0002c0002t0010g0206 a0002c0002t0010g0234 |
2 | HG02080.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.2890-956C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78971844 | |||||||
chr6:78971857 | G | A | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2890-969C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78971857 | |||||||
chr6:78971872 | G | T | 5 | a0001c0008t0003g0167 a0001c0008t0007g0164 a0001c0008t0007g0165 others(2): Show |
5 | HG02280.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.2890-984C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78971872 | |||||||
chr6:78971884 | C | T | 5 | a0001c0008t0003g0167 a0001c0008t0007g0164 a0001c0008t0007g0165 others(2): Show |
5 | HG02280.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.2890-996G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78971884 | |||||||
chr6:78971933 | C | T | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2890-1045G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78971933 | |||||||
chr6:78971934 | G | A | 124 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(121): Show |
125 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.2890-1046C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78971934 | |||||||
chr6:78971997 | C | A | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2890-1109G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78971997 | |||||||
chr6:78971998 | G | A | 3 | a0001c0001t0001g0101 a0001c0001t0001g0110 a0001c0001t0040g0080 |
3 | HG00642.hp1 HG02698.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.2890-1110C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78971998 | |||||||
chr6:78972007 | G | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2890-1119C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78972007 | |||||||
chr6:78972164 | T | C | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2890-1276A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78972164 | |||||||
chr6:78972166 | C | T | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2890-1278G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78972166 | |||||||
chr6:78972168 | C | A | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2890-1280G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78972168 | |||||||
chr6:78972221 | C | T | 9 | a0001c0001t0011g0029 a0001c0001t0017g0023 a0001c0001t0017g0026 others(6): Show |
9 | HG01891.hp1 HG02109.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.2890-1333G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78972221 | |||||||
chr6:78972292 | C | T | 1 | a0001c0001t0033g0021 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2890-1404G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78972292 | |||||||
chr6:78972330 | A | C | 9 | a0001c0001t0001g0066 a0001c0001t0001g0068 a0001c0001t0001g0088 others(6): Show |
9 | HG00673.hp1 HG02165.hp1 NA18612.hp1 others(6): Show |
intron_variant | MODIFIER | c.2890-1442T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78972330 | |||||||
chr6:78972470 | C | T | 1 | a0001c0005t0003g0001 | 3 | HG02280.hp1 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2890-1582G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78972470 | |||||||
chr6:78972519 | C | G | 1 | a0001c0021t0036g0070 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2890-1631G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78972519 | |||||||
chr6:78972566 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2890-1678C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78972566 | |||||||
chr6:78972566 | G | T | 2 | a0001c0005t0054g0038 a0001c0005t0055g0045 |
2 | HG02723.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2890-1678C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78972566 | |||||||
chr6:78972587 | A | G | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2890-1699T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78972587 | |||||||
chr6:78972609 | C | G | 5 | a0001c0001t0001g0068 a0001c0001t0001g0088 a0001c0001t0001g0089 others(2): Show |
5 | HG00673.hp1 NA18943.hp2 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.2890-1721G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78972609 | |||||||
chr6:78972649 | G | A | 3 | a0004c0004t0013g0181 a0004c0004t0013g0183 a0004c0004t0065g0182 |
3 | HG02895.hp1 HG02897.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2890-1761C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78972649 | |||||||
chr6:78972649 | G | T | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2890-1761C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78972649 | |||||||
chr6:78972650 | T | C | 86 | a0001c0008t0003g0167 a0001c0008t0007g0164 a0001c0008t0007g0165 others(83): Show |
91 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.2890-1762A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78972650 | |||||||
chr6:78972692 | T | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2890-1804A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78972692 | |||||||
chr6:78972721 | T | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2890-1833A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78972721 | |||||||
chr6:78972754 | G | A | 94 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(91): Show |
95 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.2890-1866C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78972754 | |||||||
chr6:78972757 | G | T | 1 | a0001c0001t0001g0068 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.2890-1869C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78972757 | |||||||
chr6:78972780 | A | G | 1 | a0001c0005t0049g0036 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2890-1892T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78972780 | |||||||
chr6:78972789 | T | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2890-1901A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78972789 | |||||||
chr6:78972804 | G | T | 1 | a0004c0004t0006g0180 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2890-1916C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78972804 | |||||||
chr6:78972808 | C | T | 1 | a0001c0001t0014g0160 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2890-1920G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78972808 | |||||||
chr6:78972823 | A | G | 4 | a0001c0005t0003g0001 a0001c0005t0019g0012 a0001c0005t0019g0264 others(1): Show |
7 | HG02280.hp1 HG02965.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.2890-1935T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78972823 | |||||||
chr6:78972848 | G | C | 2 | a0001c0005t0038g0047 a0001c0005t0045g0046 |
2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2890-1960C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78972848 | |||||||
chr6:78972850 | G | A | 128 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(125): Show |
129 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.2890-1962C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78972850 | |||||||
chr6:78972897 | G | A | 19 | a0001c0001t0011g0150 a0001c0001t0011g0151 a0001c0001t0011g0153 others(16): Show |
19 | HG00280.hp2 HG00639.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.2890-2009C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78972897 | |||||||
chr6:78972903 | T | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2890-2015A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78972903 | |||||||
chr6:78972950 | A | ACT | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2890-2064_2890-206 others(6): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78972950 | |||||||
chr6:78972980 | CA | C | 80 | a0002c0002t0003g0010 a0002c0002t0003g0011 a0002c0002t0003g0041 others(77): Show |
85 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.2890-2093delT | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78972980 | |||||||
chr6:78973150 | G | T | 40 | a0001c0006t0002g0013 a0001c0006t0002g0014 a0001c0006t0002g0265 others(37): Show |
46 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.2890-2262C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78973150 | |||||||
chr6:78973171 | C | T | 1 | a0001c0005t0054g0038 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2890-2283G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78973171 | |||||||
chr6:78973181 | A | G | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2890-2293T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78973181 | |||||||
chr6:78973206 | G | A | 1 | a0001c0001t0026g0154 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2890-2318C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78973206 | |||||||
chr6:78973306 | A | C | 2 | a0001c0006t0020g0006 a0001c0006t0020g0148 |
3 | NA18944.hp1 NA18965.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.2890-2418T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78973306 | |||||||
chr6:78973315 | A | G | 3 | a0001c0005t0019g0012 a0001c0005t0019g0264 a0001c0005t0046g0263 |
4 | HG03041.hp1 HG03130.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2890-2427T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78973315 | |||||||
chr6:78973359 | C | A | 1 | a0001c0021t0036g0070 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2890-2471G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78973359 | |||||||
chr6:78973378 | C | T | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2890-2490G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78973378 | |||||||
chr6:78973412 | G | A | 81 | a0001c0010t0057g0163 a0002c0002t0003g0010 a0002c0002t0003g0011 others(78): Show |
86 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.2890-2524C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78973412 | |||||||
chr6:78973430 | A | C | 1 | a0001c0001t0033g0021 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2890-2542T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78973430 | |||||||
chr6:78973443 | T | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2890-2555A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78973443 | |||||||
chr6:78973473 | T | C | 282 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(279): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.2890-2585A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78973473 | |||||||
chr6:78973474 | G | A | 1 | a0001c0006t0002g0267 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2890-2586C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78973474 | |||||||
chr6:78973544 | C | A | 296 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(293): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.2890-2656G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78973544 | |||||||
chr6:78973548 | G | A | 1 | a0001c0006t0008g0037 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2890-2660C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78973548 | |||||||
chr6:78973557 | T | G | 296 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(293): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.2890-2669A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78973557 | |||||||
chr6:78973586 | T | C | 295 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(292): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.2890-2698A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78973586 | |||||||
chr6:78973595 | C | G | 296 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(293): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.2890-2707G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78973595 | |||||||
chr6:78973624 | A | G | 9 | a0001c0001t0011g0029 a0001c0001t0017g0023 a0001c0001t0017g0026 others(6): Show |
9 | HG01891.hp1 HG02109.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.2890-2736T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78973624 | |||||||
chr6:78973640 | C | G | 1 | a0002c0002t0008g0192 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2890-2752G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78973640 | |||||||
chr6:78973696 | A | C | 1 | a0003c0003t0061g0283 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2890-2808T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78973696 | |||||||
chr6:78973778 | A | G | 6 | a0001c0005t0023g0049 a0001c0005t0023g0051 a0001c0005t0030g0048 others(3): Show |
6 | HG01884.hp2 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2890-2890T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78973778 | |||||||
chr6:78973945 | C | T | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2890-3057G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78973945 | |||||||
chr6:78973980 | T | G | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2890-3092A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78973980 | |||||||
chr6:78973983 | C | G | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2890-3095G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78973983 | |||||||
chr6:78974030 | T | C | 3 | a0001c0005t0027g0033 a0001c0012t0024g0034 a0001c0015t0024g0035 |
3 | HG01109.hp2 HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2890-3142A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78974030 | |||||||
chr6:78974070 | T | C | 2 | a0001c0006t0020g0006 a0001c0006t0020g0148 |
3 | NA18944.hp1 NA18965.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.2890-3182A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78974070 | |||||||
chr6:78974107 | A | G | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2890-3219T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78974107 | |||||||
chr6:78974119 | C | G | 3 | a0002c0002t0003g0041 a0002c0002t0003g0042 a0002c0002t0007g0044 |
3 | HG02109.hp2 HG02451.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2890-3231G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78974119 | |||||||
chr6:78974119 | C | T | 1 | a0001c0001t0021g0030 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2890-3231G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78974119 | |||||||
chr6:78974174 | A | G | 124 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(121): Show |
125 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.2890-3286T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78974174 | |||||||
chr6:78974190 | A | T | 1 | a0002c0002t0063g0176 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2890-3302T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78974190 | |||||||
chr6:78974280 | G | C | 1 | a0001c0001t0001g0122 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2890-3392C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78974280 | |||||||
chr6:78974296 | A | G | 4 | a0001c0001t0011g0255 a0001c0001t0011g0256 a0001c0001t0018g0257 others(1): Show |
4 | HG02258.hp2 HG02896.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.2890-3408T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78974296 | |||||||
chr6:78974330 | A | G | 1 | a0001c0001t0035g0067 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2890-3442T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78974330 | |||||||
chr6:78974365 | G | A | 2 | a0001c0001t0026g0149 a0001c0001t0026g0154 |
2 | HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2890-3477C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78974365 | |||||||
chr6:78974391 | A | G | 1 | a0002c0014t0003g0210 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2890-3503T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78974391 | |||||||
chr6:78974418 | T | A | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2890-3530A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78974418 | |||||||
chr6:78974445 | C | T | 6 | a0001c0005t0023g0049 a0001c0005t0023g0051 a0001c0005t0030g0048 others(3): Show |
6 | HG01884.hp2 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2890-3557G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78974445 | |||||||
chr6:78974521 | A | C | 9 | a0001c0001t0014g0158 a0001c0001t0014g0160 a0001c0001t0014g0161 others(6): Show |
9 | HG00280.hp2 HG00639.hp1 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.2890-3633T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78974521 | |||||||
chr6:78974621 | A | G | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2890-3733T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78974621 | |||||||
chr6:78974623 | C | G | 94 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(91): Show |
95 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.2890-3735G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78974623 | |||||||
chr6:78974700 | G | A | 124 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(121): Show |
125 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.2890-3812C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78974700 | |||||||
chr6:78974728 | G | C | 40 | a0001c0006t0002g0013 a0001c0006t0002g0014 a0001c0006t0002g0265 others(37): Show |
46 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.2890-3840C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78974728 | |||||||
chr6:78974856 | A | G | 280 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(277): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.2889+3736T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78974856 | |||||||
chr6:78974985 | T | C | 4 | a0001c0005t0027g0033 a0001c0006t0008g0037 a0001c0012t0024g0034 others(1): Show |
4 | HG01109.hp2 HG02572.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2889+3607A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78974985 | |||||||
chr6:78975014 | C | G | 80 | a0002c0002t0003g0010 a0002c0002t0003g0011 a0002c0002t0003g0041 others(77): Show |
85 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.2889+3578G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78975014 | |||||||
chr6:78975052 | T | C | 279 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(276): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.2889+3540A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78975052 | |||||||
chr6:78975068 | C | A | 1 | a0001c0005t0003g0001 | 3 | HG02280.hp1 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2889+3524G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78975068 | |||||||
chr6:78975077 | T | G | 3 | a0001c0005t0003g0001 a0001c0010t0029g0053 a0001c0010t0029g0054 |
5 | HG02280.hp1 HG02965.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.2889+3515A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78975077 | |||||||
chr6:78975142 | G | A | 40 | a0001c0006t0002g0013 a0001c0006t0002g0014 a0001c0006t0002g0265 others(37): Show |
46 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.2889+3450C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78975142 | |||||||
chr6:78975164 | G | C | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2889+3428C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78975164 | |||||||
chr6:78975223 | G | A | 19 | a0001c0001t0011g0150 a0001c0001t0011g0151 a0001c0001t0011g0153 others(16): Show |
19 | HG00280.hp2 HG00639.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.2889+3369C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78975223 | |||||||
chr6:78975259 | C | G | 2 | a0002c0002t0004g0208 a0002c0002t0008g0209 |
2 | HG03669.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.2889+3333G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78975259 | |||||||
chr6:78975316 | A | T | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2889+3276T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78975316 | |||||||
chr6:78975364 | G | T | 40 | a0001c0006t0002g0013 a0001c0006t0002g0014 a0001c0006t0002g0265 others(37): Show |
46 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.2889+3228C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78975364 | |||||||
chr6:78975398 | C | G | 6 | a0001c0005t0023g0049 a0001c0005t0023g0051 a0001c0005t0030g0048 others(3): Show |
6 | HG01884.hp2 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2889+3194G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78975398 | |||||||
chr6:78975505 | T | G | 1 | a0003c0003t0002g0290 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2889+3087A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78975505 | |||||||
chr6:78975530 | TAGGC | T | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2889+3058_2889+306 others(8): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78975530 | |||||||
chr6:78975606 | A | G | 1 | a0002c0002t0003g0201 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2889+2986T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78975606 | |||||||
chr6:78975732 | G | A | 1 | a0001c0005t0003g0001 | 3 | HG02280.hp1 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2889+2860C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78975732 | |||||||
chr6:78975741 | G | A | 7 | a0001c0007t0012g0169 a0001c0007t0012g0170 a0001c0007t0012g0171 others(4): Show |
7 | HG02559.hp2 HG02622.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.2889+2851C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78975741 | |||||||
chr6:78975774 | A | G | 2 | a0001c0001t0001g0101 a0001c0001t0001g0110 |
2 | HG02698.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.2889+2818T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78975774 | |||||||
chr6:78975821 | T | C | 7 | a0001c0007t0012g0169 a0001c0007t0012g0170 a0001c0007t0012g0171 others(4): Show |
7 | HG02559.hp2 HG02622.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.2889+2771A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78975821 | |||||||
chr6:78975832 | T | C | 2 | a0001c0010t0029g0053 a0001c0010t0029g0054 |
2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2889+2760A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78975832 | |||||||
chr6:78975887 | A | T | 28 | a0001c0001t0011g0029 a0001c0001t0011g0150 a0001c0001t0011g0151 others(25): Show |
28 | HG00280.hp2 HG00639.hp1 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.2889+2705T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78975887 | |||||||
chr6:78975932 | G | T | 1 | a0001c0005t0003g0001 | 3 | HG02280.hp1 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2889+2660C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78975932 | |||||||
chr6:78975977 | C | A | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2889+2615G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78975977 | |||||||
chr6:78976060 | T | G | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2889+2532A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78976060 | |||||||
chr6:78976100 | C | A | 5 | a0001c0008t0003g0167 a0001c0008t0007g0164 a0001c0008t0007g0165 others(2): Show |
5 | HG02280.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.2889+2492G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78976100 | |||||||
chr6:78976164 | G | T | 4 | a0001c0001t0005g0103 a0001c0005t0019g0012 a0001c0005t0019g0264 others(1): Show |
5 | HG03041.hp1 HG03130.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.2889+2428C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78976164 | |||||||
chr6:78976166 | C | T | 3 | a0001c0005t0019g0012 a0001c0005t0019g0264 a0001c0005t0046g0263 |
4 | HG03041.hp1 HG03130.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2889+2426G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78976166 | |||||||
chr6:78976172 | C | T | 3 | a0001c0005t0019g0012 a0001c0005t0019g0264 a0001c0005t0046g0263 |
4 | HG03041.hp1 HG03130.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2889+2420G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78976172 | |||||||
chr6:78976219 | C | T | 2 | a0001c0005t0038g0047 a0001c0005t0045g0046 |
2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2889+2373G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78976219 | |||||||
chr6:78976256 | GA | G | 95 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(92): Show |
96 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.2889+2335delT | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78976256 | |||||||
chr6:78976426 | A | G | 3 | a0002c0002t0003g0041 a0002c0002t0003g0042 a0002c0002t0007g0044 |
3 | HG02109.hp2 HG02451.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2889+2166T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78976426 | |||||||
chr6:78976428 | G | A | 1 | a0001c0005t0055g0045 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2889+2164C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78976428 | |||||||
chr6:78976436 | A | G | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2889+2156T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78976436 | |||||||
chr6:78976455 | A | G | 273 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(270): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.2889+2137T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78976455 | |||||||
chr6:78976488 | A | C | 280 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(277): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.2889+2104T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78976488 | |||||||
chr6:78976494 | G | A | 1 | a0001c0005t0049g0036 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2889+2098C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78976494 | |||||||
chr6:78976559 | A | G | 5 | a0001c0008t0003g0167 a0001c0008t0007g0164 a0001c0008t0007g0165 others(2): Show |
5 | HG02280.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.2889+2033T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78976559 | |||||||
chr6:78976580 | G | T | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2889+2012C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78976580 | |||||||
chr6:78976597 | A | C | 1 | a0001c0001t0011g0029 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2889+1995T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78976597 | |||||||
chr6:78976614 | G | A | 124 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(121): Show |
125 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.2889+1978C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78976614 | |||||||
chr6:78976618 | T | C | 4 | a0001c0006t0002g0271 a0001c0011t0016g0017 a0001c0011t0016g0018 others(1): Show |
4 | HG01123.hp1 NA19003.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.2889+1974A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78976618 | |||||||
chr6:78976644 | T | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2889+1948A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78976644 | |||||||
chr6:78976718 | C | T | 80 | a0002c0002t0003g0010 a0002c0002t0003g0011 a0002c0002t0003g0041 others(77): Show |
85 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.2889+1874G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78976718 | |||||||
chr6:78976791 | C | G | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2889+1801G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78976791 | |||||||
chr6:78976845 | A | G | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2889+1747T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78976845 | |||||||
chr6:78976874 | C | T | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2889+1718G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78976874 | |||||||
chr6:78976940 | A | G | 1 | a0004c0004t0013g0178 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2889+1652T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78976940 | |||||||
chr6:78976941 | A | G | 281 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(278): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.2889+1651T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78976941 | |||||||
chr6:78976980 | G | T | 123 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(120): Show |
124 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.2889+1612C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78976980 | |||||||
chr6:78977024 | G | C | 4 | a0001c0005t0027g0033 a0001c0006t0008g0037 a0001c0012t0024g0034 others(1): Show |
4 | HG01109.hp2 HG02572.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2889+1568C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78977024 | |||||||
chr6:78977089 | T | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2889+1503A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78977089 | |||||||
chr6:78977136 | A | T | 1 | a0004c0004t0013g0188 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2889+1456T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78977136 | |||||||
chr6:78977147 | C | A | 276 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(273): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.2889+1445G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78977147 | |||||||
chr6:78977318 | T | C | 3 | a0001c0001t0021g0027 a0001c0001t0021g0028 a0001c0001t0021g0030 |
3 | HG02922.hp2 NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2889+1274A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78977318 | |||||||
chr6:78977389 | G | A | 40 | a0001c0006t0002g0013 a0001c0006t0002g0014 a0001c0006t0002g0265 others(37): Show |
46 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.2889+1203C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78977389 | |||||||
chr6:78977472 | G | A | 3 | a0001c0001t0011g0151 a0001c0001t0018g0152 a0001c0005t0003g0001 |
5 | HG02055.hp1 HG02280.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.2889+1120C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78977472 | |||||||
chr6:78977513 | C | T | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2889+1079G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78977513 | |||||||
chr6:78977521 | A | T | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2889+1071T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78977521 | |||||||
chr6:78977530 | C | A | 1 | a0001c0001t0032g0093 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2889+1062G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78977530 | |||||||
chr6:78977587 | G | GACCTTCA others(3): Show |
131 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(128): Show |
132 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.2889+995_2889+1004 others(13): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78977587 | |||||||
chr6:78977628 | T | C | 2 | a0001c0005t0038g0047 a0001c0005t0045g0046 |
2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2889+964A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78977628 | |||||||
chr6:78977629 | T | G | 4 | a0001c0001t0011g0150 a0001c0001t0011g0151 a0001c0001t0011g0153 others(1): Show |
4 | HG02055.hp1 HG02809.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.2889+963A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78977629 | |||||||
chr6:78977677 | G | A | 2 | a0001c0001t0001g0121 a0001c0001t0001g0131 |
2 | HG00140.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.2889+915C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78977677 | |||||||
chr6:78977705 | T | C | 4 | a0001c0001t0011g0255 a0001c0001t0011g0256 a0001c0001t0018g0257 others(1): Show |
4 | HG02258.hp2 HG02896.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.2889+887A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78977705 | |||||||
chr6:78977760 | T | C | 2 | a0001c0005t0038g0047 a0001c0005t0045g0046 |
2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2889+832A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78977760 | |||||||
chr6:78977867 | T | C | 1 | a0002c0002t0010g0206 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2889+725A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78977867 | |||||||
chr6:78977999 | G | A | 2 | a0003c0003t0002g0278 a0003c0003t0009g0277 |
2 | NA18950.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.2889+593C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78977999 | |||||||
chr6:78978200 | C | G | 1 | a0002c0002t0028g0260 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2889+392G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78978200 | |||||||
chr6:78978259 | A | C | 6 | a0001c0001t0011g0150 a0001c0001t0011g0151 a0001c0001t0011g0153 others(3): Show |
6 | HG02055.hp1 HG02809.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.2889+333T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78978259 | |||||||
chr6:78978262 | A | G | 1 | a0001c0005t0023g0051 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2889+330T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78978262 | |||||||
chr6:78978334 | A | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2889+258T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78978334 | |||||||
chr6:78978373 | C | G | 4 | a0001c0001t0011g0150 a0001c0001t0011g0151 a0001c0001t0011g0153 others(1): Show |
4 | HG02055.hp1 HG02809.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.2889+219G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78978373 | |||||||
chr6:78978431 | C | T | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2889+161G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78978431 | |||||||
chr6:78978460 | C | T | 1 | a0001c0005t0045g0046 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2889+132G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78978460 | |||||||
chr6:78978462 | T | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2889+130A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 24/39 | chr6 | 78978462 | |||||||
chr6:78978823 | T | C | 3 | a0002c0002t0003g0041 a0002c0002t0003g0042 a0002c0002t0007g0044 |
3 | HG02109.hp2 HG02451.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2770-112A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78978823 | |||||||
chr6:78978914 | A | C | 1 | a0001c0001t0015g0157 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2770-203T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78978914 | |||||||
chr6:78978915 | A | C | 1 | a0001c0001t0001g0135 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2770-204T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78978915 | |||||||
chr6:78979036 | C | T | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2770-325G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78979036 | |||||||
chr6:78979045 | T | C | 4 | a0001c0005t0027g0033 a0001c0006t0008g0037 a0001c0012t0024g0034 others(1): Show |
4 | HG01109.hp2 HG02572.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2770-334A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78979045 | |||||||
chr6:78979115 | G | A | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2770-404C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78979115 | |||||||
chr6:78979613 | G | C | 2 | a0001c0005t0038g0047 a0001c0005t0045g0046 |
2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2770-902C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78979613 | |||||||
chr6:78979733 | C | T | 133 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(130): Show |
134 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.2770-1022G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78979733 | |||||||
chr6:78979753 | T | G | 1 | a0001c0001t0005g0106 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2770-1042A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78979753 | |||||||
chr6:78979778 | CTTGT | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2770-1071_2770-106 others(8): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78979778 | |||||||
chr6:78979786 | T | C | 1 | a0001c0005t0027g0033 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2770-1075A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78979786 | |||||||
chr6:78979950 | C | T | 1 | a0001c0011t0016g0017 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2770-1239G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78979950 | |||||||
chr6:78980251 | G | GA | 80 | a0002c0002t0003g0010 a0002c0002t0003g0011 a0002c0002t0003g0041 others(77): Show |
85 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.2770-1541dupT | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78980251 | |||||||
chr6:78980330 | A | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2770-1619T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78980330 | |||||||
chr6:78980442 | C | A | 9 | a0001c0001t0011g0029 a0001c0001t0017g0023 a0001c0001t0017g0026 others(6): Show |
9 | HG01891.hp1 HG02109.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.2770-1731G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78980442 | |||||||
chr6:78980573 | G | A | 133 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(130): Show |
134 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.2770-1862C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78980573 | |||||||
chr6:78980710 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2770-1999G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78980710 | |||||||
chr6:78980859 | C | T | 124 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(121): Show |
125 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.2769+2027G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78980859 | |||||||
chr6:78980935 | A | T | 1 | a0001c0005t0030g0048 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2769+1951T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78980935 | |||||||
chr6:78981151 | T | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2769+1735A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78981151 | |||||||
chr6:78981186 | A | C | 1 | a0002c0002t0008g0240 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2769+1700T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78981186 | |||||||
chr6:78981187 | G | C | 6 | a0001c0005t0023g0049 a0001c0005t0023g0051 a0001c0005t0030g0048 others(3): Show |
6 | HG01884.hp2 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2769+1699C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78981187 | |||||||
chr6:78981367 | C | T | 1 | a0002c0002t0063g0176 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2769+1519G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78981367 | |||||||
chr6:78981381 | C | T | 1 | a0001c0021t0036g0070 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2769+1505G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78981381 | |||||||
chr6:78981440 | A | G | 1 | a0002c0002t0010g0222 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2769+1446T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78981440 | |||||||
chr6:78981458 | A | G | 36 | a0001c0006t0002g0013 a0001c0006t0002g0014 a0001c0006t0002g0268 others(33): Show |
42 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.2769+1428T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78981458 | |||||||
chr6:78981525 | G | A | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2769+1361C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78981525 | |||||||
chr6:78981676 | C | A | 4 | a0001c0001t0001g0005 a0001c0001t0001g0140 a0001c0001t0005g0139 others(1): Show |
5 | HG02257.hp2 HG02717.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.2769+1210G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78981676 | |||||||
chr6:78981857 | T | C | 1 | a0001c0001t0005g0064 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2769+1029A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78981857 | |||||||
chr6:78982002 | T | C | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2769+884A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78982002 | |||||||
chr6:78982015 | T | G | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2769+871A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78982015 | |||||||
chr6:78982029 | G | A | 9 | a0001c0007t0012g0169 a0001c0007t0012g0170 a0001c0007t0012g0171 others(6): Show |
9 | HG02559.hp2 HG02622.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.2769+857C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78982029 | |||||||
chr6:78982249 | A | G | 3 | a0001c0010t0029g0053 a0001c0010t0029g0054 a0002c0002t0010g0224 |
3 | HG00558.hp1 HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2769+637T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78982249 | |||||||
chr6:78982372 | A | G | 1 | a0001c0005t0049g0036 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2769+514T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78982372 | |||||||
chr6:78982459 | G | A | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2769+427C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78982459 | |||||||
chr6:78982481 | T | C | 1 | a0001c0010t0029g0054 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2769+405A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78982481 | |||||||
chr6:78982682 | A | C | 80 | a0002c0002t0003g0010 a0002c0002t0003g0011 a0002c0002t0003g0041 others(77): Show |
85 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.2769+204T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78982682 | |||||||
chr6:78982731 | T | G | 1 | a0002c0002t0004g0211 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2769+155A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 23/39 | chr6 | 78982731 | |||||||
chr6:78983377 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2538-260G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 22/39 | chr6 | 78983377 | |||||||
chr6:78983745 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2538-628C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 22/39 | chr6 | 78983745 | |||||||
chr6:78983902 | T | C | 2 | a0001c0005t0038g0047 a0001c0005t0045g0046 |
2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2538-785A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 22/39 | chr6 | 78983902 | |||||||
chr6:78983939 | G | A | 1 | a0001c0005t0003g0001 | 3 | HG02280.hp1 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2538-822C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 22/39 | chr6 | 78983939 | |||||||
chr6:78983946 | TTTAC | T | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2538-833_2538-830d others(6): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 22/39 | chr6 | 78983946 | |||||||
chr6:78984193 | A | G | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2538-1076T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 22/39 | chr6 | 78984193 | |||||||
chr6:78984235 | T | C | 8 | a0001c0005t0003g0001 a0001c0005t0019g0012 a0001c0005t0019g0264 others(5): Show |
11 | HG01109.hp2 HG02280.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.2537+1117A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 22/39 | chr6 | 78984235 | |||||||
chr6:78984252 | G | C | 3 | a0001c0001t0001g0083 a0001c0001t0005g0102 a0001c0001t0039g0084 |
3 | NA18974.hp2 NA19065.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.2537+1100C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 22/39 | chr6 | 78984252 | |||||||
chr6:78984391 | C | CT | 4 | a0003c0003t0002g0015 a0003c0003t0002g0286 a0003c0003t0009g0276 others(1): Show |
5 | HG00099.hp2 HG01070.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.2537+960_2537+961i others(3): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 22/39 | chr6 | 78984391 | |||||||
chr6:78984418 | A | AGT | 80 | a0002c0002t0003g0010 a0002c0002t0003g0011 a0002c0002t0003g0041 others(77): Show |
85 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.2537+932_2537+933d others(4): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 22/39 | chr6 | 78984418 | |||||||
chr6:78984442 | T | A | 1 | a0001c0010t0029g0053 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2537+910A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 22/39 | chr6 | 78984442 | |||||||
chr6:78984498 | C | T | 4 | a0001c0005t0003g0001 a0001c0005t0019g0012 a0001c0005t0019g0264 others(1): Show |
7 | HG02280.hp1 HG02965.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.2537+854G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 22/39 | chr6 | 78984498 | |||||||
chr6:78984617 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2537+735C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 22/39 | chr6 | 78984617 | |||||||
chr6:78984753 | T | C | 2 | a0004c0004t0013g0181 a0004c0004t0065g0182 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2537+599A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 22/39 | chr6 | 78984753 | |||||||
chr6:78984759 | G | C | 3 | a0001c0005t0049g0036 a0001c0005t0054g0038 a0001c0005t0055g0045 |
3 | HG02723.hp1 HG03225.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2537+593C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 22/39 | chr6 | 78984759 | |||||||
chr6:78984769 | A | G | 2 | a0001c0001t0014g0160 a0001c0001t0015g0159 |
2 | HG00639.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.2537+583T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 22/39 | chr6 | 78984769 | |||||||
chr6:78984882 | T | C | 3 | a0001c0001t0001g0066 a0001c0001t0001g0146 a0001c0001t0005g0145 |
3 | NA18612.hp1 NA18988.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.2537+470A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 22/39 | chr6 | 78984882 | |||||||
chr6:78984932 | C | G | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2537+420G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 22/39 | chr6 | 78984932 | |||||||
chr6:78985012 | A | G | 1 | a0001c0005t0055g0045 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2537+340T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 22/39 | chr6 | 78985012 | |||||||
chr6:78985014 | GA | G | 6 | a0002c0002t0003g0193 a0002c0002t0003g0195 a0002c0002t0008g0197 others(3): Show |
6 | HG01109.hp1 HG02486.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.2537+337delT | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 22/39 | chr6 | 78985014 | |||||||
chr6:78985016 | T | G | 6 | a0002c0002t0003g0193 a0002c0002t0003g0195 a0002c0002t0008g0197 others(3): Show |
6 | HG01109.hp1 HG02486.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.2537+336A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 22/39 | chr6 | 78985016 | |||||||
chr6:78985019 | TTAACTCA | T | 6 | a0002c0002t0003g0193 a0002c0002t0003g0195 a0002c0002t0008g0197 others(3): Show |
6 | HG01109.hp1 HG02486.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.2537+326_2537+332d others(9): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 22/39 | chr6 | 78985019 | |||||||
chr6:78985087 | C | T | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2537+265G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 22/39 | chr6 | 78985087 | |||||||
chr6:78985099 | A | G | 2 | a0001c0001t0001g0097 a0001c0001t0001g0098 |
2 | NA18941.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.2537+253T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 22/39 | chr6 | 78985099 | |||||||
chr6:78985286 | T | TA | 40 | a0001c0006t0002g0013 a0001c0006t0002g0014 a0001c0006t0002g0265 others(37): Show |
46 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.2537+65dupT | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 22/39 | chr6 | 78985286 | |||||||
chr6:78985312 | C | T | 133 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(130): Show |
134 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.2537+40G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 22/39 | chr6 | 78985312 | |||||||
chr6:78985569 | T | C | 1 | a0002c0002t0022g0235 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.2461-141A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 21/39 | chr6 | 78985569 | |||||||
chr6:78985607 | A | G | 280 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(277): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.2461-179T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 21/39 | chr6 | 78985607 | |||||||
chr6:78985614 | G | A | 1 | a0001c0001t0015g0157 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2461-186C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 21/39 | chr6 | 78985614 | |||||||
chr6:78985656 | C | T | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2461-228G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 21/39 | chr6 | 78985656 | |||||||
chr6:78985746 | G | A | 1 | a0001c0005t0055g0045 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2461-318C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 21/39 | chr6 | 78985746 | |||||||
chr6:78985751 | G | A | 40 | a0001c0006t0002g0013 a0001c0006t0002g0014 a0001c0006t0002g0265 others(37): Show |
46 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.2461-323C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 21/39 | chr6 | 78985751 | |||||||
chr6:78986314 | T | C | 1 | a0001c0001t0005g0094 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2461-886A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 21/39 | chr6 | 78986314 | |||||||
chr6:78986398 | T | G | 1 | a0001c0021t0036g0070 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2461-970A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 21/39 | chr6 | 78986398 | |||||||
chr6:78986481 | T | C | 7 | a0001c0007t0012g0169 a0001c0007t0012g0170 a0001c0007t0012g0171 others(4): Show |
7 | HG02559.hp2 HG02622.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.2461-1053A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 21/39 | chr6 | 78986481 | |||||||
chr6:78986552 | C | T | 1 | a0001c0001t0026g0154 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2461-1124G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 21/39 | chr6 | 78986552 | |||||||
chr6:78986756 | T | G | 1 | a0001c0005t0054g0038 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2461-1328A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 21/39 | chr6 | 78986756 | |||||||
chr6:78986948 | GAAT | G | 124 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(121): Show |
125 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.2460+1258_2460+126 others(7): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 21/39 | chr6 | 78986948 | |||||||
chr6:78986957 | C | A | 4 | a0001c0005t0027g0033 a0001c0006t0008g0037 a0001c0012t0024g0034 others(1): Show |
4 | HG01109.hp2 HG02572.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2460+1252G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 21/39 | chr6 | 78986957 | |||||||
chr6:78986986 | C | T | 1 | a0003c0003t0002g0287 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2460+1223G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 21/39 | chr6 | 78986986 | |||||||
chr6:78987089 | A | C | 4 | a0001c0005t0027g0033 a0001c0006t0008g0037 a0001c0012t0024g0034 others(1): Show |
4 | HG01109.hp2 HG02572.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2460+1120T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 21/39 | chr6 | 78987089 | |||||||
chr6:78987222 | A | G | 1 | a0001c0001t0005g0052 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2460+987T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 21/39 | chr6 | 78987222 | |||||||
chr6:78987313 | T | C | 1 | a0001c0005t0055g0045 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2460+896A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 21/39 | chr6 | 78987313 | |||||||
chr6:78987468 | T | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2460+741A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 21/39 | chr6 | 78987468 | |||||||
chr6:78987594 | A | G | 1 | a0001c0007t0012g0169 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2460+615T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 21/39 | chr6 | 78987594 | |||||||
chr6:78987732 | A | C | 11 | a0001c0005t0003g0001 a0001c0005t0019g0012 a0001c0005t0019g0264 others(8): Show |
14 | HG01109.hp2 HG02280.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.2460+477T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 21/39 | chr6 | 78987732 | |||||||
chr6:78987960 | G | C | 2 | a0001c0001t0059g0118 a0001c0010t0057g0163 |
2 | HG01358.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.2460+249C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 21/39 | chr6 | 78987960 | |||||||
chr6:78988138 | G | A | 10 | a0004c0004t0006g0007 a0004c0004t0006g0008 a0004c0004t0006g0179 others(7): Show |
12 | HG00735.hp2 HG01106.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.2460+71C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 21/39 | chr6 | 78988138 | |||||||
chr6:78988155 | T | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2460+54A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 21/39 | chr6 | 78988155 | |||||||
chr6:78988479 | T | C | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2320-130A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 20/39 | chr6 | 78988479 | |||||||
chr6:78988528 | T | A | 2 | a0001c0005t0038g0047 a0001c0005t0045g0046 |
2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2320-179A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 20/39 | chr6 | 78988528 | |||||||
chr6:78988528 | T | C | 1 | a0001c0006t0002g0014 | 2 | HG02258.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2320-179A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 20/39 | chr6 | 78988528 | |||||||
chr6:78988663 | C | T | 127 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(124): Show |
128 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.2320-314G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 20/39 | chr6 | 78988663 | |||||||
chr6:78988665 | T | C | 19 | a0001c0001t0011g0150 a0001c0001t0011g0151 a0001c0001t0011g0153 others(16): Show |
19 | HG00280.hp2 HG00639.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.2320-316A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 20/39 | chr6 | 78988665 | |||||||
chr6:78988698 | G | A | 6 | a0001c0005t0030g0048 a0001c0008t0003g0167 a0001c0008t0007g0164 others(3): Show |
6 | HG01884.hp2 HG02280.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.2320-349C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 20/39 | chr6 | 78988698 | |||||||
chr6:78988699 | A | T | 6 | a0001c0005t0030g0048 a0001c0008t0003g0167 a0001c0008t0007g0164 others(3): Show |
6 | HG01884.hp2 HG02280.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.2320-350T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 20/39 | chr6 | 78988699 | |||||||
chr6:78988735 | GT | G | 59 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0005g0116 others(56): Show |
65 | HG00099.hp2 HG00438.hp2 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.2320-387delA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 20/39 | chr6 | 78988735 | |||||||
chr6:78988748 | C | T | 1 | a0001c0001t0005g0114 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.2320-399G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 20/39 | chr6 | 78988748 | |||||||
chr6:78988806 | T | A | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2320-457A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 20/39 | chr6 | 78988806 | |||||||
chr6:78988928 | A | C | 4 | a0002c0002t0003g0010 a0002c0002t0003g0244 a0002c0002t0003g0245 others(1): Show |
5 | HG01074.hp2 HG02055.hp2 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.2320-579T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 20/39 | chr6 | 78988928 | |||||||
chr6:78989083 | C | T | 2 | a0001c0005t0038g0047 a0001c0005t0045g0046 |
2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2320-734G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 20/39 | chr6 | 78989083 | |||||||
chr6:78989094 | C | CA | 127 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(124): Show |
128 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.2320-746dupT | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 20/39 | chr6 | 78989094 | |||||||
chr6:78989220 | C | A | 1 | a0002c0002t0063g0176 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2320-871G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 20/39 | chr6 | 78989220 | |||||||
chr6:78989228 | G | A | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2320-879C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 20/39 | chr6 | 78989228 | |||||||
chr6:78989430 | C | T | 1 | a0002c0002t0022g0235 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.2320-1081G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 20/39 | chr6 | 78989430 | |||||||
chr6:78989632 | T | C | 4 | a0001c0001t0011g0029 a0001c0001t0021g0027 a0001c0001t0021g0028 others(1): Show |
4 | HG02922.hp2 HG03130.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.2319+1236A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 20/39 | chr6 | 78989632 | |||||||
chr6:78989640 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2319+1228G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 20/39 | chr6 | 78989640 | |||||||
chr6:78989689 | G | C | 8 | a0002c0002t0003g0041 a0002c0002t0003g0042 a0002c0002t0007g0003 others(5): Show |
10 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(7): Show |
intron_variant | MODIFIER | c.2319+1179C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 20/39 | chr6 | 78989689 | |||||||
chr6:78989802 | T | C | 2 | a0001c0006t0020g0006 a0001c0006t0020g0148 |
3 | NA18944.hp1 NA18965.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.2319+1066A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 20/39 | chr6 | 78989802 | |||||||
chr6:78990044 | GAGA | G | 7 | a0001c0005t0030g0048 a0001c0008t0003g0167 a0001c0008t0007g0164 others(4): Show |
7 | HG01884.hp2 HG02280.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2319+821_2319+823d others(5): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 20/39 | chr6 | 78990044 | |||||||
chr6:78990120 | C | T | 94 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(91): Show |
95 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.2319+748G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 20/39 | chr6 | 78990120 | |||||||
chr6:78990190 | A | G | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2319+678T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 20/39 | chr6 | 78990190 | |||||||
chr6:78990321 | G | A | 273 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(270): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.2319+547C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 20/39 | chr6 | 78990321 | |||||||
chr6:78990440 | T | C | 1 | a0001c0001t0001g0074 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.2319+428A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 20/39 | chr6 | 78990440 | |||||||
chr6:78990442 | A | G | 280 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(277): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.2319+426T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 20/39 | chr6 | 78990442 | |||||||
chr6:78990472 | A | G | 3 | a0001c0005t0019g0012 a0001c0005t0019g0264 a0001c0005t0046g0263 |
4 | HG03041.hp1 HG03130.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2319+396T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 20/39 | chr6 | 78990472 | |||||||
chr6:78990608 | G | C | 96 | a0001c0005t0030g0048 a0001c0007t0012g0169 a0001c0007t0012g0170 others(93): Show |
101 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.2319+260C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 20/39 | chr6 | 78990608 | |||||||
chr6:78990635 | A | C | 1 | a0002c0002t0004g0223 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2319+233T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 20/39 | chr6 | 78990635 | |||||||
chr6:78990721 | T | C | 1 | a0001c0021t0036g0070 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2319+147A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 20/39 | chr6 | 78990721 | |||||||
chr6:78991013 | T | A | 2 | a0001c0005t0038g0047 a0001c0005t0045g0046 |
2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2202-28A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78991013 | |||||||
chr6:78991121 | A | G | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2202-136T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78991121 | |||||||
chr6:78991147 | C | G | 1 | a0001c0005t0019g0264 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2202-162G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78991147 | |||||||
chr6:78991149 | G | C | 9 | a0001c0007t0012g0169 a0001c0007t0012g0170 a0001c0007t0012g0171 others(6): Show |
9 | HG02559.hp2 HG02622.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.2202-164C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78991149 | |||||||
chr6:78991156 | C | T | 2 | a0001c0010t0029g0053 a0001c0010t0029g0054 |
2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2202-171G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78991156 | |||||||
chr6:78991263 | T | C | 133 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(130): Show |
134 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.2202-278A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78991263 | |||||||
chr6:78991302 | T | A | 3 | a0001c0005t0049g0036 a0001c0005t0054g0038 a0001c0005t0055g0045 |
3 | HG02723.hp1 HG03225.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2202-317A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78991302 | |||||||
chr6:78991352 | CTGT | C | 40 | a0001c0006t0002g0013 a0001c0006t0002g0014 a0001c0006t0002g0265 others(37): Show |
46 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.2202-370_2202-368d others(5): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78991352 | |||||||
chr6:78991392 | T | C | 1 | a0001c0005t0049g0036 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2202-407A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78991392 | |||||||
chr6:78991442 | T | G | 2 | a0001c0001t0001g0101 a0001c0001t0001g0110 |
2 | HG02698.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.2202-457A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78991442 | |||||||
chr6:78991560 | G | GAGA | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2202-578_2202-576d others(5): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78991560 | |||||||
chr6:78991615 | T | C | 5 | a0001c0005t0023g0049 a0001c0005t0023g0051 a0001c0005t0030g0050 others(2): Show |
5 | HG02818.hp1 HG02886.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.2202-630A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78991615 | |||||||
chr6:78991853 | AT | A | 33 | a0001c0001t0001g0100 a0001c0001t0001g0110 a0001c0001t0011g0029 others(30): Show |
36 | HG01109.hp2 HG01358.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.2202-869delA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78991853 | |||||||
chr6:78991854 | T | A | 1 | a0001c0021t0036g0070 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2202-869A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78991854 | |||||||
chr6:78991865 | T | A | 2 | a0001c0011t0016g0017 a0001c0011t0016g0018 |
2 | NA19003.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.2202-880A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78991865 | |||||||
chr6:78991960 | G | C | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2202-975C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78991960 | |||||||
chr6:78992035 | C | A | 2 | a0002c0002t0028g0260 a0002c0002t0028g0261 |
2 | HG01981.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.2202-1050G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78992035 | |||||||
chr6:78992054 | C | T | 1 | a0004c0004t0006g0184 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2202-1069G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78992054 | |||||||
chr6:78992058 | G | T | 80 | a0002c0002t0003g0010 a0002c0002t0003g0011 a0002c0002t0003g0041 others(77): Show |
85 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.2202-1073C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78992058 | |||||||
chr6:78992136 | G | A | 1 | a0001c0001t0001g0108 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.2202-1151C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78992136 | |||||||
chr6:78992183 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2202-1198G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78992183 | |||||||
chr6:78992184 | G | A | 1 | a0001c0001t0001g0138 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2202-1199C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78992184 | |||||||
chr6:78992203 | C | T | 1 | a0001c0001t0015g0156 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.2202-1218G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78992203 | |||||||
chr6:78992207 | C | G | 1 | a0001c0021t0036g0070 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2202-1222G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78992207 | |||||||
chr6:78992245 | G | C | 27 | a0002c0002t0004g0022 a0002c0002t0004g0198 a0002c0002t0004g0207 others(24): Show |
27 | HG00558.hp1 HG00621.hp1 HG02080.hp2 others(24): Show |
intron_variant | MODIFIER | c.2202-1260C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78992245 | |||||||
chr6:78992255 | G | A | 124 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(121): Show |
125 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.2202-1270C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78992255 | |||||||
chr6:78992257 | C | T | 1 | a0003c0003t0009g0276 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2202-1272G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78992257 | |||||||
chr6:78992482 | AT | A | 7 | a0001c0005t0023g0049 a0001c0005t0023g0051 a0001c0005t0030g0050 others(4): Show |
7 | HG02976.hp1 NA18522.hp2 NA18906.hp2 others(4): Show |
intron_variant | MODIFIER | c.2202-1498delA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78992482 | |||||||
chr6:78992496 | C | G | 1 | a0003c0003t0002g0274 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2202-1511G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78992496 | |||||||
chr6:78992583 | G | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2202-1598C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78992583 | |||||||
chr6:78992631 | T | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2202-1646A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78992631 | |||||||
chr6:78992813 | A | T | 2 | a0001c0001t0014g0160 a0001c0001t0015g0159 |
2 | HG00639.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.2202-1828T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78992813 | |||||||
chr6:78992891 | C | T | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2202-1906G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78992891 | |||||||
chr6:78992966 | C | T | 40 | a0001c0006t0002g0013 a0001c0006t0002g0014 a0001c0006t0002g0265 others(37): Show |
46 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.2202-1981G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78992966 | |||||||
chr6:78993018 | G | A | 36 | a0002c0002t0004g0022 a0002c0002t0004g0198 a0002c0002t0004g0207 others(33): Show |
37 | HG00558.hp1 HG00621.hp1 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.2202-2033C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78993018 | |||||||
chr6:78993079 | C | T | 94 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(91): Show |
95 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.2202-2094G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78993079 | |||||||
chr6:78993161 | T | G | 1 | a0002c0002t0062g0199 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.2202-2176A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78993161 | |||||||
chr6:78993180 | G | A | 1 | a0001c0001t0005g0094 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2202-2195C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78993180 | |||||||
chr6:78993220 | G | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2202-2235C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78993220 | |||||||
chr6:78993495 | A | G | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2202-2510T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78993495 | |||||||
chr6:78993688 | A | T | 1 | a0001c0005t0054g0038 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2202-2703T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78993688 | |||||||
chr6:78993774 | G | C | 5 | a0001c0008t0003g0167 a0001c0008t0007g0164 a0001c0008t0007g0165 others(2): Show |
5 | HG02280.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.2202-2789C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78993774 | |||||||
chr6:78994011 | C | T | 9 | a0001c0007t0012g0169 a0001c0007t0012g0170 a0001c0007t0012g0171 others(6): Show |
9 | HG02559.hp2 HG02622.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.2202-3026G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78994011 | |||||||
chr6:78994015 | A | T | 2 | a0001c0001t0001g0096 a0001c0001t0001g0143 |
2 | NA18999.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.2202-3030T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78994015 | |||||||
chr6:78994053 | C | G | 1 | a0002c0009t0004g0259 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2202-3068G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78994053 | |||||||
chr6:78994104 | G | A | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2202-3119C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78994104 | |||||||
chr6:78994187 | G | A | 6 | a0001c0005t0023g0049 a0001c0005t0023g0051 a0001c0005t0030g0048 others(3): Show |
6 | HG01884.hp2 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2202-3202C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78994187 | |||||||
chr6:78994230 | C | T | 10 | a0004c0004t0006g0007 a0004c0004t0006g0008 a0004c0004t0006g0179 others(7): Show |
12 | HG00735.hp2 HG01106.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.2201+3184G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78994230 | |||||||
chr6:78994305 | C | T | 1 | a0002c0002t0056g0196 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2201+3109G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78994305 | |||||||
chr6:78994347 | G | A | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2201+3067C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78994347 | |||||||
chr6:78994449 | C | T | 1 | a0001c0006t0002g0267 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2201+2965G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78994449 | |||||||
chr6:78994450 | G | A | 1 | a0001c0001t0021g0027 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2201+2964C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78994450 | |||||||
chr6:78994518 | G | A | 9 | a0001c0001t0011g0029 a0001c0001t0017g0023 a0001c0001t0017g0026 others(6): Show |
9 | HG01891.hp1 HG02109.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.2201+2896C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78994518 | |||||||
chr6:78994577 | A | AAAAAG | 274 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(271): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.2201+2832_2201+283 others(9): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78994577 | |||||||
chr6:78994615 | G | C | 1 | a0001c0021t0036g0070 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2201+2799C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78994615 | |||||||
chr6:78994746 | A | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2201+2668T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78994746 | |||||||
chr6:78994983 | A | G | 1 | a0004c0004t0006g0008 | 2 | HG00735.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.2201+2431T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78994983 | |||||||
chr6:78995070 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2201+2344C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78995070 | |||||||
chr6:78995183 | C | T | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2201+2231G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78995183 | |||||||
chr6:78995212 | T | C | 3 | a0001c0001t0001g0083 a0001c0001t0005g0102 a0001c0001t0039g0084 |
3 | NA18974.hp2 NA19065.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.2201+2202A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78995212 | |||||||
chr6:78995267 | A | G | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2201+2147T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78995267 | |||||||
chr6:78995418 | T | C | 6 | a0001c0005t0030g0048 a0001c0008t0003g0167 a0001c0008t0007g0164 others(3): Show |
6 | HG01884.hp2 HG02280.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.2201+1996A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78995418 | |||||||
chr6:78995495 | A | G | 6 | a0001c0005t0023g0049 a0001c0005t0023g0051 a0001c0005t0030g0048 others(3): Show |
6 | HG01884.hp2 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2201+1919T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78995495 | |||||||
chr6:78995541 | C | G | 2 | a0002c0002t0004g0208 a0002c0002t0008g0209 |
2 | HG03669.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.2201+1873G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78995541 | |||||||
chr6:78995804 | G | A | 4 | a0001c0001t0001g0005 a0001c0001t0001g0140 a0001c0001t0005g0139 others(1): Show |
5 | HG02257.hp2 HG02717.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.2201+1610C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78995804 | |||||||
chr6:78995866 | G | C | 95 | a0001c0007t0012g0169 a0001c0007t0012g0170 a0001c0007t0012g0171 others(92): Show |
100 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.2201+1548C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78995866 | |||||||
chr6:78995890 | A | G | 4 | a0001c0006t0002g0265 a0001c0006t0002g0267 a0001c0006t0009g0266 others(1): Show |
4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.2201+1524T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78995890 | |||||||
chr6:78996128 | C | T | 124 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(121): Show |
125 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.2201+1286G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78996128 | |||||||
chr6:78996200 | C | A | 1 | a0003c0003t0009g0272 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2201+1214G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78996200 | |||||||
chr6:78996257 | T | C | 1 | a0002c0020t0022g0253 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.2201+1157A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78996257 | |||||||
chr6:78996380 | G | A | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2201+1034C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78996380 | |||||||
chr6:78996413 | G | T | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2201+1001C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78996413 | |||||||
chr6:78996499 | C | T | 3 | a0003c0003t0002g0279 a0003c0003t0002g0288 a0003c0003t0060g0280 |
3 | HG00735.hp1 HG01255.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.2201+915G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78996499 | |||||||
chr6:78996554 | G | A | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2201+860C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78996554 | |||||||
chr6:78996579 | C | T | 1 | a0001c0011t0016g0019 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2201+835G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78996579 | |||||||
chr6:78996713 | T | C | 2 | a0001c0007t0012g0169 a0001c0007t0012g0170 |
2 | HG02559.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2201+701A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78996713 | |||||||
chr6:78996821 | C | T | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2201+593G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78996821 | |||||||
chr6:78996892 | C | T | 2 | a0001c0006t0002g0265 a0001c0006t0009g0266 |
2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.2201+522G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78996892 | |||||||
chr6:78996919 | T | G | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2201+495A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78996919 | |||||||
chr6:78996996 | C | A | 2 | a0001c0005t0038g0047 a0001c0005t0045g0046 |
2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2201+418G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78996996 | |||||||
chr6:78997184 | A | C | 1 | a0001c0005t0049g0036 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2201+230T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78997184 | |||||||
chr6:78997276 | C | G | 1 | a0001c0001t0001g0122 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2201+138G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78997276 | |||||||
chr6:78997297 | G | A | 1 | a0001c0001t0059g0118 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2201+117C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78997297 | |||||||
chr6:78997386 | G | C | 1 | a0001c0001t0005g0125 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2201+28C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 19/39 | chr6 | 78997386 | |||||||
chr6:78997814 | T | A | 2 | a0001c0006t0020g0006 a0001c0006t0020g0148 |
3 | NA18944.hp1 NA18965.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.2018-217A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 18/39 | chr6 | 78997814 | |||||||
chr6:78997853 | T | TA | 8 | a0001c0005t0003g0001 a0001c0005t0019g0012 a0001c0005t0019g0264 others(5): Show |
11 | HG01109.hp2 HG02280.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.2018-257dupT | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 18/39 | chr6 | 78997853 | |||||||
chr6:78997868 | T | C | 40 | a0001c0006t0002g0013 a0001c0006t0002g0014 a0001c0006t0002g0265 others(37): Show |
46 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.2018-271A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 18/39 | chr6 | 78997868 | |||||||
chr6:78998023 | T | C | 4 | a0002c0002t0007g0003 a0002c0002t0007g0004 a0002c0002t0007g0039 others(1): Show |
6 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(3): Show |
intron_variant | MODIFIER | c.2017+231A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 18/39 | chr6 | 78998023 | |||||||
chr6:78998147 | T | C | 1 | a0001c0015t0024g0035 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2017+107A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 18/39 | chr6 | 78998147 | |||||||
chr6:78998206 | C | T | 95 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(92): Show |
96 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.2017+48G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 18/39 | chr6 | 78998206 | |||||||
chr6:78998435 | T | G | 3 | a0001c0005t0049g0036 a0001c0005t0054g0038 a0001c0005t0055g0045 |
3 | HG02723.hp1 HG03225.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1880-44A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 17/39 | chr6 | 78998435 | |||||||
chr6:78998536 | T | TA | 7 | a0001c0001t0001g0100 a0001c0001t0011g0150 a0001c0001t0011g0151 others(4): Show |
7 | HG02055.hp1 HG02809.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1880-146dupT | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 17/39 | chr6 | 78998536 | |||||||
chr6:78998725 | A | T | 1 | a0003c0003t0002g0284 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1880-334T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 17/39 | chr6 | 78998725 | |||||||
chr6:78998816 | T | A | 9 | a0001c0001t0011g0029 a0001c0001t0017g0023 a0001c0001t0017g0026 others(6): Show |
9 | HG01891.hp1 HG02109.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.1880-425A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 17/39 | chr6 | 78998816 | |||||||
chr6:78998917 | C | T | 1 | a0001c0021t0036g0070 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1880-526G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 17/39 | chr6 | 78998917 | |||||||
chr6:78998958 | ACAATAAC | A | 9 | a0001c0007t0012g0169 a0001c0007t0012g0170 a0001c0007t0012g0171 others(6): Show |
9 | HG02559.hp2 HG02622.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1880-574_1880-568d others(9): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 17/39 | chr6 | 78998958 | |||||||
chr6:78998974 | T | C | 1 | a0001c0001t0015g0157 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1880-583A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 17/39 | chr6 | 78998974 | |||||||
chr6:78999182 | G | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1880-791C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 17/39 | chr6 | 78999182 | |||||||
chr6:78999220 | C | T | 4 | a0001c0005t0003g0001 a0001c0005t0019g0012 a0001c0005t0019g0264 others(1): Show |
7 | HG02280.hp1 HG02965.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.1880-829G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 17/39 | chr6 | 78999220 | |||||||
chr6:78999257 | G | C | 4 | a0001c0005t0003g0001 a0001c0005t0019g0012 a0001c0005t0019g0264 others(1): Show |
7 | HG02280.hp1 HG02965.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.1880-866C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 17/39 | chr6 | 78999257 | |||||||
chr6:78999517 | C | A | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1880-1126G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 17/39 | chr6 | 78999517 | |||||||
chr6:78999641 | A | G | 1 | a0002c0009t0004g0259 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1880-1250T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 17/39 | chr6 | 78999641 | |||||||
chr6:78999740 | G | A | 1 | a0003c0003t0009g0272 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1880-1349C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 17/39 | chr6 | 78999740 | |||||||
chr6:78999795 | T | G | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1880-1404A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 17/39 | chr6 | 78999795 | |||||||
chr6:79000249 | T | G | 5 | a0001c0008t0003g0167 a0001c0008t0007g0164 a0001c0008t0007g0165 others(2): Show |
5 | HG02280.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1879+1650A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 17/39 | chr6 | 79000249 | |||||||
chr6:79000382 | G | A | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1879+1517C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 17/39 | chr6 | 79000382 | |||||||
chr6:79000396 | T | C | 3 | a0002c0002t0003g0041 a0002c0002t0003g0042 a0002c0002t0007g0044 |
3 | HG02109.hp2 HG02451.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1879+1503A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 17/39 | chr6 | 79000396 | |||||||
chr6:79000441 | C | T | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1879+1458G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 17/39 | chr6 | 79000441 | |||||||
chr6:79000632 | T | C | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1879+1267A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 17/39 | chr6 | 79000632 | |||||||
chr6:79000771 | T | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1879+1128A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 17/39 | chr6 | 79000771 | |||||||
chr6:79000908 | C | T | 1 | a0001c0007t0012g0173 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1879+991G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 17/39 | chr6 | 79000908 | |||||||
chr6:79000939 | C | T | 19 | a0001c0001t0011g0150 a0001c0001t0011g0151 a0001c0001t0011g0153 others(16): Show |
19 | HG00280.hp2 HG00639.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.1879+960G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 17/39 | chr6 | 79000939 | |||||||
chr6:79001089 | C | T | 95 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(92): Show |
96 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.1879+810G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 17/39 | chr6 | 79001089 | |||||||
chr6:79001228 | C | A | 3 | a0001c0005t0019g0012 a0001c0005t0019g0264 a0001c0005t0046g0263 |
4 | HG03041.hp1 HG03130.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1879+671G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 17/39 | chr6 | 79001228 | |||||||
chr6:79001461 | A | G | 6 | a0002c0002t0003g0193 a0002c0002t0003g0195 a0002c0002t0008g0197 others(3): Show |
6 | HG01109.hp1 HG02486.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1879+438T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 17/39 | chr6 | 79001461 | |||||||
chr6:79001627 | T | G | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1879+272A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 17/39 | chr6 | 79001627 | |||||||
chr6:79001724 | T | A | 7 | a0001c0007t0012g0169 a0001c0007t0012g0170 a0001c0007t0012g0171 others(4): Show |
7 | HG02559.hp2 HG02622.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1879+175A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 17/39 | chr6 | 79001724 | |||||||
chr6:79002224 | C | T | 2 | a0001c0005t0038g0047 a0001c0005t0045g0046 |
2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1654-100G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 16/39 | chr6 | 79002224 | |||||||
chr6:79002255 | A | G | 80 | a0002c0002t0003g0010 a0002c0002t0003g0011 a0002c0002t0003g0041 others(77): Show |
85 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.1654-131T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 16/39 | chr6 | 79002255 | |||||||
chr6:79002284 | G | C | 1 | a0008c0019t0013g0190 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1654-160C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 16/39 | chr6 | 79002284 | |||||||
chr6:79002294 | T | C | 1 | a0001c0001t0005g0076 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1654-170A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 16/39 | chr6 | 79002294 | |||||||
chr6:79002412 | T | C | 1 | a0001c0021t0036g0070 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1654-288A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 16/39 | chr6 | 79002412 | |||||||
chr6:79002481 | C | T | 1 | a0001c0021t0036g0070 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1654-357G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 16/39 | chr6 | 79002481 | |||||||
chr6:79002637 | G | A | 4 | a0001c0006t0002g0265 a0001c0006t0002g0267 a0001c0006t0009g0266 others(1): Show |
4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1654-513C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 16/39 | chr6 | 79002637 | |||||||
chr6:79002895 | G | C | 1 | a0001c0001t0001g0128 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1654-771C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 16/39 | chr6 | 79002895 | |||||||
chr6:79003222 | T | C | 2 | a0001c0001t0014g0160 a0001c0001t0015g0159 |
2 | HG00639.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.1653+508A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 16/39 | chr6 | 79003222 | |||||||
chr6:79003321 | A | T | 7 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0133 others(4): Show |
7 | HG02145.hp2 NA18960.hp1 NA18991.hp1 others(4): Show |
intron_variant | MODIFIER | c.1653+409T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 16/39 | chr6 | 79003321 | |||||||
chr6:79003331 | G | C | 1 | a0001c0005t0003g0001 | 3 | HG02280.hp1 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1653+399C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 16/39 | chr6 | 79003331 | |||||||
chr6:79003429 | C | G | 1 | a0001c0021t0036g0070 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1653+301G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 16/39 | chr6 | 79003429 | |||||||
chr6:79003448 | T | C | 8 | a0001c0005t0003g0001 a0001c0005t0019g0012 a0001c0005t0019g0264 others(5): Show |
11 | HG01109.hp2 HG02280.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1653+282A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 16/39 | chr6 | 79003448 | |||||||
chr6:79003485 | G | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1653+245C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 16/39 | chr6 | 79003485 | |||||||
chr6:79003536 | C | T | 2 | a0001c0005t0038g0047 a0001c0005t0045g0046 |
2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1653+194G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 16/39 | chr6 | 79003536 | |||||||
chr6:79003569 | C | A | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1653+161G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 16/39 | chr6 | 79003569 | |||||||
chr6:79003673 | C | A | 2 | a0003c0003t0002g0286 a0003c0003t0031g0273 |
2 | HG00099.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.1653+57G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 16/39 | chr6 | 79003673 | |||||||
chr6:79003895 | T | G | 5 | a0001c0008t0003g0167 a0001c0008t0007g0164 a0001c0008t0007g0165 others(2): Show |
5 | HG02280.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1525-37A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79003895 | |||||||
chr6:79004224 | C | T | 1 | a0001c0006t0009g0297 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1525-366G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79004224 | |||||||
chr6:79004228 | T | G | 1 | a0001c0001t0001g0079 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1525-370A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79004228 | |||||||
chr6:79004313 | G | A | 1 | a0001c0001t0050g0061 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1525-455C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79004313 | |||||||
chr6:79004350 | G | A | 2 | a0002c0002t0004g0219 a0002c0002t0010g0218 |
2 | NA19002.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1525-492C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79004350 | |||||||
chr6:79004991 | C | T | 143 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(140): Show |
147 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.1525-1133G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79004991 | |||||||
chr6:79005070 | T | G | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1525-1212A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79005070 | |||||||
chr6:79005150 | T | C | 124 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(121): Show |
125 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.1525-1292A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79005150 | |||||||
chr6:79005213 | T | C | 5 | a0001c0005t0023g0049 a0001c0005t0023g0051 a0001c0005t0030g0050 others(2): Show |
5 | HG02818.hp1 HG02886.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1525-1355A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79005213 | |||||||
chr6:79005236 | T | C | 1 | a0002c0002t0004g0022 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1525-1378A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79005236 | |||||||
chr6:79005252 | T | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1525-1394A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79005252 | |||||||
chr6:79005308 | A | G | 1 | a0001c0001t0040g0080 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1525-1450T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79005308 | |||||||
chr6:79005776 | T | C | 8 | a0001c0001t0014g0158 a0001c0001t0014g0160 a0001c0001t0014g0161 others(5): Show |
8 | HG00280.hp2 HG00639.hp1 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.1525-1918A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79005776 | |||||||
chr6:79005881 | C | A | 1 | a0001c0001t0001g0095 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1525-2023G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79005881 | |||||||
chr6:79005903 | G | A | 143 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(140): Show |
147 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.1525-2045C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79005903 | |||||||
chr6:79006050 | T | A | 1 | a0001c0001t0001g0134 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1525-2192A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79006050 | |||||||
chr6:79006380 | C | CTGGTTTT others(8): Show |
3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1525-2537_1525-252 others(19): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79006380 | |||||||
chr6:79006396 | T | C | 5 | a0001c0005t0023g0049 a0001c0005t0023g0051 a0001c0005t0030g0050 others(2): Show |
5 | HG02818.hp1 HG02886.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1525-2538A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79006396 | |||||||
chr6:79006407 | A | G | 1 | a0001c0001t0018g0258 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1525-2549T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79006407 | |||||||
chr6:79006493 | A | C | 1 | a0001c0006t0008g0037 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1525-2635T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79006493 | |||||||
chr6:79006523 | T | G | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1525-2665A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79006523 | |||||||
chr6:79006623 | G | A | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1525-2765C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79006623 | |||||||
chr6:79006945 | A | AAAAG | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1525-3088_1525-308 others(8): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79006945 | |||||||
chr6:79007000 | G | A | 6 | a0001c0001t0011g0150 a0001c0001t0011g0151 a0001c0001t0011g0153 others(3): Show |
6 | HG02055.hp1 HG02809.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1525-3142C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79007000 | |||||||
chr6:79007047 | T | A | 4 | a0001c0001t0011g0029 a0001c0001t0021g0027 a0001c0001t0021g0028 others(1): Show |
4 | HG02922.hp2 HG03130.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.1525-3189A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79007047 | |||||||
chr6:79007603 | T | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1525-3745A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79007603 | |||||||
chr6:79007609 | T | C | 40 | a0001c0006t0002g0013 a0001c0006t0002g0014 a0001c0006t0002g0265 others(37): Show |
46 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.1525-3751A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79007609 | |||||||
chr6:79007613 | G | C | 1 | a0001c0001t0069g0117 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1525-3755C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79007613 | |||||||
chr6:79007654 | C | CT | 11 | a0001c0006t0002g0013 a0001c0006t0002g0268 a0001c0008t0003g0167 others(8): Show |
12 | HG01358.hp1 HG02280.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1525-3797dupA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79007654 | |||||||
chr6:79007654 | CT | C | 27 | a0001c0001t0011g0029 a0001c0001t0011g0255 a0001c0001t0014g0158 others(24): Show |
27 | HG00280.hp2 HG00639.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.1525-3797delA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79007654 | |||||||
chr6:79007654 | CTT | C | 8 | a0001c0001t0011g0256 a0001c0001t0017g0023 a0001c0001t0017g0026 others(5): Show |
8 | HG00642.hp1 HG01891.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1525-3798_1525-379 others(6): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79007654 | |||||||
chr6:79007654 | CTTT | C | 91 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(88): Show |
92 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.1525-3799_1525-379 others(7): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79007654 | |||||||
chr6:79007686 | G | A | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1525-3828C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79007686 | |||||||
chr6:79007698 | A | C | 1 | a0001c0006t0008g0037 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1525-3840T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79007698 | |||||||
chr6:79007766 | T | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1525-3908A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79007766 | |||||||
chr6:79007783 | C | T | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1525-3925G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79007783 | |||||||
chr6:79007807 | G | A | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1525-3949C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79007807 | |||||||
chr6:79007870 | CT | C | 3 | a0001c0001t0021g0027 a0001c0001t0021g0028 a0001c0001t0021g0030 |
3 | HG02922.hp2 NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1525-4013delA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79007870 | |||||||
chr6:79007883 | G | A | 1 | a0002c0002t0008g0192 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1525-4025C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79007883 | |||||||
chr6:79007941 | T | C | 1 | a0001c0001t0001g0068 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1525-4083A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79007941 | |||||||
chr6:79008021 | C | T | 5 | a0001c0001t0001g0005 a0001c0001t0001g0140 a0001c0001t0005g0139 others(2): Show |
6 | HG01358.hp1 HG02257.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1525-4163G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79008021 | |||||||
chr6:79008026 | G | A | 2 | a0001c0001t0026g0149 a0001c0001t0026g0154 |
2 | HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1525-4168C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79008026 | |||||||
chr6:79008066 | A | AG | 282 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(279): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.1525-4209_1525-420 others(5): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79008066 | |||||||
chr6:79008088 | G | A | 1 | a0001c0001t0011g0256 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1525-4230C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79008088 | |||||||
chr6:79008199 | A | T | 1 | a0001c0007t0012g0173 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1525-4341T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79008199 | |||||||
chr6:79008205 | C | T | 3 | a0001c0005t0019g0012 a0001c0005t0019g0264 a0001c0005t0046g0263 |
4 | HG03041.hp1 HG03130.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1525-4347G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79008205 | |||||||
chr6:79008355 | T | C | 4 | a0002c0002t0003g0201 a0002c0002t0003g0202 a0002c0002t0003g0203 others(1): Show |
4 | NA18945.hp2 NA18974.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1525-4497A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79008355 | |||||||
chr6:79008374 | T | C | 1 | a0001c0001t0014g0160 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1525-4516A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79008374 | |||||||
chr6:79008584 | CT | C | 133 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(130): Show |
134 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.1525-4727delA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79008584 | |||||||
chr6:79008780 | C | T | 1 | a0001c0001t0026g0149 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1525-4922G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79008780 | |||||||
chr6:79008797 | C | T | 15 | a0002c0002t0003g0201 a0002c0002t0003g0202 a0002c0002t0003g0203 others(12): Show |
15 | HG00642.hp2 HG01123.hp2 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.1525-4939G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79008797 | |||||||
chr6:79009013 | TCCTA | T | 1 | a0001c0005t0003g0001 | 3 | HG02280.hp1 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1525-5159_1525-515 others(8): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79009013 | |||||||
chr6:79009078 | T | G | 127 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(124): Show |
128 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.1525-5220A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79009078 | |||||||
chr6:79009121 | C | G | 1 | a0001c0001t0001g0100 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1525-5263G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79009121 | |||||||
chr6:79009132 | G | A | 1 | a0001c0005t0054g0038 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1525-5274C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79009132 | |||||||
chr6:79009411 | C | G | 3 | a0001c0006t0002g0013 a0001c0006t0002g0268 a0001c0006t0002g0275 |
4 | NA19011.hp1 NA19057.hp1 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.1525-5553G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79009411 | |||||||
chr6:79009496 | T | C | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1524+5586A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79009496 | |||||||
chr6:79009739 | G | A | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1524+5343C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79009739 | |||||||
chr6:79009818 | C | A | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1524+5264G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79009818 | |||||||
chr6:79009877 | A | T | 1 | a0001c0001t0033g0021 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1524+5205T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79009877 | |||||||
chr6:79009878 | G | A | 1 | a0001c0001t0033g0021 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1524+5204C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79009878 | |||||||
chr6:79009906 | C | G | 127 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(124): Show |
128 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.1524+5176G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79009906 | |||||||
chr6:79009908 | T | TGAAA | 133 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(130): Show |
134 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.1524+5170_1524+517 others(8): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79009908 | |||||||
chr6:79010042 | T | A | 1 | a0001c0021t0036g0070 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1524+5040A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79010042 | |||||||
chr6:79010052 | TAGGAAGA others(4): Show |
T | 5 | a0001c0005t0023g0049 a0001c0005t0023g0051 a0001c0005t0030g0050 others(2): Show |
5 | HG02818.hp1 HG02886.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1524+5019_1524+502 others(15): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79010052 | |||||||
chr6:79010220 | T | C | 4 | a0001c0005t0027g0033 a0001c0006t0008g0037 a0001c0012t0024g0034 others(1): Show |
4 | HG01109.hp2 HG02572.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1524+4862A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79010220 | |||||||
chr6:79010403 | T | A | 37 | a0001c0005t0054g0038 a0001c0006t0002g0013 a0001c0006t0002g0014 others(34): Show |
43 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.1524+4679A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79010403 | |||||||
chr6:79010505 | C | CA | 133 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(130): Show |
134 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.1524+4576dupT | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79010505 | |||||||
chr6:79010862 | G | A | 5 | a0001c0001t0005g0099 a0001c0006t0002g0265 a0001c0006t0002g0267 others(2): Show |
5 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1524+4220C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79010862 | |||||||
chr6:79011023 | AG | A | 3 | a0001c0005t0049g0036 a0001c0005t0054g0038 a0001c0005t0055g0045 |
3 | HG02723.hp1 HG03225.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1524+4058delC | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79011023 | |||||||
chr6:79011090 | G | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1524+3992C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79011090 | |||||||
chr6:79011150 | T | A | 126 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(123): Show |
127 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.1524+3932A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79011150 | |||||||
chr6:79011150 | T | G | 1 | a0001c0001t0014g0158 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1524+3932A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79011150 | |||||||
chr6:79011151 | G | A | 2 | a0002c0002t0004g0216 a0002c0002t0004g0217 |
2 | HG00733.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1524+3931C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79011151 | |||||||
chr6:79011152 | T | G | 2 | a0001c0001t0014g0158 a0001c0001t0015g0155 |
2 | HG03942.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1524+3930A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79011152 | |||||||
chr6:79011322 | AGTTT | A | 3 | a0001c0001t0001g0083 a0001c0001t0005g0102 a0001c0001t0039g0084 |
3 | NA18974.hp2 NA19065.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1524+3756_1524+375 others(8): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79011322 | |||||||
chr6:79011445 | C | T | 4 | a0001c0001t0011g0255 a0001c0001t0011g0256 a0001c0001t0018g0257 others(1): Show |
4 | HG02258.hp2 HG02896.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1524+3637G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79011445 | |||||||
chr6:79011505 | G | A | 9 | a0001c0007t0012g0169 a0001c0007t0012g0170 a0001c0007t0012g0171 others(6): Show |
9 | HG02559.hp2 HG02622.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1524+3577C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79011505 | |||||||
chr6:79011623 | C | G | 1 | a0002c0002t0008g0247 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1524+3459G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79011623 | |||||||
chr6:79011692 | C | A | 40 | a0001c0006t0002g0013 a0001c0006t0002g0014 a0001c0006t0002g0265 others(37): Show |
46 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.1524+3390G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79011692 | |||||||
chr6:79011905 | AG | A | 4 | a0001c0006t0002g0265 a0001c0006t0002g0267 a0001c0006t0009g0266 others(1): Show |
4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1524+3176delC | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79011905 | |||||||
chr6:79012183 | T | C | 2 | a0001c0005t0038g0047 a0001c0005t0045g0046 |
2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1524+2899A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79012183 | |||||||
chr6:79012236 | G | T | 8 | a0002c0002t0003g0041 a0002c0002t0003g0042 a0002c0002t0007g0003 others(5): Show |
10 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1524+2846C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79012236 | |||||||
chr6:79012266 | G | C | 1 | a0002c0002t0004g0215 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1524+2816C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79012266 | |||||||
chr6:79012307 | T | C | 1 | a0002c0002t0003g0262 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1524+2775A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79012307 | |||||||
chr6:79012318 | T | C | 1 | a0002c0002t0004g0213 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1524+2764A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79012318 | |||||||
chr6:79012329 | C | T | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1524+2753G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79012329 | |||||||
chr6:79012354 | T | C | 9 | a0001c0007t0012g0169 a0001c0007t0012g0170 a0001c0007t0012g0171 others(6): Show |
9 | HG02559.hp2 HG02622.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1524+2728A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79012354 | |||||||
chr6:79012922 | A | G | 127 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(124): Show |
128 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.1524+2160T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79012922 | |||||||
chr6:79012955 | A | G | 280 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(277): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.1524+2127T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79012955 | |||||||
chr6:79013112 | CA | C | 4 | a0001c0005t0003g0001 a0001c0005t0019g0012 a0001c0005t0019g0264 others(1): Show |
7 | HG02280.hp1 HG02965.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.1524+1969delT | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79013112 | |||||||
chr6:79013135 | T | C | 11 | a0001c0005t0003g0001 a0001c0005t0019g0012 a0001c0005t0019g0264 others(8): Show |
14 | HG01109.hp2 HG02280.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.1524+1947A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79013135 | |||||||
chr6:79013298 | G | A | 1 | a0001c0005t0003g0001 | 3 | HG02280.hp1 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1524+1784C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79013298 | |||||||
chr6:79013372 | C | A | 1 | a0004c0004t0006g0008 | 2 | HG00735.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.1524+1710G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79013372 | |||||||
chr6:79013437 | A | T | 1 | a0001c0001t0001g0115 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1524+1645T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79013437 | |||||||
chr6:79013719 | C | T | 1 | a0001c0001t0011g0029 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1524+1363G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79013719 | |||||||
chr6:79013934 | C | A | 143 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(140): Show |
147 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.1524+1148G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79013934 | |||||||
chr6:79014038 | T | A | 97 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(94): Show |
98 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.1524+1044A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79014038 | |||||||
chr6:79014039 | T | C | 97 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(94): Show |
98 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.1524+1043A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79014039 | |||||||
chr6:79014058 | T | C | 1 | a0003c0003t0009g0272 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1524+1024A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79014058 | |||||||
chr6:79014067 | T | TTACAAAC others(208): Show |
4 | a0001c0006t0002g0013 a0001c0006t0002g0268 a0001c0006t0002g0271 others(1): Show |
5 | HG01123.hp1 NA19011.hp1 NA19057.hp1 others(2): Show |
intron_variant | MODIFIER | c.1524+1014_1524+101 others(219): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79014067 | |||||||
chr6:79014067 | T | TTACAAAC others(216): Show |
1 | a0001c0006t0002g0265 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1524+1014_1524+101 others(227): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79014067 | |||||||
chr6:79014067 | T | TTACAAAC others(217): Show |
29 | a0001c0006t0002g0014 a0001c0006t0002g0267 a0001c0006t0002g0269 others(26): Show |
33 | HG00099.hp2 HG01070.hp1 HG01346.hp2 others(30): Show |
intron_variant | MODIFIER | c.1524+1014_1524+101 others(228): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79014067 | |||||||
chr6:79014067 | T | TTACAAAC others(217): Show |
3 | a0003c0003t0002g0279 a0003c0003t0002g0288 a0003c0003t0060g0280 |
3 | HG00735.hp1 HG01255.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.1524+1014_1524+101 others(228): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79014067 | |||||||
chr6:79014067 | T | TTACAAAC others(218): Show |
2 | a0003c0003t0002g0032 a0003c0003t0009g0016 |
3 | NA18955.hp1 NA19002.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1524+1014_1524+101 others(229): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79014067 | |||||||
chr6:79014067 | T | TTACAAAC others(219): Show |
1 | a0003c0003t0052g0298 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1524+1014_1524+101 others(230): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79014067 | |||||||
chr6:79014171 | G | A | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1524+911C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79014171 | |||||||
chr6:79014354 | A | T | 1 | a0001c0005t0049g0036 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1524+728T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79014354 | |||||||
chr6:79014489 | T | C | 3 | a0001c0001t0001g0075 a0001c0001t0001g0108 a0001c0001t0069g0117 |
3 | NA18950.hp1 NA19012.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1524+593A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79014489 | |||||||
chr6:79014569 | A | T | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1524+513T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79014569 | |||||||
chr6:79014662 | G | T | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1524+420C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79014662 | |||||||
chr6:79014707 | C | CCAT | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1524+374_1524+375i others(5): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79014707 | |||||||
chr6:79014709 | A | G | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1524+373T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79014709 | |||||||
chr6:79014712 | G | A | 127 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(124): Show |
128 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.1524+370C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79014712 | |||||||
chr6:79014983 | A | C | 1 | a0001c0001t0043g0085 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1524+99T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79014983 | |||||||
chr6:79015023 | C | A | 36 | a0001c0006t0002g0013 a0001c0006t0002g0014 a0001c0006t0002g0268 others(33): Show |
42 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.1524+59G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 15/39 | chr6 | 79015023 | |||||||
chr6:79015395 | C | T | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1390-179G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 14/39 | chr6 | 79015395 | |||||||
chr6:79015905 | G | A | 2 | a0001c0005t0038g0047 a0001c0005t0045g0046 |
2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1236-122C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 13/39 | chr6 | 79015905 | |||||||
chr6:79015943 | C | T | 2 | a0001c0001t0001g0005 a0001c0001t0005g0139 |
3 | HG02257.hp2 HG02717.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1236-160G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 13/39 | chr6 | 79015943 | |||||||
chr6:79016008 | T | A | 5 | a0002c0002t0004g0022 a0002c0002t0004g0221 a0002c0002t0004g0229 others(2): Show |
5 | HG02523.hp2 NA18612.hp2 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.1236-225A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 13/39 | chr6 | 79016008 | |||||||
chr6:79016018 | A | G | 1 | a0001c0001t0001g0300 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1236-235T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 13/39 | chr6 | 79016018 | |||||||
chr6:79016423 | T | C | 1 | a0001c0001t0005g0102 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1235+121A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 13/39 | chr6 | 79016423 | |||||||
chr6:79016535 | A | T | 5 | a0001c0001t0017g0023 a0001c0001t0017g0026 a0001c0001t0017g0031 others(2): Show |
5 | HG01891.hp1 HG02109.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1235+9T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 13/39 | chr6 | 79016535 | |||||||
chr6:79016722 | T | C | 5 | a0001c0001t0001g0075 a0001c0001t0001g0108 a0001c0001t0005g0076 others(2): Show |
5 | NA18950.hp1 NA18975.hp2 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.1137-80A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 12/39 | chr6 | 79016722 | |||||||
chr6:79016791 | A | C | 4 | a0002c0002t0004g0022 a0002c0002t0004g0221 a0002c0002t0004g0229 others(1): Show |
4 | HG02523.hp2 NA18612.hp2 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.1137-149T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 12/39 | chr6 | 79016791 | |||||||
chr6:79016889 | C | T | 4 | a0001c0001t0011g0150 a0001c0001t0011g0151 a0001c0001t0011g0153 others(1): Show |
4 | HG02055.hp1 HG02809.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1137-247G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 12/39 | chr6 | 79016889 | |||||||
chr6:79017033 | T | A | 72 | a0002c0002t0003g0010 a0002c0002t0003g0011 a0002c0002t0003g0193 others(69): Show |
75 | HG00558.hp1 HG00621.hp1 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.1136+313A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 12/39 | chr6 | 79017033 | |||||||
chr6:79017306 | A | C | 1 | a0002c0002t0008g0192 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1136+40T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 12/39 | chr6 | 79017306 | |||||||
chr6:79017422 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1096-36C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 11/39 | chr6 | 79017422 | |||||||
chr6:79017621 | T | C | 1 | a0002c0002t0028g0260 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.995-38A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 10/39 | chr6 | 79017621 | |||||||
chr6:79017661 | C | T | 2 | a0001c0001t0005g0064 a0001c0001t0014g0158 |
2 | HG04115.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.995-78G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 10/39 | chr6 | 79017661 | |||||||
chr6:79017671 | G | A | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.995-88C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 10/39 | chr6 | 79017671 | |||||||
chr6:79017739 | T | G | 1 | a0002c0002t0004g0217 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.995-156A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 10/39 | chr6 | 79017739 | |||||||
chr6:79017770 | C | CTT | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.995-188_995-187ins others(2): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 10/39 | chr6 | 79017770 | |||||||
chr6:79017976 | A | C | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.995-393T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 10/39 | chr6 | 79017976 | |||||||
chr6:79018180 | C | A | 1 | a0003c0003t0002g0274 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.995-597G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 10/39 | chr6 | 79018180 | |||||||
chr6:79018361 | G | A | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.994+728C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 10/39 | chr6 | 79018361 | |||||||
chr6:79018431 | C | T | 2 | a0001c0001t0001g0300 a0001c0001t0005g0299 |
2 | HG00621.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.994+658G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 10/39 | chr6 | 79018431 | |||||||
chr6:79018495 | C | T | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.994+594G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 10/39 | chr6 | 79018495 | |||||||
chr6:79018588 | T | C | 2 | a0001c0005t0049g0036 a0001c0005t0054g0038 |
2 | HG02723.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.994+501A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 10/39 | chr6 | 79018588 | |||||||
chr6:79018611 | T | G | 80 | a0002c0002t0003g0010 a0002c0002t0003g0011 a0002c0002t0003g0041 others(77): Show |
85 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.994+478A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 10/39 | chr6 | 79018611 | |||||||
chr6:79018671 | C | T | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.994+418G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 10/39 | chr6 | 79018671 | |||||||
chr6:79018721 | ACTATAGA others(4): Show |
A | 1 | a0003c0003t0002g0289 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.994+357_994+367del others(11): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 10/39 | chr6 | 79018721 | |||||||
chr6:79018778 | T | C | 1 | a0003c0003t0009g0276 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.994+311A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 10/39 | chr6 | 79018778 | |||||||
chr6:79018867 | T | G | 1 | a0001c0005t0054g0038 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.994+222A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 10/39 | chr6 | 79018867 | |||||||
chr6:79019016 | A | T | 2 | a0001c0011t0016g0017 a0001c0011t0016g0018 |
2 | NA19003.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.994+73T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 10/39 | chr6 | 79019016 | |||||||
chr6:79019189 | T | C | 1 | a0001c0001t0001g0147 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.924-30A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79019189 | |||||||
chr6:79019286 | A | G | 1 | a0001c0001t0005g0065 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.924-127T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79019286 | |||||||
chr6:79019321 | G | T | 1 | a0002c0002t0004g0022 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.924-162C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79019321 | |||||||
chr6:79019381 | A | G | 1 | a0001c0001t0001g0136 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.924-222T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79019381 | |||||||
chr6:79019665 | A | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.924-506T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79019665 | |||||||
chr6:79019736 | C | T | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.924-577G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79019736 | |||||||
chr6:79019772 | A | C | 128 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(125): Show |
129 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.924-613T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79019772 | |||||||
chr6:79019772 | A | G | 1 | a0004c0004t0006g0179 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.924-613T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79019772 | |||||||
chr6:79019856 | T | C | 1 | a0003c0003t0031g0273 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.924-697A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79019856 | |||||||
chr6:79019867 | C | T | 3 | a0001c0005t0019g0012 a0001c0005t0019g0264 a0001c0005t0046g0263 |
4 | HG03041.hp1 HG03130.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.924-708G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79019867 | |||||||
chr6:79019931 | A | G | 128 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(125): Show |
129 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.924-772T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79019931 | |||||||
chr6:79019947 | G | C | 1 | a0001c0001t0001g0136 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.924-788C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79019947 | |||||||
chr6:79020170 | T | A | 134 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0060 others(131): Show |
141 | HG00099.hp2 HG00140.hp1 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.924-1011A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79020170 | |||||||
chr6:79020171 | A | T | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.924-1012T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79020171 | |||||||
chr6:79020286 | A | C | 40 | a0001c0006t0002g0013 a0001c0006t0002g0014 a0001c0006t0002g0265 others(37): Show |
46 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.924-1127T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79020286 | |||||||
chr6:79020333 | T | C | 40 | a0001c0006t0002g0013 a0001c0006t0002g0014 a0001c0006t0002g0265 others(37): Show |
46 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.924-1174A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79020333 | |||||||
chr6:79020495 | A | G | 1 | a0001c0006t0002g0268 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.924-1336T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79020495 | |||||||
chr6:79020573 | A | T | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.924-1414T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79020573 | |||||||
chr6:79021286 | A | G | 1 | a0001c0001t0005g0103 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.924-2127T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79021286 | |||||||
chr6:79021356 | C | T | 1 | a0001c0006t0008g0037 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.924-2197G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79021356 | |||||||
chr6:79021482 | C | T | 1 | a0001c0006t0008g0037 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.924-2323G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79021482 | |||||||
chr6:79021524 | C | A | 1 | a0001c0001t0011g0029 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.924-2365G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79021524 | |||||||
chr6:79022045 | A | C | 2 | a0001c0005t0038g0047 a0001c0005t0045g0046 |
2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.924-2886T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79022045 | |||||||
chr6:79022085 | G | A | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.924-2926C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79022085 | |||||||
chr6:79022123 | G | A | 1 | a0001c0001t0026g0149 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.924-2964C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79022123 | |||||||
chr6:79022170 | G | A | 9 | a0001c0001t0011g0029 a0001c0001t0017g0023 a0001c0001t0017g0026 others(6): Show |
9 | HG01891.hp1 HG02109.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.924-3011C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79022170 | |||||||
chr6:79022269 | G | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.924-3110C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79022269 | |||||||
chr6:79022332 | T | C | 11 | a0001c0005t0003g0001 a0001c0005t0019g0012 a0001c0005t0019g0264 others(8): Show |
14 | HG01109.hp2 HG02280.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.924-3173A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79022332 | |||||||
chr6:79022365 | A | G | 1 | a0001c0005t0027g0033 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.923+3154T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79022365 | |||||||
chr6:79022473 | C | T | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.923+3046G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79022473 | |||||||
chr6:79022484 | C | T | 5 | a0002c0002t0003g0193 a0002c0002t0003g0195 a0002c0002t0008g0197 others(2): Show |
5 | HG01109.hp1 HG02486.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.923+3035G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79022484 | |||||||
chr6:79022534 | G | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.923+2985C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79022534 | |||||||
chr6:79022881 | G | C | 1 | a0001c0005t0054g0038 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.923+2638C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79022881 | |||||||
chr6:79022965 | T | A | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.923+2554A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79022965 | |||||||
chr6:79023123 | G | A | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.923+2396C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79023123 | |||||||
chr6:79023459 | A | G | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.923+2060T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79023459 | |||||||
chr6:79023631 | T | C | 1 | a0001c0021t0036g0070 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.923+1888A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79023631 | |||||||
chr6:79023701 | T | C | 1 | a0002c0020t0022g0253 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.923+1818A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79023701 | |||||||
chr6:79023965 | C | G | 2 | a0001c0005t0038g0047 a0001c0005t0045g0046 |
2 | HG02818.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.923+1554G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79023965 | |||||||
chr6:79024049 | C | T | 1 | a0001c0005t0049g0036 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.923+1470G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79024049 | |||||||
chr6:79024050 | G | A | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.923+1469C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79024050 | |||||||
chr6:79024247 | C | T | 9 | a0001c0007t0012g0169 a0001c0007t0012g0170 a0001c0007t0012g0171 others(6): Show |
9 | HG02559.hp2 HG02622.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.923+1272G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79024247 | |||||||
chr6:79024326 | C | A | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.923+1193G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79024326 | |||||||
chr6:79024514 | T | C | 1 | a0002c0002t0010g0206 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.923+1005A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79024514 | |||||||
chr6:79024527 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.923+992C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79024527 | |||||||
chr6:79024530 | C | T | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.923+989G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79024530 | |||||||
chr6:79024532 | C | T | 91 | a0001c0005t0038g0047 a0001c0005t0045g0046 a0001c0008t0003g0167 others(88): Show |
97 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.923+987G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79024532 | |||||||
chr6:79024579 | C | T | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.923+940G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79024579 | |||||||
chr6:79024652 | A | C | 129 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(126): Show |
130 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.923+867T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79024652 | |||||||
chr6:79024661 | C | T | 1 | a0001c0001t0005g0141 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.923+858G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79024661 | |||||||
chr6:79024667 | T | C | 8 | a0001c0005t0003g0001 a0001c0005t0019g0012 a0001c0005t0019g0264 others(5): Show |
11 | HG01109.hp2 HG02280.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.923+852A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79024667 | |||||||
chr6:79024713 | G | A | 1 | a0001c0005t0027g0033 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.923+806C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79024713 | |||||||
chr6:79024760 | G | A | 11 | a0001c0005t0003g0001 a0001c0005t0019g0012 a0001c0005t0019g0264 others(8): Show |
14 | HG01109.hp2 HG02280.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.923+759C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79024760 | |||||||
chr6:79024806 | A | AAAAT | 11 | a0001c0001t0011g0150 a0001c0001t0011g0151 a0001c0001t0011g0153 others(8): Show |
11 | HG01496.hp2 HG02055.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.923+709_923+712dup others(4): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79024806 | |||||||
chr6:79024836 | A | G | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.923+683T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79024836 | |||||||
chr6:79025009 | C | T | 131 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(128): Show |
132 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.923+510G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79025009 | |||||||
chr6:79025226 | T | C | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.923+293A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79025226 | |||||||
chr6:79025281 | G | T | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.923+238C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79025281 | |||||||
chr6:79025306 | G | GA | 252 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0060 others(249): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.923+212dupT | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79025306 | |||||||
chr6:79025437 | C | T | 5 | a0001c0001t0011g0255 a0001c0001t0011g0256 a0001c0001t0018g0257 others(2): Show |
5 | HG02258.hp2 HG02602.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.923+82G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79025437 | |||||||
chr6:79025460 | T | C | 1 | a0003c0003t0002g0294 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.923+59A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 9/39 | chr6 | 79025460 | |||||||
chr6:79025899 | T | TAACAACA others(5): Show |
3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.822+32_822+43dupGT others(10): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 8/39 | chr6 | 79025899 | |||||||
chr6:79026239 | C | T | 1 | a0002c0002t0004g0232 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.601-75G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79026239 | |||||||
chr6:79026369 | C | G | 280 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(277): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.601-205G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79026369 | |||||||
chr6:79026397 | C | T | 1 | a0003c0003t0002g0291 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.601-233G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79026397 | |||||||
chr6:79026467 | TA | T | 282 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(279): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.601-304delT | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79026467 | |||||||
chr6:79026722 | G | GT | 4 | a0001c0005t0003g0001 a0001c0005t0019g0012 a0001c0005t0019g0264 others(1): Show |
7 | HG02280.hp1 HG02965.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.601-559dupA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79026722 | |||||||
chr6:79026889 | A | G | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.601-725T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79026889 | |||||||
chr6:79026892 | G | A | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.601-728C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79026892 | |||||||
chr6:79027121 | T | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.601-957A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79027121 | |||||||
chr6:79027169 | A | G | 1 | a0002c0002t0063g0176 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.601-1005T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79027169 | |||||||
chr6:79027306 | C | T | 2 | a0002c0002t0010g0206 a0002c0002t0010g0234 |
2 | HG02080.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.601-1142G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79027306 | |||||||
chr6:79027389 | A | G | 125 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(122): Show |
126 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.601-1225T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79027389 | |||||||
chr6:79027394 | T | C | 1 | a0001c0001t0001g0098 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.601-1230A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79027394 | |||||||
chr6:79027466 | G | A | 1 | a0003c0003t0002g0291 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.601-1302C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79027466 | |||||||
chr6:79027812 | T | C | 1 | a0001c0005t0055g0045 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.601-1648A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79027812 | |||||||
chr6:79027834 | C | G | 4 | a0001c0001t0011g0255 a0001c0001t0011g0256 a0001c0001t0018g0257 others(1): Show |
4 | HG02258.hp2 HG02896.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.601-1670G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79027834 | |||||||
chr6:79027905 | G | A | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.601-1741C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79027905 | |||||||
chr6:79027915 | G | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.601-1751C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79027915 | |||||||
chr6:79028089 | A | G | 3 | a0001c0001t0001g0066 a0001c0001t0001g0146 a0001c0001t0005g0145 |
3 | NA18612.hp1 NA18988.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.601-1925T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79028089 | |||||||
chr6:79028307 | C | G | 1 | a0001c0001t0050g0061 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.601-2143G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79028307 | |||||||
chr6:79028330 | TA | T | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.601-2167delT | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79028330 | |||||||
chr6:79028632 | T | C | 2 | a0001c0012t0024g0034 a0001c0015t0024g0035 |
2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.601-2468A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79028632 | |||||||
chr6:79028873 | T | C | 2 | a0004c0004t0013g0181 a0004c0004t0065g0182 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.601-2709A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79028873 | |||||||
chr6:79029174 | T | A | 5 | a0001c0001t0017g0023 a0001c0001t0017g0026 a0001c0001t0017g0031 others(2): Show |
5 | HG01891.hp1 HG02109.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.601-3010A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79029174 | |||||||
chr6:79029242 | C | T | 2 | a0002c0002t0007g0004 a0002c0002t0007g0040 |
3 | HG00099.hp1 HG00140.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.601-3078G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79029242 | |||||||
chr6:79029255 | T | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.601-3091A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79029255 | |||||||
chr6:79029272 | G | A | 5 | a0001c0001t0011g0255 a0001c0001t0011g0256 a0001c0001t0018g0257 others(2): Show |
5 | HG01358.hp1 HG02258.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.601-3108C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79029272 | |||||||
chr6:79029291 | C | T | 279 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(276): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.601-3127G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79029291 | |||||||
chr6:79029293 | G | A | 124 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(121): Show |
125 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.601-3129C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79029293 | |||||||
chr6:79029350 | A | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.601-3186T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79029350 | |||||||
chr6:79029388 | G | A | 296 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(293): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.601-3224C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79029388 | |||||||
chr6:79029415 | CTATACAA | C | 1 | a0001c0005t0003g0001 | 3 | HG02280.hp1 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.601-3258_601-3252d others(9): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79029415 | |||||||
chr6:79029576 | C | G | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.601-3412G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79029576 | |||||||
chr6:79029633 | G | A | 80 | a0002c0002t0003g0010 a0002c0002t0003g0011 a0002c0002t0003g0041 others(77): Show |
85 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.601-3469C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79029633 | |||||||
chr6:79029688 | C | T | 1 | a0001c0015t0024g0035 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.601-3524G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79029688 | |||||||
chr6:79029793 | G | T | 9 | a0001c0007t0012g0169 a0001c0007t0012g0170 a0001c0007t0012g0171 others(6): Show |
9 | HG02559.hp2 HG02622.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.601-3629C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79029793 | |||||||
chr6:79029872 | A | T | 3 | a0003c0003t0002g0279 a0003c0003t0002g0288 a0003c0003t0060g0280 |
3 | HG00735.hp1 HG01255.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.601-3708T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79029872 | |||||||
chr6:79029905 | G | A | 134 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(131): Show |
135 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.601-3741C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79029905 | |||||||
chr6:79030050 | G | A | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.601-3886C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79030050 | |||||||
chr6:79030083 | T | C | 3 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 |
3 | NA18941.hp1 NA19056.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.601-3919A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79030083 | |||||||
chr6:79030196 | G | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.601-4032C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79030196 | |||||||
chr6:79030377 | T | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.601-4213A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79030377 | |||||||
chr6:79030441 | AAAGT | A | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.601-4281_601-4278d others(6): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79030441 | |||||||
chr6:79030556 | C | T | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.601-4392G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79030556 | |||||||
chr6:79030685 | T | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.601-4521A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79030685 | |||||||
chr6:79030698 | G | A | 1 | a0001c0006t0002g0014 | 2 | HG02258.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.601-4534C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79030698 | |||||||
chr6:79030715 | T | C | 1 | a0002c0002t0003g0249 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.601-4551A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79030715 | |||||||
chr6:79030729 | A | C | 3 | a0001c0001t0001g0075 a0001c0001t0001g0108 a0001c0001t0069g0117 |
3 | NA18950.hp1 NA19012.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.601-4565T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79030729 | |||||||
chr6:79030817 | T | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.601-4653A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79030817 | |||||||
chr6:79030849 | C | T | 1 | a0001c0011t0016g0018 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.601-4685G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79030849 | |||||||
chr6:79030887 | AAAGAT | A | 3 | a0001c0005t0049g0036 a0001c0005t0054g0038 a0001c0005t0055g0045 |
3 | HG02723.hp1 HG03225.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.601-4728_601-4724d others(7): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79030887 | |||||||
chr6:79030931 | G | GT | 4 | a0001c0005t0003g0001 a0001c0006t0008g0037 a0001c0011t0016g0018 others(1): Show |
6 | HG02280.hp1 HG02572.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.601-4768dupA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79030931 | |||||||
chr6:79030937 | T | G | 2 | a0001c0001t0001g0136 a0001c0001t0005g0065 |
2 | HG02451.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.601-4773A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79030937 | |||||||
chr6:79030940 | T | A | 1 | a0001c0005t0055g0045 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.601-4776A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79030940 | |||||||
chr6:79030941 | G | T | 5 | a0001c0006t0002g0013 a0001c0006t0002g0268 a0001c0011t0016g0017 others(2): Show |
6 | NA19003.hp1 NA19011.hp1 NA19057.hp1 others(3): Show |
intron_variant | MODIFIER | c.601-4777C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79030941 | |||||||
chr6:79031004 | T | C | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.601-4840A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79031004 | |||||||
chr6:79031060 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.601-4896G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79031060 | |||||||
chr6:79031100 | C | T | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.601-4936G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79031100 | |||||||
chr6:79031203 | T | C | 280 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(277): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.601-5039A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79031203 | |||||||
chr6:79031219 | T | C | 1 | a0001c0005t0003g0001 | 3 | HG02280.hp1 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.601-5055A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79031219 | |||||||
chr6:79031304 | C | T | 4 | a0001c0005t0027g0033 a0001c0006t0008g0037 a0001c0012t0024g0034 others(1): Show |
4 | HG01109.hp2 HG02572.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.601-5140G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79031304 | |||||||
chr6:79031502 | T | C | 4 | a0001c0005t0003g0001 a0001c0005t0019g0012 a0001c0005t0019g0264 others(1): Show |
7 | HG02280.hp1 HG02965.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.601-5338A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79031502 | |||||||
chr6:79032055 | G | A | 1 | a0004c0004t0013g0178 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.601-5891C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79032055 | |||||||
chr6:79032105 | A | T | 7 | a0001c0007t0012g0169 a0001c0007t0012g0170 a0001c0007t0012g0171 others(4): Show |
7 | HG02559.hp2 HG02622.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.601-5941T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79032105 | |||||||
chr6:79032109 | A | G | 7 | a0001c0007t0012g0169 a0001c0007t0012g0170 a0001c0007t0012g0171 others(4): Show |
7 | HG02559.hp2 HG02622.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.601-5945T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79032109 | |||||||
chr6:79032137 | T | C | 1 | a0004c0004t0006g0185 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.601-5973A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79032137 | |||||||
chr6:79032156 | T | G | 9 | a0001c0001t0011g0029 a0001c0001t0017g0023 a0001c0001t0017g0026 others(6): Show |
9 | HG01891.hp1 HG02109.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.601-5992A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79032156 | |||||||
chr6:79032197 | AG | A | 3 | a0001c0005t0019g0012 a0001c0005t0019g0264 a0001c0005t0046g0263 |
4 | HG03041.hp1 HG03130.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.601-6034delC | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79032197 | |||||||
chr6:79032241 | A | G | 124 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(121): Show |
125 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.601-6077T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79032241 | |||||||
chr6:79032384 | C | T | 124 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(121): Show |
125 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.601-6220G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79032384 | |||||||
chr6:79032509 | T | C | 1 | a0003c0003t0002g0294 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.601-6345A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79032509 | |||||||
chr6:79032634 | T | C | 10 | a0001c0005t0003g0001 a0001c0005t0019g0012 a0001c0005t0019g0264 others(7): Show |
13 | HG01109.hp2 HG02280.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.601-6470A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79032634 | |||||||
chr6:79032661 | G | A | 4 | a0001c0001t0011g0029 a0001c0001t0021g0027 a0001c0001t0021g0028 others(1): Show |
4 | HG02922.hp2 HG03130.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.601-6497C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79032661 | |||||||
chr6:79033096 | G | A | 5 | a0001c0008t0003g0167 a0001c0008t0007g0164 a0001c0008t0007g0165 others(2): Show |
5 | HG02280.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.601-6932C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79033096 | |||||||
chr6:79033120 | C | T | 2 | a0001c0005t0054g0038 a0001c0005t0055g0045 |
2 | HG02723.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.601-6956G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79033120 | |||||||
chr6:79033230 | G | A | 95 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(92): Show |
96 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.601-7066C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79033230 | |||||||
chr6:79033315 | T | C | 3 | a0001c0001t0001g0083 a0001c0001t0005g0102 a0001c0001t0039g0084 |
3 | NA18974.hp2 NA19065.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.601-7151A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79033315 | |||||||
chr6:79033339 | T | A | 4 | a0001c0001t0001g0073 a0001c0001t0001g0086 a0001c0001t0001g0107 others(1): Show |
4 | HG02074.hp2 HG02155.hp1 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.601-7175A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79033339 | |||||||
chr6:79033375 | C | G | 1 | a0002c0002t0010g0228 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.601-7211G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79033375 | |||||||
chr6:79033402 | G | A | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.601-7238C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79033402 | |||||||
chr6:79033485 | T | C | 2 | a0001c0005t0054g0038 a0001c0005t0055g0045 |
2 | HG02723.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.601-7321A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79033485 | |||||||
chr6:79033494 | T | C | 2 | a0001c0012t0024g0034 a0001c0015t0024g0035 |
2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.601-7330A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79033494 | |||||||
chr6:79033601 | T | G | 3 | a0004c0004t0013g0181 a0004c0004t0013g0183 a0004c0004t0065g0182 |
3 | HG02895.hp1 HG02897.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.601-7437A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79033601 | |||||||
chr6:79033803 | A | G | 5 | a0002c0002t0003g0201 a0002c0002t0003g0202 a0002c0002t0003g0203 others(2): Show |
5 | NA18945.hp2 NA18974.hp1 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.601-7639T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79033803 | |||||||
chr6:79034006 | A | T | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.601-7842T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79034006 | |||||||
chr6:79034018 | G | T | 141 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(138): Show |
145 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.601-7854C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79034018 | |||||||
chr6:79034063 | T | C | 1 | a0002c0002t0003g0251 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.601-7899A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79034063 | |||||||
chr6:79034160 | G | A | 1 | a0008c0019t0013g0190 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.601-7996C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79034160 | |||||||
chr6:79034327 | T | C | 9 | a0001c0007t0012g0169 a0001c0007t0012g0170 a0001c0007t0012g0171 others(6): Show |
9 | HG02559.hp2 HG02622.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.601-8163A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79034327 | |||||||
chr6:79034363 | C | T | 19 | a0001c0001t0011g0150 a0001c0001t0011g0151 a0001c0001t0011g0153 others(16): Show |
19 | HG00280.hp2 HG00639.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.601-8199G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79034363 | |||||||
chr6:79034865 | C | T | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.600+7978G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79034865 | |||||||
chr6:79035128 | T | C | 1 | a0002c0020t0022g0253 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.600+7715A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79035128 | |||||||
chr6:79035151 | C | A | 95 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(92): Show |
96 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.600+7692G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79035151 | |||||||
chr6:79035270 | T | C | 1 | a0001c0011t0016g0019 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.600+7573A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79035270 | |||||||
chr6:79035332 | C | A | 1 | a0001c0001t0015g0157 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.600+7511G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79035332 | |||||||
chr6:79035390 | C | T | 134 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(131): Show |
135 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.600+7453G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79035390 | |||||||
chr6:79035402 | C | T | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.600+7441G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79035402 | |||||||
chr6:79035410 | T | C | 1 | a0001c0001t0001g0128 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.600+7433A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79035410 | |||||||
chr6:79035432 | A | G | 4 | a0003c0003t0002g0002 a0003c0003t0002g0278 a0003c0003t0009g0277 others(1): Show |
6 | NA18950.hp2 NA18960.hp2 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.600+7411T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79035432 | |||||||
chr6:79035504 | A | G | 4 | a0001c0005t0003g0001 a0001c0005t0019g0012 a0001c0005t0019g0264 others(1): Show |
7 | HG02280.hp1 HG02965.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.600+7339T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79035504 | |||||||
chr6:79035560 | C | G | 36 | a0001c0006t0002g0013 a0001c0006t0002g0014 a0001c0006t0002g0268 others(33): Show |
42 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.600+7283G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79035560 | |||||||
chr6:79035758 | A | G | 1 | a0001c0001t0001g0112 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.600+7085T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79035758 | |||||||
chr6:79035788 | G | A | 6 | a0002c0002t0003g0193 a0002c0002t0003g0195 a0002c0002t0008g0197 others(3): Show |
6 | HG01109.hp1 HG02486.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.600+7055C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79035788 | |||||||
chr6:79035820 | G | A | 1 | a0003c0003t0052g0298 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.600+7023C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79035820 | |||||||
chr6:79035839 | T | C | 35 | a0001c0001t0001g0066 a0001c0001t0001g0068 a0001c0001t0001g0069 others(32): Show |
35 | HG00438.hp1 HG00621.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.600+7004A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79035839 | |||||||
chr6:79035855 | C | G | 1 | a0002c0002t0008g0192 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.600+6988G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79035855 | |||||||
chr6:79035870 | C | T | 1 | a0002c0002t0068g0220 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.600+6973G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79035870 | |||||||
chr6:79035964 | C | T | 10 | a0001c0005t0003g0001 a0001c0005t0019g0012 a0001c0005t0019g0264 others(7): Show |
13 | HG01109.hp2 HG02280.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.600+6879G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79035964 | |||||||
chr6:79036034 | A | G | 40 | a0001c0006t0002g0013 a0001c0006t0002g0014 a0001c0006t0002g0265 others(37): Show |
46 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.600+6809T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79036034 | |||||||
chr6:79036195 | C | T | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.600+6648G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79036195 | |||||||
chr6:79036331 | T | A | 1 | a0001c0001t0015g0156 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.600+6512A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79036331 | |||||||
chr6:79036349 | T | G | 6 | a0001c0005t0023g0049 a0001c0005t0023g0051 a0001c0005t0030g0048 others(3): Show |
6 | HG01884.hp2 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.600+6494A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79036349 | |||||||
chr6:79036405 | ACT | A | 9 | a0001c0001t0014g0158 a0001c0001t0014g0160 a0001c0001t0014g0161 others(6): Show |
9 | HG00280.hp2 HG00639.hp1 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.600+6436_600+6437d others(4): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79036405 | |||||||
chr6:79036435 | T | C | 1 | a0001c0001t0059g0118 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.600+6408A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79036435 | |||||||
chr6:79036437 | C | T | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.600+6406G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79036437 | |||||||
chr6:79036636 | C | T | 1 | a0001c0005t0049g0036 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.600+6207G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79036636 | |||||||
chr6:79036688 | G | A | 1 | a0001c0001t0005g0099 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.600+6155C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79036688 | |||||||
chr6:79036756 | C | A | 2 | a0001c0010t0029g0053 a0001c0010t0029g0054 |
2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.600+6087G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79036756 | |||||||
chr6:79036757 | T | A | 2 | a0001c0010t0029g0053 a0001c0010t0029g0054 |
2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.600+6086A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79036757 | |||||||
chr6:79036921 | C | CA | 111 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(108): Show |
114 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.600+5921dupT | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79036921 | |||||||
chr6:79036921 | C | CAA | 26 | a0001c0001t0001g0069 a0001c0001t0001g0100 a0001c0001t0001g0101 others(23): Show |
26 | HG00621.hp2 HG00738.hp2 HG01496.hp1 others(23): Show |
intron_variant | MODIFIER | c.600+5920_600+5921d others(4): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79036921 | |||||||
chr6:79036921 | CA | C | 9 | a0001c0005t0038g0047 a0001c0007t0012g0169 a0001c0007t0012g0170 others(6): Show |
9 | HG01070.hp1 HG01358.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.600+5921delT | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79036921 | |||||||
chr6:79036921 | CAA | C | 7 | a0001c0001t0026g0149 a0001c0005t0023g0049 a0001c0005t0023g0051 others(4): Show |
7 | HG01884.hp2 HG02886.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.600+5920_600+5921d others(4): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79036921 | |||||||
chr6:79037076 | A | T | 1 | a0001c0001t0001g0079 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.600+5767T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79037076 | |||||||
chr6:79037103 | T | C | 1 | a0001c0021t0036g0070 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.600+5740A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79037103 | |||||||
chr6:79037174 | C | T | 290 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(287): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.600+5669G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79037174 | |||||||
chr6:79037267 | A | C | 1 | a0001c0001t0001g0122 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.600+5576T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79037267 | |||||||
chr6:79037321 | C | A | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.600+5522G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79037321 | |||||||
chr6:79037378 | C | T | 1 | a0001c0005t0055g0045 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.600+5465G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79037378 | |||||||
chr6:79037506 | G | A | 1 | a0002c0002t0003g0254 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.600+5337C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79037506 | |||||||
chr6:79037727 | A | G | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.600+5116T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79037727 | |||||||
chr6:79037879 | A | C | 1 | a0001c0006t0008g0037 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.600+4964T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79037879 | |||||||
chr6:79037880 | T | C | 4 | a0001c0001t0011g0255 a0001c0001t0011g0256 a0001c0001t0018g0257 others(1): Show |
4 | HG02258.hp2 HG02896.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.600+4963A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79037880 | |||||||
chr6:79037880 | T | TAAC | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.600+4960_600+4962d others(5): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79037880 | |||||||
chr6:79037915 | T | C | 1 | a0001c0001t0005g0076 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.600+4928A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79037915 | |||||||
chr6:79037965 | T | C | 40 | a0001c0006t0002g0013 a0001c0006t0002g0014 a0001c0006t0002g0265 others(37): Show |
46 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.600+4878A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79037965 | |||||||
chr6:79037978 | T | C | 1 | a0001c0001t0015g0157 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.600+4865A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79037978 | |||||||
chr6:79038011 | C | T | 1 | a0002c0002t0063g0176 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.600+4832G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79038011 | |||||||
chr6:79038117 | T | C | 1 | a0002c0002t0063g0176 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.600+4726A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79038117 | |||||||
chr6:79038288 | T | G | 1 | a0002c0002t0063g0176 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.600+4555A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79038288 | |||||||
chr6:79038336 | C | T | 279 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(276): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.600+4507G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79038336 | |||||||
chr6:79038392 | C | T | 2 | a0002c0002t0004g0219 a0002c0002t0010g0218 |
2 | NA19002.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.600+4451G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79038392 | |||||||
chr6:79038464 | G | C | 4 | a0001c0005t0003g0001 a0001c0005t0019g0012 a0001c0005t0019g0264 others(1): Show |
7 | HG02280.hp1 HG02965.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.600+4379C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79038464 | |||||||
chr6:79038611 | C | T | 282 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(279): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.600+4232G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79038611 | |||||||
chr6:79038666 | CTTT | C | 279 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(276): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.600+4174_600+4176d others(5): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79038666 | |||||||
chr6:79038704 | A | G | 3 | a0001c0005t0019g0012 a0001c0005t0019g0264 a0001c0005t0046g0263 |
4 | HG03041.hp1 HG03130.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.600+4139T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79038704 | |||||||
chr6:79038724 | T | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.600+4119A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79038724 | |||||||
chr6:79039005 | C | A | 9 | a0001c0007t0012g0169 a0001c0007t0012g0170 a0001c0007t0012g0171 others(6): Show |
9 | HG02559.hp2 HG02622.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.600+3838G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79039005 | |||||||
chr6:79039160 | CCACAT | C | 4 | a0001c0005t0027g0033 a0001c0006t0008g0037 a0001c0012t0024g0034 others(1): Show |
4 | HG01109.hp2 HG02572.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.600+3678_600+3682d others(7): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79039160 | |||||||
chr6:79039254 | G | A | 1 | a0001c0006t0009g0266 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.600+3589C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79039254 | |||||||
chr6:79039415 | T | G | 1 | a0001c0001t0001g0111 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.600+3428A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79039415 | |||||||
chr6:79039449 | CTT | C | 144 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(141): Show |
148 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.600+3392_600+3393d others(4): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79039449 | |||||||
chr6:79039460 | AT | A | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.600+3382delA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79039460 | |||||||
chr6:79039515 | T | C | 6 | a0001c0005t0023g0049 a0001c0005t0023g0051 a0001c0005t0030g0048 others(3): Show |
6 | HG01884.hp2 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.600+3328A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79039515 | |||||||
chr6:79039732 | T | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.600+3111A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79039732 | |||||||
chr6:79039877 | T | C | 95 | a0001c0007t0012g0169 a0001c0007t0012g0170 a0001c0007t0012g0171 others(92): Show |
100 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.600+2966A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79039877 | |||||||
chr6:79039940 | C | G | 2 | a0001c0005t0054g0038 a0001c0005t0055g0045 |
2 | HG02723.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.600+2903G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79039940 | |||||||
chr6:79039947 | A | G | 3 | a0001c0005t0019g0012 a0001c0005t0019g0264 a0001c0005t0046g0263 |
4 | HG03041.hp1 HG03130.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.600+2896T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79039947 | |||||||
chr6:79040003 | C | T | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.600+2840G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79040003 | |||||||
chr6:79040092 | T | C | 283 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(280): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.600+2751A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79040092 | |||||||
chr6:79040179 | T | C | 2 | a0001c0001t0001g0146 a0001c0001t0005g0145 |
2 | NA18988.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.600+2664A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79040179 | |||||||
chr6:79040476 | A | T | 2 | a0001c0001t0014g0161 a0001c0001t0014g0162 |
2 | HG02145.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.600+2367T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79040476 | |||||||
chr6:79040668 | T | C | 134 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(131): Show |
135 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(132): Show |
intron_variant | MODIFIER | c.600+2175A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79040668 | |||||||
chr6:79040863 | C | A | 1 | a0001c0001t0059g0118 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.600+1980G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79040863 | |||||||
chr6:79040896 | C | CT | 279 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(276): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.600+1946dupA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79040896 | |||||||
chr6:79041031 | A | T | 1 | a0001c0001t0001g0121 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.600+1812T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79041031 | |||||||
chr6:79041058 | T | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.600+1785A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79041058 | |||||||
chr6:79041300 | T | C | 9 | a0001c0007t0012g0169 a0001c0007t0012g0170 a0001c0007t0012g0171 others(6): Show |
9 | HG02559.hp2 HG02622.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.600+1543A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79041300 | |||||||
chr6:79041477 | C | A | 1 | a0002c0002t0008g0240 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.600+1366G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79041477 | |||||||
chr6:79041724 | A | C | 8 | a0002c0002t0003g0237 a0002c0002t0003g0238 a0002c0002t0003g0249 others(5): Show |
8 | HG00642.hp2 HG01123.hp2 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.600+1119T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79041724 | |||||||
chr6:79041761 | C | G | 280 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(277): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.600+1082G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79041761 | |||||||
chr6:79041764 | A | T | 1 | a0002c0002t0003g0244 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.600+1079T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79041764 | |||||||
chr6:79042273 | T | C | 1 | a0001c0005t0055g0045 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.600+570A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79042273 | |||||||
chr6:79042346 | A | C | 2 | a0001c0006t0020g0006 a0001c0006t0020g0148 |
3 | NA18944.hp1 NA18965.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.600+497T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79042346 | |||||||
chr6:79042490 | C | A | 1 | a0002c0002t0003g0042 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.600+353G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79042490 | |||||||
chr6:79042587 | G | A | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.600+256C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79042587 | |||||||
chr6:79042623 | T | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.600+220A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79042623 | |||||||
chr6:79042750 | A | T | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.600+93T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79042750 | |||||||
chr6:79042786 | A | T | 1 | a0001c0005t0027g0033 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.600+57T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 7/39 | chr6 | 79042786 | |||||||
chr6:79043075 | T | C | 125 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(122): Show |
126 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.440-72A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79043075 | |||||||
chr6:79043268 | A | ATTACTTG others(9): Show |
2 | a0002c0002t0004g0216 a0002c0002t0004g0217 |
2 | HG00733.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.440-266_440-265ins others(16): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79043268 | |||||||
chr6:79043269 | A | G | 4 | a0002c0002t0004g0215 a0002c0009t0004g0009 a0002c0009t0004g0214 others(1): Show |
5 | HG00738.hp1 HG01106.hp1 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.440-266T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79043269 | |||||||
chr6:79043308 | G | A | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.440-305C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79043308 | |||||||
chr6:79043345 | C | T | 1 | a0001c0006t0002g0269 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.440-342G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79043345 | |||||||
chr6:79043356 | G | C | 126 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(123): Show |
127 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.440-353C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79043356 | |||||||
chr6:79043569 | T | C | 94 | a0001c0007t0012g0169 a0001c0007t0012g0170 a0001c0007t0012g0171 others(91): Show |
99 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.440-566A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79043569 | |||||||
chr6:79043677 | T | C | 128 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(125): Show |
129 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.440-674A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79043677 | |||||||
chr6:79043702 | TC | T | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.440-700delG | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79043702 | |||||||
chr6:79043705 | ATCTAAAT others(19): Show |
A | 3 | a0002c0002t0003g0041 a0002c0002t0003g0042 a0002c0002t0007g0044 |
3 | HG02109.hp2 HG02451.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.440-728_440-703del others(26): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79043705 | |||||||
chr6:79043792 | G | A | 1 | a0002c0002t0003g0243 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.440-789C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79043792 | |||||||
chr6:79043826 | A | G | 1 | a0001c0001t0005g0076 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.440-823T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79043826 | |||||||
chr6:79043829 | C | CT | 39 | a0001c0006t0002g0013 a0001c0006t0002g0014 a0001c0006t0002g0265 others(36): Show |
45 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.440-827dupA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79043829 | |||||||
chr6:79043829 | CT | C | 8 | a0001c0008t0003g0167 a0001c0008t0007g0164 a0001c0008t0007g0165 others(5): Show |
8 | HG02280.hp2 HG02622.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.440-827delA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79043829 | |||||||
chr6:79043958 | C | T | 1 | a0001c0005t0055g0045 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.440-955G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79043958 | |||||||
chr6:79044255 | G | A | 6 | a0001c0005t0023g0049 a0001c0005t0023g0051 a0001c0005t0030g0048 others(3): Show |
6 | HG01884.hp2 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.440-1252C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79044255 | |||||||
chr6:79044294 | T | C | 1 | a0003c0003t0061g0283 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.440-1291A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79044294 | |||||||
chr6:79044377 | T | A | 2 | a0001c0006t0020g0006 a0001c0006t0020g0148 |
3 | NA18944.hp1 NA18965.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.440-1374A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79044377 | |||||||
chr6:79044442 | A | G | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.440-1439T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79044442 | |||||||
chr6:79044603 | A | G | 11 | a0001c0005t0003g0001 a0001c0005t0019g0012 a0001c0005t0019g0264 others(8): Show |
14 | HG01109.hp2 HG02280.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.440-1600T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79044603 | |||||||
chr6:79044643 | G | A | 280 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(277): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.440-1640C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79044643 | |||||||
chr6:79044651 | T | A | 3 | a0001c0005t0049g0036 a0001c0005t0054g0038 a0001c0005t0055g0045 |
3 | HG02723.hp1 HG03225.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.440-1648A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79044651 | |||||||
chr6:79044757 | G | A | 1 | a0001c0001t0005g0103 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.440-1754C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79044757 | |||||||
chr6:79044975 | T | C | 1 | a0002c0002t0062g0199 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.440-1972A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79044975 | |||||||
chr6:79045058 | T | C | 1 | a0002c0002t0058g0043 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.440-2055A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79045058 | |||||||
chr6:79045170 | G | T | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.440-2167C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79045170 | |||||||
chr6:79045221 | C | T | 1 | a0002c0002t0063g0176 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.440-2218G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79045221 | |||||||
chr6:79045307 | T | C | 4 | a0001c0001t0011g0150 a0001c0001t0011g0151 a0001c0001t0011g0153 others(1): Show |
4 | HG02055.hp1 HG02809.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.440-2304A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79045307 | |||||||
chr6:79045368 | A | T | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.440-2365T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79045368 | |||||||
chr6:79045536 | A | G | 1 | a0001c0001t0001g0300 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.440-2533T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79045536 | |||||||
chr6:79045714 | T | C | 40 | a0001c0006t0002g0013 a0001c0006t0002g0014 a0001c0006t0002g0265 others(37): Show |
46 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.440-2711A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79045714 | |||||||
chr6:79045820 | T | C | 1 | a0001c0001t0005g0065 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.440-2817A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79045820 | |||||||
chr6:79045990 | C | T | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.440-2987G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79045990 | |||||||
chr6:79046092 | G | A | 1 | a0002c0002t0008g0240 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.440-3089C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79046092 | |||||||
chr6:79046138 | G | A | 11 | a0001c0005t0003g0001 a0001c0005t0019g0012 a0001c0005t0019g0264 others(8): Show |
14 | HG01109.hp2 HG02280.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.440-3135C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79046138 | |||||||
chr6:79046238 | T | C | 2 | a0001c0010t0029g0053 a0001c0010t0029g0054 |
2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.440-3235A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79046238 | |||||||
chr6:79046329 | C | T | 2 | a0002c0002t0007g0003 a0002c0002t0007g0039 |
3 | HG00280.hp1 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.440-3326G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79046329 | |||||||
chr6:79046371 | T | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.440-3368A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79046371 | |||||||
chr6:79046375 | A | T | 1 | a0001c0001t0001g0077 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.440-3372T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79046375 | |||||||
chr6:79046484 | A | G | 40 | a0001c0006t0002g0013 a0001c0006t0002g0014 a0001c0006t0002g0265 others(37): Show |
46 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.440-3481T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79046484 | |||||||
chr6:79046605 | A | G | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.440-3602T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79046605 | |||||||
chr6:79046627 | A | T | 6 | a0001c0005t0023g0049 a0001c0005t0023g0051 a0001c0005t0030g0048 others(3): Show |
6 | HG01884.hp2 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.440-3624T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79046627 | |||||||
chr6:79046674 | C | G | 1 | a0001c0001t0015g0155 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.440-3671G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79046674 | |||||||
chr6:79046776 | T | G | 2 | a0002c0002t0004g0229 a0002c0002t0010g0228 |
2 | NA18612.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.440-3773A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79046776 | |||||||
chr6:79046876 | A | AAAC | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.440-3876_440-3874d others(5): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79046876 | |||||||
chr6:79046903 | T | TA | 9 | a0001c0001t0001g0104 a0001c0001t0001g0131 a0001c0005t0019g0012 others(6): Show |
10 | HG01175.hp2 HG01261.hp1 HG03041.hp1 others(7): Show |
intron_variant | MODIFIER | c.440-3901dupT | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79046903 | |||||||
chr6:79046903 | TA | T | 23 | a0001c0001t0001g0077 a0001c0001t0001g0112 a0001c0001t0005g0078 others(20): Show |
23 | HG01884.hp2 HG02559.hp2 HG02622.hp2 others(20): Show |
intron_variant | MODIFIER | c.440-3901delT | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79046903 | |||||||
chr6:79047050 | G | A | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.440-4047C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79047050 | |||||||
chr6:79047057 | T | C | 4 | a0001c0005t0027g0033 a0001c0006t0008g0037 a0001c0012t0024g0034 others(1): Show |
4 | HG01109.hp2 HG02572.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.440-4054A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79047057 | |||||||
chr6:79047217 | A | G | 80 | a0002c0002t0003g0010 a0002c0002t0003g0011 a0002c0002t0003g0041 others(77): Show |
85 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.440-4214T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79047217 | |||||||
chr6:79047227 | C | T | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.440-4224G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79047227 | |||||||
chr6:79047338 | C | G | 1 | a0001c0005t0003g0001 | 3 | HG02280.hp1 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.440-4335G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79047338 | |||||||
chr6:79047456 | T | C | 3 | a0001c0001t0021g0027 a0001c0001t0021g0028 a0001c0001t0021g0030 |
3 | HG02922.hp2 NA18906.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.440-4453A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79047456 | |||||||
chr6:79047637 | G | A | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.440-4634C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79047637 | |||||||
chr6:79047716 | T | C | 1 | a0004c0004t0013g0183 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.440-4713A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79047716 | |||||||
chr6:79047721 | A | C | 96 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(93): Show |
97 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.440-4718T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79047721 | |||||||
chr6:79047756 | T | A | 1 | a0001c0001t0001g0075 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.440-4753A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79047756 | |||||||
chr6:79047762 | T | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.440-4759A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79047762 | |||||||
chr6:79047794 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.440-4791G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79047794 | |||||||
chr6:79047988 | T | A | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.440-4985A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79047988 | |||||||
chr6:79047998 | T | C | 1 | a0003c0003t0002g0289 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.440-4995A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79047998 | |||||||
chr6:79048003 | A | AT | 8 | a0001c0010t0057g0163 a0003c0003t0002g0015 a0003c0003t0002g0286 others(5): Show |
9 | HG00099.hp2 HG01070.hp1 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.440-5001dupA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79048003 | |||||||
chr6:79048273 | C | T | 1 | a0001c0021t0036g0070 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.440-5270G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79048273 | |||||||
chr6:79048286 | G | C | 1 | a0004c0004t0006g0189 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.440-5283C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79048286 | |||||||
chr6:79048289 | G | A | 1 | a0001c0021t0036g0070 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.440-5286C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79048289 | |||||||
chr6:79048450 | A | T | 42 | a0001c0006t0002g0013 a0001c0006t0002g0014 a0001c0006t0002g0265 others(39): Show |
48 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.440-5447T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79048450 | |||||||
chr6:79048501 | C | A | 125 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(122): Show |
126 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.440-5498G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79048501 | |||||||
chr6:79048506 | T | G | 125 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(122): Show |
126 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.440-5503A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79048506 | |||||||
chr6:79048810 | A | C | 1 | a0001c0005t0055g0045 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.440-5807T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79048810 | |||||||
chr6:79049121 | G | C | 1 | a0001c0001t0015g0157 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.440-6118C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79049121 | |||||||
chr6:79049149 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.440-6146C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79049149 | |||||||
chr6:79049231 | C | T | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.440-6228G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79049231 | |||||||
chr6:79049278 | T | G | 4 | a0001c0005t0003g0001 a0001c0005t0019g0012 a0001c0005t0019g0264 others(1): Show |
7 | HG02280.hp1 HG02965.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.440-6275A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79049278 | |||||||
chr6:79049366 | C | T | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.440-6363G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79049366 | |||||||
chr6:79049414 | C | T | 1 | a0003c0003t0009g0272 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.440-6411G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79049414 | |||||||
chr6:79049587 | C | T | 39 | a0001c0006t0002g0013 a0001c0006t0002g0014 a0001c0006t0002g0265 others(36): Show |
45 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.440-6584G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79049587 | |||||||
chr6:79049616 | G | A | 2 | a0003c0003t0002g0284 a0003c0003t0002g0285 |
2 | NA18977.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.440-6613C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79049616 | |||||||
chr6:79049771 | T | C | 40 | a0001c0006t0002g0013 a0001c0006t0002g0014 a0001c0006t0002g0265 others(37): Show |
46 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.440-6768A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79049771 | |||||||
chr6:79049843 | T | C | 2 | a0001c0012t0024g0034 a0001c0015t0024g0035 |
2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.440-6840A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79049843 | |||||||
chr6:79050010 | A | G | 1 | a0001c0006t0009g0297 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.440-7007T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79050010 | |||||||
chr6:79050015 | C | T | 279 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(276): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.440-7012G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79050015 | |||||||
chr6:79050077 | G | GT | 4 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0060 others(1): Show |
4 | HG00733.hp2 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.440-7075dupA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79050077 | |||||||
chr6:79050121 | C | T | 1 | a0002c0002t0003g0251 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.440-7118G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79050121 | |||||||
chr6:79050259 | A | G | 1 | a0002c0002t0051g0248 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.440-7256T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79050259 | |||||||
chr6:79050308 | A | G | 1 | a0001c0006t0002g0267 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.440-7305T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79050308 | |||||||
chr6:79050445 | G | A | 3 | a0001c0006t0002g0013 a0001c0006t0002g0268 a0001c0006t0002g0275 |
4 | NA19011.hp1 NA19057.hp1 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.440-7442C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79050445 | |||||||
chr6:79050556 | G | A | 1 | a0001c0005t0023g0051 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.440-7553C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79050556 | |||||||
chr6:79050590 | T | A | 1 | a0001c0005t0055g0045 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.440-7587A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79050590 | |||||||
chr6:79050607 | T | C | 1 | a0001c0001t0001g0112 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.440-7604A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79050607 | |||||||
chr6:79050696 | G | T | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.440-7693C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79050696 | |||||||
chr6:79050825 | C | T | 4 | a0001c0005t0027g0033 a0001c0006t0008g0037 a0001c0012t0024g0034 others(1): Show |
4 | HG01109.hp2 HG02572.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.440-7822G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79050825 | |||||||
chr6:79050979 | C | T | 1 | a0001c0021t0036g0070 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.440-7976G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79050979 | |||||||
chr6:79051103 | T | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.440-8100A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79051103 | |||||||
chr6:79051107 | C | T | 5 | a0001c0008t0003g0167 a0001c0008t0007g0164 a0001c0008t0007g0165 others(2): Show |
5 | HG02280.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.440-8104G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79051107 | |||||||
chr6:79051152 | G | A | 3 | a0001c0005t0027g0033 a0001c0012t0024g0034 a0001c0015t0024g0035 |
3 | HG01109.hp2 HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.440-8149C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79051152 | |||||||
chr6:79051266 | G | C | 8 | a0002c0002t0003g0237 a0002c0002t0003g0238 a0002c0002t0003g0249 others(5): Show |
8 | HG00642.hp2 HG01123.hp2 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.440-8263C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79051266 | |||||||
chr6:79051280 | C | T | 124 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(121): Show |
125 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.440-8277G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79051280 | |||||||
chr6:79051336 | G | T | 3 | a0001c0005t0027g0033 a0001c0012t0024g0034 a0001c0015t0024g0035 |
3 | HG01109.hp2 HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.440-8333C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79051336 | |||||||
chr6:79051401 | T | C | 1 | a0001c0001t0034g0132 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.440-8398A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79051401 | |||||||
chr6:79051525 | T | C | 40 | a0001c0006t0002g0013 a0001c0006t0002g0014 a0001c0006t0002g0265 others(37): Show |
46 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.440-8522A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79051525 | |||||||
chr6:79051614 | G | T | 8 | a0002c0002t0003g0041 a0002c0002t0003g0042 a0002c0002t0007g0003 others(5): Show |
10 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(7): Show |
intron_variant | MODIFIER | c.440-8611C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79051614 | |||||||
chr6:79051793 | C | T | 1 | a0001c0006t0009g0297 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.439+8685G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79051793 | |||||||
chr6:79051920 | G | GT | 17 | a0001c0001t0011g0150 a0001c0001t0011g0151 a0001c0001t0011g0153 others(14): Show |
17 | HG00280.hp2 HG00639.hp1 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.439+8557dupA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79051920 | |||||||
chr6:79051920 | G | T | 2 | a0001c0001t0014g0161 a0001c0001t0014g0162 |
2 | HG02145.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.439+8558C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79051920 | |||||||
chr6:79051928 | T | A | 4 | a0001c0005t0027g0033 a0001c0006t0008g0037 a0001c0012t0024g0034 others(1): Show |
4 | HG01109.hp2 HG02572.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.439+8550A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79051928 | |||||||
chr6:79052169 | T | C | 40 | a0001c0006t0002g0013 a0001c0006t0002g0014 a0001c0006t0002g0265 others(37): Show |
46 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.439+8309A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79052169 | |||||||
chr6:79052196 | G | A | 4 | a0002c0002t0003g0010 a0002c0002t0003g0244 a0002c0002t0003g0245 others(1): Show |
5 | HG01074.hp2 HG02055.hp2 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.439+8282C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79052196 | |||||||
chr6:79052333 | T | C | 5 | a0001c0001t0017g0023 a0001c0001t0017g0026 a0001c0001t0017g0031 others(2): Show |
5 | HG01891.hp1 HG02109.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.439+8145A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79052333 | |||||||
chr6:79052428 | G | A | 1 | a0001c0001t0001g0107 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.439+8050C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79052428 | |||||||
chr6:79052455 | G | A | 124 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(121): Show |
125 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.439+8023C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79052455 | |||||||
chr6:79052467 | T | G | 1 | a0002c0002t0066g0230 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.439+8011A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79052467 | |||||||
chr6:79052488 | C | T | 4 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 others(1): Show |
4 | HG02698.hp1 NA19003.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.439+7990G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79052488 | |||||||
chr6:79052979 | A | G | 1 | a0001c0001t0005g0109 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.439+7499T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79052979 | |||||||
chr6:79053106 | G | A | 6 | a0001c0005t0023g0049 a0001c0005t0023g0051 a0001c0005t0030g0048 others(3): Show |
6 | HG01884.hp2 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.439+7372C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79053106 | |||||||
chr6:79053110 | T | A | 1 | a0002c0002t0004g0207 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.439+7368A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79053110 | |||||||
chr6:79053183 | G | A | 1 | a0001c0001t0005g0076 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.439+7295C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79053183 | |||||||
chr6:79053258 | G | A | 1 | a0004c0004t0006g0180 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.439+7220C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79053258 | |||||||
chr6:79053263 | G | A | 39 | a0001c0006t0002g0013 a0001c0006t0002g0014 a0001c0006t0002g0265 others(36): Show |
45 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.439+7215C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79053263 | |||||||
chr6:79053271 | G | A | 19 | a0001c0001t0011g0150 a0001c0001t0011g0151 a0001c0001t0011g0153 others(16): Show |
19 | HG00280.hp2 HG00639.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.439+7207C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79053271 | |||||||
chr6:79053549 | G | C | 80 | a0002c0002t0003g0010 a0002c0002t0003g0011 a0002c0002t0003g0041 others(77): Show |
85 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.439+6929C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79053549 | |||||||
chr6:79053599 | G | A | 1 | a0001c0001t0015g0156 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.439+6879C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79053599 | |||||||
chr6:79053647 | C | T | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.439+6831G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79053647 | |||||||
chr6:79053655 | T | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.439+6823A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79053655 | |||||||
chr6:79053739 | T | C | 1 | a0001c0006t0009g0297 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.439+6739A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79053739 | |||||||
chr6:79053877 | C | T | 5 | a0001c0001t0001g0075 a0001c0001t0001g0108 a0001c0001t0005g0076 others(2): Show |
5 | NA18950.hp1 NA18975.hp2 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.439+6601G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79053877 | |||||||
chr6:79053980 | G | A | 2 | a0001c0010t0029g0053 a0001c0010t0029g0054 |
2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.439+6498C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79053980 | |||||||
chr6:79054103 | A | G | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.439+6375T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79054103 | |||||||
chr6:79054342 | C | CA | 118 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(115): Show |
119 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.439+6135dupT | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79054342 | |||||||
chr6:79054386 | T | C | 1 | a0001c0001t0015g0156 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.439+6092A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79054386 | |||||||
chr6:79054595 | C | T | 2 | a0001c0001t0014g0161 a0001c0001t0014g0162 |
2 | HG02145.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.439+5883G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79054595 | |||||||
chr6:79054650 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.439+5828G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79054650 | |||||||
chr6:79054739 | C | A | 1 | a0001c0001t0005g0065 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.439+5739G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79054739 | |||||||
chr6:79054739 | C | G | 6 | a0001c0005t0023g0049 a0001c0005t0023g0051 a0001c0005t0030g0048 others(3): Show |
6 | HG01884.hp2 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.439+5739G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79054739 | |||||||
chr6:79054898 | C | T | 282 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(279): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.439+5580G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79054898 | |||||||
chr6:79054943 | C | CT | 83 | a0001c0005t0038g0047 a0001c0005t0045g0046 a0001c0010t0057g0163 others(80): Show |
88 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.439+5534dupA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79054943 | |||||||
chr6:79054956 | T | TA | 4 | a0001c0005t0023g0049 a0001c0005t0023g0051 a0001c0005t0030g0048 others(1): Show |
4 | HG01884.hp2 HG02976.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.439+5521dupT | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79054956 | |||||||
chr6:79055163 | G | A | 1 | a0001c0005t0003g0001 | 3 | HG02280.hp1 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.439+5315C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79055163 | |||||||
chr6:79055377 | T | C | 1 | a0001c0005t0003g0001 | 3 | HG02280.hp1 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.439+5101A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79055377 | |||||||
chr6:79055444 | G | A | 1 | a0001c0001t0011g0255 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.439+5034C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79055444 | |||||||
chr6:79055478 | T | A | 80 | a0002c0002t0003g0010 a0002c0002t0003g0011 a0002c0002t0003g0041 others(77): Show |
85 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.439+5000A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79055478 | |||||||
chr6:79055624 | T | C | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.439+4854A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79055624 | |||||||
chr6:79055668 | G | A | 3 | a0001c0005t0027g0033 a0001c0012t0024g0034 a0001c0015t0024g0035 |
3 | HG01109.hp2 HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.439+4810C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79055668 | |||||||
chr6:79056227 | G | A | 8 | a0002c0002t0003g0041 a0002c0002t0003g0042 a0002c0002t0007g0003 others(5): Show |
10 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(7): Show |
intron_variant | MODIFIER | c.439+4251C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79056227 | |||||||
chr6:79056366 | G | A | 4 | a0001c0001t0011g0150 a0001c0001t0011g0151 a0001c0001t0011g0153 others(1): Show |
4 | HG02055.hp1 HG02809.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.439+4112C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79056366 | |||||||
chr6:79056479 | G | C | 1 | a0001c0001t0001g0113 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.439+3999C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79056479 | |||||||
chr6:79056486 | G | T | 39 | a0001c0006t0002g0013 a0001c0006t0002g0014 a0001c0006t0002g0265 others(36): Show |
45 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.439+3992C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79056486 | |||||||
chr6:79056541 | C | T | 2 | a0001c0010t0029g0053 a0001c0010t0029g0054 |
2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.439+3937G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79056541 | |||||||
chr6:79056649 | A | G | 1 | a0001c0005t0054g0038 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.439+3829T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79056649 | |||||||
chr6:79056657 | C | T | 279 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(276): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.439+3821G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79056657 | |||||||
chr6:79056699 | T | A | 1 | a0002c0002t0008g0192 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.439+3779A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79056699 | |||||||
chr6:79056834 | A | G | 40 | a0001c0006t0002g0013 a0001c0006t0002g0014 a0001c0006t0002g0265 others(37): Show |
46 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.439+3644T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79056834 | |||||||
chr6:79056878 | A | G | 3 | a0001c0001t0001g0066 a0001c0001t0001g0146 a0001c0001t0005g0145 |
3 | NA18612.hp1 NA18988.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.439+3600T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79056878 | |||||||
chr6:79056883 | T | G | 1 | a0001c0001t0005g0106 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.439+3595A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79056883 | |||||||
chr6:79057010 | G | A | 1 | a0001c0001t0005g0064 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.439+3468C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79057010 | |||||||
chr6:79057060 | T | C | 29 | a0001c0001t0011g0029 a0001c0001t0011g0150 a0001c0001t0011g0151 others(26): Show |
29 | HG00280.hp2 HG00639.hp1 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.439+3418A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79057060 | |||||||
chr6:79057300 | A | C | 1 | a0001c0001t0015g0157 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.439+3178T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79057300 | |||||||
chr6:79057306 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.439+3172G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79057306 | |||||||
chr6:79057597 | G | A | 1 | a0001c0001t0026g0154 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.439+2881C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79057597 | |||||||
chr6:79057714 | T | C | 9 | a0001c0007t0012g0169 a0001c0007t0012g0170 a0001c0007t0012g0171 others(6): Show |
9 | HG02559.hp2 HG02622.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.439+2764A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79057714 | |||||||
chr6:79057757 | C | T | 1 | a0001c0006t0009g0297 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.439+2721G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79057757 | |||||||
chr6:79058113 | G | A | 39 | a0001c0006t0002g0013 a0001c0006t0002g0014 a0001c0006t0002g0265 others(36): Show |
45 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.439+2365C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79058113 | |||||||
chr6:79058186 | G | A | 1 | a0001c0001t0001g0107 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.439+2292C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79058186 | |||||||
chr6:79058368 | T | TGTCA | 5 | a0001c0008t0003g0167 a0001c0008t0007g0164 a0001c0008t0007g0165 others(2): Show |
5 | HG02280.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.439+2106_439+2109d others(6): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79058368 | |||||||
chr6:79058641 | T | C | 1 | a0001c0021t0036g0070 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.439+1837A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79058641 | |||||||
chr6:79058855 | T | C | 2 | a0001c0001t0001g0133 a0001c0001t0001g0134 |
2 | NA18960.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.439+1623A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79058855 | |||||||
chr6:79058884 | C | T | 2 | a0001c0005t0054g0038 a0001c0005t0055g0045 |
2 | HG02723.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.439+1594G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79058884 | |||||||
chr6:79059225 | T | C | 1 | a0001c0001t0005g0299 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.439+1253A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059225 | |||||||
chr6:79059339 | A | T | 124 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(121): Show |
125 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.439+1139T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059339 | |||||||
chr6:79059473 | A | G | 2 | a0002c0002t0003g0193 a0002c0002t0008g0197 |
2 | HG01109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.439+1005T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059473 | |||||||
chr6:79059591 | T | TTA | 36 | a0001c0001t0021g0027 a0001c0008t0007g0168 a0002c0002t0003g0011 others(33): Show |
37 | HG00558.hp1 HG00673.hp2 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.439+885_439+886dup others(2): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059591 | |||||||
chr6:79059591 | T | TTATA | 22 | a0001c0001t0011g0029 a0001c0001t0021g0028 a0001c0001t0021g0030 others(19): Show |
27 | HG00621.hp1 HG00735.hp2 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.439+883_439+886dup others(4): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059591 | |||||||
chr6:79059591 | T | TTATATA | 6 | a0001c0010t0029g0054 a0002c0002t0010g0234 a0002c0002t0027g0239 others(3): Show |
6 | HG00738.hp1 HG01978.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.439+881_439+886dup others(6): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059591 | |||||||
chr6:79059591 | T | TTATATAT others(1): Show |
7 | a0001c0001t0015g0156 a0001c0001t0017g0023 a0001c0001t0017g0031 others(4): Show |
7 | HG01358.hp2 HG01891.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.439+879_439+886dup others(8): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059591 | |||||||
chr6:79059591 | T | TTATATAT others(3): Show |
3 | a0001c0001t0014g0161 a0001c0001t0015g0159 a0008c0019t0013g0190 |
3 | HG00639.hp1 HG03654.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.439+877_439+886dup others(10): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059591 | |||||||
chr6:79059591 | T | TTATATAT others(5): Show |
6 | a0001c0001t0011g0150 a0001c0001t0014g0160 a0001c0001t0015g0157 others(3): Show |
6 | HG00280.hp2 HG01175.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.439+875_439+886dup others(12): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059591 | |||||||
chr6:79059591 | T | TTATATAT others(7): Show |
10 | a0001c0001t0011g0151 a0001c0001t0011g0256 a0001c0001t0014g0162 others(7): Show |
10 | HG02055.hp1 HG02145.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.439+873_439+886dup others(14): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059591 | |||||||
chr6:79059591 | T | TTATATAT others(9): Show |
1 | a0001c0001t0011g0255 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.439+871_439+886dup others(16): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059591 | |||||||
chr6:79059591 | T | TTATATAT others(11): Show |
6 | a0001c0001t0011g0153 a0001c0007t0012g0170 a0001c0007t0012g0171 others(3): Show |
6 | HG02559.hp2 HG02809.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.439+869_439+886dup others(18): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059591 | |||||||
chr6:79059591 | T | TTATATAT others(13): Show |
2 | a0001c0007t0012g0174 a0001c0010t0057g0163 |
2 | HG01358.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.439+867_439+886dup others(20): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059591 | |||||||
chr6:79059591 | T | TTATTTAT others(11): Show |
1 | a0001c0001t0026g0149 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.439+886_439+887ins others(18): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059591 | |||||||
chr6:79059591 | TTA | T | 13 | a0001c0006t0002g0269 a0001c0006t0002g0270 a0001c0006t0002g0275 others(10): Show |
14 | HG00099.hp2 HG01109.hp1 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.439+885_439+886del others(2): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059591 | |||||||
chr6:79059591 | TTATA | T | 29 | a0001c0006t0002g0013 a0001c0006t0002g0014 a0001c0006t0002g0265 others(26): Show |
35 | HG00438.hp2 HG00735.hp1 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.439+883_439+886del others(4): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059591 | |||||||
chr6:79059591 | TTATATA | T | 4 | a0001c0006t0002g0267 a0001c0006t0002g0271 a0001c0006t0009g0297 others(1): Show |
4 | HG01123.hp1 HG02886.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.439+881_439+886del others(6): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059591 | |||||||
chr6:79059591 | TTATATAT others(3): Show |
T | 1 | a0001c0005t0049g0036 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.439+877_439+886del others(10): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059591 | |||||||
chr6:79059591 | TTATATAT others(7): Show |
T | 4 | a0002c0002t0007g0003 a0002c0002t0007g0004 a0002c0002t0007g0039 others(1): Show |
6 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(3): Show |
intron_variant | MODIFIER | c.439+873_439+886del others(14): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059591 | |||||||
chr6:79059591 | TTATATAT others(9): Show |
T | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.439+871_439+886del others(16): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059591 | |||||||
chr6:79059595 | A | T | 1 | a0001c0001t0026g0154 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.439+883T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059595 | |||||||
chr6:79059608 | TATATATA others(11): Show |
T | 4 | a0001c0005t0027g0033 a0001c0006t0008g0037 a0001c0012t0024g0034 others(1): Show |
4 | HG01109.hp2 HG02572.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.439+852_439+869del others(18): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059608 | |||||||
chr6:79059612 | TATATATA others(7): Show |
T | 4 | a0001c0005t0023g0049 a0001c0005t0023g0051 a0001c0005t0030g0048 others(1): Show |
4 | HG01884.hp2 HG02976.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.439+852_439+865del others(14): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059612 | |||||||
chr6:79059614 | TATATATA others(5): Show |
T | 4 | a0001c0001t0014g0158 a0001c0001t0015g0155 a0001c0005t0038g0047 others(1): Show |
4 | HG02818.hp1 HG02886.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.439+852_439+863del others(12): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059614 | |||||||
chr6:79059616 | TATATATA others(3): Show |
T | 5 | a0001c0001t0059g0118 a0001c0005t0019g0012 a0001c0005t0019g0264 others(2): Show |
6 | HG02559.hp1 HG02723.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.439+852_439+861del others(10): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059616 | |||||||
chr6:79059618 | TATATATA others(1): Show |
T | 3 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0005t0055g0045 |
3 | HG03225.hp1 NA18991.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.439+852_439+859del others(8): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059618 | |||||||
chr6:79059620 | TATATAA | T | 76 | a0001c0001t0001g0005 a0001c0001t0001g0066 a0001c0001t0001g0068 others(73): Show |
77 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.439+852_439+857del others(6): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059620 | |||||||
chr6:79059622 | TATAA | T | 9 | a0001c0001t0001g0077 a0001c0001t0001g0097 a0001c0001t0001g0119 others(6): Show |
9 | HG01074.hp1 HG01496.hp1 HG01934.hp2 others(6): Show |
intron_variant | MODIFIER | c.439+852_439+855del others(4): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059622 | |||||||
chr6:79059624 | TAA | T | 8 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0060 others(5): Show |
8 | HG00733.hp2 HG01070.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.439+852_439+853del others(2): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059624 | |||||||
chr6:79059626 | A | T | 25 | a0001c0001t0011g0029 a0001c0001t0011g0150 a0001c0001t0011g0151 others(22): Show |
27 | HG00280.hp2 HG00639.hp1 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.439+852T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059626 | |||||||
chr6:79059627 | A | T | 1 | a0001c0001t0025g0024 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.439+851T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059627 | |||||||
chr6:79059851 | T | C | 1 | a0002c0002t0003g0251 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.439+627A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059851 | |||||||
chr6:79059884 | G | A | 3 | a0001c0005t0049g0036 a0001c0005t0054g0038 a0001c0005t0055g0045 |
3 | HG02723.hp1 HG03225.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.439+594C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059884 | |||||||
chr6:79059997 | G | C | 5 | a0001c0008t0003g0167 a0001c0008t0007g0164 a0001c0008t0007g0165 others(2): Show |
5 | HG02280.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.439+481C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79059997 | |||||||
chr6:79060106 | GA | G | 276 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(273): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.439+371delT | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79060106 | |||||||
chr6:79060140 | A | G | 7 | a0001c0007t0012g0169 a0001c0007t0012g0170 a0001c0007t0012g0171 others(4): Show |
7 | HG02559.hp2 HG02622.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.439+338T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79060140 | |||||||
chr6:79060193 | T | C | 1 | a0001c0001t0059g0118 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.439+285A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79060193 | |||||||
chr6:79060234 | T | C | 1 | a0001c0005t0049g0036 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.439+244A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79060234 | |||||||
chr6:79060298 | T | C | 1 | a0001c0005t0055g0045 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.439+180A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 6/39 | chr6 | 79060298 | |||||||
chr6:79060635 | T | C | 1 | a0001c0005t0003g0001 | 3 | HG02280.hp1 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.340+33A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 5/39 | chr6 | 79060635 | |||||||
chr6:79060638 | T | A | 1 | a0002c0002t0022g0235 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.340+30A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 5/39 | chr6 | 79060638 | |||||||
chr6:79060651 | T | C | 1 | a0001c0006t0008g0037 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.340+17A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 5/39 | chr6 | 79060651 | |||||||
chr6:79060927 | G | A | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.190-109C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79060927 | |||||||
chr6:79060963 | A | G | 1 | a0001c0005t0049g0036 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.190-145T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79060963 | |||||||
chr6:79061058 | C | T | 2 | a0001c0012t0024g0034 a0001c0015t0024g0035 |
2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.190-240G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79061058 | |||||||
chr6:79061136 | G | A | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.190-318C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79061136 | |||||||
chr6:79061204 | T | G | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.190-386A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79061204 | |||||||
chr6:79061489 | A | G | 1 | a0001c0001t0001g0072 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.190-671T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79061489 | |||||||
chr6:79061614 | T | C | 9 | a0001c0001t0011g0029 a0001c0001t0017g0023 a0001c0001t0017g0026 others(6): Show |
9 | HG01891.hp1 HG02109.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.190-796A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79061614 | |||||||
chr6:79061842 | G | T | 1 | a0003c0003t0002g0296 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.190-1024C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79061842 | |||||||
chr6:79061912 | CCATGAAT others(10): Show |
C | 2 | a0001c0005t0049g0036 a0001c0005t0054g0038 |
2 | HG02723.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.190-1111_190-1095d others(19): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79061912 | |||||||
chr6:79062158 | T | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.190-1340A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79062158 | |||||||
chr6:79062257 | C | T | 5 | a0001c0008t0003g0167 a0001c0008t0007g0164 a0001c0008t0007g0165 others(2): Show |
5 | HG02280.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.190-1439G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79062257 | |||||||
chr6:79062584 | T | A | 3 | a0001c0006t0002g0265 a0001c0006t0009g0266 a0001c0006t0009g0297 |
3 | HG01891.hp2 HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.190-1766A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79062584 | |||||||
chr6:79062633 | T | C | 2 | a0001c0001t0026g0149 a0001c0001t0026g0154 |
2 | HG02976.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.190-1815A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79062633 | |||||||
chr6:79062636 | T | G | 94 | a0001c0007t0012g0169 a0001c0007t0012g0170 a0001c0007t0012g0171 others(91): Show |
99 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.190-1818A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79062636 | |||||||
chr6:79062834 | T | C | 1 | a0001c0001t0033g0021 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.190-2016A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79062834 | |||||||
chr6:79062852 | A | AC | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.190-2035dupG | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79062852 | |||||||
chr6:79062931 | T | G | 2 | a0002c0002t0007g0004 a0002c0002t0007g0040 |
3 | HG00099.hp1 HG00140.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.190-2113A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79062931 | |||||||
chr6:79062968 | G | A | 3 | a0001c0005t0019g0012 a0001c0005t0019g0264 a0001c0005t0046g0263 |
4 | HG03041.hp1 HG03130.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.190-2150C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79062968 | |||||||
chr6:79063067 | C | T | 1 | a0002c0002t0008g0240 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.190-2249G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79063067 | |||||||
chr6:79063087 | A | T | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.190-2269T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79063087 | |||||||
chr6:79063136 | C | T | 3 | a0001c0005t0019g0012 a0001c0005t0019g0264 a0001c0005t0046g0263 |
4 | HG03041.hp1 HG03130.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.190-2318G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79063136 | |||||||
chr6:79063191 | T | C | 1 | a0001c0001t0014g0158 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.190-2373A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79063191 | |||||||
chr6:79063302 | G | C | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.190-2484C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79063302 | |||||||
chr6:79063377 | T | A | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.190-2559A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79063377 | |||||||
chr6:79063389 | G | A | 3 | a0001c0005t0027g0033 a0001c0012t0024g0034 a0001c0015t0024g0035 |
3 | HG01109.hp2 HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.190-2571C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79063389 | |||||||
chr6:79063529 | G | C | 4 | a0001c0001t0011g0255 a0001c0001t0011g0256 a0001c0001t0018g0257 others(1): Show |
4 | HG02258.hp2 HG02896.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.190-2711C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79063529 | |||||||
chr6:79063636 | C | T | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.190-2818G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79063636 | |||||||
chr6:79063660 | G | A | 1 | a0001c0001t0018g0258 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.190-2842C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79063660 | |||||||
chr6:79064097 | C | T | 1 | a0001c0001t0005g0071 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.190-3279G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79064097 | |||||||
chr6:79064432 | T | C | 1 | a0003c0003t0002g0290 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.190-3614A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79064432 | |||||||
chr6:79064630 | A | G | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.190-3812T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79064630 | |||||||
chr6:79064708 | T | C | 1 | a0004c0004t0006g0189 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.190-3890A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79064708 | |||||||
chr6:79064912 | T | C | 1 | a0001c0005t0003g0001 | 3 | HG02280.hp1 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.190-4094A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79064912 | |||||||
chr6:79065195 | T | G | 1 | a0001c0005t0055g0045 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.190-4377A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79065195 | |||||||
chr6:79065201 | A | T | 1 | a0001c0005t0055g0045 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.190-4383T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79065201 | |||||||
chr6:79065331 | G | C | 2 | a0001c0006t0020g0006 a0001c0006t0020g0148 |
3 | NA18944.hp1 NA18965.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.190-4513C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79065331 | |||||||
chr6:79065764 | C | CCA | 66 | a0001c0001t0001g0108 a0001c0001t0001g0110 a0001c0001t0001g0111 others(63): Show |
73 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(70): Show |
intron_variant | MODIFIER | c.190-4948_190-4947d others(4): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79065764 | |||||||
chr6:79065764 | C | CCACA | 15 | a0001c0001t0001g0115 a0001c0001t0005g0114 a0001c0005t0027g0033 others(12): Show |
15 | HG01109.hp2 HG01255.hp2 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.190-4950_190-4947d others(6): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79065764 | |||||||
chr6:79065764 | C | CCACACA | 3 | a0001c0001t0001g0138 a0001c0001t0005g0116 a0003c0003t0002g0295 |
3 | HG02080.hp1 HG03540.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.190-4952_190-4947d others(8): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79065764 | |||||||
chr6:79065764 | C | CCACACAC others(5): Show |
1 | a0002c0002t0003g0011 | 2 | NA18998.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.190-4958_190-4947d others(14): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79065764 | |||||||
chr6:79065764 | CCA | C | 32 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0120 others(29): Show |
35 | HG00280.hp2 HG00621.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.190-4948_190-4947d others(4): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79065764 | |||||||
chr6:79065764 | CCACA | C | 55 | a0001c0001t0001g0066 a0001c0001t0001g0146 a0001c0001t0005g0145 others(52): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.190-4950_190-4947d others(6): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79065764 | |||||||
chr6:79065764 | CCACACA | C | 10 | a0001c0001t0001g0119 a0001c0001t0059g0118 a0002c0002t0003g0201 others(7): Show |
10 | HG02080.hp2 HG02559.hp1 HG02602.hp2 others(7): Show |
intron_variant | MODIFIER | c.190-4952_190-4947d others(8): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79065764 | |||||||
chr6:79065764 | CCACACAC others(1): Show |
C | 7 | a0002c0002t0003g0193 a0002c0002t0003g0195 a0002c0002t0008g0192 others(4): Show |
7 | HG01109.hp1 HG02486.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.190-4954_190-4947d others(10): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79065764 | |||||||
chr6:79065764 | CCACACAC others(3): Show |
C | 1 | a0001c0001t0005g0065 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.190-4956_190-4947d others(12): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79065764 | |||||||
chr6:79065892 | T | A | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.190-5074A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79065892 | |||||||
chr6:79065978 | T | C | 4 | a0001c0005t0027g0033 a0001c0006t0008g0037 a0001c0012t0024g0034 others(1): Show |
4 | HG01109.hp2 HG02572.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.190-5160A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79065978 | |||||||
chr6:79065979 | A | T | 2 | a0001c0010t0029g0053 a0001c0010t0029g0054 |
2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.190-5161T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79065979 | |||||||
chr6:79066110 | A | G | 6 | a0001c0005t0023g0049 a0001c0005t0023g0051 a0001c0005t0030g0048 others(3): Show |
6 | HG01884.hp2 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.190-5292T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79066110 | |||||||
chr6:79066161 | C | T | 6 | a0001c0007t0012g0169 a0001c0007t0012g0170 a0001c0007t0012g0171 others(3): Show |
6 | HG02559.hp2 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.190-5343G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79066161 | |||||||
chr6:79066275 | T | C | 1 | a0002c0020t0022g0253 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.190-5457A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79066275 | |||||||
chr6:79066286 | C | A | 1 | a0001c0001t0069g0117 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.190-5468G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79066286 | |||||||
chr6:79066387 | A | G | 125 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(122): Show |
126 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.190-5569T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79066387 | |||||||
chr6:79066446 | A | G | 80 | a0002c0002t0003g0010 a0002c0002t0003g0011 a0002c0002t0003g0041 others(77): Show |
85 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.190-5628T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79066446 | |||||||
chr6:79066529 | T | A | 1 | a0001c0001t0059g0118 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.190-5711A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79066529 | |||||||
chr6:79066670 | T | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.190-5852A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79066670 | |||||||
chr6:79066848 | C | T | 5 | a0001c0001t0017g0023 a0001c0001t0017g0026 a0001c0001t0017g0031 others(2): Show |
5 | HG01891.hp1 HG02109.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.190-6030G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79066848 | |||||||
chr6:79066890 | G | A | 1 | a0004c0004t0013g0188 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.190-6072C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79066890 | |||||||
chr6:79066994 | T | C | 6 | a0001c0005t0023g0049 a0001c0005t0023g0051 a0001c0005t0030g0048 others(3): Show |
6 | HG01884.hp2 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.190-6176A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79066994 | |||||||
chr6:79067140 | G | T | 1 | a0001c0001t0011g0255 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.190-6322C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79067140 | |||||||
chr6:79067175 | C | T | 5 | a0001c0001t0017g0023 a0001c0001t0017g0026 a0001c0001t0017g0031 others(2): Show |
5 | HG01891.hp1 HG02109.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.190-6357G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79067175 | |||||||
chr6:79067525 | A | G | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.190-6707T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79067525 | |||||||
chr6:79067716 | G | A | 1 | a0001c0005t0054g0038 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.190-6898C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79067716 | |||||||
chr6:79067764 | G | C | 1 | a0001c0007t0047g0175 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.190-6946C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79067764 | |||||||
chr6:79067944 | C | T | 6 | a0001c0005t0023g0049 a0001c0005t0023g0051 a0001c0005t0030g0048 others(3): Show |
6 | HG01884.hp2 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.190-7126G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79067944 | |||||||
chr6:79068043 | T | C | 1 | a0002c0002t0003g0254 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.190-7225A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79068043 | |||||||
chr6:79068333 | C | T | 1 | a0001c0001t0005g0052 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.190-7515G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79068333 | |||||||
chr6:79068385 | C | T | 1 | a0001c0011t0016g0018 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.190-7567G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79068385 | |||||||
chr6:79068662 | G | A | 39 | a0001c0006t0002g0013 a0001c0006t0002g0014 a0001c0006t0002g0265 others(36): Show |
45 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.190-7844C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79068662 | |||||||
chr6:79069029 | A | G | 1 | a0002c0002t0004g0198 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.190-8211T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79069029 | |||||||
chr6:79069098 | T | C | 1 | a0004c0004t0006g0189 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.190-8280A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79069098 | |||||||
chr6:79069107 | T | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.190-8289A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79069107 | |||||||
chr6:79069267 | C | T | 7 | a0001c0001t0001g0147 a0001c0001t0001g0300 a0001c0001t0005g0062 others(4): Show |
7 | HG00621.hp2 HG01952.hp1 NA18955.hp2 others(4): Show |
intron_variant | MODIFIER | c.189+8181G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79069267 | |||||||
chr6:79069361 | G | T | 1 | a0002c0002t0008g0192 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.189+8087C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79069361 | |||||||
chr6:79069416 | C | T | 1 | a0001c0005t0027g0033 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.189+8032G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79069416 | |||||||
chr6:79069464 | A | G | 8 | a0001c0005t0003g0001 a0001c0005t0019g0012 a0001c0005t0019g0264 others(5): Show |
11 | HG01109.hp2 HG02280.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.189+7984T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79069464 | |||||||
chr6:79069611 | T | C | 1 | a0001c0006t0008g0037 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.189+7837A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79069611 | |||||||
chr6:79069743 | C | A | 1 | a0001c0006t0008g0037 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.189+7705G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79069743 | |||||||
chr6:79069813 | T | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.189+7635A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79069813 | |||||||
chr6:79069855 | A | AC | 9 | a0001c0007t0012g0169 a0001c0007t0012g0170 a0001c0007t0012g0171 others(6): Show |
9 | HG02559.hp2 HG02622.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.189+7592_189+7593i others(3): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79069855 | |||||||
chr6:79070050 | T | G | 30 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0060 others(27): Show |
30 | HG00140.hp1 HG00558.hp2 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.189+7398A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79070050 | |||||||
chr6:79070374 | A | G | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.189+7074T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79070374 | |||||||
chr6:79070850 | A | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.189+6598T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79070850 | |||||||
chr6:79070857 | T | C | 2 | a0001c0010t0029g0053 a0001c0010t0029g0054 |
2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.189+6591A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79070857 | |||||||
chr6:79070859 | T | C | 2 | a0001c0010t0029g0053 a0001c0010t0029g0054 |
2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.189+6589A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79070859 | |||||||
chr6:79071067 | C | T | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.189+6381G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79071067 | |||||||
chr6:79071109 | C | A | 1 | a0001c0005t0055g0045 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.189+6339G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79071109 | |||||||
chr6:79071172 | T | C | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.189+6276A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79071172 | |||||||
chr6:79071313 | GA | G | 4 | a0001c0001t0011g0255 a0001c0001t0011g0256 a0001c0001t0018g0257 others(1): Show |
4 | HG02258.hp2 HG02896.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.189+6134delT | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79071313 | |||||||
chr6:79071379 | T | C | 6 | a0001c0005t0023g0049 a0001c0005t0023g0051 a0001c0005t0030g0048 others(3): Show |
6 | HG01884.hp2 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.189+6069A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79071379 | |||||||
chr6:79071496 | T | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.189+5952A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79071496 | |||||||
chr6:79071578 | T | G | 4 | a0001c0001t0001g0005 a0001c0001t0001g0140 a0001c0001t0005g0139 others(1): Show |
5 | HG02257.hp2 HG02717.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.189+5870A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79071578 | |||||||
chr6:79071608 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.189+5840C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79071608 | |||||||
chr6:79071841 | G | A | 1 | a0001c0001t0017g0031 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.189+5607C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79071841 | |||||||
chr6:79071897 | CTAT | C | 5 | a0001c0008t0003g0167 a0001c0008t0007g0164 a0001c0008t0007g0165 others(2): Show |
5 | HG02280.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.189+5548_189+5550d others(5): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79071897 | |||||||
chr6:79072072 | A | T | 1 | a0001c0001t0017g0023 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.189+5376T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79072072 | |||||||
chr6:79072188 | C | T | 1 | a0001c0005t0055g0045 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.189+5260G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79072188 | |||||||
chr6:79072293 | C | G | 4 | a0001c0005t0027g0033 a0001c0006t0008g0037 a0001c0012t0024g0034 others(1): Show |
4 | HG01109.hp2 HG02572.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.189+5155G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79072293 | |||||||
chr6:79072388 | C | T | 1 | a0001c0011t0016g0017 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.189+5060G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79072388 | |||||||
chr6:79072438 | T | C | 1 | a0001c0005t0054g0038 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.189+5010A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79072438 | |||||||
chr6:79072481 | A | AT | 133 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(130): Show |
134 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.189+4966dupA | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79072481 | |||||||
chr6:79072615 | T | C | 39 | a0001c0006t0002g0013 a0001c0006t0002g0014 a0001c0006t0002g0265 others(36): Show |
45 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.189+4833A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79072615 | |||||||
chr6:79072643 | C | T | 5 | a0001c0008t0003g0167 a0001c0008t0007g0164 a0001c0008t0007g0165 others(2): Show |
5 | HG02280.hp2 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.189+4805G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79072643 | |||||||
chr6:79072738 | C | T | 3 | a0001c0006t0002g0014 a0001c0006t0002g0269 a0001c0006t0002g0270 |
4 | HG02258.hp1 HG03195.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.189+4710G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79072738 | |||||||
chr6:79072740 | G | C | 2 | a0001c0001t0014g0160 a0001c0001t0015g0159 |
2 | HG00639.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.189+4708C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79072740 | |||||||
chr6:79072800 | A | C | 1 | a0001c0006t0008g0037 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.189+4648T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79072800 | |||||||
chr6:79072819 | T | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.189+4629A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79072819 | |||||||
chr6:79072854 | C | T | 2 | a0001c0006t0002g0013 a0001c0006t0002g0268 |
3 | NA19011.hp1 NA19057.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.189+4594G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79072854 | |||||||
chr6:79072891 | A | G | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.189+4557T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79072891 | |||||||
chr6:79072928 | T | C | 1 | a0001c0001t0001g0143 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.189+4520A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79072928 | |||||||
chr6:79072942 | C | A | 1 | a0008c0019t0013g0190 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.189+4506G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79072942 | |||||||
chr6:79073116 | T | A | 1 | a0004c0004t0006g0191 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.189+4332A>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79073116 | |||||||
chr6:79073157 | T | C | 126 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(123): Show |
127 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.189+4291A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79073157 | |||||||
chr6:79073178 | A | AT | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.189+4269_189+4270i others(3): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79073178 | |||||||
chr6:79073197 | T | C | 11 | a0001c0005t0003g0001 a0001c0005t0019g0012 a0001c0005t0019g0264 others(8): Show |
14 | HG01109.hp2 HG02280.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.189+4251A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79073197 | |||||||
chr6:79073226 | A | C | 1 | a0001c0001t0026g0149 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.189+4222T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79073226 | |||||||
chr6:79073298 | T | C | 1 | a0002c0002t0007g0044 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.189+4150A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79073298 | |||||||
chr6:79073319 | CGCCTA | C | 4 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0060 others(1): Show |
4 | HG00733.hp2 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.189+4124_189+4128d others(7): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79073319 | |||||||
chr6:79073320 | G | A | 292 | a0001c0001t0001g0005 a0001c0001t0001g0066 a0001c0001t0001g0068 others(289): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.189+4128C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79073320 | |||||||
chr6:79073327 | A | C | 4 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0060 others(1): Show |
4 | HG00733.hp2 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.189+4121T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79073327 | |||||||
chr6:79073549 | A | C | 2 | a0001c0010t0029g0053 a0001c0010t0029g0054 |
2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.189+3899T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79073549 | |||||||
chr6:79073560 | TATG | T | 6 | a0001c0005t0023g0049 a0001c0005t0023g0051 a0001c0005t0030g0048 others(3): Show |
6 | HG01884.hp2 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.189+3885_189+3887d others(5): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79073560 | |||||||
chr6:79073630 | C | T | 7 | a0002c0002t0003g0193 a0002c0002t0003g0195 a0002c0002t0008g0192 others(4): Show |
7 | HG01109.hp1 HG02486.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.189+3818G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79073630 | |||||||
chr6:79073650 | C | A | 1 | a0003c0003t0002g0296 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.189+3798G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79073650 | |||||||
chr6:79073978 | C | G | 1 | a0001c0005t0049g0036 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.189+3470G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79073978 | |||||||
chr6:79074096 | A | G | 11 | a0001c0005t0003g0001 a0001c0005t0019g0012 a0001c0005t0019g0264 others(8): Show |
14 | HG01109.hp2 HG02280.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.189+3352T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79074096 | |||||||
chr6:79074263 | G | T | 1 | a0001c0010t0057g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.189+3185C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79074263 | |||||||
chr6:79074381 | T | C | 2 | a0001c0001t0014g0161 a0001c0001t0014g0162 |
2 | HG02145.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.189+3067A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79074381 | |||||||
chr6:79074427 | G | T | 1 | a0001c0005t0055g0045 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.189+3021C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79074427 | |||||||
chr6:79074431 | T | C | 1 | a0001c0005t0055g0045 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.189+3017A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79074431 | |||||||
chr6:79074557 | T | G | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.189+2891A>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79074557 | |||||||
chr6:79074640 | T | C | 1 | a0001c0006t0002g0267 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.189+2808A>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79074640 | |||||||
chr6:79074678 | C | T | 4 | a0001c0006t0002g0265 a0001c0006t0002g0267 a0001c0006t0009g0266 others(1): Show |
4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.189+2770G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79074678 | |||||||
chr6:79074704 | G | C | 80 | a0002c0002t0003g0010 a0002c0002t0003g0011 a0002c0002t0003g0041 others(77): Show |
85 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(82): Show |
intron_variant | MODIFIER | c.189+2744C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79074704 | |||||||
chr6:79074849 | A | C | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.189+2599T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79074849 | |||||||
chr6:79075013 | C | T | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.189+2435G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79075013 | |||||||
chr6:79075146 | G | T | 19 | a0001c0001t0011g0150 a0001c0001t0011g0151 a0001c0001t0011g0153 others(16): Show |
19 | HG00280.hp2 HG00639.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.189+2302C>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79075146 | |||||||
chr6:79075165 | A | T | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.189+2283T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79075165 | |||||||
chr6:79075334 | G | A | 9 | a0001c0001t0011g0029 a0001c0001t0017g0023 a0001c0001t0017g0026 others(6): Show |
9 | HG01891.hp1 HG02109.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.189+2114C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79075334 | |||||||
chr6:79075355 | G | A | 2 | a0001c0001t0001g0146 a0001c0001t0005g0145 |
2 | NA18988.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.189+2093C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79075355 | |||||||
chr6:79075378 | A | G | 2 | a0001c0006t0020g0006 a0001c0006t0020g0148 |
3 | NA18944.hp1 NA18965.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.189+2070T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79075378 | |||||||
chr6:79075419 | G | A | 2 | a0001c0012t0024g0034 a0001c0015t0024g0035 |
2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.189+2029C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79075419 | |||||||
chr6:79075422 | C | G | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.189+2026G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79075422 | |||||||
chr6:79075604 | C | T | 2 | a0001c0001t0037g0055 a0001c0001t0044g0056 |
2 | HG00639.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.189+1844G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79075604 | |||||||
chr6:79075634 | G | GA | 6 | a0001c0001t0001g0147 a0001c0001t0011g0255 a0001c0001t0011g0256 others(3): Show |
6 | HG00738.hp1 HG02258.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.189+1813dupT | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79075634 | |||||||
chr6:79075634 | GA | G | 6 | a0001c0005t0023g0049 a0001c0005t0023g0051 a0001c0005t0030g0048 others(3): Show |
6 | HG01884.hp2 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.189+1813delT | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79075634 | |||||||
chr6:79075635 | A | G | 1 | a0003c0003t0002g0032 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.189+1813T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79075635 | |||||||
chr6:79075645 | C | A | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.189+1803G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79075645 | |||||||
chr6:79075669 | CGAG | C | 6 | a0001c0005t0023g0049 a0001c0005t0023g0051 a0001c0005t0030g0048 others(3): Show |
6 | HG01884.hp2 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.189+1776_189+1778d others(5): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79075669 | |||||||
chr6:79075695 | G | C | 1 | a0001c0005t0055g0045 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.189+1753C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79075695 | |||||||
chr6:79075812 | A | C | 3 | a0001c0006t0002g0265 a0001c0006t0009g0266 a0001c0006t0009g0297 |
3 | HG01891.hp2 HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.189+1636T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79075812 | |||||||
chr6:79075890 | C | T | 105 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0058 others(102): Show |
106 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.189+1558G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79075890 | |||||||
chr6:79075949 | A | T | 1 | a0001c0005t0046g0263 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.189+1499T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79075949 | |||||||
chr6:79076216 | C | A | 2 | a0002c0002t0028g0260 a0002c0002t0028g0261 |
2 | HG01981.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.189+1232G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79076216 | |||||||
chr6:79076228 | C | T | 2 | a0001c0010t0029g0053 a0001c0010t0029g0054 |
2 | HG02965.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.189+1220G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79076228 | |||||||
chr6:79076494 | C | G | 3 | a0001c0005t0027g0033 a0001c0012t0024g0034 a0001c0015t0024g0035 |
3 | HG01109.hp2 HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.189+954G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79076494 | |||||||
chr6:79076617 | C | T | 1 | a0001c0001t0005g0052 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.189+831G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79076617 | |||||||
chr6:79076695 | C | T | 3 | a0001c0005t0019g0012 a0001c0005t0019g0264 a0001c0005t0046g0263 |
4 | HG03041.hp1 HG03130.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.189+753G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79076695 | |||||||
chr6:79076761 | C | T | 6 | a0001c0005t0023g0049 a0001c0005t0023g0051 a0001c0005t0030g0048 others(3): Show |
6 | HG01884.hp2 HG02818.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.189+687G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79076761 | |||||||
chr6:79076922 | A | C | 1 | a0001c0005t0055g0045 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.189+526T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79076922 | |||||||
chr6:79076922 | A | G | 18 | a0001c0005t0003g0001 a0001c0005t0019g0012 a0001c0005t0019g0264 others(15): Show |
23 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(20): Show |
intron_variant | MODIFIER | c.189+526T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79076922 | |||||||
chr6:79076928 | A | C | 40 | a0001c0006t0002g0013 a0001c0006t0002g0014 a0001c0006t0002g0265 others(37): Show |
46 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.189+520T>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79076928 | |||||||
chr6:79077070 | G | A | 1 | a0001c0006t0009g0297 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.189+378C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79077070 | |||||||
chr6:79077074 | G | C | 1 | a0002c0002t0003g0262 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.189+374C>G | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79077074 | |||||||
chr6:79077091 | C | T | 9 | a0001c0001t0011g0029 a0001c0001t0017g0023 a0001c0001t0017g0026 others(6): Show |
9 | HG01891.hp1 HG02109.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.189+357G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79077091 | |||||||
chr6:79077265 | A | G | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.189+183T>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79077265 | |||||||
chr6:79077277 | C | A | 3 | a0001c0005t0019g0012 a0001c0005t0019g0264 a0001c0005t0046g0263 |
4 | HG03041.hp1 HG03130.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.189+171G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79077277 | |||||||
chr6:79077279 | C | G | 1 | a0001c0005t0003g0001 | 3 | HG02280.hp1 HG02965.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.189+169G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 4/39 | chr6 | 79077279 | |||||||
chr6:79077524 | C | A | 1 | a0003c0003t0052g0298 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.130-17G>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 3/39 | chr6 | 79077524 | |||||||
chr6:79077621 | C | G | 3 | a0001c0011t0016g0017 a0001c0011t0016g0018 a0001c0011t0016g0019 |
3 | NA19003.hp1 NA19065.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.129+79G>C | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 3/39 | chr6 | 79077621 | |||||||
chr6:79077739 | C | T | 1 | a0002c0002t0004g0022 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.100-10G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 2/39 | chr6 | 79077739 | |||||||
chr6:79077772 | C | T | 1 | a0002c0002t0048g0020 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.100-43G>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 2/39 | chr6 | 79077772 | |||||||
chr6:79077779 | C | CCCG | 4 | a0001c0001t0033g0021 a0001c0011t0016g0017 a0001c0011t0016g0018 others(1): Show |
4 | HG00280.hp2 NA19003.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-53_100-51dupCG others(1): Show |
PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 2/39 | chr6 | 79077779 | |||||||
chr6:79077938 | G | A | 39 | a0001c0006t0002g0013 a0001c0006t0002g0014 a0001c0006t0002g0265 others(36): Show |
45 | HG00099.hp2 HG00438.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.41-25C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 1/39 | chr6 | 79077938 | |||||||
chr6:79077945 | A | T | 1 | a0002c0002t0048g0020 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.41-32T>A | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 1/39 | chr6 | 79077945 | |||||||
chr6:79077973 | G | A | 2 | a0001c0001t0001g0300 a0001c0001t0005g0299 |
2 | HG00621.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.40+56C>T | PHIP | ENSG00000146247.15 | transcript | ENST00000275034.5 | protein_coding | 1/39 | chr6 | 79077973 |