Item | Value |
---|---|
geneid | 54103 |
ensemblid | ENSG00000186088.16 |
hgncid | 28042 |
symbol | GSAP |
name | gamma-secretase activating protein |
refseq_nuc | NM_017439.4 |
refseq_prot | NP_059135.2 |
ensembl_nuc | ENST00000257626.12 |
ensembl_prot | ENSP00000257626.7 |
mane_status | MANE Select |
chr | chr7 |
start | 77310751 |
end | 77416349 |
strand | - |
ver | v1.2 |
region | chr7:77310751-77416349 |
region5000 | chr7:77305751-77421349 |
regionname0 | GSAP_chr7_77310751_77416349 |
regionname5000 | GSAP_chr7_77305751_77421349 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 854 | 208 | 35 | 45 | 110 | 6 | 11 | 81 | GSAP_chr7_77305751_77421349 | GSAP | MALRL others(849): Show |
chr7 | 77305751 | 77421349 |
a0002 | 0/0 | 854 | 63 | 15 | 5 | 25 | 4 | 14 | 24 | GSAP_chr7_77305751_77421349 | GSAP | MALRL others(849): Show |
chr7 | 77305751 | 77421349 |
a0003 | 0/0 | 854 | 27 | 14 | 4 | 4 | 3 | 2 | 3 | GSAP_chr7_77305751_77421349 | GSAP | MALRL others(849): Show |
chr7 | 77305751 | 77421349 |
a0004 | 0/0 | 854 | 20 | 2 | 2 | 13 | 0 | 3 | 10 | GSAP_chr7_77305751_77421349 | GSAP | MALRL others(849): Show |
chr7 | 77305751 | 77421349 |
a0005 | 1/0 | 854 | 11 | 0 | 3 | 0 | 5 | 2 | 0 | GSAP_chr7_77305751_77421349 | GSAP | MALRL others(849): Show |
chr7 | 77305751 | 77421349 |
a0006 | 0/0 | 854 | 9 | 6 | 2 | 0 | 0 | 1 | 0 | GSAP_chr7_77305751_77421349 | GSAP | MALRL others(849): Show |
chr7 | 77305751 | 77421349 |
a0007 | 0/0 | 854 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | MALRL others(849): Show |
chr7 | 77305751 | 77421349 |
a0008 | 0/0 | 854 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | MALRL others(849): Show |
chr7 | 77305751 | 77421349 |
a0009 | 0/0 | 854 | 2 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | MALRL others(849): Show |
chr7 | 77305751 | 77421349 |
a0010 | 0/0 | 854 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | MALRL others(849): Show |
chr7 | 77305751 | 77421349 |
a0011 | 0/0 | 854 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | MALRL others(849): Show |
chr7 | 77305751 | 77421349 |
a0012 | 0/0 | 854 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | MALRL others(849): Show |
chr7 | 77305751 | 77421349 |
a0013 | 0/0 | 854 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GSAP_chr7_77305751_77421349 | GSAP | MALRL others(849): Show |
chr7 | 77305751 | 77421349 |
a0014 | 0/0 | 854 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | MALRL others(849): Show |
chr7 | 77305751 | 77421349 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 2562 | 107 | 6 | 25 | 62 | 6 | 7 | GSAP_chr7_77305751_77421349 | GSAP | ATGGC others(2557): Show |
chr7 | 77305751 | 77421349 | ||
a0001c0002 | 0/0 | 2562 | 90 | 20 | 19 | 48 | 0 | 3 | GSAP_chr7_77305751_77421349 | GSAP | ATGGC others(2557): Show |
chr7 | 77305751 | 77421349 | ||
a0001c0010 | 0/0 | 2562 | 6 | 6 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | ATGGC others(2557): Show |
chr7 | 77305751 | 77421349 | ||
a0001c0013 | 0/0 | 2562 | 2 | 2 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | ATGGC others(2557): Show |
chr7 | 77305751 | 77421349 | ||
a0001c0021 | 0/0 | 2562 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | ATGGC others(2557): Show |
chr7 | 77305751 | 77421349 | ||
a0001c0023 | 0/0 | 2562 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | ATGGC others(2557): Show |
chr7 | 77305751 | 77421349 | ||
a0001c0028 | 0/0 | 2562 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | ATGGC others(2557): Show |
chr7 | 77305751 | 77421349 | ||
a0002c0003 | 0/0 | 2562 | 50 | 14 | 4 | 15 | 4 | 13 | GSAP_chr7_77305751_77421349 | GSAP | ATGGC others(2557): Show |
chr7 | 77305751 | 77421349 | ||
a0002c0007 | 0/0 | 2562 | 10 | 0 | 0 | 10 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | ATGGC others(2557): Show |
chr7 | 77305751 | 77421349 | ||
a0002c0018 | 0/0 | 2562 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | ATGGC others(2557): Show |
chr7 | 77305751 | 77421349 | ||
a0002c0019 | 0/0 | 2562 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | ATGGC others(2557): Show |
chr7 | 77305751 | 77421349 | ||
a0002c0027 | 0/0 | 2562 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | ATGGC others(2557): Show |
chr7 | 77305751 | 77421349 | ||
a0003c0004 | 0/0 | 2562 | 21 | 11 | 4 | 1 | 3 | 2 | GSAP_chr7_77305751_77421349 | GSAP | ATGGC others(2557): Show |
chr7 | 77305751 | 77421349 | ||
a0003c0009 | 0/0 | 2562 | 6 | 3 | 0 | 3 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | ATGGC others(2557): Show |
chr7 | 77305751 | 77421349 | ||
a0004c0005 | 0/0 | 2562 | 19 | 2 | 2 | 12 | 0 | 3 | GSAP_chr7_77305751_77421349 | GSAP | ATGGC others(2557): Show |
chr7 | 77305751 | 77421349 | ||
a0004c0015 | 0/0 | 2562 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | ATGGC others(2557): Show |
chr7 | 77305751 | 77421349 | ||
a0005c0006 | 1/0 | 2562 | 11 | 0 | 3 | 0 | 5 | 2 | GSAP_chr7_77305751_77421349 | GSAP | ATGGC others(2557): Show |
chr7 | 77305751 | 77421349 | ||
a0006c0008 | 0/0 | 2562 | 8 | 6 | 2 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | ATGGC others(2557): Show |
chr7 | 77305751 | 77421349 | ||
a0006c0020 | 0/0 | 2562 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | ATGGC others(2557): Show |
chr7 | 77305751 | 77421349 | ||
a0007c0011 | 0/0 | 2562 | 5 | 5 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | ATGGC others(2557): Show |
chr7 | 77305751 | 77421349 | ||
a0008c0012 | 0/0 | 2562 | 2 | 0 | 2 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | ATGGC others(2557): Show |
chr7 | 77305751 | 77421349 | ||
a0009c0024 | 0/0 | 2562 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | ATGGC others(2557): Show |
chr7 | 77305751 | 77421349 | ||
a0009c0026 | 0/0 | 2562 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | ATGGC others(2557): Show |
chr7 | 77305751 | 77421349 | ||
a0010c0025 | 0/0 | 2562 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | ATGGC others(2557): Show |
chr7 | 77305751 | 77421349 | ||
a0011c0022 | 0/0 | 2562 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | ATGGC others(2557): Show |
chr7 | 77305751 | 77421349 | ||
a0012c0014 | 0/0 | 2562 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | ATGGC others(2557): Show |
chr7 | 77305751 | 77421349 | ||
a0013c0016 | 0/0 | 2562 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | ATGGC others(2557): Show |
chr7 | 77305751 | 77421349 | ||
a0014c0017 | 0/0 | 2562 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | ATGGC others(2557): Show |
chr7 | 77305751 | 77421349 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 3200 | 106 | 6 | 24 | 62 | 6 | 7 | GSAP_chr7_77305751_77421349 | GSAP | AGAGC others(3195): Show |
chr7 | 77305751 | 77421349 |
a0001c0001t0003 | 0/0 | 3196 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | AGAGC others(3191): Show |
chr7 | 77305751 | 77421349 |
a0001c0002t0001 | 0/0 | 3200 | 66 | 0 | 16 | 47 | 0 | 3 | GSAP_chr7_77305751_77421349 | GSAP | AGAGC others(3195): Show |
chr7 | 77305751 | 77421349 |
a0001c0002t0002 | 0/0 | 3200 | 22 | 20 | 2 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | AGAGC others(3195): Show |
chr7 | 77305751 | 77421349 |
a0001c0002t0004 | 0/0 | 3200 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | AGAGC others(3195): Show |
chr7 | 77305751 | 77421349 |
a0001c0002t0006 | 0/0 | 3200 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | AGAGC others(3195): Show |
chr7 | 77305751 | 77421349 |
a0001c0010t0001 | 0/0 | 3200 | 6 | 6 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | AGAGC others(3195): Show |
chr7 | 77305751 | 77421349 |
a0001c0013t0001 | 0/0 | 3200 | 2 | 2 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | AGAGC others(3195): Show |
chr7 | 77305751 | 77421349 |
a0001c0021t0001 | 0/0 | 3200 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | AGAGC others(3195): Show |
chr7 | 77305751 | 77421349 |
a0001c0023t0001 | 0/0 | 3200 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | AGAGC others(3195): Show |
chr7 | 77305751 | 77421349 |
a0001c0028t0002 | 0/0 | 3200 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | AGAGC others(3195): Show |
chr7 | 77305751 | 77421349 |
a0002c0003t0001 | 0/0 | 3200 | 48 | 13 | 4 | 15 | 4 | 12 | GSAP_chr7_77305751_77421349 | GSAP | AGAGC others(3195): Show |
chr7 | 77305751 | 77421349 |
a0002c0003t0002 | 0/0 | 3200 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | AGAGC others(3195): Show |
chr7 | 77305751 | 77421349 |
a0002c0003t0003 | 0/0 | 3196 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | AGAGC others(3191): Show |
chr7 | 77305751 | 77421349 |
a0002c0007t0001 | 0/0 | 3200 | 10 | 0 | 0 | 10 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | AGAGC others(3195): Show |
chr7 | 77305751 | 77421349 |
a0002c0018t0001 | 0/0 | 3200 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | AGAGC others(3195): Show |
chr7 | 77305751 | 77421349 |
a0002c0019t0001 | 0/0 | 3200 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | AGAGC others(3195): Show |
chr7 | 77305751 | 77421349 |
a0002c0027t0001 | 0/0 | 3200 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | AGAGC others(3195): Show |
chr7 | 77305751 | 77421349 |
a0003c0004t0001 | 0/0 | 3200 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | AGAGC others(3195): Show |
chr7 | 77305751 | 77421349 |
a0003c0004t0002 | 0/0 | 3200 | 19 | 10 | 4 | 0 | 3 | 2 | GSAP_chr7_77305751_77421349 | GSAP | AGAGC others(3195): Show |
chr7 | 77305751 | 77421349 |
a0003c0004t0005 | 0/0 | 3200 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | AGAGC others(3195): Show |
chr7 | 77305751 | 77421349 |
a0003c0009t0001 | 0/0 | 3200 | 6 | 3 | 0 | 3 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | AGAGC others(3195): Show |
chr7 | 77305751 | 77421349 |
a0004c0005t0001 | 0/0 | 3200 | 3 | 0 | 0 | 1 | 0 | 2 | GSAP_chr7_77305751_77421349 | GSAP | AGAGC others(3195): Show |
chr7 | 77305751 | 77421349 |
a0004c0005t0003 | 0/0 | 3196 | 16 | 2 | 2 | 11 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | AGAGC others(3191): Show |
chr7 | 77305751 | 77421349 |
a0004c0015t0003 | 0/0 | 3196 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | AGAGC others(3191): Show |
chr7 | 77305751 | 77421349 |
a0005c0006t0001 | 1/0 | 3200 | 11 | 0 | 3 | 0 | 5 | 2 | GSAP_chr7_77305751_77421349 | GSAP | AGAGC others(3195): Show |
chr7 | 77305751 | 77421349 |
a0006c0008t0001 | 0/0 | 3200 | 8 | 6 | 2 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | AGAGC others(3195): Show |
chr7 | 77305751 | 77421349 |
a0006c0020t0003 | 0/0 | 3196 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | AGAGC others(3191): Show |
chr7 | 77305751 | 77421349 |
a0007c0011t0002 | 0/0 | 3200 | 5 | 5 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | AGAGC others(3195): Show |
chr7 | 77305751 | 77421349 |
a0008c0012t0001 | 0/0 | 3200 | 2 | 0 | 2 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | AGAGC others(3195): Show |
chr7 | 77305751 | 77421349 |
a0009c0024t0003 | 0/0 | 3196 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | AGAGC others(3191): Show |
chr7 | 77305751 | 77421349 |
a0009c0026t0001 | 0/0 | 3200 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | AGAGC others(3195): Show |
chr7 | 77305751 | 77421349 |
a0010c0025t0001 | 0/0 | 3200 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | AGAGC others(3195): Show |
chr7 | 77305751 | 77421349 |
a0011c0022t0001 | 0/0 | 3200 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | AGAGC others(3195): Show |
chr7 | 77305751 | 77421349 |
a0012c0014t0001 | 0/0 | 3200 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | AGAGC others(3195): Show |
chr7 | 77305751 | 77421349 |
a0013c0016t0001 | 0/0 | 3200 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | AGAGC others(3195): Show |
chr7 | 77305751 | 77421349 |
a0014c0017t0001 | 0/0 | 3200 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | AGAGC others(3195): Show |
chr7 | 77305751 | 77421349 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0095 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0001t0003g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0001g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0001g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0001g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0002g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0002g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0004g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0002t0006g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0010t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0010t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0010t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0010t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0010t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0010t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0013t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0013t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0021t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0023t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0001c0028t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0002c0003t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0002c0003t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0002c0003t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0002c0003t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0002c0003t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0002c0003t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0002c0003t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0002c0003t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0002c0003t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0002c0003t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0002c0003t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0002c0003t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0002c0003t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0002c0003t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0002c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0002c0003t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0002c0003t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0002c0003t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0002c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0002c0003t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0002c0003t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0002c0003t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0002c0003t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0002c0003t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0002c0003t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0002c0003t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0002c0003t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0002c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0002c0003t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0002c0003t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0002c0003t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0002c0003t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0002c0003t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0002c0003t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0002c0003t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0002c0003t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0002c0003t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0002c0003t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0002c0003t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0002c0003t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0002c0003t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0002c0003t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0002c0003t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0002c0003t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0002c0003t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0002c0003t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0002c0003t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0002c0003t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0002c0003t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0002c0007t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0002c0007t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0002c0007t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0002c0007t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0002c0007t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0002c0007t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0002c0007t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0002c0007t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0002c0007t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0002c0018t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0002c0019t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0002c0027t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0003c0004t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0003c0004t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0003c0004t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0003c0004t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0003c0004t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0003c0004t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0003c0004t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0003c0004t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0003c0004t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0003c0004t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0003c0004t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0003c0004t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0003c0004t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0003c0004t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0003c0004t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0003c0004t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0003c0004t0002g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0003c0004t0002g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0003c0004t0002g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0003c0004t0002g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0003c0004t0005g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0003c0009t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0003c0009t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0003c0009t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0003c0009t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0003c0009t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0003c0009t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0004c0005t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0004c0005t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0004c0005t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0004c0005t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0004c0005t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0004c0005t0003g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0004c0005t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0004c0005t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0004c0005t0003g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0004c0005t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0004c0005t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0004c0005t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0004c0005t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0004c0005t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0004c0005t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0004c0005t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0004c0005t0003g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0004c0005t0003g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0004c0005t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0004c0015t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0005c0006t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0005c0006t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0005c0006t0001g0148 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0005c0006t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0005c0006t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0005c0006t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0005c0006t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0005c0006t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0005c0006t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0005c0006t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0005c0006t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0006c0008t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0006c0008t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0006c0008t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0006c0008t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0006c0008t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0006c0008t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0006c0008t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0006c0008t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0006c0020t0003g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0007c0011t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0007c0011t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0007c0011t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0007c0011t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0007c0011t0002g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0008c0012t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0008c0012t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0009c0024t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0009c0026t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0010c0025t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0011c0022t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0012c0014t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0013c0016t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
a0014c0017t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0005 | c0006 | t0001 | g0131 | EUR | GBR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0057 | EUR | GBR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG00140 | hp1 | a0003 | c0004 | t0002 | g0124 | EUR | GBR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0200 | EUR | GBR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0073 | EUR | FIN | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG00280 | hp2 | a0002 | c0003 | t0001 | g0005 | EUR | FIN | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG00323 | hp1 | a0005 | c0006 | t0001 | g0168 | EUR | FIN | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG00323 | hp2 | a0002 | c0003 | t0001 | g0005 | EUR | FIN | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG00408 | hp1 | a0001 | c0002 | t0001 | g0253 | EAS | CHS | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | CHS | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG00423 | hp1 | a0001 | c0002 | t0001 | g0278 | EAS | CHS | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0334 | EAS | CHS | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG00544 | hp2 | a0001 | c0002 | t0001 | g0239 | EAS | CHS | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG00558 | hp1 | a0001 | c0002 | t0001 | g0157 | EAS | CHS | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG00558 | hp2 | a0004 | c0005 | t0003 | g0159 | EAS | CHS | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG00597 | hp1 | a0001 | c0002 | t0001 | g0117 | EAS | CHS | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | CHS | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG00609 | hp1 | a0001 | c0002 | t0001 | g0299 | EAS | CHS | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | CHS | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | CHS | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG00621 | hp2 | a0004 | c0005 | t0003 | g0177 | EAS | CHS | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG00639 | hp1 | a0006 | c0008 | t0001 | g0141 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG00642 | hp1 | a0003 | c0004 | t0002 | g0341 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG00673 | hp1 | a0001 | c0002 | t0001 | g0274 | EAS | CHS | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG00673 | hp2 | a0001 | c0002 | t0001 | g0281 | EAS | CHS | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG00733 | hp2 | a0005 | c0006 | t0001 | g0122 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG00735 | hp2 | a0001 | c0002 | t0001 | g0244 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG00738 | hp1 | a0008 | c0012 | t0001 | g0170 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG01069 | hp2 | a0001 | c0002 | t0001 | g0267 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG01070 | hp2 | a0001 | c0001 | t0003 | g0293 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG01071 | hp2 | a0001 | c0002 | t0001 | g0272 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG01074 | hp1 | a0006 | c0008 | t0001 | g0136 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG01074 | hp2 | a0001 | c0002 | t0001 | g0271 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG01099 | hp1 | a0001 | c0002 | t0001 | g0342 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG01099 | hp2 | a0010 | c0025 | t0001 | g0306 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG01106 | hp1 | a0003 | c0004 | t0002 | g0340 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG01109 | hp1 | a0005 | c0006 | t0001 | g0172 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG01109 | hp2 | a0002 | c0027 | t0001 | g0214 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG01167 | hp1 | a0004 | c0005 | t0003 | g0161 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG01167 | hp2 | a0001 | c0002 | t0001 | g0275 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG01168 | hp2 | a0001 | c0002 | t0001 | g0345 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG01169 | hp1 | a0004 | c0005 | t0003 | g0158 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG01169 | hp2 | a0001 | c0002 | t0001 | g0343 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG01175 | hp1 | a0001 | c0002 | t0001 | g0344 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG01192 | hp2 | a0001 | c0002 | t0002 | g0130 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG01243 | hp1 | a0001 | c0002 | t0004 | g0034 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG01243 | hp2 | a0002 | c0003 | t0001 | g0286 | AMR | PUR | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG01255 | hp1 | a0005 | c0006 | t0001 | g0180 | AMR | CLM | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG01257 | hp2 | a0008 | c0012 | t0001 | g0169 | AMR | CLM | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG01258 | hp1 | a0003 | c0004 | t0002 | g0339 | AMR | CLM | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | CLM | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG01261 | hp1 | a0002 | c0003 | t0001 | g0147 | AMR | CLM | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | CLM | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG01361 | hp2 | a0001 | c0002 | t0001 | g0237 | AMR | CLM | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG01433 | hp1 | a0001 | c0002 | t0001 | g0301 | AMR | CLM | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG01433 | hp2 | a0001 | c0002 | t0002 | g0128 | AMR | CLM | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0195 | EUR | IBS | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG01515 | hp2 | a0005 | c0006 | t0001 | g0167 | EUR | IBS | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG01516 | hp1 | a0002 | c0003 | t0001 | g0102 | EUR | IBS | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG01516 | hp2 | a0003 | c0004 | t0002 | g0203 | EUR | IBS | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG01517 | hp1 | a0005 | c0006 | t0001 | g0166 | EUR | IBS | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG01517 | hp2 | a0002 | c0003 | t0001 | g0103 | EUR | IBS | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG01884 | hp1 | a0001 | c0002 | t0002 | g0219 | AFR | ACB | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG01884 | hp2 | a0002 | c0003 | t0001 | g0064 | AFR | ACB | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG01891 | hp1 | a0003 | c0004 | t0002 | g0132 | AFR | ACB | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG01891 | hp2 | a0007 | c0011 | t0002 | g0037 | AFR | ACB | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG01934 | hp1 | a0001 | c0002 | t0001 | g0217 | AMR | PEL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG01952 | hp1 | a0001 | c0002 | t0001 | g0268 | AMR | PEL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG01975 | hp1 | a0001 | c0002 | t0001 | g0116 | AMR | PEL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG01975 | hp2 | a0001 | c0021 | t0001 | g0249 | AMR | PEL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PEL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG01981 | hp1 | a0001 | c0002 | t0001 | g0283 | AMR | PEL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG01993 | hp1 | a0003 | c0004 | t0002 | g0133 | AMR | PEL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | KHV | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG02015 | hp2 | a0002 | c0003 | t0001 | g0335 | EAS | KHV | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG02027 | hp1 | a0001 | c0002 | t0001 | g0238 | EAS | KHV | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG02027 | hp2 | a0009 | c0024 | t0003 | g0181 | EAS | KHV | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG02055 | hp1 | a0003 | c0004 | t0002 | g0186 | AFR | ACB | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG02055 | hp2 | a0004 | c0005 | t0003 | g0222 | AFR | ACB | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0333 | EAS | KHV | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG02071 | hp2 | a0001 | c0002 | t0001 | g0193 | EAS | KHV | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG02074 | hp2 | a0001 | c0002 | t0001 | g0273 | EAS | KHV | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG02129 | hp1 | a0004 | c0005 | t0003 | g0115 | EAS | KHV | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG02132 | hp1 | a0001 | c0002 | t0001 | g0263 | EAS | KHV | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG02155 | hp1 | a0001 | c0002 | t0001 | g0277 | EAS | CDX | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | CDX | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG02165 | hp1 | a0001 | c0002 | t0001 | g0266 | EAS | CDX | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG02165 | hp2 | a0001 | c0002 | t0001 | g0230 | EAS | CDX | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG02273 | hp1 | a0001 | c0002 | t0001 | g0308 | AMR | PEL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG02273 | hp2 | a0002 | c0003 | t0001 | g0059 | AMR | PEL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG02280 | hp1 | a0006 | c0008 | t0001 | g0100 | AFR | ACB | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG02280 | hp2 | a0002 | c0003 | t0001 | g0312 | AFR | ACB | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG02451 | hp1 | a0001 | c0002 | t0002 | g0014 | AFR | ACB | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG02451 | hp2 | a0002 | c0003 | t0001 | g0311 | AFR | ACB | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | KHV | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG02523 | hp2 | a0003 | c0004 | t0001 | g0190 | EAS | KHV | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG02572 | hp1 | a0001 | c0002 | t0002 | g0011 | AFR | GWD | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG02572 | hp2 | a0001 | c0002 | t0002 | g0207 | AFR | GWD | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG02615 | hp1 | a0001 | c0002 | t0002 | g0320 | AFR | GWD | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | GWD | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG02622 | hp1 | a0006 | c0008 | t0001 | g0017 | AFR | GWD | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG02622 | hp2 | a0001 | c0002 | t0002 | g0010 | AFR | GWD | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG02630 | hp2 | a0002 | c0003 | t0001 | g0211 | AFR | GWD | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG02683 | hp1 | a0002 | c0003 | t0001 | g0030 | SAS | PJL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG02683 | hp2 | a0002 | c0018 | t0001 | g0099 | SAS | PJL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG02717 | hp1 | a0003 | c0009 | t0001 | g0027 | AFR | GWD | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG02717 | hp2 | a0001 | c0002 | t0002 | g0125 | AFR | GWD | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG02723 | hp1 | a0007 | c0011 | t0002 | g0144 | AFR | GWD | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG02723 | hp2 | a0006 | c0008 | t0001 | g0134 | AFR | GWD | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG02735 | hp1 | a0006 | c0020 | t0003 | g0024 | SAS | PJL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG02738 | hp1 | a0001 | c0023 | t0001 | g0094 | SAS | PJL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG02738 | hp2 | a0003 | c0004 | t0002 | g0113 | SAS | PJL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG02809 | hp1 | a0001 | c0010 | t0001 | g0016 | AFR | GWD | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG02809 | hp2 | a0003 | c0009 | t0001 | g0029 | AFR | GWD | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG02886 | hp1 | a0006 | c0008 | t0001 | g0137 | AFR | GWD | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG02886 | hp2 | a0003 | c0004 | t0002 | g0338 | AFR | GWD | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG02896 | hp1 | a0002 | c0003 | t0001 | g0224 | AFR | GWD | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG02896 | hp2 | a0002 | c0003 | t0001 | g0215 | AFR | GWD | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG02897 | hp1 | a0006 | c0008 | t0001 | g0139 | AFR | GWD | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG02897 | hp2 | a0002 | c0003 | t0001 | g0216 | AFR | GWD | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG02922 | hp1 | a0001 | c0002 | t0002 | g0127 | AFR | ESN | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG02922 | hp2 | a0002 | c0003 | t0001 | g0063 | AFR | ESN | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG02965 | hp1 | a0003 | c0004 | t0002 | g0187 | AFR | ESN | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG02965 | hp2 | a0001 | c0002 | t0002 | g0009 | AFR | ESN | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG02970 | hp1 | a0001 | c0002 | t0002 | g0002 | AFR | ESN | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ESN | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG02976 | hp1 | a0007 | c0011 | t0002 | g0310 | AFR | ESN | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG02976 | hp2 | a0011 | c0022 | t0001 | g0129 | AFR | ESN | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG03017 | hp1 | a0002 | c0003 | t0001 | g0060 | SAS | PJL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG03017 | hp2 | a0004 | c0005 | t0001 | g0105 | SAS | PJL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG03041 | hp1 | a0003 | c0004 | t0002 | g0146 | AFR | GWD | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG03041 | hp2 | a0003 | c0009 | t0001 | g0028 | AFR | GWD | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG03098 | hp1 | a0003 | c0004 | t0005 | g0185 | AFR | MSL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG03098 | hp2 | a0003 | c0004 | t0002 | g0152 | AFR | MSL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG03130 | hp1 | a0003 | c0004 | t0002 | g0183 | AFR | ESN | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG03130 | hp2 | a0001 | c0002 | t0002 | g0108 | AFR | ESN | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG03139 | hp1 | a0001 | c0013 | t0001 | g0218 | AFR | ESN | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG03139 | hp2 | a0001 | c0010 | t0001 | g0149 | AFR | ESN | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG03195 | hp1 | a0007 | c0011 | t0002 | g0138 | AFR | ESN | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG03195 | hp2 | a0003 | c0004 | t0002 | g0184 | AFR | ESN | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG03209 | hp1 | a0001 | c0002 | t0002 | g0012 | AFR | MSL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG03209 | hp2 | a0002 | c0003 | t0001 | g0210 | AFR | MSL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG03225 | hp1 | a0001 | c0002 | t0002 | g0002 | AFR | MSL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG03225 | hp2 | a0001 | c0002 | t0002 | g0140 | AFR | MSL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG03239 | hp1 | a0005 | c0006 | t0001 | g0165 | SAS | PJL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG03453 | hp1 | a0001 | c0002 | t0002 | g0013 | AFR | MSL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG03453 | hp2 | a0009 | c0026 | t0001 | g0054 | AFR | MSL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG03492 | hp1 | a0002 | c0003 | t0001 | g0120 | SAS | PJL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG03516 | hp1 | a0001 | c0010 | t0001 | g0145 | AFR | ESN | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG03516 | hp2 | a0001 | c0013 | t0001 | g0221 | AFR | ESN | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG03579 | hp1 | a0002 | c0003 | t0002 | g0055 | AFR | MSL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG03579 | hp2 | a0001 | c0002 | t0002 | g0119 | AFR | MSL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG03654 | hp1 | a0004 | c0005 | t0001 | g0106 | SAS | PJL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG03654 | hp2 | a0001 | c0002 | t0001 | g0265 | SAS | PJL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG03669 | hp1 | a0002 | c0003 | t0001 | g0019 | SAS | PJL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG03704 | hp1 | a0002 | c0003 | t0001 | g0155 | SAS | PJL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG03704 | hp2 | a0002 | c0003 | t0001 | g0061 | SAS | PJL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG03831 | hp1 | a0001 | c0002 | t0001 | g0243 | SAS | BEB | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG03831 | hp2 | a0002 | c0003 | t0001 | g0065 | SAS | BEB | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG03834 | hp1 | a0002 | c0003 | t0001 | g0080 | SAS | BEB | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG03834 | hp2 | a0004 | c0005 | t0003 | g0223 | SAS | BEB | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | BEB | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG03942 | hp2 | a0002 | c0003 | t0001 | g0066 | SAS | BEB | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | STU | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG04115 | hp2 | a0002 | c0003 | t0001 | g0067 | SAS | STU | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG04184 | hp1 | a0002 | c0003 | t0001 | g0069 | SAS | BEB | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG04184 | hp2 | a0005 | c0006 | t0001 | g0206 | SAS | BEB | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG04199 | hp1 | a0001 | c0002 | t0001 | g0118 | SAS | STU | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | STU | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG04204 | hp1 | a0002 | c0003 | t0003 | g0068 | SAS | STU | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG04204 | hp2 | a0002 | c0003 | t0001 | g0093 | SAS | STU | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18612 | hp1 | a0012 | c0014 | t0001 | g0173 | EAS | CHB | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18612 | hp2 | a0001 | c0002 | t0001 | g0242 | EAS | CHB | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18906 | hp1 | a0001 | c0010 | t0001 | g0151 | AFR | YRI | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18906 | hp2 | a0003 | c0004 | t0002 | g0153 | AFR | YRI | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18939 | hp2 | a0003 | c0009 | t0001 | g0188 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18940 | hp1 | a0002 | c0003 | t0001 | g0089 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18940 | hp2 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18942 | hp1 | a0001 | c0002 | t0006 | g0007 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18943 | hp1 | a0004 | c0005 | t0003 | g0176 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18943 | hp2 | a0001 | c0002 | t0001 | g0276 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18946 | hp2 | a0002 | c0007 | t0001 | g0337 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18948 | hp2 | a0001 | c0002 | t0001 | g0309 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18949 | hp1 | a0002 | c0003 | t0001 | g0247 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18949 | hp2 | a0001 | c0002 | t0001 | g0284 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18952 | hp1 | a0001 | c0002 | t0001 | g0233 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18959 | hp1 | a0001 | c0002 | t0001 | g0262 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18959 | hp2 | a0002 | c0003 | t0001 | g0121 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18960 | hp1 | a0001 | c0002 | t0001 | g0298 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18961 | hp2 | a0002 | c0003 | t0001 | g0090 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18962 | hp2 | a0004 | c0005 | t0003 | g0163 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18963 | hp1 | a0002 | c0003 | t0001 | g0245 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18963 | hp2 | a0004 | c0005 | t0003 | g0288 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18964 | hp1 | a0001 | c0002 | t0001 | g0302 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18964 | hp2 | a0004 | c0005 | t0003 | g0164 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18966 | hp1 | a0002 | c0003 | t0001 | g0287 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18967 | hp1 | a0002 | c0003 | t0001 | g0048 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18969 | hp1 | a0003 | c0009 | t0001 | g0189 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18971 | hp2 | a0002 | c0003 | t0001 | g0088 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18975 | hp1 | a0001 | c0002 | t0001 | g0264 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18975 | hp2 | a0002 | c0003 | t0001 | g0058 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18978 | hp2 | a0002 | c0007 | t0001 | g0227 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18979 | hp2 | a0001 | c0002 | t0001 | g0241 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18981 | hp1 | a0002 | c0007 | t0001 | g0323 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18982 | hp1 | a0001 | c0002 | t0001 | g0318 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18983 | hp2 | a0002 | c0007 | t0001 | g0228 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18984 | hp1 | a0004 | c0015 | t0003 | g0175 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18984 | hp2 | a0001 | c0002 | t0001 | g0240 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18987 | hp2 | a0001 | c0002 | t0001 | g0109 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18988 | hp1 | a0001 | c0002 | t0001 | g0270 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18989 | hp2 | a0001 | c0002 | t0001 | g0297 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18995 | hp1 | a0001 | c0002 | t0001 | g0336 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18997 | hp1 | a0003 | c0009 | t0001 | g0191 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18997 | hp2 | a0001 | c0002 | t0001 | g0232 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA18999 | hp2 | a0001 | c0002 | t0001 | g0269 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA19000 | hp1 | a0001 | c0002 | t0001 | g0143 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA19001 | hp1 | a0001 | c0002 | t0001 | g0300 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA19002 | hp2 | a0001 | c0002 | t0001 | g0303 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA19003 | hp1 | a0002 | c0003 | t0001 | g0285 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA19005 | hp2 | a0001 | c0002 | t0001 | g0280 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA19006 | hp2 | a0001 | c0002 | t0001 | g0317 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA19007 | hp1 | a0001 | c0002 | t0001 | g0261 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA19011 | hp1 | a0001 | c0002 | t0001 | g0110 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA19011 | hp2 | a0001 | c0002 | t0001 | g0234 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | LWK | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA19030 | hp2 | a0002 | c0019 | t0001 | g0126 | AFR | LWK | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA19043 | hp1 | a0007 | c0011 | t0002 | g0208 | AFR | LWK | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA19043 | hp2 | a0006 | c0008 | t0001 | g0052 | AFR | LWK | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA19054 | hp2 | a0004 | c0005 | t0003 | g0160 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA19060 | hp1 | a0004 | c0005 | t0001 | g0171 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA19062 | hp2 | a0002 | c0007 | t0001 | g0324 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA19063 | hp1 | a0001 | c0002 | t0001 | g0282 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA19063 | hp2 | a0004 | c0005 | t0003 | g0162 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA19064 | hp1 | a0004 | c0005 | t0003 | g0178 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA19065 | hp2 | a0001 | c0002 | t0001 | g0053 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA19066 | hp1 | a0001 | c0002 | t0001 | g0279 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA19076 | hp1 | a0002 | c0003 | t0001 | g0021 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA19076 | hp2 | a0001 | c0002 | t0001 | g0307 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA19077 | hp2 | a0002 | c0007 | t0001 | g0229 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA19081 | hp1 | a0002 | c0007 | t0001 | g0322 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA19082 | hp2 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA19084 | hp2 | a0002 | c0003 | t0001 | g0087 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA19085 | hp1 | a0002 | c0007 | t0001 | g0004 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA19085 | hp2 | a0002 | c0003 | t0001 | g0246 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA19087 | hp1 | a0002 | c0007 | t0001 | g0004 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA19090 | hp1 | a0002 | c0007 | t0001 | g0325 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA19091 | hp1 | a0004 | c0005 | t0003 | g0174 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA19091 | hp2 | a0002 | c0003 | t0001 | g0248 | EAS | JPT | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA19240 | hp1 | a0001 | c0028 | t0002 | g0142 | AFR | YRI | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA19240 | hp2 | a0001 | c0010 | t0001 | g0150 | AFR | YRI | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | ASW | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA20129 | hp2 | a0002 | c0003 | t0001 | g0062 | AFR | ASW | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0199 | EUR | TSI | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA20752 | hp2 | a0003 | c0004 | t0002 | g0123 | EUR | TSI | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA20805 | hp1 | a0005 | c0006 | t0001 | g0179 | EUR | TSI | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0201 | EUR | TSI | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA20905 | hp1 | a0013 | c0016 | t0001 | g0039 | SAS | GIH | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA20905 | hp2 | a0003 | c0004 | t0002 | g0156 | SAS | GIH | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | CLM | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG01123 | hp2 | a0002 | c0003 | t0001 | g0101 | AMR | CLM | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG02109 | hp1 | a0001 | c0002 | t0002 | g0107 | AFR | ACB | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG02109 | hp2 | a0001 | c0002 | t0002 | g0220 | AFR | ACB | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG02486 | hp1 | a0002 | c0003 | t0001 | g0038 | AFR | ACB | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG02486 | hp2 | a0001 | c0010 | t0001 | g0026 | AFR | ACB | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG02559 | hp1 | a0002 | c0003 | t0001 | g0346 | AFR | ACB | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG02559 | hp2 | a0001 | c0002 | t0002 | g0182 | AFR | ACB | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG03471 | hp1 | a0001 | c0002 | t0002 | g0135 | AFR | MSL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG03471 | hp2 | a0002 | c0003 | t0001 | g0319 | AFR | MSL | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG06807 | hp1 | a0003 | c0004 | t0002 | g0033 | AFR | USA | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
HG06807 | hp2 | a0004 | c0005 | t0003 | g0104 | AFR | USA | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | LWK | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
NA21309 | hp2 | a0014 | c0017 | t0001 | g0347 | AFR | LWK | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0095 | REF | REF | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
homoSapiens | grch38p0 | a0005 | c0006 | t0001 | g0148 | REF | REF | GSAP_chr7_77305751_77421349 | GSAP | chr7 | 77305751 | 77421349 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:77313523 | T | G | 1 | a0010 | 1 | HG01099.hp2 | missense_variant | MODERATE | c.2236A>C | p.Lys746Gln | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 28/31 | 2264/3200 | 2236/2565 | 746/854 | chr7 | 77313523 | |||
chr7:77321369 | C | A | 3 | a0004 a0006 a0009 |
31 | HG00558.hp2 HG00621.hp2 HG00639.hp1 others(28): Show |
missense_variant | MODERATE | c.1958G>T | p.Trp653Leu | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 25/31 | 1986/3200 | 1958/2565 | 653/854 | chr7 | 77321369 | |||
chr7:77321382 | C | T | 4 | a0003 a0011 a0012 others(1): Show |
30 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(27): Show |
missense_variant | MODERATE | c.1945G>A | p.Val649Ile | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 25/31 | 1973/3200 | 1945/2565 | 649/854 | chr7 | 77321382 | |||
chr7:77323718 | A | T | 1 | a0007 | 5 | HG01891.hp2 HG02723.hp1 HG02976.hp1 others(2): Show |
missense_variant | MODERATE | c.1852T>A | p.Phe618Ile | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 24/31 | 1880/3200 | 1852/2565 | 618/854 | chr7 | 77323718 | |||
chr7:77362618 | C | T | 5 | a0002 a0003 a0006 others(2): Show |
106 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(103): Show |
missense_variant | MODERATE | c.914G>A | p.Gly305Glu | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 13/31 | 942/3200 | 914/2565 | 305/854 | chr7 | 77362618 | |||
chr7:77382615 | G | T | 1 | a0014 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.485C>A | p.Pro162His | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 7/31 | 513/3200 | 485/2565 | 162/854 | chr7 | 77382615 | |||
chr7:77382617 | A | T | 1 | a0014 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.483T>A | p.His161Gln | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 7/31 | 511/3200 | 483/2565 | 161/854 | chr7 | 77382617 | |||
chr7:77406072 | A | G | 1 | a0013 | 1 | NA20905.hp1 | missense_variant | MODERATE | c.143T>C | p.Val48Ala | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 2/31 | 171/3200 | 143/2565 | 48/854 | chr7 | 77406072 | |||
chr7:77406075 | T | C | 10 | a0001 a0002 a0003 others(7): Show |
317 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(314): Show |
missense_variant | MODERATE | c.140A>G | p.His47Arg | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 2/31 | 168/3200 | 140/2565 | 47/854 | chr7 | 77406075 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:77311379 | G | A | 1 | a0001c0010 | 6 | HG02486.hp2 HG02809.hp1 HG03139.hp2 others(3): Show |
synonymous_variant | LOW | c.2544C>T | p.Thr848Thr | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 31/31 | 2572/3200 | 2544/2565 | 848/854 | chr7 | 77311379 | |||
chr7:77312128 | C | T | 1 | a0001c0023 | 1 | HG02738.hp1 | synonymous_variant | LOW | c.2346G>A | p.Thr782Thr | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 29/31 | 2374/3200 | 2346/2565 | 782/854 | chr7 | 77312128 | |||
chr7:77314461 | C | G | 5 | a0001c0013 a0002c0019 a0003c0009 others(2): Show |
11 | HG02717.hp1 HG02809.hp2 HG02976.hp2 others(8): Show |
synonymous_variant | LOW | c.2118G>C | p.Gly706Gly | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 27/31 | 2146/3200 | 2118/2565 | 706/854 | chr7 | 77314461 | |||
chr7:77353007 | T | C | 1 | a0004c0015 | 1 | NA18984.hp1 | synonymous_variant | LOW | c.1428A>G | p.Val476Val | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/31 | 1456/3200 | 1428/2565 | 476/854 | chr7 | 77353007 | |||
chr7:77355255 | G | A | 16 | a0001c0002 a0001c0013 a0001c0021 others(13): Show |
201 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(198): Show |
synonymous_variant | LOW | c.1296C>T | p.Cys432Cys | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 16/31 | 1324/3200 | 1296/2565 | 432/854 | chr7 | 77355255 | |||
chr7:77360861 | C | G | 12 | a0001c0021 a0002c0003 a0002c0007 others(9): Show |
107 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(104): Show |
synonymous_variant | LOW | c.990G>C | p.Gly330Gly | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/31 | 1018/3200 | 990/2565 | 330/854 | chr7 | 77360861 | |||
chr7:77374074 | A | G | 1 | a0002c0007 | 10 | NA18946.hp2 NA18978.hp2 NA18981.hp1 others(7): Show |
synonymous_variant | LOW | c.867T>C | p.His289His | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/31 | 895/3200 | 867/2565 | 289/854 | chr7 | 77374074 | |||
chr7:77381344 | T | C | 3 | a0001c0028 a0002c0027 a0006c0008 |
10 | HG00639.hp1 HG01074.hp1 HG01109.hp2 others(7): Show |
synonymous_variant | LOW | c.537A>G | p.Gln179Gln | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/31 | 565/3200 | 537/2565 | 179/854 | chr7 | 77381344 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:77310814 | A | T | 1 | a0001c0002t0004 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*544T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 31/31 | 544 | chr7 | 77310814 | ||||||
chr7:77310814 | AAAAT | A | 6 | a0001c0001t0003 a0002c0003t0003 a0004c0005t0003 others(3): Show |
21 | HG00558.hp2 HG00621.hp2 HG01070.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*540_*543delATTT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 31/31 | 540 | chr7 | 77310814 | ||||||
chr7:77311211 | T | C | 1 | a0001c0002t0006 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*147A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 31/31 | 147 | chr7 | 77311211 | ||||||
chr7:77311236 | T | C | 1 | a0003c0004t0005 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*122A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 31/31 | 122 | chr7 | 77311236 | ||||||
chr7:77311296 | A | G | 7 | a0001c0002t0002 a0001c0002t0004 a0001c0028t0002 others(4): Show |
50 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*62T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 31/31 | 62 | chr7 | 77311296 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:77311477 | A | G | 1 | a0001c0001t0001g0257 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2474-28T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 30/30 | chr7 | 77311477 | |||||||
chr7:77311627 | G | A | 9 | a0003c0004t0002g0113 a0003c0004t0002g0123 a0003c0004t0002g0124 others(6): Show |
9 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.2474-178C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 30/30 | chr7 | 77311627 | |||||||
chr7:77311677 | TTTACTCT others(6): Show |
T | 1 | a0001c0001t0001g0198 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.2473+151_2473+163d others(15): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 30/30 | chr7 | 77311677 | |||||||
chr7:77311715 | C | T | 13 | a0001c0002t0002g0135 a0001c0002t0002g0140 a0002c0003t0002g0055 others(10): Show |
13 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.2473+126G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 30/30 | chr7 | 77311715 | |||||||
chr7:77311755 | T | C | 2 | a0003c0004t0002g0033 a0003c0004t0002g0338 |
2 | HG02886.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2473+86A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 30/30 | chr7 | 77311755 | |||||||
chr7:77311972 | A | G | 31 | a0001c0001t0001g0036 a0001c0001t0001g0043 a0001c0001t0001g0195 others(28): Show |
32 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.2374-32T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 29/30 | chr7 | 77311972 | |||||||
chr7:77312023 | C | T | 13 | a0001c0013t0001g0218 a0001c0013t0001g0221 a0002c0019t0001g0126 others(10): Show |
13 | HG02717.hp1 HG02809.hp2 HG02886.hp2 others(10): Show |
intron_variant | MODIFIER | c.2373+78G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 29/30 | chr7 | 77312023 | |||||||
chr7:77312046 | C | T | 1 | a0001c0002t0001g0265 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2373+55G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 29/30 | chr7 | 77312046 | |||||||
chr7:77312230 | C | A | 146 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(143): Show |
150 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.2272-28G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 28/30 | chr7 | 77312230 | |||||||
chr7:77312232 | A | AAT | 146 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(143): Show |
150 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.2272-32_2272-31dup others(2): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 28/30 | chr7 | 77312232 | |||||||
chr7:77312236 | C | T | 1 | a0005c0006t0001g0206 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2272-34G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 28/30 | chr7 | 77312236 | |||||||
chr7:77312513 | C | A | 176 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(173): Show |
180 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.2272-311G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 28/30 | chr7 | 77312513 | |||||||
chr7:77312567 | C | T | 11 | a0001c0013t0001g0218 a0001c0013t0001g0221 a0002c0019t0001g0126 others(8): Show |
11 | HG02717.hp1 HG02809.hp2 HG02976.hp2 others(8): Show |
intron_variant | MODIFIER | c.2272-365G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 28/30 | chr7 | 77312567 | |||||||
chr7:77312879 | C | T | 18 | a0001c0001t0001g0036 a0001c0001t0001g0043 a0001c0001t0001g0195 others(15): Show |
19 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.2271+609G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 28/30 | chr7 | 77312879 | |||||||
chr7:77312927 | T | C | 4 | a0001c0001t0001g0328 a0001c0001t0001g0329 a0001c0001t0001g0333 others(1): Show |
4 | HG00597.hp1 HG02015.hp1 HG02071.hp1 others(1): Show |
intron_variant | MODIFIER | c.2271+561A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 28/30 | chr7 | 77312927 | |||||||
chr7:77312953 | T | G | 2 | a0001c0001t0001g0334 a0001c0002t0001g0239 |
2 | HG00544.hp1 HG00544.hp2 |
intron_variant | MODIFIER | c.2271+535A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 28/30 | chr7 | 77312953 | |||||||
chr7:77312954 | C | A | 1 | a0001c0002t0001g0239 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2271+534G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 28/30 | chr7 | 77312954 | |||||||
chr7:77313010 | C | T | 1 | a0001c0002t0001g0253 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2271+478G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 28/30 | chr7 | 77313010 | |||||||
chr7:77313138 | C | A | 75 | a0001c0001t0001g0015 a0001c0001t0001g0036 a0001c0001t0001g0043 others(72): Show |
76 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.2271+350G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 28/30 | chr7 | 77313138 | |||||||
chr7:77313287 | C | CCT | 31 | a0001c0001t0003g0293 a0002c0003t0003g0068 a0004c0005t0001g0106 others(28): Show |
31 | HG00558.hp2 HG00621.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.2271+200_2271+201i others(4): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 28/30 | chr7 | 77313287 | |||||||
chr7:77313289 | A | T | 31 | a0001c0001t0003g0293 a0002c0003t0003g0068 a0004c0005t0001g0106 others(28): Show |
31 | HG00558.hp2 HG00621.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.2271+199T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 28/30 | chr7 | 77313289 | |||||||
chr7:77313327 | A | G | 98 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(95): Show |
101 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.2271+161T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 28/30 | chr7 | 77313327 | |||||||
chr7:77313345 | G | T | 5 | a0001c0021t0001g0249 a0002c0003t0001g0059 a0002c0003t0001g0067 others(2): Show |
5 | HG00733.hp2 HG01257.hp2 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.2271+143C>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 28/30 | chr7 | 77313345 | |||||||
chr7:77313425 | G | A | 1 | a0002c0003t0001g0093 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2271+63C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 28/30 | chr7 | 77313425 | |||||||
chr7:77313469 | A | T | 11 | a0002c0003t0002g0055 a0003c0004t0002g0132 a0003c0004t0002g0183 others(8): Show |
11 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.2271+19T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 28/30 | chr7 | 77313469 | |||||||
chr7:77313624 | G | C | 1 | a0002c0003t0001g0346 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2210-75C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 27/30 | chr7 | 77313624 | |||||||
chr7:77313642 | G | A | 94 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0015 others(91): Show |
97 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.2210-93C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 27/30 | chr7 | 77313642 | |||||||
chr7:77313703 | ACT | A | 10 | a0001c0013t0001g0218 a0001c0013t0001g0221 a0003c0009t0001g0027 others(7): Show |
10 | HG02717.hp1 HG02809.hp2 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.2210-156_2210-155d others(4): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 27/30 | chr7 | 77313703 | |||||||
chr7:77313921 | T | C | 1 | a0001c0001t0001g0070 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2210-372A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 27/30 | chr7 | 77313921 | |||||||
chr7:77314026 | T | G | 11 | a0002c0003t0002g0055 a0003c0004t0002g0132 a0003c0004t0002g0183 others(8): Show |
11 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.2209+344A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 27/30 | chr7 | 77314026 | |||||||
chr7:77314041 | T | A | 2 | a0003c0004t0002g0033 a0003c0004t0002g0338 |
2 | HG02886.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2209+329A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 27/30 | chr7 | 77314041 | |||||||
chr7:77314050 | T | C | 21 | a0001c0002t0002g0002 a0001c0002t0002g0125 a0001c0002t0002g0130 others(18): Show |
22 | HG01192.hp2 HG01884.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.2209+320A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 27/30 | chr7 | 77314050 | |||||||
chr7:77314135 | T | C | 4 | a0001c0001t0001g0199 a0001c0002t0001g0267 a0001c0002t0001g0271 others(1): Show |
4 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(1): Show |
intron_variant | MODIFIER | c.2209+235A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 27/30 | chr7 | 77314135 | |||||||
chr7:77314149 | C | A | 11 | a0001c0013t0001g0218 a0001c0013t0001g0221 a0002c0019t0001g0126 others(8): Show |
11 | HG02717.hp1 HG02809.hp2 HG02976.hp2 others(8): Show |
intron_variant | MODIFIER | c.2209+221G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 27/30 | chr7 | 77314149 | |||||||
chr7:77314154 | T | C | 18 | a0001c0001t0001g0036 a0001c0001t0001g0043 a0001c0001t0001g0195 others(15): Show |
19 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.2209+216A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 27/30 | chr7 | 77314154 | |||||||
chr7:77314200 | C | T | 46 | a0001c0001t0001g0015 a0001c0001t0001g0050 a0001c0001t0001g0051 others(43): Show |
46 | HG00099.hp1 HG00733.hp2 HG01099.hp1 others(43): Show |
intron_variant | MODIFIER | c.2209+170G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 27/30 | chr7 | 77314200 | |||||||
chr7:77314228 | T | C | 2 | a0004c0005t0003g0159 a0009c0024t0003g0181 |
2 | HG00558.hp2 HG02027.hp2 |
intron_variant | MODIFIER | c.2209+142A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 27/30 | chr7 | 77314228 | |||||||
chr7:77314290 | C | T | 1 | a0001c0001t0001g0316 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2209+80G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 27/30 | chr7 | 77314290 | |||||||
chr7:77314810 | C | G | 22 | a0001c0001t0003g0293 a0002c0003t0003g0068 a0004c0005t0001g0106 others(19): Show |
22 | HG00558.hp2 HG00621.hp2 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.2090-321G>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77314810 | |||||||
chr7:77315059 | G | C | 2 | a0001c0001t0001g0036 a0001c0001t0001g0043 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.2090-570C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77315059 | |||||||
chr7:77315239 | G | A | 2 | a0001c0013t0001g0218 a0001c0013t0001g0221 |
2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2090-750C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77315239 | |||||||
chr7:77315715 | C | A | 2 | a0001c0001t0001g0045 a0001c0001t0001g0078 |
2 | NA19084.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.2090-1226G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77315715 | |||||||
chr7:77315896 | G | A | 1 | a0001c0001t0001g0304 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2090-1407C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77315896 | |||||||
chr7:77316399 | G | A | 1 | a0003c0004t0001g0190 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2090-1910C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77316399 | |||||||
chr7:77316429 | GTC | G | 68 | a0001c0001t0001g0006 a0001c0001t0001g0070 a0001c0001t0001g0326 others(65): Show |
69 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.2090-1942_2090-194 others(6): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77316429 | |||||||
chr7:77316598 | A | T | 1 | a0002c0003t0001g0048 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2090-2109T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77316598 | |||||||
chr7:77316723 | C | T | 31 | a0002c0003t0002g0055 a0003c0004t0001g0190 a0003c0004t0002g0033 others(28): Show |
31 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.2090-2234G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77316723 | |||||||
chr7:77316829 | A | G | 16 | a0001c0002t0001g0275 a0002c0003t0001g0005 a0002c0003t0001g0019 others(13): Show |
17 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.2090-2340T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77316829 | |||||||
chr7:77316879 | A | G | 1 | a0002c0003t0001g0346 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2090-2390T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77316879 | |||||||
chr7:77316883 | C | T | 2 | a0005c0006t0001g0172 a0005c0006t0001g0179 |
2 | HG01109.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.2090-2394G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77316883 | |||||||
chr7:77316999 | C | T | 16 | a0001c0002t0001g0275 a0002c0003t0001g0005 a0002c0003t0001g0019 others(13): Show |
17 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.2090-2510G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77316999 | |||||||
chr7:77317116 | T | TC | 16 | a0001c0002t0001g0275 a0002c0003t0001g0005 a0002c0003t0001g0019 others(13): Show |
17 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.2090-2628dupG | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77317116 | |||||||
chr7:77317153 | C | T | 16 | a0001c0002t0001g0275 a0002c0003t0001g0005 a0002c0003t0001g0019 others(13): Show |
17 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.2090-2664G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77317153 | |||||||
chr7:77317200 | G | A | 16 | a0001c0002t0001g0275 a0002c0003t0001g0005 a0002c0003t0001g0019 others(13): Show |
17 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.2090-2711C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77317200 | |||||||
chr7:77317239 | C | T | 16 | a0001c0002t0001g0275 a0002c0003t0001g0005 a0002c0003t0001g0019 others(13): Show |
17 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.2090-2750G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77317239 | |||||||
chr7:77317295 | A | G | 16 | a0001c0002t0001g0275 a0002c0003t0001g0005 a0002c0003t0001g0019 others(13): Show |
17 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.2090-2806T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77317295 | |||||||
chr7:77317304 | C | T | 1 | a0001c0002t0001g0309 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2090-2815G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77317304 | |||||||
chr7:77317344 | T | G | 16 | a0001c0002t0001g0275 a0002c0003t0001g0005 a0002c0003t0001g0019 others(13): Show |
17 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.2090-2855A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77317344 | |||||||
chr7:77317365 | T | C | 16 | a0001c0002t0001g0275 a0002c0003t0001g0005 a0002c0003t0001g0019 others(13): Show |
17 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.2090-2876A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77317365 | |||||||
chr7:77317377 | T | TGGGGTTG | 136 | a0001c0001t0001g0006 a0001c0001t0001g0070 a0001c0001t0001g0326 others(133): Show |
138 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(135): Show |
intron_variant | MODIFIER | c.2090-2895_2090-288 others(11): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77317377 | |||||||
chr7:77317655 | G | C | 16 | a0001c0002t0001g0275 a0002c0003t0001g0005 a0002c0003t0001g0019 others(13): Show |
17 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.2089+3070C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77317655 | |||||||
chr7:77317775 | C | A | 26 | a0002c0003t0002g0055 a0003c0004t0001g0190 a0003c0004t0002g0113 others(23): Show |
26 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.2089+2950G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77317775 | |||||||
chr7:77317781 | C | T | 16 | a0001c0002t0001g0275 a0002c0003t0001g0005 a0002c0003t0001g0019 others(13): Show |
17 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.2089+2944G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77317781 | |||||||
chr7:77317924 | A | G | 17 | a0001c0002t0001g0275 a0002c0003t0001g0005 a0002c0003t0001g0019 others(14): Show |
18 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.2089+2801T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77317924 | |||||||
chr7:77317971 | A | C | 30 | a0003c0004t0001g0190 a0003c0004t0002g0033 a0003c0004t0002g0113 others(27): Show |
30 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.2089+2754T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77317971 | |||||||
chr7:77318155 | A | G | 17 | a0001c0002t0001g0275 a0002c0003t0001g0005 a0002c0003t0001g0019 others(14): Show |
18 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.2089+2570T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77318155 | |||||||
chr7:77318202 | C | T | 17 | a0001c0002t0001g0275 a0002c0003t0001g0005 a0002c0003t0001g0019 others(14): Show |
18 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.2089+2523G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77318202 | |||||||
chr7:77318284 | C | G | 16 | a0001c0002t0001g0275 a0002c0003t0001g0005 a0002c0003t0001g0019 others(13): Show |
17 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.2089+2441G>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77318284 | |||||||
chr7:77318342 | A | AC | 17 | a0001c0002t0001g0275 a0002c0003t0001g0005 a0002c0003t0001g0019 others(14): Show |
18 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.2089+2382_2089+238 others(5): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77318342 | |||||||
chr7:77318393 | G | C | 17 | a0001c0002t0001g0275 a0002c0003t0001g0005 a0002c0003t0001g0019 others(14): Show |
18 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.2089+2332C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77318393 | |||||||
chr7:77318469 | T | C | 1 | a0002c0003t0002g0055 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2089+2256A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77318469 | |||||||
chr7:77318486 | T | A | 17 | a0001c0002t0001g0275 a0002c0003t0001g0005 a0002c0003t0001g0019 others(14): Show |
18 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.2089+2239A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77318486 | |||||||
chr7:77318556 | T | C | 17 | a0001c0002t0001g0275 a0002c0003t0001g0005 a0002c0003t0001g0019 others(14): Show |
18 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.2089+2169A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77318556 | |||||||
chr7:77318567 | T | A | 47 | a0001c0002t0001g0275 a0002c0003t0001g0005 a0002c0003t0001g0019 others(44): Show |
48 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.2089+2158A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77318567 | |||||||
chr7:77318758 | A | G | 17 | a0001c0002t0001g0275 a0002c0003t0001g0005 a0002c0003t0001g0019 others(14): Show |
18 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.2089+1967T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77318758 | |||||||
chr7:77318908 | G | T | 2 | a0001c0001t0001g0036 a0001c0001t0001g0043 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.2089+1817C>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77318908 | |||||||
chr7:77318913 | T | C | 30 | a0003c0004t0001g0190 a0003c0004t0002g0033 a0003c0004t0002g0113 others(27): Show |
30 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.2089+1812A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77318913 | |||||||
chr7:77318954 | G | A | 16 | a0001c0002t0001g0275 a0002c0003t0001g0005 a0002c0003t0001g0019 others(13): Show |
17 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.2089+1771C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77318954 | |||||||
chr7:77318965 | A | G | 1 | a0001c0002t0001g0284 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.2089+1760T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77318965 | |||||||
chr7:77319034 | G | T | 49 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0209 others(46): Show |
50 | HG00099.hp1 HG00733.hp2 HG01070.hp1 others(47): Show |
intron_variant | MODIFIER | c.2089+1691C>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77319034 | |||||||
chr7:77319041 | T | G | 30 | a0003c0004t0001g0190 a0003c0004t0002g0033 a0003c0004t0002g0113 others(27): Show |
30 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.2089+1684A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77319041 | |||||||
chr7:77319172 | C | T | 1 | a0002c0003t0001g0248 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2089+1553G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77319172 | |||||||
chr7:77319329 | C | T | 2 | a0001c0002t0002g0107 a0001c0002t0002g0108 |
2 | HG02109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2089+1396G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77319329 | |||||||
chr7:77319427 | T | C | 226 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0070 others(223): Show |
229 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.2089+1298A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77319427 | |||||||
chr7:77319511 | A | G | 16 | a0001c0002t0001g0275 a0002c0003t0001g0005 a0002c0003t0001g0019 others(13): Show |
17 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.2089+1214T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77319511 | |||||||
chr7:77319655 | T | C | 184 | a0001c0001t0001g0006 a0001c0001t0001g0070 a0001c0001t0001g0326 others(181): Show |
187 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.2089+1070A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77319655 | |||||||
chr7:77319758 | T | TA | 153 | a0001c0001t0001g0006 a0001c0001t0001g0070 a0001c0001t0001g0326 others(150): Show |
156 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.2089+966dupT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77319758 | |||||||
chr7:77319846 | A | G | 6 | a0003c0004t0002g0132 a0003c0004t0002g0183 a0003c0004t0002g0184 others(3): Show |
6 | HG01891.hp1 HG02055.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.2089+879T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77319846 | |||||||
chr7:77319874 | C | T | 88 | a0001c0001t0001g0015 a0001c0002t0001g0275 a0001c0002t0001g0342 others(85): Show |
89 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.2089+851G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77319874 | |||||||
chr7:77320025 | C | CATGTT | 226 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0070 others(223): Show |
229 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.2089+699_2089+700i others(7): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77320025 | |||||||
chr7:77320060 | T | C | 1 | a0001c0002t0001g0309 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2089+665A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77320060 | |||||||
chr7:77320076 | C | A | 226 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0070 others(223): Show |
229 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.2089+649G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77320076 | |||||||
chr7:77320181 | C | T | 2 | a0002c0003t0001g0060 a0002c0003t0003g0068 |
2 | HG03017.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.2089+544G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77320181 | |||||||
chr7:77320190 | G | A | 12 | a0001c0001t0001g0071 a0001c0001t0001g0079 a0001c0001t0001g0111 others(9): Show |
12 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.2089+535C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77320190 | |||||||
chr7:77320216 | A | G | 340 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(337): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.2089+509T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77320216 | |||||||
chr7:77320423 | G | A | 1 | a0001c0001t0001g0076 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2089+302C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77320423 | |||||||
chr7:77320522 | T | G | 1 | a0001c0002t0001g0241 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2089+203A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77320522 | |||||||
chr7:77320603 | A | G | 22 | a0004c0005t0001g0105 a0004c0005t0001g0106 a0004c0005t0001g0171 others(19): Show |
22 | HG00558.hp2 HG00621.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.2089+122T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77320603 | |||||||
chr7:77320690 | T | G | 1 | a0002c0003t0002g0055 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2089+35A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77320690 | |||||||
chr7:77320698 | C | T | 1 | a0001c0001t0001g0081 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.2089+27G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77320698 | |||||||
chr7:77320718 | C | T | 42 | a0001c0001t0001g0015 a0001c0002t0001g0342 a0001c0002t0001g0343 others(39): Show |
42 | HG00099.hp1 HG00733.hp2 HG01099.hp1 others(39): Show |
splice_region_variant&intron_variant | LOW | c.2089+7G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 26/30 | chr7 | 77320718 | |||||||
chr7:77320852 | A | G | 4 | a0001c0001t0001g0326 a0001c0002t0001g0217 a0001c0002t0001g0234 others(1): Show |
4 | HG01934.hp1 HG02165.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.1995-33T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 25/30 | chr7 | 77320852 | |||||||
chr7:77320913 | T | C | 1 | a0003c0004t0001g0190 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1995-94A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 25/30 | chr7 | 77320913 | |||||||
chr7:77320951 | C | T | 8 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0011 others(5): Show |
8 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1995-132G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 25/30 | chr7 | 77320951 | |||||||
chr7:77321263 | A | G | 1 | a0007c0011t0002g0144 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1994+70T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 25/30 | chr7 | 77321263 | |||||||
chr7:77321273 | T | C | 22 | a0003c0004t0001g0190 a0003c0004t0002g0033 a0003c0004t0002g0113 others(19): Show |
22 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.1994+60A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 25/30 | chr7 | 77321273 | |||||||
chr7:77321560 | C | T | 1 | a0002c0003t0002g0055 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1924-157G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 24/30 | chr7 | 77321560 | |||||||
chr7:77321581 | T | C | 2 | a0001c0002t0002g0107 a0001c0002t0002g0108 |
2 | HG02109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1924-178A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 24/30 | chr7 | 77321581 | |||||||
chr7:77321611 | T | A | 57 | a0001c0002t0001g0275 a0001c0002t0001g0342 a0001c0002t0001g0343 others(54): Show |
58 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.1924-208A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 24/30 | chr7 | 77321611 | |||||||
chr7:77321668 | C | T | 130 | a0001c0001t0001g0006 a0001c0001t0001g0070 a0001c0001t0001g0326 others(127): Show |
132 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(129): Show |
intron_variant | MODIFIER | c.1924-265G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 24/30 | chr7 | 77321668 | |||||||
chr7:77321859 | T | A | 220 | a0001c0001t0001g0006 a0001c0001t0001g0070 a0001c0001t0001g0326 others(217): Show |
223 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.1924-456A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 24/30 | chr7 | 77321859 | |||||||
chr7:77322323 | G | A | 4 | a0003c0004t0002g0203 a0003c0004t0002g0339 a0003c0004t0002g0340 others(1): Show |
4 | HG00642.hp1 HG01106.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1924-920C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 24/30 | chr7 | 77322323 | |||||||
chr7:77322401 | C | T | 1 | a0002c0003t0001g0319 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1924-998G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 24/30 | chr7 | 77322401 | |||||||
chr7:77322462 | T | C | 30 | a0003c0004t0001g0190 a0003c0004t0002g0033 a0003c0004t0002g0113 others(27): Show |
30 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.1924-1059A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 24/30 | chr7 | 77322462 | |||||||
chr7:77322582 | G | GT | 17 | a0001c0001t0001g0032 a0001c0001t0001g0072 a0001c0001t0001g0079 others(14): Show |
17 | HG00544.hp1 HG00597.hp2 HG00639.hp1 others(14): Show |
intron_variant | MODIFIER | c.1923+1064dupA | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 24/30 | chr7 | 77322582 | |||||||
chr7:77322582 | GT | G | 112 | a0001c0001t0001g0006 a0001c0001t0001g0070 a0001c0001t0001g0292 others(109): Show |
114 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.1923+1064delA | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 24/30 | chr7 | 77322582 | |||||||
chr7:77322591 | T | G | 1 | a0014c0017t0001g0347 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1923+1056A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 24/30 | chr7 | 77322591 | |||||||
chr7:77322604 | T | A | 6 | a0001c0002t0001g0343 a0001c0021t0001g0249 a0002c0003t0001g0224 others(3): Show |
6 | HG00099.hp1 HG01169.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.1923+1043A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 24/30 | chr7 | 77322604 | |||||||
chr7:77322604 | T | TA | 76 | a0001c0002t0001g0275 a0001c0002t0001g0342 a0001c0002t0001g0345 others(73): Show |
77 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.1923+1042dupT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 24/30 | chr7 | 77322604 | |||||||
chr7:77322604 | T | TTA | 6 | a0001c0002t0001g0344 a0002c0003t0001g0048 a0003c0004t0002g0132 others(3): Show |
6 | HG01175.hp1 HG01891.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1923+1042_1923+104 others(6): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 24/30 | chr7 | 77322604 | |||||||
chr7:77322948 | C | A | 24 | a0003c0004t0001g0190 a0003c0004t0002g0033 a0003c0004t0002g0113 others(21): Show |
24 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.1923+699G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 24/30 | chr7 | 77322948 | |||||||
chr7:77322972 | A | T | 30 | a0003c0004t0001g0190 a0003c0004t0002g0033 a0003c0004t0002g0113 others(27): Show |
30 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.1923+675T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 24/30 | chr7 | 77322972 | |||||||
chr7:77322986 | GTTCT | G | 6 | a0003c0004t0002g0132 a0003c0004t0002g0183 a0003c0004t0002g0184 others(3): Show |
6 | HG01891.hp1 HG02055.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1923+657_1923+660d others(6): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 24/30 | chr7 | 77322986 | |||||||
chr7:77322993 | C | A | 1 | a0002c0003t0002g0055 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1923+654G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 24/30 | chr7 | 77322993 | |||||||
chr7:77323000 | T | C | 1 | a0004c0005t0003g0174 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1923+647A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 24/30 | chr7 | 77323000 | |||||||
chr7:77323325 | A | G | 2 | a0001c0001t0001g0035 a0001c0001t0001g0084 |
2 | HG03669.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1923+322T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 24/30 | chr7 | 77323325 | |||||||
chr7:77323363 | T | C | 5 | a0003c0004t0002g0033 a0003c0004t0002g0146 a0003c0004t0002g0152 others(2): Show |
5 | HG02886.hp2 HG03041.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1923+284A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 24/30 | chr7 | 77323363 | |||||||
chr7:77323549 | T | C | 9 | a0003c0004t0002g0113 a0003c0004t0002g0123 a0003c0004t0002g0124 others(6): Show |
9 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.1923+98A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 24/30 | chr7 | 77323549 | |||||||
chr7:77323588 | A | G | 8 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0011 others(5): Show |
8 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1923+59T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 24/30 | chr7 | 77323588 | |||||||
chr7:77324000 | C | T | 2 | a0001c0013t0001g0218 a0001c0013t0001g0221 |
2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1828-258G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 23/30 | chr7 | 77324000 | |||||||
chr7:77324007 | C | A | 1 | a0002c0003t0001g0346 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1828-265G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 23/30 | chr7 | 77324007 | |||||||
chr7:77324042 | A | C | 1 | a0001c0001t0001g0205 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1828-300T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 23/30 | chr7 | 77324042 | |||||||
chr7:77324122 | A | G | 1 | a0001c0001t0001g0316 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1828-380T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 23/30 | chr7 | 77324122 | |||||||
chr7:77324168 | G | C | 5 | a0007c0011t0002g0037 a0007c0011t0002g0138 a0007c0011t0002g0144 others(2): Show |
5 | HG01891.hp2 HG02723.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1828-426C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 23/30 | chr7 | 77324168 | |||||||
chr7:77324174 | C | G | 13 | a0003c0004t0001g0190 a0003c0004t0002g0033 a0003c0004t0002g0146 others(10): Show |
13 | HG02523.hp2 HG02717.hp1 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.1828-432G>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 23/30 | chr7 | 77324174 | |||||||
chr7:77324236 | C | G | 25 | a0003c0004t0001g0190 a0003c0004t0002g0113 a0003c0004t0002g0123 others(22): Show |
25 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.1828-494G>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 23/30 | chr7 | 77324236 | |||||||
chr7:77324468 | T | C | 5 | a0007c0011t0002g0037 a0007c0011t0002g0138 a0007c0011t0002g0144 others(2): Show |
5 | HG01891.hp2 HG02723.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1828-726A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 23/30 | chr7 | 77324468 | |||||||
chr7:77324536 | A | G | 1 | a0001c0002t0002g0012 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1828-794T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 23/30 | chr7 | 77324536 | |||||||
chr7:77324576 | G | C | 5 | a0007c0011t0002g0037 a0007c0011t0002g0138 a0007c0011t0002g0144 others(2): Show |
5 | HG01891.hp2 HG02723.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1828-834C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 23/30 | chr7 | 77324576 | |||||||
chr7:77324615 | T | C | 1 | a0001c0001t0001g0236 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1828-873A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 23/30 | chr7 | 77324615 | |||||||
chr7:77324685 | T | A | 1 | a0005c0006t0001g0206 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1828-943A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 23/30 | chr7 | 77324685 | |||||||
chr7:77324756 | G | GT | 6 | a0001c0001t0001g0111 a0001c0001t0001g0326 a0001c0002t0001g0284 others(3): Show |
6 | HG01175.hp1 HG04184.hp1 NA18949.hp2 others(3): Show |
intron_variant | MODIFIER | c.1828-1015dupA | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 23/30 | chr7 | 77324756 | |||||||
chr7:77324825 | ACT | A | 8 | a0001c0002t0001g0193 a0001c0002t0001g0230 a0001c0002t0001g0242 others(5): Show |
8 | HG02071.hp2 HG02132.hp1 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.1828-1085_1828-108 others(6): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 23/30 | chr7 | 77324825 | |||||||
chr7:77324826 | C | CT | 68 | a0001c0001t0001g0001 a0001c0001t0001g0085 a0001c0001t0001g0258 others(65): Show |
68 | HG00140.hp1 HG00558.hp2 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.1828-1085dupA | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 23/30 | chr7 | 77324826 | |||||||
chr7:77324826 | C | CTT | 6 | a0001c0001t0001g0333 a0001c0002t0002g0135 a0001c0002t0002g0140 others(3): Show |
6 | HG00621.hp2 HG02027.hp2 HG02071.hp1 others(3): Show |
intron_variant | MODIFIER | c.1828-1086_1828-108 others(6): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 23/30 | chr7 | 77324826 | |||||||
chr7:77324826 | CT | C | 109 | a0001c0001t0001g0006 a0001c0001t0001g0192 a0001c0001t0001g0326 others(106): Show |
111 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.1828-1085delA | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 23/30 | chr7 | 77324826 | |||||||
chr7:77325024 | T | C | 51 | a0001c0002t0001g0275 a0002c0003t0001g0005 a0002c0003t0001g0019 others(48): Show |
52 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.1827+1188A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 23/30 | chr7 | 77325024 | |||||||
chr7:77325027 | G | A | 1 | a0002c0027t0001g0214 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1827+1185C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 23/30 | chr7 | 77325027 | |||||||
chr7:77325404 | C | G | 1 | a0002c0003t0002g0055 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1827+808G>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 23/30 | chr7 | 77325404 | |||||||
chr7:77325407 | A | G | 46 | a0001c0002t0001g0275 a0002c0003t0001g0005 a0002c0003t0001g0019 others(43): Show |
47 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.1827+805T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 23/30 | chr7 | 77325407 | |||||||
chr7:77325439 | T | C | 1 | a0001c0002t0001g0118 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1827+773A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 23/30 | chr7 | 77325439 | |||||||
chr7:77326358 | T | G | 1 | a0001c0002t0004g0034 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1766-85A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 22/30 | chr7 | 77326358 | |||||||
chr7:77326438 | T | G | 31 | a0004c0005t0001g0105 a0004c0005t0001g0106 a0004c0005t0001g0171 others(28): Show |
31 | HG00558.hp2 HG00621.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.1766-165A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 22/30 | chr7 | 77326438 | |||||||
chr7:77326445 | A | C | 2 | a0001c0002t0002g0135 a0001c0002t0002g0140 |
2 | HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1766-172T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 22/30 | chr7 | 77326445 | |||||||
chr7:77326446 | G | C | 1 | a0014c0017t0001g0347 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1766-173C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 22/30 | chr7 | 77326446 | |||||||
chr7:77326627 | C | T | 4 | a0001c0002t0001g0342 a0001c0002t0001g0343 a0001c0002t0001g0344 others(1): Show |
4 | HG01099.hp1 HG01168.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.1766-354G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 22/30 | chr7 | 77326627 | |||||||
chr7:77326683 | A | G | 46 | a0001c0002t0001g0275 a0002c0003t0001g0005 a0002c0003t0001g0019 others(43): Show |
47 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.1766-410T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 22/30 | chr7 | 77326683 | |||||||
chr7:77326813 | C | T | 46 | a0001c0002t0001g0275 a0002c0003t0001g0005 a0002c0003t0001g0019 others(43): Show |
47 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.1766-540G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 22/30 | chr7 | 77326813 | |||||||
chr7:77326831 | C | T | 1 | a0006c0020t0003g0024 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1766-558G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 22/30 | chr7 | 77326831 | |||||||
chr7:77326930 | T | G | 16 | a0001c0002t0001g0275 a0002c0003t0001g0005 a0002c0003t0001g0019 others(13): Show |
17 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.1766-657A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 22/30 | chr7 | 77326930 | |||||||
chr7:77327007 | G | A | 23 | a0004c0005t0001g0105 a0004c0005t0001g0106 a0004c0005t0001g0171 others(20): Show |
23 | HG00558.hp2 HG00621.hp2 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.1766-734C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 22/30 | chr7 | 77327007 | |||||||
chr7:77327180 | G | A | 2 | a0001c0010t0001g0145 a0001c0010t0001g0149 |
2 | HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1766-907C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 22/30 | chr7 | 77327180 | |||||||
chr7:77327280 | C | T | 24 | a0003c0004t0001g0190 a0003c0004t0002g0113 a0003c0004t0002g0123 others(21): Show |
24 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.1766-1007G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 22/30 | chr7 | 77327280 | |||||||
chr7:77327322 | G | A | 145 | a0001c0001t0001g0006 a0001c0001t0001g0305 a0001c0001t0001g0326 others(142): Show |
147 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.1766-1049C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 22/30 | chr7 | 77327322 | |||||||
chr7:77327341 | C | T | 1 | a0002c0003t0001g0346 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1766-1068G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 22/30 | chr7 | 77327341 | |||||||
chr7:77327370 | A | AAC | 104 | a0001c0001t0001g0006 a0001c0001t0001g0305 a0001c0001t0001g0326 others(101): Show |
106 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.1766-1099_1766-109 others(6): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 22/30 | chr7 | 77327370 | |||||||
chr7:77327382 | C | A | 1 | a0001c0001t0001g0226 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1766-1109G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 22/30 | chr7 | 77327382 | |||||||
chr7:77327388 | C | G | 1 | a0002c0003t0001g0120 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1766-1115G>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 22/30 | chr7 | 77327388 | |||||||
chr7:77327457 | T | C | 223 | a0001c0001t0001g0006 a0001c0001t0001g0305 a0001c0001t0001g0326 others(220): Show |
226 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.1765+1149A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 22/30 | chr7 | 77327457 | |||||||
chr7:77327502 | C | T | 3 | a0007c0011t0002g0037 a0007c0011t0002g0208 a0007c0011t0002g0310 |
3 | HG01891.hp2 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1765+1104G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 22/30 | chr7 | 77327502 | |||||||
chr7:77327541 | T | C | 1 | a0002c0003t0001g0066 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1765+1065A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 22/30 | chr7 | 77327541 | |||||||
chr7:77327605 | CATAAAAC others(15): Show |
C | 9 | a0003c0004t0002g0113 a0003c0004t0002g0123 a0003c0004t0002g0124 others(6): Show |
9 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.1765+979_1765+1000 others(25): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 22/30 | chr7 | 77327605 | |||||||
chr7:77327637 | C | T | 6 | a0003c0004t0002g0132 a0003c0004t0002g0183 a0003c0004t0002g0184 others(3): Show |
6 | HG01891.hp1 HG02055.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1765+969G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 22/30 | chr7 | 77327637 | |||||||
chr7:77327723 | T | C | 5 | a0007c0011t0002g0037 a0007c0011t0002g0138 a0007c0011t0002g0144 others(2): Show |
5 | HG01891.hp2 HG02723.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1765+883A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 22/30 | chr7 | 77327723 | |||||||
chr7:77327730 | C | T | 3 | a0002c0003t0001g0059 a0002c0003t0001g0067 a0008c0012t0001g0169 |
3 | HG01257.hp2 HG02273.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1765+876G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 22/30 | chr7 | 77327730 | |||||||
chr7:77327836 | G | A | 23 | a0004c0005t0001g0105 a0004c0005t0001g0106 a0004c0005t0001g0171 others(20): Show |
23 | HG00558.hp2 HG00621.hp2 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.1765+770C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 22/30 | chr7 | 77327836 | |||||||
chr7:77327871 | G | C | 6 | a0003c0004t0002g0132 a0003c0004t0002g0183 a0003c0004t0002g0184 others(3): Show |
6 | HG01891.hp1 HG02055.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1765+735C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 22/30 | chr7 | 77327871 | |||||||
chr7:77328228 | G | A | 1 | a0002c0003t0001g0058 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1765+378C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 22/30 | chr7 | 77328228 | |||||||
chr7:77328264 | C | T | 41 | a0001c0002t0001g0342 a0001c0002t0001g0343 a0001c0002t0001g0344 others(38): Show |
41 | HG00099.hp1 HG00733.hp2 HG01099.hp1 others(38): Show |
intron_variant | MODIFIER | c.1765+342G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 22/30 | chr7 | 77328264 | |||||||
chr7:77328360 | C | T | 137 | a0001c0001t0001g0006 a0001c0001t0001g0305 a0001c0001t0001g0326 others(134): Show |
139 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.1765+246G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 22/30 | chr7 | 77328360 | |||||||
chr7:77328434 | A | T | 16 | a0001c0002t0001g0275 a0002c0003t0001g0005 a0002c0003t0001g0019 others(13): Show |
17 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.1765+172T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 22/30 | chr7 | 77328434 | |||||||
chr7:77328447 | G | A | 1 | a0007c0011t0002g0310 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1765+159C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 22/30 | chr7 | 77328447 | |||||||
chr7:77328509 | A | T | 32 | a0004c0005t0001g0105 a0004c0005t0001g0106 a0004c0005t0001g0171 others(29): Show |
32 | HG00558.hp2 HG00621.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.1765+97T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 22/30 | chr7 | 77328509 | |||||||
chr7:77328794 | T | C | 1 | a0001c0002t0001g0280 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1734-157A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 21/30 | chr7 | 77328794 | |||||||
chr7:77329013 | T | A | 16 | a0001c0002t0001g0275 a0002c0003t0001g0005 a0002c0003t0001g0019 others(13): Show |
17 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.1733+320A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 21/30 | chr7 | 77329013 | |||||||
chr7:77329013 | TA | T | 65 | a0001c0001t0001g0023 a0001c0001t0001g0294 a0001c0001t0003g0293 others(62): Show |
65 | HG00099.hp1 HG00733.hp2 HG01070.hp2 others(62): Show |
intron_variant | MODIFIER | c.1733+319delT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 21/30 | chr7 | 77329013 | |||||||
chr7:77329048 | C | A | 1 | a0001c0001t0001g0251 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1733+285G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 21/30 | chr7 | 77329048 | |||||||
chr7:77329206 | C | T | 5 | a0007c0011t0002g0037 a0007c0011t0002g0138 a0007c0011t0002g0144 others(2): Show |
5 | HG01891.hp2 HG02723.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1733+127G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 21/30 | chr7 | 77329206 | |||||||
chr7:77329240 | A | G | 40 | a0001c0002t0001g0275 a0002c0003t0001g0005 a0002c0003t0001g0019 others(37): Show |
41 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.1733+93T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 21/30 | chr7 | 77329240 | |||||||
chr7:77329408 | G | A | 1 | a0001c0001t0001g0075 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1675-17C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 20/30 | chr7 | 77329408 | |||||||
chr7:77329413 | A | G | 340 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(337): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.1675-22T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 20/30 | chr7 | 77329413 | |||||||
chr7:77329424 | G | T | 6 | a0003c0004t0002g0132 a0003c0004t0002g0183 a0003c0004t0002g0184 others(3): Show |
6 | HG01891.hp1 HG02055.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1675-33C>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 20/30 | chr7 | 77329424 | |||||||
chr7:77329634 | G | C | 1 | a0001c0002t0002g0140 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1675-243C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 20/30 | chr7 | 77329634 | |||||||
chr7:77329663 | C | A | 102 | a0001c0001t0001g0006 a0001c0001t0001g0305 a0001c0001t0001g0326 others(99): Show |
104 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.1675-272G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 20/30 | chr7 | 77329663 | |||||||
chr7:77329708 | T | C | 1 | a0001c0001t0001g0205 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1675-317A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 20/30 | chr7 | 77329708 | |||||||
chr7:77329786 | C | CT | 87 | a0001c0001t0001g0006 a0001c0001t0001g0305 a0001c0001t0001g0326 others(84): Show |
89 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.1675-396_1675-395i others(3): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 20/30 | chr7 | 77329786 | |||||||
chr7:77329884 | C | T | 1 | a0001c0001t0001g0236 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1674+355G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 20/30 | chr7 | 77329884 | |||||||
chr7:77330059 | TAGG | T | 102 | a0001c0001t0001g0006 a0001c0001t0001g0305 a0001c0001t0001g0326 others(99): Show |
104 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.1674+177_1674+179d others(5): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 20/30 | chr7 | 77330059 | |||||||
chr7:77330150 | T | C | 2 | a0002c0003t0001g0215 a0002c0003t0001g0216 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1674+89A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 20/30 | chr7 | 77330150 | |||||||
chr7:77330414 | G | T | 101 | a0001c0001t0001g0006 a0001c0001t0001g0305 a0001c0001t0001g0326 others(98): Show |
103 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.1546-47C>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77330414 | |||||||
chr7:77330428 | G | A | 1 | a0006c0008t0001g0100 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1546-61C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77330428 | |||||||
chr7:77330467 | T | C | 101 | a0001c0001t0001g0006 a0001c0001t0001g0305 a0001c0001t0001g0326 others(98): Show |
103 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.1546-100A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77330467 | |||||||
chr7:77330496 | G | T | 1 | a0014c0017t0001g0347 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1546-129C>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77330496 | |||||||
chr7:77330498 | A | G | 146 | a0001c0001t0001g0006 a0001c0001t0001g0305 a0001c0001t0001g0326 others(143): Show |
149 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.1546-131T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77330498 | |||||||
chr7:77330573 | C | CT | 8 | a0001c0001t0001g0040 a0001c0001t0001g0057 a0001c0001t0001g0079 others(5): Show |
8 | HG00099.hp2 HG00323.hp1 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.1546-207dupA | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77330573 | |||||||
chr7:77330573 | CT | C | 8 | a0001c0001t0001g0073 a0001c0001t0001g0112 a0001c0001t0001g0226 others(5): Show |
8 | HG00280.hp1 HG00609.hp2 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.1546-207delA | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77330573 | |||||||
chr7:77330578 | T | G | 99 | a0001c0001t0001g0006 a0001c0001t0001g0305 a0001c0001t0001g0331 others(96): Show |
101 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.1546-211A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77330578 | |||||||
chr7:77330588 | T | G | 2 | a0001c0002t0001g0283 a0003c0004t0002g0146 |
2 | HG01981.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1546-221A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77330588 | |||||||
chr7:77330591 | T | G | 101 | a0001c0001t0001g0006 a0001c0001t0001g0305 a0001c0001t0001g0326 others(98): Show |
103 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.1546-224A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77330591 | |||||||
chr7:77330591 | T | TG | 23 | a0002c0003t0001g0021 a0003c0004t0001g0190 a0003c0004t0002g0113 others(20): Show |
23 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.1546-225_1546-224i others(3): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77330591 | |||||||
chr7:77330591 | T | TTG | 15 | a0002c0003t0001g0005 a0002c0003t0001g0019 a0002c0003t0001g0030 others(12): Show |
16 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.1546-225_1546-224i others(4): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77330591 | |||||||
chr7:77330591 | T | TTTG | 7 | a0001c0002t0001g0275 a0007c0011t0002g0037 a0007c0011t0002g0138 others(4): Show |
7 | HG01167.hp2 HG01891.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1546-227_1546-225d others(5): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77330591 | |||||||
chr7:77330696 | C | T | 101 | a0001c0001t0001g0006 a0001c0001t0001g0305 a0001c0001t0001g0326 others(98): Show |
103 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.1546-329G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77330696 | |||||||
chr7:77330788 | T | C | 37 | a0004c0005t0001g0106 a0004c0005t0001g0171 a0004c0005t0003g0104 others(34): Show |
37 | HG00099.hp1 HG00558.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.1546-421A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77330788 | |||||||
chr7:77330805 | C | T | 1 | a0001c0001t0001g0250 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1546-438G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77330805 | |||||||
chr7:77330866 | A | G | 3 | a0002c0003t0001g0038 a0002c0003t0001g0062 a0002c0003t0001g0064 |
3 | HG01884.hp2 HG02486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1546-499T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77330866 | |||||||
chr7:77330883 | T | G | 45 | a0001c0002t0001g0275 a0002c0003t0001g0005 a0002c0003t0001g0019 others(42): Show |
46 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.1546-516A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77330883 | |||||||
chr7:77331060 | T | C | 1 | a0001c0001t0001g0022 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1546-693A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77331060 | |||||||
chr7:77331098 | A | G | 109 | a0001c0001t0001g0006 a0001c0001t0001g0305 a0001c0001t0001g0326 others(106): Show |
111 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.1546-731T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77331098 | |||||||
chr7:77331257 | T | C | 2 | a0002c0003t0001g0215 a0002c0003t0001g0216 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1546-890A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77331257 | |||||||
chr7:77331293 | T | C | 1 | a0001c0002t0001g0242 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1546-926A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77331293 | |||||||
chr7:77331502 | G | A | 101 | a0001c0001t0001g0006 a0001c0001t0001g0305 a0001c0001t0001g0326 others(98): Show |
103 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.1546-1135C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77331502 | |||||||
chr7:77331567 | C | T | 34 | a0001c0002t0001g0342 a0001c0002t0001g0343 a0001c0002t0001g0344 others(31): Show |
34 | HG00733.hp2 HG01099.hp1 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.1546-1200G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77331567 | |||||||
chr7:77331800 | T | C | 101 | a0001c0001t0001g0006 a0001c0001t0001g0305 a0001c0001t0001g0326 others(98): Show |
103 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.1546-1433A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77331800 | |||||||
chr7:77331892 | G | GA | 22 | a0003c0004t0001g0190 a0003c0004t0002g0113 a0003c0004t0002g0123 others(19): Show |
22 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.1546-1526dupT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77331892 | |||||||
chr7:77331892 | GA | G | 135 | a0001c0001t0001g0112 a0001c0001t0001g0254 a0001c0001t0001g0305 others(132): Show |
138 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.1546-1526delT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77331892 | |||||||
chr7:77331894 | A | G | 1 | a0002c0003t0001g0019 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1546-1527T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77331894 | |||||||
chr7:77332007 | A | G | 16 | a0001c0002t0001g0275 a0002c0003t0001g0005 a0002c0003t0001g0019 others(13): Show |
17 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.1546-1640T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77332007 | |||||||
chr7:77332158 | G | A | 1 | a0001c0002t0001g0284 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1546-1791C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77332158 | |||||||
chr7:77332334 | T | C | 29 | a0004c0005t0001g0105 a0004c0005t0001g0106 a0004c0005t0001g0171 others(26): Show |
29 | HG00099.hp1 HG00558.hp2 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.1546-1967A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77332334 | |||||||
chr7:77332417 | T | A | 45 | a0001c0002t0001g0275 a0002c0003t0001g0005 a0002c0003t0001g0019 others(42): Show |
46 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.1546-2050A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77332417 | |||||||
chr7:77332420 | A | T | 5 | a0003c0004t0002g0033 a0003c0004t0002g0146 a0003c0004t0002g0152 others(2): Show |
5 | HG02886.hp2 HG03041.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1546-2053T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77332420 | |||||||
chr7:77332564 | G | A | 2 | a0002c0003t0001g0215 a0002c0003t0001g0216 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1546-2197C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77332564 | |||||||
chr7:77332617 | G | A | 5 | a0007c0011t0002g0037 a0007c0011t0002g0138 a0007c0011t0002g0144 others(2): Show |
5 | HG01891.hp2 HG02723.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1546-2250C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77332617 | |||||||
chr7:77332968 | A | G | 1 | a0001c0002t0001g0244 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1546-2601T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77332968 | |||||||
chr7:77333080 | A | T | 45 | a0001c0002t0001g0275 a0002c0003t0001g0005 a0002c0003t0001g0019 others(42): Show |
46 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.1546-2713T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77333080 | |||||||
chr7:77333116 | A | G | 45 | a0001c0002t0001g0275 a0002c0003t0001g0005 a0002c0003t0001g0019 others(42): Show |
46 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.1546-2749T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77333116 | |||||||
chr7:77333140 | G | A | 45 | a0001c0002t0001g0275 a0002c0003t0001g0005 a0002c0003t0001g0019 others(42): Show |
46 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.1546-2773C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77333140 | |||||||
chr7:77333551 | C | G | 245 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(242): Show |
250 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.1546-3184G>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77333551 | |||||||
chr7:77333688 | T | C | 9 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0011 others(6): Show |
9 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1546-3321A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77333688 | |||||||
chr7:77333803 | T | C | 1 | a0001c0001t0001g0084 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1546-3436A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77333803 | |||||||
chr7:77334504 | A | G | 1 | a0014c0017t0001g0347 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1546-4137T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77334504 | |||||||
chr7:77334523 | C | T | 5 | a0007c0011t0002g0037 a0007c0011t0002g0138 a0007c0011t0002g0144 others(2): Show |
5 | HG01891.hp2 HG02723.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1546-4156G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77334523 | |||||||
chr7:77334579 | T | TAAAAAAA others(3): Show |
1 | a0003c0004t0002g0132 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1546-4213_1546-421 others(14): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77334579 | |||||||
chr7:77334579 | T | TAAAAAAA others(4): Show |
4 | a0003c0009t0001g0028 a0003c0009t0001g0189 a0003c0009t0001g0191 others(1): Show |
4 | HG03041.hp2 NA18969.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.1546-4213_1546-421 others(15): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77334579 | |||||||
chr7:77334579 | T | TAAAAAAA others(5): Show |
9 | a0003c0004t0001g0190 a0003c0004t0002g0113 a0003c0004t0002g0203 others(6): Show |
9 | HG00642.hp1 HG01106.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1546-4213_1546-421 others(16): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77334579 | |||||||
chr7:77334579 | T | TAAAAAAA others(6): Show |
2 | a0003c0004t0002g0123 a0003c0004t0002g0124 |
2 | HG00140.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1546-4213_1546-421 others(17): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77334579 | |||||||
chr7:77334579 | T | TAAAAAAA others(8): Show |
14 | a0001c0002t0001g0275 a0002c0003t0001g0005 a0002c0003t0001g0019 others(11): Show |
15 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.1546-4213_1546-421 others(19): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77334579 | |||||||
chr7:77334579 | T | TAAAAAAA others(9): Show |
2 | a0002c0003t0001g0245 a0002c0003t0001g0335 |
2 | HG02015.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.1546-4213_1546-421 others(20): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77334579 | |||||||
chr7:77334579 | T | TAAAAAAA others(10): Show |
2 | a0003c0004t0002g0133 a0003c0004t0002g0156 |
2 | HG01993.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1546-4213_1546-421 others(21): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77334579 | |||||||
chr7:77334579 | TTA | T | 4 | a0007c0011t0002g0037 a0007c0011t0002g0138 a0007c0011t0002g0144 others(1): Show |
4 | HG01891.hp2 HG02723.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1546-4214_1546-421 others(6): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77334579 | |||||||
chr7:77334580 | T | A | 39 | a0001c0002t0001g0275 a0002c0003t0001g0005 a0002c0003t0001g0019 others(36): Show |
40 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(37): Show |
intron_variant | MODIFIER | c.1546-4213A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77334580 | |||||||
chr7:77334580 | T | TA | 49 | a0001c0001t0001g0050 a0001c0001t0001g0086 a0001c0001t0001g0097 others(46): Show |
50 | HG00099.hp1 HG00323.hp1 HG00558.hp2 others(47): Show |
intron_variant | MODIFIER | c.1546-4214dupT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77334580 | |||||||
chr7:77334580 | T | TAA | 47 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0032 others(44): Show |
49 | HG00733.hp2 HG01071.hp1 HG01099.hp1 others(46): Show |
intron_variant | MODIFIER | c.1546-4215_1546-421 others(6): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77334580 | |||||||
chr7:77334580 | T | TAAA | 7 | a0001c0001t0001g0082 a0002c0003t0001g0090 a0002c0003t0001g0215 others(4): Show |
7 | HG02896.hp2 HG02897.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1546-4216_1546-421 others(7): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77334580 | |||||||
chr7:77334580 | TA | T | 27 | a0001c0001t0001g0008 a0001c0001t0001g0036 a0001c0001t0001g0057 others(24): Show |
27 | HG00099.hp2 HG00408.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.1546-4214delT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77334580 | |||||||
chr7:77334797 | A | G | 1 | a0014c0017t0001g0347 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1546-4430T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77334797 | |||||||
chr7:77334851 | G | A | 2 | a0001c0010t0001g0016 a0001c0010t0001g0026 |
2 | HG02486.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1546-4484C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77334851 | |||||||
chr7:77334856 | G | A | 1 | a0014c0017t0001g0347 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1546-4489C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77334856 | |||||||
chr7:77334939 | C | T | 40 | a0001c0002t0001g0275 a0002c0003t0001g0005 a0002c0003t0001g0019 others(37): Show |
41 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.1546-4572G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77334939 | |||||||
chr7:77335019 | C | G | 1 | a0007c0011t0002g0138 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1546-4652G>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77335019 | |||||||
chr7:77335061 | C | T | 3 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0304 |
3 | NA18966.hp2 NA18986.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.1546-4694G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77335061 | |||||||
chr7:77335086 | T | TA | 91 | a0001c0001t0001g0006 a0001c0001t0001g0305 a0001c0001t0001g0326 others(88): Show |
93 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.1546-4720dupT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77335086 | |||||||
chr7:77335117 | A | G | 9 | a0002c0007t0001g0004 a0002c0007t0001g0227 a0002c0007t0001g0228 others(6): Show |
10 | NA18946.hp2 NA18978.hp2 NA18981.hp1 others(7): Show |
intron_variant | MODIFIER | c.1546-4750T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77335117 | |||||||
chr7:77335182 | T | C | 5 | a0007c0011t0002g0037 a0007c0011t0002g0138 a0007c0011t0002g0144 others(2): Show |
5 | HG01891.hp2 HG02723.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1546-4815A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77335182 | |||||||
chr7:77335205 | G | A | 5 | a0003c0004t0002g0033 a0003c0004t0002g0146 a0003c0004t0002g0152 others(2): Show |
5 | HG02886.hp2 HG03041.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1546-4838C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77335205 | |||||||
chr7:77335258 | C | T | 1 | a0006c0008t0001g0137 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1546-4891G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77335258 | |||||||
chr7:77335356 | C | A | 5 | a0007c0011t0002g0037 a0007c0011t0002g0138 a0007c0011t0002g0144 others(2): Show |
5 | HG01891.hp2 HG02723.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1546-4989G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77335356 | |||||||
chr7:77335366 | C | A | 1 | a0001c0001t0001g0328 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1546-4999G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77335366 | |||||||
chr7:77335454 | C | G | 50 | a0001c0002t0001g0275 a0002c0003t0001g0005 a0002c0003t0001g0019 others(47): Show |
51 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.1546-5087G>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77335454 | |||||||
chr7:77335455 | A | G | 1 | a0002c0003t0002g0055 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1546-5088T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77335455 | |||||||
chr7:77335623 | T | C | 9 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0011 others(6): Show |
9 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1546-5256A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77335623 | |||||||
chr7:77335638 | C | CA | 9 | a0001c0002t0001g0237 a0003c0004t0002g0113 a0003c0004t0002g0123 others(6): Show |
9 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.1546-5272dupT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77335638 | |||||||
chr7:77335642 | A | C | 1 | a0001c0002t0001g0303 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1546-5275T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77335642 | |||||||
chr7:77335809 | G | A | 1 | a0002c0003t0001g0060 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1546-5442C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77335809 | |||||||
chr7:77335826 | C | G | 6 | a0003c0004t0002g0132 a0003c0004t0002g0183 a0003c0004t0002g0184 others(3): Show |
6 | HG01891.hp1 HG02055.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1546-5459G>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77335826 | |||||||
chr7:77336073 | G | C | 22 | a0001c0001t0001g0331 a0001c0002t0001g0116 a0001c0002t0001g0232 others(19): Show |
23 | HG00423.hp1 HG01433.hp1 HG01952.hp1 others(20): Show |
intron_variant | MODIFIER | c.1546-5706C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77336073 | |||||||
chr7:77336132 | C | T | 5 | a0007c0011t0002g0037 a0007c0011t0002g0138 a0007c0011t0002g0144 others(2): Show |
5 | HG01891.hp2 HG02723.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1546-5765G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77336132 | |||||||
chr7:77336176 | T | C | 1 | a0002c0003t0001g0063 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1546-5809A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77336176 | |||||||
chr7:77336379 | C | T | 1 | a0004c0005t0001g0106 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1546-6012G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77336379 | |||||||
chr7:77336481 | C | CT | 54 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0032 others(51): Show |
56 | HG00323.hp1 HG00733.hp2 HG01070.hp1 others(53): Show |
intron_variant | MODIFIER | c.1546-6115dupA | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77336481 | |||||||
chr7:77336485 | T | G | 49 | a0001c0002t0001g0275 a0002c0003t0001g0005 a0002c0003t0001g0019 others(46): Show |
50 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.1546-6118A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77336485 | |||||||
chr7:77336614 | A | G | 50 | a0001c0002t0001g0275 a0002c0003t0001g0005 a0002c0003t0001g0019 others(47): Show |
51 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.1546-6247T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77336614 | |||||||
chr7:77336668 | T | C | 1 | a0003c0004t0002g0152 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1546-6301A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77336668 | |||||||
chr7:77336729 | T | C | 50 | a0001c0002t0001g0275 a0002c0003t0001g0005 a0002c0003t0001g0019 others(47): Show |
51 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.1546-6362A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77336729 | |||||||
chr7:77336790 | T | C | 29 | a0004c0005t0001g0105 a0004c0005t0001g0106 a0004c0005t0001g0171 others(26): Show |
29 | HG00099.hp1 HG00558.hp2 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.1546-6423A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77336790 | |||||||
chr7:77337143 | C | T | 1 | a0014c0017t0001g0347 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1546-6776G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77337143 | |||||||
chr7:77337284 | C | T | 16 | a0001c0002t0001g0275 a0002c0003t0001g0005 a0002c0003t0001g0019 others(13): Show |
17 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.1546-6917G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77337284 | |||||||
chr7:77337285 | G | A | 1 | a0001c0023t0001g0094 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1546-6918C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77337285 | |||||||
chr7:77337301 | TG | T | 50 | a0001c0002t0001g0275 a0002c0003t0001g0005 a0002c0003t0001g0019 others(47): Show |
51 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.1546-6935delC | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77337301 | |||||||
chr7:77337305 | G | GGT | 91 | a0001c0001t0001g0006 a0001c0001t0001g0305 a0001c0001t0001g0326 others(88): Show |
93 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.1546-6939_1546-693 others(6): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77337305 | |||||||
chr7:77337309 | G | A | 1 | a0001c0001t0001g0081 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1546-6942C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77337309 | |||||||
chr7:77337319 | C | T | 1 | a0001c0001t0001g0295 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1546-6952G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77337319 | |||||||
chr7:77337701 | C | A | 1 | a0001c0001t0003g0293 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1546-7334G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77337701 | |||||||
chr7:77337758 | A | G | 5 | a0007c0011t0002g0037 a0007c0011t0002g0138 a0007c0011t0002g0144 others(2): Show |
5 | HG01891.hp2 HG02723.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1546-7391T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77337758 | |||||||
chr7:77338051 | A | C | 1 | a0002c0003t0001g0087 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1546-7684T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77338051 | |||||||
chr7:77338195 | A | G | 7 | a0004c0005t0003g0222 a0005c0006t0001g0131 a0005c0006t0001g0165 others(4): Show |
7 | HG00099.hp1 HG01109.hp1 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.1546-7828T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77338195 | |||||||
chr7:77338247 | C | T | 16 | a0001c0002t0001g0275 a0002c0003t0001g0005 a0002c0003t0001g0019 others(13): Show |
17 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.1546-7880G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77338247 | |||||||
chr7:77338433 | C | T | 50 | a0001c0002t0001g0275 a0002c0003t0001g0005 a0002c0003t0001g0019 others(47): Show |
51 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.1546-8066G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77338433 | |||||||
chr7:77338459 | A | G | 1 | a0003c0004t0002g0133 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1546-8092T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77338459 | |||||||
chr7:77338559 | A | C | 34 | a0003c0004t0001g0190 a0003c0004t0002g0033 a0003c0004t0002g0113 others(31): Show |
34 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.1546-8192T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77338559 | |||||||
chr7:77338621 | G | A | 38 | a0004c0005t0001g0105 a0004c0005t0001g0106 a0004c0005t0001g0171 others(35): Show |
38 | HG00099.hp1 HG00558.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.1546-8254C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77338621 | |||||||
chr7:77338641 | G | A | 5 | a0001c0002t0002g0002 a0001c0002t0002g0207 a0001c0002t0002g0219 others(2): Show |
6 | HG01884.hp1 HG02109.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1546-8274C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77338641 | |||||||
chr7:77338652 | G | A | 95 | a0001c0001t0001g0006 a0001c0001t0001g0305 a0001c0001t0001g0326 others(92): Show |
97 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.1546-8285C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77338652 | |||||||
chr7:77338800 | A | T | 1 | a0006c0008t0001g0139 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1546-8433T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77338800 | |||||||
chr7:77338878 | A | G | 1 | a0006c0020t0003g0024 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1546-8511T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77338878 | |||||||
chr7:77338925 | A | C | 29 | a0003c0004t0001g0190 a0003c0004t0002g0033 a0003c0004t0002g0113 others(26): Show |
29 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.1546-8558T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77338925 | |||||||
chr7:77338948 | A | G | 5 | a0007c0011t0002g0037 a0007c0011t0002g0138 a0007c0011t0002g0144 others(2): Show |
5 | HG01891.hp2 HG02723.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1546-8581T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77338948 | |||||||
chr7:77339061 | G | A | 1 | a0005c0006t0001g0122 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1546-8694C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77339061 | |||||||
chr7:77339064 | A | G | 2 | a0002c0003t0001g0059 a0002c0003t0001g0067 |
2 | HG02273.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1546-8697T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77339064 | |||||||
chr7:77339081 | C | T | 90 | a0001c0001t0001g0006 a0001c0001t0001g0305 a0001c0001t0001g0326 others(87): Show |
92 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.1546-8714G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77339081 | |||||||
chr7:77339149 | A | C | 2 | a0006c0008t0001g0134 a0006c0008t0001g0141 |
2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1546-8782T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77339149 | |||||||
chr7:77339225 | G | T | 1 | a0011c0022t0001g0129 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1546-8858C>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77339225 | |||||||
chr7:77339278 | G | A | 240 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(237): Show |
245 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.1546-8911C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77339278 | |||||||
chr7:77339291 | G | A | 4 | a0003c0004t0001g0190 a0003c0009t0001g0188 a0003c0009t0001g0189 others(1): Show |
4 | HG02523.hp2 NA18939.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.1546-8924C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77339291 | |||||||
chr7:77339331 | G | A | 3 | a0001c0001t0001g0077 a0001c0001t0001g0085 a0005c0006t0001g0206 |
3 | HG04115.hp1 HG04184.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1546-8964C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77339331 | |||||||
chr7:77339353 | C | G | 1 | a0013c0016t0001g0039 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1546-8986G>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77339353 | |||||||
chr7:77339417 | G | A | 1 | a0002c0003t0001g0065 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1546-9050C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77339417 | |||||||
chr7:77339424 | G | A | 1 | a0001c0001t0001g0226 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1546-9057C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77339424 | |||||||
chr7:77339586 | A | G | 29 | a0003c0004t0001g0190 a0003c0004t0002g0033 a0003c0004t0002g0113 others(26): Show |
29 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.1546-9219T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77339586 | |||||||
chr7:77339621 | A | C | 1 | a0004c0005t0003g0115 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1546-9254T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77339621 | |||||||
chr7:77339643 | A | G | 4 | a0006c0008t0001g0052 a0006c0008t0001g0134 a0006c0008t0001g0137 others(1): Show |
4 | HG00639.hp1 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1546-9276T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77339643 | |||||||
chr7:77339671 | A | AGGAGGAC others(10): Show |
90 | a0001c0001t0001g0006 a0001c0001t0001g0305 a0001c0001t0001g0326 others(87): Show |
92 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.1546-9321_1546-930 others(21): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77339671 | |||||||
chr7:77339688 | T | TGGAGGAC others(10): Show |
10 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0011 others(7): Show |
10 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1546-9322_1546-932 others(21): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77339688 | |||||||
chr7:77339712 | TAC | T | 90 | a0001c0001t0001g0006 a0001c0001t0001g0305 a0001c0001t0001g0326 others(87): Show |
92 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.1546-9347_1546-934 others(6): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77339712 | |||||||
chr7:77339737 | A | T | 1 | a0002c0003t0001g0285 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1546-9370T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77339737 | |||||||
chr7:77340034 | T | G | 1 | a0001c0002t0001g0244 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1545+9317A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77340034 | |||||||
chr7:77340175 | C | A | 9 | a0006c0008t0001g0017 a0006c0008t0001g0052 a0006c0008t0001g0100 others(6): Show |
9 | HG00639.hp1 HG01074.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1545+9176G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77340175 | |||||||
chr7:77340232 | C | T | 10 | a0001c0002t0001g0238 a0002c0007t0001g0004 a0002c0007t0001g0227 others(7): Show |
11 | HG02027.hp1 NA18946.hp2 NA18978.hp2 others(8): Show |
intron_variant | MODIFIER | c.1545+9119G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77340232 | |||||||
chr7:77340378 | C | T | 5 | a0001c0002t0001g0020 a0001c0002t0001g0025 a0001c0002t0001g0297 others(2): Show |
5 | HG00609.hp1 NA18940.hp2 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.1545+8973G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77340378 | |||||||
chr7:77340414 | G | A | 1 | a0001c0002t0001g0118 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1545+8937C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77340414 | |||||||
chr7:77340517 | G | A | 24 | a0003c0004t0001g0190 a0003c0004t0002g0113 a0003c0004t0002g0123 others(21): Show |
24 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.1545+8834C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77340517 | |||||||
chr7:77340522 | T | C | 110 | a0001c0001t0001g0006 a0001c0001t0001g0305 a0001c0001t0001g0326 others(107): Show |
112 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.1545+8829A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77340522 | |||||||
chr7:77340795 | A | C | 90 | a0001c0001t0001g0006 a0001c0001t0001g0305 a0001c0001t0001g0326 others(87): Show |
92 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.1545+8556T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77340795 | |||||||
chr7:77340858 | C | T | 9 | a0006c0008t0001g0017 a0006c0008t0001g0052 a0006c0008t0001g0100 others(6): Show |
9 | HG00639.hp1 HG01074.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1545+8493G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77340858 | |||||||
chr7:77340999 | T | G | 24 | a0003c0004t0001g0190 a0003c0004t0002g0113 a0003c0004t0002g0123 others(21): Show |
24 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.1545+8352A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77340999 | |||||||
chr7:77341059 | T | C | 243 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(240): Show |
248 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.1545+8292A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77341059 | |||||||
chr7:77341115 | A | G | 1 | a0004c0005t0003g0164 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1545+8236T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77341115 | |||||||
chr7:77341160 | C | T | 24 | a0003c0004t0001g0190 a0003c0004t0002g0113 a0003c0004t0002g0123 others(21): Show |
24 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.1545+8191G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77341160 | |||||||
chr7:77341181 | T | G | 6 | a0002c0003t0002g0055 a0003c0004t0002g0033 a0003c0004t0002g0146 others(3): Show |
6 | HG02886.hp2 HG03041.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1545+8170A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77341181 | |||||||
chr7:77341188 | T | A | 7 | a0001c0002t0002g0002 a0001c0002t0002g0207 a0001c0002t0002g0219 others(4): Show |
8 | HG01884.hp1 HG02109.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1545+8163A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77341188 | |||||||
chr7:77341386 | A | C | 9 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0011 others(6): Show |
9 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1545+7965T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77341386 | |||||||
chr7:77341457 | G | A | 1 | a0003c0004t0002g0123 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1545+7894C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77341457 | |||||||
chr7:77341751 | C | T | 1 | a0003c0004t0002g0152 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1545+7600G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77341751 | |||||||
chr7:77341914 | C | T | 1 | a0001c0001t0001g0018 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1545+7437G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77341914 | |||||||
chr7:77341983 | C | G | 1 | a0005c0006t0001g0172 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1545+7368G>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77341983 | |||||||
chr7:77342079 | G | A | 5 | a0007c0011t0002g0037 a0007c0011t0002g0138 a0007c0011t0002g0144 others(2): Show |
5 | HG01891.hp2 HG02723.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1545+7272C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77342079 | |||||||
chr7:77342125 | TCTGA | T | 9 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0011 others(6): Show |
9 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1545+7222_1545+722 others(8): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77342125 | |||||||
chr7:77342161 | G | A | 118 | a0001c0001t0001g0006 a0001c0001t0001g0305 a0001c0001t0001g0326 others(115): Show |
120 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.1545+7190C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77342161 | |||||||
chr7:77342201 | T | C | 1 | a0002c0003t0001g0245 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1545+7150A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77342201 | |||||||
chr7:77342202 | G | T | 1 | a0002c0003t0001g0245 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1545+7149C>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77342202 | |||||||
chr7:77342224 | C | T | 16 | a0001c0002t0001g0275 a0002c0003t0001g0005 a0002c0003t0001g0019 others(13): Show |
17 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.1545+7127G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77342224 | |||||||
chr7:77342249 | T | C | 129 | a0001c0001t0001g0006 a0001c0001t0001g0305 a0001c0001t0001g0326 others(126): Show |
131 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.1545+7102A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77342249 | |||||||
chr7:77342269 | C | T | 1 | a0002c0003t0002g0055 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1545+7082G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77342269 | |||||||
chr7:77342452 | T | C | 129 | a0001c0001t0001g0006 a0001c0001t0001g0305 a0001c0001t0001g0326 others(126): Show |
131 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.1545+6899A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77342452 | |||||||
chr7:77342459 | A | C | 8 | a0002c0003t0001g0019 a0002c0003t0001g0021 a0002c0003t0001g0030 others(5): Show |
8 | HG02015.hp2 HG02683.hp1 HG03669.hp1 others(5): Show |
intron_variant | MODIFIER | c.1545+6892T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77342459 | |||||||
chr7:77342495 | T | C | 1 | a0002c0003t0001g0058 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1545+6856A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77342495 | |||||||
chr7:77342531 | T | TC | 39 | a0004c0005t0001g0105 a0004c0005t0001g0106 a0004c0005t0001g0171 others(36): Show |
39 | HG00099.hp1 HG00558.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.1545+6819dupG | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77342531 | |||||||
chr7:77342535 | T | C | 39 | a0004c0005t0001g0105 a0004c0005t0001g0106 a0004c0005t0001g0171 others(36): Show |
39 | HG00099.hp1 HG00558.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.1545+6816A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77342535 | |||||||
chr7:77342618 | G | A | 1 | a0002c0018t0001g0099 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1545+6733C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77342618 | |||||||
chr7:77342624 | T | C | 1 | a0001c0002t0001g0309 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1545+6727A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77342624 | |||||||
chr7:77342819 | G | T | 1 | a0002c0003t0001g0245 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1545+6532C>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77342819 | |||||||
chr7:77342824 | C | T | 1 | a0001c0002t0001g0277 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1545+6527G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77342824 | |||||||
chr7:77342873 | A | G | 105 | a0001c0001t0001g0006 a0001c0001t0001g0305 a0001c0001t0001g0326 others(102): Show |
107 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.1545+6478T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77342873 | |||||||
chr7:77343058 | A | G | 241 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(238): Show |
246 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.1545+6293T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77343058 | |||||||
chr7:77343184 | G | A | 1 | a0001c0001t0001g0330 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1545+6167C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77343184 | |||||||
chr7:77343185 | C | CT | 105 | a0001c0001t0001g0006 a0001c0001t0001g0305 a0001c0001t0001g0326 others(102): Show |
107 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.1545+6165_1545+616 others(5): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77343185 | |||||||
chr7:77343251 | T | G | 6 | a0002c0003t0002g0055 a0003c0004t0002g0033 a0003c0004t0002g0146 others(3): Show |
6 | HG02886.hp2 HG03041.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1545+6100A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77343251 | |||||||
chr7:77343568 | G | A | 16 | a0003c0004t0001g0190 a0003c0004t0002g0113 a0003c0004t0002g0123 others(13): Show |
16 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.1545+5783C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77343568 | |||||||
chr7:77343801 | A | G | 149 | a0001c0001t0001g0006 a0001c0001t0001g0305 a0001c0001t0001g0331 others(146): Show |
152 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.1545+5550T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77343801 | |||||||
chr7:77343861 | C | T | 2 | a0002c0003t0001g0090 a0011c0022t0001g0129 |
2 | HG02976.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.1545+5490G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77343861 | |||||||
chr7:77344069 | A | G | 24 | a0003c0004t0001g0190 a0003c0004t0002g0113 a0003c0004t0002g0123 others(21): Show |
24 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.1545+5282T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77344069 | |||||||
chr7:77344406 | G | A | 1 | a0001c0001t0001g0078 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1545+4945C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77344406 | |||||||
chr7:77344523 | G | A | 16 | a0001c0002t0001g0275 a0002c0003t0001g0005 a0002c0003t0001g0019 others(13): Show |
17 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.1545+4828C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77344523 | |||||||
chr7:77344763 | A | C | 117 | a0001c0001t0001g0006 a0001c0001t0001g0305 a0001c0002t0001g0020 others(114): Show |
118 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.1545+4588T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77344763 | |||||||
chr7:77344906 | C | T | 6 | a0003c0004t0002g0132 a0003c0004t0002g0183 a0003c0004t0002g0184 others(3): Show |
6 | HG01891.hp1 HG02055.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1545+4445G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77344906 | |||||||
chr7:77345108 | T | C | 2 | a0006c0008t0001g0137 a0007c0011t0002g0138 |
2 | HG02886.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1545+4243A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77345108 | |||||||
chr7:77345231 | G | C | 117 | a0001c0001t0001g0006 a0001c0001t0001g0258 a0001c0001t0001g0305 others(114): Show |
118 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.1545+4120C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77345231 | |||||||
chr7:77345502 | G | A | 2 | a0003c0004t0002g0340 a0003c0004t0002g0341 |
2 | HG00642.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.1545+3849C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77345502 | |||||||
chr7:77345572 | A | T | 53 | a0001c0001t0001g0003 a0001c0001t0001g0209 a0001c0001t0001g0250 others(50): Show |
55 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(52): Show |
intron_variant | MODIFIER | c.1545+3779T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77345572 | |||||||
chr7:77345689 | C | T | 16 | a0001c0002t0001g0275 a0002c0003t0001g0005 a0002c0003t0001g0019 others(13): Show |
17 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.1545+3662G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77345689 | |||||||
chr7:77345690 | C | A | 50 | a0001c0001t0001g0003 a0001c0001t0001g0209 a0001c0001t0001g0250 others(47): Show |
52 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.1545+3661G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77345690 | |||||||
chr7:77345692 | C | T | 1 | a0002c0003t0001g0245 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1545+3659G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77345692 | |||||||
chr7:77345696 | T | C | 116 | a0001c0001t0001g0006 a0001c0001t0001g0305 a0001c0002t0001g0020 others(113): Show |
117 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.1545+3655A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77345696 | |||||||
chr7:77345839 | C | G | 6 | a0002c0003t0002g0055 a0007c0011t0002g0037 a0007c0011t0002g0138 others(3): Show |
6 | HG01891.hp2 HG02723.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1545+3512G>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77345839 | |||||||
chr7:77345870 | C | T | 1 | a0014c0017t0001g0347 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1545+3481G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77345870 | |||||||
chr7:77345963 | T | A | 53 | a0001c0001t0001g0003 a0001c0001t0001g0209 a0001c0001t0001g0250 others(50): Show |
55 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(52): Show |
intron_variant | MODIFIER | c.1545+3388A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77345963 | |||||||
chr7:77346067 | C | T | 1 | a0002c0018t0001g0099 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1545+3284G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77346067 | |||||||
chr7:77346252 | G | A | 87 | a0001c0001t0001g0006 a0001c0002t0001g0020 a0001c0002t0001g0025 others(84): Show |
88 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.1545+3099C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77346252 | |||||||
chr7:77346265 | C | T | 2 | a0001c0002t0001g0157 a0001c0002t0001g0239 |
2 | HG00544.hp2 HG00558.hp1 |
intron_variant | MODIFIER | c.1545+3086G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77346265 | |||||||
chr7:77346270 | C | CA | 10 | a0001c0001t0001g0212 a0001c0001t0001g0315 a0001c0002t0001g0275 others(7): Show |
10 | HG00738.hp2 HG01074.hp1 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.1545+3080dupT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77346270 | |||||||
chr7:77346270 | C | CAAAA | 8 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0012 others(5): Show |
8 | HG01433.hp2 HG02615.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1545+3077_1545+308 others(8): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77346270 | |||||||
chr7:77346270 | C | CAAAAA | 26 | a0001c0002t0006g0007 a0003c0004t0001g0190 a0003c0004t0002g0033 others(23): Show |
26 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.1545+3076_1545+308 others(9): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77346270 | |||||||
chr7:77346270 | C | CAAAAAAA | 63 | a0001c0001t0001g0006 a0001c0002t0001g0020 a0001c0002t0001g0025 others(60): Show |
64 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.1545+3074_1545+308 others(11): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77346270 | |||||||
chr7:77346270 | C | CAAAAAAA others(1): Show |
10 | a0001c0002t0001g0110 a0001c0002t0001g0233 a0001c0002t0001g0234 others(7): Show |
10 | HG01952.hp1 HG03516.hp2 NA18612.hp2 others(7): Show |
intron_variant | MODIFIER | c.1545+3073_1545+308 others(12): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77346270 | |||||||
chr7:77346270 | CA | C | 7 | a0001c0001t0001g0008 a0001c0001t0001g0305 a0001c0001t0001g0313 others(4): Show |
7 | HG01070.hp2 HG03704.hp1 NA18957.hp1 others(4): Show |
intron_variant | MODIFIER | c.1545+3080delT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77346270 | |||||||
chr7:77346287 | A | G | 1 | a0005c0006t0001g0165 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1545+3064T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77346287 | |||||||
chr7:77346311 | T | A | 121 | a0001c0001t0001g0006 a0001c0002t0001g0020 a0001c0002t0001g0025 others(118): Show |
122 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.1545+3040A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77346311 | |||||||
chr7:77346377 | C | A | 1 | a0001c0023t0001g0094 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1545+2974G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77346377 | |||||||
chr7:77346537 | C | CA | 85 | a0001c0001t0001g0006 a0001c0001t0001g0049 a0001c0001t0001g0075 others(82): Show |
86 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.1545+2813dupT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77346537 | |||||||
chr7:77346621 | G | A | 40 | a0004c0005t0001g0105 a0004c0005t0001g0106 a0004c0005t0001g0171 others(37): Show |
40 | HG00099.hp1 HG00558.hp2 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.1545+2730C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77346621 | |||||||
chr7:77346659 | G | A | 10 | a0001c0001t0001g0001 a0001c0001t0001g0032 a0001c0001t0001g0047 others(7): Show |
11 | HG00323.hp1 HG01934.hp2 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.1545+2692C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77346659 | |||||||
chr7:77346717 | GAA | G | 86 | a0001c0001t0001g0006 a0001c0002t0001g0020 a0001c0002t0001g0025 others(83): Show |
87 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.1545+2632_1545+263 others(6): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77346717 | |||||||
chr7:77346757 | T | C | 86 | a0001c0001t0001g0006 a0001c0002t0001g0020 a0001c0002t0001g0025 others(83): Show |
87 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.1545+2594A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77346757 | |||||||
chr7:77346867 | G | A | 1 | a0004c0005t0003g0176 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1545+2484C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77346867 | |||||||
chr7:77346872 | A | ACT | 243 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(240): Show |
248 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.1545+2477_1545+247 others(6): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77346872 | |||||||
chr7:77346934 | A | ACCACCAC others(8): Show |
1 | a0001c0001t0001g0258 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1545+2402_1545+241 others(19): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77346934 | |||||||
chr7:77346950 | C | A | 1 | a0001c0001t0001g0112 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1545+2401G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77346950 | |||||||
chr7:77347004 | T | C | 87 | a0001c0001t0001g0006 a0001c0002t0001g0020 a0001c0002t0001g0025 others(84): Show |
88 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.1545+2347A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77347004 | |||||||
chr7:77347204 | G | T | 6 | a0002c0003t0002g0055 a0007c0011t0002g0037 a0007c0011t0002g0138 others(3): Show |
6 | HG01891.hp2 HG02723.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1545+2147C>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77347204 | |||||||
chr7:77347295 | G | A | 1 | a0001c0001t0001g0305 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1545+2056C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77347295 | |||||||
chr7:77347416 | G | A | 1 | a0002c0003t0001g0093 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1545+1935C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77347416 | |||||||
chr7:77347517 | T | C | 40 | a0004c0005t0001g0105 a0004c0005t0001g0106 a0004c0005t0001g0171 others(37): Show |
40 | HG00099.hp1 HG00558.hp2 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.1545+1834A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77347517 | |||||||
chr7:77347704 | A | G | 6 | a0002c0003t0002g0055 a0007c0011t0002g0037 a0007c0011t0002g0138 others(3): Show |
6 | HG01891.hp2 HG02723.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1545+1647T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77347704 | |||||||
chr7:77347798 | G | A | 1 | a0001c0002t0001g0244 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1545+1553C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77347798 | |||||||
chr7:77347822 | T | G | 2 | a0001c0002t0002g0135 a0001c0002t0002g0140 |
2 | HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1545+1529A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77347822 | |||||||
chr7:77347854 | T | C | 2 | a0002c0003t0001g0247 a0002c0003t0001g0287 |
2 | NA18949.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.1545+1497A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77347854 | |||||||
chr7:77347893 | T | C | 1 | a0001c0001t0001g0008 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1545+1458A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77347893 | |||||||
chr7:77347987 | C | CA | 43 | a0001c0001t0001g0085 a0001c0001t0001g0304 a0001c0001t0001g0326 others(40): Show |
43 | HG00099.hp1 HG00558.hp2 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.1545+1363dupT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77347987 | |||||||
chr7:77347987 | CA | C | 20 | a0001c0001t0001g0057 a0001c0001t0001g0079 a0001c0002t0001g0273 others(17): Show |
21 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(18): Show |
intron_variant | MODIFIER | c.1545+1363delT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77347987 | |||||||
chr7:77348000 | A | T | 123 | a0001c0001t0001g0006 a0001c0002t0001g0020 a0001c0002t0001g0025 others(120): Show |
124 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.1545+1351T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77348000 | |||||||
chr7:77348003 | T | A | 3 | a0005c0006t0001g0131 a0005c0006t0001g0166 a0005c0006t0001g0167 |
3 | HG00099.hp1 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1545+1348A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77348003 | |||||||
chr7:77348113 | G | A | 1 | a0001c0001t0001g0292 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1545+1238C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77348113 | |||||||
chr7:77348152 | A | G | 1 | a0002c0003t0001g0319 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1545+1199T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77348152 | |||||||
chr7:77348502 | G | A | 5 | a0001c0002t0001g0238 a0001c0002t0001g0264 a0001c0002t0001g0274 others(2): Show |
5 | HG00673.hp1 HG01099.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.1545+849C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77348502 | |||||||
chr7:77348596 | G | A | 1 | a0001c0001t0001g0081 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1545+755C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77348596 | |||||||
chr7:77348768 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1545+583C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77348768 | |||||||
chr7:77348779 | G | A | 7 | a0005c0006t0001g0131 a0005c0006t0001g0165 a0005c0006t0001g0166 others(4): Show |
7 | HG00099.hp1 HG01109.hp1 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.1545+572C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77348779 | |||||||
chr7:77348936 | C | CTG | 20 | a0001c0001t0001g0015 a0001c0001t0001g0035 a0001c0002t0001g0020 others(17): Show |
20 | HG00733.hp2 HG01433.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.1545+413_1545+414d others(4): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77348936 | |||||||
chr7:77348936 | CTGTG | C | 3 | a0001c0001t0001g0259 a0001c0013t0001g0218 a0001c0013t0001g0221 |
3 | HG00609.hp2 HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1545+411_1545+414d others(6): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77348936 | |||||||
chr7:77348967 | C | T | 75 | a0001c0001t0001g0006 a0001c0002t0001g0020 a0001c0002t0001g0025 others(72): Show |
76 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.1545+384G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77348967 | |||||||
chr7:77349203 | T | G | 9 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0011 others(6): Show |
9 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1545+148A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77349203 | |||||||
chr7:77349259 | A | G | 6 | a0003c0004t0002g0132 a0003c0004t0002g0183 a0003c0004t0002g0184 others(3): Show |
6 | HG01891.hp1 HG02055.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1545+92T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77349259 | |||||||
chr7:77349277 | A | G | 1 | a0001c0001t0001g0008 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1545+74T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 19/30 | chr7 | 77349277 | |||||||
chr7:77349459 | G | C | 1 | a0001c0001t0001g0194 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1492-55C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77349459 | |||||||
chr7:77349560 | G | A | 9 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0011 others(6): Show |
9 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1492-156C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77349560 | |||||||
chr7:77349590 | A | G | 228 | a0001c0001t0001g0006 a0001c0002t0001g0020 a0001c0002t0001g0025 others(225): Show |
231 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.1492-186T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77349590 | |||||||
chr7:77349667 | TAGAG | T | 29 | a0001c0002t0001g0342 a0001c0002t0001g0343 a0001c0002t0001g0344 others(26): Show |
29 | HG00140.hp1 HG00642.hp1 HG01099.hp1 others(26): Show |
intron_variant | MODIFIER | c.1492-267_1492-264d others(6): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77349667 | |||||||
chr7:77349709 | C | T | 1 | a0003c0004t0002g0203 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1492-305G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77349709 | |||||||
chr7:77349736 | A | C | 3 | a0001c0001t0001g0015 a0001c0010t0001g0016 a0001c0010t0001g0026 |
3 | HG02486.hp2 HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1492-332T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77349736 | |||||||
chr7:77349779 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1492-375G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77349779 | |||||||
chr7:77349970 | C | T | 1 | a0001c0002t0001g0237 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1492-566G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77349970 | |||||||
chr7:77349971 | G | A | 9 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0011 others(6): Show |
9 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1492-567C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77349971 | |||||||
chr7:77350036 | A | G | 1 | a0001c0002t0001g0269 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1492-632T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77350036 | |||||||
chr7:77350285 | A | G | 14 | a0001c0002t0001g0118 a0001c0002t0001g0157 a0001c0002t0001g0239 others(11): Show |
14 | HG00544.hp2 HG00558.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.1492-881T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77350285 | |||||||
chr7:77350285 | AG | A | 71 | a0001c0001t0001g0006 a0001c0002t0001g0020 a0001c0002t0001g0025 others(68): Show |
72 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.1492-882delC | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77350285 | |||||||
chr7:77350286 | G | A | 13 | a0001c0002t0001g0118 a0001c0002t0001g0157 a0001c0002t0001g0239 others(10): Show |
13 | HG00544.hp2 HG00558.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.1492-882C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77350286 | |||||||
chr7:77350293 | G | A | 1 | a0002c0003t0001g0120 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1492-889C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77350293 | |||||||
chr7:77350471 | C | T | 31 | a0004c0005t0001g0105 a0004c0005t0001g0106 a0004c0005t0001g0171 others(28): Show |
31 | HG00099.hp1 HG00558.hp2 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.1492-1067G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77350471 | |||||||
chr7:77350472 | G | C | 23 | a0001c0002t0002g0135 a0001c0002t0002g0140 a0003c0004t0001g0190 others(20): Show |
23 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.1492-1068C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77350472 | |||||||
chr7:77350572 | T | TA | 119 | a0001c0002t0001g0342 a0001c0002t0001g0343 a0001c0002t0001g0344 others(116): Show |
121 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.1492-1169dupT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77350572 | |||||||
chr7:77350572 | T | TAA | 14 | a0002c0003t0001g0060 a0002c0003t0001g0065 a0002c0003t0001g0090 others(11): Show |
14 | HG01891.hp1 HG02055.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.1492-1170_1492-116 others(6): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77350572 | |||||||
chr7:77350572 | TA | T | 92 | a0001c0001t0001g0006 a0001c0001t0001g0091 a0001c0001t0001g0195 others(89): Show |
93 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.1492-1169delT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77350572 | |||||||
chr7:77350616 | G | A | 2 | a0002c0003t0001g0210 a0002c0003t0001g0211 |
2 | HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1492-1212C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77350616 | |||||||
chr7:77350925 | T | A | 3 | a0001c0002t0001g0267 a0001c0002t0001g0271 a0001c0002t0001g0272 |
3 | HG01069.hp2 HG01071.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.1492-1521A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77350925 | |||||||
chr7:77350947 | T | C | 16 | a0002c0003t0001g0005 a0002c0003t0001g0019 a0002c0003t0001g0021 others(13): Show |
17 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.1492-1543A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77350947 | |||||||
chr7:77351009 | A | T | 1 | a0001c0001t0001g0081 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1492-1605T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77351009 | |||||||
chr7:77351091 | C | A | 1 | a0001c0001t0001g0292 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1492-1687G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77351091 | |||||||
chr7:77351147 | A | G | 2 | a0002c0003t0001g0210 a0002c0003t0001g0211 |
2 | HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1492-1743T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77351147 | |||||||
chr7:77351324 | AGGGCATC others(4): Show |
A | 144 | a0001c0002t0001g0342 a0001c0002t0001g0343 a0001c0002t0001g0344 others(141): Show |
146 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.1491+1609_1491+161 others(15): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77351324 | |||||||
chr7:77351448 | T | TAAGAGAA others(307): Show |
5 | a0007c0011t0002g0037 a0007c0011t0002g0138 a0007c0011t0002g0144 others(2): Show |
5 | HG01891.hp2 HG02723.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1491+1495_1491+149 others(318): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77351448 | |||||||
chr7:77351448 | T | TAAGAGAA others(308): Show |
1 | a0002c0003t0002g0055 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1491+1495_1491+149 others(319): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77351448 | |||||||
chr7:77351499 | T | C | 75 | a0001c0001t0001g0006 a0001c0002t0001g0020 a0001c0002t0001g0025 others(72): Show |
76 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.1491+1445A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77351499 | |||||||
chr7:77351515 | G | A | 30 | a0004c0005t0001g0105 a0004c0005t0001g0106 a0004c0005t0001g0171 others(27): Show |
30 | HG00099.hp1 HG00558.hp2 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.1491+1429C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77351515 | |||||||
chr7:77351566 | T | C | 1 | a0001c0002t0001g0273 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1491+1378A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77351566 | |||||||
chr7:77351979 | G | A | 5 | a0001c0002t0002g0002 a0001c0002t0002g0207 a0001c0002t0002g0219 others(2): Show |
6 | HG01884.hp1 HG02109.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1491+965C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77351979 | |||||||
chr7:77352227 | A | G | 1 | a0001c0002t0001g0263 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1491+717T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77352227 | |||||||
chr7:77352341 | C | T | 136 | a0001c0002t0001g0342 a0001c0002t0001g0343 a0001c0002t0001g0344 others(133): Show |
138 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.1491+603G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77352341 | |||||||
chr7:77352351 | T | C | 3 | a0007c0011t0002g0037 a0007c0011t0002g0208 a0007c0011t0002g0310 |
3 | HG01891.hp2 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1491+593A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77352351 | |||||||
chr7:77352457 | G | A | 2 | a0002c0003t0001g0088 a0002c0003t0001g0089 |
2 | NA18940.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.1491+487C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77352457 | |||||||
chr7:77352792 | AC | A | 137 | a0001c0002t0001g0342 a0001c0002t0001g0343 a0001c0002t0001g0344 others(134): Show |
139 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.1491+151delG | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 18/30 | chr7 | 77352792 | |||||||
chr7:77353101 | C | G | 16 | a0002c0003t0001g0005 a0002c0003t0001g0019 a0002c0003t0001g0021 others(13): Show |
17 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.1409-75G>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 17/30 | chr7 | 77353101 | |||||||
chr7:77353163 | C | T | 137 | a0001c0002t0001g0342 a0001c0002t0001g0343 a0001c0002t0001g0344 others(134): Show |
139 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.1409-137G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 17/30 | chr7 | 77353163 | |||||||
chr7:77353231 | A | G | 1 | a0001c0002t0001g0274 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1409-205T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 17/30 | chr7 | 77353231 | |||||||
chr7:77353234 | T | G | 1 | a0001c0001t0001g0075 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1409-208A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 17/30 | chr7 | 77353234 | |||||||
chr7:77353327 | A | T | 34 | a0001c0021t0001g0249 a0002c0003t0001g0038 a0002c0003t0001g0048 others(31): Show |
35 | HG00738.hp1 HG01257.hp2 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.1408+245T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 17/30 | chr7 | 77353327 | |||||||
chr7:77353351 | A | G | 1 | a0001c0001t0001g0328 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1408+221T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 17/30 | chr7 | 77353351 | |||||||
chr7:77353433 | G | A | 3 | a0003c0009t0001g0188 a0003c0009t0001g0189 a0003c0009t0001g0191 |
3 | NA18939.hp2 NA18969.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.1408+139C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 17/30 | chr7 | 77353433 | |||||||
chr7:77353444 | G | GT | 29 | a0001c0001t0001g0001 a0001c0001t0001g0032 a0001c0001t0001g0042 others(26): Show |
31 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.1408+127dupA | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 17/30 | chr7 | 77353444 | |||||||
chr7:77353496 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1408+76G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 17/30 | chr7 | 77353496 | |||||||
chr7:77353678 | A | C | 1 | a0001c0001t0001g0291 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1339-37T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 16/30 | chr7 | 77353678 | |||||||
chr7:77353820 | G | A | 1 | a0001c0002t0001g0244 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1339-179C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 16/30 | chr7 | 77353820 | |||||||
chr7:77353889 | C | T | 2 | a0001c0002t0001g0261 a0001c0002t0001g0298 |
2 | NA18960.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1339-248G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 16/30 | chr7 | 77353889 | |||||||
chr7:77353905 | G | A | 1 | a0001c0002t0001g0053 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1339-264C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 16/30 | chr7 | 77353905 | |||||||
chr7:77353926 | G | A | 13 | a0002c0003t0001g0286 a0002c0003t0001g0311 a0002c0003t0001g0312 others(10): Show |
13 | HG00639.hp1 HG01074.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1339-285C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 16/30 | chr7 | 77353926 | |||||||
chr7:77353997 | A | G | 209 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(206): Show |
212 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.1339-356T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 16/30 | chr7 | 77353997 | |||||||
chr7:77354166 | T | C | 1 | a0001c0001t0003g0293 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1339-525A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 16/30 | chr7 | 77354166 | |||||||
chr7:77354198 | C | T | 45 | a0001c0002t0001g0342 a0001c0002t0001g0343 a0001c0002t0001g0344 others(42): Show |
46 | HG00738.hp1 HG01099.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.1339-557G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 16/30 | chr7 | 77354198 | |||||||
chr7:77354300 | G | A | 115 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(112): Show |
117 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.1339-659C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 16/30 | chr7 | 77354300 | |||||||
chr7:77354516 | A | T | 1 | a0002c0003t0002g0055 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1338+697T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 16/30 | chr7 | 77354516 | |||||||
chr7:77354677 | C | CT | 16 | a0001c0002t0001g0282 a0001c0002t0002g0009 a0001c0002t0002g0010 others(13): Show |
16 | HG01433.hp2 HG01891.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.1338+535dupA | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 16/30 | chr7 | 77354677 | |||||||
chr7:77354677 | C | CTT | 82 | a0001c0002t0001g0020 a0001c0002t0001g0025 a0001c0002t0001g0053 others(79): Show |
83 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.1338+534_1338+535d others(4): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 16/30 | chr7 | 77354677 | |||||||
chr7:77354677 | CT | C | 131 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(128): Show |
133 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.1338+535delA | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 16/30 | chr7 | 77354677 | |||||||
chr7:77354827 | G | A | 1 | a0001c0001t0001g0194 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1338+386C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 16/30 | chr7 | 77354827 | |||||||
chr7:77354916 | T | A | 1 | a0001c0002t0002g0207 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1338+297A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 16/30 | chr7 | 77354916 | |||||||
chr7:77354973 | G | A | 1 | a0001c0001t0001g0201 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1338+240C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 16/30 | chr7 | 77354973 | |||||||
chr7:77355002 | G | A | 1 | a0011c0022t0001g0129 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1338+211C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 16/30 | chr7 | 77355002 | |||||||
chr7:77355109 | T | C | 110 | a0001c0002t0001g0342 a0001c0002t0001g0343 a0001c0002t0001g0344 others(107): Show |
112 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.1338+104A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 16/30 | chr7 | 77355109 | |||||||
chr7:77355132 | C | A | 18 | a0001c0002t0002g0135 a0001c0002t0002g0140 a0003c0004t0001g0190 others(15): Show |
18 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.1338+81G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 16/30 | chr7 | 77355132 | |||||||
chr7:77355149 | C | T | 5 | a0003c0004t0002g0033 a0003c0004t0002g0146 a0003c0004t0002g0152 others(2): Show |
5 | HG02886.hp2 HG03041.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1338+64G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 16/30 | chr7 | 77355149 | |||||||
chr7:77355435 | C | CA | 48 | a0001c0002t0001g0110 a0001c0002t0001g0234 a0001c0002t0001g0342 others(45): Show |
49 | HG00738.hp1 HG01099.hp1 HG01168.hp2 others(46): Show |
splice_region_variant&intron_variant | LOW | c.1121-6dupT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 15/30 | chr7 | 77355435 | |||||||
chr7:77355435 | CA | C | 122 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(119): Show |
124 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(121): Show |
splice_region_variant&intron_variant | LOW | c.1121-6delT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 15/30 | chr7 | 77355435 | |||||||
chr7:77355714 | T | C | 2 | a0002c0003t0001g0038 a0002c0003t0001g0062 |
2 | HG02486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1028-67A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77355714 | |||||||
chr7:77355787 | G | GTTTTTTT others(1): Show |
38 | a0001c0002t0001g0342 a0001c0002t0001g0343 a0001c0002t0001g0345 others(35): Show |
39 | HG00738.hp1 HG01099.hp1 HG01168.hp2 others(36): Show |
intron_variant | MODIFIER | c.1028-148_1028-141d others(10): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77355787 | |||||||
chr7:77355787 | G | GTTTTTTT others(2): Show |
48 | a0001c0002t0001g0344 a0001c0002t0002g0135 a0001c0002t0002g0140 others(45): Show |
49 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.1028-149_1028-141d others(11): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77355787 | |||||||
chr7:77355787 | G | GTTTTTTT others(3): Show |
16 | a0002c0003t0001g0021 a0002c0003t0001g0101 a0002c0003t0001g0311 others(13): Show |
16 | HG00639.hp1 HG00642.hp1 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.1028-150_1028-141d others(12): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77355787 | |||||||
chr7:77355787 | G | GTTTTTTT others(4): Show |
8 | a0002c0003t0001g0019 a0002c0003t0001g0286 a0002c0003t0001g0335 others(5): Show |
8 | HG01109.hp2 HG01243.hp2 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.1028-151_1028-141d others(13): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77355787 | |||||||
chr7:77355787 | GT | G | 177 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(174): Show |
180 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.1028-141delA | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77355787 | |||||||
chr7:77355787 | GTT | G | 14 | a0001c0001t0001g0031 a0001c0001t0001g0260 a0001c0002t0001g0275 others(11): Show |
14 | HG00423.hp2 HG01167.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.1028-142_1028-141d others(4): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77355787 | |||||||
chr7:77355807 | A | T | 110 | a0001c0002t0001g0342 a0001c0002t0001g0343 a0001c0002t0001g0344 others(107): Show |
112 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.1028-160T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77355807 | |||||||
chr7:77355878 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1028-231G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77355878 | |||||||
chr7:77355971 | T | C | 23 | a0001c0002t0002g0135 a0001c0002t0002g0140 a0003c0004t0001g0190 others(20): Show |
23 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.1028-324A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77355971 | |||||||
chr7:77355995 | T | C | 1 | a0001c0002t0001g0241 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1028-348A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77355995 | |||||||
chr7:77356024 | TCAAG | T | 110 | a0001c0002t0001g0342 a0001c0002t0001g0343 a0001c0002t0001g0344 others(107): Show |
112 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.1028-381_1028-378d others(6): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77356024 | |||||||
chr7:77356027 | A | G | 1 | a0001c0002t0001g0143 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1028-380T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77356027 | |||||||
chr7:77356174 | A | G | 9 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0011 others(6): Show |
9 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1028-527T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77356174 | |||||||
chr7:77356353 | C | T | 2 | a0001c0001t0001g0077 a0001c0001t0001g0085 |
2 | HG04115.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1028-706G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77356353 | |||||||
chr7:77356464 | TATC | T | 9 | a0002c0007t0001g0004 a0002c0007t0001g0227 a0002c0007t0001g0228 others(6): Show |
10 | NA18946.hp2 NA18978.hp2 NA18981.hp1 others(7): Show |
intron_variant | MODIFIER | c.1028-820_1028-818d others(5): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77356464 | |||||||
chr7:77356533 | G | A | 4 | a0001c0002t0001g0232 a0001c0002t0001g0233 a0001c0002t0001g0240 others(1): Show |
4 | NA18952.hp1 NA18982.hp1 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.1028-886C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77356533 | |||||||
chr7:77356563 | A | T | 4 | a0001c0002t0001g0157 a0001c0002t0001g0239 a0001c0002t0001g0261 others(1): Show |
4 | HG00544.hp2 HG00558.hp1 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.1028-916T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77356563 | |||||||
chr7:77356603 | T | C | 3 | a0006c0008t0001g0017 a0006c0008t0001g0136 a0009c0026t0001g0054 |
3 | HG01074.hp1 HG02622.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1028-956A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77356603 | |||||||
chr7:77356641 | TTG | T | 27 | a0002c0003t0001g0048 a0002c0003t0001g0058 a0002c0003t0001g0059 others(24): Show |
28 | HG00738.hp1 HG01257.hp2 HG02273.hp2 others(25): Show |
intron_variant | MODIFIER | c.1028-996_1028-995d others(4): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77356641 | |||||||
chr7:77356713 | A | G | 1 | a0004c0005t0003g0104 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1028-1066T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77356713 | |||||||
chr7:77356874 | G | T | 1 | a0006c0008t0001g0052 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1028-1227C>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77356874 | |||||||
chr7:77356997 | C | A | 110 | a0001c0002t0001g0342 a0001c0002t0001g0343 a0001c0002t0001g0344 others(107): Show |
112 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.1028-1350G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77356997 | |||||||
chr7:77357343 | A | G | 1 | a0002c0003t0001g0211 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1028-1696T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77357343 | |||||||
chr7:77357493 | C | T | 106 | a0001c0002t0002g0135 a0001c0002t0002g0140 a0002c0003t0001g0005 others(103): Show |
108 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.1028-1846G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77357493 | |||||||
chr7:77357501 | C | T | 6 | a0003c0004t0002g0132 a0003c0004t0002g0183 a0003c0004t0002g0184 others(3): Show |
6 | HG01891.hp1 HG02055.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1028-1854G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77357501 | |||||||
chr7:77357534 | G | A | 1 | a0003c0004t0002g0152 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1028-1887C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77357534 | |||||||
chr7:77357569 | GGAA | G | 5 | a0002c0003t0002g0055 a0007c0011t0002g0138 a0007c0011t0002g0144 others(2): Show |
5 | HG02723.hp1 HG02976.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1028-1925_1028-192 others(7): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77357569 | |||||||
chr7:77357663 | A | G | 1 | a0001c0002t0002g0140 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1028-2016T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77357663 | |||||||
chr7:77357737 | TGGAG | T | 5 | a0002c0003t0002g0055 a0007c0011t0002g0138 a0007c0011t0002g0144 others(2): Show |
5 | HG02723.hp1 HG02976.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1028-2094_1028-209 others(8): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77357737 | |||||||
chr7:77357812 | G | A | 47 | a0001c0002t0001g0342 a0001c0002t0001g0343 a0001c0002t0001g0344 others(44): Show |
48 | HG00738.hp1 HG01099.hp1 HG01168.hp2 others(45): Show |
intron_variant | MODIFIER | c.1028-2165C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77357812 | |||||||
chr7:77358105 | C | T | 1 | a0002c0003t0001g0224 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1028-2458G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77358105 | |||||||
chr7:77358161 | C | A | 3 | a0001c0010t0001g0145 a0001c0010t0001g0149 a0001c0010t0001g0151 |
3 | HG03139.hp2 HG03516.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1028-2514G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77358161 | |||||||
chr7:77358162 | A | G | 64 | a0001c0002t0002g0135 a0001c0002t0002g0140 a0002c0003t0001g0005 others(61): Show |
65 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.1028-2515T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77358162 | |||||||
chr7:77358186 | T | C | 128 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(125): Show |
132 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.1028-2539A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77358186 | |||||||
chr7:77358203 | A | C | 1 | a0003c0004t0002g0184 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1028-2556T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77358203 | |||||||
chr7:77358366 | G | A | 105 | a0001c0002t0001g0342 a0001c0002t0001g0343 a0001c0002t0001g0344 others(102): Show |
107 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.1027+2458C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77358366 | |||||||
chr7:77358367 | G | A | 1 | a0001c0001t0001g0290 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1027+2457C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77358367 | |||||||
chr7:77358840 | A | G | 110 | a0001c0002t0001g0342 a0001c0002t0001g0343 a0001c0002t0001g0344 others(107): Show |
112 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.1027+1984T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77358840 | |||||||
chr7:77359015 | C | T | 110 | a0001c0002t0001g0342 a0001c0002t0001g0343 a0001c0002t0001g0344 others(107): Show |
112 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.1027+1809G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77359015 | |||||||
chr7:77359059 | C | T | 5 | a0002c0003t0001g0038 a0002c0003t0001g0062 a0002c0003t0001g0063 others(2): Show |
5 | HG01884.hp2 HG01891.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1027+1765G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77359059 | |||||||
chr7:77359060 | G | A | 2 | a0001c0001t0001g0331 a0002c0003t0001g0005 |
3 | HG00280.hp2 HG00323.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.1027+1764C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77359060 | |||||||
chr7:77359126 | C | G | 110 | a0001c0002t0001g0342 a0001c0002t0001g0343 a0001c0002t0001g0344 others(107): Show |
112 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.1027+1698G>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77359126 | |||||||
chr7:77359142 | A | G | 1 | a0001c0001t0001g0041 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1027+1682T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77359142 | |||||||
chr7:77359200 | C | CA | 56 | a0001c0002t0001g0342 a0001c0002t0001g0343 a0001c0002t0001g0344 others(53): Show |
57 | HG00738.hp1 HG01099.hp1 HG01168.hp2 others(54): Show |
intron_variant | MODIFIER | c.1027+1623dupT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77359200 | |||||||
chr7:77359207 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1027+1617T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77359207 | |||||||
chr7:77359209 | A | G | 18 | a0001c0002t0002g0135 a0001c0002t0002g0140 a0003c0004t0001g0190 others(15): Show |
18 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.1027+1615T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77359209 | |||||||
chr7:77359241 | A | G | 1 | a0001c0002t0001g0143 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1027+1583T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77359241 | |||||||
chr7:77359706 | A | G | 112 | a0001c0002t0001g0342 a0001c0002t0001g0343 a0001c0002t0001g0344 others(109): Show |
114 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.1027+1118T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77359706 | |||||||
chr7:77360065 | T | C | 1 | a0001c0001t0001g0289 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1027+759A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77360065 | |||||||
chr7:77360075 | T | C | 110 | a0001c0002t0001g0342 a0001c0002t0001g0343 a0001c0002t0001g0344 others(107): Show |
112 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.1027+749A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77360075 | |||||||
chr7:77360129 | T | A | 5 | a0003c0004t0002g0033 a0003c0004t0002g0146 a0003c0004t0002g0152 others(2): Show |
5 | HG02886.hp2 HG03041.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1027+695A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77360129 | |||||||
chr7:77360336 | G | A | 2 | a0001c0002t0002g0119 a0001c0002t0002g0182 |
2 | HG02559.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1027+488C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77360336 | |||||||
chr7:77360719 | C | T | 6 | a0003c0004t0002g0132 a0003c0004t0002g0183 a0003c0004t0002g0184 others(3): Show |
6 | HG01891.hp1 HG02055.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1027+105G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77360719 | |||||||
chr7:77360764 | G | A | 1 | a0001c0002t0001g0117 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1027+60C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77360764 | |||||||
chr7:77360809 | C | T | 104 | a0002c0003t0001g0005 a0002c0003t0001g0019 a0002c0003t0001g0021 others(101): Show |
106 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.1027+15G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 14/30 | chr7 | 77360809 | |||||||
chr7:77361055 | C | A | 80 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0304 others(77): Show |
81 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.950-154G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 13/30 | chr7 | 77361055 | |||||||
chr7:77361197 | A | C | 1 | a0001c0002t0001g0275 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.950-296T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 13/30 | chr7 | 77361197 | |||||||
chr7:77361209 | A | G | 2 | a0001c0002t0002g0107 a0001c0002t0002g0108 |
2 | HG02109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.950-308T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 13/30 | chr7 | 77361209 | |||||||
chr7:77361566 | T | C | 1 | a0011c0022t0001g0129 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.950-665A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 13/30 | chr7 | 77361566 | |||||||
chr7:77361618 | G | A | 1 | a0014c0017t0001g0347 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.950-717C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 13/30 | chr7 | 77361618 | |||||||
chr7:77361648 | C | A | 1 | a0002c0003t0001g0346 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.950-747G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 13/30 | chr7 | 77361648 | |||||||
chr7:77361682 | T | C | 111 | a0001c0002t0001g0342 a0001c0002t0001g0343 a0001c0002t0001g0344 others(108): Show |
113 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.950-781A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 13/30 | chr7 | 77361682 | |||||||
chr7:77361794 | G | A | 2 | a0001c0002t0001g0157 a0001c0002t0001g0239 |
2 | HG00544.hp2 HG00558.hp1 |
intron_variant | MODIFIER | c.949+789C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 13/30 | chr7 | 77361794 | |||||||
chr7:77361832 | T | C | 314 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(311): Show |
319 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(316): Show |
intron_variant | MODIFIER | c.949+751A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 13/30 | chr7 | 77361832 | |||||||
chr7:77362153 | T | C | 108 | a0001c0002t0001g0342 a0001c0002t0001g0343 a0001c0002t0001g0344 others(105): Show |
110 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.949+430A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 13/30 | chr7 | 77362153 | |||||||
chr7:77362257 | C | T | 1 | a0002c0003t0001g0120 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.949+326G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 13/30 | chr7 | 77362257 | |||||||
chr7:77362453 | T | G | 1 | a0002c0003t0001g0147 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.949+130A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 13/30 | chr7 | 77362453 | |||||||
chr7:77362458 | G | C | 1 | a0002c0003t0003g0068 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.949+125C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 13/30 | chr7 | 77362458 | |||||||
chr7:77362506 | C | T | 1 | a0001c0001t0001g0071 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.949+77G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 13/30 | chr7 | 77362506 | |||||||
chr7:77362696 | A | G | 10 | a0002c0018t0001g0099 a0003c0004t0002g0113 a0003c0004t0002g0123 others(7): Show |
10 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.872-36T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77362696 | |||||||
chr7:77362932 | G | A | 1 | a0001c0002t0001g0273 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.872-272C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77362932 | |||||||
chr7:77362961 | A | G | 109 | a0001c0002t0001g0342 a0001c0002t0001g0343 a0001c0002t0001g0344 others(106): Show |
111 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.872-301T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77362961 | |||||||
chr7:77363038 | C | T | 1 | a0002c0027t0001g0214 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.872-378G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77363038 | |||||||
chr7:77363305 | C | T | 104 | a0002c0003t0001g0005 a0002c0003t0001g0019 a0002c0003t0001g0021 others(101): Show |
106 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.872-645G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77363305 | |||||||
chr7:77363597 | G | A | 1 | a0001c0002t0001g0284 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.872-937C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77363597 | |||||||
chr7:77363867 | T | C | 314 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(311): Show |
319 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(316): Show |
intron_variant | MODIFIER | c.872-1207A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77363867 | |||||||
chr7:77363915 | AATAATT | A | 3 | a0001c0002t0001g0267 a0001c0002t0001g0271 a0001c0002t0001g0272 |
3 | HG01069.hp2 HG01071.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.872-1261_872-1256d others(8): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77363915 | |||||||
chr7:77364260 | C | T | 110 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(107): Show |
112 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.872-1600G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77364260 | |||||||
chr7:77364335 | C | T | 1 | a0002c0003t0001g0120 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.872-1675G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77364335 | |||||||
chr7:77364461 | A | G | 110 | a0001c0002t0001g0342 a0001c0002t0001g0343 a0001c0002t0001g0344 others(107): Show |
112 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.872-1801T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77364461 | |||||||
chr7:77364478 | C | A | 13 | a0002c0003t0001g0286 a0002c0003t0001g0311 a0002c0003t0001g0312 others(10): Show |
13 | HG00639.hp1 HG01074.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.872-1818G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77364478 | |||||||
chr7:77364534 | A | G | 1 | a0001c0002t0001g0109 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.872-1874T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77364534 | |||||||
chr7:77364668 | G | A | 108 | a0001c0002t0001g0342 a0001c0002t0001g0343 a0001c0002t0001g0344 others(105): Show |
110 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.872-2008C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77364668 | |||||||
chr7:77364672 | TAATAA | T | 3 | a0003c0004t0002g0340 a0003c0004t0002g0341 a0005c0006t0001g0172 |
3 | HG00642.hp1 HG01106.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.872-2017_872-2013d others(7): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77364672 | |||||||
chr7:77364736 | A | C | 2 | a0001c0001t0001g0056 a0001c0001t0001g0070 |
2 | HG00639.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.872-2076T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77364736 | |||||||
chr7:77364930 | T | C | 10 | a0004c0005t0001g0171 a0004c0005t0003g0159 a0004c0005t0003g0160 others(7): Show |
10 | HG00558.hp2 HG00621.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.872-2270A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77364930 | |||||||
chr7:77364933 | C | T | 100 | a0001c0002t0002g0135 a0001c0002t0002g0140 a0002c0003t0001g0005 others(97): Show |
102 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.872-2273G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77364933 | |||||||
chr7:77365111 | T | A | 7 | a0002c0003t0001g0286 a0002c0003t0001g0311 a0002c0003t0001g0312 others(4): Show |
7 | HG01074.hp1 HG01109.hp2 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.872-2451A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77365111 | |||||||
chr7:77365144 | G | A | 1 | a0005c0006t0001g0165 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.872-2484C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77365144 | |||||||
chr7:77365172 | TC | T | 100 | a0002c0003t0001g0005 a0002c0003t0001g0019 a0002c0003t0001g0021 others(97): Show |
102 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.872-2513delG | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77365172 | |||||||
chr7:77365244 | T | A | 17 | a0001c0001t0001g0204 a0002c0003t0001g0005 a0002c0003t0001g0019 others(14): Show |
18 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.872-2584A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77365244 | |||||||
chr7:77365304 | G | A | 2 | a0001c0002t0002g0135 a0001c0002t0002g0140 |
2 | HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.872-2644C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77365304 | |||||||
chr7:77365445 | A | G | 62 | a0001c0002t0001g0342 a0001c0002t0001g0343 a0001c0002t0001g0344 others(59): Show |
63 | HG00639.hp1 HG00738.hp1 HG01074.hp1 others(60): Show |
intron_variant | MODIFIER | c.872-2785T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77365445 | |||||||
chr7:77365716 | T | C | 10 | a0002c0027t0001g0214 a0006c0008t0001g0017 a0006c0008t0001g0052 others(7): Show |
10 | HG00639.hp1 HG01074.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.872-3056A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77365716 | |||||||
chr7:77365834 | C | T | 1 | a0014c0017t0001g0347 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.872-3174G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77365834 | |||||||
chr7:77365898 | G | GT | 28 | a0001c0001t0001g0023 a0001c0001t0001g0070 a0001c0001t0001g0260 others(25): Show |
28 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(25): Show |
intron_variant | MODIFIER | c.872-3239dupA | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77365898 | |||||||
chr7:77365898 | GT | G | 122 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0031 others(119): Show |
125 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.872-3239delA | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77365898 | |||||||
chr7:77365908 | T | G | 52 | a0001c0001t0001g0003 a0001c0001t0001g0209 a0001c0001t0001g0250 others(49): Show |
54 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(51): Show |
intron_variant | MODIFIER | c.872-3248A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77365908 | |||||||
chr7:77365953 | G | A | 5 | a0001c0001t0001g0294 a0001c0001t0001g0313 a0001c0001t0001g0314 others(2): Show |
5 | NA18939.hp1 NA18946.hp1 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.872-3293C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77365953 | |||||||
chr7:77365962 | T | C | 1 | a0014c0017t0001g0347 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.872-3302A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77365962 | |||||||
chr7:77366149 | G | A | 114 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(111): Show |
116 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.872-3489C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77366149 | |||||||
chr7:77366262 | GCTT | G | 4 | a0007c0011t0002g0138 a0007c0011t0002g0144 a0007c0011t0002g0208 others(1): Show |
4 | HG02723.hp1 HG02976.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.872-3605_872-3603d others(5): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77366262 | |||||||
chr7:77366320 | C | T | 1 | a0003c0009t0001g0189 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.872-3660G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77366320 | |||||||
chr7:77366323 | G | A | 1 | a0007c0011t0002g0144 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.872-3663C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77366323 | |||||||
chr7:77366835 | A | G | 80 | a0001c0001t0001g0003 a0001c0001t0001g0209 a0001c0001t0001g0250 others(77): Show |
82 | HG00140.hp1 HG00642.hp1 HG00738.hp1 others(79): Show |
intron_variant | MODIFIER | c.872-4175T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77366835 | |||||||
chr7:77367037 | G | C | 78 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0304 others(75): Show |
79 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.872-4377C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77367037 | |||||||
chr7:77367158 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.872-4498C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77367158 | |||||||
chr7:77367172 | A | T | 1 | a0009c0026t0001g0054 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.872-4512T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77367172 | |||||||
chr7:77367207 | C | T | 1 | a0001c0001t0001g0032 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.872-4547G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77367207 | |||||||
chr7:77367276 | T | C | 1 | a0001c0001t0001g0154 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.872-4616A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77367276 | |||||||
chr7:77367314 | T | G | 17 | a0001c0001t0001g0204 a0002c0003t0001g0005 a0002c0003t0001g0019 others(14): Show |
18 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.872-4654A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77367314 | |||||||
chr7:77367755 | G | C | 1 | a0006c0008t0001g0052 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.872-5095C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77367755 | |||||||
chr7:77367795 | C | T | 1 | a0014c0017t0001g0347 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.872-5135G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77367795 | |||||||
chr7:77367875 | G | C | 1 | a0006c0008t0001g0141 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.872-5215C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77367875 | |||||||
chr7:77367948 | G | A | 2 | a0001c0002t0001g0020 a0001c0002t0001g0025 |
2 | NA18940.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.872-5288C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77367948 | |||||||
chr7:77368250 | C | T | 1 | a0001c0002t0002g0127 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.872-5590G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77368250 | |||||||
chr7:77368384 | C | A | 1 | a0014c0017t0001g0347 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.871+5686G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77368384 | |||||||
chr7:77368608 | A | G | 2 | a0004c0005t0003g0158 a0004c0005t0003g0161 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.871+5462T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77368608 | |||||||
chr7:77368645 | G | T | 5 | a0002c0003t0002g0055 a0007c0011t0002g0138 a0007c0011t0002g0144 others(2): Show |
5 | HG02723.hp1 HG02976.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.871+5425C>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77368645 | |||||||
chr7:77368649 | G | A | 1 | a0014c0017t0001g0347 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.871+5421C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77368649 | |||||||
chr7:77368738 | T | C | 49 | a0001c0001t0001g0290 a0001c0002t0001g0342 a0001c0002t0001g0343 others(46): Show |
50 | HG00738.hp1 HG01099.hp1 HG01168.hp2 others(47): Show |
intron_variant | MODIFIER | c.871+5332A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77368738 | |||||||
chr7:77368746 | T | C | 1 | a0014c0017t0001g0347 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.871+5324A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77368746 | |||||||
chr7:77368927 | G | C | 1 | a0002c0003t0001g0346 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.871+5143C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77368927 | |||||||
chr7:77368953 | G | A | 6 | a0003c0004t0002g0132 a0003c0004t0002g0183 a0003c0004t0002g0184 others(3): Show |
6 | HG01891.hp1 HG02055.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.871+5117C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77368953 | |||||||
chr7:77368969 | C | T | 55 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0304 others(52): Show |
55 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.871+5101G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77368969 | |||||||
chr7:77369194 | A | G | 1 | a0001c0002t0006g0007 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.871+4876T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77369194 | |||||||
chr7:77369225 | G | C | 17 | a0001c0001t0001g0204 a0002c0003t0001g0005 a0002c0003t0001g0019 others(14): Show |
18 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.871+4845C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77369225 | |||||||
chr7:77369266 | G | A | 1 | a0001c0021t0001g0249 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.871+4804C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77369266 | |||||||
chr7:77369591 | T | C | 1 | a0001c0023t0001g0094 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.871+4479A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77369591 | |||||||
chr7:77369605 | G | A | 131 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0204 others(128): Show |
134 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.871+4465C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77369605 | |||||||
chr7:77369740 | C | T | 1 | a0014c0017t0001g0347 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.871+4330G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77369740 | |||||||
chr7:77369782 | T | TA | 23 | a0001c0001t0001g0008 a0002c0018t0001g0099 a0003c0004t0001g0190 others(20): Show |
23 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.871+4287dupT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77369782 | |||||||
chr7:77369803 | T | G | 1 | a0001c0002t0001g0301 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.871+4267A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77369803 | |||||||
chr7:77369901 | C | CTTTTT | 9 | a0002c0007t0001g0004 a0002c0007t0001g0227 a0002c0007t0001g0228 others(6): Show |
10 | NA18946.hp2 NA18978.hp2 NA18981.hp1 others(7): Show |
intron_variant | MODIFIER | c.871+4168_871+4169i others(7): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77369901 | |||||||
chr7:77369902 | G | GTTTTT | 121 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0204 others(118): Show |
123 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.871+4163_871+4167d others(7): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77369902 | |||||||
chr7:77369902 | G | T | 9 | a0002c0007t0001g0004 a0002c0007t0001g0227 a0002c0007t0001g0228 others(6): Show |
10 | NA18946.hp2 NA18978.hp2 NA18981.hp1 others(7): Show |
intron_variant | MODIFIER | c.871+4168C>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77369902 | |||||||
chr7:77369986 | A | G | 17 | a0001c0001t0001g0204 a0002c0003t0001g0005 a0002c0003t0001g0019 others(14): Show |
18 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.871+4084T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77369986 | |||||||
chr7:77370255 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.871+3815G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77370255 | |||||||
chr7:77370260 | C | T | 1 | a0001c0002t0001g0281 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.871+3810G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77370260 | |||||||
chr7:77370265 | G | A | 1 | a0001c0001t0001g0251 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.871+3805C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77370265 | |||||||
chr7:77370286 | C | T | 1 | a0001c0001t0001g0231 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.871+3784G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77370286 | |||||||
chr7:77370422 | T | C | 3 | a0001c0001t0001g0071 a0001c0001t0001g0079 a0001c0001t0001g0111 |
3 | NA18945.hp1 NA19003.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.871+3648A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77370422 | |||||||
chr7:77370840 | A | AC | 11 | a0001c0028t0002g0142 a0002c0027t0001g0214 a0006c0008t0001g0017 others(8): Show |
11 | HG00639.hp1 HG01074.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.871+3229dupG | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77370840 | |||||||
chr7:77370967 | A | G | 9 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0011 others(6): Show |
9 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.871+3103T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77370967 | |||||||
chr7:77371085 | G | C | 1 | a0014c0017t0001g0347 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.871+2985C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77371085 | |||||||
chr7:77371099 | C | CA | 3 | a0001c0002t0002g0119 a0001c0002t0002g0182 a0001c0002t0004g0034 |
3 | HG01243.hp1 HG02559.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.871+2970dupT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77371099 | |||||||
chr7:77371415 | G | A | 1 | a0014c0017t0001g0347 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.871+2655C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77371415 | |||||||
chr7:77371431 | CT | C | 36 | a0001c0001t0001g0204 a0001c0001t0001g0295 a0001c0001t0001g0296 others(33): Show |
37 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.871+2638delA | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77371431 | |||||||
chr7:77371431 | CTT | C | 83 | a0001c0001t0001g0195 a0001c0001t0001g0202 a0001c0002t0001g0020 others(80): Show |
84 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.871+2637_871+2638d others(4): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77371431 | |||||||
chr7:77371431 | CTTT | C | 192 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(189): Show |
195 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.871+2636_871+2638d others(5): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77371431 | |||||||
chr7:77371434 | T | C | 1 | a0001c0002t0001g0303 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.871+2636A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77371434 | |||||||
chr7:77371437 | T | C | 2 | a0001c0002t0002g0135 a0001c0002t0002g0140 |
2 | HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.871+2633A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77371437 | |||||||
chr7:77371439 | T | C | 16 | a0001c0001t0001g0195 a0001c0001t0001g0202 a0001c0028t0002g0142 others(13): Show |
16 | HG00639.hp1 HG01074.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.871+2631A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77371439 | |||||||
chr7:77371440 | T | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(178): Show |
184 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.871+2630A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77371440 | |||||||
chr7:77371441 | T | C | 1 | a0002c0003t0001g0121 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.871+2629A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77371441 | |||||||
chr7:77371450 | T | C | 22 | a0002c0018t0001g0099 a0003c0004t0001g0190 a0003c0004t0002g0033 others(19): Show |
22 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.871+2620A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77371450 | |||||||
chr7:77371520 | C | T | 1 | a0014c0017t0001g0347 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.871+2550G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77371520 | |||||||
chr7:77371665 | G | A | 3 | a0001c0002t0001g0270 a0001c0002t0001g0300 a0001c0002t0001g0317 |
3 | NA18988.hp1 NA19001.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.871+2405C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77371665 | |||||||
chr7:77371717 | G | A | 103 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(100): Show |
104 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.871+2353C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77371717 | |||||||
chr7:77371726 | C | T | 1 | a0001c0002t0002g0012 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.871+2344G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77371726 | |||||||
chr7:77371808 | A | G | 1 | a0001c0002t0001g0307 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.871+2262T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77371808 | |||||||
chr7:77371811 | C | T | 1 | a0001c0002t0001g0278 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.871+2259G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77371811 | |||||||
chr7:77371884 | G | A | 104 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(101): Show |
105 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.871+2186C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77371884 | |||||||
chr7:77371895 | A | G | 2 | a0001c0002t0002g0119 a0001c0002t0002g0182 |
2 | HG02559.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.871+2175T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77371895 | |||||||
chr7:77371937 | A | G | 4 | a0001c0002t0001g0232 a0001c0002t0001g0233 a0001c0002t0001g0240 others(1): Show |
4 | NA18952.hp1 NA18982.hp1 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.871+2133T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77371937 | |||||||
chr7:77372001 | T | TA | 5 | a0001c0028t0002g0142 a0006c0008t0001g0134 a0006c0008t0001g0137 others(2): Show |
5 | HG00639.hp1 HG02723.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.871+2068dupT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77372001 | |||||||
chr7:77372069 | C | T | 1 | a0001c0002t0001g0239 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.871+2001G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77372069 | |||||||
chr7:77372146 | A | G | 1 | a0014c0017t0001g0347 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.871+1924T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77372146 | |||||||
chr7:77372320 | G | A | 1 | a0004c0005t0003g0177 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.871+1750C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77372320 | |||||||
chr7:77372334 | T | C | 1 | a0014c0017t0001g0347 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.871+1736A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77372334 | |||||||
chr7:77372378 | A | C | 4 | a0007c0011t0002g0138 a0007c0011t0002g0144 a0007c0011t0002g0208 others(1): Show |
4 | HG02723.hp1 HG02976.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.871+1692T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77372378 | |||||||
chr7:77372511 | A | C | 1 | a0003c0004t0002g0156 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.871+1559T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77372511 | |||||||
chr7:77372826 | G | A | 2 | a0001c0001t0001g0008 a0001c0001t0001g0023 |
2 | NA18960.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.871+1244C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77372826 | |||||||
chr7:77372843 | C | T | 1 | a0006c0008t0001g0100 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.871+1227G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77372843 | |||||||
chr7:77372991 | C | T | 9 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0011 others(6): Show |
9 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.871+1079G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77372991 | |||||||
chr7:77373238 | A | G | 6 | a0003c0004t0002g0132 a0003c0004t0002g0183 a0003c0004t0002g0184 others(3): Show |
6 | HG01891.hp1 HG02055.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.871+832T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77373238 | |||||||
chr7:77373461 | C | T | 1 | a0014c0017t0001g0347 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.871+609G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77373461 | |||||||
chr7:77373484 | G | T | 9 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0011 others(6): Show |
9 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.871+586C>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77373484 | |||||||
chr7:77373580 | G | A | 1 | a0001c0002t0001g0299 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.871+490C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77373580 | |||||||
chr7:77373960 | A | G | 10 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0011 others(7): Show |
10 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.871+110T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77373960 | |||||||
chr7:77374022 | A | C | 1 | a0001c0002t0001g0275 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.871+48T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 12/30 | chr7 | 77374022 | |||||||
chr7:77374285 | A | C | 10 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0011 others(7): Show |
10 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.786-130T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 11/30 | chr7 | 77374285 | |||||||
chr7:77374485 | C | T | 5 | a0002c0003t0002g0055 a0007c0011t0002g0138 a0007c0011t0002g0144 others(2): Show |
5 | HG02723.hp1 HG02976.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.786-330G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 11/30 | chr7 | 77374485 | |||||||
chr7:77374602 | G | A | 1 | a0001c0002t0004g0034 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.786-447C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 11/30 | chr7 | 77374602 | |||||||
chr7:77374646 | GA | G | 9 | a0001c0002t0001g0269 a0001c0028t0002g0142 a0002c0027t0001g0214 others(6): Show |
9 | HG00639.hp1 HG01109.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.785+411delT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 11/30 | chr7 | 77374646 | |||||||
chr7:77374660 | C | A | 3 | a0001c0001t0001g0255 a0003c0004t0001g0190 a0014c0017t0001g0347 |
3 | HG02523.hp2 NA18978.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.785+398G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 11/30 | chr7 | 77374660 | |||||||
chr7:77374919 | T | G | 1 | a0002c0003t0002g0055 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.785+139A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 11/30 | chr7 | 77374919 | |||||||
chr7:77374992 | G | A | 5 | a0002c0003t0002g0055 a0007c0011t0002g0138 a0007c0011t0002g0144 others(2): Show |
5 | HG02723.hp1 HG02976.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.785+66C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 11/30 | chr7 | 77374992 | |||||||
chr7:77375026 | T | C | 4 | a0001c0002t0001g0342 a0001c0002t0001g0343 a0001c0002t0001g0344 others(1): Show |
4 | HG01099.hp1 HG01168.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.785+32A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 11/30 | chr7 | 77375026 | |||||||
chr7:77375045 | A | C | 1 | a0014c0017t0001g0347 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.785+13T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 11/30 | chr7 | 77375045 | |||||||
chr7:77375199 | T | C | 1 | a0014c0017t0001g0347 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.742-98A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 10/30 | chr7 | 77375199 | |||||||
chr7:77375369 | A | G | 1 | a0001c0001t0001g0018 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.742-268T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 10/30 | chr7 | 77375369 | |||||||
chr7:77375380 | A | G | 1 | a0001c0001t0001g0081 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.742-279T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 10/30 | chr7 | 77375380 | |||||||
chr7:77375451 | A | C | 81 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0304 others(78): Show |
82 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.742-350T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 10/30 | chr7 | 77375451 | |||||||
chr7:77375486 | A | G | 1 | a0001c0001t0001g0081 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.742-385T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 10/30 | chr7 | 77375486 | |||||||
chr7:77375574 | G | T | 49 | a0002c0003t0001g0038 a0002c0003t0001g0048 a0002c0003t0001g0058 others(46): Show |
50 | HG00738.hp1 HG01257.hp2 HG01884.hp2 others(47): Show |
intron_variant | MODIFIER | c.742-473C>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 10/30 | chr7 | 77375574 | |||||||
chr7:77375739 | G | A | 1 | a0002c0003t0001g0121 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.742-638C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 10/30 | chr7 | 77375739 | |||||||
chr7:77375810 | C | T | 70 | a0002c0003t0001g0038 a0002c0003t0001g0048 a0002c0003t0001g0058 others(67): Show |
71 | HG00140.hp1 HG00642.hp1 HG00738.hp1 others(68): Show |
intron_variant | MODIFIER | c.742-709G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 10/30 | chr7 | 77375810 | |||||||
chr7:77375843 | TA | T | 283 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(280): Show |
287 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.742-743delT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 10/30 | chr7 | 77375843 | |||||||
chr7:77375855 | A | C | 3 | a0001c0001t0001g0194 a0004c0005t0003g0104 a0005c0006t0001g0206 |
3 | HG04184.hp2 HG06807.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.742-754T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 10/30 | chr7 | 77375855 | |||||||
chr7:77375858 | AC | A | 5 | a0003c0004t0002g0132 a0003c0004t0002g0183 a0003c0004t0002g0184 others(2): Show |
5 | HG01891.hp1 HG02055.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.742-758delG | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 10/30 | chr7 | 77375858 | |||||||
chr7:77375859 | C | A | 2 | a0003c0004t0005g0185 a0014c0017t0001g0347 |
2 | HG03098.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.742-758G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 10/30 | chr7 | 77375859 | |||||||
chr7:77376064 | C | T | 1 | a0014c0017t0001g0347 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.741+784G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 10/30 | chr7 | 77376064 | |||||||
chr7:77376310 | T | C | 315 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(312): Show |
320 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(317): Show |
intron_variant | MODIFIER | c.741+538A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 10/30 | chr7 | 77376310 | |||||||
chr7:77376380 | A | G | 302 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(299): Show |
307 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(304): Show |
intron_variant | MODIFIER | c.741+468T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 10/30 | chr7 | 77376380 | |||||||
chr7:77376417 | C | T | 6 | a0003c0004t0002g0132 a0003c0004t0002g0183 a0003c0004t0002g0184 others(3): Show |
6 | HG01891.hp1 HG02055.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.741+431G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 10/30 | chr7 | 77376417 | |||||||
chr7:77376511 | C | T | 6 | a0003c0004t0002g0132 a0003c0004t0002g0183 a0003c0004t0002g0184 others(3): Show |
6 | HG01891.hp1 HG02055.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.741+337G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 10/30 | chr7 | 77376511 | |||||||
chr7:77376518 | G | A | 1 | a0014c0017t0001g0347 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.741+330C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 10/30 | chr7 | 77376518 | |||||||
chr7:77376620 | A | C | 1 | a0014c0017t0001g0347 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.741+228T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 10/30 | chr7 | 77376620 | |||||||
chr7:77376646 | G | A | 1 | a0002c0003t0001g0048 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.741+202C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 10/30 | chr7 | 77376646 | |||||||
chr7:77376651 | C | A | 79 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0304 others(76): Show |
80 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.741+197G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 10/30 | chr7 | 77376651 | |||||||
chr7:77376663 | G | C | 1 | a0004c0005t0001g0106 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.741+185C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 10/30 | chr7 | 77376663 | |||||||
chr7:77376748 | CGTGTGCG others(5): Show |
C | 1 | a0001c0001t0001g0326 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.741+88_741+99delTC others(10): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 10/30 | chr7 | 77376748 | |||||||
chr7:77376767 | C | A | 1 | a0004c0005t0003g0288 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.741+81G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 10/30 | chr7 | 77376767 | |||||||
chr7:77376775 | C | CA | 8 | a0001c0001t0001g0018 a0001c0001t0001g0085 a0004c0005t0003g0158 others(5): Show |
8 | HG01074.hp1 HG01167.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.741+72dupT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 10/30 | chr7 | 77376775 | |||||||
chr7:77376775 | C | CAA | 10 | a0001c0028t0002g0142 a0002c0027t0001g0214 a0006c0008t0001g0100 others(7): Show |
10 | HG00639.hp1 HG01109.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.741+71_741+72dupTT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 10/30 | chr7 | 77376775 | |||||||
chr7:77376775 | C | CAAA | 7 | a0002c0003t0002g0055 a0003c0004t0002g0033 a0003c0004t0002g0146 others(4): Show |
7 | HG02622.hp1 HG02886.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.741+70_741+72dupTT others(1): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 10/30 | chr7 | 77376775 | |||||||
chr7:77376775 | CA | C | 83 | a0001c0001t0001g0041 a0001c0001t0001g0112 a0001c0001t0001g0209 others(80): Show |
85 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.741+72delT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 10/30 | chr7 | 77376775 | |||||||
chr7:77376775 | CAAAAAA | C | 11 | a0001c0002t0002g0002 a0001c0002t0002g0119 a0001c0002t0002g0125 others(8): Show |
12 | HG01192.hp2 HG01243.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.741+67_741+72delTT others(4): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 10/30 | chr7 | 77376775 | |||||||
chr7:77376788 | AAAAAAAA others(1): Show |
A | 66 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0304 others(63): Show |
66 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.741+52_741+59delCT others(6): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 10/30 | chr7 | 77376788 | |||||||
chr7:77376797 | A | G | 16 | a0002c0003t0001g0005 a0002c0003t0001g0019 a0002c0003t0001g0021 others(13): Show |
17 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.741+51T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 10/30 | chr7 | 77376797 | |||||||
chr7:77376922 | A | G | 1 | a0001c0002t0001g0274 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.682-15T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 9/30 | chr7 | 77376922 | |||||||
chr7:77377217 | T | TA | 16 | a0002c0003t0001g0005 a0002c0003t0001g0019 a0002c0003t0001g0021 others(13): Show |
17 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.681+68dupT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 9/30 | chr7 | 77377217 | |||||||
chr7:77377237 | T | TA | 124 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(121): Show |
127 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.681+48dupT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 9/30 | chr7 | 77377237 | |||||||
chr7:77377237 | T | TAA | 21 | a0001c0001t0001g0044 a0001c0001t0001g0050 a0001c0001t0001g0051 others(18): Show |
21 | HG00099.hp2 HG00735.hp1 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.681+47_681+48dupTT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 9/30 | chr7 | 77377237 | |||||||
chr7:77377237 | T | TAAAAAAA | 24 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0011 others(21): Show |
25 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(22): Show |
intron_variant | MODIFIER | c.681+42_681+48dupTT others(5): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 9/30 | chr7 | 77377237 | |||||||
chr7:77377237 | T | TAAAAAAA others(4): Show |
1 | a0014c0017t0001g0347 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.681+38_681+48dupTT others(9): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 9/30 | chr7 | 77377237 | |||||||
chr7:77377237 | T | TAAAAAAA others(6): Show |
3 | a0003c0004t0002g0183 a0003c0004t0002g0184 a0003c0004t0002g0187 |
3 | HG02965.hp1 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.681+36_681+48dupTT others(11): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 9/30 | chr7 | 77377237 | |||||||
chr7:77377237 | T | TAAAAAAA others(7): Show |
3 | a0003c0004t0002g0132 a0003c0004t0002g0186 a0003c0004t0005g0185 |
3 | HG01891.hp1 HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.681+35_681+48dupTT others(12): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 9/30 | chr7 | 77377237 | |||||||
chr7:77377237 | T | TAAAAAAA others(8): Show |
1 | a0002c0003t0001g0060 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.681+34_681+48dupTT others(13): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 9/30 | chr7 | 77377237 | |||||||
chr7:77377237 | T | TAAAAAAA others(9): Show |
7 | a0001c0002t0001g0342 a0001c0002t0001g0343 a0001c0002t0001g0345 others(4): Show |
7 | HG01099.hp1 HG01168.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.681+33_681+48dupTT others(14): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 9/30 | chr7 | 77377237 | |||||||
chr7:77377237 | T | TAAAAAAA others(10): Show |
23 | a0001c0002t0001g0344 a0002c0003t0001g0058 a0002c0003t0001g0059 others(20): Show |
23 | HG00140.hp1 HG00738.hp1 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.681+32_681+48dupTT others(15): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 9/30 | chr7 | 77377237 | |||||||
chr7:77377237 | T | TAAAAAAA others(11): Show |
17 | a0002c0003t0001g0063 a0002c0003t0001g0064 a0002c0003t0001g0066 others(14): Show |
17 | HG01258.hp1 HG01516.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.681+31_681+48dupTT others(16): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 9/30 | chr7 | 77377237 | |||||||
chr7:77377237 | T | TAAAAAAA others(12): Show |
8 | a0002c0003t0001g0069 a0002c0003t0001g0089 a0002c0003t0001g0319 others(5): Show |
8 | HG00642.hp1 HG01106.hp1 HG03471.hp2 others(5): Show |
intron_variant | MODIFIER | c.681+30_681+48dupTT others(17): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 9/30 | chr7 | 77377237 | |||||||
chr7:77377237 | T | TAAAAAAA others(13): Show |
4 | a0002c0007t0001g0004 a0002c0007t0001g0227 a0002c0007t0001g0324 others(1): Show |
5 | NA18978.hp2 NA19062.hp2 NA19085.hp1 others(2): Show |
intron_variant | MODIFIER | c.681+29_681+48dupTT others(18): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 9/30 | chr7 | 77377237 | |||||||
chr7:77377237 | T | TAAAAAAA others(14): Show |
1 | a0002c0003t0001g0048 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.681+28_681+48dupTT others(19): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 9/30 | chr7 | 77377237 | |||||||
chr7:77377237 | T | TAAAAAAA others(19): Show |
1 | a0002c0003t0001g0062 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.681+48_681+49insTT others(24): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 9/30 | chr7 | 77377237 | |||||||
chr7:77377237 | T | TAAAAAAA others(21): Show |
1 | a0002c0003t0001g0038 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.681+48_681+49insTT others(26): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 9/30 | chr7 | 77377237 | |||||||
chr7:77377268 | G | A | 2 | a0006c0008t0001g0134 a0006c0008t0001g0141 |
2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.681+18C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 9/30 | chr7 | 77377268 | |||||||
chr7:77377400 | C | CA | 74 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0304 others(71): Show |
75 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.577-11dupT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77377400 | |||||||
chr7:77377400 | C | CAA | 13 | a0001c0002t0001g0117 a0001c0002t0001g0143 a0001c0002t0001g0232 others(10): Show |
13 | HG00597.hp1 HG01099.hp2 HG01361.hp2 others(10): Show |
intron_variant | MODIFIER | c.577-12_577-11dupTT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77377400 | |||||||
chr7:77377400 | CA | C | 18 | a0001c0001t0001g0035 a0001c0001t0001g0057 a0001c0001t0001g0082 others(15): Show |
18 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.577-11delT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77377400 | |||||||
chr7:77377400 | CAA | C | 116 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(113): Show |
118 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.577-12_577-11delTT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77377400 | |||||||
chr7:77377400 | CAAA | C | 72 | a0001c0001t0001g0292 a0001c0001t0001g0294 a0001c0002t0001g0342 others(69): Show |
73 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(70): Show |
intron_variant | MODIFIER | c.577-13_577-11delTT others(1): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77377400 | |||||||
chr7:77377400 | CAAAA | C | 10 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0011 others(7): Show |
10 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.577-14_577-11delTT others(2): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77377400 | |||||||
chr7:77377400 | CAAAAAA | C | 17 | a0001c0001t0001g0334 a0002c0003t0001g0005 a0002c0003t0001g0019 others(14): Show |
18 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(15): Show |
intron_variant | MODIFIER | c.577-16_577-11delTT others(4): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77377400 | |||||||
chr7:77377609 | A | G | 16 | a0003c0004t0001g0190 a0003c0004t0002g0113 a0003c0004t0002g0123 others(13): Show |
16 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.577-219T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77377609 | |||||||
chr7:77377850 | A | G | 1 | a0002c0003t0001g0059 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.577-460T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77377850 | |||||||
chr7:77377880 | T | G | 1 | a0014c0017t0001g0347 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.577-490A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77377880 | |||||||
chr7:77377937 | C | G | 1 | a0011c0022t0001g0129 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.577-547G>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77377937 | |||||||
chr7:77378327 | T | A | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.577-937A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77378327 | |||||||
chr7:77378430 | G | A | 2 | a0002c0003t0001g0088 a0002c0003t0001g0089 |
2 | NA18940.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.577-1040C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77378430 | |||||||
chr7:77378433 | A | G | 1 | a0014c0017t0001g0347 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.577-1043T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77378433 | |||||||
chr7:77378436 | A | T | 4 | a0007c0011t0002g0138 a0007c0011t0002g0144 a0007c0011t0002g0208 others(1): Show |
4 | HG02723.hp1 HG02976.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.577-1046T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77378436 | |||||||
chr7:77378461 | G | A | 1 | a0002c0003t0001g0319 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.577-1071C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77378461 | |||||||
chr7:77378465 | C | T | 6 | a0003c0004t0002g0132 a0003c0004t0002g0183 a0003c0004t0002g0184 others(3): Show |
6 | HG01891.hp1 HG02055.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.577-1075G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77378465 | |||||||
chr7:77378520 | C | CA | 6 | a0001c0001t0001g0042 a0001c0002t0001g0283 a0001c0002t0002g0135 others(3): Show |
6 | HG01099.hp2 HG01255.hp1 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.577-1131dupT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77378520 | |||||||
chr7:77378520 | C | CAA | 10 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0011 others(7): Show |
10 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.577-1132_577-1131d others(4): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77378520 | |||||||
chr7:77378523 | A | C | 26 | a0002c0003t0001g0059 a0002c0003t0001g0066 a0002c0003t0001g0067 others(23): Show |
26 | HG00140.hp1 HG00642.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.577-1133T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77378523 | |||||||
chr7:77378526 | A | C | 1 | a0003c0004t0002g0113 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.577-1136T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77378526 | |||||||
chr7:77378527 | AAAC | A | 5 | a0002c0003t0002g0055 a0007c0011t0002g0138 a0007c0011t0002g0144 others(2): Show |
5 | HG02723.hp1 HG02976.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.577-1140_577-1138d others(5): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77378527 | |||||||
chr7:77378529 | AC | A | 9 | a0002c0003t0001g0058 a0002c0003t0001g0065 a0002c0003t0001g0069 others(6): Show |
9 | HG01891.hp1 HG02055.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.577-1140delG | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77378529 | |||||||
chr7:77378530 | C | A | 63 | a0001c0001t0001g0003 a0001c0001t0001g0209 a0001c0001t0001g0250 others(60): Show |
65 | HG00140.hp1 HG00642.hp1 HG00738.hp1 others(62): Show |
intron_variant | MODIFIER | c.577-1140G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77378530 | |||||||
chr7:77378680 | A | C | 7 | a0001c0001t0001g0045 a0001c0001t0001g0078 a0001c0001t0001g0192 others(4): Show |
7 | HG00544.hp1 NA18983.hp1 NA18987.hp1 others(4): Show |
intron_variant | MODIFIER | c.577-1290T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77378680 | |||||||
chr7:77378953 | G | A | 3 | a0001c0002t0001g0270 a0001c0002t0001g0300 a0001c0002t0001g0317 |
3 | NA18988.hp1 NA19001.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.577-1563C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77378953 | |||||||
chr7:77379149 | A | G | 2 | a0001c0002t0002g0135 a0001c0002t0002g0140 |
2 | HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.577-1759T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77379149 | |||||||
chr7:77379231 | T | C | 1 | a0002c0003t0001g0286 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.577-1841A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77379231 | |||||||
chr7:77379461 | G | A | 2 | a0007c0011t0002g0208 a0007c0011t0002g0310 |
2 | HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.576+1844C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77379461 | |||||||
chr7:77379916 | A | T | 1 | a0001c0001t0001g0015 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.576+1389T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77379916 | |||||||
chr7:77379943 | C | T | 314 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(311): Show |
319 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(316): Show |
intron_variant | MODIFIER | c.576+1362G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77379943 | |||||||
chr7:77380002 | T | C | 6 | a0003c0004t0002g0132 a0003c0004t0002g0183 a0003c0004t0002g0184 others(3): Show |
6 | HG01891.hp1 HG02055.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.576+1303A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77380002 | |||||||
chr7:77380188 | G | C | 26 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0011 others(23): Show |
27 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(24): Show |
intron_variant | MODIFIER | c.576+1117C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77380188 | |||||||
chr7:77380231 | A | G | 98 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0304 others(95): Show |
99 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.576+1074T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77380231 | |||||||
chr7:77380259 | G | A | 4 | a0001c0001t0001g0235 a0001c0001t0001g0254 a0001c0001t0001g0255 others(1): Show |
4 | NA18971.hp1 NA18978.hp1 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.576+1046C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77380259 | |||||||
chr7:77380353 | T | C | 1 | a0001c0002t0001g0269 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.576+952A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77380353 | |||||||
chr7:77380366 | A | C | 1 | a0001c0002t0001g0269 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.576+939T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77380366 | |||||||
chr7:77380382 | G | A | 1 | a0014c0017t0001g0347 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.576+923C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77380382 | |||||||
chr7:77380724 | T | C | 1 | a0007c0011t0002g0144 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.576+581A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77380724 | |||||||
chr7:77380813 | G | T | 97 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0018 others(94): Show |
97 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.576+492C>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77380813 | |||||||
chr7:77380832 | C | T | 1 | a0001c0001t0001g0305 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.576+473G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77380832 | |||||||
chr7:77380893 | C | T | 15 | a0002c0003t0001g0005 a0002c0003t0001g0019 a0002c0003t0001g0021 others(12): Show |
16 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.576+412G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77380893 | |||||||
chr7:77380903 | T | C | 1 | a0014c0017t0001g0347 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.576+402A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77380903 | |||||||
chr7:77381263 | G | GA | 81 | a0001c0001t0001g0018 a0001c0001t0001g0197 a0001c0001t0001g0295 others(78): Show |
82 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.576+41dupT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 8/30 | chr7 | 77381263 | |||||||
chr7:77381365 | AAAAC | A | 78 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0304 others(75): Show |
79 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.527-15_527-12delGT others(2): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 7/30 | chr7 | 77381365 | |||||||
chr7:77381369 | C | G | 1 | a0001c0021t0001g0249 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.527-15G>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 7/30 | chr7 | 77381369 | |||||||
chr7:77381392 | A | T | 21 | a0003c0004t0001g0190 a0003c0004t0002g0033 a0003c0004t0002g0113 others(18): Show |
21 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.527-38T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 7/30 | chr7 | 77381392 | |||||||
chr7:77381607 | T | C | 3 | a0001c0002t0001g0234 a0001c0002t0001g0280 a0001c0002t0001g0282 |
3 | NA19005.hp2 NA19011.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.527-253A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 7/30 | chr7 | 77381607 | |||||||
chr7:77381749 | T | C | 7 | a0001c0002t0001g0267 a0001c0002t0001g0271 a0001c0002t0001g0272 others(4): Show |
7 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.527-395A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 7/30 | chr7 | 77381749 | |||||||
chr7:77381819 | T | C | 1 | a0001c0001t0001g0023 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.527-465A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 7/30 | chr7 | 77381819 | |||||||
chr7:77381991 | T | C | 1 | a0001c0010t0001g0150 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.526+583A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 7/30 | chr7 | 77381991 | |||||||
chr7:77382011 | G | A | 1 | a0001c0002t0001g0116 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.526+563C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 7/30 | chr7 | 77382011 | |||||||
chr7:77382120 | T | C | 10 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0011 others(7): Show |
10 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.526+454A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 7/30 | chr7 | 77382120 | |||||||
chr7:77382183 | A | G | 1 | a0014c0017t0001g0347 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.526+391T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 7/30 | chr7 | 77382183 | |||||||
chr7:77382334 | T | A | 1 | a0002c0018t0001g0099 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.526+240A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 7/30 | chr7 | 77382334 | |||||||
chr7:77382410 | A | G | 7 | a0001c0001t0001g0003 a0001c0001t0001g0209 a0001c0001t0001g0250 others(4): Show |
8 | HG01070.hp1 HG01071.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.526+164T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 7/30 | chr7 | 77382410 | |||||||
chr7:77382500 | T | G | 11 | a0001c0028t0002g0142 a0002c0027t0001g0214 a0006c0008t0001g0017 others(8): Show |
11 | HG00639.hp1 HG01074.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.526+74A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 7/30 | chr7 | 77382500 | |||||||
chr7:77382725 | C | T | 60 | a0001c0001t0001g0003 a0001c0001t0001g0209 a0001c0001t0001g0250 others(57): Show |
62 | HG00738.hp1 HG01070.hp1 HG01071.hp1 others(59): Show |
intron_variant | MODIFIER | c.457-82G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77382725 | |||||||
chr7:77382726 | T | C | 7 | a0001c0001t0001g0045 a0001c0001t0001g0078 a0001c0001t0001g0192 others(4): Show |
7 | HG00544.hp1 NA18983.hp1 NA18987.hp1 others(4): Show |
intron_variant | MODIFIER | c.457-83A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77382726 | |||||||
chr7:77382950 | C | G | 1 | a0005c0006t0001g0165 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.457-307G>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77382950 | |||||||
chr7:77383036 | G | A | 1 | a0014c0017t0001g0347 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.457-393C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77383036 | |||||||
chr7:77383098 | G | T | 1 | a0001c0002t0001g0297 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.457-455C>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77383098 | |||||||
chr7:77383185 | T | C | 74 | a0001c0002t0001g0342 a0001c0002t0001g0343 a0001c0002t0001g0344 others(71): Show |
75 | HG00140.hp1 HG00642.hp1 HG00738.hp1 others(72): Show |
intron_variant | MODIFIER | c.457-542A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77383185 | |||||||
chr7:77383318 | T | TCA | 10 | a0001c0001t0001g0258 a0001c0002t0001g0157 a0001c0002t0001g0193 others(7): Show |
10 | HG00558.hp1 HG01261.hp1 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.457-677_457-676dup others(2): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77383318 | |||||||
chr7:77383318 | TCA | T | 152 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(149): Show |
154 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.457-677_457-676del others(2): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77383318 | |||||||
chr7:77383318 | TCACA | T | 23 | a0001c0002t0002g0009 a0001c0002t0002g0011 a0001c0002t0002g0014 others(20): Show |
23 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.457-679_457-676del others(4): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77383318 | |||||||
chr7:77383520 | T | A | 81 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0304 others(78): Show |
82 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.457-877A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77383520 | |||||||
chr7:77383648 | A | G | 83 | a0001c0001t0001g0008 a0001c0001t0001g0295 a0001c0001t0001g0296 others(80): Show |
84 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.457-1005T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77383648 | |||||||
chr7:77383714 | C | A | 1 | a0001c0001t0001g0197 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.457-1071G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77383714 | |||||||
chr7:77383728 | C | T | 74 | a0001c0002t0001g0342 a0001c0002t0001g0343 a0001c0002t0001g0344 others(71): Show |
75 | HG00140.hp1 HG00642.hp1 HG00738.hp1 others(72): Show |
intron_variant | MODIFIER | c.457-1085G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77383728 | |||||||
chr7:77383854 | G | C | 2 | a0001c0002t0002g0135 a0001c0002t0002g0140 |
2 | HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.457-1211C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77383854 | |||||||
chr7:77383860 | T | A | 1 | a0001c0002t0001g0193 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.457-1217A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77383860 | |||||||
chr7:77383930 | A | C | 1 | a0001c0002t0001g0281 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.457-1287T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77383930 | |||||||
chr7:77384000 | T | C | 1 | a0014c0017t0001g0347 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.457-1357A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77384000 | |||||||
chr7:77384075 | A | G | 16 | a0001c0028t0002g0142 a0002c0027t0001g0214 a0003c0004t0002g0033 others(13): Show |
16 | HG00639.hp1 HG01074.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.457-1432T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77384075 | |||||||
chr7:77384275 | A | G | 1 | a0001c0001t0001g0073 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.457-1632T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77384275 | |||||||
chr7:77384277 | G | A | 16 | a0002c0003t0001g0005 a0002c0003t0001g0019 a0002c0003t0001g0021 others(13): Show |
17 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.457-1634C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77384277 | |||||||
chr7:77384406 | G | T | 5 | a0002c0003t0002g0055 a0007c0011t0002g0138 a0007c0011t0002g0144 others(2): Show |
5 | HG02723.hp1 HG02976.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.457-1763C>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77384406 | |||||||
chr7:77384578 | G | A | 1 | a0004c0005t0003g0160 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.457-1935C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77384578 | |||||||
chr7:77384660 | G | A | 10 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0011 others(7): Show |
10 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.457-2017C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77384660 | |||||||
chr7:77384868 | G | A | 1 | a0006c0008t0001g0100 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.457-2225C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77384868 | |||||||
chr7:77384947 | T | G | 4 | a0001c0001t0001g0044 a0001c0001t0001g0072 a0001c0001t0001g0074 others(1): Show |
4 | HG00735.hp1 HG00738.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.457-2304A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77384947 | |||||||
chr7:77385034 | C | CT | 15 | a0001c0001t0001g0257 a0001c0002t0002g0009 a0001c0002t0002g0010 others(12): Show |
15 | HG01167.hp1 HG01169.hp1 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.456+2325dupA | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77385034 | |||||||
chr7:77385090 | A | G | 10 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0011 others(7): Show |
10 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.456+2270T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77385090 | |||||||
chr7:77385113 | A | C | 25 | a0001c0001t0001g0044 a0001c0001t0001g0072 a0001c0001t0001g0074 others(22): Show |
25 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.456+2247T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77385113 | |||||||
chr7:77385158 | C | T | 1 | a0001c0002t0001g0302 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.456+2202G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77385158 | |||||||
chr7:77385190 | C | T | 1 | a0002c0003t0001g0121 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.456+2170G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77385190 | |||||||
chr7:77385220 | G | T | 1 | a0001c0001t0001g0114 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.456+2140C>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77385220 | |||||||
chr7:77385432 | T | C | 1 | a0001c0002t0001g0118 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.456+1928A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77385432 | |||||||
chr7:77385830 | A | G | 1 | a0001c0002t0001g0265 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.456+1530T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77385830 | |||||||
chr7:77385974 | A | G | 3 | a0001c0002t0002g0119 a0001c0002t0002g0182 a0001c0002t0004g0034 |
3 | HG01243.hp1 HG02559.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.456+1386T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77385974 | |||||||
chr7:77385979 | A | C | 1 | a0001c0002t0001g0241 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.456+1381T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77385979 | |||||||
chr7:77385990 | T | G | 3 | a0001c0001t0001g0036 a0001c0001t0001g0043 a0001c0001t0001g0205 |
3 | HG01257.hp1 HG01258.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.456+1370A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77385990 | |||||||
chr7:77386059 | G | GA | 132 | a0001c0001t0001g0003 a0001c0001t0001g0044 a0001c0001t0001g0072 others(129): Show |
135 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.456+1300dupT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77386059 | |||||||
chr7:77386094 | C | T | 12 | a0002c0003t0001g0058 a0002c0003t0001g0247 a0002c0003t0001g0287 others(9): Show |
13 | NA18946.hp2 NA18949.hp1 NA18966.hp1 others(10): Show |
intron_variant | MODIFIER | c.456+1266G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77386094 | |||||||
chr7:77386381 | T | C | 164 | a0001c0001t0001g0003 a0001c0001t0001g0044 a0001c0001t0001g0072 others(161): Show |
167 | HG00140.hp1 HG00423.hp1 HG00544.hp2 others(164): Show |
intron_variant | MODIFIER | c.456+979A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77386381 | |||||||
chr7:77386412 | G | A | 1 | a0001c0002t0002g0140 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.456+948C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77386412 | |||||||
chr7:77386547 | C | T | 1 | a0001c0001t0001g0226 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.456+813G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77386547 | |||||||
chr7:77386558 | G | A | 15 | a0004c0005t0001g0171 a0004c0005t0003g0115 a0004c0005t0003g0159 others(12): Show |
15 | HG00558.hp2 HG00621.hp2 HG02027.hp2 others(12): Show |
intron_variant | MODIFIER | c.456+802C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77386558 | |||||||
chr7:77386617 | C | T | 4 | a0001c0010t0001g0145 a0001c0010t0001g0149 a0001c0010t0001g0150 others(1): Show |
4 | HG03139.hp2 HG03516.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.456+743G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77386617 | |||||||
chr7:77386716 | G | A | 14 | a0001c0028t0002g0142 a0002c0003t0002g0055 a0002c0027t0001g0214 others(11): Show |
14 | HG00639.hp1 HG01109.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.456+644C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77386716 | |||||||
chr7:77386746 | T | C | 1 | a0014c0017t0001g0347 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.456+614A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77386746 | |||||||
chr7:77386805 | G | A | 4 | a0002c0003t0001g0021 a0002c0003t0001g0245 a0002c0003t0001g0246 others(1): Show |
4 | NA18963.hp1 NA19003.hp1 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.456+555C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77386805 | |||||||
chr7:77386865 | C | T | 11 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0011 others(8): Show |
11 | HG01433.hp2 HG02280.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.456+495G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77386865 | |||||||
chr7:77386960 | G | T | 2 | a0001c0002t0001g0264 a0001c0002t0001g0274 |
2 | HG00673.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.456+400C>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77386960 | |||||||
chr7:77386991 | T | C | 4 | a0001c0002t0002g0002 a0001c0002t0002g0207 a0001c0002t0002g0219 others(1): Show |
5 | HG01884.hp1 HG02109.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.456+369A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77386991 | |||||||
chr7:77387033 | C | T | 2 | a0001c0002t0002g0135 a0001c0002t0002g0140 |
2 | HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.456+327G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77387033 | |||||||
chr7:77387043 | T | C | 1 | a0014c0017t0001g0347 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.456+317A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77387043 | |||||||
chr7:77387143 | T | C | 10 | a0001c0028t0002g0142 a0002c0027t0001g0214 a0006c0008t0001g0017 others(7): Show |
10 | HG00639.hp1 HG01074.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.456+217A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77387143 | |||||||
chr7:77387169 | T | C | 1 | a0002c0003t0001g0319 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.456+191A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77387169 | |||||||
chr7:77387230 | G | A | 1 | a0005c0006t0001g0122 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.456+130C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77387230 | |||||||
chr7:77387242 | T | A | 2 | a0001c0002t0002g0135 a0001c0002t0002g0140 |
2 | HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.456+118A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77387242 | |||||||
chr7:77387332 | A | G | 1 | a0014c0017t0001g0347 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.456+28T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 6/30 | chr7 | 77387332 | |||||||
chr7:77387510 | A | C | 1 | a0014c0017t0001g0347 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.368-62T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77387510 | |||||||
chr7:77387563 | A | T | 1 | a0001c0002t0001g0276 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.368-115T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77387563 | |||||||
chr7:77387650 | C | T | 1 | a0014c0017t0001g0347 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.368-202G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77387650 | |||||||
chr7:77387651 | G | A | 2 | a0002c0003t0001g0069 a0002c0003t0003g0068 |
2 | HG04184.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.368-203C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77387651 | |||||||
chr7:77387747 | C | T | 7 | a0001c0001t0001g0045 a0001c0001t0001g0078 a0001c0001t0001g0192 others(4): Show |
7 | HG00544.hp1 NA18983.hp1 NA18987.hp1 others(4): Show |
intron_variant | MODIFIER | c.368-299G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77387747 | |||||||
chr7:77387787 | T | C | 1 | a0014c0017t0001g0347 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.368-339A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77387787 | |||||||
chr7:77387953 | G | A | 1 | a0001c0002t0001g0277 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.368-505C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77387953 | |||||||
chr7:77388026 | T | C | 10 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0011 others(7): Show |
10 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.368-578A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77388026 | |||||||
chr7:77388081 | A | G | 1 | a0001c0023t0001g0094 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.368-633T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77388081 | |||||||
chr7:77388125 | T | C | 198 | a0001c0001t0001g0204 a0001c0001t0001g0295 a0001c0001t0001g0296 others(195): Show |
201 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.368-677A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77388125 | |||||||
chr7:77388269 | G | A | 1 | a0006c0008t0001g0100 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.368-821C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77388269 | |||||||
chr7:77388345 | T | C | 10 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0011 others(7): Show |
10 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.368-897A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77388345 | |||||||
chr7:77388577 | C | T | 5 | a0001c0001t0001g0031 a0001c0001t0001g0040 a0001c0001t0001g0041 others(2): Show |
5 | HG00408.hp2 HG00423.hp2 HG02129.hp2 others(2): Show |
intron_variant | MODIFIER | c.368-1129G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77388577 | |||||||
chr7:77388578 | G | A | 4 | a0003c0004t0002g0123 a0003c0004t0002g0124 a0003c0004t0002g0133 others(1): Show |
4 | HG00140.hp1 HG01993.hp1 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.368-1130C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77388578 | |||||||
chr7:77388779 | C | T | 1 | a0001c0002t0002g0140 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.368-1331G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77388779 | |||||||
chr7:77388866 | CAGTA | C | 6 | a0001c0001t0001g0326 a0001c0001t0001g0328 a0001c0001t0001g0329 others(3): Show |
6 | HG00597.hp2 HG02015.hp1 HG02071.hp1 others(3): Show |
intron_variant | MODIFIER | c.368-1422_368-1419d others(6): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77388866 | |||||||
chr7:77388996 | A | G | 1 | a0011c0022t0001g0129 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.368-1548T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77388996 | |||||||
chr7:77389108 | T | C | 6 | a0001c0028t0002g0142 a0006c0008t0001g0052 a0006c0008t0001g0134 others(3): Show |
6 | HG00639.hp1 HG02723.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.368-1660A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77389108 | |||||||
chr7:77389132 | A | G | 2 | a0001c0002t0001g0193 a0001c0002t0001g0273 |
2 | HG02071.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.368-1684T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77389132 | |||||||
chr7:77389195 | G | A | 2 | a0001c0002t0001g0243 a0001c0002t0001g0262 |
2 | HG03831.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.368-1747C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77389195 | |||||||
chr7:77389225 | C | T | 314 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(311): Show |
319 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(316): Show |
intron_variant | MODIFIER | c.368-1777G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77389225 | |||||||
chr7:77389232 | G | A | 1 | a0001c0002t0001g0143 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.368-1784C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77389232 | |||||||
chr7:77389260 | A | T | 16 | a0001c0001t0001g0258 a0003c0004t0001g0190 a0003c0004t0002g0113 others(13): Show |
16 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.368-1812T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77389260 | |||||||
chr7:77389262 | T | A | 1 | a0001c0002t0002g0128 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.368-1814A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77389262 | |||||||
chr7:77389289 | G | GTA | 3 | a0001c0002t0002g0135 a0001c0002t0002g0140 a0002c0027t0001g0214 |
3 | HG01109.hp2 HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.368-1843_368-1842d others(4): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77389289 | |||||||
chr7:77389291 | A | G | 5 | a0001c0002t0001g0342 a0001c0002t0001g0343 a0001c0002t0001g0344 others(2): Show |
5 | HG01099.hp1 HG01168.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.368-1843T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77389291 | |||||||
chr7:77389303 | A | T | 14 | a0001c0001t0001g0204 a0001c0002t0001g0276 a0001c0002t0001g0302 others(11): Show |
14 | HG00642.hp2 HG02523.hp2 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.368-1855T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77389303 | |||||||
chr7:77389323 | G | A | 1 | a0001c0001t0001g0035 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.368-1875C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77389323 | |||||||
chr7:77389325 | TTTG | T | 15 | a0001c0028t0002g0142 a0002c0003t0002g0055 a0002c0027t0001g0214 others(12): Show |
15 | HG00639.hp1 HG01074.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.368-1880_368-1878d others(5): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77389325 | |||||||
chr7:77389379 | T | TA | 8 | a0001c0001t0001g0036 a0001c0001t0001g0043 a0001c0001t0001g0044 others(5): Show |
8 | HG00735.hp1 HG01257.hp1 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.368-1932dupT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77389379 | |||||||
chr7:77389409 | G | T | 1 | a0014c0017t0001g0347 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.368-1961C>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77389409 | |||||||
chr7:77389431 | T | TC | 13 | a0001c0001t0001g0086 a0001c0001t0001g0291 a0001c0001t0001g0329 others(10): Show |
13 | HG00597.hp1 HG01993.hp2 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.368-1984dupG | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77389431 | |||||||
chr7:77389437 | C | T | 2 | a0006c0008t0001g0017 a0006c0008t0001g0136 |
2 | HG01074.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.368-1989G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77389437 | |||||||
chr7:77389438 | C | G | 1 | a0001c0001t0001g0204 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.368-1990G>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77389438 | |||||||
chr7:77389457 | C | T | 1 | a0003c0004t0002g0123 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.368-2009G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77389457 | |||||||
chr7:77389528 | G | A | 1 | a0001c0001t0001g0075 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.368-2080C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77389528 | |||||||
chr7:77389530 | G | A | 59 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0011 others(56): Show |
60 | HG00738.hp1 HG01257.hp2 HG01433.hp2 others(57): Show |
intron_variant | MODIFIER | c.368-2082C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77389530 | |||||||
chr7:77389668 | T | G | 1 | a0002c0003t0001g0285 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.368-2220A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77389668 | |||||||
chr7:77389844 | T | C | 1 | a0014c0017t0001g0347 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.368-2396A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77389844 | |||||||
chr7:77389912 | T | C | 10 | a0001c0028t0002g0142 a0002c0027t0001g0214 a0006c0008t0001g0017 others(7): Show |
10 | HG00639.hp1 HG01074.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.368-2464A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77389912 | |||||||
chr7:77389917 | C | T | 10 | a0001c0028t0002g0142 a0002c0027t0001g0214 a0006c0008t0001g0017 others(7): Show |
10 | HG00639.hp1 HG01074.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.368-2469G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77389917 | |||||||
chr7:77389992 | A | G | 2 | a0001c0001t0001g0051 a0001c0002t0002g0140 |
2 | HG02074.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.368-2544T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77389992 | |||||||
chr7:77390007 | T | A | 1 | a0001c0001t0001g0225 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.368-2559A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390007 | |||||||
chr7:77390020 | G | T | 4 | a0001c0001t0001g0051 a0002c0003t0001g0215 a0002c0003t0001g0216 others(1): Show |
4 | HG02074.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.368-2572C>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390020 | |||||||
chr7:77390039 | C | G | 1 | a0001c0001t0001g0051 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.368-2591G>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390039 | |||||||
chr7:77390141 | C | T | 95 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0011 others(92): Show |
97 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.368-2693G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390141 | |||||||
chr7:77390170 | G | C | 1 | a0002c0003t0001g0005 | 2 | HG00280.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.368-2722C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390170 | |||||||
chr7:77390295 | C | T | 2 | a0001c0010t0001g0016 a0014c0017t0001g0347 |
2 | HG02809.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.368-2847G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390295 | |||||||
chr7:77390425 | A | G | 1 | a0001c0002t0001g0020 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.368-2977T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390425 | |||||||
chr7:77390452 | A | G | 73 | a0001c0002t0001g0342 a0001c0002t0001g0343 a0001c0002t0001g0344 others(70): Show |
74 | HG00140.hp1 HG00642.hp1 HG00738.hp1 others(71): Show |
intron_variant | MODIFIER | c.368-3004T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390452 | |||||||
chr7:77390549 | A | C | 120 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(117): Show |
122 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.368-3101T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390549 | |||||||
chr7:77390656 | T | C | 115 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(112): Show |
117 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.368-3208A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390656 | |||||||
chr7:77390821 | C | T | 49 | a0002c0003t0001g0038 a0002c0003t0001g0048 a0002c0003t0001g0058 others(46): Show |
50 | HG00738.hp1 HG01257.hp2 HG01884.hp2 others(47): Show |
intron_variant | MODIFIER | c.368-3373G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390821 | |||||||
chr7:77390939 | C | T | 2 | a0003c0004t0002g0152 a0003c0004t0002g0153 |
2 | HG03098.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.368-3491G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390939 | |||||||
chr7:77390946 | T | TA | 49 | a0001c0001t0001g0015 a0001c0001t0001g0040 a0001c0001t0001g0046 others(46): Show |
49 | HG00140.hp2 HG00408.hp2 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.368-3499dupT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390946 | |||||||
chr7:77390946 | T | TAA | 48 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0023 others(45): Show |
48 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.368-3500_368-3499d others(4): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390946 | |||||||
chr7:77390946 | T | TAAA | 28 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0032 others(25): Show |
29 | HG00099.hp2 HG00597.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.368-3501_368-3499d others(5): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390946 | |||||||
chr7:77390946 | T | TAAAA | 6 | a0001c0001t0001g0042 a0001c0001t0001g0049 a0001c0001t0001g0072 others(3): Show |
6 | HG01070.hp2 HG01517.hp2 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.368-3502_368-3499d others(6): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390946 | |||||||
chr7:77390946 | T | TAAAAA | 6 | a0001c0001t0001g0044 a0001c0001t0001g0074 a0001c0001t0001g0081 others(3): Show |
6 | HG00735.hp1 HG00738.hp2 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.368-3503_368-3499d others(7): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390946 | |||||||
chr7:77390946 | T | TAAAAAAA others(4): Show |
1 | a0003c0004t0002g0187 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.368-3509_368-3499d others(13): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390946 | |||||||
chr7:77390946 | T | TAAAAAAA others(5): Show |
3 | a0003c0004t0002g0183 a0003c0004t0002g0184 a0003c0004t0005g0185 |
3 | HG03098.hp1 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.368-3510_368-3499d others(14): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390946 | |||||||
chr7:77390946 | T | TAAAAAAA others(6): Show |
1 | a0003c0004t0002g0132 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.368-3511_368-3499d others(15): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390946 | |||||||
chr7:77390946 | T | TAAAAAAA others(8): Show |
1 | a0003c0004t0002g0186 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.368-3513_368-3499d others(17): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390946 | |||||||
chr7:77390946 | T | TTAAAAAA others(4): Show |
1 | a0003c0004t0002g0146 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.368-3499_368-3498i others(13): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390946 | |||||||
chr7:77390946 | TA | T | 23 | a0001c0002t0001g0117 a0001c0002t0001g0230 a0001c0002t0001g0233 others(20): Show |
23 | HG00597.hp1 HG00639.hp1 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.368-3499delT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390946 | |||||||
chr7:77390946 | TAA | T | 11 | a0001c0002t0001g0118 a0001c0002t0001g0239 a0001c0002t0001g0265 others(8): Show |
12 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(9): Show |
intron_variant | MODIFIER | c.368-3500_368-3499d others(4): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390946 | |||||||
chr7:77390946 | TAAA | T | 25 | a0001c0002t0001g0020 a0001c0002t0001g0025 a0001c0002t0001g0110 others(22): Show |
26 | HG00423.hp1 HG00558.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.368-3501_368-3499d others(5): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390946 | |||||||
chr7:77390946 | TAAAA | T | 31 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0304 others(28): Show |
31 | HG01069.hp2 HG01071.hp2 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.368-3502_368-3499d others(6): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390946 | |||||||
chr7:77390946 | TAAAAAAA others(1): Show |
T | 7 | a0003c0004t0002g0113 a0003c0004t0002g0123 a0003c0004t0002g0124 others(4): Show |
7 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.368-3506_368-3499d others(10): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390946 | |||||||
chr7:77390946 | TAAAAAAA others(3): Show |
T | 1 | a0014c0017t0001g0347 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.368-3508_368-3499d others(12): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390946 | |||||||
chr7:77390946 | TAAAAAAA others(6): Show |
T | 1 | a0003c0009t0001g0027 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.368-3511_368-3499d others(15): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390946 | |||||||
chr7:77390946 | TAAAAAAA others(7): Show |
T | 1 | a0011c0022t0001g0129 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.368-3512_368-3499d others(16): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390946 | |||||||
chr7:77390946 | TAAAAAAA others(8): Show |
T | 1 | a0001c0002t0001g0268 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.368-3513_368-3499d others(17): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390946 | |||||||
chr7:77390946 | TAAAAAAA others(12): Show |
T | 1 | a0003c0004t0001g0190 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.368-3517_368-3499d others(21): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390946 | |||||||
chr7:77390946 | TAAAAAAA others(16): Show |
T | 2 | a0002c0003t0001g0247 a0002c0007t0001g0325 |
2 | NA18949.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.368-3521_368-3499d others(25): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390946 | |||||||
chr7:77390946 | TAAAAAAA others(17): Show |
T | 50 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0096 others(47): Show |
51 | HG00738.hp1 HG01099.hp1 HG01168.hp2 others(48): Show |
intron_variant | MODIFIER | c.368-3522_368-3499d others(26): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390946 | |||||||
chr7:77390946 | TAAAAAAA others(18): Show |
T | 2 | a0003c0004t0002g0152 a0003c0004t0002g0153 |
2 | HG03098.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.368-3523_368-3499d others(27): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390946 | |||||||
chr7:77390954 | A | T | 1 | a0003c0004t0002g0156 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.368-3506T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390954 | |||||||
chr7:77390955 | A | T | 7 | a0003c0004t0002g0113 a0003c0004t0002g0123 a0003c0004t0002g0124 others(4): Show |
7 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.368-3507T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390955 | |||||||
chr7:77390956 | A | T | 1 | a0003c0004t0002g0203 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.368-3508T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390956 | |||||||
chr7:77390960 | A | T | 1 | a0003c0009t0001g0027 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.368-3512T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390960 | |||||||
chr7:77390966 | A | T | 1 | a0003c0004t0001g0190 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.368-3518T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390966 | |||||||
chr7:77390972 | A | T | 2 | a0003c0004t0002g0152 a0003c0004t0002g0153 |
2 | HG03098.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.368-3524T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77390972 | |||||||
chr7:77391020 | G | A | 9 | a0001c0002t0002g0002 a0001c0002t0002g0125 a0001c0002t0002g0130 others(6): Show |
10 | HG01192.hp2 HG01884.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.368-3572C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77391020 | |||||||
chr7:77391120 | C | T | 1 | a0003c0009t0001g0191 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.368-3672G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77391120 | |||||||
chr7:77391125 | C | CA | 46 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0042 others(43): Show |
46 | HG00140.hp2 HG00408.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.368-3678dupT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77391125 | |||||||
chr7:77391125 | C | CAA | 19 | a0001c0001t0001g0003 a0001c0001t0001g0250 a0001c0001t0001g0252 others(16): Show |
21 | HG01069.hp2 HG01071.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.368-3679_368-3678d others(4): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77391125 | |||||||
chr7:77391125 | C | CAAA | 61 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0304 others(58): Show |
61 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.368-3680_368-3678d others(5): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77391125 | |||||||
chr7:77391125 | CA | C | 26 | a0001c0001t0001g0045 a0001c0001t0001g0056 a0001c0002t0001g0343 others(23): Show |
26 | HG00639.hp1 HG00639.hp2 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.368-3678delT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77391125 | |||||||
chr7:77391125 | CAA | C | 20 | a0002c0003t0001g0005 a0002c0003t0001g0019 a0002c0003t0001g0030 others(17): Show |
21 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.368-3679_368-3678d others(4): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77391125 | |||||||
chr7:77391125 | CAAA | C | 66 | a0002c0003t0001g0021 a0002c0003t0001g0038 a0002c0003t0001g0048 others(63): Show |
67 | HG00140.hp1 HG00642.hp1 HG00738.hp1 others(64): Show |
intron_variant | MODIFIER | c.368-3680_368-3678d others(5): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77391125 | |||||||
chr7:77391136 | A | G | 1 | a0002c0003t0001g0147 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.368-3688T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77391136 | |||||||
chr7:77391142 | A | G | 40 | a0001c0002t0002g0107 a0001c0002t0002g0108 a0001c0002t0002g0320 others(37): Show |
41 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.368-3694T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77391142 | |||||||
chr7:77391150 | A | G | 1 | a0001c0001t0001g0305 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.368-3702T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77391150 | |||||||
chr7:77391164 | A | C | 1 | a0014c0017t0001g0347 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.368-3716T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77391164 | |||||||
chr7:77391178 | C | CT | 23 | a0001c0002t0001g0109 a0001c0002t0001g0110 a0001c0002t0001g0217 others(20): Show |
23 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.368-3731dupA | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77391178 | |||||||
chr7:77391179 | T | A | 1 | a0002c0003t0001g0030 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.368-3731A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77391179 | |||||||
chr7:77391188 | T | A | 1 | a0001c0002t0001g0143 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.368-3740A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77391188 | |||||||
chr7:77391195 | G | C | 12 | a0001c0002t0001g0117 a0001c0002t0001g0193 a0001c0002t0001g0230 others(9): Show |
12 | HG00597.hp1 HG00673.hp2 HG02071.hp2 others(9): Show |
intron_variant | MODIFIER | c.368-3747C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77391195 | |||||||
chr7:77391305 | A | G | 1 | a0014c0017t0001g0347 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.368-3857T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77391305 | |||||||
chr7:77391364 | T | C | 6 | a0003c0004t0002g0132 a0003c0004t0002g0183 a0003c0004t0002g0184 others(3): Show |
6 | HG01891.hp1 HG02055.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.368-3916A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77391364 | |||||||
chr7:77391416 | A | G | 1 | a0001c0002t0001g0237 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.368-3968T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77391416 | |||||||
chr7:77391419 | G | A | 1 | a0001c0002t0006g0007 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.368-3971C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77391419 | |||||||
chr7:77391546 | A | T | 64 | a0002c0003t0001g0038 a0002c0003t0001g0048 a0002c0003t0001g0058 others(61): Show |
65 | HG00140.hp1 HG00642.hp1 HG00738.hp1 others(62): Show |
intron_variant | MODIFIER | c.368-4098T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77391546 | |||||||
chr7:77391561 | C | T | 5 | a0002c0003t0001g0038 a0002c0003t0001g0062 a0002c0003t0001g0063 others(2): Show |
5 | HG01884.hp2 HG01891.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.368-4113G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77391561 | |||||||
chr7:77391627 | C | T | 78 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0304 others(75): Show |
79 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.368-4179G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77391627 | |||||||
chr7:77391690 | C | CTGGACAT others(7): Show |
1 | a0001c0002t0001g0282 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.368-4256_368-4243d others(16): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77391690 | |||||||
chr7:77391906 | C | T | 4 | a0004c0005t0001g0171 a0004c0005t0003g0159 a0004c0005t0003g0164 others(1): Show |
4 | HG00558.hp2 HG02027.hp2 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.368-4458G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77391906 | |||||||
chr7:77391998 | G | A | 1 | a0006c0008t0001g0134 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.368-4550C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77391998 | |||||||
chr7:77392053 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.368-4605G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77392053 | |||||||
chr7:77392063 | A | G | 4 | a0002c0003t0001g0021 a0002c0003t0001g0245 a0002c0003t0001g0246 others(1): Show |
4 | NA18963.hp1 NA19003.hp1 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.368-4615T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77392063 | |||||||
chr7:77392087 | T | C | 10 | a0001c0028t0002g0142 a0002c0027t0001g0214 a0006c0008t0001g0017 others(7): Show |
10 | HG00639.hp1 HG01074.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.368-4639A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77392087 | |||||||
chr7:77392170 | C | T | 1 | a0002c0003t0001g0066 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.368-4722G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77392170 | |||||||
chr7:77392180 | C | G | 2 | a0001c0002t0002g0107 a0001c0002t0002g0108 |
2 | HG02109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.368-4732G>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77392180 | |||||||
chr7:77392224 | G | GAA | 80 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0304 others(77): Show |
81 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.367+4756_367+4757d others(4): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77392224 | |||||||
chr7:77392266 | G | A | 79 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0304 others(76): Show |
80 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.367+4716C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77392266 | |||||||
chr7:77392458 | G | A | 16 | a0002c0003t0001g0005 a0002c0003t0001g0019 a0002c0003t0001g0021 others(13): Show |
17 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.367+4524C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77392458 | |||||||
chr7:77392463 | G | A | 14 | a0001c0001t0001g0031 a0001c0001t0001g0040 a0001c0001t0001g0041 others(11): Show |
14 | HG00408.hp2 HG00423.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.367+4519C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77392463 | |||||||
chr7:77392543 | G | A | 1 | a0001c0002t0002g0125 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.367+4439C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77392543 | |||||||
chr7:77392644 | A | G | 1 | a0001c0002t0001g0241 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.367+4338T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77392644 | |||||||
chr7:77392697 | A | G | 80 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0304 others(77): Show |
81 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.367+4285T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77392697 | |||||||
chr7:77392758 | T | A | 21 | a0002c0018t0001g0099 a0003c0004t0001g0190 a0003c0004t0002g0033 others(18): Show |
21 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(18): Show |
intron_variant | MODIFIER | c.367+4224A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77392758 | |||||||
chr7:77393159 | A | C | 81 | a0001c0001t0001g0213 a0001c0001t0001g0295 a0001c0001t0001g0296 others(78): Show |
82 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.367+3823T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77393159 | |||||||
chr7:77393262 | C | A | 15 | a0001c0028t0002g0142 a0002c0003t0002g0055 a0002c0027t0001g0214 others(12): Show |
15 | HG00639.hp1 HG01074.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.367+3720G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77393262 | |||||||
chr7:77393559 | C | T | 80 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0304 others(77): Show |
81 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.367+3423G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77393559 | |||||||
chr7:77393674 | C | CT | 26 | a0001c0001t0001g0023 a0001c0002t0001g0275 a0001c0002t0001g0276 others(23): Show |
26 | HG01167.hp2 HG01433.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.367+3307dupA | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77393674 | |||||||
chr7:77393674 | C | CTT | 70 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0305 others(67): Show |
71 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.367+3306_367+3307d others(4): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77393674 | |||||||
chr7:77393674 | C | CTTT | 6 | a0001c0001t0001g0304 a0001c0002t0001g0109 a0001c0002t0001g0232 others(3): Show |
6 | HG02132.hp1 NA18948.hp2 NA18949.hp2 others(3): Show |
intron_variant | MODIFIER | c.367+3305_367+3307d others(5): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77393674 | |||||||
chr7:77393818 | C | T | 1 | a0006c0008t0001g0052 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.367+3164G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77393818 | |||||||
chr7:77393834 | C | T | 1 | a0014c0017t0001g0347 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.367+3148G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77393834 | |||||||
chr7:77393865 | G | C | 80 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0304 others(77): Show |
81 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.367+3117C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77393865 | |||||||
chr7:77393866 | G | C | 1 | a0001c0002t0001g0053 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.367+3116C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77393866 | |||||||
chr7:77394038 | T | C | 80 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0304 others(77): Show |
81 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.367+2944A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77394038 | |||||||
chr7:77394090 | C | T | 67 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0304 others(64): Show |
67 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.367+2892G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77394090 | |||||||
chr7:77394098 | A | G | 1 | a0002c0003t0001g0346 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.367+2884T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77394098 | |||||||
chr7:77394185 | T | C | 20 | a0001c0028t0002g0142 a0002c0003t0002g0055 a0002c0027t0001g0214 others(17): Show |
20 | HG00639.hp1 HG01074.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.367+2797A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77394185 | |||||||
chr7:77394646 | G | A | 1 | a0001c0002t0001g0282 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.367+2336C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77394646 | |||||||
chr7:77394715 | T | C | 2 | a0001c0002t0002g0107 a0001c0002t0002g0108 |
2 | HG02109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.367+2267A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77394715 | |||||||
chr7:77394740 | T | A | 1 | a0001c0002t0001g0253 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.367+2242A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77394740 | |||||||
chr7:77394745 | C | T | 1 | a0006c0008t0001g0100 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.367+2237G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77394745 | |||||||
chr7:77394813 | T | C | 1 | a0002c0003t0002g0055 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.367+2169A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77394813 | |||||||
chr7:77394814 | A | G | 5 | a0002c0003t0002g0055 a0007c0011t0002g0138 a0007c0011t0002g0144 others(2): Show |
5 | HG02723.hp1 HG02976.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.367+2168T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77394814 | |||||||
chr7:77394960 | C | T | 174 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0304 others(171): Show |
176 | HG00140.hp1 HG00423.hp1 HG00544.hp2 others(173): Show |
intron_variant | MODIFIER | c.367+2022G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77394960 | |||||||
chr7:77394983 | C | T | 191 | a0001c0001t0001g0204 a0001c0001t0001g0295 a0001c0001t0001g0296 others(188): Show |
194 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.367+1999G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77394983 | |||||||
chr7:77395162 | G | C | 17 | a0001c0001t0001g0204 a0002c0003t0001g0005 a0002c0003t0001g0019 others(14): Show |
18 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.367+1820C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77395162 | |||||||
chr7:77395170 | TAGAC | T | 77 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0304 others(74): Show |
78 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.367+1808_367+1811d others(6): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77395170 | |||||||
chr7:77395292 | A | C | 1 | a0001c0010t0001g0016 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.367+1690T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77395292 | |||||||
chr7:77395370 | A | G | 1 | a0002c0003t0001g0285 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.367+1612T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77395370 | |||||||
chr7:77395442 | G | A | 3 | a0001c0002t0002g0107 a0001c0002t0002g0108 a0001c0028t0002g0142 |
3 | HG02109.hp1 HG03130.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.367+1540C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77395442 | |||||||
chr7:77395497 | A | G | 1 | a0006c0008t0001g0100 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.367+1485T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77395497 | |||||||
chr7:77395813 | G | A | 1 | a0004c0005t0001g0105 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.367+1169C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77395813 | |||||||
chr7:77395845 | A | T | 312 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(309): Show |
317 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(314): Show |
intron_variant | MODIFIER | c.367+1137T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77395845 | |||||||
chr7:77396190 | T | G | 2 | a0001c0002t0002g0107 a0001c0002t0002g0108 |
2 | HG02109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.367+792A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77396190 | |||||||
chr7:77396240 | C | A | 47 | a0002c0003t0001g0038 a0002c0003t0001g0048 a0002c0003t0001g0058 others(44): Show |
48 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(45): Show |
intron_variant | MODIFIER | c.367+742G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77396240 | |||||||
chr7:77396343 | T | C | 1 | a0006c0008t0001g0100 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.367+639A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77396343 | |||||||
chr7:77396449 | G | T | 9 | a0003c0004t0002g0113 a0003c0004t0002g0123 a0003c0004t0002g0124 others(6): Show |
9 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.367+533C>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77396449 | |||||||
chr7:77396723 | T | C | 120 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(117): Show |
122 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.367+259A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77396723 | |||||||
chr7:77396818 | AT | A | 12 | a0001c0002t0002g0002 a0001c0002t0002g0119 a0001c0002t0002g0125 others(9): Show |
13 | HG01192.hp2 HG01243.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.367+163delA | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77396818 | |||||||
chr7:77396819 | T | A | 48 | a0001c0001t0001g0192 a0001c0001t0001g0292 a0002c0003t0001g0038 others(45): Show |
49 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(46): Show |
intron_variant | MODIFIER | c.367+163A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 5/30 | chr7 | 77396819 | |||||||
chr7:77397047 | A | G | 2 | a0001c0002t0002g0107 a0001c0002t0002g0108 |
2 | HG02109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.314-12T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 4/30 | chr7 | 77397047 | |||||||
chr7:77397133 | A | G | 2 | a0003c0004t0002g0152 a0003c0004t0002g0153 |
2 | HG03098.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.314-98T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 4/30 | chr7 | 77397133 | |||||||
chr7:77397143 | G | A | 62 | a0002c0003t0001g0038 a0002c0003t0001g0048 a0002c0003t0001g0058 others(59): Show |
63 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(60): Show |
intron_variant | MODIFIER | c.314-108C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 4/30 | chr7 | 77397143 | |||||||
chr7:77397759 | A | C | 81 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0304 others(78): Show |
82 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.244-344T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77397759 | |||||||
chr7:77397778 | T | A | 1 | a0006c0008t0001g0139 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.244-363A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77397778 | |||||||
chr7:77398036 | T | G | 4 | a0007c0011t0002g0138 a0007c0011t0002g0144 a0007c0011t0002g0208 others(1): Show |
4 | HG02723.hp1 HG02976.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.244-621A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77398036 | |||||||
chr7:77398211 | G | T | 16 | a0002c0003t0001g0005 a0002c0003t0001g0019 a0002c0003t0001g0021 others(13): Show |
17 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.244-796C>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77398211 | |||||||
chr7:77398397 | TCTAA | T | 10 | a0001c0028t0002g0142 a0002c0027t0001g0214 a0006c0008t0001g0017 others(7): Show |
10 | HG00639.hp1 HG01074.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.244-986_244-983del others(4): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77398397 | |||||||
chr7:77398614 | A | T | 6 | a0001c0002t0001g0265 a0001c0002t0002g0135 a0001c0002t0002g0140 others(3): Show |
6 | HG02896.hp2 HG02897.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.244-1199T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77398614 | |||||||
chr7:77398771 | C | CA | 79 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0304 others(76): Show |
80 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.244-1357dupT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77398771 | |||||||
chr7:77398973 | C | T | 80 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0304 others(77): Show |
81 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.244-1558G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77398973 | |||||||
chr7:77399013 | G | T | 1 | a0001c0002t0002g0011 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.244-1598C>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77399013 | |||||||
chr7:77399137 | T | A | 80 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0304 others(77): Show |
81 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.244-1722A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77399137 | |||||||
chr7:77399182 | T | A | 1 | a0003c0009t0001g0191 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.244-1767A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77399182 | |||||||
chr7:77399335 | G | T | 7 | a0002c0007t0001g0227 a0002c0007t0001g0228 a0002c0007t0001g0229 others(4): Show |
7 | NA18946.hp2 NA18978.hp2 NA18981.hp1 others(4): Show |
intron_variant | MODIFIER | c.244-1920C>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77399335 | |||||||
chr7:77399504 | C | A | 1 | a0001c0002t0002g0002 | 2 | HG02970.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.244-2089G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77399504 | |||||||
chr7:77399528 | C | T | 1 | a0010c0025t0001g0306 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.244-2113G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77399528 | |||||||
chr7:77399667 | T | C | 80 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0304 others(77): Show |
81 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.244-2252A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77399667 | |||||||
chr7:77399703 | TG | T | 58 | a0001c0001t0001g0075 a0001c0001t0001g0198 a0001c0001t0001g0199 others(55): Show |
59 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.244-2289delC | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77399703 | |||||||
chr7:77399711 | G | A | 2 | a0001c0002t0002g0135 a0001c0002t0002g0140 |
2 | HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.244-2296C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77399711 | |||||||
chr7:77399713 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.244-2298G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77399713 | |||||||
chr7:77399786 | T | A | 1 | a0001c0001t0001g0031 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.244-2371A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77399786 | |||||||
chr7:77400020 | A | G | 80 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0304 others(77): Show |
81 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.244-2605T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77400020 | |||||||
chr7:77400053 | G | C | 80 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0304 others(77): Show |
81 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.244-2638C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77400053 | |||||||
chr7:77400074 | G | T | 1 | a0004c0005t0003g0115 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.244-2659C>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77400074 | |||||||
chr7:77400139 | T | C | 15 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0011 others(12): Show |
15 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.244-2724A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77400139 | |||||||
chr7:77400149 | T | G | 1 | a0001c0002t0001g0277 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.244-2734A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77400149 | |||||||
chr7:77400232 | G | C | 1 | a0014c0017t0001g0347 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.244-2817C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77400232 | |||||||
chr7:77400921 | A | T | 81 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0304 others(78): Show |
82 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.244-3506T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77400921 | |||||||
chr7:77400936 | A | AT | 144 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0304 others(141): Show |
146 | HG00140.hp1 HG00423.hp1 HG00544.hp2 others(143): Show |
intron_variant | MODIFIER | c.244-3522dupA | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77400936 | |||||||
chr7:77400936 | AT | A | 24 | a0001c0001t0001g0008 a0001c0001t0001g0032 a0001c0001t0001g0225 others(21): Show |
24 | HG00099.hp1 HG00639.hp1 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.244-3522delA | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77400936 | |||||||
chr7:77400986 | T | G | 1 | a0001c0001t0001g0071 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.244-3571A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77400986 | |||||||
chr7:77401016 | T | C | 9 | a0001c0002t0002g0002 a0001c0002t0002g0125 a0001c0002t0002g0130 others(6): Show |
10 | HG01192.hp2 HG01884.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.243+3543A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77401016 | |||||||
chr7:77401025 | T | G | 2 | a0005c0006t0001g0166 a0005c0006t0001g0167 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.243+3534A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77401025 | |||||||
chr7:77401057 | A | G | 81 | a0001c0001t0001g0213 a0001c0001t0001g0295 a0001c0001t0001g0296 others(78): Show |
82 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.243+3502T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77401057 | |||||||
chr7:77401089 | G | A | 1 | a0001c0001t0001g0201 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.243+3470C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77401089 | |||||||
chr7:77401225 | G | A | 1 | a0002c0003t0001g0093 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.243+3334C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77401225 | |||||||
chr7:77401238 | A | G | 1 | a0002c0003t0001g0335 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.243+3321T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77401238 | |||||||
chr7:77401244 | G | A | 5 | a0002c0003t0002g0055 a0007c0011t0002g0138 a0007c0011t0002g0144 others(2): Show |
5 | HG02723.hp1 HG02976.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.243+3315C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77401244 | |||||||
chr7:77401323 | A | G | 1 | a0001c0002t0002g0108 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.243+3236T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77401323 | |||||||
chr7:77401620 | C | A | 80 | a0001c0001t0001g0213 a0001c0001t0001g0295 a0001c0001t0001g0296 others(77): Show |
81 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.243+2939G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77401620 | |||||||
chr7:77401789 | C | T | 6 | a0003c0004t0002g0132 a0003c0004t0002g0183 a0003c0004t0002g0184 others(3): Show |
6 | HG01891.hp1 HG02055.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.243+2770G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77401789 | |||||||
chr7:77401839 | A | T | 9 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0011 others(6): Show |
9 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.243+2720T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77401839 | |||||||
chr7:77401930 | A | T | 2 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
2 | HG01168.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.243+2629T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77401930 | |||||||
chr7:77402017 | T | C | 2 | a0002c0003t0001g0247 a0002c0003t0001g0287 |
2 | NA18949.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.243+2542A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402017 | |||||||
chr7:77402042 | G | C | 1 | a0001c0002t0001g0241 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.243+2517C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402042 | |||||||
chr7:77402076 | C | G | 80 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0304 others(77): Show |
81 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.243+2483G>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402076 | |||||||
chr7:77402402 | G | GA | 11 | a0003c0004t0002g0132 a0003c0004t0002g0152 a0003c0004t0002g0153 others(8): Show |
11 | HG01891.hp1 HG02055.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.243+2156dupT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402402 | |||||||
chr7:77402402 | GAA | G | 68 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0304 others(65): Show |
69 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.243+2155_243+2156d others(4): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402402 | |||||||
chr7:77402404 | A | G | 1 | a0001c0002t0001g0232 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.243+2155T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402404 | |||||||
chr7:77402409 | A | AT | 33 | a0001c0002t0001g0342 a0001c0002t0001g0343 a0001c0002t0001g0344 others(30): Show |
33 | HG01099.hp1 HG01168.hp2 HG01169.hp2 others(30): Show |
intron_variant | MODIFIER | c.243+2149_243+2150i others(3): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402409 | |||||||
chr7:77402409 | A | T | 9 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0011 others(6): Show |
9 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.243+2150T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402409 | |||||||
chr7:77402411 | A | AT | 24 | a0001c0001t0001g0254 a0002c0003t0001g0065 a0002c0003t0001g0247 others(21): Show |
25 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.243+2147_243+2148i others(3): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402411 | |||||||
chr7:77402411 | A | T | 179 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(176): Show |
181 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.243+2148T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402411 | |||||||
chr7:77402411 | AAT | A | 10 | a0001c0002t0001g0193 a0001c0002t0001g0234 a0001c0002t0001g0242 others(7): Show |
10 | HG00673.hp2 HG02071.hp2 HG02132.hp1 others(7): Show |
intron_variant | MODIFIER | c.243+2146_243+2147d others(4): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402411 | |||||||
chr7:77402413 | T | A | 4 | a0003c0004t0001g0190 a0003c0009t0001g0029 a0003c0009t0001g0191 others(1): Show |
4 | HG01255.hp1 HG02523.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.243+2146A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402413 | |||||||
chr7:77402425 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.243+2134G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402425 | |||||||
chr7:77402435 | G | A | 88 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0304 others(85): Show |
89 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.243+2124C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402435 | |||||||
chr7:77402435 | G | C | 21 | a0002c0003t0001g0005 a0002c0003t0001g0019 a0002c0003t0001g0021 others(18): Show |
22 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.243+2124C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402435 | |||||||
chr7:77402455 | C | T | 22 | a0002c0018t0001g0099 a0003c0004t0001g0190 a0003c0004t0002g0033 others(19): Show |
22 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.243+2104G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402455 | |||||||
chr7:77402497 | A | AG | 3 | a0005c0006t0001g0131 a0005c0006t0001g0166 a0005c0006t0001g0167 |
3 | HG00099.hp1 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.243+2061dupC | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402497 | |||||||
chr7:77402593 | C | CAAAAAA | 9 | a0002c0018t0001g0099 a0003c0004t0002g0123 a0003c0004t0002g0124 others(6): Show |
9 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.243+1960_243+1965d others(8): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402593 | |||||||
chr7:77402593 | C | CAAAAAAA | 11 | a0003c0004t0001g0190 a0003c0004t0002g0033 a0003c0004t0002g0113 others(8): Show |
11 | HG02523.hp2 HG02717.hp1 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.243+1959_243+1965d others(9): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402593 | |||||||
chr7:77402593 | C | CAAAAAAA others(6): Show |
2 | a0001c0002t0002g0107 a0001c0002t0002g0108 |
2 | HG02109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.243+1953_243+1965d others(15): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402593 | |||||||
chr7:77402593 | C | CAAAAAAA others(13): Show |
2 | a0002c0003t0001g0005 a0002c0003t0001g0030 |
3 | HG00280.hp2 HG00323.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.243+1946_243+1965d others(22): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402593 | |||||||
chr7:77402593 | C | CAAAAAAA others(14): Show |
2 | a0002c0003t0001g0080 a0006c0020t0003g0024 |
2 | HG02735.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.243+1945_243+1965d others(23): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402593 | |||||||
chr7:77402593 | C | CAAAAAAA others(15): Show |
4 | a0001c0001t0001g0204 a0002c0003t0001g0019 a0002c0003t0001g0155 others(1): Show |
4 | HG00642.hp2 HG02015.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.243+1944_243+1965d others(24): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402593 | |||||||
chr7:77402593 | C | CAAAAAAA others(16): Show |
1 | a0002c0003t0001g0102 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.243+1943_243+1965d others(25): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402593 | |||||||
chr7:77402593 | C | CAAAAAAA others(17): Show |
3 | a0002c0003t0001g0101 a0002c0003t0001g0103 a0011c0022t0001g0129 |
3 | HG01123.hp2 HG01517.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.243+1965_243+1966i others(26): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402593 | |||||||
chr7:77402593 | CA | C | 52 | a0001c0001t0001g0305 a0001c0002t0001g0278 a0001c0002t0001g0343 others(49): Show |
53 | HG00423.hp1 HG01168.hp2 HG01169.hp2 others(50): Show |
intron_variant | MODIFIER | c.243+1965delT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402593 | |||||||
chr7:77402593 | CAA | C | 81 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0304 others(78): Show |
82 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.243+1964_243+1965d others(4): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402593 | |||||||
chr7:77402593 | CAAAA | C | 14 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0011 others(11): Show |
14 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.243+1962_243+1965d others(6): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402593 | |||||||
chr7:77402616 | A | AAAAAAAA others(24): Show |
1 | a0001c0001t0001g0035 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.243+1942_243+1943i others(33): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402616 | |||||||
chr7:77402616 | A | AAAAAAAA others(23): Show |
1 | a0001c0001t0001g0084 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.243+1942_243+1943i others(32): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402616 | |||||||
chr7:77402616 | A | AAAAAAAA others(22): Show |
1 | a0001c0001t0001g0333 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.243+1942_243+1943i others(31): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402616 | |||||||
chr7:77402616 | A | AAAAAAAA others(21): Show |
2 | a0001c0001t0001g0329 a0001c0001t0001g0330 |
2 | HG00597.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.243+1942_243+1943i others(30): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402616 | |||||||
chr7:77402616 | A | AAAAAAAA others(20): Show |
7 | a0001c0001t0001g0045 a0001c0001t0001g0078 a0001c0001t0001g0081 others(4): Show |
7 | HG01243.hp2 HG02280.hp2 HG04115.hp1 others(4): Show |
intron_variant | MODIFIER | c.243+1942_243+1943i others(29): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402616 | |||||||
chr7:77402616 | A | AAAAAAAA others(19): Show |
2 | a0001c0001t0001g0015 a0001c0001t0001g0077 |
2 | HG02630.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.243+1942_243+1943i others(28): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402616 | |||||||
chr7:77402616 | A | AAAAAAAA others(18): Show |
4 | a0001c0001t0001g0112 a0001c0001t0001g0321 a0001c0001t0001g0332 others(1): Show |
4 | HG02155.hp2 HG02451.hp2 NA18987.hp1 others(1): Show |
intron_variant | MODIFIER | c.243+1942_243+1943i others(27): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402616 | |||||||
chr7:77402616 | A | AAAAAAAA others(17): Show |
4 | a0001c0001t0001g0001 a0001c0001t0001g0047 a0001c0001t0001g0114 others(1): Show |
5 | HG01361.hp1 HG01934.hp2 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.243+1942_243+1943i others(26): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402616 | |||||||
chr7:77402616 | A | AAAAAAAA others(16): Show |
7 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0086 others(4): Show |
7 | HG01070.hp1 HG01993.hp2 NA18906.hp1 others(4): Show |
intron_variant | MODIFIER | c.243+1942_243+1943i others(25): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402616 | |||||||
chr7:77402616 | A | AAAAAAAA others(15): Show |
27 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0032 others(24): Show |
27 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(24): Show |
intron_variant | MODIFIER | c.243+1942_243+1943i others(24): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402616 | |||||||
chr7:77402616 | A | AAAAAAAA others(14): Show |
20 | a0001c0001t0001g0043 a0001c0001t0001g0050 a0001c0001t0001g0072 others(17): Show |
20 | HG00733.hp1 HG00738.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.243+1942_243+1943i others(23): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402616 | |||||||
chr7:77402616 | A | AAAAAAAA others(13): Show |
8 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0022 others(5): Show |
9 | HG01070.hp2 HG01071.hp1 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.243+1942_243+1943i others(22): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402616 | |||||||
chr7:77402616 | A | AAAAAAAA others(11): Show |
2 | a0001c0001t0001g0083 a0001c0001t0001g0328 |
2 | HG02015.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.243+1942_243+1943i others(20): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402616 | |||||||
chr7:77402616 | A | AAAAAAAA others(10): Show |
1 | a0001c0001t0001g0042 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.243+1942_243+1943i others(19): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402616 | |||||||
chr7:77402616 | A | AAAAAAAA others(9): Show |
1 | a0001c0001t0001g0226 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.243+1942_243+1943i others(18): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402616 | |||||||
chr7:77402616 | A | AAAAAAAA others(8): Show |
1 | a0001c0001t0001g0235 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.243+1942_243+1943i others(17): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402616 | |||||||
chr7:77402616 | A | AAAAAAAA others(5): Show |
2 | a0001c0001t0001g0070 a0001c0001t0001g0200 |
2 | HG00140.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.243+1942_243+1943i others(14): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402616 | |||||||
chr7:77402616 | A | AAAAAAAA others(4): Show |
1 | a0001c0001t0001g0056 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.243+1942_243+1943i others(13): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402616 | |||||||
chr7:77402616 | A | AAAAAAAA others(3): Show |
3 | a0001c0001t0001g0049 a0001c0001t0001g0082 a0001c0001t0001g0334 |
3 | HG00544.hp1 NA18967.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.243+1942_243+1943i others(12): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402616 | |||||||
chr7:77402616 | A | AAT | 6 | a0001c0001t0001g0031 a0001c0001t0001g0040 a0001c0001t0001g0041 others(3): Show |
6 | HG00423.hp2 HG02129.hp2 NA18945.hp1 others(3): Show |
intron_variant | MODIFIER | c.243+1942_243+1943i others(4): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402616 | |||||||
chr7:77402684 | T | TA | 14 | a0001c0001t0001g0085 a0001c0001t0001g0254 a0001c0002t0002g0009 others(11): Show |
14 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.243+1874dupT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402684 | |||||||
chr7:77402684 | T | TAA | 76 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0304 others(73): Show |
77 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.243+1873_243+1874d others(4): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402684 | |||||||
chr7:77402737 | G | C | 1 | a0002c0003t0001g0101 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.243+1822C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402737 | |||||||
chr7:77402746 | A | G | 1 | a0002c0003t0001g0147 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.243+1813T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402746 | |||||||
chr7:77402764 | C | T | 1 | a0001c0001t0001g0226 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.243+1795G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402764 | |||||||
chr7:77402955 | A | G | 5 | a0002c0003t0002g0055 a0007c0011t0002g0138 a0007c0011t0002g0144 others(2): Show |
5 | HG02723.hp1 HG02976.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.243+1604T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77402955 | |||||||
chr7:77403000 | G | C | 2 | a0004c0005t0003g0158 a0004c0005t0003g0161 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.243+1559C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77403000 | |||||||
chr7:77403057 | G | T | 14 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0011 others(11): Show |
14 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.243+1502C>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77403057 | |||||||
chr7:77403181 | C | T | 69 | a0002c0003t0001g0038 a0002c0003t0001g0048 a0002c0003t0001g0058 others(66): Show |
70 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(67): Show |
intron_variant | MODIFIER | c.243+1378G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77403181 | |||||||
chr7:77403210 | C | A | 1 | a0001c0002t0001g0279 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.243+1349G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77403210 | |||||||
chr7:77403327 | T | C | 6 | a0003c0004t0002g0132 a0003c0004t0002g0183 a0003c0004t0002g0184 others(3): Show |
6 | HG01891.hp1 HG02055.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.243+1232A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77403327 | |||||||
chr7:77403379 | G | A | 2 | a0003c0004t0002g0033 a0003c0004t0002g0338 |
2 | HG02886.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.243+1180C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77403379 | |||||||
chr7:77403471 | A | T | 1 | a0002c0003t0001g0346 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.243+1088T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77403471 | |||||||
chr7:77403547 | C | T | 3 | a0001c0001t0001g0199 a0001c0010t0001g0145 a0001c0010t0001g0149 |
3 | HG03139.hp2 HG03516.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.243+1012G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77403547 | |||||||
chr7:77403569 | G | GA | 71 | a0001c0013t0001g0218 a0001c0013t0001g0221 a0002c0003t0001g0038 others(68): Show |
72 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(69): Show |
intron_variant | MODIFIER | c.243+989dupT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77403569 | |||||||
chr7:77403647 | A | C | 47 | a0002c0003t0001g0038 a0002c0003t0001g0048 a0002c0003t0001g0058 others(44): Show |
48 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(45): Show |
intron_variant | MODIFIER | c.243+912T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77403647 | |||||||
chr7:77403680 | C | T | 174 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0304 others(171): Show |
176 | HG00140.hp1 HG00423.hp1 HG00544.hp2 others(173): Show |
intron_variant | MODIFIER | c.243+879G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77403680 | |||||||
chr7:77403843 | C | A | 7 | a0002c0003t0001g0038 a0002c0003t0001g0062 a0002c0003t0001g0063 others(4): Show |
7 | HG01884.hp2 HG01891.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.243+716G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77403843 | |||||||
chr7:77404118 | C | A | 79 | a0001c0001t0001g0213 a0001c0001t0001g0295 a0001c0001t0001g0296 others(76): Show |
80 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.243+441G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77404118 | |||||||
chr7:77404148 | T | C | 4 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0304 others(1): Show |
4 | NA18957.hp1 NA18966.hp2 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.243+411A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77404148 | |||||||
chr7:77404180 | T | G | 15 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0011 others(12): Show |
15 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.243+379A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77404180 | |||||||
chr7:77404186 | A | G | 26 | a0001c0013t0001g0218 a0001c0013t0001g0221 a0002c0003t0001g0065 others(23): Show |
26 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.243+373T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77404186 | |||||||
chr7:77404401 | T | C | 1 | a0002c0003t0001g0319 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.243+158A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77404401 | |||||||
chr7:77404478 | G | C | 15 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0011 others(12): Show |
15 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.243+81C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 3/30 | chr7 | 77404478 | |||||||
chr7:77404620 | A | G | 81 | a0001c0001t0001g0213 a0001c0001t0001g0295 a0001c0001t0001g0296 others(78): Show |
82 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(79): Show |
splice_region_variant&intron_variant | LOW | c.187-5T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 2/30 | chr7 | 77404620 | |||||||
chr7:77404698 | AACTC | A | 11 | a0001c0002t0001g0117 a0001c0002t0001g0193 a0001c0002t0001g0234 others(8): Show |
11 | HG00597.hp1 HG00673.hp2 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.187-87_187-84delGA others(2): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 2/30 | chr7 | 77404698 | |||||||
chr7:77404768 | C | T | 10 | a0001c0028t0002g0142 a0002c0027t0001g0214 a0006c0008t0001g0017 others(7): Show |
10 | HG00639.hp1 HG01074.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.187-153G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 2/30 | chr7 | 77404768 | |||||||
chr7:77404807 | A | C | 10 | a0001c0028t0002g0142 a0002c0027t0001g0214 a0006c0008t0001g0017 others(7): Show |
10 | HG00639.hp1 HG01074.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.187-192T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 2/30 | chr7 | 77404807 | |||||||
chr7:77405060 | C | A | 15 | a0002c0003t0001g0005 a0002c0003t0001g0019 a0002c0003t0001g0021 others(12): Show |
16 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.187-445G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 2/30 | chr7 | 77405060 | |||||||
chr7:77405094 | TTATAG | T | 15 | a0002c0003t0001g0005 a0002c0003t0001g0019 a0002c0003t0001g0021 others(12): Show |
16 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.187-484_187-480del others(5): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 2/30 | chr7 | 77405094 | |||||||
chr7:77405161 | A | C | 1 | a0001c0002t0001g0263 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.187-546T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 2/30 | chr7 | 77405161 | |||||||
chr7:77405235 | G | C | 15 | a0002c0003t0001g0005 a0002c0003t0001g0019 a0002c0003t0001g0021 others(12): Show |
16 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.187-620C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 2/30 | chr7 | 77405235 | |||||||
chr7:77405308 | AAAT | A | 10 | a0001c0028t0002g0142 a0002c0027t0001g0214 a0006c0008t0001g0017 others(7): Show |
10 | HG00639.hp1 HG01074.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.187-696_187-694del others(3): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 2/30 | chr7 | 77405308 | |||||||
chr7:77405346 | G | A | 10 | a0001c0028t0002g0142 a0002c0027t0001g0214 a0006c0008t0001g0017 others(7): Show |
10 | HG00639.hp1 HG01074.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.186+683C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 2/30 | chr7 | 77405346 | |||||||
chr7:77405364 | T | C | 1 | a0001c0001t0001g0081 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.186+665A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 2/30 | chr7 | 77405364 | |||||||
chr7:77405377 | C | T | 1 | a0011c0022t0001g0129 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.186+652G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 2/30 | chr7 | 77405377 | |||||||
chr7:77405533 | T | TA | 36 | a0001c0013t0001g0218 a0001c0013t0001g0221 a0001c0028t0002g0142 others(33): Show |
36 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.186+495dupT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 2/30 | chr7 | 77405533 | |||||||
chr7:77405570 | C | T | 2 | a0001c0002t0002g0009 a0001c0002t0002g0011 |
2 | HG02572.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.186+459G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 2/30 | chr7 | 77405570 | |||||||
chr7:77405651 | C | T | 2 | a0001c0001t0001g0057 a0001c0001t0001g0209 |
2 | HG00099.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.186+378G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 2/30 | chr7 | 77405651 | |||||||
chr7:77405847 | C | G | 1 | a0007c0011t0002g0144 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.186+182G>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 2/30 | chr7 | 77405847 | |||||||
chr7:77405905 | T | C | 15 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0011 others(12): Show |
15 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.186+124A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 2/30 | chr7 | 77405905 | |||||||
chr7:77406163 | C | G | 10 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0011 others(7): Show |
10 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.110-58G>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77406163 | |||||||
chr7:77406331 | C | A | 15 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0011 others(12): Show |
15 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.110-226G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77406331 | |||||||
chr7:77406332 | G | A | 10 | a0001c0028t0002g0142 a0002c0027t0001g0214 a0006c0008t0001g0017 others(7): Show |
10 | HG00639.hp1 HG01074.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.110-227C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77406332 | |||||||
chr7:77406488 | C | T | 1 | a0002c0003t0001g0346 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.110-383G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77406488 | |||||||
chr7:77406535 | T | G | 1 | a0001c0001t0001g0316 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.110-430A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77406535 | |||||||
chr7:77406565 | T | C | 2 | a0001c0002t0001g0243 a0001c0002t0001g0262 |
2 | HG03831.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.110-460A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77406565 | |||||||
chr7:77406597 | A | G | 1 | a0001c0001t0001g0256 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.110-492T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77406597 | |||||||
chr7:77406661 | G | C | 80 | a0001c0001t0001g0213 a0001c0001t0001g0295 a0001c0001t0001g0296 others(77): Show |
81 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.110-556C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77406661 | |||||||
chr7:77406695 | A | G | 1 | a0001c0001t0001g0192 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.110-590T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77406695 | |||||||
chr7:77406708 | A | G | 195 | a0001c0001t0001g0213 a0001c0001t0001g0295 a0001c0001t0001g0296 others(192): Show |
198 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.110-603T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77406708 | |||||||
chr7:77406759 | C | A | 1 | a0006c0008t0001g0100 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.110-654G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77406759 | |||||||
chr7:77406965 | G | T | 1 | a0001c0002t0001g0299 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.110-860C>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77406965 | |||||||
chr7:77406984 | G | A | 2 | a0001c0001t0001g0056 a0001c0001t0001g0070 |
2 | HG00639.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.110-879C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77406984 | |||||||
chr7:77407160 | C | A | 10 | a0001c0028t0002g0142 a0002c0027t0001g0214 a0006c0008t0001g0017 others(7): Show |
10 | HG00639.hp1 HG01074.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.110-1055G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77407160 | |||||||
chr7:77407258 | A | G | 50 | a0001c0002t0001g0342 a0001c0002t0001g0343 a0001c0002t0001g0344 others(47): Show |
51 | HG01099.hp1 HG01168.hp2 HG01169.hp2 others(48): Show |
intron_variant | MODIFIER | c.110-1153T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77407258 | |||||||
chr7:77407389 | C | G | 83 | a0001c0001t0001g0213 a0001c0001t0001g0295 a0001c0001t0001g0296 others(80): Show |
84 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.110-1284G>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77407389 | |||||||
chr7:77407668 | CTG | C | 6 | a0001c0001t0001g0326 a0001c0001t0001g0328 a0001c0001t0001g0329 others(3): Show |
6 | HG00597.hp2 HG02015.hp1 HG02071.hp1 others(3): Show |
intron_variant | MODIFIER | c.110-1565_110-1564d others(4): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77407668 | |||||||
chr7:77407913 | G | T | 1 | a0001c0002t0001g0262 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.110-1808C>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77407913 | |||||||
chr7:77407949 | T | C | 1 | a0002c0003t0001g0335 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.110-1844A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77407949 | |||||||
chr7:77408047 | G | C | 14 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0011 others(11): Show |
14 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.110-1942C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77408047 | |||||||
chr7:77408537 | A | G | 14 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0011 others(11): Show |
14 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.110-2432T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77408537 | |||||||
chr7:77408689 | C | CA | 32 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(29): Show |
33 | HG00280.hp2 HG00323.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.110-2585dupT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77408689 | |||||||
chr7:77408689 | C | CAAAAA | 10 | a0001c0002t0002g0009 a0001c0002t0002g0011 a0001c0002t0002g0012 others(7): Show |
10 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.110-2589_110-2585d others(7): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77408689 | |||||||
chr7:77408689 | CA | C | 79 | a0001c0001t0001g0326 a0001c0001t0003g0293 a0001c0002t0001g0020 others(76): Show |
80 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.110-2585delT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77408689 | |||||||
chr7:77408689 | CAA | C | 67 | a0001c0002t0001g0116 a0001c0002t0001g0262 a0001c0002t0002g0135 others(64): Show |
68 | HG00140.hp1 HG00639.hp1 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.110-2586_110-2585d others(4): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77408689 | |||||||
chr7:77408689 | CAAA | C | 6 | a0003c0004t0002g0132 a0003c0004t0002g0183 a0003c0004t0002g0184 others(3): Show |
6 | HG01891.hp1 HG02055.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.110-2587_110-2585d others(5): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77408689 | |||||||
chr7:77408877 | A | G | 1 | a0009c0026t0001g0054 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.110-2772T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77408877 | |||||||
chr7:77408897 | G | A | 2 | a0001c0002t0001g0283 a0010c0025t0001g0306 |
2 | HG01099.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.110-2792C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77408897 | |||||||
chr7:77408946 | AG | A | 14 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0011 others(11): Show |
14 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.110-2842delC | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77408946 | |||||||
chr7:77409332 | G | T | 59 | a0001c0001t0001g0056 a0001c0001t0001g0070 a0001c0028t0002g0142 others(56): Show |
60 | HG00639.hp1 HG00639.hp2 HG01074.hp1 others(57): Show |
intron_variant | MODIFIER | c.110-3227C>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77409332 | |||||||
chr7:77409628 | C | T | 291 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(288): Show |
295 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.110-3523G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77409628 | |||||||
chr7:77409713 | C | T | 2 | a0001c0002t0001g0261 a0001c0002t0001g0298 |
2 | NA18960.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.110-3608G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77409713 | |||||||
chr7:77409741 | G | T | 14 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0011 others(11): Show |
14 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.110-3636C>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77409741 | |||||||
chr7:77409928 | G | C | 1 | a0011c0022t0001g0129 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.110-3823C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77409928 | |||||||
chr7:77410092 | A | C | 1 | a0001c0002t0001g0297 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.110-3987T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77410092 | |||||||
chr7:77410119 | G | A | 15 | a0002c0003t0001g0005 a0002c0003t0001g0019 a0002c0003t0001g0021 others(12): Show |
16 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.110-4014C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77410119 | |||||||
chr7:77410166 | T | G | 79 | a0001c0001t0001g0213 a0001c0001t0001g0295 a0001c0001t0001g0296 others(76): Show |
80 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.110-4061A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77410166 | |||||||
chr7:77410585 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.110-4480G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77410585 | |||||||
chr7:77410879 | T | C | 1 | a0002c0003t0002g0055 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.110-4774A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77410879 | |||||||
chr7:77411037 | G | A | 15 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0011 others(12): Show |
15 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.110-4932C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77411037 | |||||||
chr7:77411098 | T | TA | 10 | a0001c0002t0002g0002 a0001c0002t0002g0009 a0001c0002t0002g0207 others(7): Show |
11 | HG01516.hp2 HG01884.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.110-4994dupT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77411098 | |||||||
chr7:77411098 | T | TAA | 45 | a0001c0001t0001g0114 a0001c0001t0001g0204 a0001c0002t0002g0010 others(42): Show |
46 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.110-4995_110-4994d others(4): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77411098 | |||||||
chr7:77411098 | TA | T | 221 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(218): Show |
223 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(220): Show |
intron_variant | MODIFIER | c.110-4994delT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77411098 | |||||||
chr7:77411098 | TAA | T | 6 | a0001c0001t0001g0036 a0001c0001t0001g0198 a0001c0001t0001g0209 others(3): Show |
6 | HG01070.hp1 HG01070.hp2 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.110-4995_110-4994d others(4): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77411098 | |||||||
chr7:77411230 | C | A | 7 | a0002c0003t0001g0048 a0002c0003t0001g0087 a0002c0003t0001g0088 others(4): Show |
7 | NA18940.hp1 NA18959.hp2 NA18961.hp2 others(4): Show |
intron_variant | MODIFIER | c.109+4983G>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77411230 | |||||||
chr7:77411471 | T | C | 1 | a0001c0002t0006g0007 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.109+4742A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77411471 | |||||||
chr7:77411511 | G | A | 4 | a0007c0011t0002g0138 a0007c0011t0002g0144 a0007c0011t0002g0208 others(1): Show |
4 | HG02723.hp1 HG02976.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.109+4702C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77411511 | |||||||
chr7:77411620 | CTAAA | C | 3 | a0001c0002t0002g0125 a0001c0002t0002g0130 a0002c0019t0001g0126 |
3 | HG01192.hp2 HG02717.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.109+4589_109+4592d others(6): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77411620 | |||||||
chr7:77411668 | A | G | 1 | a0014c0017t0001g0347 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.109+4545T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77411668 | |||||||
chr7:77411703 | T | C | 1 | a0001c0001t0001g0294 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.109+4510A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77411703 | |||||||
chr7:77411770 | A | AAT | 25 | a0001c0001t0001g0114 a0001c0013t0001g0218 a0001c0013t0001g0221 others(22): Show |
25 | HG00140.hp1 HG00642.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.109+4441_109+4442d others(4): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77411770 | |||||||
chr7:77411954 | C | G | 15 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0011 others(12): Show |
15 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.109+4259G>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77411954 | |||||||
chr7:77411955 | G | A | 1 | a0001c0002t0002g0119 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.109+4258C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77411955 | |||||||
chr7:77411970 | A | G | 15 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0011 others(12): Show |
15 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.109+4243T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77411970 | |||||||
chr7:77411973 | G | A | 239 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(236): Show |
243 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.109+4240C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77411973 | |||||||
chr7:77412039 | C | T | 2 | a0001c0001t0001g0057 a0001c0001t0001g0209 |
2 | HG00099.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.109+4174G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77412039 | |||||||
chr7:77412055 | C | T | 1 | a0003c0009t0001g0191 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.109+4158G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77412055 | |||||||
chr7:77412406 | G | A | 4 | a0001c0001t0001g0006 a0001c0001t0001g0049 a0001c0001t0001g0091 others(1): Show |
4 | NA18945.hp2 NA18967.hp2 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.109+3807C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77412406 | |||||||
chr7:77412480 | A | T | 4 | a0007c0011t0002g0138 a0007c0011t0002g0144 a0007c0011t0002g0208 others(1): Show |
4 | HG02723.hp1 HG02976.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.109+3733T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77412480 | |||||||
chr7:77412486 | T | C | 160 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(157): Show |
163 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.109+3727A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77412486 | |||||||
chr7:77412543 | G | C | 12 | a0001c0028t0002g0142 a0002c0003t0001g0215 a0002c0003t0001g0216 others(9): Show |
12 | HG00639.hp1 HG01074.hp1 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.109+3670C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77412543 | |||||||
chr7:77412604 | A | G | 4 | a0001c0010t0001g0145 a0001c0010t0001g0149 a0001c0010t0001g0150 others(1): Show |
4 | HG03139.hp2 HG03516.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.109+3609T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77412604 | |||||||
chr7:77412759 | T | C | 2 | a0004c0005t0003g0162 a0004c0005t0003g0163 |
2 | NA18962.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.109+3454A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77412759 | |||||||
chr7:77412760 | A | C | 2 | a0004c0005t0003g0162 a0004c0005t0003g0163 |
2 | NA18962.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.109+3453T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77412760 | |||||||
chr7:77412776 | CA | C | 261 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(258): Show |
265 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.109+3436delT | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77412776 | |||||||
chr7:77412883 | A | G | 1 | a0001c0002t0001g0143 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.109+3330T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77412883 | |||||||
chr7:77413123 | C | G | 15 | a0002c0003t0001g0005 a0002c0003t0001g0019 a0002c0003t0001g0021 others(12): Show |
16 | HG00280.hp2 HG00323.hp2 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.109+3090G>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77413123 | |||||||
chr7:77413209 | C | T | 10 | a0001c0028t0002g0142 a0002c0027t0001g0214 a0006c0008t0001g0017 others(7): Show |
10 | HG00639.hp1 HG01074.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.109+3004G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77413209 | |||||||
chr7:77413231 | G | A | 15 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0011 others(12): Show |
15 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.109+2982C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77413231 | |||||||
chr7:77413268 | A | G | 1 | a0002c0003t0001g0120 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.109+2945T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77413268 | |||||||
chr7:77413314 | C | T | 79 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0304 others(76): Show |
80 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.109+2899G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77413314 | |||||||
chr7:77413406 | A | G | 1 | a0002c0003t0001g0030 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.109+2807T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77413406 | |||||||
chr7:77413597 | G | A | 5 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0096 others(2): Show |
5 | HG02074.hp1 NA18948.hp1 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.109+2616C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77413597 | |||||||
chr7:77413839 | C | T | 10 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0011 others(7): Show |
10 | HG01433.hp2 HG02451.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.109+2374G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77413839 | |||||||
chr7:77413845 | T | A | 2 | a0001c0002t0002g0135 a0001c0002t0002g0140 |
2 | HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.109+2368A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77413845 | |||||||
chr7:77413857 | G | GT | 160 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(157): Show |
163 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.109+2355dupA | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77413857 | |||||||
chr7:77413857 | G | GTT | 29 | a0001c0001t0001g0035 a0001c0001t0001g0204 a0001c0002t0002g0009 others(26): Show |
30 | HG00280.hp2 HG00323.hp2 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.109+2354_109+2355d others(4): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77413857 | |||||||
chr7:77413857 | G | GTTT | 96 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0304 others(93): Show |
97 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.109+2353_109+2355d others(5): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77413857 | |||||||
chr7:77413857 | G | GTTTT | 22 | a0001c0001t0001g0114 a0001c0002t0001g0053 a0001c0013t0001g0218 others(19): Show |
22 | HG00140.hp1 HG01361.hp1 HG01993.hp1 others(19): Show |
intron_variant | MODIFIER | c.109+2352_109+2355d others(6): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77413857 | |||||||
chr7:77413857 | G | T | 1 | a0001c0001t0001g0056 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.109+2356C>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77413857 | |||||||
chr7:77413865 | C | T | 178 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(175): Show |
181 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.109+2348G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77413865 | |||||||
chr7:77414069 | T | A | 81 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0002t0001g0020 others(78): Show |
82 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.109+2144A>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77414069 | |||||||
chr7:77414227 | A | C | 2 | a0003c0004t0002g0152 a0003c0004t0002g0153 |
2 | HG03098.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.109+1986T>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77414227 | |||||||
chr7:77414250 | A | T | 1 | a0003c0004t0002g0146 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.109+1963T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77414250 | |||||||
chr7:77414546 | A | G | 193 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0015 others(190): Show |
195 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.109+1667T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77414546 | |||||||
chr7:77414772 | T | C | 1 | a0001c0028t0002g0142 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.109+1441A>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77414772 | |||||||
chr7:77414844 | C | CTTTTT | 8 | a0001c0001t0001g0313 a0001c0001t0001g0314 a0001c0001t0001g0315 others(5): Show |
8 | HG02280.hp2 HG02451.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.109+1364_109+1368d others(7): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77414844 | |||||||
chr7:77414844 | C | CTTTTTT | 40 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0022 others(37): Show |
41 | HG00140.hp2 HG00609.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.109+1363_109+1368d others(8): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77414844 | |||||||
chr7:77414844 | C | CTTTTTTT | 50 | a0001c0001t0001g0018 a0001c0001t0001g0194 a0001c0001t0001g0195 others(47): Show |
50 | HG00408.hp1 HG00423.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.109+1362_109+1368d others(9): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77414844 | |||||||
chr7:77414844 | C | CTTTTTTT others(1): Show |
14 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0001c0002t0001g0193 others(11): Show |
14 | HG00544.hp2 HG00621.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.109+1361_109+1368d others(10): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77414844 | |||||||
chr7:77414844 | C | CTTTTTTT others(2): Show |
6 | a0001c0001t0001g0015 a0001c0001t0001g0231 a0001c0002t0001g0232 others(3): Show |
6 | HG00639.hp1 HG02630.hp1 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.109+1360_109+1368d others(11): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77414844 | |||||||
chr7:77414844 | C | CTTTTTTT others(3): Show |
1 | a0001c0002t0002g0140 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.109+1359_109+1368d others(12): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77414844 | |||||||
chr7:77414844 | C | CTTTTTTT others(5): Show |
3 | a0001c0002t0001g0230 a0006c0008t0001g0139 a0007c0011t0002g0138 |
3 | HG02165.hp2 HG02897.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.109+1357_109+1368d others(14): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77414844 | |||||||
chr7:77414844 | C | CTTTTTTT others(6): Show |
2 | a0006c0008t0001g0136 a0006c0008t0001g0137 |
2 | HG01074.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.109+1356_109+1368d others(15): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77414844 | |||||||
chr7:77414844 | C | CTTTTTTT others(7): Show |
3 | a0001c0002t0002g0135 a0003c0004t0001g0190 a0006c0008t0001g0017 |
3 | HG02523.hp2 HG02622.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.109+1355_109+1368d others(16): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77414844 | |||||||
chr7:77414844 | C | CTTTTTTT others(8): Show |
1 | a0006c0008t0001g0134 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.109+1354_109+1368d others(17): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77414844 | |||||||
chr7:77414844 | C | CTTTTTTT others(12): Show |
1 | a0003c0009t0001g0189 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.109+1350_109+1368d others(21): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77414844 | |||||||
chr7:77414844 | C | CTTTTTTT others(13): Show |
1 | a0003c0009t0001g0188 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.109+1349_109+1368d others(22): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77414844 | |||||||
chr7:77414844 | CTT | C | 6 | a0001c0010t0001g0149 a0001c0010t0001g0150 a0001c0010t0001g0151 others(3): Show |
6 | HG02683.hp1 HG03098.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.109+1367_109+1368d others(4): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77414844 | |||||||
chr7:77414844 | CTTT | C | 6 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0002t0004g0034 others(3): Show |
6 | HG00423.hp2 HG01243.hp1 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.109+1366_109+1368d others(5): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77414844 | |||||||
chr7:77414844 | CTTTT | C | 25 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0040 others(22): Show |
25 | HG00408.hp2 HG00735.hp1 HG01257.hp1 others(22): Show |
intron_variant | MODIFIER | c.109+1365_109+1368d others(6): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77414844 | |||||||
chr7:77414844 | CTTTTT | C | 106 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0056 others(103): Show |
109 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.109+1364_109+1368d others(7): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77414844 | |||||||
chr7:77414844 | CTTTTTT | C | 11 | a0001c0002t0001g0345 a0001c0002t0002g0125 a0001c0013t0001g0221 others(8): Show |
11 | HG00140.hp1 HG00733.hp2 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.109+1363_109+1368d others(8): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77414844 | |||||||
chr7:77414844 | CTTTTTTT | C | 10 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0011 others(7): Show |
10 | HG01192.hp2 HG01433.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.109+1362_109+1368d others(9): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77414844 | |||||||
chr7:77414844 | CTTTTTTT others(3): Show |
C | 1 | a0003c0004t0002g0156 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.109+1359_109+1368d others(12): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77414844 | |||||||
chr7:77414844 | CTTTTTTT others(4): Show |
C | 29 | a0001c0002t0001g0157 a0001c0002t0002g0182 a0004c0005t0001g0171 others(26): Show |
29 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.109+1358_109+1368d others(13): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77414844 | |||||||
chr7:77414844 | CTTTTTTT others(5): Show |
C | 1 | a0002c0003t0001g0224 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.109+1357_109+1368d others(14): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77414844 | |||||||
chr7:77414844 | CTTTTTTT others(6): Show |
C | 7 | a0001c0001t0001g0225 a0003c0004t0002g0132 a0003c0004t0002g0183 others(4): Show |
7 | HG01069.hp1 HG01891.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.109+1356_109+1368d others(15): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77414844 | |||||||
chr7:77414844 | CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0001g0226 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.109+1354_109+1368d others(17): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77414844 | |||||||
chr7:77414903 | G | C | 4 | a0003c0004t0001g0190 a0003c0009t0001g0188 a0003c0009t0001g0189 others(1): Show |
4 | HG02523.hp2 NA18939.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.109+1310C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77414903 | |||||||
chr7:77414904 | C | T | 3 | a0002c0007t0001g0227 a0002c0007t0001g0228 a0002c0007t0001g0229 |
3 | NA18978.hp2 NA18983.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.109+1309G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77414904 | |||||||
chr7:77415019 | A | G | 1 | a0003c0004t0002g0133 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.109+1194T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77415019 | |||||||
chr7:77415117 | C | T | 2 | a0001c0001t0001g0015 a0001c0010t0001g0016 |
2 | HG02630.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.109+1096G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77415117 | |||||||
chr7:77415131 | A | G | 162 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0015 others(159): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.109+1082T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77415131 | |||||||
chr7:77415137 | C | T | 6 | a0001c0002t0002g0009 a0001c0002t0002g0010 a0001c0002t0002g0011 others(3): Show |
6 | HG02451.hp1 HG02572.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.109+1076G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77415137 | |||||||
chr7:77415221 | A | T | 1 | a0001c0001t0001g0192 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.109+992T>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77415221 | |||||||
chr7:77415447 | T | G | 151 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(148): Show |
153 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.109+766A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77415447 | |||||||
chr7:77415515 | C | T | 1 | a0001c0001t0001g0008 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.109+698G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77415515 | |||||||
chr7:77415603 | G | A | 1 | a0003c0004t0002g0338 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.109+610C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77415603 | |||||||
chr7:77415675 | C | T | 1 | a0001c0002t0006g0007 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.109+538G>A | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77415675 | |||||||
chr7:77415675 | CCT | C | 4 | a0002c0003t0001g0005 a0003c0004t0002g0339 a0003c0004t0002g0340 others(1): Show |
5 | HG00280.hp2 HG00323.hp2 HG00642.hp1 others(2): Show |
intron_variant | MODIFIER | c.109+536_109+537del others(2): Show |
GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77415675 | |||||||
chr7:77415854 | G | C | 4 | a0001c0002t0001g0342 a0001c0002t0001g0343 a0001c0002t0001g0344 others(1): Show |
4 | HG01099.hp1 HG01168.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.109+359C>G | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77415854 | |||||||
chr7:77416055 | A | G | 1 | a0001c0001t0001g0006 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.109+158T>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77416055 | |||||||
chr7:77416160 | T | G | 1 | a0002c0003t0001g0346 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.109+53A>C | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77416160 | |||||||
chr7:77416195 | G | A | 1 | a0014c0017t0001g0347 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.109+18C>T | GSAP | ENSG00000186088.16 | transcript | ENST00000257626.12 | protein_coding | 1/30 | chr7 | 77416195 |