Item | Value |
---|---|
geneid | 257218 |
ensemblid | ENSG00000146414.17 |
hgncid | 19336 |
symbol | SHPRH |
name | SNF2 histone linker PHD RING helicase |
refseq_nuc | NM_001042683.3 |
refseq_prot | NP_001036148.2 |
ensembl_nuc | ENST00000275233.12 |
ensembl_prot | ENSP00000275233.7 |
mane_status | MANE Select |
chr | chr6 |
start | 145884807 |
end | 145964358 |
strand | - |
ver | v1.2 |
region | chr6:145884807-145964358 |
region5000 | chr6:145879807-145969358 |
regionname0 | SHPRH_chr6_145884807_145964358 |
regionname5000 | SHPRH_chr6_145879807_145969358 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1683 | 300 | 61 | 53 | 141 | 12 | 31 | 116 | SHPRH_chr6_145879807_145969358 | SHPRH | MSSRR others(1678): Show |
chr6 | 145879807 | 145969358 |
a0002 | 0/0 | 1683 | 17 | 15 | 2 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | MSSRR others(1678): Show |
chr6 | 145879807 | 145969358 |
a0003 | 0/0 | 1683 | 16 | 0 | 0 | 16 | 0 | 0 | 9 | SHPRH_chr6_145879807_145969358 | SHPRH | MSSRR others(1678): Show |
chr6 | 145879807 | 145969358 |
a0004 | 0/0 | 1683 | 6 | 0 | 0 | 6 | 0 | 0 | 4 | SHPRH_chr6_145879807_145969358 | SHPRH | MSSRR others(1678): Show |
chr6 | 145879807 | 145969358 |
a0005 | 0/0 | 1683 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | MSSRR others(1678): Show |
chr6 | 145879807 | 145969358 |
a0006 | 0/0 | 1683 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | MSSRR others(1678): Show |
chr6 | 145879807 | 145969358 |
a0007 | 0/0 | 1683 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | SHPRH_chr6_145879807_145969358 | SHPRH | MSSRR others(1678): Show |
chr6 | 145879807 | 145969358 |
a0008 | 0/0 | 1683 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | SHPRH_chr6_145879807_145969358 | SHPRH | MSSRR others(1678): Show |
chr6 | 145879807 | 145969358 |
a0009 | 0/0 | 1683 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | MSSRR others(1678): Show |
chr6 | 145879807 | 145969358 |
a0010 | 0/0 | 1683 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | MSSRR others(1678): Show |
chr6 | 145879807 | 145969358 |
a0011 | 0/0 | 1683 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | MSSRR others(1678): Show |
chr6 | 145879807 | 145969358 |
a0012 | 0/0 | 1683 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | MSSRR others(1678): Show |
chr6 | 145879807 | 145969358 |
a0013 | 0/0 | 1683 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | MSSRR others(1678): Show |
chr6 | 145879807 | 145969358 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 5049 | 203 | 36 | 44 | 91 | 9 | 22 | SHPRH_chr6_145879807_145969358 | SHPRH | ATGAG others(5044): Show |
chr6 | 145879807 | 145969358 | ||
a0001c0002 | 1/0 | 5049 | 69 | 3 | 8 | 46 | 3 | 8 | SHPRH_chr6_145879807_145969358 | SHPRH | ATGAG others(5044): Show |
chr6 | 145879807 | 145969358 | ||
a0001c0003 | 0/0 | 5049 | 22 | 21 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | ATGAG others(5044): Show |
chr6 | 145879807 | 145969358 | ||
a0001c0009 | 0/0 | 5049 | 2 | 0 | 0 | 2 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | ATGAG others(5044): Show |
chr6 | 145879807 | 145969358 | ||
a0001c0014 | 0/0 | 5049 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | ATGAG others(5044): Show |
chr6 | 145879807 | 145969358 | ||
a0001c0015 | 0/0 | 5049 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | ATGAG others(5044): Show |
chr6 | 145879807 | 145969358 | ||
a0001c0019 | 0/0 | 5049 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | ATGAG others(5044): Show |
chr6 | 145879807 | 145969358 | ||
a0001c0020 | 0/0 | 5049 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | ATGAG others(5044): Show |
chr6 | 145879807 | 145969358 | ||
a0002c0004 | 0/0 | 5049 | 17 | 15 | 2 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | ATGAG others(5044): Show |
chr6 | 145879807 | 145969358 | ||
a0003c0005 | 0/0 | 5049 | 16 | 0 | 0 | 16 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | ATGAG others(5044): Show |
chr6 | 145879807 | 145969358 | ||
a0004c0006 | 0/0 | 5049 | 6 | 0 | 0 | 6 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | ATGAG others(5044): Show |
chr6 | 145879807 | 145969358 | ||
a0005c0007 | 0/0 | 5049 | 4 | 4 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | ATGAG others(5044): Show |
chr6 | 145879807 | 145969358 | ||
a0006c0008 | 0/0 | 5049 | 2 | 1 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | ATGAG others(5044): Show |
chr6 | 145879807 | 145969358 | ||
a0007c0011 | 0/0 | 5049 | 2 | 0 | 0 | 2 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | ATGAG others(5044): Show |
chr6 | 145879807 | 145969358 | ||
a0008c0010 | 0/0 | 5049 | 2 | 0 | 0 | 2 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | ATGAG others(5044): Show |
chr6 | 145879807 | 145969358 | ||
a0009c0012 | 0/0 | 5049 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | ATGAG others(5044): Show |
chr6 | 145879807 | 145969358 | ||
a0010c0016 | 0/0 | 5049 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | ATGAG others(5044): Show |
chr6 | 145879807 | 145969358 | ||
a0011c0013 | 0/0 | 5049 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | ATGAG others(5044): Show |
chr6 | 145879807 | 145969358 | ||
a0012c0017 | 0/0 | 5049 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | ATGAG others(5044): Show |
chr6 | 145879807 | 145969358 | ||
a0013c0018 | 0/0 | 5049 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | ATGAG others(5044): Show |
chr6 | 145879807 | 145969358 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 7596 | 149 | 22 | 35 | 77 | 5 | 10 | SHPRH_chr6_145879807_145969358 | SHPRH | ACGCT others(7591): Show |
chr6 | 145879807 | 145969358 |
a0001c0001t0002 | 0/1 | 7597 | 21 | 11 | 3 | 1 | 0 | 5 | SHPRH_chr6_145879807_145969358 | SHPRH | ACGCT others(7592): Show |
chr6 | 145879807 | 145969358 |
a0001c0001t0004 | 0/0 | 7597 | 21 | 1 | 3 | 12 | 2 | 3 | SHPRH_chr6_145879807_145969358 | SHPRH | ACGCT others(7592): Show |
chr6 | 145879807 | 145969358 |
a0001c0001t0006 | 0/0 | 7596 | 8 | 0 | 3 | 0 | 1 | 4 | SHPRH_chr6_145879807_145969358 | SHPRH | ACGCT others(7591): Show |
chr6 | 145879807 | 145969358 |
a0001c0001t0010 | 0/0 | 7596 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | ACGCT others(7591): Show |
chr6 | 145879807 | 145969358 |
a0001c0001t0012 | 0/0 | 7597 | 1 | 0 | 0 | 0 | 1 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | ACGCT others(7592): Show |
chr6 | 145879807 | 145969358 |
a0001c0001t0015 | 0/0 | 7597 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | ACGCT others(7592): Show |
chr6 | 145879807 | 145969358 |
a0001c0001t0016 | 0/0 | 7597 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | ACGCT others(7592): Show |
chr6 | 145879807 | 145969358 |
a0001c0002t0002 | 0/0 | 7597 | 68 | 3 | 8 | 46 | 3 | 8 | SHPRH_chr6_145879807_145969358 | SHPRH | ACGCT others(7592): Show |
chr6 | 145879807 | 145969358 |
a0001c0002t0009 | 1/0 | 7596 | 1 | 0 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | ACGCT others(7591): Show |
chr6 | 145879807 | 145969358 |
a0001c0003t0003 | 0/0 | 7597 | 7 | 7 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | ACGCT others(7592): Show |
chr6 | 145879807 | 145969358 |
a0001c0003t0005 | 0/0 | 7597 | 14 | 13 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | ACGCT others(7592): Show |
chr6 | 145879807 | 145969358 |
a0001c0003t0009 | 0/0 | 7596 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | ACGCT others(7591): Show |
chr6 | 145879807 | 145969358 |
a0001c0009t0001 | 0/0 | 7596 | 2 | 0 | 0 | 2 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | ACGCT others(7591): Show |
chr6 | 145879807 | 145969358 |
a0001c0014t0001 | 0/0 | 7596 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | ACGCT others(7591): Show |
chr6 | 145879807 | 145969358 |
a0001c0015t0014 | 0/0 | 7597 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | ACGCT others(7592): Show |
chr6 | 145879807 | 145969358 |
a0001c0019t0001 | 0/0 | 7596 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | ACGCT others(7591): Show |
chr6 | 145879807 | 145969358 |
a0001c0020t0001 | 0/0 | 7596 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | ACGCT others(7591): Show |
chr6 | 145879807 | 145969358 |
a0002c0004t0003 | 0/0 | 7597 | 17 | 15 | 2 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | ACGCT others(7592): Show |
chr6 | 145879807 | 145969358 |
a0003c0005t0001 | 0/0 | 7596 | 15 | 0 | 0 | 15 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | ACGCT others(7591): Show |
chr6 | 145879807 | 145969358 |
a0003c0005t0011 | 0/0 | 7596 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | ACGCT others(7591): Show |
chr6 | 145879807 | 145969358 |
a0004c0006t0007 | 0/0 | 7597 | 6 | 0 | 0 | 6 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | ACGCT others(7592): Show |
chr6 | 145879807 | 145969358 |
a0005c0007t0001 | 0/0 | 7596 | 4 | 4 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | ACGCT others(7591): Show |
chr6 | 145879807 | 145969358 |
a0006c0008t0003 | 0/0 | 7597 | 2 | 1 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | ACGCT others(7592): Show |
chr6 | 145879807 | 145969358 |
a0007c0011t0008 | 0/0 | 7596 | 2 | 0 | 0 | 2 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | ACGCT others(7591): Show |
chr6 | 145879807 | 145969358 |
a0008c0010t0001 | 0/0 | 7596 | 2 | 0 | 0 | 2 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | ACGCT others(7591): Show |
chr6 | 145879807 | 145969358 |
a0009c0012t0001 | 0/0 | 7596 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | ACGCT others(7591): Show |
chr6 | 145879807 | 145969358 |
a0010c0016t0013 | 0/0 | 7597 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | ACGCT others(7592): Show |
chr6 | 145879807 | 145969358 |
a0011c0013t0005 | 0/0 | 7597 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | ACGCT others(7592): Show |
chr6 | 145879807 | 145969358 |
a0012c0017t0001 | 0/0 | 7596 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | ACGCT others(7591): Show |
chr6 | 145879807 | 145969358 |
a0013c0018t0002 | 0/0 | 7597 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | ACGCT others(7592): Show |
chr6 | 145879807 | 145969358 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0002g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0002g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0002g0181 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0004g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0004g0043 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0004g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0004g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0004g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0004g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0004g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0004g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0004g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0004g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0004g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0004g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0004g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0004g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0004g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0004g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0006g0046 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0006g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0006g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0006g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0006g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0006g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0006g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0010g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0012g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0015g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0001t0016g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0001 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0005 | 0/0 | 4 | 2 | 0 | 0 | 1 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0006 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0002t0009g0207 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0003t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0003t0003g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0003t0003g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0003t0003g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0003t0003g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0003t0003g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0003t0003g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0003t0005g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0003t0005g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0003t0005g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0003t0005g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0003t0005g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0003t0005g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0003t0005g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0003t0005g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0003t0005g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0003t0005g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0003t0005g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0003t0009g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0009t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0009t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0014t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0015t0014g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0019t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0001c0020t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0002c0004t0003g0008 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0002c0004t0003g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0002c0004t0003g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0002c0004t0003g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0002c0004t0003g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0002c0004t0003g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0002c0004t0003g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0002c0004t0003g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0002c0004t0003g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0002c0004t0003g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0002c0004t0003g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0003c0005t0001g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0003c0005t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0003c0005t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0003c0005t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0003c0005t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0003c0005t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0003c0005t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0003c0005t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0003c0005t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0003c0005t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0003c0005t0011g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0004c0006t0007g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0004c0006t0007g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0004c0006t0007g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0004c0006t0007g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0005c0007t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0005c0007t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0005c0007t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0005c0007t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0006c0008t0003g0044 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0007c0011t0008g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0008c0010t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0009c0012t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0010c0016t0013g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0011c0013t0005g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0012c0017t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
a0013c0018t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00280 | hp1 | a0001 | c0002 | t0002 | g0198 | EUR | FIN | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0083 | EUR | FIN | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | CHS | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | CHS | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | CHS | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | CHS | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG00609 | hp1 | a0003 | c0005 | t0001 | g0175 | EAS | CHS | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG00609 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | CHS | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | CHS | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG00639 | hp2 | a0001 | c0002 | t0002 | g0212 | AMR | PUR | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG00642 | hp2 | a0001 | c0001 | t0006 | g0273 | AMR | PUR | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG00735 | hp2 | a0001 | c0001 | t0006 | g0046 | AMR | PUR | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG00738 | hp2 | a0001 | c0002 | t0002 | g0215 | AMR | PUR | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG00741 | hp2 | a0001 | c0001 | t0006 | g0274 | AMR | PUR | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0216 | AMR | PUR | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01074 | hp1 | a0001 | c0001 | t0004 | g0246 | AMR | PUR | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01074 | hp2 | a0001 | c0002 | t0002 | g0006 | AMR | PUR | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01081 | hp1 | a0002 | c0004 | t0003 | g0265 | AMR | PUR | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01081 | hp2 | a0006 | c0008 | t0003 | g0044 | AMR | PUR | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01099 | hp1 | a0001 | c0002 | t0002 | g0197 | AMR | PUR | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0195 | AMR | PUR | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01109 | hp2 | a0001 | c0001 | t0004 | g0245 | AMR | PUR | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01192 | hp1 | a0001 | c0001 | t0004 | g0244 | AMR | PUR | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01255 | hp2 | a0001 | c0002 | t0002 | g0200 | AMR | CLM | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01257 | hp1 | a0001 | c0002 | t0002 | g0214 | AMR | CLM | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0224 | AMR | CLM | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01433 | hp1 | a0001 | c0003 | t0005 | g0052 | AMR | CLM | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0136 | EUR | IBS | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01515 | hp2 | a0001 | c0001 | t0004 | g0043 | EUR | IBS | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01516 | hp1 | a0001 | c0002 | t0002 | g0005 | EUR | IBS | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0018 | EUR | IBS | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01517 | hp1 | a0001 | c0001 | t0004 | g0043 | EUR | IBS | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0018 | EUR | IBS | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01884 | hp1 | a0002 | c0004 | t0003 | g0261 | AFR | ACB | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01884 | hp2 | a0001 | c0001 | t0004 | g0232 | AFR | ACB | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01891 | hp2 | a0001 | c0003 | t0003 | g0255 | AFR | ACB | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01993 | hp2 | a0001 | c0002 | t0002 | g0201 | AMR | PEL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02040 | hp2 | a0003 | c0005 | t0001 | g0003 | EAS | KHV | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0189 | AFR | ACB | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02055 | hp2 | a0001 | c0001 | t0016 | g0271 | AFR | ACB | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02056 | hp1 | a0001 | c0019 | t0001 | g0107 | EAS | KHV | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02056 | hp2 | a0001 | c0002 | t0002 | g0204 | EAS | KHV | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02074 | hp1 | a0001 | c0014 | t0001 | g0156 | EAS | KHV | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02132 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | KHV | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02132 | hp2 | a0003 | c0005 | t0001 | g0171 | EAS | KHV | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02135 | hp1 | a0003 | c0005 | t0001 | g0170 | EAS | KHV | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02135 | hp2 | a0004 | c0006 | t0007 | g0177 | EAS | KHV | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02145 | hp1 | a0002 | c0004 | t0003 | g0262 | AFR | ACB | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02145 | hp2 | a0001 | c0003 | t0003 | g0253 | AFR | ACB | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02155 | hp1 | a0003 | c0005 | t0001 | g0173 | EAS | CDX | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02155 | hp2 | a0004 | c0006 | t0007 | g0015 | EAS | CDX | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02165 | hp1 | a0003 | c0005 | t0011 | g0176 | EAS | CDX | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02165 | hp2 | a0001 | c0002 | t0002 | g0206 | EAS | CDX | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02257 | hp1 | a0001 | c0002 | t0002 | g0005 | AFR | ACB | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02451 | hp2 | a0006 | c0008 | t0003 | g0044 | AFR | ACB | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02572 | hp2 | a0001 | c0003 | t0005 | g0050 | AFR | GWD | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02602 | hp1 | a0001 | c0002 | t0002 | g0229 | SAS | PJL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0269 | AFR | GWD | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02622 | hp1 | a0001 | c0002 | t0002 | g0209 | AFR | GWD | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02630 | hp2 | a0002 | c0004 | t0003 | g0008 | AFR | GWD | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0191 | AFR | GWD | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02683 | hp2 | a0001 | c0001 | t0006 | g0275 | SAS | PJL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02717 | hp1 | a0001 | c0003 | t0005 | g0049 | AFR | GWD | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02717 | hp2 | a0001 | c0003 | t0009 | g0258 | AFR | GWD | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02723 | hp1 | a0002 | c0004 | t0003 | g0008 | AFR | GWD | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02735 | hp1 | a0009 | c0012 | t0001 | g0092 | SAS | PJL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02735 | hp2 | a0010 | c0016 | t0013 | g0217 | SAS | PJL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02809 | hp1 | a0005 | c0007 | t0001 | g0091 | AFR | GWD | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02809 | hp2 | a0001 | c0003 | t0005 | g0048 | AFR | GWD | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02818 | hp2 | a0001 | c0003 | t0005 | g0053 | AFR | GWD | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02886 | hp2 | a0002 | c0004 | t0003 | g0266 | AFR | GWD | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0038 | AFR | GWD | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02895 | hp2 | a0001 | c0003 | t0005 | g0017 | AFR | GWD | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0038 | AFR | GWD | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02896 | hp2 | a0002 | c0004 | t0003 | g0016 | AFR | GWD | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02897 | hp1 | a0002 | c0004 | t0003 | g0016 | AFR | GWD | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02897 | hp2 | a0001 | c0003 | t0005 | g0017 | AFR | GWD | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02965 | hp1 | a0011 | c0013 | t0005 | g0055 | AFR | ESN | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02970 | hp1 | a0001 | c0003 | t0005 | g0009 | AFR | ESN | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02970 | hp2 | a0002 | c0004 | t0003 | g0259 | AFR | ESN | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0268 | AFR | ESN | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02976 | hp2 | a0002 | c0004 | t0003 | g0045 | AFR | ESN | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03017 | hp1 | a0001 | c0002 | t0002 | g0231 | SAS | PJL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03017 | hp2 | a0001 | c0020 | t0001 | g0059 | SAS | PJL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03041 | hp1 | a0001 | c0003 | t0003 | g0252 | AFR | GWD | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03041 | hp2 | a0001 | c0003 | t0005 | g0009 | AFR | GWD | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | MSL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03098 | hp2 | a0001 | c0001 | t0015 | g0270 | AFR | MSL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ESN | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03195 | hp1 | a0001 | c0003 | t0003 | g0254 | AFR | ESN | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03195 | hp2 | a0001 | c0003 | t0005 | g0056 | AFR | ESN | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03209 | hp1 | a0001 | c0003 | t0005 | g0054 | AFR | MSL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03209 | hp2 | a0001 | c0015 | t0014 | g0250 | AFR | MSL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | MSL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03225 | hp2 | a0001 | c0003 | t0003 | g0257 | AFR | MSL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03239 | hp1 | a0001 | c0002 | t0002 | g0226 | SAS | PJL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03453 | hp1 | a0001 | c0003 | t0005 | g0051 | AFR | MSL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03453 | hp2 | a0001 | c0003 | t0003 | g0256 | AFR | MSL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03486 | hp1 | a0001 | c0003 | t0003 | g0251 | AFR | MSL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0190 | AFR | MSL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0228 | SAS | PJL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ESN | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0193 | AFR | ESN | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0194 | AFR | GWD | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03540 | hp2 | a0005 | c0007 | t0001 | g0090 | AFR | GWD | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03579 | hp1 | a0002 | c0004 | t0003 | g0260 | AFR | MSL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03579 | hp2 | a0005 | c0007 | t0001 | g0089 | AFR | MSL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03654 | hp2 | a0001 | c0002 | t0002 | g0213 | SAS | PJL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03669 | hp1 | a0001 | c0001 | t0006 | g0046 | SAS | PJL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03669 | hp2 | a0012 | c0017 | t0001 | g0098 | SAS | PJL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0210 | SAS | PJL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03704 | hp2 | a0001 | c0001 | t0006 | g0277 | SAS | PJL | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0039 | SAS | BEB | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | BEB | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03927 | hp1 | a0001 | c0001 | t0004 | g0241 | SAS | BEB | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03927 | hp2 | a0001 | c0002 | t0002 | g0196 | SAS | BEB | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03942 | hp1 | a0001 | c0002 | t0002 | g0005 | SAS | BEB | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | BEB | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | STU | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG04115 | hp2 | a0001 | c0002 | t0002 | g0006 | SAS | STU | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG04184 | hp1 | a0001 | c0002 | t0002 | g0225 | SAS | BEB | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0039 | SAS | BEB | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG04199 | hp1 | a0001 | c0001 | t0006 | g0272 | SAS | STU | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | STU | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0227 | SAS | STU | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG04204 | hp2 | a0001 | c0001 | t0004 | g0239 | SAS | STU | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18612 | hp1 | a0003 | c0005 | t0001 | g0169 | EAS | CHB | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CHB | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18747 | hp1 | a0001 | c0001 | t0010 | g0079 | EAS | CHB | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | CHB | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18906 | hp1 | a0005 | c0007 | t0001 | g0088 | AFR | YRI | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18906 | hp2 | a0002 | c0004 | t0003 | g0263 | AFR | YRI | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18939 | hp1 | a0001 | c0002 | t0002 | g0180 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18942 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18948 | hp2 | a0001 | c0001 | t0004 | g0234 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18950 | hp1 | a0001 | c0002 | t0002 | g0187 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18951 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18952 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18952 | hp2 | a0001 | c0009 | t0001 | g0085 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18953 | hp1 | a0007 | c0011 | t0008 | g0031 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18953 | hp2 | a0001 | c0002 | t0002 | g0183 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18956 | hp1 | a0001 | c0002 | t0002 | g0042 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18957 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18959 | hp1 | a0001 | c0002 | t0002 | g0182 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18960 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18963 | hp1 | a0004 | c0006 | t0007 | g0178 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18964 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18965 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18966 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18968 | hp2 | a0001 | c0002 | t0002 | g0221 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18970 | hp2 | a0001 | c0002 | t0002 | g0218 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18973 | hp1 | a0001 | c0002 | t0002 | g0040 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18977 | hp1 | a0001 | c0002 | t0002 | g0202 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18977 | hp2 | a0001 | c0009 | t0001 | g0063 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18979 | hp1 | a0001 | c0002 | t0002 | g0184 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18982 | hp1 | a0001 | c0001 | t0004 | g0238 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18984 | hp1 | a0003 | c0005 | t0001 | g0003 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18984 | hp2 | a0001 | c0002 | t0002 | g0041 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18986 | hp1 | a0003 | c0005 | t0001 | g0035 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18986 | hp2 | a0003 | c0005 | t0001 | g0116 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18988 | hp1 | a0001 | c0002 | t0002 | g0036 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18988 | hp2 | a0001 | c0001 | t0004 | g0242 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18990 | hp2 | a0001 | c0002 | t0002 | g0199 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18991 | hp1 | a0001 | c0002 | t0002 | g0203 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18997 | hp2 | a0001 | c0002 | t0002 | g0211 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18998 | hp2 | a0001 | c0002 | t0002 | g0042 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18999 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19000 | hp2 | a0001 | c0002 | t0002 | g0036 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19001 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19002 | hp1 | a0003 | c0005 | t0001 | g0003 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19002 | hp2 | a0004 | c0006 | t0007 | g0015 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19003 | hp2 | a0004 | c0006 | t0007 | g0179 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19007 | hp1 | a0007 | c0011 | t0008 | g0031 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19007 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19009 | hp2 | a0001 | c0002 | t0002 | g0188 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19010 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19011 | hp2 | a0001 | c0002 | t0002 | g0186 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | LWK | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19043 | hp2 | a0001 | c0003 | t0005 | g0047 | AFR | LWK | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19055 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19055 | hp2 | a0003 | c0005 | t0001 | g0172 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19056 | hp1 | a0001 | c0002 | t0002 | g0248 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19056 | hp2 | a0003 | c0005 | t0001 | g0003 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19057 | hp2 | a0003 | c0005 | t0001 | g0174 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19058 | hp1 | a0001 | c0002 | t0002 | g0041 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19060 | hp2 | a0001 | c0002 | t0002 | g0037 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19064 | hp1 | a0001 | c0002 | t0002 | g0223 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19065 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19065 | hp2 | a0008 | c0010 | t0001 | g0034 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19066 | hp2 | a0013 | c0018 | t0002 | g0230 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19070 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19072 | hp1 | a0001 | c0002 | t0002 | g0219 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19074 | hp2 | a0003 | c0005 | t0001 | g0003 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19076 | hp2 | a0001 | c0002 | t0002 | g0220 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19077 | hp2 | a0001 | c0002 | t0002 | g0185 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19079 | hp1 | a0001 | c0002 | t0002 | g0037 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19081 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19081 | hp2 | a0004 | c0006 | t0007 | g0015 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19082 | hp2 | a0001 | c0001 | t0004 | g0235 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19084 | hp1 | a0001 | c0002 | t0002 | g0222 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19084 | hp2 | a0001 | c0001 | t0004 | g0236 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19085 | hp1 | a0003 | c0005 | t0001 | g0035 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19087 | hp1 | a0008 | c0010 | t0001 | g0034 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19087 | hp2 | a0001 | c0002 | t0002 | g0040 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19088 | hp1 | a0001 | c0001 | t0004 | g0233 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19089 | hp1 | a0001 | c0001 | t0004 | g0243 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19091 | hp1 | a0001 | c0001 | t0004 | g0237 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA20129 | hp1 | a0002 | c0004 | t0003 | g0016 | AFR | ASW | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0267 | AFR | ASW | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA20752 | hp1 | a0001 | c0001 | t0012 | g0240 | EUR | TSI | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0093 | EUR | TSI | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA20805 | hp1 | a0001 | c0002 | t0002 | g0205 | EUR | TSI | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA20805 | hp2 | a0001 | c0001 | t0006 | g0276 | EUR | TSI | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | GIH | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA20905 | hp2 | a0001 | c0001 | t0004 | g0247 | SAS | GIH | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01123 | hp1 | a0001 | c0002 | t0002 | g0208 | AMR | CLM | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG01123 | hp2 | a0002 | c0004 | t0003 | g0008 | AMR | CLM | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02109 | hp1 | a0002 | c0004 | t0003 | g0045 | AFR | ACB | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0192 | AFR | ACB | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02486 | hp1 | a0002 | c0004 | t0003 | g0008 | AFR | ACB | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG02559 | hp2 | a0002 | c0004 | t0003 | g0264 | AFR | ACB | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | USA | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
HG06807 | hp2 | a0001 | c0003 | t0005 | g0009 | AFR | USA | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18955 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | LWK | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
NA21309 | hp2 | a0001 | c0002 | t0002 | g0005 | AFR | LWK | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0181 | REF | REF | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
homoSapiens | grch38p0 | a0001 | c0002 | t0009 | g0207 | REF | REF | SHPRH_chr6_145879807_145969358 | SHPRH | chr6 | 145879807 | 145969358 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:145921337 | C | T | 1 | a0013 | 1 | NA19066.hp2 | missense_variant | MODERATE | c.3838G>A | p.Val1280Met | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 21/30 | 4498/7596 | 3838/5052 | 1280/1683 | chr6 | 145921337 | |||
chr6:145921378 | G | A | 1 | a0011 | 1 | HG02965.hp1 | missense_variant | MODERATE | c.3797C>T | p.Thr1266Ile | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 21/30 | 4457/7596 | 3797/5052 | 1266/1683 | chr6 | 145921378 | |||
chr6:145921385 | C | T | 1 | a0012 | 1 | HG03669.hp2 | missense_variant | MODERATE | c.3790G>A | p.Gly1264Ser | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 21/30 | 4450/7596 | 3790/5052 | 1264/1683 | chr6 | 145921385 | |||
chr6:145922780 | T | C | 2 | a0003 a0008 |
18 | HG00609.hp1 HG02040.hp2 HG02132.hp2 others(15): Show |
missense_variant | MODERATE | c.3602A>G | p.Asn1201Ser | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 19/30 | 4262/7596 | 3602/5052 | 1201/1683 | chr6 | 145922780 | |||
chr6:145922825 | C | T | 1 | a0010 | 1 | HG02735.hp2 | missense_variant | MODERATE | c.3557G>A | p.Cys1186Tyr | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 19/30 | 4217/7596 | 3557/5052 | 1186/1683 | chr6 | 145922825 | |||
chr6:145941835 | G | T | 1 | a0006 | 2 | HG01081.hp2 HG02451.hp2 |
missense_variant | MODERATE | c.2278C>A | p.His760Asn | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 10/30 | 2938/7596 | 2278/5052 | 760/1683 | chr6 | 145941835 | |||
chr6:145943474 | A | G | 1 | a0008 | 2 | NA19065.hp2 NA19087.hp1 |
missense_variant | MODERATE | c.1907T>C | p.Leu636Pro | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 9/30 | 2567/7596 | 1907/5052 | 636/1683 | chr6 | 145943474 | |||
chr6:145943606 | A | C | 1 | a0002 | 17 | HG01081.hp1 HG01123.hp2 HG01884.hp1 others(14): Show |
missense_variant | MODERATE | c.1775T>G | p.Phe592Cys | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 9/30 | 2435/7596 | 1775/5052 | 592/1683 | chr6 | 145943606 | |||
chr6:145952478 | C | T | 1 | a0009 | 1 | HG02735.hp1 | missense_variant&splice_region_variant | MODERATE | c.634G>A | p.Val212Ile | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 3/30 | 1294/7596 | 634/5052 | 212/1683 | chr6 | 145952478 | |||
chr6:145954829 | T | C | 1 | a0007 | 2 | NA18953.hp1 NA19007.hp1 |
missense_variant | MODERATE | c.494A>G | p.Lys165Arg | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 2/30 | 1154/7596 | 494/5052 | 165/1683 | chr6 | 145954829 | |||
chr6:145954847 | T | G | 1 | a0004 | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
missense_variant | MODERATE | c.476A>C | p.Asp159Ala | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 2/30 | 1136/7596 | 476/5052 | 159/1683 | chr6 | 145954847 | |||
chr6:145955144 | C | T | 1 | a0005 | 4 | HG02809.hp1 HG03540.hp2 HG03579.hp2 others(1): Show |
missense_variant | MODERATE | c.179G>A | p.Ser60Asn | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 2/30 | 839/7596 | 179/5052 | 60/1683 | chr6 | 145955144 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:145910484 | T | C | 1 | a0001c0019 | 1 | HG02056.hp1 | synonymous_variant | LOW | c.4479A>G | p.Ser1493Ser | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/30 | 5139/7596 | 4479/5052 | 1493/1683 | chr6 | 145910484 | |||
chr6:145913508 | G | A | 17 | a0001c0001 a0001c0003 a0001c0009 others(14): Show |
282 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(279): Show |
synonymous_variant | LOW | c.4296C>T | p.Cys1432Cys | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/30 | 4956/7596 | 4296/5052 | 1432/1683 | chr6 | 145913508 | |||
chr6:145940766 | A | G | 1 | a0001c0015 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.2526T>C | p.Asn842Asn | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/30 | 3186/7596 | 2526/5052 | 842/1683 | chr6 | 145940766 | |||
chr6:145943344 | C | T | 1 | a0001c0014 | 1 | HG02074.hp1 | synonymous_variant | LOW | c.2037G>A | p.Lys679Lys | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 9/30 | 2697/7596 | 2037/5052 | 679/1683 | chr6 | 145943344 | |||
chr6:145943452 | T | G | 1 | a0001c0020 | 1 | HG03017.hp2 | synonymous_variant | LOW | c.1929A>C | p.Val643Val | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 9/30 | 2589/7596 | 1929/5052 | 643/1683 | chr6 | 145943452 | |||
chr6:145946315 | C | T | 1 | a0001c0009 | 2 | NA18952.hp2 NA18977.hp2 |
synonymous_variant | LOW | c.1239G>A | p.Pro413Pro | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 7/30 | 1899/7596 | 1239/5052 | 413/1683 | chr6 | 145946315 | |||
chr6:145950340 | A | G | 4 | a0001c0003 a0002c0004 a0006c0008 others(1): Show |
42 | HG01081.hp1 HG01081.hp2 HG01123.hp2 others(39): Show |
synonymous_variant | LOW | c.906T>C | p.Pro302Pro | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 4/30 | 1566/7596 | 906/5052 | 302/1683 | chr6 | 145950340 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:145884837 | G | T | 11 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(8): Show |
129 | HG00280.hp1 HG00609.hp2 HG00639.hp2 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*1854C>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 30/30 | 1854 | chr6 | 145884837 | ||||||
chr6:145884865 | G | A | 3 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0012 |
30 | HG00642.hp2 HG00735.hp2 HG00741.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*1826C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 30/30 | 1826 | chr6 | 145884865 | ||||||
chr6:145884950 | A | T | 1 | a0007c0011t0008 | 2 | NA18953.hp1 NA19007.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1741T>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 30/30 | 1741 | chr6 | 145884950 | ||||||
chr6:145885137 | A | G | 1 | a0001c0001t0016 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1554T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 30/30 | 1554 | chr6 | 145885137 | ||||||
chr6:145885458 | G | C | 1 | a0001c0001t0010 | 1 | NA18747.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1233C>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 30/30 | 1233 | chr6 | 145885458 | ||||||
chr6:145886119 | A | C | 1 | a0010c0016t0013 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*572T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 30/30 | 572 | chr6 | 145886119 | ||||||
chr6:145886329 | A | G | 10 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(7): Show |
123 | HG00280.hp1 HG00609.hp2 HG00639.hp2 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*362T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 30/30 | 362 | chr6 | 145886329 | ||||||
chr6:145886366 | G | GT | 16 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(13): Show |
170 | HG00280.hp1 HG00609.hp2 HG00639.hp2 others(167): Show |
3_prime_UTR_variant | MODIFIER | c.*324dupA | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 30/30 | 324 | chr6 | 145886366 | ||||||
chr6:145886372 | T | G | 1 | a0004c0006t0007 | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*319A>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 30/30 | 319 | chr6 | 145886372 | ||||||
chr6:145886427 | A | G | 11 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(8): Show |
129 | HG00280.hp1 HG00609.hp2 HG00639.hp2 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*264T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 30/30 | 264 | chr6 | 145886427 | ||||||
chr6:145886521 | A | C | 11 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(8): Show |
129 | HG00280.hp1 HG00609.hp2 HG00639.hp2 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*170T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 30/30 | 170 | chr6 | 145886521 | ||||||
chr6:145886550 | T | C | 3 | a0001c0001t0015 a0001c0001t0016 a0001c0015t0014 |
3 | HG02055.hp2 HG03098.hp2 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*141A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 30/30 | 141 | chr6 | 145886550 | ||||||
chr6:145886661 | C | T | 1 | a0001c0001t0012 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*30G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 30/30 | 30 | chr6 | 145886661 | ||||||
chr6:145963790 | C | T | 1 | a0001c0001t0015 | 1 | HG03098.hp2 | 5_prime_UTR_variant | MODIFIER | c.-92G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/30 | 8468 | chr6 | 145963790 | ||||||
chr6:145963827 | G | A | 1 | a0003c0005t0011 | 1 | HG02165.hp1 | 5_prime_UTR_variant | MODIFIER | c.-129C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/30 | 8505 | chr6 | 145963827 | ||||||
chr6:145964065 | C | G | 1 | a0004c0006t0007 | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-367G>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/30 | 8743 | chr6 | 145964065 | ||||||
chr6:145964068 | C | A | 13 | a0001c0001t0001 a0001c0001t0010 a0001c0009t0001 others(10): Show |
181 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(178): Show |
5_prime_UTR_variant | MODIFIER | c.-370G>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/30 | 8746 | chr6 | 145964068 | ||||||
chr6:145964069 | C | T | 13 | a0001c0001t0001 a0001c0001t0010 a0001c0009t0001 others(10): Show |
181 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(178): Show |
5_prime_UTR_variant | MODIFIER | c.-371G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/30 | 8747 | chr6 | 145964069 | ||||||
chr6:145964078 | T | G | 2 | a0001c0001t0015 a0001c0001t0016 |
2 | HG02055.hp2 HG03098.hp2 |
5_prime_UTR_variant | MODIFIER | c.-380A>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/30 | 8756 | chr6 | 145964078 | ||||||
chr6:145964089 | G | T | 2 | a0001c0003t0005 a0011c0013t0005 |
15 | HG01433.hp1 HG02572.hp2 HG02717.hp1 others(12): Show |
5_prime_UTR_variant | MODIFIER | c.-391C>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/30 | 8767 | chr6 | 145964089 | ||||||
chr6:145964302 | GT | G | 1 | a0001c0001t0006 | 8 | HG00642.hp2 HG00735.hp2 HG00741.hp2 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-605delA | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/30 | 8981 | chr6 | 145964302 | ||||||
chr6:145964303 | TC | T | 1 | a0004c0006t0007 | 6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-606delG | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/30 | 8982 | chr6 | 145964303 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:145886844 | A | G | 1 | a0001c0001t0001g0075 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.4956-57T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 29/29 | chr6 | 145886844 | |||||||
chr6:145886975 | T | A | 1 | a0001c0001t0001g0065 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.4956-188A>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 29/29 | chr6 | 145886975 | |||||||
chr6:145886984 | T | G | 98 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0189 others(95): Show |
129 | HG00280.hp1 HG00609.hp2 HG00639.hp2 others(126): Show |
intron_variant | MODIFIER | c.4956-197A>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 29/29 | chr6 | 145886984 | |||||||
chr6:145887027 | G | C | 3 | a0001c0003t0003g0251 a0001c0003t0003g0252 a0001c0003t0003g0253 |
3 | HG02145.hp2 HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.4956-240C>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 29/29 | chr6 | 145887027 | |||||||
chr6:145887265 | T | A | 3 | a0001c0001t0001g0119 a0001c0001t0001g0132 a0001c0001t0001g0133 |
3 | HG00738.hp1 HG02683.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.4956-478A>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 29/29 | chr6 | 145887265 | |||||||
chr6:145887529 | G | GT | 14 | a0001c0001t0001g0095 a0001c0001t0002g0193 a0001c0001t0002g0195 others(11): Show |
16 | HG01109.hp1 HG01109.hp2 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.4955+490dupA | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 29/29 | chr6 | 145887529 | |||||||
chr6:145887532 | TG | T | 5 | a0001c0001t0002g0192 a0001c0001t0002g0210 a0001c0001t0002g0268 others(2): Show |
5 | HG02109.hp2 HG02976.hp1 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.4955+487delC | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 29/29 | chr6 | 145887532 | |||||||
chr6:145887533 | G | GT | 38 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0021 others(35): Show |
47 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.4955+486dupA | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 29/29 | chr6 | 145887533 | |||||||
chr6:145887533 | G | GTT | 5 | a0001c0001t0001g0010 a0001c0001t0001g0070 a0001c0001t0001g0096 others(2): Show |
6 | HG01981.hp2 HG02109.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.4955+485_4955+486d others(4): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 29/29 | chr6 | 145887533 | |||||||
chr6:145887533 | G | T | 96 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0145 others(93): Show |
127 | HG00280.hp1 HG00609.hp2 HG00639.hp2 others(124): Show |
intron_variant | MODIFIER | c.4955+487C>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 29/29 | chr6 | 145887533 | |||||||
chr6:145887533 | GT | G | 12 | a0001c0001t0001g0011 a0001c0001t0001g0123 a0001c0003t0003g0257 others(9): Show |
17 | HG01081.hp1 HG01123.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.4955+486delA | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 29/29 | chr6 | 145887533 | |||||||
chr6:145887535 | T | G | 1 | a0001c0001t0001g0114 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.4955+485A>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 29/29 | chr6 | 145887535 | |||||||
chr6:145887606 | G | A | 2 | a0001c0003t0003g0254 a0001c0003t0003g0255 |
2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.4955+414C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 29/29 | chr6 | 145887606 | |||||||
chr6:145887627 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.4955+393G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 29/29 | chr6 | 145887627 | |||||||
chr6:145887628 | G | A | 2 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
2 | HG01069.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.4955+392C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 29/29 | chr6 | 145887628 | |||||||
chr6:145887639 | G | C | 1 | a0001c0001t0001g0102 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.4955+381C>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 29/29 | chr6 | 145887639 | |||||||
chr6:145887655 | C | T | 1 | a0001c0002t0002g0226 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.4955+365G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 29/29 | chr6 | 145887655 | |||||||
chr6:145887673 | C | T | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4955+347G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 29/29 | chr6 | 145887673 | |||||||
chr6:145887687 | A | G | 1 | a0001c0003t0003g0257 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.4955+333T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 29/29 | chr6 | 145887687 | |||||||
chr6:145887801 | T | G | 98 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0189 others(95): Show |
129 | HG00280.hp1 HG00609.hp2 HG00639.hp2 others(126): Show |
intron_variant | MODIFIER | c.4955+219A>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 29/29 | chr6 | 145887801 | |||||||
chr6:145888237 | G | A | 1 | a0001c0001t0001g0121 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.4875-137C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145888237 | |||||||
chr6:145888287 | A | C | 2 | a0001c0001t0001g0025 a0001c0001t0001g0117 |
3 | HG00642.hp1 HG01257.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.4875-187T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145888287 | |||||||
chr6:145888534 | C | T | 23 | a0001c0001t0001g0029 a0001c0001t0001g0097 a0001c0001t0001g0165 others(20): Show |
28 | HG00735.hp1 HG01081.hp2 HG01433.hp1 others(25): Show |
intron_variant | MODIFIER | c.4875-434G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145888534 | |||||||
chr6:145888626 | C | T | 30 | a0001c0003t0003g0251 a0001c0003t0003g0252 a0001c0003t0003g0253 others(27): Show |
40 | HG01081.hp1 HG01081.hp2 HG01123.hp2 others(37): Show |
intron_variant | MODIFIER | c.4875-526G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145888626 | |||||||
chr6:145888890 | G | A | 1 | a0001c0001t0001g0068 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.4875-790C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145888890 | |||||||
chr6:145888893 | T | C | 2 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
2 | HG01069.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.4875-793A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145888893 | |||||||
chr6:145888927 | G | A | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | HG02572.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.4875-827C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145888927 | |||||||
chr6:145888975 | T | C | 1 | a0005c0007t0001g0088 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.4875-875A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145888975 | |||||||
chr6:145889004 | G | A | 18 | a0001c0003t0003g0251 a0001c0003t0003g0252 a0001c0003t0003g0253 others(15): Show |
22 | HG01081.hp2 HG01433.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.4875-904C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145889004 | |||||||
chr6:145889397 | A | G | 1 | a0001c0002t0002g0200 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.4875-1297T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145889397 | |||||||
chr6:145889488 | T | C | 1 | a0001c0015t0014g0250 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4875-1388A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145889488 | |||||||
chr6:145889527 | C | A | 1 | a0001c0001t0001g0030 | 2 | HG01891.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.4875-1427G>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145889527 | |||||||
chr6:145889863 | C | A | 1 | a0001c0001t0001g0057 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.4875-1763G>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145889863 | |||||||
chr6:145889964 | G | A | 1 | a0001c0003t0003g0256 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.4875-1864C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145889964 | |||||||
chr6:145890009 | T | C | 1 | a0001c0002t0002g0199 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.4875-1909A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145890009 | |||||||
chr6:145890047 | A | C | 1 | a0001c0015t0014g0250 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4875-1947T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145890047 | |||||||
chr6:145890069 | C | G | 2 | a0001c0003t0005g0017 a0001c0003t0005g0050 |
3 | HG02572.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.4875-1969G>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145890069 | |||||||
chr6:145890290 | C | T | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4875-2190G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145890290 | |||||||
chr6:145890339 | T | A | 2 | a0004c0006t0007g0015 a0004c0006t0007g0177 |
4 | HG02135.hp2 HG02155.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.4875-2239A>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145890339 | |||||||
chr6:145890386 | T | A | 1 | a0001c0015t0014g0250 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4875-2286A>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145890386 | |||||||
chr6:145890488 | C | T | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4875-2388G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145890488 | |||||||
chr6:145890499 | T | C | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4875-2399A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145890499 | |||||||
chr6:145890697 | T | C | 31 | a0001c0003t0003g0251 a0001c0003t0003g0252 a0001c0003t0003g0253 others(28): Show |
41 | HG01081.hp1 HG01081.hp2 HG01123.hp2 others(38): Show |
intron_variant | MODIFIER | c.4874+2518A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145890697 | |||||||
chr6:145890787 | G | C | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4874+2428C>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145890787 | |||||||
chr6:145890867 | G | C | 1 | a0006c0008t0003g0044 | 2 | HG01081.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.4874+2348C>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145890867 | |||||||
chr6:145890924 | C | T | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4874+2291G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145890924 | |||||||
chr6:145890929 | T | C | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4874+2286A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145890929 | |||||||
chr6:145890963 | T | A | 1 | a0001c0001t0002g0269 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.4874+2252A>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145890963 | |||||||
chr6:145890964 | T | C | 1 | a0001c0001t0002g0269 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.4874+2251A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145890964 | |||||||
chr6:145890977 | GGATGACT others(4): Show |
G | 1 | a0001c0001t0002g0269 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.4874+2227_4874+223 others(15): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145890977 | |||||||
chr6:145890989 | T | A | 1 | a0001c0001t0002g0269 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.4874+2226A>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145890989 | |||||||
chr6:145890999 | G | C | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4874+2216C>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145890999 | |||||||
chr6:145891115 | A | C | 2 | a0001c0003t0003g0254 a0001c0003t0003g0255 |
2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.4874+2100T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145891115 | |||||||
chr6:145891149 | A | G | 98 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0189 others(95): Show |
129 | HG00280.hp1 HG00609.hp2 HG00639.hp2 others(126): Show |
intron_variant | MODIFIER | c.4874+2066T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145891149 | |||||||
chr6:145891202 | T | C | 131 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0002g0038 others(128): Show |
172 | HG00280.hp1 HG00609.hp2 HG00639.hp2 others(169): Show |
intron_variant | MODIFIER | c.4874+2013A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145891202 | |||||||
chr6:145891459 | A | G | 2 | a0003c0005t0001g0035 a0003c0005t0001g0174 |
3 | NA18986.hp1 NA19057.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.4874+1756T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145891459 | |||||||
chr6:145891501 | C | G | 1 | a0001c0001t0001g0061 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4874+1714G>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145891501 | |||||||
chr6:145891537 | C | T | 2 | a0001c0003t0003g0254 a0001c0003t0003g0255 |
2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.4874+1678G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145891537 | |||||||
chr6:145891591 | T | C | 2 | a0001c0003t0003g0254 a0001c0003t0003g0255 |
2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.4874+1624A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145891591 | |||||||
chr6:145891621 | G | A | 3 | a0001c0003t0003g0251 a0001c0003t0003g0252 a0001c0003t0003g0253 |
3 | HG02145.hp2 HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.4874+1594C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145891621 | |||||||
chr6:145891773 | T | C | 1 | a0001c0003t0003g0256 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.4874+1442A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145891773 | |||||||
chr6:145892192 | C | T | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4874+1023G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145892192 | |||||||
chr6:145892519 | G | A | 10 | a0002c0004t0003g0008 a0002c0004t0003g0016 a0002c0004t0003g0045 others(7): Show |
16 | HG01081.hp1 HG01123.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.4874+696C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145892519 | |||||||
chr6:145892569 | TC | T | 3 | a0001c0001t0002g0268 a0001c0001t0002g0269 a0001c0003t0003g0254 |
3 | HG02615.hp1 HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.4874+645delG | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145892569 | |||||||
chr6:145892570 | C | T | 126 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0189 others(123): Show |
167 | HG00280.hp1 HG00609.hp2 HG00639.hp2 others(164): Show |
intron_variant | MODIFIER | c.4874+645G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145892570 | |||||||
chr6:145892596 | A | G | 3 | a0001c0003t0003g0251 a0001c0003t0003g0252 a0001c0003t0003g0253 |
3 | HG02145.hp2 HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.4874+619T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145892596 | |||||||
chr6:145893008 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.4874+207C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 28/29 | chr6 | 145893008 | |||||||
chr6:145893427 | G | A | 2 | a0001c0001t0001g0101 a0001c0001t0001g0122 |
2 | NA18950.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.4696-34C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 27/29 | chr6 | 145893427 | |||||||
chr6:145893446 | AGTAT | A | 3 | a0001c0001t0015g0270 a0001c0001t0016g0271 a0001c0015t0014g0250 |
3 | HG02055.hp2 HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.4696-57_4696-54del others(4): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 27/29 | chr6 | 145893446 | |||||||
chr6:145893517 | C | A | 1 | a0001c0015t0014g0250 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4696-124G>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 27/29 | chr6 | 145893517 | |||||||
chr6:145893564 | A | C | 2 | a0001c0001t0015g0270 a0001c0001t0016g0271 |
2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.4696-171T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 27/29 | chr6 | 145893564 | |||||||
chr6:145893617 | T | G | 2 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
2 | HG01069.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.4696-224A>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 27/29 | chr6 | 145893617 | |||||||
chr6:145893749 | C | G | 1 | a0001c0001t0001g0071 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.4696-356G>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 27/29 | chr6 | 145893749 | |||||||
chr6:145893772 | C | T | 3 | a0001c0001t0001g0099 a0001c0001t0001g0114 a0001c0001t0001g0154 |
3 | HG01928.hp2 NA18998.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.4695+378G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 27/29 | chr6 | 145893772 | |||||||
chr6:145893773 | G | A | 1 | a0001c0001t0002g0267 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.4695+377C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 27/29 | chr6 | 145893773 | |||||||
chr6:145893788 | G | A | 3 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0145 |
3 | HG02572.hp1 HG03098.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.4695+362C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 27/29 | chr6 | 145893788 | |||||||
chr6:145893901 | T | A | 1 | a0001c0001t0001g0111 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.4695+249A>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 27/29 | chr6 | 145893901 | |||||||
chr6:145893907 | C | G | 1 | a0001c0001t0015g0270 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4695+243G>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 27/29 | chr6 | 145893907 | |||||||
chr6:145894082 | G | A | 1 | a0001c0001t0004g0233 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.4695+68C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 27/29 | chr6 | 145894082 | |||||||
chr6:145894083 | C | A | 1 | a0001c0001t0004g0233 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.4695+67G>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 27/29 | chr6 | 145894083 | |||||||
chr6:145894130 | G | A | 2 | a0001c0001t0001g0020 a0001c0001t0001g0084 |
3 | HG02965.hp2 HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.4695+20C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 27/29 | chr6 | 145894130 | |||||||
chr6:145894420 | G | GT | 109 | a0001c0001t0001g0073 a0001c0001t0001g0096 a0001c0001t0001g0126 others(106): Show |
146 | HG00280.hp1 HG00609.hp2 HG00621.hp1 others(143): Show |
intron_variant | MODIFIER | c.4609-185dupA | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 26/29 | chr6 | 145894420 | |||||||
chr6:145894420 | G | GTT | 23 | a0001c0001t0002g0189 a0001c0001t0002g0190 a0001c0002t0002g0201 others(20): Show |
27 | HG01081.hp2 HG01123.hp1 HG01433.hp1 others(24): Show |
intron_variant | MODIFIER | c.4609-186_4609-185d others(4): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 26/29 | chr6 | 145894420 | |||||||
chr6:145894420 | G | T | 1 | a0001c0001t0004g0235 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.4609-184C>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 26/29 | chr6 | 145894420 | |||||||
chr6:145894582 | C | G | 13 | a0001c0003t0005g0009 a0001c0003t0005g0017 a0001c0003t0005g0047 others(10): Show |
17 | HG01081.hp2 HG01433.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.4608+303G>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 26/29 | chr6 | 145894582 | |||||||
chr6:145894674 | A | C | 11 | a0002c0004t0003g0008 a0002c0004t0003g0016 a0002c0004t0003g0045 others(8): Show |
17 | HG01081.hp1 HG01123.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.4608+211T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 26/29 | chr6 | 145894674 | |||||||
chr6:145895048 | C | T | 129 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0189 others(126): Show |
170 | HG00280.hp1 HG00609.hp2 HG00639.hp2 others(167): Show |
intron_variant | MODIFIER | c.4516-71G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145895048 | |||||||
chr6:145895193 | G | C | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4516-216C>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145895193 | |||||||
chr6:145895243 | G | A | 129 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0189 others(126): Show |
170 | HG00280.hp1 HG00609.hp2 HG00639.hp2 others(167): Show |
intron_variant | MODIFIER | c.4516-266C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145895243 | |||||||
chr6:145895272 | T | C | 1 | a0001c0001t0001g0077 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.4516-295A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145895272 | |||||||
chr6:145895473 | G | A | 1 | a0001c0001t0001g0146 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.4516-496C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145895473 | |||||||
chr6:145895537 | G | GT | 54 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0069 others(51): Show |
76 | HG00280.hp1 HG00609.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.4516-561dupA | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145895537 | |||||||
chr6:145895614 | G | C | 1 | a0001c0002t0002g0186 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.4516-637C>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145895614 | |||||||
chr6:145895652 | T | C | 1 | a0001c0001t0001g0027 | 2 | HG01255.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.4516-675A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145895652 | |||||||
chr6:145895655 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.4516-678G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145895655 | |||||||
chr6:145896015 | A | G | 1 | a0001c0001t0001g0030 | 2 | HG01891.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.4516-1038T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145896015 | |||||||
chr6:145896172 | A | G | 3 | a0001c0003t0003g0251 a0001c0003t0003g0252 a0001c0003t0003g0253 |
3 | HG02145.hp2 HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.4516-1195T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145896172 | |||||||
chr6:145896434 | C | T | 133 | a0001c0001t0001g0033 a0001c0001t0001g0166 a0001c0001t0001g0167 others(130): Show |
175 | HG00280.hp1 HG00609.hp2 HG00639.hp2 others(172): Show |
intron_variant | MODIFIER | c.4516-1457G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145896434 | |||||||
chr6:145896514 | C | T | 2 | a0001c0001t0001g0134 a0001c0001t0001g0147 |
2 | HG01192.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.4516-1537G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145896514 | |||||||
chr6:145896530 | A | G | 1 | a0001c0001t0004g0232 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.4516-1553T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145896530 | |||||||
chr6:145896633 | T | C | 94 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0189 others(91): Show |
123 | HG00280.hp1 HG00609.hp2 HG00639.hp2 others(120): Show |
intron_variant | MODIFIER | c.4516-1656A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145896633 | |||||||
chr6:145896968 | T | G | 2 | a0002c0004t0003g0264 a0002c0004t0003g0266 |
2 | HG02559.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.4516-1991A>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145896968 | |||||||
chr6:145897045 | A | C | 1 | a0001c0001t0001g0123 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.4516-2068T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145897045 | |||||||
chr6:145897199 | A | T | 1 | a0001c0001t0012g0240 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.4516-2222T>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145897199 | |||||||
chr6:145897203 | T | A | 133 | a0001c0001t0001g0033 a0001c0001t0001g0166 a0001c0001t0001g0167 others(130): Show |
175 | HG00280.hp1 HG00609.hp2 HG00639.hp2 others(172): Show |
intron_variant | MODIFIER | c.4516-2226A>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145897203 | |||||||
chr6:145897210 | A | C | 89 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0189 others(86): Show |
118 | HG00280.hp1 HG00609.hp2 HG00639.hp2 others(115): Show |
intron_variant | MODIFIER | c.4516-2233T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145897210 | |||||||
chr6:145897265 | C | T | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4516-2288G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145897265 | |||||||
chr6:145897850 | T | C | 1 | a0001c0002t0002g0213 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.4516-2873A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145897850 | |||||||
chr6:145897913 | T | C | 98 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0189 others(95): Show |
129 | HG00280.hp1 HG00609.hp2 HG00639.hp2 others(126): Show |
intron_variant | MODIFIER | c.4516-2936A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145897913 | |||||||
chr6:145898028 | A | G | 98 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0189 others(95): Show |
129 | HG00280.hp1 HG00609.hp2 HG00639.hp2 others(126): Show |
intron_variant | MODIFIER | c.4516-3051T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145898028 | |||||||
chr6:145898042 | G | C | 1 | a0001c0001t0001g0152 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.4516-3065C>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145898042 | |||||||
chr6:145898081 | G | A | 2 | a0001c0001t0001g0013 a0001c0001t0001g0155 |
4 | NA18990.hp1 NA18999.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.4516-3104C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145898081 | |||||||
chr6:145898096 | T | C | 47 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0005 others(44): Show |
69 | HG00280.hp1 HG00609.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.4516-3119A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145898096 | |||||||
chr6:145898397 | T | A | 169 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0019 others(166): Show |
222 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(219): Show |
intron_variant | MODIFIER | c.4516-3420A>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145898397 | |||||||
chr6:145898447 | ATT | A | 63 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0189 others(60): Show |
87 | HG00280.hp1 HG00609.hp2 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.4516-3472_4516-347 others(6): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145898447 | |||||||
chr6:145898626 | T | C | 13 | a0001c0003t0005g0009 a0001c0003t0005g0017 a0001c0003t0005g0047 others(10): Show |
17 | HG01081.hp2 HG01433.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.4516-3649A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145898626 | |||||||
chr6:145898723 | C | A | 2 | a0001c0003t0003g0256 a0001c0003t0003g0257 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.4516-3746G>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145898723 | |||||||
chr6:145898727 | C | T | 1 | a0001c0002t0002g0214 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.4516-3750G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145898727 | |||||||
chr6:145898751 | A | C | 1 | a0001c0001t0001g0165 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.4516-3774T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145898751 | |||||||
chr6:145898759 | C | T | 2 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
2 | HG01069.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.4516-3782G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145898759 | |||||||
chr6:145898908 | C | T | 1 | a0001c0002t0002g0196 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.4516-3931G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145898908 | |||||||
chr6:145899114 | G | A | 99 | a0001c0001t0001g0061 a0001c0001t0002g0038 a0001c0001t0002g0039 others(96): Show |
130 | HG00280.hp1 HG00609.hp2 HG00639.hp2 others(127): Show |
intron_variant | MODIFIER | c.4516-4137C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145899114 | |||||||
chr6:145899273 | C | A | 94 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0189 others(91): Show |
123 | HG00280.hp1 HG00609.hp2 HG00639.hp2 others(120): Show |
intron_variant | MODIFIER | c.4516-4296G>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145899273 | |||||||
chr6:145899318 | T | C | 1 | a0001c0003t0003g0256 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.4516-4341A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145899318 | |||||||
chr6:145899324 | G | A | 1 | a0001c0001t0001g0022 | 2 | HG00438.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.4516-4347C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145899324 | |||||||
chr6:145899622 | G | C | 98 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0189 others(95): Show |
129 | HG00280.hp1 HG00609.hp2 HG00639.hp2 others(126): Show |
intron_variant | MODIFIER | c.4516-4645C>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145899622 | |||||||
chr6:145900046 | C | T | 212 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0018 others(209): Show |
268 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(265): Show |
intron_variant | MODIFIER | c.4516-5069G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145900046 | |||||||
chr6:145900160 | C | T | 1 | a0001c0003t0003g0252 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.4516-5183G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145900160 | |||||||
chr6:145900383 | C | G | 1 | a0001c0001t0002g0228 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.4516-5406G>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145900383 | |||||||
chr6:145900423 | T | C | 1 | a0001c0019t0001g0107 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.4516-5446A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145900423 | |||||||
chr6:145900466 | C | T | 2 | a0001c0001t0002g0268 a0001c0001t0002g0269 |
2 | HG02615.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.4516-5489G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145900466 | |||||||
chr6:145900483 | G | T | 2 | a0001c0001t0002g0268 a0001c0001t0002g0269 |
2 | HG02615.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.4516-5506C>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145900483 | |||||||
chr6:145900617 | A | G | 98 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0189 others(95): Show |
129 | HG00280.hp1 HG00609.hp2 HG00639.hp2 others(126): Show |
intron_variant | MODIFIER | c.4516-5640T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145900617 | |||||||
chr6:145900712 | T | C | 20 | a0001c0003t0003g0251 a0001c0003t0003g0252 a0001c0003t0003g0253 others(17): Show |
24 | HG01081.hp2 HG01433.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.4516-5735A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145900712 | |||||||
chr6:145901100 | A | T | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4516-6123T>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145901100 | |||||||
chr6:145901200 | G | A | 3 | a0001c0001t0001g0093 a0001c0001t0001g0110 a0001c0001t0001g0111 |
3 | HG01346.hp2 HG02004.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.4516-6223C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145901200 | |||||||
chr6:145901473 | G | C | 1 | a0001c0015t0014g0250 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4516-6496C>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145901473 | |||||||
chr6:145901656 | A | C | 2 | a0001c0003t0003g0254 a0001c0003t0003g0255 |
2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.4516-6679T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145901656 | |||||||
chr6:145901669 | C | T | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4516-6692G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145901669 | |||||||
chr6:145901738 | AAC | A | 11 | a0002c0004t0003g0008 a0002c0004t0003g0016 a0002c0004t0003g0045 others(8): Show |
17 | HG01081.hp1 HG01123.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.4516-6763_4516-676 others(6): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145901738 | |||||||
chr6:145901795 | T | C | 2 | a0001c0001t0001g0087 a0001c0001t0001g0108 |
2 | HG01361.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.4516-6818A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145901795 | |||||||
chr6:145901910 | C | T | 1 | a0001c0001t0010g0079 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.4516-6933G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145901910 | |||||||
chr6:145902217 | T | G | 1 | a0001c0003t0005g0048 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4516-7240A>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145902217 | |||||||
chr6:145902240 | T | A | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4516-7263A>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145902240 | |||||||
chr6:145902310 | A | C | 1 | a0001c0001t0002g0039 | 2 | HG03834.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.4516-7333T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145902310 | |||||||
chr6:145902405 | G | A | 1 | a0001c0003t0003g0257 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.4516-7428C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145902405 | |||||||
chr6:145902505 | T | G | 1 | a0001c0001t0001g0168 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.4516-7528A>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145902505 | |||||||
chr6:145902640 | G | GA | 98 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0189 others(95): Show |
129 | HG00280.hp1 HG00609.hp2 HG00639.hp2 others(126): Show |
intron_variant | MODIFIER | c.4516-7664dupT | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145902640 | |||||||
chr6:145902700 | G | A | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4516-7723C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145902700 | |||||||
chr6:145903219 | C | T | 1 | a0001c0015t0014g0250 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4515+7229G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145903219 | |||||||
chr6:145903342 | TA | T | 27 | a0001c0001t0004g0007 a0001c0001t0004g0043 a0001c0001t0004g0232 others(24): Show |
32 | HG00642.hp2 HG00735.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.4515+7105delT | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145903342 | |||||||
chr6:145903343 | A | T | 11 | a0002c0004t0003g0008 a0002c0004t0003g0016 a0002c0004t0003g0045 others(8): Show |
17 | HG01081.hp1 HG01123.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.4515+7105T>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145903343 | |||||||
chr6:145903369 | A | G | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4515+7079T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145903369 | |||||||
chr6:145903408 | G | A | 20 | a0001c0003t0003g0251 a0001c0003t0003g0252 a0001c0003t0003g0253 others(17): Show |
24 | HG01081.hp2 HG01433.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.4515+7040C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145903408 | |||||||
chr6:145903412 | T | C | 1 | a0001c0002t0002g0211 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.4515+7036A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145903412 | |||||||
chr6:145903427 | CAG | C | 146 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(143): Show |
182 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(179): Show |
intron_variant | MODIFIER | c.4515+7019_4515+702 others(6): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145903427 | |||||||
chr6:145903510 | C | T | 1 | a0005c0007t0001g0090 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.4515+6938G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145903510 | |||||||
chr6:145903570 | T | C | 2 | a0001c0003t0005g0017 a0001c0003t0005g0050 |
3 | HG02572.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.4515+6878A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145903570 | |||||||
chr6:145903775 | C | T | 1 | a0001c0001t0004g0244 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.4515+6673G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145903775 | |||||||
chr6:145903976 | G | A | 1 | a0001c0001t0001g0086 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.4515+6472C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145903976 | |||||||
chr6:145904012 | T | C | 3 | a0002c0004t0003g0045 a0002c0004t0003g0261 a0002c0004t0003g0265 |
4 | HG01081.hp1 HG01884.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.4515+6436A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145904012 | |||||||
chr6:145904088 | G | T | 1 | a0001c0001t0002g0192 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4515+6360C>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145904088 | |||||||
chr6:145904135 | C | A | 147 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(144): Show |
183 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(180): Show |
intron_variant | MODIFIER | c.4515+6313G>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145904135 | |||||||
chr6:145904187 | C | T | 1 | a0001c0019t0001g0107 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.4515+6261G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145904187 | |||||||
chr6:145904483 | G | A | 25 | a0001c0001t0004g0007 a0001c0001t0004g0043 a0001c0001t0004g0232 others(22): Show |
30 | HG00642.hp2 HG00735.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.4515+5965C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145904483 | |||||||
chr6:145904539 | A | C | 2 | a0001c0003t0003g0254 a0001c0003t0003g0255 |
2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.4515+5909T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145904539 | |||||||
chr6:145904626 | G | A | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4515+5822C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145904626 | |||||||
chr6:145904687 | G | A | 3 | a0001c0003t0003g0251 a0001c0003t0003g0252 a0001c0003t0003g0253 |
3 | HG02145.hp2 HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.4515+5761C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145904687 | |||||||
chr6:145904731 | T | C | 11 | a0002c0004t0003g0008 a0002c0004t0003g0016 a0002c0004t0003g0045 others(8): Show |
17 | HG01081.hp1 HG01123.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.4515+5717A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145904731 | |||||||
chr6:145904834 | G | T | 11 | a0002c0004t0003g0008 a0002c0004t0003g0016 a0002c0004t0003g0045 others(8): Show |
17 | HG01081.hp1 HG01123.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.4515+5614C>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145904834 | |||||||
chr6:145904835 | C | A | 11 | a0002c0004t0003g0008 a0002c0004t0003g0016 a0002c0004t0003g0045 others(8): Show |
17 | HG01081.hp1 HG01123.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.4515+5613G>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145904835 | |||||||
chr6:145904878 | G | A | 1 | a0001c0002t0002g0209 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4515+5570C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145904878 | |||||||
chr6:145904900 | A | G | 2 | a0001c0003t0003g0254 a0001c0003t0003g0255 |
2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.4515+5548T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145904900 | |||||||
chr6:145904952 | C | A | 20 | a0001c0003t0003g0251 a0001c0003t0003g0252 a0001c0003t0003g0253 others(17): Show |
24 | HG01081.hp2 HG01433.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.4515+5496G>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145904952 | |||||||
chr6:145905225 | G | A | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4515+5223C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145905225 | |||||||
chr6:145905371 | C | T | 1 | a0001c0001t0004g0234 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.4515+5077G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145905371 | |||||||
chr6:145905400 | T | A | 2 | a0001c0001t0001g0123 a0001c0001t0001g0131 |
2 | HG00544.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.4515+5048A>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145905400 | |||||||
chr6:145905453 | T | C | 1 | a0001c0002t0002g0209 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4515+4995A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145905453 | |||||||
chr6:145905617 | T | C | 1 | a0001c0002t0002g0203 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.4515+4831A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145905617 | |||||||
chr6:145905739 | T | C | 1 | a0013c0018t0002g0230 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.4515+4709A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145905739 | |||||||
chr6:145905753 | T | C | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4515+4695A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145905753 | |||||||
chr6:145905870 | C | A | 1 | a0001c0015t0014g0250 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4515+4578G>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145905870 | |||||||
chr6:145906118 | A | G | 1 | a0001c0001t0004g0245 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.4515+4330T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145906118 | |||||||
chr6:145906419 | C | A | 4 | a0001c0001t0001g0014 a0001c0001t0001g0158 a0001c0001t0001g0159 others(1): Show |
6 | NA18943.hp2 NA18962.hp1 NA18973.hp2 others(3): Show |
intron_variant | MODIFIER | c.4515+4029G>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145906419 | |||||||
chr6:145906896 | G | A | 1 | a0001c0003t0003g0251 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.4515+3552C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145906896 | |||||||
chr6:145907279 | A | C | 1 | a0001c0003t0009g0258 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.4515+3169T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145907279 | |||||||
chr6:145907308 | A | G | 2 | a0001c0001t0002g0268 a0001c0001t0002g0269 |
2 | HG02615.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.4515+3140T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145907308 | |||||||
chr6:145907766 | T | C | 1 | a0001c0003t0005g0017 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.4515+2682A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145907766 | |||||||
chr6:145907785 | AAAAACAA others(3): Show |
A | 25 | a0001c0001t0004g0007 a0001c0001t0004g0043 a0001c0001t0004g0232 others(22): Show |
30 | HG00642.hp2 HG00735.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.4515+2653_4515+266 others(14): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145907785 | |||||||
chr6:145907785 | AAAAACAA others(8): Show |
A | 10 | a0002c0004t0003g0008 a0002c0004t0003g0016 a0002c0004t0003g0045 others(7): Show |
16 | HG01081.hp1 HG01123.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.4515+2648_4515+266 others(19): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145907785 | |||||||
chr6:145907831 | C | G | 31 | a0001c0003t0003g0251 a0001c0003t0003g0252 a0001c0003t0003g0253 others(28): Show |
41 | HG01081.hp1 HG01081.hp2 HG01123.hp2 others(38): Show |
intron_variant | MODIFIER | c.4515+2617G>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145907831 | |||||||
chr6:145907941 | G | A | 13 | a0001c0003t0005g0009 a0001c0003t0005g0017 a0001c0003t0005g0047 others(10): Show |
17 | HG01081.hp2 HG01433.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.4515+2507C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145907941 | |||||||
chr6:145908184 | T | C | 1 | a0001c0001t0001g0151 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.4515+2264A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145908184 | |||||||
chr6:145908303 | T | C | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4515+2145A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145908303 | |||||||
chr6:145908393 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.4515+2055G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145908393 | |||||||
chr6:145908403 | T | C | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4515+2045A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145908403 | |||||||
chr6:145908503 | C | A | 1 | a0001c0001t0001g0080 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.4515+1945G>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145908503 | |||||||
chr6:145908506 | C | T | 1 | a0002c0004t0003g0259 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.4515+1942G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145908506 | |||||||
chr6:145908767 | G | A | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4515+1681C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145908767 | |||||||
chr6:145908948 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.4515+1500C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145908948 | |||||||
chr6:145909000 | A | G | 1 | a0001c0001t0001g0105 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.4515+1448T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145909000 | |||||||
chr6:145909096 | C | G | 181 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(178): Show |
229 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(226): Show |
intron_variant | MODIFIER | c.4515+1352G>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145909096 | |||||||
chr6:145909101 | A | G | 3 | a0001c0003t0005g0048 a0001c0003t0005g0051 a0001c0003t0005g0052 |
3 | HG01433.hp1 HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.4515+1347T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145909101 | |||||||
chr6:145909193 | T | C | 2 | a0001c0001t0004g0233 a0001c0001t0004g0237 |
2 | NA19088.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.4515+1255A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145909193 | |||||||
chr6:145909196 | T | C | 25 | a0001c0001t0004g0007 a0001c0001t0004g0043 a0001c0001t0004g0232 others(22): Show |
30 | HG00642.hp2 HG00735.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.4515+1252A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145909196 | |||||||
chr6:145909318 | T | C | 181 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(178): Show |
229 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(226): Show |
intron_variant | MODIFIER | c.4515+1130A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145909318 | |||||||
chr6:145909407 | G | A | 2 | a0001c0001t0015g0270 a0001c0001t0016g0271 |
2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.4515+1041C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145909407 | |||||||
chr6:145909699 | C | A | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4515+749G>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145909699 | |||||||
chr6:145909769 | GA | G | 177 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(174): Show |
223 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(220): Show |
intron_variant | MODIFIER | c.4515+678delT | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145909769 | |||||||
chr6:145909832 | T | C | 1 | a0001c0003t0005g0047 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4515+616A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145909832 | |||||||
chr6:145909843 | T | A | 10 | a0002c0004t0003g0008 a0002c0004t0003g0016 a0002c0004t0003g0045 others(7): Show |
16 | HG01081.hp1 HG01123.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.4515+605A>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145909843 | |||||||
chr6:145909981 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4515+467G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145909981 | |||||||
chr6:145910334 | C | A | 177 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(174): Show |
223 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(220): Show |
intron_variant | MODIFIER | c.4515+114G>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145910334 | |||||||
chr6:145910426 | A | G | 1 | a0003c0005t0011g0176 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.4515+22T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 25/29 | chr6 | 145910426 | |||||||
chr6:145911167 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.4327-531C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/29 | chr6 | 145911167 | |||||||
chr6:145911189 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.4327-553A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/29 | chr6 | 145911189 | |||||||
chr6:145911211 | C | T | 1 | a0001c0003t0005g0056 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.4327-575G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/29 | chr6 | 145911211 | |||||||
chr6:145911222 | C | A | 1 | a0001c0001t0015g0270 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4327-586G>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/29 | chr6 | 145911222 | |||||||
chr6:145911267 | G | C | 177 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(174): Show |
223 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(220): Show |
intron_variant | MODIFIER | c.4327-631C>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/29 | chr6 | 145911267 | |||||||
chr6:145911327 | G | A | 2 | a0001c0003t0003g0256 a0001c0003t0003g0257 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.4327-691C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/29 | chr6 | 145911327 | |||||||
chr6:145911413 | G | A | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4327-777C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/29 | chr6 | 145911413 | |||||||
chr6:145911668 | C | T | 177 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(174): Show |
223 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(220): Show |
intron_variant | MODIFIER | c.4327-1032G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/29 | chr6 | 145911668 | |||||||
chr6:145911685 | T | G | 1 | a0001c0001t0016g0271 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4327-1049A>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/29 | chr6 | 145911685 | |||||||
chr6:145911690 | A | ATAG | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4327-1055_4327-105 others(7): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/29 | chr6 | 145911690 | |||||||
chr6:145911692 | T | A | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4327-1056A>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/29 | chr6 | 145911692 | |||||||
chr6:145911697 | C | A | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4327-1061G>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/29 | chr6 | 145911697 | |||||||
chr6:145911698 | A | AGAAAG | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4327-1063_4327-106 others(9): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/29 | chr6 | 145911698 | |||||||
chr6:145911827 | C | T | 1 | a0001c0002t0002g0221 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.4327-1191G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/29 | chr6 | 145911827 | |||||||
chr6:145911842 | A | T | 181 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(178): Show |
229 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(226): Show |
intron_variant | MODIFIER | c.4327-1206T>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/29 | chr6 | 145911842 | |||||||
chr6:145911931 | T | C | 7 | a0001c0001t0002g0039 a0001c0001t0002g0210 a0001c0001t0002g0216 others(4): Show |
8 | HG01070.hp2 HG01346.hp1 HG03492.hp1 others(5): Show |
intron_variant | MODIFIER | c.4327-1295A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/29 | chr6 | 145911931 | |||||||
chr6:145912028 | A | G | 2 | a0001c0001t0002g0268 a0001c0001t0002g0269 |
2 | HG02615.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.4327-1392T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/29 | chr6 | 145912028 | |||||||
chr6:145912083 | G | T | 13 | a0001c0003t0005g0009 a0001c0003t0005g0017 a0001c0003t0005g0047 others(10): Show |
17 | HG01081.hp2 HG01433.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.4326+1395C>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/29 | chr6 | 145912083 | |||||||
chr6:145912106 | GC | G | 31 | a0001c0003t0003g0251 a0001c0003t0003g0252 a0001c0003t0003g0253 others(28): Show |
41 | HG01081.hp1 HG01081.hp2 HG01123.hp2 others(38): Show |
intron_variant | MODIFIER | c.4326+1371delG | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/29 | chr6 | 145912106 | |||||||
chr6:145912202 | A | T | 181 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(178): Show |
229 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(226): Show |
intron_variant | MODIFIER | c.4326+1276T>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/29 | chr6 | 145912202 | |||||||
chr6:145912237 | G | T | 1 | a0001c0001t0004g0247 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.4326+1241C>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/29 | chr6 | 145912237 | |||||||
chr6:145912266 | GA | G | 13 | a0001c0003t0005g0009 a0001c0003t0005g0017 a0001c0003t0005g0047 others(10): Show |
17 | HG01081.hp2 HG01433.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.4326+1211delT | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/29 | chr6 | 145912266 | |||||||
chr6:145912382 | A | C | 3 | a0001c0003t0003g0251 a0001c0003t0003g0252 a0001c0003t0003g0253 |
3 | HG02145.hp2 HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.4326+1096T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/29 | chr6 | 145912382 | |||||||
chr6:145912425 | A | G | 11 | a0002c0004t0003g0008 a0002c0004t0003g0016 a0002c0004t0003g0045 others(8): Show |
17 | HG01081.hp1 HG01123.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.4326+1053T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/29 | chr6 | 145912425 | |||||||
chr6:145912850 | G | GAT | 13 | a0001c0001t0001g0117 a0001c0001t0001g0150 a0002c0004t0003g0008 others(10): Show |
19 | HG01081.hp1 HG01123.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.4326+626_4326+627d others(4): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/29 | chr6 | 145912850 | |||||||
chr6:145912875 | T | A | 7 | a0001c0002t0002g0037 a0001c0002t0002g0182 a0001c0002t0002g0183 others(4): Show |
8 | NA18950.hp1 NA18953.hp2 NA18959.hp1 others(5): Show |
intron_variant | MODIFIER | c.4326+603A>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/29 | chr6 | 145912875 | |||||||
chr6:145912894 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.4326+584A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/29 | chr6 | 145912894 | |||||||
chr6:145912909 | G | A | 1 | a0002c0004t0003g0262 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.4326+569C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/29 | chr6 | 145912909 | |||||||
chr6:145913061 | G | A | 146 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(143): Show |
182 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(179): Show |
intron_variant | MODIFIER | c.4326+417C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/29 | chr6 | 145913061 | |||||||
chr6:145913167 | T | C | 1 | a0001c0001t0004g0233 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.4326+311A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/29 | chr6 | 145913167 | |||||||
chr6:145913178 | C | T | 1 | a0001c0001t0004g0246 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.4326+300G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/29 | chr6 | 145913178 | |||||||
chr6:145913285 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.4326+193A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/29 | chr6 | 145913285 | |||||||
chr6:145913399 | G | A | 11 | a0002c0004t0003g0008 a0002c0004t0003g0016 a0002c0004t0003g0045 others(8): Show |
17 | HG01081.hp1 HG01123.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.4326+79C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 24/29 | chr6 | 145913399 | |||||||
chr6:145913585 | G | A | 3 | a0001c0002t0002g0037 a0001c0002t0002g0182 a0001c0002t0002g0187 |
4 | NA18950.hp1 NA18959.hp1 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.4255-36C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145913585 | |||||||
chr6:145913795 | C | T | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4255-246G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145913795 | |||||||
chr6:145913797 | T | C | 3 | a0001c0003t0003g0251 a0001c0003t0003g0252 a0001c0003t0003g0253 |
3 | HG02145.hp2 HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.4255-248A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145913797 | |||||||
chr6:145913853 | A | G | 1 | a0001c0001t0004g0239 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.4255-304T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145913853 | |||||||
chr6:145913883 | A | T | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4255-334T>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145913883 | |||||||
chr6:145913931 | A | C | 3 | a0001c0002t0002g0036 a0001c0002t0002g0042 a0001c0002t0002g0223 |
5 | NA18956.hp1 NA18988.hp1 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.4255-382T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145913931 | |||||||
chr6:145913936 | T | C | 2 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
2 | HG01069.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.4255-387A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145913936 | |||||||
chr6:145914163 | T | C | 1 | a0001c0002t0002g0226 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.4255-614A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145914163 | |||||||
chr6:145914245 | C | A | 1 | a0001c0001t0001g0129 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.4255-696G>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145914245 | |||||||
chr6:145914291 | A | C | 4 | a0001c0001t0001g0066 a0001c0001t0001g0068 a0001c0001t0001g0070 others(1): Show |
4 | NA18991.hp2 NA19011.hp1 NA19072.hp2 others(1): Show |
intron_variant | MODIFIER | c.4255-742T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145914291 | |||||||
chr6:145914461 | T | C | 1 | a0001c0002t0002g0203 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.4255-912A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145914461 | |||||||
chr6:145914490 | A | G | 181 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(178): Show |
229 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(226): Show |
intron_variant | MODIFIER | c.4255-941T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145914490 | |||||||
chr6:145914708 | G | C | 2 | a0001c0009t0001g0063 a0001c0009t0001g0085 |
2 | NA18952.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.4255-1159C>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145914708 | |||||||
chr6:145914771 | G | T | 2 | a0001c0003t0003g0254 a0001c0003t0003g0255 |
2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.4255-1222C>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145914771 | |||||||
chr6:145914877 | G | C | 1 | a0001c0001t0001g0125 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.4255-1328C>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145914877 | |||||||
chr6:145914969 | T | C | 1 | a0001c0001t0001g0158 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.4255-1420A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145914969 | |||||||
chr6:145915105 | A | C | 1 | a0001c0015t0014g0250 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4255-1556T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145915105 | |||||||
chr6:145915186 | C | A | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4255-1637G>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145915186 | |||||||
chr6:145915237 | T | TAA | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4255-1690_4255-168 others(6): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145915237 | |||||||
chr6:145915352 | T | C | 34 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0020 others(31): Show |
44 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.4255-1803A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145915352 | |||||||
chr6:145915820 | TTTAC | T | 102 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(99): Show |
126 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(123): Show |
intron_variant | MODIFIER | c.4255-2275_4255-227 others(8): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145915820 | |||||||
chr6:145915824 | C | T | 1 | a0001c0002t0002g0005 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.4255-2275G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145915824 | |||||||
chr6:145915930 | ATTCTC | A | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4254+2196_4254+220 others(9): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145915930 | |||||||
chr6:145916069 | T | C | 1 | a0001c0001t0001g0078 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.4254+2062A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145916069 | |||||||
chr6:145916209 | T | C | 2 | a0001c0001t0002g0268 a0001c0001t0002g0269 |
2 | HG02615.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.4254+1922A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145916209 | |||||||
chr6:145916360 | T | C | 1 | a0001c0001t0001g0061 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4254+1771A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145916360 | |||||||
chr6:145916421 | A | G | 2 | a0001c0001t0015g0270 a0001c0001t0016g0271 |
2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.4254+1710T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145916421 | |||||||
chr6:145916510 | TA | T | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4254+1620delT | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145916510 | |||||||
chr6:145916821 | C | T | 1 | a0001c0001t0004g0233 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.4254+1310G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145916821 | |||||||
chr6:145916896 | C | T | 142 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(139): Show |
177 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(174): Show |
intron_variant | MODIFIER | c.4254+1235G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145916896 | |||||||
chr6:145917009 | C | T | 1 | a0001c0003t0005g0051 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4254+1122G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145917009 | |||||||
chr6:145917047 | C | T | 2 | a0001c0001t0001g0033 a0001c0001t0001g0166 |
3 | HG02723.hp2 HG02818.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.4254+1084G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145917047 | |||||||
chr6:145917135 | T | C | 1 | a0001c0001t0002g0268 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.4254+996A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145917135 | |||||||
chr6:145917166 | T | A | 146 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(143): Show |
182 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(179): Show |
intron_variant | MODIFIER | c.4254+965A>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145917166 | |||||||
chr6:145917196 | T | C | 8 | a0001c0001t0001g0030 a0001c0001t0001g0060 a0001c0001t0001g0139 others(5): Show |
9 | HG01891.hp1 HG02257.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.4254+935A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145917196 | |||||||
chr6:145917311 | G | A | 2 | a0001c0003t0003g0252 a0006c0008t0003g0044 |
3 | HG01081.hp2 HG02451.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.4254+820C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145917311 | |||||||
chr6:145917391 | C | T | 2 | a0001c0003t0003g0254 a0001c0003t0003g0255 |
2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.4254+740G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145917391 | |||||||
chr6:145917412 | C | T | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4254+719G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145917412 | |||||||
chr6:145917571 | G | A | 1 | a0001c0002t0002g0214 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.4254+560C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145917571 | |||||||
chr6:145917595 | G | GA | 181 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(178): Show |
229 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(226): Show |
intron_variant | MODIFIER | c.4254+535dupT | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145917595 | |||||||
chr6:145917797 | T | C | 1 | a0001c0002t0002g0214 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.4254+334A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145917797 | |||||||
chr6:145917807 | A | C | 2 | a0001c0003t0003g0254 a0001c0003t0003g0255 |
2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.4254+324T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145917807 | |||||||
chr6:145917988 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.4254+143A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145917988 | |||||||
chr6:145918109 | T | C | 2 | a0001c0001t0006g0276 a0001c0001t0006g0277 |
2 | HG03704.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.4254+22A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 23/29 | chr6 | 145918109 | |||||||
chr6:145918400 | GA | G | 5 | a0001c0001t0001g0032 a0001c0001t0001g0148 a0001c0001t0001g0149 others(2): Show |
6 | HG01993.hp1 NA18954.hp1 NA18955.hp2 others(3): Show |
intron_variant | MODIFIER | c.4153-169delT | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 22/29 | chr6 | 145918400 | |||||||
chr6:145918401 | A | AT | 4 | a0001c0001t0001g0157 a0002c0004t0003g0016 a0002c0004t0003g0045 others(1): Show |
6 | HG01081.hp2 HG02109.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.4153-170dupA | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 22/29 | chr6 | 145918401 | |||||||
chr6:145918445 | A | G | 1 | a0006c0008t0003g0044 | 2 | HG01081.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.4153-213T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 22/29 | chr6 | 145918445 | |||||||
chr6:145918538 | C | A | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4153-306G>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 22/29 | chr6 | 145918538 | |||||||
chr6:145918681 | T | A | 1 | a0001c0001t0001g0138 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.4153-449A>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 22/29 | chr6 | 145918681 | |||||||
chr6:145919104 | C | T | 2 | a0001c0003t0003g0256 a0001c0003t0003g0257 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.4152+244G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 22/29 | chr6 | 145919104 | |||||||
chr6:145919249 | C | G | 1 | a0002c0004t0003g0265 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.4152+99G>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 22/29 | chr6 | 145919249 | |||||||
chr6:145919501 | T | C | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.4009-10A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 21/29 | chr6 | 145919501 | |||||||
chr6:145919570 | CAA | C | 7 | a0001c0001t0002g0038 a0001c0001t0002g0189 a0001c0001t0002g0190 others(4): Show |
8 | HG01109.hp1 HG02055.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.4009-81_4009-80del others(2): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 21/29 | chr6 | 145919570 | |||||||
chr6:145919700 | T | G | 1 | a0002c0004t0003g0260 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4009-209A>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 21/29 | chr6 | 145919700 | |||||||
chr6:145919713 | A | C | 1 | a0001c0001t0001g0141 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.4009-222T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 21/29 | chr6 | 145919713 | |||||||
chr6:145919771 | C | T | 2 | a0001c0001t0004g0246 a0001c0001t0004g0247 |
2 | HG01074.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.4009-280G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 21/29 | chr6 | 145919771 | |||||||
chr6:145919771 | CTT | C | 3 | a0001c0001t0002g0268 a0001c0001t0002g0269 a0001c0001t0016g0271 |
3 | HG02055.hp2 HG02615.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.4009-282_4009-281d others(4): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 21/29 | chr6 | 145919771 | |||||||
chr6:145919880 | T | C | 1 | a0001c0001t0001g0153 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.4009-389A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 21/29 | chr6 | 145919880 | |||||||
chr6:145919935 | T | G | 1 | a0001c0001t0001g0069 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.4009-444A>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 21/29 | chr6 | 145919935 | |||||||
chr6:145920061 | T | C | 31 | a0001c0003t0003g0251 a0001c0003t0003g0252 a0001c0003t0003g0253 others(28): Show |
41 | HG01081.hp1 HG01081.hp2 HG01123.hp2 others(38): Show |
intron_variant | MODIFIER | c.4009-570A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 21/29 | chr6 | 145920061 | |||||||
chr6:145920105 | A | G | 25 | a0001c0001t0004g0007 a0001c0001t0004g0043 a0001c0001t0004g0232 others(22): Show |
30 | HG00642.hp2 HG00735.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.4009-614T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 21/29 | chr6 | 145920105 | |||||||
chr6:145920323 | A | G | 31 | a0001c0003t0003g0251 a0001c0003t0003g0252 a0001c0003t0003g0253 others(28): Show |
41 | HG01081.hp1 HG01081.hp2 HG01123.hp2 others(38): Show |
intron_variant | MODIFIER | c.4009-832T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 21/29 | chr6 | 145920323 | |||||||
chr6:145920336 | A | C | 186 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(183): Show |
234 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(231): Show |
intron_variant | MODIFIER | c.4008+831T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 21/29 | chr6 | 145920336 | |||||||
chr6:145920379 | G | A | 1 | a0001c0002t0002g0199 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.4008+788C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 21/29 | chr6 | 145920379 | |||||||
chr6:145920494 | ATC | A | 5 | a0001c0001t0001g0081 a0004c0006t0007g0015 a0004c0006t0007g0177 others(2): Show |
7 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(4): Show |
intron_variant | MODIFIER | c.4008+671_4008+672d others(4): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 21/29 | chr6 | 145920494 | |||||||
chr6:145920575 | A | AT | 181 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(178): Show |
229 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(226): Show |
intron_variant | MODIFIER | c.4008+591_4008+592i others(3): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 21/29 | chr6 | 145920575 | |||||||
chr6:145920862 | A | G | 3 | a0001c0001t0015g0270 a0001c0001t0016g0271 a0001c0015t0014g0250 |
3 | HG02055.hp2 HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.4008+305T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 21/29 | chr6 | 145920862 | |||||||
chr6:145921516 | C | A | 1 | a0001c0001t0001g0163 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3783-124G>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 20/29 | chr6 | 145921516 | |||||||
chr6:145921540 | GT | G | 175 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(172): Show |
222 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(219): Show |
intron_variant | MODIFIER | c.3783-149delA | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 20/29 | chr6 | 145921540 | |||||||
chr6:145921553 | TA | T | 2 | a0001c0001t0001g0020 a0001c0001t0001g0140 |
3 | HG02559.hp1 HG02965.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.3783-162delT | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 20/29 | chr6 | 145921553 | |||||||
chr6:145921554 | A | T | 1 | a0001c0001t0002g0210 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3783-162T>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 20/29 | chr6 | 145921554 | |||||||
chr6:145921691 | G | C | 1 | a0001c0002t0002g0222 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.3783-299C>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 20/29 | chr6 | 145921691 | |||||||
chr6:145921767 | A | G | 2 | a0001c0003t0005g0049 a0001c0003t0005g0053 |
2 | HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.3783-375T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 20/29 | chr6 | 145921767 | |||||||
chr6:145921806 | C | T | 146 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(143): Show |
182 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(179): Show |
intron_variant | MODIFIER | c.3783-414G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 20/29 | chr6 | 145921806 | |||||||
chr6:145921820 | T | G | 13 | a0001c0003t0005g0009 a0001c0003t0005g0017 a0001c0003t0005g0047 others(10): Show |
17 | HG01081.hp2 HG01433.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.3783-428A>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 20/29 | chr6 | 145921820 | |||||||
chr6:145921935 | T | C | 32 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0021 others(29): Show |
41 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.3782+351A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 20/29 | chr6 | 145921935 | |||||||
chr6:145921940 | A | T | 32 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0021 others(29): Show |
41 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.3782+346T>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 20/29 | chr6 | 145921940 | |||||||
chr6:145921964 | C | G | 1 | a0001c0002t0002g0206 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.3782+322G>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 20/29 | chr6 | 145921964 | |||||||
chr6:145921974 | T | G | 3 | a0003c0005t0001g0035 a0003c0005t0001g0116 a0003c0005t0001g0174 |
4 | NA18986.hp1 NA18986.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.3782+312A>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 20/29 | chr6 | 145921974 | |||||||
chr6:145922025 | G | C | 20 | a0001c0003t0003g0251 a0001c0003t0003g0252 a0001c0003t0003g0253 others(17): Show |
24 | HG01081.hp2 HG01433.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.3782+261C>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 20/29 | chr6 | 145922025 | |||||||
chr6:145922049 | A | G | 2 | a0001c0001t0001g0033 a0001c0001t0001g0166 |
3 | HG02723.hp2 HG02818.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.3782+237T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 20/29 | chr6 | 145922049 | |||||||
chr6:145922071 | T | C | 1 | a0001c0002t0002g0198 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.3782+215A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 20/29 | chr6 | 145922071 | |||||||
chr6:145922390 | C | T | 2 | a0001c0001t0002g0268 a0001c0001t0002g0269 |
2 | HG02615.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.3720-42G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 19/29 | chr6 | 145922390 | |||||||
chr6:145922445 | C | T | 177 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(174): Show |
223 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(220): Show |
intron_variant | MODIFIER | c.3720-97G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 19/29 | chr6 | 145922445 | |||||||
chr6:145922583 | T | C | 2 | a0001c0003t0005g0017 a0001c0003t0005g0050 |
3 | HG02572.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.3719+80A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 19/29 | chr6 | 145922583 | |||||||
chr6:145922855 | C | T | 1 | a0001c0001t0001g0114 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.3546-19G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 18/29 | chr6 | 145922855 | |||||||
chr6:145922876 | G | A | 25 | a0001c0001t0004g0007 a0001c0001t0004g0043 a0001c0001t0004g0232 others(22): Show |
30 | HG00642.hp2 HG00735.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.3546-40C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 18/29 | chr6 | 145922876 | |||||||
chr6:145922880 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3546-44T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 18/29 | chr6 | 145922880 | |||||||
chr6:145922912 | T | C | 13 | a0001c0003t0005g0009 a0001c0003t0005g0017 a0001c0003t0005g0047 others(10): Show |
17 | HG01081.hp2 HG01433.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.3546-76A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 18/29 | chr6 | 145922912 | |||||||
chr6:145922940 | T | C | 1 | a0001c0003t0003g0253 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3546-104A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 18/29 | chr6 | 145922940 | |||||||
chr6:145922941 | T | A | 11 | a0002c0004t0003g0008 a0002c0004t0003g0016 a0002c0004t0003g0045 others(8): Show |
17 | HG01081.hp1 HG01123.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.3546-105A>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 18/29 | chr6 | 145922941 | |||||||
chr6:145922945 | G | GT | 174 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(171): Show |
217 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(214): Show |
intron_variant | MODIFIER | c.3546-110dupA | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 18/29 | chr6 | 145922945 | |||||||
chr6:145922945 | G | GTT | 11 | a0002c0004t0003g0008 a0002c0004t0003g0016 a0002c0004t0003g0045 others(8): Show |
17 | HG01081.hp1 HG01123.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.3546-111_3546-110d others(4): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 18/29 | chr6 | 145922945 | |||||||
chr6:145922992 | A | G | 177 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(174): Show |
223 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(220): Show |
intron_variant | MODIFIER | c.3546-156T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 18/29 | chr6 | 145922992 | |||||||
chr6:145923049 | T | C | 1 | a0001c0001t0006g0276 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.3546-213A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 18/29 | chr6 | 145923049 | |||||||
chr6:145923138 | G | A | 3 | a0001c0003t0003g0251 a0001c0003t0003g0252 a0001c0003t0003g0253 |
3 | HG02145.hp2 HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3546-302C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 18/29 | chr6 | 145923138 | |||||||
chr6:145923245 | G | A | 3 | a0001c0001t0001g0029 a0001c0001t0001g0097 a0001c0001t0001g0165 |
4 | HG00735.hp1 HG01928.hp1 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.3545+398C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 18/29 | chr6 | 145923245 | |||||||
chr6:145923572 | A | G | 1 | a0001c0001t0001g0127 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.3545+71T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 18/29 | chr6 | 145923572 | |||||||
chr6:145923607 | A | G | 181 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(178): Show |
229 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(226): Show |
intron_variant | MODIFIER | c.3545+36T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 18/29 | chr6 | 145923607 | |||||||
chr6:145923904 | G | T | 2 | a0003c0005t0001g0035 a0003c0005t0001g0116 |
3 | NA18986.hp1 NA18986.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.3403-119C>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 17/29 | chr6 | 145923904 | |||||||
chr6:145923910 | C | G | 3 | a0001c0001t0015g0270 a0001c0001t0016g0271 a0001c0015t0014g0250 |
3 | HG02055.hp2 HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.3403-125G>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 17/29 | chr6 | 145923910 | |||||||
chr6:145924015 | G | A | 211 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(208): Show |
264 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(261): Show |
intron_variant | MODIFIER | c.3403-230C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 17/29 | chr6 | 145924015 | |||||||
chr6:145924038 | T | C | 3 | a0001c0001t0001g0012 a0001c0001t0001g0108 a0001c0001t0001g0126 |
5 | HG03942.hp2 NA18939.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.3403-253A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 17/29 | chr6 | 145924038 | |||||||
chr6:145924096 | A | G | 2 | a0001c0003t0003g0256 a0001c0003t0003g0257 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.3403-311T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 17/29 | chr6 | 145924096 | |||||||
chr6:145924097 | T | C | 1 | a0001c0001t0001g0064 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.3403-312A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 17/29 | chr6 | 145924097 | |||||||
chr6:145924136 | A | G | 1 | a0001c0001t0004g0244 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3403-351T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 17/29 | chr6 | 145924136 | |||||||
chr6:145924140 | A | C | 2 | a0001c0003t0003g0254 a0001c0003t0003g0255 |
2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.3403-355T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 17/29 | chr6 | 145924140 | |||||||
chr6:145924144 | C | T | 2 | a0001c0001t0015g0270 a0001c0001t0016g0271 |
2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.3403-359G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 17/29 | chr6 | 145924144 | |||||||
chr6:145924292 | AGT | A | 146 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(143): Show |
182 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(179): Show |
intron_variant | MODIFIER | c.3402+445_3402+446d others(4): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 17/29 | chr6 | 145924292 | |||||||
chr6:145924886 | T | A | 2 | a0001c0003t0005g0054 a0011c0013t0005g0055 |
2 | HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.3295-40A>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 16/29 | chr6 | 145924886 | |||||||
chr6:145925005 | A | G | 1 | a0004c0006t0007g0177 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.3295-159T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 16/29 | chr6 | 145925005 | |||||||
chr6:145925048 | A | T | 3 | a0001c0003t0003g0251 a0001c0003t0003g0252 a0001c0003t0003g0253 |
3 | HG02145.hp2 HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.3295-202T>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 16/29 | chr6 | 145925048 | |||||||
chr6:145925075 | A | G | 18 | a0001c0003t0003g0251 a0001c0003t0003g0252 a0001c0003t0003g0253 others(15): Show |
22 | HG01081.hp2 HG01433.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.3295-229T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 16/29 | chr6 | 145925075 | |||||||
chr6:145925216 | T | C | 1 | a0004c0006t0007g0178 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.3295-370A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 16/29 | chr6 | 145925216 | |||||||
chr6:145925320 | G | A | 1 | a0011c0013t0005g0055 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3295-474C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 16/29 | chr6 | 145925320 | |||||||
chr6:145925341 | T | TAC | 32 | a0001c0001t0001g0065 a0001c0001t0001g0069 a0001c0001t0001g0146 others(29): Show |
37 | HG00642.hp2 HG00735.hp2 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.3295-497_3295-496d others(4): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 16/29 | chr6 | 145925341 | |||||||
chr6:145925341 | T | TACAC | 21 | a0001c0001t0001g0033 a0001c0001t0001g0166 a0001c0001t0002g0268 others(18): Show |
30 | HG01081.hp1 HG01123.hp2 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.3295-499_3295-496d others(6): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 16/29 | chr6 | 145925341 | |||||||
chr6:145925341 | T | TACACAC | 32 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0020 others(29): Show |
41 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.3295-501_3295-496d others(8): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 16/29 | chr6 | 145925341 | |||||||
chr6:145925341 | T | TACACACA others(1): Show |
7 | a0001c0001t0001g0071 a0001c0001t0001g0074 a0001c0001t0001g0086 others(4): Show |
7 | HG00544.hp2 HG01069.hp2 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.3295-503_3295-496d others(10): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 16/29 | chr6 | 145925341 | |||||||
chr6:145925341 | T | TACACACA others(3): Show |
80 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(77): Show |
103 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(100): Show |
intron_variant | MODIFIER | c.3295-505_3295-496d others(12): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 16/29 | chr6 | 145925341 | |||||||
chr6:145925341 | T | TACACACA others(5): Show |
18 | a0001c0001t0001g0030 a0001c0001t0001g0060 a0001c0001t0001g0096 others(15): Show |
19 | HG00558.hp2 HG00738.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.3295-507_3295-496d others(14): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 16/29 | chr6 | 145925341 | |||||||
chr6:145925341 | T | TACACACA others(7): Show |
2 | a0001c0020t0001g0059 a0005c0007t0001g0089 |
2 | HG03017.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.3295-509_3295-496d others(16): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 16/29 | chr6 | 145925341 | |||||||
chr6:145925341 | TAC | T | 3 | a0001c0001t0015g0270 a0001c0001t0016g0271 a0001c0002t0002g0219 |
3 | HG02055.hp2 HG03098.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.3295-497_3295-496d others(4): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 16/29 | chr6 | 145925341 | |||||||
chr6:145925368 | A | ACACACAC others(5): Show |
3 | a0001c0001t0001g0010 a0001c0001t0001g0075 a0001c0001t0001g0078 |
5 | HG01975.hp2 HG01981.hp2 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.3295-523_3295-522i others(14): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 16/29 | chr6 | 145925368 | |||||||
chr6:145925371 | T | C | 31 | a0001c0003t0003g0251 a0001c0003t0003g0252 a0001c0003t0003g0253 others(28): Show |
41 | HG01081.hp1 HG01081.hp2 HG01123.hp2 others(38): Show |
intron_variant | MODIFIER | c.3295-525A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 16/29 | chr6 | 145925371 | |||||||
chr6:145925463 | T | C | 2 | a0001c0002t0002g0225 a0001c0002t0002g0226 |
2 | HG03239.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.3295-617A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 16/29 | chr6 | 145925463 | |||||||
chr6:145925491 | T | C | 1 | a0001c0001t0001g0103 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.3295-645A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 16/29 | chr6 | 145925491 | |||||||
chr6:145925544 | T | C | 1 | a0001c0001t0001g0112 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.3294+660A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 16/29 | chr6 | 145925544 | |||||||
chr6:145925595 | C | T | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.3294+609G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 16/29 | chr6 | 145925595 | |||||||
chr6:145925653 | C | T | 2 | a0001c0001t0015g0270 a0001c0001t0016g0271 |
2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.3294+551G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 16/29 | chr6 | 145925653 | |||||||
chr6:145925759 | C | T | 1 | a0001c0001t0001g0114 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.3294+445G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 16/29 | chr6 | 145925759 | |||||||
chr6:145925868 | A | G | 1 | a0001c0014t0001g0156 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.3294+336T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 16/29 | chr6 | 145925868 | |||||||
chr6:145925911 | A | C | 2 | a0001c0002t0002g0004 a0001c0002t0002g0041 |
7 | HG00609.hp2 NA18952.hp1 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.3294+293T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 16/29 | chr6 | 145925911 | |||||||
chr6:145925918 | T | C | 1 | a0001c0001t0004g0239 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.3294+286A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 16/29 | chr6 | 145925918 | |||||||
chr6:145926356 | C | T | 2 | a0001c0003t0003g0254 a0001c0003t0003g0255 |
2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.3202-60G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 15/29 | chr6 | 145926356 | |||||||
chr6:145926368 | T | C | 2 | a0001c0001t0006g0276 a0001c0001t0006g0277 |
2 | HG03704.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.3202-72A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 15/29 | chr6 | 145926368 | |||||||
chr6:145926399 | T | C | 1 | a0001c0002t0002g0229 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3202-103A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 15/29 | chr6 | 145926399 | |||||||
chr6:145926484 | G | C | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.3202-188C>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 15/29 | chr6 | 145926484 | |||||||
chr6:145926814 | T | C | 31 | a0001c0003t0003g0251 a0001c0003t0003g0252 a0001c0003t0003g0253 others(28): Show |
41 | HG01081.hp1 HG01081.hp2 HG01123.hp2 others(38): Show |
intron_variant | MODIFIER | c.3201+375A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 15/29 | chr6 | 145926814 | |||||||
chr6:145926817 | A | G | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.3201+372T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 15/29 | chr6 | 145926817 | |||||||
chr6:145926830 | C | T | 3 | a0001c0001t0001g0057 a0001c0001t0006g0273 a0001c0001t0006g0274 |
3 | HG00642.hp2 HG00741.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.3201+359G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 15/29 | chr6 | 145926830 | |||||||
chr6:145926910 | C | T | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.3201+279G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 15/29 | chr6 | 145926910 | |||||||
chr6:145927008 | G | A | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.3201+181C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 15/29 | chr6 | 145927008 | |||||||
chr6:145927041 | T | C | 186 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(183): Show |
234 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(231): Show |
intron_variant | MODIFIER | c.3201+148A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 15/29 | chr6 | 145927041 | |||||||
chr6:145927084 | G | C | 31 | a0001c0003t0003g0251 a0001c0003t0003g0252 a0001c0003t0003g0253 others(28): Show |
41 | HG01081.hp1 HG01081.hp2 HG01123.hp2 others(38): Show |
intron_variant | MODIFIER | c.3201+105C>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 15/29 | chr6 | 145927084 | |||||||
chr6:145927105 | C | A | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.3201+84G>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 15/29 | chr6 | 145927105 | |||||||
chr6:145927533 | T | C | 3 | a0001c0001t0015g0270 a0001c0001t0016g0271 a0001c0015t0014g0250 |
3 | HG02055.hp2 HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.3113-256A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145927533 | |||||||
chr6:145927571 | C | T | 14 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0040 others(11): Show |
27 | HG00609.hp2 HG02056.hp2 NA18942.hp1 others(24): Show |
intron_variant | MODIFIER | c.3113-294G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145927571 | |||||||
chr6:145927576 | G | C | 2 | a0001c0003t0003g0256 a0001c0003t0003g0257 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.3113-299C>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145927576 | |||||||
chr6:145927705 | A | T | 2 | a0001c0001t0002g0268 a0001c0001t0002g0269 |
2 | HG02615.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.3113-428T>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145927705 | |||||||
chr6:145927727 | C | T | 186 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(183): Show |
234 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(231): Show |
intron_variant | MODIFIER | c.3113-450G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145927727 | |||||||
chr6:145927798 | T | G | 1 | a0006c0008t0003g0044 | 2 | HG01081.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.3113-521A>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145927798 | |||||||
chr6:145927915 | A | G | 1 | a0001c0001t0001g0072 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.3113-638T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145927915 | |||||||
chr6:145928049 | C | G | 3 | a0001c0001t0001g0139 a0001c0001t0001g0142 a0001c0001t0001g0143 |
3 | HG02886.hp1 HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3113-772G>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145928049 | |||||||
chr6:145928209 | TG | T | 3 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0145 |
3 | HG02572.hp1 HG03098.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.3113-933delC | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145928209 | |||||||
chr6:145928310 | G | A | 1 | a0001c0001t0001g0152 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3113-1033C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145928310 | |||||||
chr6:145928392 | A | T | 11 | a0002c0004t0003g0008 a0002c0004t0003g0016 a0002c0004t0003g0045 others(8): Show |
17 | HG01081.hp1 HG01123.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.3113-1115T>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145928392 | |||||||
chr6:145928393 | A | T | 11 | a0002c0004t0003g0008 a0002c0004t0003g0016 a0002c0004t0003g0045 others(8): Show |
17 | HG01081.hp1 HG01123.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.3113-1116T>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145928393 | |||||||
chr6:145928394 | AAAAGGTA others(14): Show |
A | 11 | a0002c0004t0003g0008 a0002c0004t0003g0016 a0002c0004t0003g0045 others(8): Show |
17 | HG01081.hp1 HG01123.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.3113-1138_3113-111 others(25): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145928394 | |||||||
chr6:145928642 | A | T | 1 | a0004c0006t0007g0177 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.3113-1365T>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145928642 | |||||||
chr6:145928695 | G | A | 2 | a0005c0007t0001g0088 a0005c0007t0001g0089 |
2 | HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3113-1418C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145928695 | |||||||
chr6:145928837 | C | G | 1 | a0003c0005t0001g0170 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.3113-1560G>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145928837 | |||||||
chr6:145928851 | GAGA | G | 11 | a0002c0004t0003g0008 a0002c0004t0003g0016 a0002c0004t0003g0045 others(8): Show |
17 | HG01081.hp1 HG01123.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.3113-1577_3113-157 others(7): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145928851 | |||||||
chr6:145928889 | C | T | 10 | a0002c0004t0003g0008 a0002c0004t0003g0016 a0002c0004t0003g0045 others(7): Show |
16 | HG01081.hp1 HG01123.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.3113-1612G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145928889 | |||||||
chr6:145929019 | A | T | 181 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(178): Show |
229 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(226): Show |
intron_variant | MODIFIER | c.3113-1742T>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145929019 | |||||||
chr6:145929059 | A | G | 2 | a0005c0007t0001g0088 a0005c0007t0001g0089 |
2 | HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3113-1782T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145929059 | |||||||
chr6:145929242 | C | T | 2 | a0001c0001t0002g0268 a0001c0001t0002g0269 |
2 | HG02615.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.3113-1965G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145929242 | |||||||
chr6:145929311 | G | C | 1 | a0001c0002t0002g0211 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.3113-2034C>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145929311 | |||||||
chr6:145929577 | A | T | 1 | a0001c0001t0001g0152 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3113-2300T>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145929577 | |||||||
chr6:145929743 | T | A | 1 | a0001c0001t0012g0240 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.3113-2466A>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145929743 | |||||||
chr6:145929811 | T | C | 142 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(139): Show |
177 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(174): Show |
intron_variant | MODIFIER | c.3113-2534A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145929811 | |||||||
chr6:145929823 | A | G | 144 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(141): Show |
180 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(177): Show |
intron_variant | MODIFIER | c.3113-2546T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145929823 | |||||||
chr6:145929847 | G | A | 1 | a0001c0001t0015g0270 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3113-2570C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145929847 | |||||||
chr6:145929972 | G | C | 181 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(178): Show |
229 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(226): Show |
intron_variant | MODIFIER | c.3113-2695C>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145929972 | |||||||
chr6:145930078 | C | T | 1 | a0001c0002t0002g0218 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.3113-2801G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145930078 | |||||||
chr6:145930280 | G | T | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | NA18943.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.3112+2777C>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145930280 | |||||||
chr6:145930364 | T | C | 1 | a0001c0001t0001g0135 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.3112+2693A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145930364 | |||||||
chr6:145930376 | CAT | C | 31 | a0001c0003t0003g0251 a0001c0003t0003g0252 a0001c0003t0003g0253 others(28): Show |
41 | HG01081.hp1 HG01081.hp2 HG01123.hp2 others(38): Show |
intron_variant | MODIFIER | c.3112+2679_3112+268 others(6): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145930376 | |||||||
chr6:145930439 | T | C | 2 | a0001c0001t0006g0273 a0001c0001t0006g0274 |
2 | HG00642.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.3112+2618A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145930439 | |||||||
chr6:145930493 | A | C | 1 | a0003c0005t0011g0176 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.3112+2564T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145930493 | |||||||
chr6:145930696 | T | G | 2 | a0001c0002t0002g0205 a0001c0002t0002g0212 |
2 | HG00639.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.3112+2361A>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145930696 | |||||||
chr6:145930902 | G | A | 31 | a0001c0003t0003g0251 a0001c0003t0003g0252 a0001c0003t0003g0253 others(28): Show |
41 | HG01081.hp1 HG01081.hp2 HG01123.hp2 others(38): Show |
intron_variant | MODIFIER | c.3112+2155C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145930902 | |||||||
chr6:145930926 | T | C | 2 | a0001c0001t0015g0270 a0001c0001t0016g0271 |
2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.3112+2131A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145930926 | |||||||
chr6:145931196 | C | T | 2 | a0001c0003t0003g0254 a0001c0003t0003g0255 |
2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.3112+1861G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145931196 | |||||||
chr6:145931328 | G | T | 1 | a0001c0001t0001g0145 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.3112+1729C>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145931328 | |||||||
chr6:145931359 | A | C | 1 | a0001c0001t0002g0191 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3112+1698T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145931359 | |||||||
chr6:145931439 | G | A | 1 | a0004c0006t0007g0179 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.3112+1618C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145931439 | |||||||
chr6:145931498 | G | A | 2 | a0001c0003t0003g0254 a0001c0003t0003g0255 |
2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.3112+1559C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145931498 | |||||||
chr6:145931538 | A | T | 2 | a0001c0001t0001g0067 a0001c0001t0001g0083 |
2 | HG00280.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.3112+1519T>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145931538 | |||||||
chr6:145931890 | CT | C | 176 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(173): Show |
222 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(219): Show |
intron_variant | MODIFIER | c.3112+1166delA | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145931890 | |||||||
chr6:145931890 | CTT | C | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.3112+1165_3112+116 others(6): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145931890 | |||||||
chr6:145932009 | G | C | 2 | a0001c0001t0001g0139 a0001c0001t0001g0142 |
2 | HG02886.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3112+1048C>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145932009 | |||||||
chr6:145932041 | AT | A | 3 | a0001c0001t0015g0270 a0001c0001t0016g0271 a0001c0015t0014g0250 |
3 | HG02055.hp2 HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.3112+1015delA | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145932041 | |||||||
chr6:145932190 | A | C | 4 | a0001c0001t0001g0066 a0001c0001t0001g0068 a0001c0001t0001g0070 others(1): Show |
4 | NA18991.hp2 NA19011.hp1 NA19072.hp2 others(1): Show |
intron_variant | MODIFIER | c.3112+867T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145932190 | |||||||
chr6:145932285 | T | C | 1 | a0001c0002t0002g0213 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.3112+772A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145932285 | |||||||
chr6:145932314 | C | T | 1 | a0001c0001t0001g0021 | 2 | HG02080.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.3112+743G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145932314 | |||||||
chr6:145932480 | AACACTAT others(6): Show |
A | 2 | a0001c0002t0002g0200 a0001c0002t0002g0214 |
2 | HG01255.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.3112+564_3112+576d others(15): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145932480 | |||||||
chr6:145932503 | C | T | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.3112+554G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145932503 | |||||||
chr6:145932507 | C | G | 1 | a0001c0001t0001g0113 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.3112+550G>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145932507 | |||||||
chr6:145932513 | G | C | 1 | a0001c0002t0002g0215 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.3112+544C>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145932513 | |||||||
chr6:145932541 | G | A | 1 | a0006c0008t0003g0044 | 2 | HG01081.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.3112+516C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145932541 | |||||||
chr6:145932741 | T | G | 2 | a0001c0002t0002g0225 a0001c0002t0002g0226 |
2 | HG03239.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.3112+316A>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145932741 | |||||||
chr6:145932787 | C | A | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.3112+270G>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145932787 | |||||||
chr6:145932838 | ATGTT | A | 24 | a0001c0001t0004g0007 a0001c0001t0004g0043 a0001c0001t0004g0232 others(21): Show |
29 | HG00642.hp2 HG00735.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.3112+215_3112+218d others(6): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145932838 | |||||||
chr6:145932847 | T | A | 1 | a0001c0001t0002g0195 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3112+210A>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145932847 | |||||||
chr6:145932964 | T | TC | 146 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(143): Show |
182 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(179): Show |
intron_variant | MODIFIER | c.3112+92dupG | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 14/29 | chr6 | 145932964 | |||||||
chr6:145933224 | G | A | 1 | a0001c0001t0004g0241 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2991-46C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 13/29 | chr6 | 145933224 | |||||||
chr6:145933376 | T | C | 2 | a0001c0001t0002g0268 a0001c0001t0002g0269 |
2 | HG02615.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2991-198A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 13/29 | chr6 | 145933376 | |||||||
chr6:145933565 | C | G | 2 | a0001c0003t0003g0256 a0001c0003t0003g0257 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2991-387G>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 13/29 | chr6 | 145933565 | |||||||
chr6:145933669 | T | C | 1 | a0006c0008t0003g0044 | 2 | HG01081.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.2991-491A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 13/29 | chr6 | 145933669 | |||||||
chr6:145933911 | C | T | 2 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
2 | HG01069.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2991-733G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 13/29 | chr6 | 145933911 | |||||||
chr6:145933943 | A | C | 146 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(143): Show |
182 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(179): Show |
intron_variant | MODIFIER | c.2991-765T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 13/29 | chr6 | 145933943 | |||||||
chr6:145934011 | T | A | 14 | a0001c0001t0016g0271 a0001c0003t0005g0009 a0001c0003t0005g0017 others(11): Show |
18 | HG01081.hp2 HG01433.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.2991-833A>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 13/29 | chr6 | 145934011 | |||||||
chr6:145934114 | G | C | 2 | a0001c0003t0003g0256 a0001c0003t0003g0257 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2990+793C>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 13/29 | chr6 | 145934114 | |||||||
chr6:145934130 | G | A | 2 | a0001c0001t0004g0246 a0001c0001t0004g0247 |
2 | HG01074.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.2990+777C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 13/29 | chr6 | 145934130 | |||||||
chr6:145934193 | C | T | 1 | a0001c0015t0014g0250 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2990+714G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 13/29 | chr6 | 145934193 | |||||||
chr6:145934194 | G | A | 177 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(174): Show |
223 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(220): Show |
intron_variant | MODIFIER | c.2990+713C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 13/29 | chr6 | 145934194 | |||||||
chr6:145934230 | G | A | 12 | a0001c0003t0005g0009 a0001c0003t0005g0017 a0001c0003t0005g0047 others(9): Show |
15 | HG01433.hp1 HG02572.hp2 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.2990+677C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 13/29 | chr6 | 145934230 | |||||||
chr6:145934339 | G | T | 11 | a0002c0004t0003g0008 a0002c0004t0003g0016 a0002c0004t0003g0045 others(8): Show |
17 | HG01081.hp1 HG01123.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.2990+568C>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 13/29 | chr6 | 145934339 | |||||||
chr6:145934423 | GC | G | 99 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(96): Show |
123 | HG00609.hp1 HG00621.hp2 HG00639.hp1 others(120): Show |
intron_variant | MODIFIER | c.2990+483delG | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 13/29 | chr6 | 145934423 | |||||||
chr6:145934473 | T | TAAATA | 24 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0022 others(21): Show |
31 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.2990+429_2990+433d others(7): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 13/29 | chr6 | 145934473 | |||||||
chr6:145934473 | T | TAAATAAA others(3): Show |
17 | a0001c0001t0001g0019 a0001c0001t0001g0060 a0001c0001t0001g0061 others(14): Show |
18 | HG00558.hp2 HG00741.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.2990+424_2990+433d others(12): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 13/29 | chr6 | 145934473 | |||||||
chr6:145934473 | T | TAAATAAA others(8): Show |
104 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(101): Show |
133 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(130): Show |
intron_variant | MODIFIER | c.2990+419_2990+433d others(17): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 13/29 | chr6 | 145934473 | |||||||
chr6:145934473 | T | TAAATAAA others(13): Show |
13 | a0001c0001t0001g0018 a0001c0001t0001g0057 a0001c0001t0001g0132 others(10): Show |
14 | HG01496.hp1 HG01515.hp1 HG01516.hp2 others(11): Show |
intron_variant | MODIFIER | c.2990+414_2990+433d others(22): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 13/29 | chr6 | 145934473 | |||||||
chr6:145934473 | T | TAAATAAA others(18): Show |
15 | a0001c0003t0003g0254 a0001c0003t0003g0255 a0001c0003t0005g0009 others(12): Show |
20 | HG01433.hp1 HG01891.hp2 HG02809.hp2 others(17): Show |
intron_variant | MODIFIER | c.2990+409_2990+433d others(27): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 13/29 | chr6 | 145934473 | |||||||
chr6:145934473 | T | TAAATAAA others(23): Show |
8 | a0001c0015t0014g0250 a0002c0004t0003g0008 a0002c0004t0003g0045 others(5): Show |
12 | HG01081.hp1 HG01123.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.2990+404_2990+433d others(32): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 13/29 | chr6 | 145934473 | |||||||
chr6:145934473 | T | TAAATAAA others(28): Show |
2 | a0001c0003t0005g0049 a0001c0003t0005g0053 |
2 | HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.2990+399_2990+433d others(37): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 13/29 | chr6 | 145934473 | |||||||
chr6:145934507 | T | TAAAATAA others(9): Show |
4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.2990+399_2990+400i others(18): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 13/29 | chr6 | 145934507 | |||||||
chr6:145934508 | A | AAAATAAA others(7): Show |
1 | a0001c0001t0001g0071 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2990+398_2990+399i others(16): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 13/29 | chr6 | 145934508 | |||||||
chr6:145934613 | T | G | 1 | a0001c0001t0001g0166 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2990+294A>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 13/29 | chr6 | 145934613 | |||||||
chr6:145934658 | G | A | 177 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(174): Show |
223 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(220): Show |
intron_variant | MODIFIER | c.2990+249C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 13/29 | chr6 | 145934658 | |||||||
chr6:145934808 | C | T | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.2990+99G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 13/29 | chr6 | 145934808 | |||||||
chr6:145935174 | G | C | 2 | a0001c0003t0003g0256 a0001c0003t0003g0257 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2734-11C>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 12/29 | chr6 | 145935174 | |||||||
chr6:145935179 | G | GA | 17 | a0001c0001t0001g0133 a0001c0001t0001g0148 a0001c0003t0003g0251 others(14): Show |
20 | HG00738.hp1 HG01433.hp1 HG01993.hp1 others(17): Show |
intron_variant | MODIFIER | c.2734-17dupT | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 12/29 | chr6 | 145935179 | |||||||
chr6:145935179 | GA | G | 5 | a0001c0002t0002g0182 a0004c0006t0007g0015 a0004c0006t0007g0177 others(2): Show |
7 | HG02135.hp2 HG02155.hp2 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.2734-17delT | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 12/29 | chr6 | 145935179 | |||||||
chr6:145935194 | A | G | 1 | a0001c0001t0001g0158 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2734-31T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 12/29 | chr6 | 145935194 | |||||||
chr6:145935498 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2570-57C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145935498 | |||||||
chr6:145935661 | A | G | 1 | a0001c0001t0001g0070 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2570-220T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145935661 | |||||||
chr6:145935879 | T | G | 3 | a0001c0001t0015g0270 a0001c0001t0016g0271 a0001c0015t0014g0250 |
3 | HG02055.hp2 HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2570-438A>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145935879 | |||||||
chr6:145935928 | T | C | 1 | a0001c0001t0016g0271 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2570-487A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145935928 | |||||||
chr6:145935954 | TAC | T | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.2570-515_2570-514d others(4): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145935954 | |||||||
chr6:145936029 | G | C | 1 | a0001c0001t0016g0271 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2570-588C>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145936029 | |||||||
chr6:145936065 | T | C | 3 | a0001c0001t0004g0007 a0001c0001t0004g0242 a0001c0001t0004g0243 |
6 | NA18951.hp2 NA18955.hp1 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.2570-624A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145936065 | |||||||
chr6:145936209 | G | A | 1 | a0001c0002t0002g0248 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2570-768C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145936209 | |||||||
chr6:145936352 | G | A | 13 | a0001c0003t0005g0009 a0001c0003t0005g0017 a0001c0003t0005g0047 others(10): Show |
17 | HG01081.hp2 HG01433.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.2570-911C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145936352 | |||||||
chr6:145936466 | A | G | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.2570-1025T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145936466 | |||||||
chr6:145936467 | T | C | 2 | a0001c0003t0003g0254 a0001c0003t0003g0255 |
2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2570-1026A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145936467 | |||||||
chr6:145936625 | G | C | 181 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(178): Show |
229 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(226): Show |
intron_variant | MODIFIER | c.2570-1184C>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145936625 | |||||||
chr6:145936668 | C | T | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.2570-1227G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145936668 | |||||||
chr6:145936725 | C | T | 1 | a0001c0001t0006g0275 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2570-1284G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145936725 | |||||||
chr6:145936775 | T | G | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.2570-1334A>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145936775 | |||||||
chr6:145936938 | G | A | 2 | a0001c0003t0003g0254 a0001c0003t0003g0255 |
2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2570-1497C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145936938 | |||||||
chr6:145936964 | C | T | 1 | a0001c0003t0005g0056 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2570-1523G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145936964 | |||||||
chr6:145936976 | A | ATCT | 3 | a0001c0001t0002g0268 a0001c0001t0002g0269 a0001c0001t0015g0270 |
3 | HG02615.hp1 HG02976.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2570-1538_2570-153 others(7): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145936976 | |||||||
chr6:145936978 | C | CT | 5 | a0001c0001t0002g0190 a0001c0002t0002g0005 a0001c0002t0002g0202 others(2): Show |
8 | HG01516.hp1 HG02257.hp1 HG03486.hp2 others(5): Show |
intron_variant | MODIFIER | c.2570-1538dupA | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145936978 | |||||||
chr6:145936978 | CT | C | 12 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0069 others(9): Show |
13 | HG01993.hp2 HG02735.hp2 HG02965.hp1 others(10): Show |
intron_variant | MODIFIER | c.2570-1538delA | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145936978 | |||||||
chr6:145936978 | CTT | C | 154 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(151): Show |
194 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(191): Show |
intron_variant | MODIFIER | c.2570-1539_2570-153 others(6): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145936978 | |||||||
chr6:145936978 | CTTT | C | 16 | a0001c0001t0001g0105 a0001c0001t0001g0138 a0001c0001t0001g0165 others(13): Show |
22 | HG01081.hp1 HG01123.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.2570-1540_2570-153 others(7): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145936978 | |||||||
chr6:145936979 | T | TTC | 6 | a0001c0001t0002g0193 a0001c0001t0016g0271 a0004c0006t0007g0015 others(3): Show |
8 | HG02055.hp2 HG02135.hp2 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.2570-1539_2570-153 others(6): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145936979 | |||||||
chr6:145936980 | T | TC | 3 | a0001c0001t0002g0038 a0001c0001t0002g0191 a0001c0001t0002g0192 |
4 | HG02109.hp2 HG02647.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.2570-1540_2570-153 others(5): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145936980 | |||||||
chr6:145936982 | T | C | 7 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0069 others(4): Show |
7 | HG02965.hp1 HG03209.hp1 HG03942.hp2 others(4): Show |
intron_variant | MODIFIER | c.2570-1541A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145936982 | |||||||
chr6:145936983 | T | C | 154 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(151): Show |
194 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(191): Show |
intron_variant | MODIFIER | c.2570-1542A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145936983 | |||||||
chr6:145936984 | T | C | 16 | a0001c0001t0001g0138 a0001c0001t0001g0165 a0001c0003t0003g0252 others(13): Show |
22 | HG01081.hp1 HG01123.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.2570-1543A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145936984 | |||||||
chr6:145937022 | C | T | 14 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0040 others(11): Show |
27 | HG00609.hp2 HG02056.hp2 NA18942.hp1 others(24): Show |
intron_variant | MODIFIER | c.2570-1581G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145937022 | |||||||
chr6:145937042 | G | A | 1 | a0001c0001t0002g0195 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2570-1601C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145937042 | |||||||
chr6:145937086 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2570-1645G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145937086 | |||||||
chr6:145937183 | C | G | 1 | a0001c0019t0001g0107 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2570-1742G>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145937183 | |||||||
chr6:145937370 | C | G | 2 | a0001c0003t0003g0256 a0001c0003t0003g0257 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2570-1929G>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145937370 | |||||||
chr6:145937397 | A | G | 2 | a0001c0001t0001g0105 a0001c0001t0001g0106 |
2 | NA18956.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.2570-1956T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145937397 | |||||||
chr6:145937602 | G | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0027 |
4 | HG01255.hp1 HG01433.hp2 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.2570-2161C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145937602 | |||||||
chr6:145937915 | T | TAAC | 14 | a0001c0002t0002g0001 a0001c0002t0002g0004 a0001c0002t0002g0040 others(11): Show |
27 | HG00609.hp2 HG02056.hp2 NA18942.hp1 others(24): Show |
intron_variant | MODIFIER | c.2570-2475_2570-247 others(7): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145937915 | |||||||
chr6:145938369 | C | T | 177 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(174): Show |
223 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(220): Show |
intron_variant | MODIFIER | c.2569+2354G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145938369 | |||||||
chr6:145938486 | A | G | 1 | a0001c0001t0001g0058 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2569+2237T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145938486 | |||||||
chr6:145938567 | T | C | 3 | a0001c0002t0002g0036 a0001c0002t0002g0042 a0001c0002t0002g0223 |
5 | NA18956.hp1 NA18988.hp1 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.2569+2156A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145938567 | |||||||
chr6:145938645 | G | A | 25 | a0001c0001t0004g0007 a0001c0001t0004g0043 a0001c0001t0004g0232 others(22): Show |
30 | HG00642.hp2 HG00735.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.2569+2078C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145938645 | |||||||
chr6:145938874 | A | G | 177 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(174): Show |
223 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(220): Show |
intron_variant | MODIFIER | c.2569+1849T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145938874 | |||||||
chr6:145938877 | C | G | 1 | a0001c0001t0004g0244 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2569+1846G>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145938877 | |||||||
chr6:145939146 | A | G | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.2569+1577T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145939146 | |||||||
chr6:145939298 | T | C | 1 | a0001c0001t0001g0061 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2569+1425A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145939298 | |||||||
chr6:145939400 | A | G | 2 | a0001c0001t0015g0270 a0001c0001t0016g0271 |
2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2569+1323T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145939400 | |||||||
chr6:145939546 | A | G | 2 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
2 | HG01069.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2569+1177T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145939546 | |||||||
chr6:145939617 | C | T | 181 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(178): Show |
229 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(226): Show |
intron_variant | MODIFIER | c.2569+1106G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145939617 | |||||||
chr6:145939837 | A | C | 1 | a0001c0001t0015g0270 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2569+886T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145939837 | |||||||
chr6:145939880 | T | C | 1 | a0003c0005t0001g0169 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2569+843A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145939880 | |||||||
chr6:145940098 | T | C | 2 | a0001c0001t0001g0162 a0001c0001t0001g0163 |
2 | NA18966.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.2569+625A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145940098 | |||||||
chr6:145940135 | C | T | 177 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(174): Show |
223 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(220): Show |
intron_variant | MODIFIER | c.2569+588G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145940135 | |||||||
chr6:145940203 | C | T | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.2569+520G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145940203 | |||||||
chr6:145940305 | T | A | 1 | a0001c0001t0006g0275 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2569+418A>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145940305 | |||||||
chr6:145940323 | C | G | 1 | a0001c0015t0014g0250 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2569+400G>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145940323 | |||||||
chr6:145940370 | A | AC | 39 | a0001c0001t0001g0062 a0001c0001t0001g0065 a0001c0001t0001g0066 others(36): Show |
39 | HG00280.hp1 HG00438.hp1 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.2569+352dupG | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145940370 | |||||||
chr6:145940507 | C | T | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.2569+216G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145940507 | |||||||
chr6:145940663 | T | C | 2 | a0001c0001t0001g0134 a0001c0001t0001g0147 |
2 | HG01192.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.2569+60A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145940663 | |||||||
chr6:145940717 | C | A | 3 | a0001c0002t0002g0036 a0001c0002t0002g0042 a0001c0002t0002g0223 |
5 | NA18956.hp1 NA18988.hp1 NA18998.hp2 others(2): Show |
splice_region_variant&intron_variant | LOW | c.2569+6G>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 11/29 | chr6 | 145940717 | |||||||
chr6:145940871 | T | C | 1 | a0001c0002t0002g0180 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2491-70A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 10/29 | chr6 | 145940871 | |||||||
chr6:145941557 | C | T | 2 | a0001c0003t0003g0254 a0001c0003t0003g0255 |
2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2490+66G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 10/29 | chr6 | 145941557 | |||||||
chr6:145941561 | G | T | 220 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(217): Show |
274 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(271): Show |
intron_variant | MODIFIER | c.2490+62C>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 10/29 | chr6 | 145941561 | |||||||
chr6:145941954 | C | T | 2 | a0001c0001t0004g0043 a0001c0001t0004g0232 |
3 | HG01515.hp2 HG01517.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.2239-80G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 9/29 | chr6 | 145941954 | |||||||
chr6:145942016 | A | G | 1 | a0001c0001t0001g0064 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2239-142T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 9/29 | chr6 | 145942016 | |||||||
chr6:145942178 | T | A | 1 | a0001c0003t0005g0053 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2239-304A>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 9/29 | chr6 | 145942178 | |||||||
chr6:145942323 | T | C | 1 | a0001c0001t0002g0224 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2239-449A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 9/29 | chr6 | 145942323 | |||||||
chr6:145942571 | T | C | 5 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0097 others(2): Show |
7 | HG00735.hp1 HG01069.hp1 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.2238+572A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 9/29 | chr6 | 145942571 | |||||||
chr6:145942690 | A | G | 1 | a0001c0002t0002g0188 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2238+453T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 9/29 | chr6 | 145942690 | |||||||
chr6:145942750 | G | A | 12 | a0001c0003t0005g0009 a0001c0003t0005g0017 a0001c0003t0005g0047 others(9): Show |
15 | HG01433.hp1 HG02572.hp2 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.2238+393C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 9/29 | chr6 | 145942750 | |||||||
chr6:145942935 | T | C | 211 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(208): Show |
264 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(261): Show |
intron_variant | MODIFIER | c.2238+208A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 9/29 | chr6 | 145942935 | |||||||
chr6:145943002 | C | A | 1 | a0001c0003t0003g0257 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2238+141G>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 9/29 | chr6 | 145943002 | |||||||
chr6:145943073 | G | C | 2 | a0001c0003t0005g0054 a0011c0013t0005g0055 |
2 | HG02965.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2238+70C>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 9/29 | chr6 | 145943073 | |||||||
chr6:145943096 | G | A | 2 | a0001c0001t0001g0019 a0001c0001t0001g0062 |
3 | HG00741.hp1 HG02622.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.2238+47C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 9/29 | chr6 | 145943096 | |||||||
chr6:145943884 | T | C | 3 | a0001c0003t0003g0251 a0001c0003t0003g0252 a0001c0003t0003g0253 |
3 | HG02145.hp2 HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1579-82A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 8/29 | chr6 | 145943884 | |||||||
chr6:145944043 | G | T | 2 | a0001c0003t0003g0251 a0001c0003t0003g0253 |
2 | HG02145.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1579-241C>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 8/29 | chr6 | 145944043 | |||||||
chr6:145944078 | A | C | 1 | a0001c0001t0001g0097 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1579-276T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 8/29 | chr6 | 145944078 | |||||||
chr6:145944204 | C | A | 145 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(142): Show |
181 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(178): Show |
intron_variant | MODIFIER | c.1579-402G>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 8/29 | chr6 | 145944204 | |||||||
chr6:145944263 | C | T | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.1579-461G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 8/29 | chr6 | 145944263 | |||||||
chr6:145944499 | A | C | 2 | a0001c0001t0002g0268 a0001c0001t0002g0269 |
2 | HG02615.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1579-697T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 8/29 | chr6 | 145944499 | |||||||
chr6:145944500 | GGTCGAAC others(1): Show |
G | 90 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(87): Show |
113 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.1579-706_1579-699d others(10): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 8/29 | chr6 | 145944500 | |||||||
chr6:145944510 | G | C | 90 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(87): Show |
113 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.1579-708C>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 8/29 | chr6 | 145944510 | |||||||
chr6:145944511 | G | T | 90 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(87): Show |
113 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.1579-709C>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 8/29 | chr6 | 145944511 | |||||||
chr6:145945036 | T | C | 146 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(143): Show |
182 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(179): Show |
intron_variant | MODIFIER | c.1578+345A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 8/29 | chr6 | 145945036 | |||||||
chr6:145945273 | T | G | 1 | a0001c0001t0001g0030 | 2 | HG01891.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.1578+108A>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 8/29 | chr6 | 145945273 | |||||||
chr6:145946039 | G | T | 1 | a0001c0003t0005g0047 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1321+194C>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 7/29 | chr6 | 145946039 | |||||||
chr6:145946172 | G | T | 7 | a0001c0002t0002g0037 a0001c0002t0002g0182 a0001c0002t0002g0183 others(4): Show |
8 | NA18950.hp1 NA18953.hp2 NA18959.hp1 others(5): Show |
intron_variant | MODIFIER | c.1321+61C>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 7/29 | chr6 | 145946172 | |||||||
chr6:145946737 | A | G | 181 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(178): Show |
229 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(226): Show |
intron_variant | MODIFIER | c.1213-396T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 6/29 | chr6 | 145946737 | |||||||
chr6:145946743 | AT | A | 25 | a0001c0001t0004g0007 a0001c0001t0004g0043 a0001c0001t0004g0232 others(22): Show |
30 | HG00642.hp2 HG00735.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.1213-403delA | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 6/29 | chr6 | 145946743 | |||||||
chr6:145946753 | T | A | 2 | a0001c0002t0002g0225 a0001c0002t0002g0226 |
2 | HG03239.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1213-412A>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 6/29 | chr6 | 145946753 | |||||||
chr6:145946754 | A | T | 1 | a0001c0001t0001g0096 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1213-413T>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 6/29 | chr6 | 145946754 | |||||||
chr6:145946840 | G | C | 11 | a0002c0004t0003g0008 a0002c0004t0003g0016 a0002c0004t0003g0045 others(8): Show |
17 | HG01081.hp1 HG01123.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.1213-499C>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 6/29 | chr6 | 145946840 | |||||||
chr6:145946859 | T | A | 1 | a0001c0001t0002g0227 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1213-518A>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 6/29 | chr6 | 145946859 | |||||||
chr6:145947094 | A | G | 18 | a0001c0003t0003g0251 a0001c0003t0003g0252 a0001c0003t0003g0253 others(15): Show |
22 | HG01081.hp2 HG01433.hp1 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.1212+399T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 6/29 | chr6 | 145947094 | |||||||
chr6:145947243 | C | A | 2 | a0001c0001t0001g0135 a0001c0001t0001g0136 |
2 | HG01515.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.1212+250G>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 6/29 | chr6 | 145947243 | |||||||
chr6:145947301 | C | A | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.1212+192G>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 6/29 | chr6 | 145947301 | |||||||
chr6:145947382 | C | T | 2 | a0001c0003t0003g0256 a0001c0003t0003g0257 |
2 | HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1212+111G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 6/29 | chr6 | 145947382 | |||||||
chr6:145947487 | T | A | 146 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(143): Show |
182 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(179): Show |
splice_region_variant&intron_variant | LOW | c.1212+6A>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 6/29 | chr6 | 145947487 | |||||||
chr6:145947674 | T | C | 1 | a0001c0003t0003g0253 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1062-31A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 5/29 | chr6 | 145947674 | |||||||
chr6:145947883 | G | A | 1 | a0001c0001t0002g0228 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1062-240C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 5/29 | chr6 | 145947883 | |||||||
chr6:145948045 | G | A | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.1061+227C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 5/29 | chr6 | 145948045 | |||||||
chr6:145948456 | T | C | 1 | a0001c0001t0001g0137 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.983-106A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 4/29 | chr6 | 145948456 | |||||||
chr6:145948685 | T | G | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.983-335A>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 4/29 | chr6 | 145948685 | |||||||
chr6:145948746 | T | C | 1 | a0001c0003t0003g0257 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.983-396A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 4/29 | chr6 | 145948746 | |||||||
chr6:145948805 | G | A | 1 | a0001c0002t0002g0229 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.983-455C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 4/29 | chr6 | 145948805 | |||||||
chr6:145948891 | A | G | 1 | a0001c0003t0003g0254 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.983-541T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 4/29 | chr6 | 145948891 | |||||||
chr6:145948955 | C | T | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.983-605G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 4/29 | chr6 | 145948955 | |||||||
chr6:145948985 | T | C | 1 | a0006c0008t0003g0044 | 2 | HG01081.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.983-635A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 4/29 | chr6 | 145948985 | |||||||
chr6:145948998 | A | G | 13 | a0001c0003t0005g0009 a0001c0003t0005g0017 a0001c0003t0005g0047 others(10): Show |
17 | HG01081.hp2 HG01433.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.983-648T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 4/29 | chr6 | 145948998 | |||||||
chr6:145949311 | A | C | 1 | a0001c0001t0001g0165 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.982+953T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 4/29 | chr6 | 145949311 | |||||||
chr6:145950041 | T | G | 1 | a0001c0001t0001g0062 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.982+223A>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 4/29 | chr6 | 145950041 | |||||||
chr6:145950197 | C | G | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.982+67G>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 4/29 | chr6 | 145950197 | |||||||
chr6:145950533 | T | G | 3 | a0001c0003t0003g0251 a0001c0003t0003g0252 a0001c0003t0003g0253 |
3 | HG02145.hp2 HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.764-51A>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 3/29 | chr6 | 145950533 | |||||||
chr6:145950563 | A | G | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.764-81T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 3/29 | chr6 | 145950563 | |||||||
chr6:145950740 | T | TA | 11 | a0002c0004t0003g0008 a0002c0004t0003g0016 a0002c0004t0003g0045 others(8): Show |
17 | HG01081.hp1 HG01123.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.764-259dupT | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 3/29 | chr6 | 145950740 | |||||||
chr6:145950841 | C | T | 32 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0021 others(29): Show |
41 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.764-359G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 3/29 | chr6 | 145950841 | |||||||
chr6:145950847 | AGAAGCTG others(4): Show |
A | 146 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(143): Show |
182 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(179): Show |
intron_variant | MODIFIER | c.764-376_764-366del others(11): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 3/29 | chr6 | 145950847 | |||||||
chr6:145950878 | T | C | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.764-396A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 3/29 | chr6 | 145950878 | |||||||
chr6:145950917 | G | T | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | HG02572.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.764-435C>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 3/29 | chr6 | 145950917 | |||||||
chr6:145951177 | T | C | 1 | a0013c0018t0002g0230 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.764-695A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 3/29 | chr6 | 145951177 | |||||||
chr6:145951438 | A | G | 1 | a0001c0002t0002g0036 | 2 | NA18988.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.763+911T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 3/29 | chr6 | 145951438 | |||||||
chr6:145951467 | T | C | 1 | a0001c0009t0001g0085 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.763+882A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 3/29 | chr6 | 145951467 | |||||||
chr6:145951523 | C | T | 1 | a0001c0001t0001g0093 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.763+826G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 3/29 | chr6 | 145951523 | |||||||
chr6:145951655 | C | T | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.763+694G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 3/29 | chr6 | 145951655 | |||||||
chr6:145952122 | A | G | 2 | a0001c0003t0003g0254 a0001c0003t0003g0255 |
2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.763+227T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 3/29 | chr6 | 145952122 | |||||||
chr6:145952183 | A | G | 1 | a0001c0001t0001g0020 | 2 | HG02965.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.763+166T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 3/29 | chr6 | 145952183 | |||||||
chr6:145952214 | A | G | 2 | a0001c0001t0002g0268 a0001c0001t0002g0269 |
2 | HG02615.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.763+135T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 3/29 | chr6 | 145952214 | |||||||
chr6:145952562 | T | A | 1 | a0001c0001t0001g0138 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.634-84A>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 2/29 | chr6 | 145952562 | |||||||
chr6:145952633 | C | T | 145 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(142): Show |
181 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(178): Show |
intron_variant | MODIFIER | c.634-155G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 2/29 | chr6 | 145952633 | |||||||
chr6:145952829 | CAGA | C | 2 | a0001c0001t0001g0033 a0001c0001t0001g0166 |
3 | HG02723.hp2 HG02818.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.634-354_634-352del others(3): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 2/29 | chr6 | 145952829 | |||||||
chr6:145952885 | T | G | 7 | a0001c0001t0001g0030 a0001c0001t0001g0060 a0001c0001t0001g0139 others(4): Show |
8 | HG01891.hp1 HG02257.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.634-407A>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 2/29 | chr6 | 145952885 | |||||||
chr6:145953285 | G | A | 3 | a0001c0003t0003g0251 a0001c0003t0003g0252 a0001c0003t0003g0253 |
3 | HG02145.hp2 HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.634-807C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 2/29 | chr6 | 145953285 | |||||||
chr6:145953443 | C | T | 3 | a0001c0001t0001g0019 a0001c0001t0001g0061 a0001c0001t0001g0062 |
4 | HG00741.hp1 HG02451.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.634-965G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 2/29 | chr6 | 145953443 | |||||||
chr6:145953595 | A | C | 3 | a0001c0003t0003g0256 a0001c0003t0003g0257 a0001c0003t0009g0258 |
3 | HG02717.hp2 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.633+1095T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 2/29 | chr6 | 145953595 | |||||||
chr6:145953686 | T | C | 11 | a0002c0004t0003g0008 a0002c0004t0003g0016 a0002c0004t0003g0045 others(8): Show |
17 | HG01081.hp1 HG01123.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.633+1004A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 2/29 | chr6 | 145953686 | |||||||
chr6:145953826 | T | C | 1 | a0001c0002t0002g0231 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.633+864A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 2/29 | chr6 | 145953826 | |||||||
chr6:145953920 | G | A | 25 | a0001c0001t0004g0007 a0001c0001t0004g0043 a0001c0001t0004g0232 others(22): Show |
30 | HG00642.hp2 HG00735.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.633+770C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 2/29 | chr6 | 145953920 | |||||||
chr6:145953998 | CA | C | 19 | a0001c0003t0003g0251 a0001c0003t0003g0252 a0001c0003t0003g0253 others(16): Show |
23 | HG01081.hp2 HG01433.hp1 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.633+691delT | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 2/29 | chr6 | 145953998 | |||||||
chr6:145954093 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.633+597G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 2/29 | chr6 | 145954093 | |||||||
chr6:145954137 | GA | G | 25 | a0001c0001t0004g0007 a0001c0001t0004g0043 a0001c0001t0004g0232 others(22): Show |
30 | HG00642.hp2 HG00735.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.633+552delT | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 2/29 | chr6 | 145954137 | |||||||
chr6:145954217 | A | T | 1 | a0001c0001t0001g0155 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.633+473T>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 2/29 | chr6 | 145954217 | |||||||
chr6:145954259 | G | A | 11 | a0002c0004t0003g0008 a0002c0004t0003g0016 a0002c0004t0003g0045 others(8): Show |
17 | HG01081.hp1 HG01123.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.633+431C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 2/29 | chr6 | 145954259 | |||||||
chr6:145954435 | G | C | 1 | a0001c0001t0001g0144 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.633+255C>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 2/29 | chr6 | 145954435 | |||||||
chr6:145954585 | T | C | 2 | a0001c0001t0015g0270 a0001c0001t0016g0271 |
2 | HG02055.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.633+105A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 2/29 | chr6 | 145954585 | |||||||
chr6:145955644 | A | T | 145 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(142): Show |
181 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(178): Show |
intron_variant | MODIFIER | c.-32-290T>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145955644 | |||||||
chr6:145955735 | C | T | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.-32-381G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145955735 | |||||||
chr6:145955753 | T | G | 2 | a0001c0001t0006g0276 a0001c0001t0006g0277 |
2 | HG03704.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-32-399A>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145955753 | |||||||
chr6:145955955 | T | C | 6 | a0001c0001t0004g0043 a0001c0001t0004g0232 a0001c0001t0004g0244 others(3): Show |
7 | HG01074.hp1 HG01109.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.-32-601A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145955955 | |||||||
chr6:145956195 | C | T | 13 | a0001c0003t0005g0009 a0001c0003t0005g0017 a0001c0003t0005g0047 others(10): Show |
17 | HG01081.hp2 HG01433.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.-32-841G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145956195 | |||||||
chr6:145956558 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-32-1204C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145956558 | |||||||
chr6:145956626 | A | C | 1 | a0001c0001t0001g0087 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-32-1272T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145956626 | |||||||
chr6:145956691 | C | T | 177 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(174): Show |
223 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(220): Show |
intron_variant | MODIFIER | c.-32-1337G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145956691 | |||||||
chr6:145956757 | T | A | 1 | a0001c0001t0001g0086 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-32-1403A>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145956757 | |||||||
chr6:145957117 | G | A | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.-32-1763C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145957117 | |||||||
chr6:145957365 | T | G | 2 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
2 | HG01069.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-32-2011A>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145957365 | |||||||
chr6:145957784 | T | C | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.-32-2430A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145957784 | |||||||
chr6:145957823 | T | C | 104 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(101): Show |
128 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(125): Show |
intron_variant | MODIFIER | c.-32-2469A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145957823 | |||||||
chr6:145957926 | T | A | 2 | a0001c0001t0002g0268 a0001c0001t0002g0269 |
2 | HG02615.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-32-2572A>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145957926 | |||||||
chr6:145957962 | G | T | 181 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(178): Show |
229 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(226): Show |
intron_variant | MODIFIER | c.-32-2608C>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145957962 | |||||||
chr6:145957995 | GAGACTTC others(8): Show |
G | 3 | a0001c0003t0003g0256 a0001c0003t0003g0257 a0001c0003t0009g0258 |
3 | HG02717.hp2 HG03225.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-32-2656_-32-2642d others(17): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145957995 | |||||||
chr6:145958227 | C | T | 25 | a0001c0001t0004g0007 a0001c0001t0004g0043 a0001c0001t0004g0232 others(22): Show |
30 | HG00642.hp2 HG00735.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.-32-2873G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145958227 | |||||||
chr6:145958302 | A | G | 3 | a0001c0003t0003g0251 a0001c0003t0003g0252 a0001c0003t0003g0253 |
3 | HG02145.hp2 HG03041.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-32-2948T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145958302 | |||||||
chr6:145958466 | C | T | 2 | a0001c0001t0002g0268 a0001c0001t0002g0269 |
2 | HG02615.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-32-3112G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145958466 | |||||||
chr6:145958828 | C | CATTT | 3 | a0001c0001t0001g0060 a0002c0004t0003g0259 a0002c0004t0003g0260 |
3 | HG02630.hp1 HG02970.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-32-3478_-32-3475d others(6): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145958828 | |||||||
chr6:145958962 | A | C | 1 | a0001c0020t0001g0059 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-32-3608T>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145958962 | |||||||
chr6:145959001 | T | C | 1 | a0001c0001t0001g0146 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.-32-3647A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145959001 | |||||||
chr6:145959055 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-32-3701A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145959055 | |||||||
chr6:145959370 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-32-4016G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145959370 | |||||||
chr6:145959374 | T | A | 5 | a0001c0001t0001g0032 a0001c0001t0001g0148 a0001c0001t0001g0149 others(2): Show |
6 | HG01993.hp1 NA18954.hp1 NA18955.hp2 others(3): Show |
intron_variant | MODIFIER | c.-32-4020A>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145959374 | |||||||
chr6:145959513 | CT | C | 181 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(178): Show |
229 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(226): Show |
intron_variant | MODIFIER | c.-32-4160delA | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145959513 | |||||||
chr6:145959654 | G | C | 186 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(183): Show |
234 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(231): Show |
intron_variant | MODIFIER | c.-33+4077C>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145959654 | |||||||
chr6:145959655 | C | T | 2 | a0001c0001t0004g0043 a0001c0001t0004g0232 |
3 | HG01515.hp2 HG01517.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.-33+4076G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145959655 | |||||||
chr6:145959833 | C | T | 3 | a0001c0001t0001g0018 a0001c0001t0001g0057 a0001c0001t0001g0153 |
4 | HG01496.hp1 HG01516.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.-33+3898G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145959833 | |||||||
chr6:145960009 | T | C | 1 | a0001c0001t0002g0267 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-33+3722A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145960009 | |||||||
chr6:145960210 | GCAATGGT | G | 145 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(142): Show |
181 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(178): Show |
intron_variant | MODIFIER | c.-33+3514_-33+3520d others(9): Show |
SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145960210 | |||||||
chr6:145960231 | T | C | 211 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(208): Show |
264 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(261): Show |
intron_variant | MODIFIER | c.-33+3500A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145960231 | |||||||
chr6:145960232 | G | A | 1 | a0001c0001t0001g0152 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-33+3499C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145960232 | |||||||
chr6:145960402 | G | A | 1 | a0001c0003t0005g0056 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-33+3329C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145960402 | |||||||
chr6:145960493 | T | A | 1 | a0001c0002t0002g0248 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-33+3238A>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145960493 | |||||||
chr6:145960676 | A | T | 1 | a0001c0002t0002g0180 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-33+3055T>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145960676 | |||||||
chr6:145960847 | C | T | 1 | a0003c0005t0001g0169 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-33+2884G>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145960847 | |||||||
chr6:145960925 | A | G | 177 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(174): Show |
223 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(220): Show |
intron_variant | MODIFIER | c.-33+2806T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145960925 | |||||||
chr6:145960944 | T | C | 1 | a0001c0001t0001g0153 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-33+2787A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145960944 | |||||||
chr6:145961012 | T | C | 1 | a0001c0001t0001g0154 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-33+2719A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145961012 | |||||||
chr6:145961059 | G | A | 1 | a0001c0015t0014g0250 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-33+2672C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145961059 | |||||||
chr6:145961195 | G | A | 1 | a0001c0001t0002g0249 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-33+2536C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145961195 | |||||||
chr6:145961202 | C | A | 11 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0155 others(8): Show |
15 | HG02074.hp1 NA18942.hp2 NA18943.hp2 others(12): Show |
intron_variant | MODIFIER | c.-33+2529G>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145961202 | |||||||
chr6:145961263 | T | G | 1 | a0001c0001t0001g0164 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-33+2468A>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145961263 | |||||||
chr6:145961493 | T | A | 1 | a0001c0001t0001g0165 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-33+2238A>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145961493 | |||||||
chr6:145961552 | A | G | 21 | a0001c0003t0003g0251 a0001c0003t0003g0252 a0001c0003t0003g0253 others(18): Show |
25 | HG01081.hp2 HG01433.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.-33+2179T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145961552 | |||||||
chr6:145961685 | G | A | 1 | a0001c0015t0014g0250 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-33+2046C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145961685 | |||||||
chr6:145962206 | G | A | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.-33+1525C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145962206 | |||||||
chr6:145962538 | G | A | 1 | a0001c0015t0014g0250 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-33+1193C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145962538 | |||||||
chr6:145962783 | A | G | 4 | a0004c0006t0007g0015 a0004c0006t0007g0177 a0004c0006t0007g0178 others(1): Show |
6 | HG02135.hp2 HG02155.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.-33+948T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145962783 | |||||||
chr6:145963379 | G | A | 1 | a0003c0005t0001g0175 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-33+352C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145963379 | |||||||
chr6:145963424 | A | G | 141 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(138): Show |
176 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(173): Show |
intron_variant | MODIFIER | c.-33+307T>C | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145963424 | |||||||
chr6:145963485 | T | C | 183 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(180): Show |
231 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(228): Show |
intron_variant | MODIFIER | c.-33+246A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145963485 | |||||||
chr6:145963544 | T | C | 11 | a0003c0005t0001g0003 a0003c0005t0001g0035 a0003c0005t0001g0169 others(8): Show |
17 | HG00609.hp1 HG02040.hp2 HG02132.hp2 others(14): Show |
intron_variant | MODIFIER | c.-33+187A>G | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145963544 | |||||||
chr6:145963607 | G | A | 1 | a0001c0001t0002g0267 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-33+124C>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145963607 | |||||||
chr6:145963681 | G | T | 2 | a0001c0001t0002g0268 a0001c0001t0002g0269 |
2 | HG02615.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-33+50C>A | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145963681 | |||||||
chr6:145963682 | C | A | 2 | a0001c0001t0002g0268 a0001c0001t0002g0269 |
2 | HG02615.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-33+49G>T | SHPRH | ENSG00000146414.17 | transcript | ENST00000275233.12 | protein_coding | 1/29 | chr6 | 145963682 |