Item | Value |
---|---|
geneid | 2185 |
ensemblid | ENSG00000120899.18 |
hgncid | 9612 |
symbol | PTK2B |
name | protein tyrosine kinase 2 beta |
refseq_nuc | NM_173176.3 |
refseq_prot | NP_775268.1 |
ensembl_nuc | ENST00000346049.10 |
ensembl_prot | ENSP00000332816.6 |
mane_status | MANE Select |
chr | chr8 |
start | 27325552 |
end | 27459386 |
strand | + |
ver | v1.2 |
region | chr8:27325552-27459386 |
region5000 | chr8:27320552-27464386 |
regionname0 | PTK2B_chr8_27325552_27459386 |
regionname5000 | PTK2B_chr8_27320552_27464386 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 1009 | 184 | 65 | 34 | 70 | 5 | 9 | 53 | PTK2B_chr8_27320552_27464386 | PTK2B | MSGVS others(1004): Show |
chr8 | 27320552 | 27464386 |
a0002 | 0/1 | 1009 | 133 | 25 | 36 | 53 | 5 | 13 | 39 | PTK2B_chr8_27320552_27464386 | PTK2B | MSGVS others(1004): Show |
chr8 | 27320552 | 27464386 |
a0003 | 0/0 | 1009 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | MSGVS others(1004): Show |
chr8 | 27320552 | 27464386 |
a0004 | 0/0 | 1009 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | PTK2B_chr8_27320552_27464386 | PTK2B | MSGVS others(1004): Show |
chr8 | 27320552 | 27464386 |
a0005 | 0/0 | 1009 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | MSGVS others(1004): Show |
chr8 | 27320552 | 27464386 |
a0006 | 0/0 | 1009 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | MSGVS others(1004): Show |
chr8 | 27320552 | 27464386 |
a0007 | 0/0 | 1009 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | MSGVS others(1004): Show |
chr8 | 27320552 | 27464386 |
a0008 | 0/0 | 616 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | MSGVS others(611): Show |
chr8 | 27320552 | 27464386 |
a0009 | 0/0 | 1009 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | MSGVS others(1004): Show |
chr8 | 27320552 | 27464386 |
a0010 | 0/0 | 1009 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | MSGVS others(1004): Show |
chr8 | 27320552 | 27464386 |
a0011 | 0/0 | 1009 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | MSGVS others(1004): Show |
chr8 | 27320552 | 27464386 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 3027 | 68 | 28 | 14 | 18 | 3 | 5 | PTK2B_chr8_27320552_27464386 | PTK2B | ATGTC others(3022): Show |
chr8 | 27320552 | 27464386 | ||
a0001c0002 | 1/0 | 3027 | 62 | 7 | 8 | 41 | 2 | 3 | PTK2B_chr8_27320552_27464386 | PTK2B | ATGTC others(3022): Show |
chr8 | 27320552 | 27464386 | ||
a0001c0007 | 0/0 | 3027 | 11 | 5 | 6 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | ATGTC others(3022): Show |
chr8 | 27320552 | 27464386 | ||
a0001c0008 | 0/0 | 3027 | 9 | 9 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | ATGTC others(3022): Show |
chr8 | 27320552 | 27464386 | ||
a0001c0009 | 0/0 | 3027 | 8 | 1 | 1 | 6 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | ATGTC others(3022): Show |
chr8 | 27320552 | 27464386 | ||
a0001c0010 | 0/0 | 3027 | 8 | 8 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | ATGTC others(3022): Show |
chr8 | 27320552 | 27464386 | ||
a0001c0011 | 0/0 | 3027 | 6 | 0 | 1 | 5 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | ATGTC others(3022): Show |
chr8 | 27320552 | 27464386 | ||
a0001c0012 | 0/0 | 3027 | 4 | 0 | 3 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | ATGTC others(3022): Show |
chr8 | 27320552 | 27464386 | ||
a0001c0013 | 0/0 | 3027 | 3 | 2 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | ATGTC others(3022): Show |
chr8 | 27320552 | 27464386 | ||
a0001c0021 | 0/0 | 3027 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | ATGTC others(3022): Show |
chr8 | 27320552 | 27464386 | ||
a0001c0022 | 0/0 | 3027 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | ATGTC others(3022): Show |
chr8 | 27320552 | 27464386 | ||
a0001c0025 | 0/0 | 3027 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | ATGTC others(3022): Show |
chr8 | 27320552 | 27464386 | ||
a0001c0027 | 0/0 | 3027 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | ATGTC others(3022): Show |
chr8 | 27320552 | 27464386 | ||
a0001c0030 | 0/0 | 3027 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | ATGTC others(3022): Show |
chr8 | 27320552 | 27464386 | ||
a0002c0003 | 0/1 | 3027 | 58 | 8 | 18 | 24 | 3 | 4 | PTK2B_chr8_27320552_27464386 | PTK2B | ATGTC others(3022): Show |
chr8 | 27320552 | 27464386 | ||
a0002c0004 | 0/0 | 3027 | 31 | 0 | 6 | 18 | 1 | 6 | PTK2B_chr8_27320552_27464386 | PTK2B | ATGTC others(3022): Show |
chr8 | 27320552 | 27464386 | ||
a0002c0005 | 0/0 | 3027 | 19 | 0 | 8 | 8 | 0 | 3 | PTK2B_chr8_27320552_27464386 | PTK2B | ATGTC others(3022): Show |
chr8 | 27320552 | 27464386 | ||
a0002c0006 | 0/0 | 3027 | 19 | 13 | 3 | 2 | 1 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | ATGTC others(3022): Show |
chr8 | 27320552 | 27464386 | ||
a0002c0017 | 0/0 | 3027 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | ATGTC others(3022): Show |
chr8 | 27320552 | 27464386 | ||
a0002c0018 | 0/0 | 3027 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | ATGTC others(3022): Show |
chr8 | 27320552 | 27464386 | ||
a0002c0023 | 0/0 | 3027 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | ATGTC others(3022): Show |
chr8 | 27320552 | 27464386 | ||
a0002c0024 | 0/0 | 3027 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | ATGTC others(3022): Show |
chr8 | 27320552 | 27464386 | ||
a0002c0026 | 0/0 | 3027 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | ATGTC others(3022): Show |
chr8 | 27320552 | 27464386 | ||
a0002c0031 | 0/0 | 3027 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | ATGTC others(3022): Show |
chr8 | 27320552 | 27464386 | ||
a0003c0014 | 0/0 | 3027 | 2 | 0 | 2 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | ATGTC others(3022): Show |
chr8 | 27320552 | 27464386 | ||
a0004c0015 | 0/0 | 3027 | 2 | 0 | 0 | 2 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | ATGTC others(3022): Show |
chr8 | 27320552 | 27464386 | ||
a0005c0016 | 0/0 | 3027 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | ATGTC others(3022): Show |
chr8 | 27320552 | 27464386 | ||
a0006c0028 | 0/0 | 3027 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | ATGTC others(3022): Show |
chr8 | 27320552 | 27464386 | ||
a0007c0032 | 0/0 | 3027 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | ATGTC others(3022): Show |
chr8 | 27320552 | 27464386 | ||
a0008c0020 | 0/0 | 3027 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | ATGTC others(3022): Show |
chr8 | 27320552 | 27464386 | ||
a0009c0029 | 0/0 | 3027 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | ATGTC others(3022): Show |
chr8 | 27320552 | 27464386 | ||
a0010c0033 | 0/0 | 3027 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | ATGTC others(3022): Show |
chr8 | 27320552 | 27464386 | ||
a0011c0019 | 0/0 | 3027 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | ATGTC others(3022): Show |
chr8 | 27320552 | 27464386 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0003 | 0/0 | 4074 | 67 | 28 | 13 | 18 | 3 | 5 | PTK2B_chr8_27320552_27464386 | PTK2B | CCTTT others(4069): Show |
chr8 | 27320552 | 27464386 |
a0001c0001t0005 | 0/0 | 4074 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | CCTTT others(4069): Show |
chr8 | 27320552 | 27464386 |
a0001c0002t0001 | 1/0 | 4074 | 62 | 7 | 8 | 41 | 2 | 3 | PTK2B_chr8_27320552_27464386 | PTK2B | CCTTT others(4069): Show |
chr8 | 27320552 | 27464386 |
a0001c0007t0003 | 0/0 | 4074 | 11 | 5 | 6 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | CCTTT others(4069): Show |
chr8 | 27320552 | 27464386 |
a0001c0008t0003 | 0/0 | 4074 | 9 | 9 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | CCTTT others(4069): Show |
chr8 | 27320552 | 27464386 |
a0001c0009t0002 | 0/0 | 4074 | 8 | 1 | 1 | 6 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | CCTTT others(4069): Show |
chr8 | 27320552 | 27464386 |
a0001c0010t0003 | 0/0 | 4074 | 8 | 8 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | CCTTT others(4069): Show |
chr8 | 27320552 | 27464386 |
a0001c0011t0001 | 0/0 | 4074 | 6 | 0 | 1 | 5 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | CCTTT others(4069): Show |
chr8 | 27320552 | 27464386 |
a0001c0012t0004 | 0/0 | 4074 | 4 | 0 | 3 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | CCTTT others(4069): Show |
chr8 | 27320552 | 27464386 |
a0001c0013t0003 | 0/0 | 4074 | 3 | 2 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | CCTTT others(4069): Show |
chr8 | 27320552 | 27464386 |
a0001c0021t0004 | 0/0 | 4074 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | CCTTT others(4069): Show |
chr8 | 27320552 | 27464386 |
a0001c0022t0002 | 0/0 | 4074 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | CCTTT others(4069): Show |
chr8 | 27320552 | 27464386 |
a0001c0025t0001 | 0/0 | 4074 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | CCTTT others(4069): Show |
chr8 | 27320552 | 27464386 |
a0001c0027t0003 | 0/0 | 4074 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | CCTTT others(4069): Show |
chr8 | 27320552 | 27464386 |
a0001c0030t0002 | 0/0 | 4074 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | CCTTT others(4069): Show |
chr8 | 27320552 | 27464386 |
a0002c0003t0002 | 0/1 | 4074 | 56 | 8 | 17 | 23 | 3 | 4 | PTK2B_chr8_27320552_27464386 | PTK2B | CCTTT others(4069): Show |
chr8 | 27320552 | 27464386 |
a0002c0003t0004 | 0/0 | 4074 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | CCTTT others(4069): Show |
chr8 | 27320552 | 27464386 |
a0002c0003t0006 | 0/0 | 4074 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | CCTTT others(4069): Show |
chr8 | 27320552 | 27464386 |
a0002c0004t0002 | 0/0 | 4074 | 31 | 0 | 6 | 18 | 1 | 6 | PTK2B_chr8_27320552_27464386 | PTK2B | CCTTT others(4069): Show |
chr8 | 27320552 | 27464386 |
a0002c0005t0001 | 0/0 | 4074 | 19 | 0 | 8 | 8 | 0 | 3 | PTK2B_chr8_27320552_27464386 | PTK2B | CCTTT others(4069): Show |
chr8 | 27320552 | 27464386 |
a0002c0006t0001 | 0/0 | 4074 | 18 | 12 | 3 | 2 | 1 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | CCTTT others(4069): Show |
chr8 | 27320552 | 27464386 |
a0002c0006t0002 | 0/0 | 4074 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | CCTTT others(4069): Show |
chr8 | 27320552 | 27464386 |
a0002c0017t0002 | 0/0 | 4074 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | CCTTT others(4069): Show |
chr8 | 27320552 | 27464386 |
a0002c0018t0002 | 0/0 | 4074 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | CCTTT others(4069): Show |
chr8 | 27320552 | 27464386 |
a0002c0023t0001 | 0/0 | 4074 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | CCTTT others(4069): Show |
chr8 | 27320552 | 27464386 |
a0002c0024t0001 | 0/0 | 4074 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | CCTTT others(4069): Show |
chr8 | 27320552 | 27464386 |
a0002c0026t0001 | 0/0 | 4074 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | CCTTT others(4069): Show |
chr8 | 27320552 | 27464386 |
a0002c0031t0001 | 0/0 | 4074 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | CCTTT others(4069): Show |
chr8 | 27320552 | 27464386 |
a0003c0014t0003 | 0/0 | 4074 | 2 | 0 | 2 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | CCTTT others(4069): Show |
chr8 | 27320552 | 27464386 |
a0004c0015t0001 | 0/0 | 4074 | 2 | 0 | 0 | 2 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | CCTTT others(4069): Show |
chr8 | 27320552 | 27464386 |
a0005c0016t0002 | 0/0 | 4074 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | CCTTT others(4069): Show |
chr8 | 27320552 | 27464386 |
a0006c0028t0001 | 0/0 | 4074 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | CCTTT others(4069): Show |
chr8 | 27320552 | 27464386 |
a0007c0032t0003 | 0/0 | 4074 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | CCTTT others(4069): Show |
chr8 | 27320552 | 27464386 |
a0008c0020t0002 | 0/0 | 4074 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | CCTTT others(4069): Show |
chr8 | 27320552 | 27464386 |
a0009c0029t0001 | 0/0 | 4074 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | CCTTT others(4069): Show |
chr8 | 27320552 | 27464386 |
a0010c0033t0001 | 0/0 | 4074 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | CCTTT others(4069): Show |
chr8 | 27320552 | 27464386 |
a0011c0019t0002 | 0/0 | 4074 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | CCTTT others(4069): Show |
chr8 | 27320552 | 27464386 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0001t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0001t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0001t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0001t0003g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0001t0003g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0001t0003g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0001t0003g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0001t0003g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0001t0003g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0001t0003g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0001t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0001t0003g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0001t0003g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0001t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0001t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0001t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0001t0003g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0001t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0001t0003g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0001t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0001t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0001t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0001t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0001t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0001t0003g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0001t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0001t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0001t0003g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0001t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0001t0003g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0001t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0001t0003g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0001t0003g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0001t0003g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0001t0003g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0001t0003g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0001t0003g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0001t0003g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0001t0003g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0001t0003g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0001t0003g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0001t0005g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0002t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0002t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0002t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0002t0001g0132 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0002t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0002t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0002t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0002t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0002t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0002t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0002t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0002t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0002t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0002t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0002t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0002t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0002t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0007t0003g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0007t0003g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0007t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0007t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0007t0003g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0007t0003g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0007t0003g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0007t0003g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0007t0003g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0007t0003g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0007t0003g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0008t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0008t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0008t0003g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0008t0003g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0008t0003g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0008t0003g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0008t0003g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0008t0003g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0008t0003g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0009t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0009t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0009t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0009t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0009t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0009t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0009t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0009t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0010t0003g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0010t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0010t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0010t0003g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0010t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0010t0003g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0010t0003g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0010t0003g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0011t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0011t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0011t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0011t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0011t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0011t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0012t0004g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0012t0004g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0012t0004g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0012t0004g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0013t0003g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0013t0003g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0013t0003g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0021t0004g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0022t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0025t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0027t0003g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0001c0030t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0003t0002g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0003t0002g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0003t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0003t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0003t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0003t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0003t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0003t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0003t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0003t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0003t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0003t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0003t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0003t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0003t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0003t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0003t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0003t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0003t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0003t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0003t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0003t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0003t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0003t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0003t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0003t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0003t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0003t0002g0254 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0003t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0003t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0003t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0003t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0003t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0003t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0003t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0003t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0003t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0003t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0003t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0003t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0003t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0003t0002g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0003t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0003t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0003t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0003t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0003t0002g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0003t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0003t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0003t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0003t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0003t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0003t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0003t0002g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0003t0004g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0003t0006g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0004t0002g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0004t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0004t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0004t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0004t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0004t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0004t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0004t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0004t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0004t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0004t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0004t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0004t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0004t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0004t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0004t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0004t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0004t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0004t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0004t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0004t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0004t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0004t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0004t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0004t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0004t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0004t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0004t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0004t0002g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0005t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0005t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0005t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0005t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0005t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0005t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0005t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0005t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0005t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0005t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0005t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0005t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0005t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0005t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0005t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0005t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0005t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0005t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0006t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0006t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0006t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0006t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0006t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0006t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0006t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0006t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0006t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0006t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0006t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0006t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0006t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0006t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0006t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0006t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0006t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0006t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0006t0002g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0017t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0018t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0023t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0024t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0026t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0002c0031t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0003c0014t0003g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0003c0014t0003g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0004c0015t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0004c0015t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0005c0016t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0006c0028t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0007c0032t0003g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0008c0020t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0009c0029t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0010c0033t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
a0011c0019t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0001 | g0133 | EUR | GBR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG00099 | hp2 | a0002 | c0003 | t0002 | g0265 | EUR | GBR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG00323 | hp1 | a0001 | c0002 | t0001 | g0124 | EUR | FIN | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG00323 | hp2 | a0001 | c0001 | t0003 | g0096 | EUR | FIN | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG00408 | hp1 | a0002 | c0005 | t0001 | g0202 | EAS | CHS | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG00408 | hp2 | a0002 | c0003 | t0002 | g0239 | EAS | CHS | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG00423 | hp1 | a0001 | c0009 | t0002 | g0237 | EAS | CHS | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG00423 | hp2 | a0001 | c0009 | t0002 | g0107 | EAS | CHS | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG00438 | hp1 | a0001 | c0001 | t0003 | g0046 | EAS | CHS | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG00438 | hp2 | a0002 | c0004 | t0002 | g0101 | EAS | CHS | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG00544 | hp1 | a0001 | c0001 | t0003 | g0072 | EAS | CHS | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG00544 | hp2 | a0001 | c0002 | t0001 | g0160 | EAS | CHS | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG00609 | hp1 | a0002 | c0005 | t0001 | g0073 | EAS | CHS | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG00609 | hp2 | a0001 | c0009 | t0002 | g0125 | EAS | CHS | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG00621 | hp1 | a0001 | c0001 | t0003 | g0041 | EAS | CHS | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG00621 | hp2 | a0005 | c0016 | t0002 | g0106 | EAS | CHS | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG00639 | hp1 | a0001 | c0013 | t0003 | g0302 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG00639 | hp2 | a0002 | c0005 | t0001 | g0002 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG00673 | hp1 | a0001 | c0001 | t0003 | g0150 | EAS | CHS | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG00673 | hp2 | a0002 | c0003 | t0002 | g0222 | EAS | CHS | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG00733 | hp1 | a0001 | c0001 | t0003 | g0022 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG00733 | hp2 | a0002 | c0003 | t0004 | g0272 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG00735 | hp1 | a0002 | c0003 | t0002 | g0023 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG00735 | hp2 | a0001 | c0007 | t0003 | g0136 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG00738 | hp1 | a0002 | c0006 | t0001 | g0010 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG00738 | hp2 | a0001 | c0001 | t0003 | g0081 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG00741 | hp1 | a0002 | c0003 | t0002 | g0260 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG00741 | hp2 | a0002 | c0004 | t0002 | g0094 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG01069 | hp1 | a0001 | c0001 | t0005 | g0059 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG01069 | hp2 | a0002 | c0003 | t0002 | g0003 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG01070 | hp1 | a0002 | c0006 | t0001 | g0050 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG01070 | hp2 | a0001 | c0007 | t0003 | g0277 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG01071 | hp1 | a0001 | c0007 | t0003 | g0278 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG01071 | hp2 | a0002 | c0003 | t0002 | g0003 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG01074 | hp1 | a0001 | c0001 | t0003 | g0031 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG01074 | hp2 | a0002 | c0003 | t0002 | g0262 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG01081 | hp1 | a0001 | c0012 | t0004 | g0053 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG01081 | hp2 | a0002 | c0024 | t0001 | g0086 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG01099 | hp1 | a0003 | c0014 | t0003 | g0061 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG01099 | hp2 | a0002 | c0004 | t0002 | g0246 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG01106 | hp1 | a0002 | c0003 | t0002 | g0057 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG01106 | hp2 | a0002 | c0003 | t0002 | g0267 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG01109 | hp1 | a0002 | c0005 | t0001 | g0002 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG01109 | hp2 | a0001 | c0001 | t0003 | g0273 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG01168 | hp1 | a0002 | c0004 | t0002 | g0244 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG01168 | hp2 | a0001 | c0002 | t0001 | g0188 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG01169 | hp1 | a0003 | c0014 | t0003 | g0045 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG01169 | hp2 | a0002 | c0004 | t0002 | g0245 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG01175 | hp1 | a0002 | c0003 | t0002 | g0253 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG01175 | hp2 | a0001 | c0012 | t0004 | g0211 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG01192 | hp1 | a0001 | c0011 | t0001 | g0079 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG01192 | hp2 | a0001 | c0001 | t0003 | g0090 | AMR | PUR | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG01255 | hp1 | a0002 | c0004 | t0002 | g0298 | AMR | CLM | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0029 | AMR | CLM | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG01256 | hp1 | a0001 | c0001 | t0003 | g0047 | AMR | CLM | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG01256 | hp2 | a0002 | c0005 | t0001 | g0194 | AMR | CLM | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG01257 | hp1 | a0002 | c0003 | t0002 | g0067 | AMR | CLM | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG01257 | hp2 | a0002 | c0003 | t0002 | g0264 | AMR | CLM | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG01258 | hp1 | a0002 | c0003 | t0002 | g0004 | AMR | CLM | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG01258 | hp2 | a0002 | c0005 | t0001 | g0195 | AMR | CLM | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG01261 | hp1 | a0002 | c0003 | t0002 | g0247 | AMR | CLM | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG01261 | hp2 | a0001 | c0009 | t0002 | g0018 | AMR | CLM | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG01346 | hp1 | a0002 | c0003 | t0002 | g0058 | AMR | CLM | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG01346 | hp2 | a0001 | c0001 | t0003 | g0205 | AMR | CLM | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG01361 | hp1 | a0002 | c0006 | t0001 | g0070 | AMR | CLM | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG01361 | hp2 | a0002 | c0003 | t0002 | g0004 | AMR | CLM | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG01433 | hp1 | a0001 | c0001 | t0003 | g0030 | AMR | CLM | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG01433 | hp2 | a0001 | c0002 | t0001 | g0134 | AMR | CLM | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG01496 | hp1 | a0001 | c0002 | t0001 | g0168 | AMR | CLM | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG01496 | hp2 | a0001 | c0001 | t0003 | g0025 | AMR | CLM | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG01515 | hp1 | a0001 | c0001 | t0003 | g0097 | EUR | IBS | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG01515 | hp2 | a0002 | c0004 | t0002 | g0248 | EUR | IBS | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG01516 | hp1 | a0002 | c0006 | t0001 | g0068 | EUR | IBS | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG01516 | hp2 | a0002 | c0003 | t0002 | g0256 | EUR | IBS | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG01884 | hp1 | a0002 | c0003 | t0002 | g0251 | AFR | ACB | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG01884 | hp2 | a0001 | c0002 | t0001 | g0173 | AFR | ACB | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG01928 | hp1 | a0002 | c0005 | t0001 | g0033 | AMR | PEL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG01928 | hp2 | a0001 | c0002 | t0001 | g0157 | AMR | PEL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG01934 | hp1 | a0001 | c0001 | t0003 | g0028 | AMR | PEL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG01934 | hp2 | a0001 | c0002 | t0001 | g0131 | AMR | PEL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG01943 | hp1 | a0001 | c0002 | t0001 | g0147 | AMR | PEL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG01943 | hp2 | a0002 | c0005 | t0001 | g0026 | AMR | PEL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG01978 | hp1 | a0002 | c0004 | t0002 | g0242 | AMR | PEL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG01978 | hp2 | a0001 | c0012 | t0004 | g0055 | AMR | PEL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG01993 | hp1 | a0001 | c0007 | t0003 | g0137 | AMR | PEL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG01993 | hp2 | a0002 | c0003 | t0002 | g0069 | AMR | PEL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02004 | hp1 | a0001 | c0001 | t0003 | g0034 | AMR | PEL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02004 | hp2 | a0002 | c0003 | t0002 | g0299 | AMR | PEL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02015 | hp1 | a0002 | c0003 | t0002 | g0217 | EAS | KHV | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02015 | hp2 | a0001 | c0002 | t0001 | g0163 | EAS | KHV | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02040 | hp1 | a0001 | c0002 | t0001 | g0155 | EAS | KHV | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02040 | hp2 | a0002 | c0004 | t0002 | g0108 | EAS | KHV | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02055 | hp1 | a0001 | c0001 | t0003 | g0181 | AFR | ACB | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02055 | hp2 | a0001 | c0001 | t0003 | g0064 | AFR | ACB | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02056 | hp1 | a0001 | c0002 | t0001 | g0311 | EAS | KHV | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02056 | hp2 | a0001 | c0011 | t0001 | g0144 | EAS | KHV | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02071 | hp1 | a0002 | c0004 | t0002 | g0208 | EAS | KHV | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02071 | hp2 | a0001 | c0002 | t0001 | g0167 | EAS | KHV | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02074 | hp1 | a0002 | c0004 | t0002 | g0111 | EAS | KHV | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02074 | hp2 | a0002 | c0003 | t0002 | g0283 | EAS | KHV | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02080 | hp1 | a0001 | c0001 | t0003 | g0048 | EAS | KHV | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02080 | hp2 | a0002 | c0003 | t0002 | g0274 | EAS | KHV | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02135 | hp1 | a0001 | c0001 | t0003 | g0037 | EAS | KHV | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02135 | hp2 | a0001 | c0002 | t0001 | g0139 | EAS | KHV | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02145 | hp1 | a0001 | c0001 | t0003 | g0095 | AFR | ACB | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02145 | hp2 | a0002 | c0023 | t0001 | g0123 | AFR | ACB | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02165 | hp1 | a0002 | c0003 | t0002 | g0261 | EAS | CDX | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02165 | hp2 | a0002 | c0031 | t0001 | g0156 | EAS | CDX | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02257 | hp1 | a0001 | c0001 | t0003 | g0182 | AFR | ACB | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0318 | AFR | ACB | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02258 | hp1 | a0001 | c0008 | t0003 | g0316 | AFR | ACB | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02258 | hp2 | a0002 | c0003 | t0002 | g0255 | AFR | ACB | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02273 | hp1 | a0002 | c0003 | t0002 | g0054 | AMR | PEL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02273 | hp2 | a0001 | c0007 | t0003 | g0189 | AMR | PEL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02280 | hp1 | a0001 | c0001 | t0003 | g0065 | AFR | ACB | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02280 | hp2 | a0002 | c0003 | t0002 | g0249 | AFR | ACB | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02293 | hp1 | a0001 | c0002 | t0001 | g0148 | AMR | PEL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02293 | hp2 | a0001 | c0001 | t0003 | g0051 | AMR | PEL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02300 | hp1 | a0001 | c0007 | t0003 | g0135 | AMR | PEL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02300 | hp2 | a0002 | c0005 | t0001 | g0032 | AMR | PEL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02523 | hp1 | a0002 | c0003 | t0002 | g0300 | EAS | KHV | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02523 | hp2 | a0001 | c0002 | t0001 | g0143 | EAS | KHV | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02572 | hp1 | a0001 | c0001 | t0003 | g0088 | AFR | GWD | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02572 | hp2 | a0001 | c0001 | t0003 | g0228 | AFR | GWD | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02602 | hp1 | a0001 | c0002 | t0001 | g0130 | SAS | PJL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02602 | hp2 | a0001 | c0001 | t0003 | g0091 | SAS | PJL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02615 | hp1 | a0001 | c0030 | t0002 | g0007 | AFR | GWD | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02615 | hp2 | a0002 | c0006 | t0001 | g0286 | AFR | GWD | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02622 | hp1 | a0002 | c0006 | t0001 | g0323 | AFR | GWD | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02622 | hp2 | a0001 | c0001 | t0003 | g0017 | AFR | GWD | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02630 | hp1 | a0002 | c0006 | t0001 | g0291 | AFR | GWD | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02630 | hp2 | a0001 | c0007 | t0003 | g0303 | AFR | GWD | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02647 | hp1 | a0001 | c0010 | t0003 | g0232 | AFR | GWD | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02647 | hp2 | a0006 | c0028 | t0001 | g0177 | AFR | GWD | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0082 | SAS | PJL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02698 | hp2 | a0002 | c0004 | t0002 | g0112 | SAS | PJL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02717 | hp1 | a0001 | c0008 | t0003 | g0114 | AFR | GWD | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02717 | hp2 | a0001 | c0001 | t0003 | g0294 | AFR | GWD | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02723 | hp1 | a0001 | c0013 | t0003 | g0304 | AFR | GWD | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02723 | hp2 | a0001 | c0008 | t0003 | g0319 | AFR | GWD | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02809 | hp1 | a0001 | c0010 | t0003 | g0285 | AFR | GWD | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02809 | hp2 | a0002 | c0003 | t0002 | g0321 | AFR | GWD | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02818 | hp1 | a0001 | c0001 | t0003 | g0227 | AFR | GWD | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02818 | hp2 | a0001 | c0001 | t0003 | g0115 | AFR | GWD | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02895 | hp1 | a0001 | c0007 | t0003 | g0280 | AFR | GWD | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02895 | hp2 | a0001 | c0010 | t0003 | g0230 | AFR | GWD | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02896 | hp1 | a0001 | c0008 | t0003 | g0292 | AFR | GWD | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02896 | hp2 | a0002 | c0006 | t0001 | g0234 | AFR | GWD | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02897 | hp1 | a0001 | c0007 | t0003 | g0281 | AFR | GWD | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02897 | hp2 | a0002 | c0006 | t0001 | g0290 | AFR | GWD | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02922 | hp1 | a0007 | c0032 | t0003 | g0284 | AFR | ESN | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02922 | hp2 | a0001 | c0001 | t0003 | g0113 | AFR | ESN | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02965 | hp1 | a0001 | c0002 | t0001 | g0226 | AFR | ESN | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02965 | hp2 | a0002 | c0017 | t0002 | g0252 | AFR | ESN | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02970 | hp1 | a0001 | c0008 | t0003 | g0320 | AFR | ESN | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02970 | hp2 | a0001 | c0001 | t0003 | g0185 | AFR | ESN | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02976 | hp1 | a0001 | c0001 | t0003 | g0187 | AFR | ESN | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02976 | hp2 | a0001 | c0001 | t0003 | g0016 | AFR | ESN | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG03041 | hp1 | a0001 | c0010 | t0003 | g0229 | AFR | GWD | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG03041 | hp2 | a0001 | c0002 | t0001 | g0174 | AFR | GWD | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG03098 | hp1 | a0001 | c0027 | t0003 | g0293 | AFR | MSL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG03098 | hp2 | a0001 | c0010 | t0003 | g0233 | AFR | MSL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG03130 | hp1 | a0001 | c0013 | t0003 | g0301 | AFR | ESN | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG03130 | hp2 | a0002 | c0006 | t0001 | g0062 | AFR | ESN | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG03139 | hp1 | a0001 | c0001 | t0003 | g0093 | AFR | ESN | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG03139 | hp2 | a0001 | c0002 | t0001 | g0295 | AFR | ESN | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG03195 | hp1 | a0002 | c0006 | t0001 | g0020 | AFR | ESN | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG03195 | hp2 | a0002 | c0026 | t0001 | g0238 | AFR | ESN | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG03209 | hp1 | a0002 | c0006 | t0001 | g0287 | AFR | MSL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG03209 | hp2 | a0001 | c0008 | t0003 | g0296 | AFR | MSL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG03225 | hp1 | a0001 | c0001 | t0003 | g0175 | AFR | MSL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG03225 | hp2 | a0001 | c0010 | t0003 | g0289 | AFR | MSL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG03239 | hp1 | a0001 | c0012 | t0004 | g0027 | SAS | PJL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG03239 | hp2 | a0002 | c0003 | t0002 | g0259 | SAS | PJL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG03486 | hp1 | a0001 | c0002 | t0001 | g0176 | AFR | MSL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG03486 | hp2 | a0002 | c0003 | t0002 | g0266 | AFR | MSL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG03490 | hp1 | a0002 | c0004 | t0002 | g0109 | SAS | PJL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG03490 | hp2 | a0002 | c0003 | t0002 | g0275 | SAS | PJL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG03516 | hp1 | a0002 | c0003 | t0002 | g0180 | AFR | ESN | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | ESN | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG03540 | hp1 | a0001 | c0001 | t0003 | g0276 | AFR | GWD | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG03540 | hp2 | a0001 | c0001 | t0003 | g0184 | AFR | GWD | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG03579 | hp1 | a0001 | c0001 | t0003 | g0063 | AFR | MSL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG03579 | hp2 | a0001 | c0002 | t0001 | g0178 | AFR | MSL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG03669 | hp1 | a0002 | c0004 | t0002 | g0225 | SAS | PJL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG03669 | hp2 | a0002 | c0005 | t0001 | g0204 | SAS | PJL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG03704 | hp1 | a0002 | c0004 | t0002 | g0110 | SAS | PJL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG03704 | hp2 | a0002 | c0003 | t0002 | g0263 | SAS | PJL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0060 | SAS | PJL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG03710 | hp2 | a0001 | c0002 | t0001 | g0165 | SAS | PJL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG03927 | hp1 | a0002 | c0004 | t0002 | g0099 | SAS | BEB | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG03927 | hp2 | a0002 | c0005 | t0001 | g0203 | SAS | BEB | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG04115 | hp1 | a0002 | c0004 | t0002 | g0224 | SAS | STU | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG04115 | hp2 | a0002 | c0005 | t0001 | g0309 | SAS | STU | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG04199 | hp1 | a0001 | c0001 | t0003 | g0199 | SAS | STU | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG04199 | hp2 | a0001 | c0001 | t0003 | g0056 | SAS | STU | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA18522 | hp1 | a0001 | c0001 | t0003 | g0186 | AFR | YRI | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA18522 | hp2 | a0001 | c0007 | t0003 | g0279 | AFR | YRI | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA18906 | hp1 | a0002 | c0003 | t0002 | g0236 | AFR | YRI | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA18906 | hp2 | a0001 | c0001 | t0003 | g0036 | AFR | YRI | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA18943 | hp1 | a0002 | c0006 | t0001 | g0127 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA18943 | hp2 | a0001 | c0009 | t0002 | g0312 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA18945 | hp1 | a0001 | c0002 | t0001 | g0078 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA18945 | hp2 | a0001 | c0002 | t0001 | g0077 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA18946 | hp1 | a0002 | c0004 | t0002 | g0250 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA18946 | hp2 | a0001 | c0009 | t0002 | g0103 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA18947 | hp1 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA18947 | hp2 | a0002 | c0003 | t0002 | g0241 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA18949 | hp1 | a0001 | c0011 | t0001 | g0166 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA18949 | hp2 | a0008 | c0020 | t0002 | g0014 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA18956 | hp1 | a0001 | c0002 | t0001 | g0117 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA18956 | hp2 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA18957 | hp1 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA18957 | hp2 | a0001 | c0002 | t0001 | g0120 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA18960 | hp1 | a0001 | c0002 | t0001 | g0138 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA18960 | hp2 | a0002 | c0003 | t0002 | g0258 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA18961 | hp1 | a0002 | c0003 | t0002 | g0223 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA18961 | hp2 | a0001 | c0011 | t0001 | g0149 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA18962 | hp1 | a0001 | c0011 | t0001 | g0140 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA18962 | hp2 | a0002 | c0004 | t0002 | g0209 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA18966 | hp1 | a0002 | c0003 | t0002 | g0271 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA18966 | hp2 | a0004 | c0015 | t0001 | g0193 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA18967 | hp1 | a0001 | c0002 | t0001 | g0170 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA18967 | hp2 | a0002 | c0003 | t0002 | g0307 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA18968 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA18968 | hp2 | a0002 | c0004 | t0002 | g0011 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA18969 | hp1 | a0001 | c0002 | t0001 | g0122 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA18969 | hp2 | a0002 | c0003 | t0002 | g0310 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA18970 | hp1 | a0002 | c0005 | t0001 | g0201 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA18970 | hp2 | a0001 | c0011 | t0001 | g0098 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA18978 | hp1 | a0001 | c0002 | t0001 | g0164 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA18978 | hp2 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA18979 | hp1 | a0002 | c0005 | t0001 | g0083 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA18979 | hp2 | a0002 | c0003 | t0002 | g0218 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA18980 | hp1 | a0001 | c0002 | t0001 | g0145 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA18980 | hp2 | a0002 | c0004 | t0002 | g0001 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA18981 | hp1 | a0001 | c0002 | t0001 | g0172 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA18981 | hp2 | a0002 | c0004 | t0002 | g0105 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA18983 | hp1 | a0002 | c0003 | t0006 | g0040 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA18983 | hp2 | a0001 | c0002 | t0001 | g0080 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA18985 | hp1 | a0001 | c0002 | t0001 | g0152 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA18985 | hp2 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA18986 | hp1 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA18986 | hp2 | a0002 | c0004 | t0002 | g0104 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA18990 | hp1 | a0002 | c0003 | t0002 | g0012 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA18990 | hp2 | a0002 | c0003 | t0002 | g0308 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA18991 | hp1 | a0001 | c0002 | t0001 | g0161 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA18991 | hp2 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA18993 | hp1 | a0002 | c0003 | t0002 | g0219 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA18993 | hp2 | a0001 | c0002 | t0001 | g0121 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA18994 | hp1 | a0001 | c0009 | t0002 | g0313 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA18994 | hp2 | a0002 | c0003 | t0002 | g0220 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA18995 | hp1 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA18995 | hp2 | a0009 | c0029 | t0001 | g0153 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA18999 | hp1 | a0002 | c0003 | t0002 | g0240 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA18999 | hp2 | a0004 | c0015 | t0001 | g0198 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA19000 | hp1 | a0001 | c0002 | t0001 | g0128 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA19000 | hp2 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA19002 | hp1 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA19002 | hp2 | a0010 | c0033 | t0001 | g0154 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA19003 | hp1 | a0002 | c0004 | t0002 | g0001 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA19003 | hp2 | a0001 | c0002 | t0001 | g0146 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA19005 | hp1 | a0002 | c0003 | t0002 | g0270 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA19005 | hp2 | a0001 | c0002 | t0001 | g0306 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA19007 | hp1 | a0002 | c0004 | t0002 | g0215 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA19007 | hp2 | a0002 | c0005 | t0001 | g0084 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA19009 | hp1 | a0001 | c0002 | t0001 | g0129 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA19009 | hp2 | a0002 | c0003 | t0002 | g0221 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA19011 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA19011 | hp2 | a0001 | c0002 | t0001 | g0212 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA19012 | hp1 | a0001 | c0002 | t0001 | g0169 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA19012 | hp2 | a0002 | c0004 | t0002 | g0001 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA19030 | hp1 | a0001 | c0001 | t0003 | g0305 | AFR | LWK | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA19030 | hp2 | a0002 | c0006 | t0001 | g0006 | AFR | LWK | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA19043 | hp1 | a0002 | c0018 | t0002 | g0089 | AFR | LWK | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA19043 | hp2 | a0001 | c0021 | t0004 | g0009 | AFR | LWK | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA19056 | hp1 | a0002 | c0006 | t0001 | g0213 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA19056 | hp2 | a0002 | c0005 | t0001 | g0196 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA19057 | hp1 | a0002 | c0003 | t0002 | g0216 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA19057 | hp2 | a0001 | c0002 | t0001 | g0192 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA19068 | hp1 | a0002 | c0004 | t0002 | g0151 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA19068 | hp2 | a0001 | c0002 | t0001 | g0214 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA19070 | hp1 | a0002 | c0005 | t0001 | g0085 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA19070 | hp2 | a0001 | c0002 | t0001 | g0206 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA19074 | hp1 | a0002 | c0004 | t0002 | g0191 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA19074 | hp2 | a0001 | c0002 | t0001 | g0158 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA19077 | hp1 | a0002 | c0004 | t0002 | g0013 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA19077 | hp2 | a0001 | c0002 | t0001 | g0126 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA19082 | hp1 | a0002 | c0005 | t0001 | g0197 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA19082 | hp2 | a0001 | c0002 | t0001 | g0190 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA19084 | hp1 | a0001 | c0002 | t0001 | g0119 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA19084 | hp2 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA19085 | hp1 | a0001 | c0002 | t0001 | g0162 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA19085 | hp2 | a0001 | c0001 | t0003 | g0075 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA19087 | hp1 | a0001 | c0002 | t0001 | g0159 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA19087 | hp2 | a0011 | c0019 | t0002 | g0102 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA19090 | hp1 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA19090 | hp2 | a0002 | c0004 | t0002 | g0210 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA19091 | hp1 | a0001 | c0002 | t0001 | g0171 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA19091 | hp2 | a0002 | c0003 | t0002 | g0257 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA19240 | hp1 | a0001 | c0008 | t0003 | g0315 | AFR | YRI | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA19240 | hp2 | a0001 | c0009 | t0002 | g0087 | AFR | YRI | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA20129 | hp1 | a0002 | c0006 | t0002 | g0317 | AFR | ASW | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA20129 | hp2 | a0001 | c0007 | t0003 | g0179 | AFR | ASW | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA20805 | hp1 | a0001 | c0001 | t0003 | g0024 | EUR | TSI | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA20805 | hp2 | a0002 | c0003 | t0002 | g0207 | EUR | TSI | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA20905 | hp1 | a0002 | c0003 | t0002 | g0268 | SAS | GIH | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA20905 | hp2 | a0001 | c0002 | t0001 | g0142 | SAS | GIH | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG01123 | hp1 | a0001 | c0002 | t0001 | g0076 | AMR | CLM | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG01123 | hp2 | a0002 | c0005 | t0001 | g0200 | AMR | CLM | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02109 | hp1 | a0001 | c0001 | t0003 | g0322 | AFR | ACB | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02109 | hp2 | a0001 | c0008 | t0003 | g0243 | AFR | ACB | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02486 | hp1 | a0001 | c0010 | t0003 | g0231 | AFR | ACB | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02486 | hp2 | a0001 | c0008 | t0003 | g0314 | AFR | ACB | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02559 | hp1 | a0001 | c0001 | t0003 | g0288 | AFR | ACB | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG02559 | hp2 | a0002 | c0003 | t0002 | g0269 | AFR | ACB | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG03471 | hp1 | a0001 | c0002 | t0001 | g0235 | AFR | MSL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG03471 | hp2 | a0001 | c0001 | t0003 | g0183 | AFR | MSL | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG06807 | hp1 | a0001 | c0010 | t0003 | g0297 | AFR | USA | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
HG06807 | hp2 | a0002 | c0006 | t0001 | g0066 | AFR | USA | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA18955 | hp1 | a0001 | c0002 | t0001 | g0141 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA18955 | hp2 | a0002 | c0004 | t0002 | g0100 | EAS | JPT | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA20300 | hp1 | a0001 | c0025 | t0001 | g0019 | AFR | USA | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA20300 | hp2 | a0001 | c0022 | t0002 | g0008 | AFR | USA | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA21309 | hp1 | a0002 | c0006 | t0001 | g0282 | AFR | LWK | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
NA21309 | hp2 | a0002 | c0006 | t0001 | g0092 | AFR | LWK | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
homoSapiens | chm13v2 | a0002 | c0003 | t0002 | g0254 | REF | REF | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0132 | REF | REF | PTK2B_chr8_27320552_27464386 | PTK2B | chr8 | 27320552 | 27464386 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:27397637 | G | A | 1 | a0005 | 1 | HG00621.hp2 | missense_variant | MODERATE | c.53G>A | p.Arg18Gln | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/31 | 220/4074 | 53/3030 | 18/1009 | chr8 | 27397637 | |||
chr8:27430984 | A | G | 1 | a0010 | 1 | NA19002.hp2 | missense_variant | MODERATE | c.778A>G | p.Ile260Val | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 8/31 | 945/4074 | 778/3030 | 260/1009 | chr8 | 27430984 | |||
chr8:27430997 | C | A | 1 | a0003 | 2 | HG01099.hp1 HG01169.hp1 |
missense_variant | MODERATE | c.791C>A | p.Thr264Asn | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 8/31 | 958/4074 | 791/3030 | 264/1009 | chr8 | 27430997 | |||
chr8:27434530 | G | A | 1 | a0006 | 1 | HG02647.hp2 | missense_variant | MODERATE | c.1163G>A | p.Arg388Gln | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 13/31 | 1330/4074 | 1163/3030 | 388/1009 | chr8 | 27434530 | |||
chr8:27435791 | G | A | 1 | a0004 | 2 | NA18966.hp2 NA18999.hp2 |
missense_variant&splice_region_variant | MODERATE | c.1241G>A | p.Gly414Glu | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 14/31 | 1408/4074 | 1241/3030 | 414/1009 | chr8 | 27435791 | |||
chr8:27437873 | G | A | 1 | a0009 | 1 | NA18995.hp2 | missense_variant | MODERATE | c.1636G>A | p.Val546Met | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 18/31 | 1803/4074 | 1636/3030 | 546/1009 | chr8 | 27437873 | |||
chr8:27440239 | G | T | 1 | a0008 | 1 | NA18949.hp2 | missense_variant&splice_region_variant | MODERATE | c.1837G>T | p.Val613Leu | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2004/4074 | 1837/3030 | 613/1009 | chr8 | 27440239 | |||
chr8:27440247 | G | C | 1 | a0008 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.1845G>C | p.Met615Ile | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2012/4074 | 1845/3030 | 615/1009 | chr8 | 27440247 | |||
chr8:27440251 | G | T | 1 | a0008 | 1 | NA18949.hp2 | stop_gained | HIGH | c.1849G>T | p.Glu617* | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2016/4074 | 1849/3030 | 617/1009 | chr8 | 27440251 | |||
chr8:27440254 | A | T | 1 | a0008 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.1852A>T | p.Ile618Phe | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2019/4074 | 1852/3030 | 618/1009 | chr8 | 27440254 | |||
chr8:27440263 | T | A | 1 | a0008 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.1861T>A | p.Phe621Ile | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2028/4074 | 1861/3030 | 621/1009 | chr8 | 27440263 | |||
chr8:27440264 | T | A | 1 | a0008 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.1862T>A | p.Phe621Tyr | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2029/4074 | 1862/3030 | 621/1009 | chr8 | 27440264 | |||
chr8:27440265 | T | A | 1 | a0008 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.1863T>A | p.Phe621Leu | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2030/4074 | 1863/3030 | 621/1009 | chr8 | 27440265 | |||
chr8:27440266 | G | C | 1 | a0008 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.1864G>C | p.Gly622Arg | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2031/4074 | 1864/3030 | 622/1009 | chr8 | 27440266 | |||
chr8:27440267 | G | T | 1 | a0008 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.1865G>T | p.Gly622Val | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2032/4074 | 1865/3030 | 622/1009 | chr8 | 27440267 | |||
chr8:27440272 | C | A | 1 | a0008 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.1870C>A | p.Gln624Lys | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2037/4074 | 1870/3030 | 624/1009 | chr8 | 27440272 | |||
chr8:27440274 | G | T | 1 | a0008 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.1872G>T | p.Gln624His | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2039/4074 | 1872/3030 | 624/1009 | chr8 | 27440274 | |||
chr8:27440275 | C | T | 1 | a0008 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.1873C>T | p.Pro625Ser | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2040/4074 | 1873/3030 | 625/1009 | chr8 | 27440275 | |||
chr8:27440279 | T | G | 1 | a0008 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.1877T>G | p.Phe626Cys | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2044/4074 | 1877/3030 | 626/1009 | chr8 | 27440279 | |||
chr8:27440282 | T | A | 1 | a0008 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.1880T>A | p.Phe627Tyr | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2047/4074 | 1880/3030 | 627/1009 | chr8 | 27440282 | |||
chr8:27440285 | G | T | 1 | a0008 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.1883G>T | p.Trp628Leu | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2050/4074 | 1883/3030 | 628/1009 | chr8 | 27440285 | |||
chr8:27440286 | G | C | 1 | a0008 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.1884G>C | p.Trp628Cys | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2051/4074 | 1884/3030 | 628/1009 | chr8 | 27440286 | |||
chr8:27440288 | T | C | 1 | a0008 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.1886T>C | p.Leu629Pro | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2053/4074 | 1886/3030 | 629/1009 | chr8 | 27440288 | |||
chr8:27440294 | A | T | 1 | a0008 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.1892A>T | p.Asn631Ile | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2059/4074 | 1892/3030 | 631/1009 | chr8 | 27440294 | |||
chr8:27440295 | C | A | 1 | a0008 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.1893C>A | p.Asn631Lys | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2060/4074 | 1893/3030 | 631/1009 | chr8 | 27440295 | |||
chr8:27440298 | G | T | 1 | a0008 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.1896G>T | p.Lys632Asn | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2063/4074 | 1896/3030 | 632/1009 | chr8 | 27440298 | |||
chr8:27440299 | G | T | 1 | a0008 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.1897G>T | p.Asp633Tyr | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2064/4074 | 1897/3030 | 633/1009 | chr8 | 27440299 | |||
chr8:27440300 | A | T | 1 | a0008 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.1898A>T | p.Asp633Val | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2065/4074 | 1898/3030 | 633/1009 | chr8 | 27440300 | |||
chr8:27440302 | G | A | 1 | a0008 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.1900G>A | p.Val634Ile | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2067/4074 | 1900/3030 | 634/1009 | chr8 | 27440302 | |||
chr8:27440303 | T | C | 1 | a0008 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.1901T>C | p.Val634Ala | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2068/4074 | 1901/3030 | 634/1009 | chr8 | 27440303 | |||
chr8:27440306 | T | A | 1 | a0008 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.1904T>A | p.Ile635Asn | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2071/4074 | 1904/3030 | 635/1009 | chr8 | 27440306 | |||
chr8:27440311 | G | T | 1 | a0008 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.1909G>T | p.Val637Leu | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2076/4074 | 1909/3030 | 637/1009 | chr8 | 27440311 | |||
chr8:27440319 | G | C | 1 | a0008 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.1917G>C | p.Glu639Asp | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2084/4074 | 1917/3030 | 639/1009 | chr8 | 27440319 | |||
chr8:27440320 | A | T | 1 | a0008 | 1 | NA18949.hp2 | stop_gained | HIGH | c.1918A>T | p.Lys640* | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2085/4074 | 1918/3030 | 640/1009 | chr8 | 27440320 | |||
chr8:27445804 | G | T | 1 | a0007 | 1 | HG02922.hp1 | missense_variant | MODERATE | c.2225G>T | p.Gly742Val | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/31 | 2392/4074 | 2225/3030 | 742/1009 | chr8 | 27445804 | |||
chr8:27445857 | G | A | 1 | a0011 | 1 | NA19087.hp2 | missense_variant | MODERATE | c.2278G>A | p.Val760Ile | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/31 | 2445/4074 | 2278/3030 | 760/1009 | chr8 | 27445857 | |||
chr8:27451068 | A | C | 5 | a0002 a0004 a0005 others(2): Show |
137 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(134): Show |
missense_variant | MODERATE | c.2513A>C | p.Lys838Thr | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 26/31 | 2680/4074 | 2513/3030 | 838/1009 | chr8 | 27451068 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:27397611 | T | C | 11 | a0001c0009 a0001c0012 a0001c0021 others(8): Show |
107 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(104): Show |
synonymous_variant | LOW | c.27T>C | p.Ser9Ser | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/31 | 194/4074 | 27/3030 | 9/1009 | chr8 | 27397611 | |||
chr8:27397629 | G | A | 9 | a0001c0009 a0001c0012 a0002c0003 others(6): Show |
105 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(102): Show |
synonymous_variant | LOW | c.45G>A | p.Thr15Thr | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/31 | 212/4074 | 45/3030 | 15/1009 | chr8 | 27397629 | |||
chr8:27397740 | T | C | 1 | a0002c0017 | 1 | HG02965.hp2 | synonymous_variant | LOW | c.156T>C | p.Pro52Pro | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/31 | 323/4074 | 156/3030 | 52/1009 | chr8 | 27397740 | |||
chr8:27397746 | A | G | 11 | a0001c0009 a0001c0012 a0001c0021 others(8): Show |
107 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(104): Show |
synonymous_variant | LOW | c.162A>G | p.Lys54Lys | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/31 | 329/4074 | 162/3030 | 54/1009 | chr8 | 27397746 | |||
chr8:27419933 | G | A | 1 | a0002c0023 | 1 | HG02145.hp2 | synonymous_variant | LOW | c.243G>A | p.Gly81Gly | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 3/31 | 410/4074 | 243/3030 | 81/1009 | chr8 | 27419933 | |||
chr8:27420020 | G | A | 11 | a0001c0001 a0001c0013 a0001c0021 others(8): Show |
100 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(97): Show |
synonymous_variant | LOW | c.330G>A | p.Thr110Thr | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 3/31 | 497/4074 | 330/3030 | 110/1009 | chr8 | 27420020 | |||
chr8:27422366 | G | A | 1 | a0001c0013 | 3 | HG00639.hp1 HG02723.hp1 HG03130.hp1 |
synonymous_variant | LOW | c.534G>A | p.Leu178Leu | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/31 | 701/4074 | 534/3030 | 178/1009 | chr8 | 27422366 | |||
chr8:27431436 | T | C | 1 | a0002c0024 | 1 | HG01081.hp2 | synonymous_variant | LOW | c.849T>C | p.Pro283Pro | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 9/31 | 1016/4074 | 849/3030 | 283/1009 | chr8 | 27431436 | |||
chr8:27435789 | C | T | 2 | a0001c0010 a0007c0032 |
9 | HG02486.hp1 HG02647.hp1 HG02809.hp1 others(6): Show |
synonymous_variant | LOW | c.1239C>T | p.Pro413Pro | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 14/31 | 1406/4074 | 1239/3030 | 413/1009 | chr8 | 27435789 | |||
chr8:27436348 | C | T | 7 | a0001c0001 a0001c0007 a0001c0012 others(4): Show |
90 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(87): Show |
splice_region_variant&synonymous_variant | LOW | c.1341C>T | p.His447His | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 15/31 | 1508/4074 | 1341/3030 | 447/1009 | chr8 | 27436348 | |||
chr8:27440238 | C | T | 1 | a0001c0027 | 1 | HG03098.hp1 | splice_region_variant&synonymous_variant | LOW | c.1836C>T | p.Ala612Ala | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2003/4074 | 1836/3030 | 612/1009 | chr8 | 27440238 | |||
chr8:27440241 | G | T | 1 | a0008c0020 | 1 | NA18949.hp2 | synonymous_variant | LOW | c.1839G>T | p.Val613Val | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2006/4074 | 1839/3030 | 613/1009 | chr8 | 27440241 | |||
chr8:27440253 | G | A | 1 | a0008c0020 | 1 | NA18949.hp2 | synonymous_variant | LOW | c.1851G>A | p.Glu617Glu | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2018/4074 | 1851/3030 | 617/1009 | chr8 | 27440253 | |||
chr8:27440289 | G | A | 1 | a0008c0020 | 1 | NA18949.hp2 | synonymous_variant | LOW | c.1887G>A | p.Leu629Leu | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2054/4074 | 1887/3030 | 629/1009 | chr8 | 27440289 | |||
chr8:27440292 | G | A | 1 | a0008c0020 | 1 | NA18949.hp2 | synonymous_variant | LOW | c.1890G>A | p.Glu630Glu | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2057/4074 | 1890/3030 | 630/1009 | chr8 | 27440292 | |||
chr8:27440307 | C | A | 1 | a0008c0020 | 1 | NA18949.hp2 | synonymous_variant | LOW | c.1905C>A | p.Ile635Ile | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2072/4074 | 1905/3030 | 635/1009 | chr8 | 27440307 | |||
chr8:27440310 | G | C | 1 | a0008c0020 | 1 | NA18949.hp2 | synonymous_variant | LOW | c.1908G>C | p.Gly636Gly | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/31 | 2075/4074 | 1908/3030 | 636/1009 | chr8 | 27440310 | |||
chr8:27444208 | C | G | 7 | a0002c0004 a0002c0018 a0002c0026 others(4): Show |
37 | HG00438.hp2 HG00621.hp2 HG00741.hp2 others(34): Show |
splice_region_variant&synonymous_variant | LOW | c.2151C>G | p.Pro717Pro | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 23/31 | 2318/4074 | 2151/3030 | 717/1009 | chr8 | 27444208 | |||
chr8:27454186 | T | C | 26 | a0001c0001 a0001c0007 a0001c0008 others(23): Show |
247 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(244): Show |
synonymous_variant | LOW | c.2628T>C | p.Thr876Thr | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 29/31 | 2795/4074 | 2628/3030 | 876/1009 | chr8 | 27454186 | |||
chr8:27458359 | A | G | 25 | a0001c0001 a0001c0007 a0001c0008 others(22): Show |
246 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(243): Show |
synonymous_variant | LOW | c.2880A>G | p.Ala960Ala | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 31/31 | 3047/4074 | 2880/3030 | 960/1009 | chr8 | 27458359 | |||
chr8:27458383 | A | G | 24 | a0001c0001 a0001c0007 a0001c0008 others(21): Show |
245 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(242): Show |
synonymous_variant | LOW | c.2904A>G | p.Leu968Leu | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 31/31 | 3071/4074 | 2904/3030 | 968/1009 | chr8 | 27458383 | |||
chr8:27458419 | A | G | 1 | a0001c0011 | 6 | HG01192.hp1 HG02056.hp2 NA18949.hp1 others(3): Show |
synonymous_variant | LOW | c.2940A>G | p.Ser980Ser | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 31/31 | 3107/4074 | 2940/3030 | 980/1009 | chr8 | 27458419 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:27325582 | T | C | 1 | a0001c0001t0005 | 1 | HG01069.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-137T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/31 | chr8 | 27325582 | |||||||
chr8:27397563 | A | G | 15 | a0001c0009t0002 a0001c0012t0004 a0001c0021t0004 others(12): Show |
109 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(106): Show |
5_prime_UTR_variant | MODIFIER | c.-22A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/31 | 22 | chr8 | 27397563 | ||||||
chr8:27458600 | G | A | 12 | a0001c0001t0003 a0001c0001t0005 a0001c0007t0003 others(9): Show |
109 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*91G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 31/31 | 91 | chr8 | 27458600 | ||||||
chr8:27458772 | G | T | 1 | a0002c0003t0006 | 1 | NA18983.hp1 | 3_prime_UTR_variant | MODIFIER | c.*263G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 31/31 | 263 | chr8 | 27458772 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:27325768 | C | G | 3 | a0001c0001t0003g0322 a0002c0003t0002g0321 a0002c0006t0001g0323 |
3 | HG02109.hp1 HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.-38+87C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27325768 | |||||||
chr8:27325983 | G | A | 1 | a0001c0002t0001g0005 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-38+302G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27325983 | |||||||
chr8:27326044 | A | G | 2 | a0001c0008t0003g0319 a0001c0008t0003g0320 |
2 | HG02723.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-38+363A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27326044 | |||||||
chr8:27326056 | C | T | 2 | a0001c0001t0003g0318 a0002c0006t0002g0317 |
2 | HG02257.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-38+375C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27326056 | |||||||
chr8:27326057 | G | T | 6 | a0001c0001t0003g0322 a0001c0008t0003g0314 a0001c0008t0003g0315 others(3): Show |
6 | HG02109.hp1 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-38+376G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27326057 | |||||||
chr8:27326061 | C | G | 6 | a0001c0001t0003g0322 a0001c0008t0003g0314 a0001c0008t0003g0315 others(3): Show |
6 | HG02109.hp1 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-38+380C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27326061 | |||||||
chr8:27326085 | C | T | 4 | a0001c0002t0001g0311 a0001c0009t0002g0312 a0001c0009t0002g0313 others(1): Show |
4 | HG02056.hp1 NA18943.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.-38+404C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27326085 | |||||||
chr8:27326102 | G | A | 17 | a0001c0002t0001g0311 a0001c0008t0003g0314 a0001c0008t0003g0315 others(14): Show |
19 | HG00738.hp1 HG02056.hp1 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.-38+421G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27326102 | |||||||
chr8:27326112 | C | T | 1 | a0002c0005t0001g0309 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-38+431C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27326112 | |||||||
chr8:27326193 | A | G | 109 | a0001c0001t0003g0227 a0001c0001t0003g0228 a0001c0001t0003g0273 others(106): Show |
113 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.-38+512A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27326193 | |||||||
chr8:27326226 | A | ATATG | 10 | a0001c0002t0001g0214 a0002c0003t0002g0216 a0002c0003t0002g0217 others(7): Show |
10 | HG00673.hp2 HG02015.hp1 NA18961.hp1 others(7): Show |
intron_variant | MODIFIER | c.-38+546_-38+547ins others(4): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27326226 | ||||||
chr8:27326226 | A | ATG | 12 | a0001c0002t0001g0212 a0001c0008t0003g0315 a0001c0008t0003g0316 others(9): Show |
12 | HG01175.hp2 HG02071.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.-38+579_-38+580dup others(2): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27326226 | ||||||
chr8:27326226 | ATG | A | 81 | a0001c0001t0003g0021 a0001c0001t0003g0022 a0001c0001t0003g0024 others(78): Show |
83 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.-38+579_-38+580del others(2): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27326226 | ||||||
chr8:27326226 | ATGTG | A | 22 | a0001c0001t0003g0294 a0001c0001t0003g0305 a0001c0001t0003g0322 others(19): Show |
22 | HG00639.hp1 HG01255.hp1 HG02004.hp2 others(19): Show |
intron_variant | MODIFIER | c.-38+577_-38+580del others(4): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27326226 | ||||||
chr8:27326226 | ATGTGTG | A | 72 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(69): Show |
74 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.-38+575_-38+580del others(6): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27326226 | ||||||
chr8:27326226 | ATGTGTGT others(3): Show |
A | 2 | a0002c0004t0002g0224 a0002c0004t0002g0225 |
2 | HG03669.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.-38+571_-38+580del others(10): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27326226 | ||||||
chr8:27326277 | T | C | 99 | a0001c0001t0003g0227 a0001c0001t0003g0228 a0001c0001t0003g0273 others(96): Show |
101 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.-38+596T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27326277 | |||||||
chr8:27326709 | A | G | 2 | a0001c0010t0003g0285 a0007c0032t0003g0284 |
2 | HG02809.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-38+1028A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27326709 | |||||||
chr8:27326824 | C | T | 83 | a0001c0001t0003g0088 a0001c0001t0003g0273 a0001c0001t0003g0276 others(80): Show |
85 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.-38+1143C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27326824 | |||||||
chr8:27326989 | G | A | 4 | a0001c0001t0003g0227 a0001c0001t0003g0228 a0001c0002t0001g0226 others(1): Show |
4 | HG02572.hp2 HG02818.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-38+1308G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27326989 | |||||||
chr8:27327060 | G | A | 69 | a0001c0001t0003g0088 a0001c0001t0003g0273 a0001c0001t0003g0276 others(66): Show |
71 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.-38+1379G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27327060 | |||||||
chr8:27327178 | G | A | 70 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(67): Show |
70 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.-38+1497G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27327178 | |||||||
chr8:27327203 | G | A | 1 | a0002c0003t0002g0236 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-38+1522G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27327203 | |||||||
chr8:27327211 | G | T | 1 | a0001c0002t0001g0206 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-38+1530G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27327211 | |||||||
chr8:27327212 | C | T | 9 | a0001c0002t0001g0311 a0001c0009t0002g0312 a0001c0009t0002g0313 others(6): Show |
11 | HG02056.hp1 NA18943.hp2 NA18949.hp2 others(8): Show |
intron_variant | MODIFIER | c.-38+1531C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27327212 | |||||||
chr8:27327380 | C | A | 4 | a0001c0008t0003g0292 a0001c0010t0003g0289 a0002c0006t0001g0290 others(1): Show |
4 | HG02630.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-38+1699C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27327380 | |||||||
chr8:27327410 | GT | G | 68 | a0001c0001t0003g0088 a0001c0001t0003g0273 a0001c0001t0003g0276 others(65): Show |
70 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.-38+1739delT | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27327410 | ||||||
chr8:27327568 | A | C | 2 | a0001c0008t0003g0319 a0001c0008t0003g0320 |
2 | HG02723.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-38+1887A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27327568 | |||||||
chr8:27327649 | G | A | 1 | a0001c0009t0002g0237 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-38+1968G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27327649 | |||||||
chr8:27327788 | C | A | 25 | a0001c0001t0003g0095 a0001c0001t0003g0096 a0001c0001t0003g0097 others(22): Show |
25 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(22): Show |
intron_variant | MODIFIER | c.-38+2107C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27327788 | |||||||
chr8:27327863 | T | A | 1 | a0002c0026t0001g0238 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-38+2182T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27327863 | |||||||
chr8:27327951 | A | G | 1 | a0001c0002t0001g0235 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-38+2270A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27327951 | |||||||
chr8:27328050 | G | A | 7 | a0001c0001t0003g0294 a0001c0001t0003g0305 a0001c0007t0003g0303 others(4): Show |
7 | HG00639.hp1 HG02630.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.-38+2369G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27328050 | |||||||
chr8:27328411 | A | G | 2 | a0001c0010t0003g0285 a0007c0032t0003g0284 |
2 | HG02809.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-38+2730A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27328411 | |||||||
chr8:27328509 | T | C | 75 | a0001c0001t0003g0088 a0001c0001t0003g0273 a0001c0001t0003g0276 others(72): Show |
77 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.-38+2828T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27328509 | |||||||
chr8:27328561 | G | C | 1 | a0002c0004t0002g0094 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-38+2880G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27328561 | |||||||
chr8:27328934 | C | T | 186 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(183): Show |
190 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(187): Show |
intron_variant | MODIFIER | c.-38+3253C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27328934 | |||||||
chr8:27328942 | C | CTT | 82 | a0001c0001t0003g0088 a0001c0001t0003g0273 a0001c0001t0003g0276 others(79): Show |
84 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.-38+3273_-38+3274d others(4): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27328942 | ||||||
chr8:27329000 | C | T | 1 | a0001c0021t0004g0009 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-38+3319C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27329000 | |||||||
chr8:27329075 | T | C | 159 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(156): Show |
161 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.-38+3394T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27329075 | |||||||
chr8:27329135 | G | A | 84 | a0001c0001t0003g0088 a0001c0001t0003g0273 a0001c0001t0003g0276 others(81): Show |
86 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.-38+3454G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27329135 | |||||||
chr8:27329191 | C | T | 19 | a0001c0001t0003g0227 a0001c0001t0003g0228 a0001c0002t0001g0226 others(16): Show |
19 | HG02486.hp1 HG02572.hp2 HG02630.hp1 others(16): Show |
intron_variant | MODIFIER | c.-38+3510C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27329191 | |||||||
chr8:27329204 | A | G | 74 | a0001c0001t0003g0088 a0001c0001t0003g0273 a0001c0001t0003g0276 others(71): Show |
76 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.-38+3523A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27329204 | |||||||
chr8:27329206 | G | A | 3 | a0002c0003t0002g0239 a0002c0003t0002g0240 a0002c0003t0002g0241 |
3 | HG00408.hp2 NA18947.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.-38+3525G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27329206 | |||||||
chr8:27329228 | G | A | 10 | a0001c0001t0003g0294 a0001c0001t0003g0305 a0001c0007t0003g0303 others(7): Show |
10 | HG00639.hp1 HG02258.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-38+3547G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27329228 | |||||||
chr8:27329306 | C | G | 25 | a0001c0001t0003g0095 a0001c0001t0003g0096 a0001c0001t0003g0097 others(22): Show |
25 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(22): Show |
intron_variant | MODIFIER | c.-38+3625C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27329306 | |||||||
chr8:27329339 | A | G | 1 | a0002c0006t0001g0010 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-38+3658A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27329339 | |||||||
chr8:27329403 | T | C | 1 | a0002c0006t0001g0010 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-38+3722T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27329403 | |||||||
chr8:27329406 | A | G | 208 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(205): Show |
213 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(210): Show |
intron_variant | MODIFIER | c.-38+3725A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27329406 | |||||||
chr8:27329667 | T | C | 5 | a0001c0001t0003g0113 a0001c0001t0003g0115 a0001c0008t0003g0114 others(2): Show |
5 | HG00738.hp1 HG02717.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.-38+3986T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27329667 | |||||||
chr8:27329668 | T | C | 1 | a0002c0006t0001g0020 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-38+3987T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27329668 | |||||||
chr8:27329842 | G | T | 1 | a0001c0002t0001g0190 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-38+4161G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27329842 | |||||||
chr8:27329864 | A | G | 1 | a0002c0018t0002g0089 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-38+4183A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27329864 | |||||||
chr8:27329899 | G | T | 1 | a0001c0001t0003g0093 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-38+4218G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27329899 | |||||||
chr8:27329987 | C | G | 1 | a0001c0007t0003g0189 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-38+4306C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27329987 | |||||||
chr8:27330126 | C | T | 1 | a0001c0008t0003g0320 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-38+4445C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27330126 | |||||||
chr8:27330136 | A | G | 3 | a0001c0008t0003g0314 a0001c0008t0003g0315 a0001c0008t0003g0316 |
3 | HG02258.hp1 HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-38+4455A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27330136 | |||||||
chr8:27330153 | G | A | 1 | a0001c0001t0003g0021 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-38+4472G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27330153 | |||||||
chr8:27330334 | G | T | 1 | a0002c0006t0001g0287 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-38+4653G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27330334 | |||||||
chr8:27330504 | C | T | 1 | a0002c0006t0002g0317 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-38+4823C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27330504 | |||||||
chr8:27330805 | G | A | 4 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-38+5124G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27330805 | |||||||
chr8:27330838 | G | T | 1 | a0001c0002t0001g0188 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-38+5157G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27330838 | |||||||
chr8:27330968 | G | A | 1 | a0002c0004t0002g0242 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-38+5287G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27330968 | |||||||
chr8:27330985 | G | A | 3 | a0001c0008t0003g0314 a0001c0008t0003g0315 a0001c0008t0003g0316 |
3 | HG02258.hp1 HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-38+5304G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27330985 | |||||||
chr8:27331001 | G | A | 197 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(194): Show |
202 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(199): Show |
intron_variant | MODIFIER | c.-38+5320G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27331001 | |||||||
chr8:27331121 | C | T | 1 | a0002c0004t0002g0112 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-38+5440C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27331121 | |||||||
chr8:27331141 | G | A | 2 | a0001c0002t0001g0117 a0001c0002t0001g0118 |
2 | NA18956.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.-38+5460G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27331141 | |||||||
chr8:27331287 | G | A | 5 | a0001c0002t0001g0077 a0001c0002t0001g0119 a0001c0002t0001g0120 others(2): Show |
5 | NA18945.hp2 NA18957.hp2 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.-38+5606G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27331287 | |||||||
chr8:27331463 | T | C | 205 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(202): Show |
210 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(207): Show |
intron_variant | MODIFIER | c.-38+5782T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27331463 | |||||||
chr8:27331476 | C | CT | 169 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(166): Show |
172 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.-38+5802dupT | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27331476 | ||||||
chr8:27331541 | C | T | 4 | a0001c0001t0003g0071 a0001c0001t0003g0072 a0001c0001t0003g0074 others(1): Show |
4 | HG00544.hp1 HG00609.hp1 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.-38+5860C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27331541 | |||||||
chr8:27331640 | C | T | 1 | a0001c0001t0003g0205 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-38+5959C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27331640 | |||||||
chr8:27331696 | AG | A | 107 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(104): Show |
108 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.-38+6017delG | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27331696 | ||||||
chr8:27331791 | T | C | 17 | a0001c0001t0003g0294 a0001c0001t0003g0305 a0001c0002t0001g0295 others(14): Show |
17 | HG00639.hp1 HG02109.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.-38+6110T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27331791 | |||||||
chr8:27331844 | T | C | 1 | a0002c0023t0001g0123 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-38+6163T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27331844 | |||||||
chr8:27332081 | C | G | 11 | a0001c0002t0001g0311 a0001c0009t0002g0312 a0001c0009t0002g0313 others(8): Show |
13 | HG02056.hp1 HG02622.hp1 NA18943.hp2 others(10): Show |
intron_variant | MODIFIER | c.-38+6400C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27332081 | |||||||
chr8:27332454 | A | T | 1 | a0002c0006t0001g0020 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-38+6773A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27332454 | |||||||
chr8:27332535 | C | T | 2 | a0001c0001t0003g0115 a0002c0006t0002g0317 |
2 | HG02818.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-38+6854C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27332535 | |||||||
chr8:27332578 | A | AT | 20 | a0001c0001t0003g0276 a0001c0001t0003g0322 a0001c0002t0001g0235 others(17): Show |
22 | HG01070.hp2 HG01071.hp1 HG02056.hp1 others(19): Show |
intron_variant | MODIFIER | c.-38+6908dupT | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27332578 | ||||||
chr8:27332578 | A | G | 1 | a0002c0003t0002g0275 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-38+6897A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27332578 | |||||||
chr8:27332599 | C | T | 1 | a0002c0003t0002g0274 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-38+6918C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27332599 | |||||||
chr8:27332658 | A | T | 203 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(200): Show |
208 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(205): Show |
intron_variant | MODIFIER | c.-38+6977A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27332658 | |||||||
chr8:27332796 | G | T | 1 | a0001c0008t0003g0114 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-38+7115G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27332796 | |||||||
chr8:27332864 | C | A | 1 | a0001c0002t0001g0124 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-38+7183C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27332864 | |||||||
chr8:27332883 | A | G | 12 | a0001c0001t0003g0322 a0001c0002t0001g0235 a0001c0002t0001g0311 others(9): Show |
14 | HG02056.hp1 HG02109.hp1 HG03471.hp1 others(11): Show |
intron_variant | MODIFIER | c.-38+7202A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27332883 | |||||||
chr8:27332908 | C | T | 1 | a0002c0003t0002g0300 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-38+7227C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27332908 | |||||||
chr8:27332981 | T | C | 19 | a0001c0001t0003g0022 a0001c0001t0003g0294 a0001c0002t0001g0295 others(16): Show |
19 | HG00639.hp1 HG00733.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.-38+7300T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27332981 | |||||||
chr8:27333115 | G | T | 2 | a0001c0008t0003g0114 a0002c0006t0001g0010 |
2 | HG00738.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-38+7434G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27333115 | |||||||
chr8:27333182 | A | G | 2 | a0001c0010t0003g0289 a0002c0006t0001g0006 |
2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-38+7501A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27333182 | |||||||
chr8:27333376 | G | A | 1 | a0002c0003t0002g0023 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-38+7695G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27333376 | |||||||
chr8:27333386 | C | T | 12 | a0001c0001t0003g0022 a0001c0001t0003g0294 a0001c0007t0003g0303 others(9): Show |
12 | HG00639.hp1 HG00733.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.-38+7705C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27333386 | |||||||
chr8:27333428 | G | A | 11 | a0001c0001t0003g0024 a0001c0001t0003g0025 a0001c0001t0003g0028 others(8): Show |
11 | HG01074.hp1 HG01255.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.-38+7747G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27333428 | |||||||
chr8:27333493 | T | G | 18 | a0001c0001t0003g0022 a0001c0001t0003g0294 a0001c0002t0001g0295 others(15): Show |
18 | HG00639.hp1 HG00733.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.-38+7812T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27333493 | |||||||
chr8:27333661 | A | G | 1 | a0002c0006t0001g0068 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-38+7980A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27333661 | |||||||
chr8:27333839 | G | A | 2 | a0001c0008t0003g0114 a0002c0006t0001g0010 |
2 | HG00738.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-38+8158G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27333839 | |||||||
chr8:27334006 | G | A | 1 | a0002c0005t0001g0309 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-38+8325G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27334006 | |||||||
chr8:27334252 | T | C | 32 | a0001c0001t0003g0022 a0001c0001t0003g0294 a0001c0001t0003g0322 others(29): Show |
34 | HG00639.hp1 HG00733.hp1 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.-38+8571T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27334252 | |||||||
chr8:27334436 | C | T | 2 | a0001c0001t0003g0186 a0001c0001t0003g0187 |
2 | HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-38+8755C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27334436 | |||||||
chr8:27334581 | C | T | 1 | a0002c0023t0001g0123 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-38+8900C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27334581 | |||||||
chr8:27334625 | G | A | 1 | a0001c0009t0002g0125 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-38+8944G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27334625 | |||||||
chr8:27334719 | G | A | 181 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(178): Show |
184 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.-38+9038G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27334719 | |||||||
chr8:27335139 | A | G | 1 | a0002c0003t0002g0067 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-38+9458A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27335139 | |||||||
chr8:27335197 | C | T | 10 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(7): Show |
10 | HG02055.hp2 HG02257.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.-38+9516C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27335197 | |||||||
chr8:27335218 | C | T | 1 | a0001c0001t0003g0034 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-38+9537C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27335218 | |||||||
chr8:27335409 | A | G | 2 | a0001c0001t0003g0322 a0001c0002t0001g0235 |
2 | HG02109.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-38+9728A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27335409 | |||||||
chr8:27335595 | C | CA | 9 | a0001c0001t0003g0322 a0001c0002t0001g0235 a0001c0008t0003g0114 others(6): Show |
9 | HG00738.hp1 HG02109.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.-38+9933dupA | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27335595 | ||||||
chr8:27335595 | CA | C | 25 | a0001c0001t0003g0017 a0001c0001t0003g0175 a0001c0001t0003g0273 others(22): Show |
25 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.-38+9933delA | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27335595 | ||||||
chr8:27335658 | C | T | 1 | a0002c0003t0002g0241 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-38+9977C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27335658 | |||||||
chr8:27335660 | C | T | 1 | a0002c0006t0001g0006 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-38+9979C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27335660 | |||||||
chr8:27335922 | T | C | 3 | a0001c0001t0003g0081 a0001c0001t0003g0082 a0001c0001t0003g0205 |
3 | HG00738.hp2 HG01346.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.-38+10241T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27335922 | |||||||
chr8:27335936 | C | T | 22 | a0001c0001t0003g0081 a0001c0001t0003g0082 a0001c0001t0003g0199 others(19): Show |
23 | HG00408.hp1 HG00639.hp2 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.-38+10255C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27335936 | |||||||
chr8:27335977 | C | T | 6 | a0001c0002t0001g0295 a0001c0008t0003g0243 a0001c0008t0003g0296 others(3): Show |
6 | HG02109.hp2 HG02615.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.-38+10296C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27335977 | |||||||
chr8:27336006 | C | T | 1 | a0002c0003t0004g0272 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-38+10325C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27336006 | |||||||
chr8:27336049 | G | A | 181 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(178): Show |
184 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.-38+10368G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27336049 | |||||||
chr8:27336138 | A | G | 1 | a0002c0003t0002g0271 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-38+10457A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27336138 | |||||||
chr8:27336216 | C | T | 3 | a0001c0009t0002g0237 a0002c0003t0002g0270 a0002c0003t0002g0274 |
3 | HG00423.hp1 HG02080.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.-38+10535C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27336216 | |||||||
chr8:27336290 | C | T | 7 | a0001c0001t0003g0022 a0001c0001t0003g0294 a0001c0007t0003g0303 others(4): Show |
7 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-38+10609C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27336290 | |||||||
chr8:27336406 | G | T | 181 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(178): Show |
184 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.-38+10725G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27336406 | |||||||
chr8:27336490 | T | C | 3 | a0001c0008t0003g0314 a0001c0008t0003g0315 a0001c0008t0003g0316 |
3 | HG02258.hp1 HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-38+10809T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27336490 | |||||||
chr8:27336534 | TA | T | 15 | a0001c0001t0003g0322 a0001c0002t0001g0235 a0001c0002t0001g0311 others(12): Show |
17 | HG00738.hp1 HG02056.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.-38+10862delA | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27336534 | ||||||
chr8:27336562 | T | C | 12 | a0001c0001t0003g0322 a0001c0002t0001g0235 a0001c0002t0001g0311 others(9): Show |
14 | HG02056.hp1 HG02109.hp1 HG03471.hp1 others(11): Show |
intron_variant | MODIFIER | c.-38+10881T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27336562 | |||||||
chr8:27336563 | ATGTAAAC others(2): Show |
A | 3 | a0001c0008t0003g0314 a0001c0008t0003g0315 a0001c0008t0003g0316 |
3 | HG02258.hp1 HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-38+10887_-38+1089 others(13): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27336563 | ||||||
chr8:27336598 | T | C | 1 | a0002c0004t0002g0011 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-38+10917T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27336598 | |||||||
chr8:27336858 | C | T | 2 | a0001c0001t0003g0060 a0001c0001t0005g0059 |
2 | HG01069.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.-38+11177C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27336858 | |||||||
chr8:27336862 | GTCTC | G | 12 | a0001c0001t0003g0322 a0001c0002t0001g0235 a0001c0002t0001g0311 others(9): Show |
14 | HG02056.hp1 HG02109.hp1 HG03471.hp1 others(11): Show |
intron_variant | MODIFIER | c.-38+11187_-38+1119 others(8): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27336862 | ||||||
chr8:27336939 | G | A | 1 | a0002c0003t0002g0249 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-38+11258G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27336939 | |||||||
chr8:27336950 | C | T | 2 | a0001c0008t0003g0319 a0001c0008t0003g0320 |
2 | HG02723.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-38+11269C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27336950 | |||||||
chr8:27336992 | A | G | 213 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(210): Show |
218 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.-38+11311A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27336992 | |||||||
chr8:27337112 | C | T | 188 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(185): Show |
191 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.-38+11431C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27337112 | |||||||
chr8:27337271 | A | G | 210 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(207): Show |
215 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.-38+11590A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27337271 | |||||||
chr8:27337288 | A | G | 1 | a0002c0003t0002g0069 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-38+11607A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27337288 | |||||||
chr8:27337297 | G | A | 1 | a0001c0010t0003g0289 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-38+11616G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27337297 | |||||||
chr8:27337343 | G | A | 1 | a0001c0001t0003g0113 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-38+11662G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27337343 | |||||||
chr8:27337364 | T | C | 10 | a0001c0002t0001g0311 a0001c0009t0002g0312 a0001c0009t0002g0313 others(7): Show |
12 | HG02056.hp1 NA18943.hp2 NA18949.hp2 others(9): Show |
intron_variant | MODIFIER | c.-38+11683T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27337364 | |||||||
chr8:27337528 | C | T | 1 | a0002c0003t0004g0272 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-38+11847C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27337528 | |||||||
chr8:27337591 | A | G | 1 | a0002c0005t0001g0204 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-38+11910A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27337591 | |||||||
chr8:27337604 | T | C | 84 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(81): Show |
85 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.-38+11923T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27337604 | |||||||
chr8:27337623 | G | A | 1 | a0002c0003t0002g0012 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-38+11942G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27337623 | |||||||
chr8:27337760 | C | G | 1 | a0002c0005t0001g0033 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-38+12079C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27337760 | |||||||
chr8:27337766 | A | C | 9 | a0001c0002t0001g0295 a0001c0008t0003g0243 a0001c0008t0003g0296 others(6): Show |
9 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-38+12085A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27337766 | |||||||
chr8:27337851 | CAT | C | 7 | a0001c0001t0003g0022 a0001c0001t0003g0294 a0001c0007t0003g0303 others(4): Show |
7 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-38+12173_-38+1217 others(6): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27337851 | ||||||
chr8:27337897 | C | T | 1 | a0002c0023t0001g0123 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-38+12216C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27337897 | |||||||
chr8:27338044 | C | T | 10 | a0001c0002t0001g0311 a0001c0009t0002g0312 a0001c0009t0002g0313 others(7): Show |
12 | HG02056.hp1 NA18943.hp2 NA18949.hp2 others(9): Show |
intron_variant | MODIFIER | c.-38+12363C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27338044 | |||||||
chr8:27338045 | G | A | 1 | a0001c0001t0003g0090 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-38+12364G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27338045 | |||||||
chr8:27338046 | T | A | 31 | a0001c0001t0003g0022 a0001c0001t0003g0294 a0001c0002t0001g0295 others(28): Show |
33 | HG00639.hp1 HG00733.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.-38+12365T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27338046 | |||||||
chr8:27338068 | T | C | 10 | a0001c0002t0001g0311 a0001c0009t0002g0312 a0001c0009t0002g0313 others(7): Show |
12 | HG02056.hp1 NA18943.hp2 NA18949.hp2 others(9): Show |
intron_variant | MODIFIER | c.-38+12387T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27338068 | |||||||
chr8:27338201 | G | A | 1 | a0001c0001t0003g0276 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-38+12520G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27338201 | |||||||
chr8:27338455 | G | A | 2 | a0002c0004t0002g0244 a0002c0004t0002g0245 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-38+12774G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27338455 | |||||||
chr8:27338651 | A | T | 1 | a0002c0006t0002g0317 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-38+12970A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27338651 | |||||||
chr8:27338700 | T | C | 1 | a0001c0001t0003g0288 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-38+13019T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27338700 | |||||||
chr8:27339073 | G | A | 1 | a0002c0003t0002g0069 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-38+13392G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27339073 | |||||||
chr8:27339191 | G | T | 1 | a0001c0010t0003g0289 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-38+13510G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27339191 | |||||||
chr8:27339278 | T | G | 1 | a0002c0004t0002g0250 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-38+13597T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27339278 | |||||||
chr8:27339482 | C | T | 7 | a0001c0001t0003g0022 a0001c0001t0003g0294 a0001c0007t0003g0303 others(4): Show |
7 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-38+13801C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27339482 | |||||||
chr8:27339489 | T | C | 1 | a0002c0003t0002g0300 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-38+13808T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27339489 | |||||||
chr8:27339581 | A | T | 1 | a0002c0006t0001g0282 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-38+13900A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27339581 | |||||||
chr8:27339663 | G | A | 1 | a0001c0030t0002g0007 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-38+13982G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27339663 | |||||||
chr8:27339738 | A | G | 1 | a0002c0006t0001g0323 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-38+14057A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27339738 | |||||||
chr8:27340071 | G | A | 5 | a0001c0002t0001g0126 a0001c0002t0001g0128 a0001c0002t0001g0190 others(2): Show |
5 | NA18943.hp1 NA19000.hp1 NA19070.hp2 others(2): Show |
intron_variant | MODIFIER | c.-38+14390G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27340071 | |||||||
chr8:27340098 | G | C | 2 | a0001c0007t0003g0277 a0001c0007t0003g0278 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-38+14417G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27340098 | |||||||
chr8:27340175 | C | T | 4 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-38+14494C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27340175 | |||||||
chr8:27340209 | A | T | 1 | a0001c0011t0001g0098 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-38+14528A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27340209 | |||||||
chr8:27340256 | G | A | 4 | a0001c0001t0003g0071 a0001c0001t0003g0072 a0001c0001t0003g0074 others(1): Show |
4 | HG00544.hp1 HG00609.hp1 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.-38+14575G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27340256 | |||||||
chr8:27340362 | G | A | 1 | a0001c0001t0003g0035 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-38+14681G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27340362 | |||||||
chr8:27340586 | G | T | 13 | a0001c0002t0001g0311 a0001c0008t0003g0114 a0001c0009t0002g0312 others(10): Show |
15 | HG00738.hp1 HG02056.hp1 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.-38+14905G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27340586 | |||||||
chr8:27340660 | C | T | 2 | a0001c0008t0003g0114 a0002c0006t0001g0010 |
2 | HG00738.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-38+14979C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27340660 | |||||||
chr8:27340668 | C | G | 1 | a0001c0001t0003g0052 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-38+14987C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27340668 | |||||||
chr8:27340721 | T | C | 1 | a0001c0002t0001g0129 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-38+15040T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27340721 | |||||||
chr8:27340747 | C | T | 10 | a0001c0002t0001g0311 a0001c0009t0002g0312 a0001c0009t0002g0313 others(7): Show |
12 | HG02056.hp1 NA18943.hp2 NA18949.hp2 others(9): Show |
intron_variant | MODIFIER | c.-38+15066C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27340747 | |||||||
chr8:27340942 | A | G | 2 | a0001c0001t0003g0322 a0001c0002t0001g0235 |
2 | HG02109.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-38+15261A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27340942 | |||||||
chr8:27341053 | C | T | 1 | a0002c0004t0002g0111 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-38+15372C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27341053 | |||||||
chr8:27341114 | C | T | 2 | a0001c0001t0003g0322 a0001c0002t0001g0235 |
2 | HG02109.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-38+15433C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27341114 | |||||||
chr8:27341288 | G | A | 1 | a0001c0008t0003g0243 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-38+15607G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27341288 | |||||||
chr8:27341367 | G | A | 198 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(195): Show |
201 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.-38+15686G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27341367 | |||||||
chr8:27341380 | G | A | 1 | a0001c0009t0002g0237 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-38+15699G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27341380 | |||||||
chr8:27341440 | G | A | 3 | a0001c0001t0003g0081 a0001c0001t0003g0082 a0001c0001t0003g0205 |
3 | HG00738.hp2 HG01346.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.-38+15759G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27341440 | |||||||
chr8:27341518 | G | T | 13 | a0001c0002t0001g0311 a0001c0008t0003g0114 a0001c0009t0002g0312 others(10): Show |
15 | HG00738.hp1 HG02056.hp1 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.-38+15837G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27341518 | |||||||
chr8:27341519 | A | C | 1 | a0002c0005t0001g0309 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-38+15838A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27341519 | |||||||
chr8:27341664 | G | A | 7 | a0001c0001t0003g0175 a0001c0002t0001g0173 a0001c0002t0001g0174 others(4): Show |
7 | HG01884.hp2 HG02647.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.-38+15983G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27341664 | |||||||
chr8:27341666 | G | T | 3 | a0001c0001t0003g0081 a0001c0001t0003g0082 a0001c0001t0003g0205 |
3 | HG00738.hp2 HG01346.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.-38+15985G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27341666 | |||||||
chr8:27341710 | G | T | 7 | a0001c0001t0003g0022 a0001c0001t0003g0294 a0001c0007t0003g0303 others(4): Show |
7 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-38+16029G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27341710 | |||||||
chr8:27341734 | C | T | 1 | a0002c0006t0001g0020 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-38+16053C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27341734 | |||||||
chr8:27341735 | A | G | 314 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(311): Show |
319 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(316): Show |
intron_variant | MODIFIER | c.-38+16054A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27341735 | |||||||
chr8:27341753 | A | C | 1 | a0002c0003t0002g0269 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-38+16072A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27341753 | |||||||
chr8:27341928 | A | G | 1 | a0001c0030t0002g0007 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-38+16247A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27341928 | |||||||
chr8:27341961 | A | G | 1 | a0002c0003t0002g0300 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-38+16280A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27341961 | |||||||
chr8:27341991 | A | T | 13 | a0001c0002t0001g0311 a0001c0008t0003g0114 a0001c0009t0002g0312 others(10): Show |
15 | HG00738.hp1 HG02056.hp1 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.-38+16310A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27341991 | |||||||
chr8:27342021 | A | G | 2 | a0001c0002t0001g0171 a0001c0002t0001g0172 |
2 | NA18981.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.-38+16340A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27342021 | |||||||
chr8:27342099 | C | T | 1 | a0001c0002t0001g0235 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-38+16418C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27342099 | |||||||
chr8:27342118 | G | C | 10 | a0001c0002t0001g0311 a0001c0009t0002g0312 a0001c0009t0002g0313 others(7): Show |
12 | HG02056.hp1 NA18943.hp2 NA18949.hp2 others(9): Show |
intron_variant | MODIFIER | c.-38+16437G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27342118 | |||||||
chr8:27342217 | A | T | 10 | a0001c0002t0001g0311 a0001c0009t0002g0312 a0001c0009t0002g0313 others(7): Show |
12 | HG02056.hp1 NA18943.hp2 NA18949.hp2 others(9): Show |
intron_variant | MODIFIER | c.-38+16536A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27342217 | |||||||
chr8:27342289 | CT | C | 7 | a0001c0001t0003g0022 a0001c0001t0003g0294 a0001c0007t0003g0303 others(4): Show |
7 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-38+16620delT | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27342289 | ||||||
chr8:27342299 | T | C | 1 | a0001c0001t0003g0113 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-38+16618T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27342299 | |||||||
chr8:27342302 | C | G | 1 | a0002c0006t0001g0287 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-38+16621C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27342302 | |||||||
chr8:27342364 | T | G | 212 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(209): Show |
217 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.-38+16683T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27342364 | |||||||
chr8:27342562 | G | A | 10 | a0001c0002t0001g0126 a0001c0002t0001g0128 a0001c0002t0001g0138 others(7): Show |
10 | HG00735.hp2 HG01993.hp1 HG02273.hp2 others(7): Show |
intron_variant | MODIFIER | c.-38+16881G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27342562 | |||||||
chr8:27342570 | C | T | 191 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(188): Show |
194 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.-38+16889C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27342570 | |||||||
chr8:27342629 | C | G | 3 | a0001c0002t0001g0295 a0001c0008t0003g0243 a0001c0008t0003g0296 |
3 | HG02109.hp2 HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-38+16948C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27342629 | |||||||
chr8:27342685 | G | T | 1 | a0002c0003t0002g0067 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-38+17004G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27342685 | |||||||
chr8:27342759 | A | T | 1 | a0001c0009t0002g0237 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-38+17078A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27342759 | |||||||
chr8:27342819 | A | G | 3 | a0001c0008t0003g0314 a0001c0008t0003g0315 a0001c0008t0003g0316 |
3 | HG02258.hp1 HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-38+17138A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27342819 | |||||||
chr8:27342825 | C | T | 2 | a0001c0008t0003g0319 a0001c0008t0003g0320 |
2 | HG02723.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-38+17144C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27342825 | |||||||
chr8:27342862 | T | A | 4 | a0001c0002t0001g0295 a0001c0008t0003g0243 a0001c0008t0003g0296 others(1): Show |
4 | HG02109.hp2 HG02615.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-38+17181T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27342862 | |||||||
chr8:27343055 | T | G | 7 | a0001c0001t0003g0022 a0001c0001t0003g0294 a0001c0007t0003g0303 others(4): Show |
7 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-38+17374T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27343055 | |||||||
chr8:27343447 | G | A | 215 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(212): Show |
220 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.-38+17766G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27343447 | |||||||
chr8:27343563 | C | T | 7 | a0001c0001t0003g0022 a0001c0001t0003g0294 a0001c0007t0003g0303 others(4): Show |
7 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-38+17882C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27343563 | |||||||
chr8:27343564 | G | A | 1 | a0001c0001t0003g0115 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-38+17883G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27343564 | |||||||
chr8:27343801 | A | G | 2 | a0001c0010t0003g0289 a0002c0006t0001g0006 |
2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-38+18120A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27343801 | |||||||
chr8:27343876 | G | A | 194 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(191): Show |
197 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.-38+18195G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27343876 | |||||||
chr8:27343998 | G | A | 1 | a0001c0007t0003g0279 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-38+18317G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27343998 | |||||||
chr8:27344043 | T | C | 1 | a0002c0003t0002g0251 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-38+18362T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27344043 | |||||||
chr8:27344137 | G | A | 1 | a0001c0010t0003g0297 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-38+18456G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27344137 | |||||||
chr8:27344228 | A | G | 1 | a0002c0003t0002g0223 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-38+18547A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27344228 | |||||||
chr8:27344262 | C | T | 7 | a0001c0001t0003g0181 a0001c0001t0003g0182 a0001c0001t0003g0183 others(4): Show |
7 | HG02055.hp1 HG02257.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.-38+18581C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27344262 | |||||||
chr8:27344275 | G | A | 1 | a0001c0001t0003g0024 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-38+18594G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27344275 | |||||||
chr8:27344339 | C | T | 1 | a0001c0013t0003g0304 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-38+18658C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27344339 | |||||||
chr8:27344384 | C | T | 7 | a0001c0001t0003g0088 a0001c0001t0003g0273 a0002c0003t0002g0180 others(4): Show |
7 | HG01106.hp2 HG01109.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-38+18703C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27344384 | |||||||
chr8:27344534 | T | C | 2 | a0001c0010t0003g0289 a0002c0006t0001g0006 |
2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-38+18853T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27344534 | |||||||
chr8:27344688 | C | G | 1 | a0001c0010t0003g0233 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-38+19007C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27344688 | |||||||
chr8:27344752 | G | A | 1 | a0001c0002t0001g0139 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-38+19071G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27344752 | |||||||
chr8:27344757 | G | T | 1 | a0001c0002t0001g0170 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-38+19076G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27344757 | |||||||
chr8:27344780 | A | T | 13 | a0001c0001t0003g0227 a0001c0001t0003g0228 a0001c0001t0003g0288 others(10): Show |
13 | HG02486.hp1 HG02559.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.-38+19099A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27344780 | |||||||
chr8:27344793 | C | T | 1 | a0002c0003t0002g0265 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-38+19112C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27344793 | |||||||
chr8:27344833 | C | G | 2 | a0001c0001t0003g0113 a0001c0001t0003g0115 |
2 | HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-38+19152C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27344833 | |||||||
chr8:27344927 | C | CT | 200 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(197): Show |
203 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.-38+19248dupT | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27344927 | ||||||
chr8:27345110 | C | T | 10 | a0001c0002t0001g0311 a0001c0009t0002g0312 a0001c0009t0002g0313 others(7): Show |
12 | HG02056.hp1 NA18943.hp2 NA18949.hp2 others(9): Show |
intron_variant | MODIFIER | c.-38+19429C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27345110 | |||||||
chr8:27345187 | C | T | 10 | a0001c0002t0001g0311 a0001c0009t0002g0312 a0001c0009t0002g0313 others(7): Show |
12 | HG02056.hp1 NA18943.hp2 NA18949.hp2 others(9): Show |
intron_variant | MODIFIER | c.-38+19506C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27345187 | |||||||
chr8:27345290 | G | A | 1 | a0001c0022t0002g0008 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-38+19609G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27345290 | |||||||
chr8:27345304 | A | G | 1 | a0001c0001t0003g0113 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-38+19623A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27345304 | |||||||
chr8:27345519 | A | G | 1 | a0002c0006t0002g0317 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-38+19838A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27345519 | |||||||
chr8:27345522 | C | T | 253 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(250): Show |
258 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(255): Show |
intron_variant | MODIFIER | c.-38+19841C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27345522 | |||||||
chr8:27345549 | T | A | 10 | a0001c0002t0001g0311 a0001c0009t0002g0312 a0001c0009t0002g0313 others(7): Show |
12 | HG02056.hp1 NA18943.hp2 NA18949.hp2 others(9): Show |
intron_variant | MODIFIER | c.-38+19868T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27345549 | |||||||
chr8:27345628 | T | C | 1 | a0001c0002t0001g0192 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-38+19947T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27345628 | |||||||
chr8:27345635 | A | G | 1 | a0002c0005t0001g0203 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-38+19954A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27345635 | |||||||
chr8:27345640 | A | G | 1 | a0001c0021t0004g0009 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-38+19959A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27345640 | |||||||
chr8:27345666 | A | G | 1 | a0001c0010t0003g0229 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-38+19985A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27345666 | |||||||
chr8:27345699 | A | T | 2 | a0001c0010t0003g0289 a0002c0006t0001g0006 |
2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-38+20018A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27345699 | |||||||
chr8:27346125 | A | G | 3 | a0001c0008t0003g0314 a0001c0008t0003g0315 a0001c0008t0003g0316 |
3 | HG02258.hp1 HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-38+20444A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27346125 | |||||||
chr8:27346336 | A | T | 1 | a0002c0004t0002g0250 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-38+20655A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27346336 | |||||||
chr8:27346338 | T | C | 1 | a0002c0006t0002g0317 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-38+20657T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27346338 | |||||||
chr8:27346355 | C | T | 1 | a0002c0005t0001g0202 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-38+20674C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27346355 | |||||||
chr8:27346499 | T | C | 1 | a0001c0002t0001g0226 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-38+20818T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27346499 | |||||||
chr8:27346605 | A | G | 2 | a0001c0001t0003g0113 a0001c0001t0003g0115 |
2 | HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-38+20924A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27346605 | |||||||
chr8:27346607 | G | A | 1 | a0002c0005t0001g0309 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-38+20926G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27346607 | |||||||
chr8:27346638 | A | G | 1 | a0001c0030t0002g0007 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-38+20957A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27346638 | |||||||
chr8:27346767 | G | A | 1 | a0002c0003t0002g0180 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-38+21086G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27346767 | |||||||
chr8:27347000 | C | G | 1 | a0001c0022t0002g0008 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-38+21319C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27347000 | |||||||
chr8:27347081 | A | G | 69 | a0001c0001t0003g0056 a0001c0001t0003g0088 a0001c0001t0003g0273 others(66): Show |
71 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.-38+21400A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27347081 | |||||||
chr8:27347146 | A | G | 199 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(196): Show |
202 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.-38+21465A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27347146 | |||||||
chr8:27347214 | T | TA | 17 | a0001c0001t0003g0175 a0001c0001t0003g0322 a0001c0002t0001g0173 others(14): Show |
17 | HG00738.hp1 HG01169.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-38+21549dupA | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27347214 | ||||||
chr8:27347214 | T | TAA | 197 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(194): Show |
202 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.-38+21548_-38+2154 others(6): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27347214 | ||||||
chr8:27347214 | T | TAAA | 10 | a0001c0001t0003g0022 a0001c0001t0003g0294 a0001c0007t0003g0303 others(7): Show |
10 | HG00639.hp1 HG00733.hp1 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.-38+21547_-38+2154 others(7): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27347214 | ||||||
chr8:27347246 | G | A | 4 | a0001c0002t0001g0295 a0001c0008t0003g0243 a0001c0008t0003g0296 others(1): Show |
4 | HG02109.hp2 HG02615.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-38+21565G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27347246 | |||||||
chr8:27347253 | G | A | 1 | a0001c0001t0003g0036 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-38+21572G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27347253 | |||||||
chr8:27347340 | A | G | 214 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(211): Show |
219 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.-38+21659A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27347340 | |||||||
chr8:27347529 | AG | A | 110 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(107): Show |
111 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.-38+21850delG | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27347529 | ||||||
chr8:27347718 | G | A | 14 | a0001c0001t0003g0175 a0001c0001t0003g0276 a0001c0002t0001g0173 others(11): Show |
14 | HG01070.hp2 HG01071.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-38+22037G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27347718 | |||||||
chr8:27347765 | A | T | 2 | a0001c0002t0001g0117 a0001c0002t0001g0118 |
2 | NA18956.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.-38+22084A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27347765 | |||||||
chr8:27347772 | C | G | 2 | a0001c0001t0003g0113 a0001c0001t0003g0115 |
2 | HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-38+22091C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27347772 | |||||||
chr8:27347938 | A | G | 2 | a0001c0007t0003g0277 a0001c0007t0003g0278 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-38+22257A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27347938 | |||||||
chr8:27348029 | G | A | 1 | a0001c0001t0003g0288 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-38+22348G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27348029 | |||||||
chr8:27348177 | A | G | 1 | a0001c0008t0003g0320 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-38+22496A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27348177 | |||||||
chr8:27348260 | G | A | 214 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(211): Show |
219 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.-38+22579G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27348260 | |||||||
chr8:27348267 | G | A | 2 | a0001c0001t0003g0322 a0001c0002t0001g0235 |
2 | HG02109.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-38+22586G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27348267 | |||||||
chr8:27348279 | G | C | 3 | a0001c0008t0003g0114 a0002c0006t0001g0010 a0002c0006t0002g0317 |
3 | HG00738.hp1 HG02717.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-38+22598G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27348279 | |||||||
chr8:27348305 | G | A | 1 | a0001c0010t0003g0231 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-38+22624G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27348305 | |||||||
chr8:27348317 | G | A | 1 | a0002c0023t0001g0123 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-38+22636G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27348317 | |||||||
chr8:27348350 | C | T | 3 | a0001c0008t0003g0114 a0002c0006t0001g0010 a0002c0006t0002g0317 |
3 | HG00738.hp1 HG02717.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-38+22669C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27348350 | |||||||
chr8:27348385 | A | G | 2 | a0001c0001t0003g0113 a0001c0001t0003g0115 |
2 | HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-38+22704A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27348385 | |||||||
chr8:27348488 | C | T | 1 | a0001c0021t0004g0009 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-38+22807C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27348488 | |||||||
chr8:27348599 | G | A | 3 | a0001c0008t0003g0114 a0002c0006t0001g0010 a0002c0006t0002g0317 |
3 | HG00738.hp1 HG02717.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-38+22918G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27348599 | |||||||
chr8:27348665 | C | T | 3 | a0001c0008t0003g0314 a0001c0008t0003g0315 a0001c0008t0003g0316 |
3 | HG02258.hp1 HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-38+22984C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27348665 | |||||||
chr8:27348674 | A | G | 1 | a0001c0008t0003g0114 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-38+22993A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27348674 | |||||||
chr8:27348727 | C | T | 7 | a0001c0002t0001g0295 a0001c0008t0003g0243 a0001c0008t0003g0296 others(4): Show |
7 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.-38+23046C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27348727 | |||||||
chr8:27348754 | C | T | 2 | a0002c0003t0002g0004 a0002c0003t0002g0264 |
3 | HG01257.hp2 HG01258.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.-38+23073C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27348754 | |||||||
chr8:27348884 | C | T | 2 | a0001c0010t0003g0289 a0002c0006t0001g0006 |
2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-38+23203C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27348884 | |||||||
chr8:27349095 | C | A | 10 | a0001c0002t0001g0311 a0001c0009t0002g0312 a0001c0009t0002g0313 others(7): Show |
12 | HG02056.hp1 NA18943.hp2 NA18949.hp2 others(9): Show |
intron_variant | MODIFIER | c.-38+23414C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27349095 | |||||||
chr8:27349181 | A | G | 2 | a0002c0004t0002g0109 a0002c0004t0002g0110 |
2 | HG03490.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.-38+23500A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27349181 | |||||||
chr8:27349380 | C | T | 1 | a0002c0005t0001g0201 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-38+23699C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27349380 | |||||||
chr8:27349673 | A | G | 2 | a0001c0010t0003g0289 a0002c0006t0001g0006 |
2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-38+23992A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27349673 | |||||||
chr8:27350128 | A | G | 4 | a0001c0002t0001g0295 a0001c0008t0003g0243 a0001c0008t0003g0296 others(1): Show |
4 | HG02109.hp2 HG02615.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-38+24447A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350128 | |||||||
chr8:27350249 | G | A | 4 | a0001c0002t0001g0130 a0001c0008t0003g0114 a0002c0006t0001g0010 others(1): Show |
4 | HG00738.hp1 HG02602.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-38+24568G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350249 | |||||||
chr8:27350254 | G | A | 1 | a0001c0001t0003g0288 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-38+24573G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350254 | |||||||
chr8:27350378 | CCCAG | C | 199 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(196): Show |
202 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.-38+24702_-38+2470 others(8): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350378 | ||||||
chr8:27350548 | C | G | 1 | a0002c0004t0002g0298 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-38+24867C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350548 | |||||||
chr8:27350548 | C | T | 1 | a0001c0002t0001g0169 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-38+24867C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350548 | |||||||
chr8:27350575 | G | GCCTCC | 71 | a0001c0001t0003g0056 a0001c0001t0003g0088 a0001c0001t0003g0273 others(68): Show |
73 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.-38+24895_-38+2489 others(9): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350575 | ||||||
chr8:27350601 | C | A | 2 | a0001c0008t0003g0114 a0002c0006t0001g0010 |
2 | HG00738.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-38+24920C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350601 | |||||||
chr8:27350609 | G | A | 109 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(106): Show |
110 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.-38+24928G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350609 | |||||||
chr8:27350646 | C | G | 1 | a0001c0002t0001g0192 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-38+24965C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350646 | |||||||
chr8:27350712 | C | A | 2 | a0001c0008t0003g0114 a0002c0006t0001g0010 |
2 | HG00738.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-38+25031C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350712 | |||||||
chr8:27350718 | C | T | 5 | a0001c0002t0001g0168 a0001c0002t0001g0295 a0001c0008t0003g0243 others(2): Show |
5 | HG01496.hp1 HG02109.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-38+25037C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350718 | |||||||
chr8:27350739 | G | T | 1 | a0001c0002t0001g0138 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-38+25058G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350739 | |||||||
chr8:27350745 | G | T | 192 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(189): Show |
195 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.-38+25064G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350745 | |||||||
chr8:27350775 | C | CAA | 10 | a0001c0002t0001g0311 a0001c0009t0002g0312 a0001c0009t0002g0313 others(7): Show |
12 | HG02056.hp1 NA18943.hp2 NA18949.hp2 others(9): Show |
intron_variant | MODIFIER | c.-38+25095_-38+2509 others(6): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350775 | ||||||
chr8:27350900 | C | T | 3 | a0001c0008t0003g0114 a0002c0006t0001g0010 a0002c0006t0002g0317 |
3 | HG00738.hp1 HG02717.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-38+25219C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350900 | |||||||
chr8:27350975 | C | CA | 6 | a0001c0008t0003g0296 a0001c0010t0003g0229 a0001c0011t0001g0140 others(3): Show |
6 | HG01256.hp2 HG01258.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.-38+25310dupA | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350975 | ||||||
chr8:27350975 | C | CAA | 6 | a0001c0001t0003g0047 a0001c0002t0001g0173 a0001c0002t0001g0174 others(3): Show |
6 | HG01070.hp2 HG01071.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.-38+25309_-38+2531 others(6): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350975 | ||||||
chr8:27350975 | C | CAAAAAAA others(4): Show |
3 | a0001c0002t0001g0295 a0001c0010t0003g0231 a0001c0010t0003g0233 |
3 | HG02486.hp1 HG03098.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-38+25300_-38+2531 others(15): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350975 | ||||||
chr8:27350975 | C | CAAAAAAA others(5): Show |
1 | a0002c0006t0001g0287 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-38+25299_-38+2531 others(16): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350975 | ||||||
chr8:27350975 | C | CAAAAAAA others(6): Show |
2 | a0001c0010t0003g0232 a0002c0005t0001g0002 |
3 | HG00639.hp2 HG01109.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-38+25298_-38+2531 others(17): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350975 | ||||||
chr8:27350975 | C | CAAAAAAA others(7): Show |
4 | a0001c0001t0003g0063 a0001c0001t0003g0227 a0001c0010t0003g0285 others(1): Show |
4 | HG02809.hp1 HG02818.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-38+25297_-38+2531 others(18): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350975 | ||||||
chr8:27350975 | C | CAAAAAAA others(8): Show |
1 | a0001c0001t0003g0017 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-38+25296_-38+2531 others(19): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350975 | ||||||
chr8:27350975 | C | CAAAAAAA others(11): Show |
2 | a0001c0001t0003g0046 a0002c0006t0001g0286 |
2 | HG00438.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.-38+25310_-38+2531 others(22): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350975 | ||||||
chr8:27350975 | C | CAAAAAAA others(12): Show |
6 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0075 others(3): Show |
6 | HG01099.hp1 HG01169.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.-38+25310_-38+2531 others(23): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350975 | ||||||
chr8:27350975 | C | CAAAAAAA others(13): Show |
4 | a0001c0001t0003g0042 a0001c0025t0001g0019 a0002c0006t0001g0062 others(1): Show |
4 | HG02922.hp1 HG03130.hp2 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.-38+25310_-38+2531 others(24): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350975 | ||||||
chr8:27350975 | C | CAAAAAAA others(14): Show |
5 | a0001c0001t0003g0021 a0001c0001t0003g0034 a0001c0001t0003g0041 others(2): Show |
5 | HG00621.hp1 HG02004.hp1 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.-38+25310_-38+2531 others(25): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350975 | ||||||
chr8:27350975 | C | CAAAAAAA others(15): Show |
5 | a0001c0001t0003g0025 a0001c0001t0003g0039 a0001c0001t0005g0059 others(2): Show |
5 | HG01069.hp1 HG01496.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-38+25310_-38+2531 others(26): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350975 | ||||||
chr8:27350975 | C | CAAAAAAA others(16): Show |
2 | a0001c0001t0003g0037 a0001c0001t0003g0038 |
2 | HG02135.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.-38+25310_-38+2531 others(27): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350975 | ||||||
chr8:27350975 | C | CAAAAAAA others(17): Show |
1 | a0001c0001t0003g0052 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-38+25310_-38+2531 others(28): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350975 | ||||||
chr8:27350988 | A | ATATATAT others(4): Show |
1 | a0001c0002t0001g0165 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-38+25307_-38+2530 others(15): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350988 | |||||||
chr8:27350988 | A | ATATATAT others(6): Show |
1 | a0001c0011t0001g0166 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-38+25307_-38+2530 others(17): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350988 | |||||||
chr8:27350988 | A | T | 1 | a0001c0002t0001g0167 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-38+25307A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350988 | |||||||
chr8:27350988 | AAAATATA others(13): Show |
A | 1 | a0001c0001t0003g0322 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-38+25309_-38+2532 others(24): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350988 | ||||||
chr8:27350989 | AAATATAT others(4): Show |
A | 2 | a0001c0002t0001g0164 a0002c0006t0001g0282 |
2 | NA18978.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-38+25310_-38+2532 others(15): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350989 | ||||||
chr8:27350989 | AAATATAT others(8): Show |
A | 1 | a0001c0002t0001g0163 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-38+25310_-38+2532 others(19): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350989 | ||||||
chr8:27350989 | AAATATAT others(10): Show |
A | 5 | a0001c0002t0001g0158 a0001c0002t0001g0159 a0001c0002t0001g0160 others(2): Show |
5 | HG00544.hp2 NA18991.hp1 NA19074.hp2 others(2): Show |
intron_variant | MODIFIER | c.-38+25310_-38+2532 others(21): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350989 | ||||||
chr8:27350989 | AAATATAT others(12): Show |
A | 6 | a0001c0002t0001g0080 a0001c0002t0001g0155 a0001c0002t0001g0157 others(3): Show |
6 | HG01928.hp2 HG02040.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.-38+25310_-38+2532 others(23): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350989 | ||||||
chr8:27350989 | AAATATAT others(26): Show |
A | 3 | a0001c0002t0001g0005 a0001c0002t0001g0129 a0009c0029t0001g0153 |
3 | NA18968.hp1 NA18995.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.-38+25310_-38+2534 others(37): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350989 | ||||||
chr8:27350989 | AAATATAT others(30): Show |
A | 1 | a0001c0002t0001g0212 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-38+25310_-38+2534 others(41): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350989 | ||||||
chr8:27350990 | A | AAAAAAAA others(25): Show |
1 | a0001c0001t0003g0060 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-38+25310_-38+2531 others(36): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | ||||||
chr8:27350990 | A | AAAAAAAA others(33): Show |
1 | a0002c0006t0001g0050 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-38+25310_-38+2531 others(44): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | ||||||
chr8:27350990 | A | AAAAAAAA others(19): Show |
1 | a0001c0001t0003g0228 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-38+25310_-38+2531 others(30): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | ||||||
chr8:27350990 | A | AAAAAAAA others(23): Show |
2 | a0001c0001t0003g0031 a0001c0001t0003g0305 |
2 | HG01074.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-38+25310_-38+2531 others(34): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | ||||||
chr8:27350990 | A | AAAAAAAA others(31): Show |
1 | a0001c0001t0003g0072 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-38+25310_-38+2531 others(42): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | ||||||
chr8:27350990 | A | AAAAAAAA others(18): Show |
1 | a0001c0001t0003g0049 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-38+25310_-38+2531 others(29): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | ||||||
chr8:27350990 | A | AAAAAAAA others(24): Show |
2 | a0001c0001t0003g0074 a0002c0005t0001g0032 |
2 | HG02300.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.-38+25310_-38+2531 others(35): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | ||||||
chr8:27350990 | A | AAAAAAAA others(26): Show |
1 | a0001c0001t0003g0015 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-38+25310_-38+2531 others(37): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | ||||||
chr8:27350990 | A | AAAAAAAA others(28): Show |
1 | a0001c0001t0003g0036 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-38+25310_-38+2531 others(39): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | ||||||
chr8:27350990 | A | AAAAAAAA others(23): Show |
1 | a0001c0010t0003g0230 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-38+25310_-38+2531 others(34): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | ||||||
chr8:27350990 | A | AAAAAAAA others(32): Show |
1 | a0001c0001t0003g0029 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-38+25310_-38+2531 others(43): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | ||||||
chr8:27350990 | A | AAAAAAAA others(38): Show |
1 | a0001c0001t0003g0028 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-38+25310_-38+2531 others(49): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | ||||||
chr8:27350990 | A | AAAAAAAA others(23): Show |
1 | a0001c0012t0004g0027 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-38+25310_-38+2531 others(34): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | ||||||
chr8:27350990 | A | AAAAAAAA others(22): Show |
1 | a0002c0006t0001g0323 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-38+25310_-38+2531 others(33): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | ||||||
chr8:27350990 | A | AAAAAAAA others(26): Show |
1 | a0001c0001t0003g0030 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-38+25310_-38+2531 others(37): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | ||||||
chr8:27350990 | A | AAAAAAAA others(28): Show |
1 | a0002c0006t0001g0066 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-38+25310_-38+2531 others(39): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | ||||||
chr8:27350990 | A | AAAAAAAA others(13): Show |
1 | a0001c0002t0001g0116 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-38+25310_-38+2531 others(24): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | ||||||
chr8:27350990 | A | AAAAAAAA others(26): Show |
2 | a0002c0005t0001g0033 a0002c0026t0001g0238 |
2 | HG01928.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-38+25310_-38+2531 others(37): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | ||||||
chr8:27350990 | A | AAAAAAAA others(11): Show |
1 | a0001c0001t0003g0318 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-38+25310_-38+2531 others(22): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | ||||||
chr8:27350990 | A | AAAAAAAA others(12): Show |
1 | a0001c0008t0003g0320 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-38+25310_-38+2531 others(23): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | ||||||
chr8:27350990 | A | AAAAAAAA others(9): Show |
1 | a0001c0008t0003g0319 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-38+25310_-38+2531 others(20): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | ||||||
chr8:27350990 | A | AAAAAAAA others(11): Show |
1 | a0001c0001t0003g0093 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-38+25310_-38+2531 others(22): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | ||||||
chr8:27350990 | A | AAAAAAAA others(3): Show |
1 | a0001c0001t0003g0024 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-38+25310_-38+2531 others(14): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | ||||||
chr8:27350990 | A | AAAAAAAA others(5): Show |
1 | a0001c0002t0001g0176 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-38+25310_-38+2531 others(16): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | ||||||
chr8:27350990 | A | AAAAAAAT others(8): Show |
1 | a0001c0002t0001g0178 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-38+25310_-38+2531 others(19): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | ||||||
chr8:27350990 | A | AAAAAATA others(7): Show |
1 | a0001c0007t0003g0179 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-38+25310_-38+2531 others(18): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | ||||||
chr8:27350990 | A | AAAAAATA others(9): Show |
1 | a0001c0001t0003g0175 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-38+25310_-38+2531 others(20): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | ||||||
chr8:27350990 | A | AAAATATA others(5): Show |
1 | a0001c0002t0001g0134 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-38+25310_-38+2531 others(16): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | ||||||
chr8:27350990 | A | AAATATAT others(10): Show |
1 | a0001c0002t0001g0119 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-38+25310_-38+2531 others(21): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | ||||||
chr8:27350990 | A | AAATATAT others(18): Show |
1 | a0001c0002t0001g0120 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-38+25310_-38+2531 others(29): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | ||||||
chr8:27350990 | A | AAATATAT others(20): Show |
1 | a0001c0002t0001g0133 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-38+25310_-38+2531 others(31): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | ||||||
chr8:27350990 | A | AATATATA others(5): Show |
1 | a0001c0007t0003g0135 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-38+25349_-38+2536 others(16): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | ||||||
chr8:27350990 | A | AATATATA others(7): Show |
1 | a0001c0002t0001g0122 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-38+25347_-38+2536 others(18): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | ||||||
chr8:27350990 | A | T | 6 | a0001c0002t0001g0077 a0001c0002t0001g0078 a0001c0002t0001g0118 others(3): Show |
6 | HG02071.hp2 HG03710.hp2 NA18945.hp1 others(3): Show |
intron_variant | MODIFIER | c.-38+25309A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350990 | |||||||
chr8:27350990 | AATAT | A | 7 | a0001c0002t0001g0147 a0001c0002t0001g0169 a0001c0011t0001g0079 others(4): Show |
7 | HG01192.hp1 HG01361.hp1 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.-38+25357_-38+2536 others(8): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | ||||||
chr8:27350990 | AATATATA others(1): Show |
A | 8 | a0001c0001t0003g0048 a0001c0002t0001g0128 a0001c0007t0003g0280 others(5): Show |
8 | HG02074.hp1 HG02080.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-38+25353_-38+2536 others(12): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | ||||||
chr8:27350990 | AATATATA others(3): Show |
A | 3 | a0001c0002t0001g0214 a0001c0012t0004g0211 a0002c0004t0002g0109 |
3 | HG01175.hp2 HG03490.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.-38+25351_-38+2536 others(14): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | ||||||
chr8:27350990 | AATATATA others(5): Show |
A | 9 | a0001c0001t0003g0095 a0001c0009t0002g0103 a0001c0009t0002g0107 others(6): Show |
9 | HG00423.hp2 HG00438.hp2 HG00621.hp2 others(6): Show |
intron_variant | MODIFIER | c.-38+25349_-38+2536 others(16): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | ||||||
chr8:27350990 | AATATATA others(7): Show |
A | 6 | a0001c0007t0003g0279 a0001c0011t0001g0098 a0002c0003t0002g0218 others(3): Show |
6 | HG03927.hp1 NA18522.hp2 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-38+25347_-38+2536 others(18): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | ||||||
chr8:27350990 | AATATATA others(9): Show |
A | 14 | a0001c0009t0002g0018 a0001c0009t0002g0087 a0001c0012t0004g0053 others(11): Show |
14 | HG00733.hp2 HG01081.hp1 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.-38+25345_-38+2536 others(20): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | ||||||
chr8:27350990 | AATATATA others(11): Show |
A | 8 | a0001c0001t0003g0088 a0001c0001t0003g0113 a0001c0001t0003g0115 others(5): Show |
8 | HG01168.hp1 HG01516.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.-38+25343_-38+2536 others(22): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | ||||||
chr8:27350990 | AATATATA others(13): Show |
A | 1 | a0001c0002t0001g0235 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-38+25341_-38+2536 others(24): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | ||||||
chr8:27350990 | AATATATA others(17): Show |
A | 1 | a0002c0003t0002g0264 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-38+25337_-38+2536 others(28): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | ||||||
chr8:27350990 | AATATATA others(19): Show |
A | 1 | a0001c0010t0003g0289 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-38+25335_-38+2536 others(30): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | ||||||
chr8:27350990 | AATATATA others(21): Show |
A | 2 | a0001c0008t0003g0114 a0002c0006t0001g0010 |
2 | HG00738.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-38+25333_-38+2536 others(32): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27350990 | ||||||
chr8:27350991 | AT | A | 12 | a0001c0001t0003g0081 a0001c0002t0001g0138 a0001c0002t0001g0170 others(9): Show |
12 | HG00609.hp2 HG00735.hp2 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.-38+25311delT | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350991 | |||||||
chr8:27350991 | ATAT | A | 8 | a0001c0001t0003g0294 a0001c0002t0001g0139 a0001c0002t0001g0190 others(5): Show |
8 | HG00639.hp1 HG02135.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-38+25311_-38+2531 others(7): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350991 | |||||||
chr8:27350991 | ATATAT | A | 4 | a0001c0001t0003g0182 a0001c0001t0003g0186 a0001c0002t0001g0206 others(1): Show |
4 | HG00741.hp2 HG02257.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-38+25311_-38+2531 others(9): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350991 | |||||||
chr8:27350991 | ATATATAT others(4): Show |
A | 2 | a0002c0004t0002g0110 a0002c0004t0002g0151 |
2 | HG03704.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.-38+25311_-38+2532 others(15): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350991 | |||||||
chr8:27350991 | ATATATAT others(6): Show |
A | 10 | a0001c0001t0003g0096 a0001c0001t0003g0097 a0002c0003t0002g0057 others(7): Show |
10 | HG00323.hp2 HG01106.hp1 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-38+25311_-38+2532 others(17): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350991 | |||||||
chr8:27350991 | ATATATAT others(8): Show |
A | 29 | a0001c0001t0003g0056 a0001c0001t0003g0276 a0001c0002t0001g0141 others(26): Show |
30 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(27): Show |
intron_variant | MODIFIER | c.-38+25311_-38+2532 others(19): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350991 | |||||||
chr8:27350991 | ATATATAT others(10): Show |
A | 15 | a0001c0001t0003g0150 a0001c0001t0003g0181 a0001c0001t0003g0273 others(12): Show |
15 | HG00408.hp2 HG00673.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-38+25311_-38+2532 others(21): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350991 | |||||||
chr8:27350991 | ATATATAT others(12): Show |
A | 2 | a0001c0001t0003g0184 a0002c0003t0002g0268 |
2 | HG03540.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-38+25311_-38+2532 others(23): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350991 | |||||||
chr8:27350991 | ATATATAT others(16): Show |
A | 2 | a0002c0003t0002g0004 a0002c0003t0002g0207 |
3 | HG01258.hp1 HG01361.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-38+25311_-38+2533 others(27): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350991 | |||||||
chr8:27350991 | ATATATAT others(18): Show |
A | 8 | a0001c0002t0001g0311 a0001c0009t0002g0312 a0002c0003t0002g0012 others(5): Show |
10 | HG02056.hp1 NA18943.hp2 NA18949.hp2 others(7): Show |
intron_variant | MODIFIER | c.-38+25311_-38+2533 others(29): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350991 | |||||||
chr8:27350991 | ATATATAT others(20): Show |
A | 1 | a0002c0006t0001g0006 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-38+25311_-38+2533 others(31): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350991 | |||||||
chr8:27350991 | ATATATAT others(22): Show |
A | 1 | a0002c0006t0002g0317 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-38+25311_-38+2533 others(33): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350991 | |||||||
chr8:27350991 | ATATATAT others(30): Show |
A | 1 | a0001c0002t0001g0121 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-38+25311_-38+2534 others(41): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350991 | |||||||
chr8:27350992 | T | A | 70 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0034 others(67): Show |
71 | HG00438.hp1 HG00609.hp1 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.-38+25311T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350992 | |||||||
chr8:27350994 | T | A | 70 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0022 others(67): Show |
71 | HG00438.hp1 HG00609.hp1 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.-38+25313T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350994 | |||||||
chr8:27350996 | T | A | 69 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0022 others(66): Show |
70 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.-38+25315T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350996 | |||||||
chr8:27350998 | T | A | 65 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0022 others(62): Show |
65 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.-38+25317T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27350998 | |||||||
chr8:27351000 | T | A | 63 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0022 others(60): Show |
63 | HG00609.hp1 HG00639.hp1 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.-38+25319T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27351000 | |||||||
chr8:27351002 | T | A | 58 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0022 others(55): Show |
58 | HG00609.hp1 HG00639.hp1 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.-38+25321T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27351002 | |||||||
chr8:27351004 | T | A | 58 | a0001c0001t0003g0016 a0001c0001t0003g0022 a0001c0001t0003g0035 others(55): Show |
58 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.-38+25323T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27351004 | |||||||
chr8:27351006 | T | A | 54 | a0001c0001t0003g0016 a0001c0001t0003g0035 a0001c0001t0003g0048 others(51): Show |
54 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.-38+25325T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27351006 | |||||||
chr8:27351008 | T | A | 78 | a0001c0001t0003g0016 a0001c0001t0003g0035 a0001c0001t0003g0048 others(75): Show |
79 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.-38+25327T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27351008 | |||||||
chr8:27351010 | T | A | 88 | a0001c0001t0003g0035 a0001c0001t0003g0048 a0001c0001t0003g0056 others(85): Show |
89 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.-38+25329T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27351010 | |||||||
chr8:27351012 | T | A | 82 | a0001c0001t0003g0035 a0001c0001t0003g0048 a0001c0001t0003g0056 others(79): Show |
83 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.-38+25331T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27351012 | |||||||
chr8:27351014 | T | A | 74 | a0001c0001t0003g0035 a0001c0001t0003g0048 a0001c0001t0003g0056 others(71): Show |
75 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.-38+25333T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27351014 | |||||||
chr8:27351016 | T | A | 63 | a0001c0001t0003g0048 a0001c0001t0003g0056 a0001c0001t0003g0088 others(60): Show |
64 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.-38+25335T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27351016 | |||||||
chr8:27351016 | TATATATA others(19): Show |
T | 1 | a0002c0004t0002g0191 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-38+25336_-38+2536 others(30): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27351016 | |||||||
chr8:27351018 | T | A | 42 | a0001c0001t0003g0048 a0001c0001t0003g0095 a0001c0001t0003g0096 others(39): Show |
45 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(42): Show |
intron_variant | MODIFIER | c.-38+25337T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27351018 | |||||||
chr8:27351018 | TATATATA others(17): Show |
T | 1 | a0001c0009t0002g0313 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-38+25338_-38+2536 others(28): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27351018 | |||||||
chr8:27351020 | T | A | 23 | a0001c0001t0003g0048 a0001c0001t0003g0095 a0001c0001t0003g0096 others(20): Show |
25 | HG00323.hp2 HG00733.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.-38+25339T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27351020 | |||||||
chr8:27351022 | T | A | 20 | a0001c0001t0003g0048 a0001c0001t0003g0095 a0001c0001t0003g0096 others(17): Show |
22 | HG00323.hp2 HG00738.hp1 HG01515.hp1 others(19): Show |
intron_variant | MODIFIER | c.-38+25341T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27351022 | |||||||
chr8:27351024 | T | A | 14 | a0001c0001t0003g0113 a0001c0001t0003g0115 a0001c0002t0001g0311 others(11): Show |
16 | HG00738.hp1 HG02056.hp1 HG02818.hp2 others(13): Show |
intron_variant | MODIFIER | c.-38+25343T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27351024 | |||||||
chr8:27351026 | T | A | 1 | a0002c0006t0002g0317 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-38+25345T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27351026 | |||||||
chr8:27351032 | TATATATA others(3): Show |
T | 3 | a0001c0008t0003g0314 a0001c0008t0003g0315 a0001c0008t0003g0316 |
3 | HG02258.hp1 HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-38+25352_-38+2536 others(14): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27351032 | |||||||
chr8:27351038 | TATAC | T | 4 | a0001c0001t0003g0016 a0001c0001t0003g0183 a0001c0001t0003g0185 others(1): Show |
4 | HG02970.hp2 HG02976.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-38+25358_-38+2536 others(8): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27351038 | |||||||
chr8:27351040 | T | C | 10 | a0001c0001t0003g0022 a0001c0001t0003g0294 a0001c0007t0003g0303 others(7): Show |
10 | HG00639.hp1 HG00733.hp1 HG02165.hp1 others(7): Show |
intron_variant | MODIFIER | c.-38+25359T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27351040 | |||||||
chr8:27351042 | C | T | 18 | a0001c0001t0003g0181 a0001c0001t0003g0182 a0001c0001t0003g0184 others(15): Show |
20 | HG00609.hp1 HG02055.hp1 HG02056.hp1 others(17): Show |
intron_variant | MODIFIER | c.-38+25361C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27351042 | |||||||
chr8:27351247 | T | C | 4 | a0001c0001t0003g0063 a0001c0001t0003g0064 a0001c0001t0003g0065 others(1): Show |
4 | HG02055.hp2 HG02280.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-38+25566T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27351247 | |||||||
chr8:27351315 | A | G | 3 | a0001c0001t0003g0095 a0001c0001t0003g0096 a0001c0001t0003g0097 |
3 | HG00323.hp2 HG01515.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.-38+25634A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27351315 | |||||||
chr8:27351604 | T | A | 1 | a0002c0006t0002g0317 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-38+25923T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27351604 | |||||||
chr8:27351731 | A | C | 3 | a0001c0001t0003g0081 a0001c0001t0003g0082 a0001c0001t0003g0205 |
3 | HG00738.hp2 HG01346.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.-38+26050A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27351731 | |||||||
chr8:27351738 | T | G | 1 | a0001c0010t0003g0289 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-38+26057T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27351738 | |||||||
chr8:27352033 | G | A | 2 | a0002c0003t0002g0249 a0002c0017t0002g0252 |
2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-38+26352G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27352033 | |||||||
chr8:27352069 | C | A | 6 | a0002c0005t0001g0083 a0002c0005t0001g0084 a0002c0005t0001g0085 others(3): Show |
6 | NA18970.hp1 NA18979.hp1 NA19007.hp2 others(3): Show |
intron_variant | MODIFIER | c.-38+26388C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27352069 | |||||||
chr8:27352080 | CAG | C | 7 | a0001c0001t0003g0022 a0001c0001t0003g0294 a0001c0007t0003g0303 others(4): Show |
7 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-38+26400_-38+2640 others(6): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27352080 | |||||||
chr8:27352095 | G | A | 1 | a0001c0022t0002g0008 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-38+26414G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27352095 | |||||||
chr8:27352230 | T | G | 1 | a0002c0005t0001g0204 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-38+26549T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27352230 | |||||||
chr8:27352373 | A | G | 3 | a0001c0008t0003g0314 a0001c0008t0003g0315 a0001c0008t0003g0316 |
3 | HG02258.hp1 HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-38+26692A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27352373 | |||||||
chr8:27352414 | C | T | 3 | a0001c0008t0003g0292 a0001c0008t0003g0319 a0001c0008t0003g0320 |
3 | HG02723.hp2 HG02896.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-38+26733C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27352414 | |||||||
chr8:27352573 | A | C | 4 | a0001c0002t0001g0295 a0001c0008t0003g0243 a0001c0008t0003g0296 others(1): Show |
4 | HG02109.hp2 HG02615.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-38+26892A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27352573 | |||||||
chr8:27352638 | G | A | 1 | a0002c0024t0001g0086 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-38+26957G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27352638 | |||||||
chr8:27352872 | A | G | 4 | a0001c0001t0003g0036 a0002c0006t0001g0286 a0002c0006t0001g0287 others(1): Show |
4 | HG02615.hp2 HG03195.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-38+27191A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27352872 | |||||||
chr8:27353000 | G | A | 1 | a0001c0001t0003g0276 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-38+27319G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27353000 | |||||||
chr8:27353001 | G | T | 199 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(196): Show |
202 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.-38+27320G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27353001 | |||||||
chr8:27353127 | G | A | 6 | a0001c0001t0003g0294 a0001c0007t0003g0303 a0001c0013t0003g0301 others(3): Show |
6 | HG00639.hp1 HG02630.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-38+27446G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27353127 | |||||||
chr8:27353172 | G | A | 2 | a0001c0001t0003g0322 a0001c0002t0001g0235 |
2 | HG02109.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-38+27491G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27353172 | |||||||
chr8:27353293 | A | G | 2 | a0002c0003t0002g0257 a0002c0003t0002g0258 |
2 | NA18960.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.-38+27612A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27353293 | |||||||
chr8:27353335 | T | C | 1 | a0001c0021t0004g0009 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-38+27654T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27353335 | |||||||
chr8:27353476 | T | A | 8 | a0001c0002t0001g0295 a0001c0008t0003g0243 a0001c0008t0003g0296 others(5): Show |
8 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-38+27795T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27353476 | |||||||
chr8:27353491 | A | C | 4 | a0001c0009t0002g0237 a0002c0003t0002g0270 a0002c0003t0002g0274 others(1): Show |
4 | HG00423.hp1 HG02074.hp2 HG02080.hp2 others(1): Show |
intron_variant | MODIFIER | c.-38+27810A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27353491 | |||||||
chr8:27353500 | T | C | 4 | a0001c0009t0002g0237 a0002c0003t0002g0270 a0002c0003t0002g0274 others(1): Show |
4 | HG00423.hp1 HG02074.hp2 HG02080.hp2 others(1): Show |
intron_variant | MODIFIER | c.-38+27819T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27353500 | |||||||
chr8:27353551 | T | G | 2 | a0001c0010t0003g0289 a0002c0006t0001g0006 |
2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-38+27870T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27353551 | |||||||
chr8:27353560 | A | AAC | 75 | a0001c0001t0003g0056 a0001c0001t0003g0088 a0001c0001t0003g0273 others(72): Show |
77 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.-38+27891_-38+2789 others(6): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27353560 | ||||||
chr8:27353632 | C | T | 1 | a0002c0006t0002g0317 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-38+27951C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27353632 | |||||||
chr8:27353640 | G | A | 7 | a0001c0001t0003g0022 a0001c0001t0003g0294 a0001c0007t0003g0303 others(4): Show |
7 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-38+27959G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27353640 | |||||||
chr8:27353667 | T | C | 26 | a0001c0001t0003g0021 a0001c0001t0003g0035 a0001c0001t0003g0037 others(23): Show |
26 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.-38+27986T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27353667 | |||||||
chr8:27353671 | C | A | 3 | a0001c0008t0003g0314 a0001c0008t0003g0315 a0001c0008t0003g0316 |
3 | HG02258.hp1 HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-38+27990C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27353671 | |||||||
chr8:27353816 | C | A | 217 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(214): Show |
222 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(219): Show |
intron_variant | MODIFIER | c.-38+28135C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27353816 | |||||||
chr8:27353829 | C | T | 2 | a0001c0008t0003g0114 a0002c0006t0001g0010 |
2 | HG00738.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-38+28148C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27353829 | |||||||
chr8:27353838 | G | T | 3 | a0001c0008t0003g0114 a0002c0006t0001g0010 a0002c0006t0002g0317 |
3 | HG00738.hp1 HG02717.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-38+28157G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27353838 | |||||||
chr8:27353859 | A | G | 13 | a0001c0001t0003g0227 a0001c0001t0003g0228 a0001c0001t0003g0288 others(10): Show |
13 | HG02486.hp1 HG02559.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.-38+28178A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27353859 | |||||||
chr8:27353908 | G | T | 1 | a0001c0002t0001g0134 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-38+28227G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27353908 | |||||||
chr8:27354042 | T | G | 30 | a0001c0001t0003g0022 a0001c0001t0003g0113 a0001c0001t0003g0115 others(27): Show |
32 | HG00639.hp1 HG00733.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.-38+28361T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27354042 | |||||||
chr8:27354198 | C | T | 2 | a0002c0003t0002g0249 a0002c0017t0002g0252 |
2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-38+28517C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27354198 | |||||||
chr8:27354358 | G | A | 1 | a0002c0004t0002g0094 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-38+28677G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27354358 | |||||||
chr8:27354393 | G | A | 110 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(107): Show |
111 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.-38+28712G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27354393 | |||||||
chr8:27354423 | A | T | 2 | a0001c0009t0002g0018 a0001c0009t0002g0087 |
2 | HG01261.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-38+28742A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27354423 | |||||||
chr8:27354548 | G | A | 4 | a0001c0008t0003g0114 a0001c0030t0002g0007 a0002c0006t0001g0010 others(1): Show |
4 | HG00738.hp1 HG02615.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-38+28867G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27354548 | |||||||
chr8:27354631 | C | T | 3 | a0001c0001t0003g0093 a0002c0006t0001g0020 a0002c0006t0001g0323 |
3 | HG02622.hp1 HG03139.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-38+28950C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27354631 | |||||||
chr8:27354716 | C | T | 1 | a0001c0001t0003g0025 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-38+29035C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27354716 | |||||||
chr8:27354759 | A | C | 103 | a0001c0001t0003g0022 a0001c0001t0003g0056 a0001c0001t0003g0113 others(100): Show |
107 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.-38+29078A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27354759 | |||||||
chr8:27354833 | C | G | 1 | a0002c0004t0002g0225 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-38+29152C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27354833 | |||||||
chr8:27354881 | C | T | 18 | a0001c0001t0003g0022 a0001c0001t0003g0113 a0001c0001t0003g0115 others(15): Show |
18 | HG00639.hp1 HG00733.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.-38+29200C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27354881 | |||||||
chr8:27355324 | GGAAGAGA others(4): Show |
G | 1 | a0001c0007t0003g0279 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-38+29653_-38+2966 others(15): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27355324 | ||||||
chr8:27355637 | G | A | 4 | a0001c0008t0003g0114 a0001c0030t0002g0007 a0002c0006t0001g0010 others(1): Show |
4 | HG00738.hp1 HG02615.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-38+29956G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27355637 | |||||||
chr8:27355671 | C | G | 1 | a0001c0001t0003g0115 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-38+29990C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27355671 | |||||||
chr8:27355955 | A | C | 7 | a0001c0001t0003g0022 a0001c0001t0003g0294 a0001c0007t0003g0303 others(4): Show |
7 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-38+30274A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27355955 | |||||||
chr8:27355994 | G | A | 1 | a0002c0003t0002g0275 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-38+30313G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27355994 | |||||||
chr8:27356001 | C | A | 73 | a0001c0001t0003g0056 a0001c0001t0003g0273 a0001c0001t0003g0322 others(70): Show |
75 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.-38+30320C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27356001 | |||||||
chr8:27356020 | C | CA | 8 | a0001c0001t0003g0022 a0001c0001t0003g0090 a0001c0001t0003g0294 others(5): Show |
8 | HG00639.hp1 HG00733.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.-38+30354dupA | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27356020 | ||||||
chr8:27356122 | C | T | 214 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(211): Show |
219 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.-38+30441C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27356122 | |||||||
chr8:27356204 | G | A | 1 | a0001c0021t0004g0009 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-38+30523G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27356204 | |||||||
chr8:27356287 | C | T | 73 | a0001c0001t0003g0056 a0001c0001t0003g0273 a0001c0001t0003g0322 others(70): Show |
75 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.-38+30606C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27356287 | |||||||
chr8:27356461 | C | G | 1 | a0001c0021t0004g0009 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-38+30780C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27356461 | |||||||
chr8:27356476 | A | G | 1 | a0001c0007t0003g0303 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-38+30795A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27356476 | |||||||
chr8:27356559 | T | C | 3 | a0002c0003t0002g0180 a0002c0003t0002g0266 a0002c0003t0002g0269 |
3 | HG02559.hp2 HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-38+30878T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27356559 | |||||||
chr8:27356653 | G | A | 2 | a0001c0001t0003g0113 a0001c0001t0003g0115 |
2 | HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-38+30972G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27356653 | |||||||
chr8:27356663 | A | G | 7 | a0001c0001t0003g0022 a0001c0001t0003g0294 a0001c0007t0003g0303 others(4): Show |
7 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-38+30982A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27356663 | |||||||
chr8:27356827 | A | G | 2 | a0001c0002t0001g0117 a0001c0002t0001g0118 |
2 | NA18956.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.-38+31146A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27356827 | |||||||
chr8:27356865 | T | G | 3 | a0002c0006t0001g0234 a0002c0006t0001g0290 a0002c0006t0001g0291 |
3 | HG02630.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-38+31184T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27356865 | |||||||
chr8:27356929 | G | A | 1 | a0002c0003t0002g0207 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-38+31248G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27356929 | |||||||
chr8:27357071 | G | C | 1 | a0002c0003t0002g0257 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-38+31390G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27357071 | |||||||
chr8:27357092 | G | C | 1 | a0001c0007t0003g0135 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-38+31411G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27357092 | |||||||
chr8:27357379 | A | C | 1 | a0001c0009t0002g0312 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-38+31698A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27357379 | |||||||
chr8:27357575 | G | T | 4 | a0001c0001t0003g0276 a0001c0007t0003g0279 a0001c0007t0003g0280 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-38+31894G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27357575 | |||||||
chr8:27357994 | C | A | 7 | a0001c0001t0003g0021 a0001c0001t0003g0037 a0001c0001t0003g0042 others(4): Show |
7 | HG00438.hp1 HG02135.hp1 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.-38+32313C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27357994 | |||||||
chr8:27358040 | G | A | 28 | a0001c0001t0003g0022 a0001c0001t0003g0113 a0001c0001t0003g0115 others(25): Show |
30 | HG00639.hp1 HG00733.hp1 HG02056.hp1 others(27): Show |
intron_variant | MODIFIER | c.-38+32359G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27358040 | |||||||
chr8:27358085 | A | G | 1 | a0002c0003t0002g0251 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-38+32404A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27358085 | |||||||
chr8:27358208 | C | T | 2 | a0001c0030t0002g0007 a0002c0006t0002g0317 |
2 | HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-38+32527C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27358208 | |||||||
chr8:27358294 | T | C | 4 | a0001c0001t0003g0113 a0001c0001t0003g0115 a0001c0021t0004g0009 others(1): Show |
4 | HG02818.hp2 HG02922.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.-38+32613T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27358294 | |||||||
chr8:27358376 | A | G | 1 | a0001c0001t0003g0097 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-38+32695A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27358376 | |||||||
chr8:27359020 | T | C | 9 | a0001c0002t0001g0311 a0001c0009t0002g0312 a0001c0009t0002g0313 others(6): Show |
11 | HG02056.hp1 NA18943.hp2 NA18949.hp2 others(8): Show |
intron_variant | MODIFIER | c.-38+33339T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27359020 | |||||||
chr8:27359165 | G | C | 1 | a0002c0006t0001g0287 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-38+33484G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27359165 | |||||||
chr8:27359178 | C | T | 10 | a0001c0001t0003g0093 a0001c0001t0003g0113 a0001c0001t0003g0115 others(7): Show |
10 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-38+33497C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27359178 | |||||||
chr8:27359275 | T | A | 1 | a0001c0001t0003g0036 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-38+33594T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27359275 | |||||||
chr8:27359367 | C | T | 1 | a0001c0002t0001g0170 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-38+33686C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27359367 | |||||||
chr8:27359371 | C | T | 1 | a0001c0001t0003g0051 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-38+33690C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27359371 | |||||||
chr8:27359396 | G | A | 1 | a0001c0001t0003g0063 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-38+33715G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27359396 | |||||||
chr8:27359422 | A | T | 1 | a0002c0004t0002g0011 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-38+33741A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27359422 | |||||||
chr8:27359443 | G | C | 4 | a0001c0009t0002g0237 a0002c0003t0002g0270 a0002c0003t0002g0274 others(1): Show |
4 | HG00423.hp1 HG02074.hp2 HG02080.hp2 others(1): Show |
intron_variant | MODIFIER | c.-38+33762G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27359443 | |||||||
chr8:27359496 | G | T | 7 | a0001c0001t0003g0063 a0001c0001t0003g0064 a0001c0001t0003g0065 others(4): Show |
7 | HG02055.hp2 HG02280.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-38+33815G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27359496 | |||||||
chr8:27359501 | T | C | 1 | a0002c0005t0001g0204 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-38+33820T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27359501 | |||||||
chr8:27359531 | A | T | 1 | a0002c0004t0002g0011 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-38+33850A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27359531 | |||||||
chr8:27359942 | A | AACATCCT others(3): Show |
1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+34263_-38+3427 others(14): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27359942 | ||||||
chr8:27359945 | A | G | 1 | a0001c0010t0003g0229 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-38+34264A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27359945 | |||||||
chr8:27360246 | C | T | 69 | a0001c0001t0003g0056 a0001c0001t0003g0273 a0001c0001t0003g0322 others(66): Show |
71 | HG00099.hp2 HG00408.hp2 HG00673.hp2 others(68): Show |
intron_variant | MODIFIER | c.-38+34565C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27360246 | |||||||
chr8:27360392 | C | T | 1 | a0001c0030t0002g0007 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-38+34711C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27360392 | |||||||
chr8:27360574 | G | A | 1 | a0002c0006t0001g0092 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-38+34893G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27360574 | |||||||
chr8:27360612 | G | A | 1 | a0001c0022t0002g0008 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-38+34931G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27360612 | |||||||
chr8:27360663 | T | C | 1 | a0002c0006t0001g0068 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-38+34982T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27360663 | |||||||
chr8:27360716 | T | G | 1 | a0001c0001t0003g0036 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-38+35035T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27360716 | |||||||
chr8:27360815 | C | T | 9 | a0001c0002t0001g0311 a0001c0009t0002g0312 a0001c0009t0002g0313 others(6): Show |
11 | HG02056.hp1 NA18943.hp2 NA18949.hp2 others(8): Show |
intron_variant | MODIFIER | c.-38+35134C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27360815 | |||||||
chr8:27360859 | A | G | 211 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(208): Show |
216 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.-38+35178A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27360859 | |||||||
chr8:27360875 | A | T | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35194A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27360875 | |||||||
chr8:27360882 | C | G | 1 | a0001c0002t0001g0077 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-38+35201C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27360882 | |||||||
chr8:27360948 | A | C | 19 | a0001c0001t0003g0022 a0001c0001t0003g0113 a0001c0001t0003g0115 others(16): Show |
19 | HG00639.hp1 HG00733.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.-38+35267A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27360948 | |||||||
chr8:27360975 | G | C | 2 | a0001c0001t0003g0113 a0001c0001t0003g0115 |
2 | HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-38+35294G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27360975 | |||||||
chr8:27360993 | A | C | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35312A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27360993 | |||||||
chr8:27360994 | C | A | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35313C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27360994 | |||||||
chr8:27361047 | G | A | 2 | a0002c0003t0002g0249 a0002c0017t0002g0252 |
2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-38+35366G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361047 | |||||||
chr8:27361060 | C | A | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35379C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361060 | |||||||
chr8:27361074 | C | T | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35393C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361074 | |||||||
chr8:27361075 | T | C | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35394T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361075 | |||||||
chr8:27361115 | C | G | 1 | a0001c0001t0003g0051 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-38+35434C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361115 | |||||||
chr8:27361119 | C | T | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35438C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361119 | |||||||
chr8:27361134 | C | T | 1 | a0001c0002t0001g0152 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-38+35453C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361134 | |||||||
chr8:27361139 | A | G | 2 | a0001c0001t0003g0113 a0001c0001t0003g0115 |
2 | HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-38+35458A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361139 | |||||||
chr8:27361220 | T | C | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35539T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361220 | |||||||
chr8:27361231 | T | A | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35550T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361231 | |||||||
chr8:27361265 | C | G | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35584C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361265 | |||||||
chr8:27361283 | A | G | 1 | a0002c0003t0002g0253 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-38+35602A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361283 | |||||||
chr8:27361327 | T | C | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35646T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361327 | |||||||
chr8:27361329 | C | A | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35648C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361329 | |||||||
chr8:27361340 | T | C | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35659T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361340 | |||||||
chr8:27361341 | C | T | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35660C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361341 | |||||||
chr8:27361343 | C | A | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35662C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361343 | |||||||
chr8:27361351 | T | A | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35670T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361351 | |||||||
chr8:27361359 | C | T | 2 | a0001c0009t0002g0107 a0005c0016t0002g0106 |
2 | HG00423.hp2 HG00621.hp2 |
intron_variant | MODIFIER | c.-38+35678C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361359 | |||||||
chr8:27361373 | C | A | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35692C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361373 | |||||||
chr8:27361374 | A | T | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35693A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361374 | |||||||
chr8:27361375 | T | G | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35694T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361375 | |||||||
chr8:27361390 | T | G | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35709T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361390 | |||||||
chr8:27361395 | T | A | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35714T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361395 | |||||||
chr8:27361398 | C | A | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35717C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361398 | |||||||
chr8:27361399 | T | C | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35718T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361399 | |||||||
chr8:27361401 | T | A | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35720T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361401 | |||||||
chr8:27361424 | T | A | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35743T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361424 | |||||||
chr8:27361442 | T | A | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35761T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361442 | |||||||
chr8:27361450 | C | A | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35769C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361450 | |||||||
chr8:27361451 | T | G | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35770T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361451 | |||||||
chr8:27361453 | G | A | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35772G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361453 | |||||||
chr8:27361455 | C | A | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35774C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361455 | |||||||
chr8:27361463 | A | T | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35782A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361463 | |||||||
chr8:27361464 | T | A | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35783T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361464 | |||||||
chr8:27361480 | T | G | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35799T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361480 | |||||||
chr8:27361482 | C | T | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35801C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361482 | |||||||
chr8:27361489 | G | T | 1 | a0001c0002t0001g0172 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-38+35808G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361489 | |||||||
chr8:27361491 | T | A | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35810T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361491 | |||||||
chr8:27361512 | C | G | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35831C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361512 | |||||||
chr8:27361513 | C | A | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35832C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361513 | |||||||
chr8:27361515 | C | A | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35834C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361515 | |||||||
chr8:27361518 | C | T | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35837C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361518 | |||||||
chr8:27361521 | G | A | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35840G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361521 | |||||||
chr8:27361530 | T | A | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35849T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361530 | |||||||
chr8:27361537 | T | A | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35856T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361537 | |||||||
chr8:27361538 | T | A | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35857T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361538 | |||||||
chr8:27361539 | A | T | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35858A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361539 | |||||||
chr8:27361546 | A | T | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35865A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361546 | |||||||
chr8:27361548 | A | G | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35867A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361548 | |||||||
chr8:27361549 | G | A | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35868G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361549 | |||||||
chr8:27361550 | C | A | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35869C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361550 | |||||||
chr8:27361554 | C | G | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35873C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361554 | |||||||
chr8:27361555 | C | G | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35874C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361555 | |||||||
chr8:27361559 | G | T | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35878G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361559 | |||||||
chr8:27361560 | A | T | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35879A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361560 | |||||||
chr8:27361561 | C | A | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35880C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361561 | |||||||
chr8:27361563 | G | C | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35882G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361563 | |||||||
chr8:27361564 | G | T | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35883G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361564 | |||||||
chr8:27361566 | C | G | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35885C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361566 | |||||||
chr8:27361571 | T | A | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35890T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361571 | |||||||
chr8:27361571 | T | G | 1 | a0002c0004t0002g0011 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-38+35890T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361571 | |||||||
chr8:27361572 | G | T | 2 | a0001c0001t0003g0043 a0002c0004t0002g0011 |
2 | NA18956.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.-38+35891G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361572 | |||||||
chr8:27361573 | G | T | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35892G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361573 | |||||||
chr8:27361601 | T | A | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35920T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361601 | |||||||
chr8:27361611 | G | T | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35930G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361611 | |||||||
chr8:27361614 | C | G | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-38+35933C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361614 | |||||||
chr8:27361615 | T | A | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35933T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361615 | |||||||
chr8:27361620 | T | G | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35928T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361620 | |||||||
chr8:27361621 | A | G | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35927A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361621 | |||||||
chr8:27361622 | G | A | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35926G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361622 | |||||||
chr8:27361623 | G | T | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35925G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361623 | |||||||
chr8:27361629 | T | A | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35919T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361629 | |||||||
chr8:27361632 | G | A | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35916G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361632 | |||||||
chr8:27361639 | A | C | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35909A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361639 | |||||||
chr8:27361640 | G | A | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35908G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361640 | |||||||
chr8:27361646 | T | C | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35902T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361646 | |||||||
chr8:27361654 | A | T | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35894A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361654 | |||||||
chr8:27361667 | A | T | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35881A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361667 | |||||||
chr8:27361675 | A | T | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35873A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361675 | |||||||
chr8:27361685 | C | G | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35863C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361685 | |||||||
chr8:27361688 | T | C | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35860T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361688 | |||||||
chr8:27361702 | T | A | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35846T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361702 | |||||||
chr8:27361711 | G | A | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35837G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361711 | |||||||
chr8:27361713 | C | T | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35835C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361713 | |||||||
chr8:27361715 | C | A | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35833C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361715 | |||||||
chr8:27361717 | C | A | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35831C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361717 | |||||||
chr8:27361732 | G | T | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35816G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361732 | |||||||
chr8:27361752 | G | T | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35796G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361752 | |||||||
chr8:27361758 | C | T | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35790C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361758 | |||||||
chr8:27361759 | T | C | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35789T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361759 | |||||||
chr8:27361760 | G | T | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35788G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361760 | |||||||
chr8:27361808 | C | A | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35740C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361808 | |||||||
chr8:27361828 | G | C | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35720G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361828 | |||||||
chr8:27361829 | C | G | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35719C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361829 | |||||||
chr8:27361841 | G | A | 1 | a0002c0026t0001g0238 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-37-35707G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361841 | |||||||
chr8:27361851 | C | T | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35697C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361851 | |||||||
chr8:27361858 | T | A | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35690T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361858 | |||||||
chr8:27361859 | G | A | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35689G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361859 | |||||||
chr8:27361864 | T | A | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35684T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361864 | |||||||
chr8:27361880 | T | A | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35668T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361880 | |||||||
chr8:27361909 | T | C | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35639T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361909 | |||||||
chr8:27361910 | C | T | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35638C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361910 | |||||||
chr8:27361911 | T | A | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35637T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361911 | |||||||
chr8:27361913 | A | C | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35635A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361913 | |||||||
chr8:27361918 | C | T | 19 | a0001c0009t0002g0103 a0001c0009t0002g0107 a0001c0012t0004g0211 others(16): Show |
19 | HG00423.hp2 HG00438.hp2 HG00621.hp2 others(16): Show |
intron_variant | MODIFIER | c.-37-35630C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361918 | |||||||
chr8:27361928 | A | C | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35620A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361928 | |||||||
chr8:27361956 | G | T | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35592G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361956 | |||||||
chr8:27361980 | A | T | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35568A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361980 | |||||||
chr8:27361981 | G | A | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35567G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361981 | |||||||
chr8:27361991 | C | A | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35557C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361991 | |||||||
chr8:27361995 | C | A | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35553C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27361995 | |||||||
chr8:27362000 | C | A | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35548C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27362000 | |||||||
chr8:27362013 | T | A | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35535T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27362013 | |||||||
chr8:27362024 | C | CACTGTCC others(6): Show |
1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35524_-37-3552 others(17): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27362024 | |||||||
chr8:27362032 | G | T | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35516G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27362032 | |||||||
chr8:27362033 | T | A | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35515T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27362033 | |||||||
chr8:27362035 | T | A | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35513T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27362035 | |||||||
chr8:27362045 | A | C | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35503A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27362045 | |||||||
chr8:27362059 | T | A | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35489T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27362059 | |||||||
chr8:27362060 | T | A | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35488T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27362060 | |||||||
chr8:27362074 | C | T | 15 | a0001c0009t0002g0103 a0001c0012t0004g0211 a0002c0004t0002g0094 others(12): Show |
15 | HG00438.hp2 HG00741.hp2 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.-37-35474C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27362074 | |||||||
chr8:27362076 | T | A | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35472T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27362076 | |||||||
chr8:27362083 | G | T | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35465G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27362083 | |||||||
chr8:27362093 | G | A | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35455G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27362093 | |||||||
chr8:27362100 | T | A | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35448T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27362100 | |||||||
chr8:27362200 | T | A | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35348T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27362200 | |||||||
chr8:27362201 | A | G | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35347A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27362201 | |||||||
chr8:27362202 | G | T | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35346G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27362202 | |||||||
chr8:27362211 | G | T | 1 | a0001c0001t0003g0063 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-37-35337G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27362211 | |||||||
chr8:27362212 | GCAGCACC others(6): Show |
G | 1 | a0001c0001t0003g0063 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-37-35334_-37-3532 others(17): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27362212 | ||||||
chr8:27362219 | C | T | 2 | a0001c0030t0002g0007 a0002c0006t0002g0317 |
2 | HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-37-35329C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27362219 | |||||||
chr8:27362227 | T | C | 1 | a0001c0001t0003g0063 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-37-35321T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27362227 | |||||||
chr8:27362234 | T | A | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-35314T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27362234 | |||||||
chr8:27362337 | C | A | 7 | a0001c0001t0003g0022 a0001c0001t0003g0294 a0001c0007t0003g0303 others(4): Show |
7 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-37-35211C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27362337 | |||||||
chr8:27362470 | C | T | 84 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(81): Show |
85 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.-37-35078C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27362470 | |||||||
chr8:27362771 | C | T | 2 | a0001c0008t0003g0114 a0002c0006t0001g0010 |
2 | HG00738.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-37-34777C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27362771 | |||||||
chr8:27362793 | G | A | 112 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(109): Show |
113 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.-37-34755G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27362793 | |||||||
chr8:27362808 | TCTCCCAC others(16): Show |
T | 2 | a0002c0004t0002g0109 a0002c0004t0002g0110 |
2 | HG03490.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.-37-34710_-37-3468 others(27): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27362808 | ||||||
chr8:27363116 | GA | G | 4 | a0001c0008t0003g0114 a0001c0030t0002g0007 a0002c0006t0001g0010 others(1): Show |
4 | HG00738.hp1 HG02615.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37-34431delA | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27363116 | |||||||
chr8:27363249 | C | T | 9 | a0001c0002t0001g0311 a0001c0009t0002g0312 a0001c0009t0002g0313 others(6): Show |
11 | HG02056.hp1 NA18943.hp2 NA18949.hp2 others(8): Show |
intron_variant | MODIFIER | c.-37-34299C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27363249 | |||||||
chr8:27363254 | C | T | 9 | a0001c0002t0001g0311 a0001c0009t0002g0312 a0001c0009t0002g0313 others(6): Show |
11 | HG02056.hp1 NA18943.hp2 NA18949.hp2 others(8): Show |
intron_variant | MODIFIER | c.-37-34294C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27363254 | |||||||
chr8:27363291 | G | A | 3 | a0002c0003t0002g0239 a0002c0003t0002g0240 a0002c0003t0002g0241 |
3 | HG00408.hp2 NA18947.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.-37-34257G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27363291 | |||||||
chr8:27363311 | G | A | 7 | a0001c0012t0004g0053 a0001c0012t0004g0055 a0002c0003t0002g0023 others(4): Show |
7 | HG00735.hp1 HG01081.hp1 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.-37-34237G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27363311 | |||||||
chr8:27363323 | A | C | 1 | a0001c0001t0003g0043 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-37-34225A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27363323 | |||||||
chr8:27363323 | A | G | 6 | a0001c0001t0003g0021 a0001c0001t0003g0037 a0001c0001t0003g0042 others(3): Show |
6 | HG00438.hp1 HG02135.hp1 NA18985.hp2 others(3): Show |
intron_variant | MODIFIER | c.-37-34225A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27363323 | |||||||
chr8:27363592 | G | A | 9 | a0001c0002t0001g0311 a0001c0009t0002g0312 a0001c0009t0002g0313 others(6): Show |
11 | HG02056.hp1 NA18943.hp2 NA18949.hp2 others(8): Show |
intron_variant | MODIFIER | c.-37-33956G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27363592 | |||||||
chr8:27363665 | T | A | 1 | a0001c0010t0003g0229 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-37-33883T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27363665 | |||||||
chr8:27363701 | T | C | 1 | a0001c0010t0003g0289 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-37-33847T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27363701 | |||||||
chr8:27363944 | G | C | 3 | a0001c0001t0003g0088 a0001c0001t0003g0113 a0001c0001t0003g0115 |
3 | HG02572.hp1 HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-37-33604G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27363944 | |||||||
chr8:27364133 | A | G | 3 | a0001c0002t0001g0295 a0001c0008t0003g0243 a0001c0008t0003g0296 |
3 | HG02109.hp2 HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-37-33415A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27364133 | |||||||
chr8:27364166 | T | C | 2 | a0001c0002t0001g0142 a0001c0002t0001g0165 |
2 | HG03710.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.-37-33382T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27364166 | |||||||
chr8:27364375 | C | T | 2 | a0002c0004t0002g0109 a0002c0004t0002g0110 |
2 | HG03490.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.-37-33173C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27364375 | |||||||
chr8:27364470 | G | A | 1 | a0001c0022t0002g0008 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-37-33078G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27364470 | |||||||
chr8:27364470 | G | C | 4 | a0001c0008t0003g0114 a0001c0030t0002g0007 a0002c0006t0001g0010 others(1): Show |
4 | HG00738.hp1 HG02615.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37-33078G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27364470 | |||||||
chr8:27364489 | C | T | 2 | a0001c0030t0002g0007 a0002c0006t0002g0317 |
2 | HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-37-33059C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27364489 | |||||||
chr8:27364563 | A | T | 4 | a0001c0008t0003g0114 a0001c0030t0002g0007 a0002c0006t0001g0010 others(1): Show |
4 | HG00738.hp1 HG02615.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37-32985A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27364563 | |||||||
chr8:27364670 | G | A | 2 | a0001c0001t0003g0060 a0001c0001t0005g0059 |
2 | HG01069.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.-37-32878G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27364670 | |||||||
chr8:27364945 | A | G | 1 | a0002c0005t0001g0309 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-37-32603A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27364945 | |||||||
chr8:27364962 | C | T | 2 | a0001c0021t0004g0009 a0001c0022t0002g0008 |
2 | NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-37-32586C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27364962 | |||||||
chr8:27365026 | C | A | 3 | a0001c0008t0003g0314 a0001c0008t0003g0315 a0001c0008t0003g0316 |
3 | HG02258.hp1 HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-37-32522C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27365026 | |||||||
chr8:27365188 | G | A | 2 | a0001c0010t0003g0289 a0002c0006t0001g0006 |
2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-37-32360G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27365188 | |||||||
chr8:27365298 | G | A | 1 | a0001c0022t0002g0008 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-37-32250G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27365298 | |||||||
chr8:27365370 | T | C | 3 | a0001c0002t0001g0295 a0001c0008t0003g0243 a0001c0008t0003g0296 |
3 | HG02109.hp2 HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-37-32178T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27365370 | |||||||
chr8:27365448 | C | T | 1 | a0001c0002t0001g0174 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-37-32100C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27365448 | |||||||
chr8:27365637 | G | T | 2 | a0001c0001t0003g0322 a0001c0002t0001g0235 |
2 | HG02109.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-37-31911G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27365637 | |||||||
chr8:27365655 | C | CTTT | 31 | a0001c0001t0003g0022 a0001c0001t0003g0088 a0001c0001t0003g0113 others(28): Show |
33 | HG00639.hp1 HG00733.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.-37-31893_-37-3189 others(7): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27365655 | |||||||
chr8:27365811 | G | A | 2 | a0001c0010t0003g0289 a0002c0006t0001g0006 |
2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-37-31737G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27365811 | |||||||
chr8:27365825 | T | C | 75 | a0001c0001t0003g0056 a0001c0001t0003g0273 a0001c0001t0003g0322 others(72): Show |
77 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.-37-31723T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27365825 | |||||||
chr8:27365840 | C | T | 2 | a0001c0010t0003g0285 a0007c0032t0003g0284 |
2 | HG02809.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-37-31708C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27365840 | |||||||
chr8:27365900 | A | G | 2 | a0001c0001t0003g0036 a0001c0013t0003g0304 |
2 | HG02723.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-37-31648A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27365900 | |||||||
chr8:27365957 | T | C | 2 | a0001c0030t0002g0007 a0002c0006t0002g0317 |
2 | HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-37-31591T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27365957 | |||||||
chr8:27366121 | G | A | 2 | a0001c0010t0003g0289 a0002c0006t0001g0006 |
2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-37-31427G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27366121 | |||||||
chr8:27366165 | G | A | 75 | a0001c0001t0003g0056 a0001c0001t0003g0273 a0001c0001t0003g0322 others(72): Show |
77 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.-37-31383G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27366165 | |||||||
chr8:27366279 | A | G | 19 | a0001c0009t0002g0103 a0001c0009t0002g0107 a0001c0012t0004g0211 others(16): Show |
19 | HG00423.hp2 HG00438.hp2 HG00621.hp2 others(16): Show |
intron_variant | MODIFIER | c.-37-31269A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27366279 | |||||||
chr8:27366339 | A | G | 7 | a0001c0001t0003g0022 a0001c0001t0003g0294 a0001c0007t0003g0303 others(4): Show |
7 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-37-31209A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27366339 | |||||||
chr8:27366579 | T | C | 1 | a0002c0026t0001g0238 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-37-30969T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27366579 | |||||||
chr8:27366803 | TG | T | 3 | a0002c0003t0002g0247 a0002c0004t0002g0224 a0002c0004t0002g0225 |
3 | HG01261.hp1 HG03669.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.-37-30743delG | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27366803 | ||||||
chr8:27366816 | A | G | 9 | a0001c0002t0001g0311 a0001c0009t0002g0312 a0001c0009t0002g0313 others(6): Show |
11 | HG02056.hp1 NA18943.hp2 NA18949.hp2 others(8): Show |
intron_variant | MODIFIER | c.-37-30732A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27366816 | |||||||
chr8:27366880 | G | A | 1 | a0001c0025t0001g0019 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-37-30668G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27366880 | |||||||
chr8:27366909 | C | T | 1 | a0002c0003t0002g0258 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-37-30639C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27366909 | |||||||
chr8:27366993 | G | A | 18 | a0001c0001t0003g0022 a0001c0001t0003g0088 a0001c0001t0003g0113 others(15): Show |
18 | HG00639.hp1 HG00733.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.-37-30555G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27366993 | |||||||
chr8:27367229 | C | T | 1 | a0001c0010t0003g0289 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-37-30319C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27367229 | |||||||
chr8:27367280 | T | C | 31 | a0001c0001t0003g0022 a0001c0001t0003g0088 a0001c0001t0003g0113 others(28): Show |
33 | HG00639.hp1 HG00733.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.-37-30268T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27367280 | |||||||
chr8:27367290 | A | G | 1 | a0001c0001t0003g0113 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-37-30258A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27367290 | |||||||
chr8:27367390 | G | A | 1 | a0001c0001t0003g0072 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-37-30158G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27367390 | |||||||
chr8:27367409 | C | T | 2 | a0001c0007t0003g0280 a0001c0007t0003g0281 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-37-30139C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27367409 | |||||||
chr8:27367439 | G | A | 1 | a0002c0003t0002g0271 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-37-30109G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27367439 | |||||||
chr8:27367503 | C | G | 2 | a0001c0010t0003g0289 a0002c0006t0001g0006 |
2 | HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-37-30045C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27367503 | |||||||
chr8:27367799 | A | G | 4 | a0001c0008t0003g0114 a0001c0030t0002g0007 a0002c0006t0001g0010 others(1): Show |
4 | HG00738.hp1 HG02615.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37-29749A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27367799 | |||||||
chr8:27367801 | A | G | 4 | a0001c0008t0003g0114 a0001c0030t0002g0007 a0002c0006t0001g0010 others(1): Show |
4 | HG00738.hp1 HG02615.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37-29747A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27367801 | |||||||
chr8:27368125 | C | T | 4 | a0001c0001t0003g0276 a0001c0007t0003g0279 a0001c0007t0003g0280 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37-29423C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27368125 | |||||||
chr8:27368126 | G | A | 1 | a0001c0025t0001g0019 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-37-29422G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27368126 | |||||||
chr8:27368278 | G | A | 1 | a0001c0001t0003g0318 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-37-29270G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27368278 | |||||||
chr8:27368452 | C | T | 1 | a0002c0003t0002g0267 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-37-29096C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27368452 | |||||||
chr8:27368513 | C | G | 3 | a0001c0001t0003g0047 a0002c0005t0001g0194 a0002c0005t0001g0195 |
3 | HG01256.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-37-29035C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27368513 | |||||||
chr8:27368669 | A | T | 1 | a0001c0010t0003g0289 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-37-28879A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27368669 | |||||||
chr8:27368824 | G | C | 7 | a0001c0001t0003g0088 a0001c0001t0003g0113 a0001c0001t0003g0115 others(4): Show |
7 | HG02258.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.-37-28724G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27368824 | |||||||
chr8:27368895 | G | T | 3 | a0001c0002t0001g0120 a0001c0002t0001g0121 a0001c0002t0001g0122 |
3 | NA18957.hp2 NA18969.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.-37-28653G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27368895 | |||||||
chr8:27368915 | G | C | 7 | a0001c0001t0003g0022 a0001c0001t0003g0294 a0001c0007t0003g0303 others(4): Show |
7 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-37-28633G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27368915 | |||||||
chr8:27368919 | G | A | 1 | a0001c0002t0001g0170 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-37-28629G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27368919 | |||||||
chr8:27369219 | C | G | 1 | a0001c0010t0003g0289 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-37-28329C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27369219 | |||||||
chr8:27369239 | T | C | 8 | a0001c0009t0002g0312 a0001c0009t0002g0313 a0002c0003t0002g0012 others(5): Show |
10 | NA18943.hp2 NA18949.hp2 NA18968.hp2 others(7): Show |
intron_variant | MODIFIER | c.-37-28309T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27369239 | |||||||
chr8:27369241 | C | T | 1 | a0001c0021t0004g0009 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-37-28307C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27369241 | |||||||
chr8:27369273 | A | C | 124 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(121): Show |
125 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.-37-28275A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27369273 | |||||||
chr8:27369401 | G | A | 1 | a0001c0001t0003g0322 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-37-28147G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27369401 | |||||||
chr8:27369533 | G | A | 1 | a0002c0004t0002g0248 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-37-28015G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27369533 | |||||||
chr8:27369536 | G | C | 3 | a0001c0002t0001g0295 a0001c0008t0003g0243 a0001c0008t0003g0296 |
3 | HG02109.hp2 HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-37-28012G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27369536 | |||||||
chr8:27369609 | G | A | 6 | a0001c0001t0003g0088 a0001c0001t0003g0113 a0001c0001t0003g0115 others(3): Show |
6 | HG02258.hp1 HG02486.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-37-27939G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27369609 | |||||||
chr8:27369714 | C | G | 3 | a0001c0008t0003g0314 a0001c0008t0003g0315 a0001c0008t0003g0316 |
3 | HG02258.hp1 HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-37-27834C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27369714 | |||||||
chr8:27369819 | A | G | 1 | a0001c0001t0003g0022 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-37-27729A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27369819 | |||||||
chr8:27369887 | G | C | 3 | a0001c0001t0003g0088 a0001c0001t0003g0113 a0001c0001t0003g0115 |
3 | HG02572.hp1 HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-37-27661G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27369887 | |||||||
chr8:27369909 | G | A | 4 | a0001c0008t0003g0114 a0001c0030t0002g0007 a0002c0006t0001g0010 others(1): Show |
4 | HG00738.hp1 HG02615.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37-27639G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27369909 | |||||||
chr8:27369925 | T | C | 28 | a0001c0001t0003g0022 a0001c0001t0003g0088 a0001c0001t0003g0113 others(25): Show |
30 | HG00639.hp1 HG00733.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.-37-27623T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27369925 | |||||||
chr8:27369934 | A | G | 1 | a0002c0005t0001g0309 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-37-27614A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27369934 | |||||||
chr8:27369936 | C | T | 109 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(106): Show |
110 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.-37-27612C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27369936 | |||||||
chr8:27370037 | A | G | 82 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(79): Show |
83 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.-37-27511A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27370037 | |||||||
chr8:27370117 | C | T | 2 | a0001c0021t0004g0009 a0001c0022t0002g0008 |
2 | NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-37-27431C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27370117 | |||||||
chr8:27370169 | G | T | 8 | a0001c0001t0003g0022 a0001c0001t0003g0175 a0001c0001t0003g0294 others(5): Show |
8 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-37-27379G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27370169 | |||||||
chr8:27370321 | C | T | 1 | a0002c0006t0002g0317 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-37-27227C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27370321 | |||||||
chr8:27370322 | G | A | 1 | a0002c0004t0002g0094 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-37-27226G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27370322 | |||||||
chr8:27370496 | C | T | 1 | a0001c0010t0003g0233 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-37-27052C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27370496 | |||||||
chr8:27370545 | A | C | 4 | a0001c0008t0003g0114 a0001c0030t0002g0007 a0002c0006t0001g0010 others(1): Show |
4 | HG00738.hp1 HG02615.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37-27003A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27370545 | |||||||
chr8:27370559 | G | A | 13 | a0001c0001t0003g0022 a0001c0001t0003g0175 a0001c0001t0003g0294 others(10): Show |
13 | HG00639.hp1 HG00733.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-37-26989G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27370559 | |||||||
chr8:27370567 | T | G | 1 | a0001c0010t0003g0289 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-37-26981T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27370567 | |||||||
chr8:27370600 | G | T | 1 | a0001c0001t0003g0072 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-37-26948G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27370600 | |||||||
chr8:27370677 | T | C | 2 | a0001c0002t0001g0192 a0002c0005t0001g0202 |
2 | HG00408.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.-37-26871T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27370677 | |||||||
chr8:27370839 | C | G | 8 | a0001c0009t0002g0312 a0001c0009t0002g0313 a0002c0003t0002g0012 others(5): Show |
10 | NA18943.hp2 NA18949.hp2 NA18968.hp2 others(7): Show |
intron_variant | MODIFIER | c.-37-26709C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27370839 | |||||||
chr8:27370897 | C | G | 4 | a0001c0001t0003g0024 a0002c0005t0001g0026 a0002c0005t0001g0032 others(1): Show |
4 | HG01928.hp1 HG01943.hp2 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.-37-26651C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27370897 | |||||||
chr8:27370986 | C | T | 5 | a0001c0001t0003g0047 a0002c0005t0001g0194 a0002c0005t0001g0195 others(2): Show |
5 | HG01081.hp2 HG01123.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.-37-26562C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27370986 | |||||||
chr8:27371045 | G | A | 8 | a0001c0009t0002g0312 a0001c0009t0002g0313 a0002c0003t0002g0012 others(5): Show |
10 | NA18943.hp2 NA18949.hp2 NA18968.hp2 others(7): Show |
intron_variant | MODIFIER | c.-37-26503G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27371045 | |||||||
chr8:27371061 | A | G | 1 | a0001c0012t0004g0211 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-37-26487A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27371061 | |||||||
chr8:27371110 | G | C | 1 | a0001c0002t0001g0192 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-37-26438G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27371110 | |||||||
chr8:27371149 | C | A | 112 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(109): Show |
113 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.-37-26399C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27371149 | |||||||
chr8:27371158 | C | T | 8 | a0001c0001t0003g0022 a0001c0001t0003g0175 a0001c0001t0003g0294 others(5): Show |
8 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-37-26390C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27371158 | |||||||
chr8:27371185 | C | T | 1 | a0002c0004t0002g0110 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-37-26363C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27371185 | |||||||
chr8:27371292 | G | A | 1 | a0002c0023t0001g0123 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-37-26256G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27371292 | |||||||
chr8:27371325 | G | A | 8 | a0001c0001t0003g0022 a0001c0001t0003g0175 a0001c0001t0003g0294 others(5): Show |
8 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-37-26223G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27371325 | |||||||
chr8:27371338 | G | A | 1 | a0002c0003t0002g0267 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-37-26210G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27371338 | |||||||
chr8:27371443 | C | T | 1 | a0002c0018t0002g0089 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-37-26105C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27371443 | |||||||
chr8:27371545 | T | TTA | 18 | a0001c0001t0003g0022 a0001c0001t0003g0175 a0001c0001t0003g0276 others(15): Show |
18 | HG00639.hp1 HG00733.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.-37-25987_-37-2598 others(6): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27371545 | ||||||
chr8:27371545 | T | TTATA | 109 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(106): Show |
110 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.-37-25989_-37-2598 others(8): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27371545 | ||||||
chr8:27371793 | C | T | 3 | a0001c0001t0003g0088 a0001c0001t0003g0113 a0001c0001t0003g0115 |
3 | HG02572.hp1 HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-37-25755C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27371793 | |||||||
chr8:27371905 | C | T | 2 | a0001c0030t0002g0007 a0002c0006t0002g0317 |
2 | HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-37-25643C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27371905 | |||||||
chr8:27371910 | C | T | 3 | a0001c0008t0003g0292 a0001c0008t0003g0319 a0001c0008t0003g0320 |
3 | HG02723.hp2 HG02896.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-37-25638C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27371910 | |||||||
chr8:27371927 | G | A | 4 | a0001c0002t0001g0078 a0001c0002t0001g0170 a0001c0002t0001g0171 others(1): Show |
4 | NA18945.hp1 NA18967.hp1 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37-25621G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27371927 | |||||||
chr8:27371944 | A | G | 1 | a0002c0006t0001g0068 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-37-25604A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27371944 | |||||||
chr8:27371987 | CAT | C | 3 | a0001c0002t0001g0295 a0001c0008t0003g0243 a0001c0008t0003g0296 |
3 | HG02109.hp2 HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-37-25558_-37-2555 others(6): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27371987 | ||||||
chr8:27372004 | G | A | 2 | a0002c0003t0002g0307 a0002c0003t0002g0308 |
2 | NA18967.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.-37-25544G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27372004 | |||||||
chr8:27372040 | T | C | 2 | a0001c0011t0001g0140 a0001c0011t0001g0166 |
2 | NA18949.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.-37-25508T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27372040 | |||||||
chr8:27372076 | G | A | 2 | a0001c0021t0004g0009 a0001c0022t0002g0008 |
2 | NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-37-25472G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27372076 | |||||||
chr8:27372109 | T | C | 1 | a0002c0026t0001g0238 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-37-25439T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27372109 | |||||||
chr8:27372126 | A | G | 1 | a0001c0010t0003g0289 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-37-25422A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27372126 | |||||||
chr8:27372199 | G | A | 8 | a0001c0009t0002g0312 a0001c0009t0002g0313 a0002c0003t0002g0012 others(5): Show |
10 | NA18943.hp2 NA18949.hp2 NA18968.hp2 others(7): Show |
intron_variant | MODIFIER | c.-37-25349G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27372199 | |||||||
chr8:27372220 | G | T | 1 | a0001c0002t0001g0162 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-37-25328G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27372220 | |||||||
chr8:27372520 | G | A | 11 | a0001c0001t0003g0022 a0001c0001t0003g0175 a0001c0001t0003g0294 others(8): Show |
11 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.-37-25028G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27372520 | |||||||
chr8:27372947 | G | A | 2 | a0001c0021t0004g0009 a0001c0022t0002g0008 |
2 | NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-37-24601G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27372947 | |||||||
chr8:27372948 | C | T | 2 | a0001c0008t0003g0114 a0002c0006t0001g0010 |
2 | HG00738.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-37-24600C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27372948 | |||||||
chr8:27372955 | A | T | 1 | a0001c0030t0002g0007 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-37-24593A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27372955 | |||||||
chr8:27372961 | T | C | 2 | a0002c0003t0002g0004 a0002c0003t0002g0264 |
3 | HG01257.hp2 HG01258.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.-37-24587T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27372961 | |||||||
chr8:27373058 | A | G | 1 | a0001c0001t0003g0093 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-37-24490A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27373058 | |||||||
chr8:27373061 | T | C | 8 | a0001c0001t0003g0022 a0001c0001t0003g0175 a0001c0001t0003g0294 others(5): Show |
8 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-37-24487T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27373061 | |||||||
chr8:27373120 | A | G | 122 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(119): Show |
123 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.-37-24428A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27373120 | |||||||
chr8:27373159 | G | A | 1 | a0001c0001t0003g0046 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-37-24389G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27373159 | |||||||
chr8:27373301 | C | T | 8 | a0001c0002t0001g0295 a0001c0008t0003g0243 a0001c0008t0003g0296 others(5): Show |
8 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-37-24247C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27373301 | |||||||
chr8:27373302 | A | G | 148 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(145): Show |
151 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.-37-24246A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27373302 | |||||||
chr8:27373408 | T | G | 222 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(219): Show |
227 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.-37-24140T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27373408 | |||||||
chr8:27373698 | T | A | 17 | a0001c0001t0003g0022 a0001c0001t0003g0049 a0001c0001t0003g0088 others(14): Show |
17 | HG00733.hp1 HG00738.hp1 HG01070.hp2 others(14): Show |
intron_variant | MODIFIER | c.-37-23850T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27373698 | |||||||
chr8:27373699 | A | T | 9 | a0001c0002t0001g0173 a0001c0002t0001g0174 a0001c0002t0001g0176 others(6): Show |
9 | HG01884.hp2 HG02647.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.-37-23849A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27373699 | |||||||
chr8:27373803 | A | G | 1 | a0002c0003t0006g0040 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-37-23745A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27373803 | |||||||
chr8:27373890 | G | T | 2 | a0001c0030t0002g0007 a0002c0006t0002g0317 |
2 | HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-37-23658G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27373890 | |||||||
chr8:27373976 | G | A | 8 | a0001c0001t0003g0022 a0001c0001t0003g0175 a0001c0001t0003g0294 others(5): Show |
8 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-37-23572G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27373976 | |||||||
chr8:27374040 | G | A | 1 | a0002c0006t0002g0317 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-37-23508G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27374040 | |||||||
chr8:27374071 | A | T | 73 | a0001c0001t0003g0056 a0001c0009t0002g0018 a0001c0009t0002g0087 others(70): Show |
75 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.-37-23477A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27374071 | |||||||
chr8:27374092 | G | A | 8 | a0001c0001t0003g0022 a0001c0001t0003g0175 a0001c0001t0003g0294 others(5): Show |
8 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-37-23456G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27374092 | |||||||
chr8:27374170 | T | G | 9 | a0001c0002t0001g0143 a0001c0002t0001g0155 a0001c0002t0001g0158 others(6): Show |
9 | HG00544.hp2 HG02015.hp2 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.-37-23378T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27374170 | |||||||
chr8:27374256 | G | A | 2 | a0001c0030t0002g0007 a0002c0006t0002g0317 |
2 | HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-37-23292G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27374256 | |||||||
chr8:27374304 | CTTGGGAT others(3): Show |
C | 2 | a0001c0011t0001g0098 a0001c0011t0001g0149 |
2 | NA18961.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.-37-23241_-37-2323 others(14): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27374304 | ||||||
chr8:27374346 | C | T | 8 | a0001c0009t0002g0312 a0001c0009t0002g0313 a0002c0003t0002g0012 others(5): Show |
10 | NA18943.hp2 NA18949.hp2 NA18968.hp2 others(7): Show |
intron_variant | MODIFIER | c.-37-23202C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27374346 | |||||||
chr8:27374462 | G | A | 1 | a0002c0005t0001g0002 | 2 | HG00639.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.-37-23086G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27374462 | |||||||
chr8:27374501 | T | C | 142 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(139): Show |
145 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(142): Show |
intron_variant | MODIFIER | c.-37-23047T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27374501 | |||||||
chr8:27374547 | C | T | 26 | a0001c0001t0003g0022 a0001c0001t0003g0175 a0001c0001t0003g0294 others(23): Show |
28 | HG00639.hp1 HG00733.hp1 HG02109.hp2 others(25): Show |
intron_variant | MODIFIER | c.-37-23001C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27374547 | |||||||
chr8:27374548 | G | A | 2 | a0002c0004t0002g0109 a0002c0004t0002g0110 |
2 | HG03490.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.-37-23000G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27374548 | |||||||
chr8:27374673 | C | G | 1 | a0002c0006t0001g0006 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-37-22875C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27374673 | |||||||
chr8:27374707 | A | G | 1 | a0002c0004t0002g0242 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-37-22841A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27374707 | |||||||
chr8:27374777 | G | A | 8 | a0001c0001t0003g0022 a0001c0001t0003g0175 a0001c0001t0003g0294 others(5): Show |
8 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-37-22771G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27374777 | |||||||
chr8:27374808 | G | A | 1 | a0002c0004t0002g0101 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-37-22740G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27374808 | |||||||
chr8:27374894 | ATG | A | 6 | a0001c0002t0001g0295 a0001c0008t0003g0243 a0001c0008t0003g0296 others(3): Show |
6 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-37-22651_-37-2265 others(6): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27374894 | ||||||
chr8:27375430 | T | C | 8 | a0001c0001t0003g0022 a0001c0001t0003g0175 a0001c0001t0003g0294 others(5): Show |
8 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-37-22118T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27375430 | |||||||
chr8:27375492 | C | T | 3 | a0001c0008t0003g0314 a0001c0008t0003g0315 a0001c0008t0003g0316 |
3 | HG02258.hp1 HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-37-22056C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27375492 | |||||||
chr8:27375569 | A | G | 2 | a0002c0003t0002g0249 a0002c0017t0002g0252 |
2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-37-21979A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27375569 | |||||||
chr8:27375665 | G | A | 1 | a0001c0021t0004g0009 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-37-21883G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27375665 | |||||||
chr8:27375678 | G | A | 2 | a0001c0009t0002g0018 a0001c0009t0002g0087 |
2 | HG01261.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-37-21870G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27375678 | |||||||
chr8:27375726 | C | T | 2 | a0002c0004t0002g0109 a0002c0004t0002g0110 |
2 | HG03490.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.-37-21822C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27375726 | |||||||
chr8:27375815 | C | T | 8 | a0001c0009t0002g0312 a0001c0009t0002g0313 a0002c0003t0002g0012 others(5): Show |
10 | NA18943.hp2 NA18949.hp2 NA18968.hp2 others(7): Show |
intron_variant | MODIFIER | c.-37-21733C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27375815 | |||||||
chr8:27376070 | A | G | 3 | a0001c0001t0003g0095 a0001c0001t0003g0096 a0001c0001t0003g0097 |
3 | HG00323.hp2 HG01515.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.-37-21478A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27376070 | |||||||
chr8:27376179 | C | A | 8 | a0001c0001t0003g0022 a0001c0001t0003g0175 a0001c0001t0003g0294 others(5): Show |
8 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-37-21369C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27376179 | |||||||
chr8:27376216 | G | A | 6 | a0001c0002t0001g0295 a0001c0008t0003g0243 a0001c0008t0003g0296 others(3): Show |
6 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-37-21332G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27376216 | |||||||
chr8:27376316 | T | A | 1 | a0002c0003t0002g0207 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-37-21232T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27376316 | |||||||
chr8:27376387 | G | C | 4 | a0001c0002t0001g0078 a0001c0002t0001g0170 a0001c0002t0001g0171 others(1): Show |
4 | NA18945.hp1 NA18967.hp1 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37-21161G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27376387 | |||||||
chr8:27376507 | C | G | 8 | a0001c0001t0003g0022 a0001c0001t0003g0175 a0001c0001t0003g0294 others(5): Show |
8 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-37-21041C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27376507 | |||||||
chr8:27376633 | G | A | 2 | a0002c0004t0002g0244 a0002c0004t0002g0245 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-37-20915G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27376633 | |||||||
chr8:27376661 | G | A | 2 | a0001c0008t0003g0319 a0001c0008t0003g0320 |
2 | HG02723.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-37-20887G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27376661 | |||||||
chr8:27376776 | A | G | 4 | a0001c0001t0003g0063 a0001c0001t0003g0064 a0001c0001t0003g0065 others(1): Show |
4 | HG02055.hp2 HG02109.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37-20772A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27376776 | |||||||
chr8:27376849 | G | A | 2 | a0001c0007t0003g0280 a0001c0007t0003g0281 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-37-20699G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27376849 | |||||||
chr8:27376884 | C | T | 1 | a0001c0002t0001g0192 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-37-20664C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27376884 | |||||||
chr8:27376930 | C | T | 8 | a0001c0001t0003g0022 a0001c0001t0003g0175 a0001c0001t0003g0294 others(5): Show |
8 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-37-20618C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27376930 | |||||||
chr8:27376994 | C | A | 1 | a0001c0002t0001g0226 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-37-20554C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27376994 | |||||||
chr8:27377074 | G | A | 4 | a0001c0007t0003g0135 a0001c0007t0003g0136 a0001c0007t0003g0137 others(1): Show |
4 | HG00735.hp2 HG01993.hp1 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.-37-20474G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27377074 | |||||||
chr8:27377103 | C | G | 1 | a0001c0001t0003g0017 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-37-20445C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27377103 | |||||||
chr8:27377154 | C | T | 1 | a0002c0003t0002g0251 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-37-20394C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27377154 | |||||||
chr8:27377171 | C | T | 6 | a0001c0001t0003g0063 a0001c0001t0003g0064 a0001c0001t0003g0065 others(3): Show |
6 | HG02055.hp2 HG02109.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-37-20377C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27377171 | |||||||
chr8:27377215 | G | A | 1 | a0002c0006t0002g0317 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-37-20333G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27377215 | |||||||
chr8:27377314 | C | A | 3 | a0001c0002t0001g0295 a0001c0008t0003g0243 a0001c0008t0003g0296 |
3 | HG02109.hp2 HG03139.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-37-20234C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27377314 | |||||||
chr8:27377360 | G | A | 1 | a0001c0002t0001g0161 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-37-20188G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27377360 | |||||||
chr8:27377363 | A | C | 1 | a0001c0002t0001g0161 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-37-20185A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27377363 | |||||||
chr8:27377416 | G | A | 6 | a0001c0002t0001g0295 a0001c0008t0003g0243 a0001c0008t0003g0296 others(3): Show |
6 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-37-20132G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27377416 | |||||||
chr8:27377479 | T | C | 1 | a0001c0002t0001g0161 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-37-20069T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27377479 | |||||||
chr8:27377703 | C | T | 6 | a0001c0001t0003g0063 a0001c0001t0003g0064 a0001c0001t0003g0065 others(3): Show |
6 | HG02055.hp2 HG02109.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-37-19845C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27377703 | |||||||
chr8:27377794 | C | G | 1 | a0002c0004t0002g0215 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-37-19754C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27377794 | |||||||
chr8:27377934 | T | C | 1 | a0001c0002t0001g0295 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-37-19614T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27377934 | |||||||
chr8:27378011 | C | T | 2 | a0001c0001t0003g0060 a0001c0001t0005g0059 |
2 | HG01069.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.-37-19537C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27378011 | |||||||
chr8:27378274 | T | G | 1 | a0001c0001t0003g0036 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-37-19274T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27378274 | |||||||
chr8:27378301 | G | A | 72 | a0001c0001t0003g0056 a0001c0009t0002g0018 a0001c0009t0002g0087 others(69): Show |
74 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.-37-19247G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27378301 | |||||||
chr8:27378372 | G | T | 2 | a0001c0009t0002g0018 a0001c0009t0002g0087 |
2 | HG01261.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-37-19176G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27378372 | |||||||
chr8:27378480 | C | T | 1 | a0002c0006t0002g0317 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-37-19068C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27378480 | |||||||
chr8:27378601 | C | CTG | 9 | a0001c0001t0003g0294 a0001c0002t0001g0078 a0001c0002t0001g0122 others(6): Show |
9 | HG01433.hp2 HG01993.hp1 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.-37-18899_-37-1889 others(6): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27378601 | ||||||
chr8:27378601 | C | CTGTG | 5 | a0001c0002t0001g0076 a0001c0002t0001g0133 a0001c0002t0001g0147 others(2): Show |
5 | HG00099.hp1 HG00544.hp2 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.-37-18901_-37-1889 others(8): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27378601 | ||||||
chr8:27378601 | CTG | C | 29 | a0001c0001t0003g0175 a0001c0002t0001g0117 a0001c0002t0001g0118 others(26): Show |
31 | HG00323.hp1 HG00423.hp2 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.-37-18899_-37-1889 others(6): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27378601 | ||||||
chr8:27378601 | CTGTG | C | 59 | a0001c0001t0003g0056 a0001c0002t0001g0080 a0001c0002t0001g0126 others(56): Show |
59 | HG00438.hp2 HG00621.hp2 HG00733.hp2 others(56): Show |
intron_variant | MODIFIER | c.-37-18901_-37-1889 others(8): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27378601 | ||||||
chr8:27378601 | CTGTGTG | C | 29 | a0001c0002t0001g0142 a0001c0008t0003g0114 a0001c0008t0003g0315 others(26): Show |
30 | HG00673.hp2 HG00735.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.-37-18903_-37-1889 others(10): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27378601 | ||||||
chr8:27378601 | CTGTGTGT others(1): Show |
C | 16 | a0001c0001t0003g0022 a0001c0002t0001g0161 a0001c0009t0002g0237 others(13): Show |
16 | HG00423.hp1 HG00733.hp1 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.-37-18905_-37-1889 others(12): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27378601 | ||||||
chr8:27378601 | CTGTGTGT others(3): Show |
C | 2 | a0001c0001t0003g0038 a0002c0003t0002g0259 |
2 | HG03239.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.-37-18907_-37-1889 others(14): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27378601 | ||||||
chr8:27378601 | CTGTGTGT others(5): Show |
C | 18 | a0001c0001t0003g0021 a0001c0001t0003g0037 a0001c0001t0003g0042 others(15): Show |
19 | HG00099.hp2 HG00438.hp1 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.-37-18909_-37-1889 others(16): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27378601 | ||||||
chr8:27378601 | CTGTGTGT others(7): Show |
C | 28 | a0001c0001t0003g0024 a0001c0001t0003g0031 a0001c0001t0003g0035 others(25): Show |
28 | HG00323.hp2 HG00544.hp1 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.-37-18911_-37-1889 others(18): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27378601 | ||||||
chr8:27378601 | CTGTGTGT others(9): Show |
C | 53 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(50): Show |
54 | HG00408.hp1 HG00408.hp2 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.-37-18913_-37-1889 others(20): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27378601 | ||||||
chr8:27378601 | CTGTGTGT others(11): Show |
C | 1 | a0001c0010t0003g0232 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-37-18915_-37-1889 others(22): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27378601 | ||||||
chr8:27378601 | CTGTGTGT others(13): Show |
C | 12 | a0001c0001t0003g0227 a0001c0001t0003g0228 a0001c0001t0003g0288 others(9): Show |
12 | HG02486.hp1 HG02559.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.-37-18917_-37-1889 others(24): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27378601 | ||||||
chr8:27378601 | CTGTGTGT others(19): Show |
C | 7 | a0001c0001t0003g0181 a0001c0001t0003g0182 a0001c0001t0003g0183 others(4): Show |
7 | HG02055.hp1 HG02257.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.-37-18923_-37-1889 others(30): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27378601 | ||||||
chr8:27378602 | T | C | 2 | a0001c0008t0003g0314 a0002c0006t0001g0006 |
2 | HG02486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-37-18946T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27378602 | |||||||
chr8:27378604 | T | C | 6 | a0001c0009t0002g0107 a0002c0003t0002g0249 a0002c0004t0002g0094 others(3): Show |
6 | HG00423.hp2 HG00741.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-37-18944T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27378604 | |||||||
chr8:27378606 | T | C | 47 | a0001c0001t0003g0056 a0001c0002t0001g0295 a0001c0008t0003g0243 others(44): Show |
47 | HG00438.hp2 HG00621.hp2 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.-37-18942T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27378606 | |||||||
chr8:27378608 | T | C | 27 | a0001c0008t0003g0114 a0001c0008t0003g0315 a0001c0008t0003g0316 others(24): Show |
28 | HG00673.hp2 HG00735.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.-37-18940T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27378608 | |||||||
chr8:27378610 | T | C | 12 | a0001c0009t0002g0237 a0001c0012t0004g0027 a0002c0003t0002g0223 others(9): Show |
12 | HG00423.hp1 HG01175.hp1 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.-37-18938T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27378610 | |||||||
chr8:27378612 | T | C | 1 | a0002c0003t0002g0259 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-37-18936T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27378612 | |||||||
chr8:27378614 | T | C | 7 | a0002c0003t0002g0003 a0002c0003t0002g0260 a0002c0003t0002g0262 others(4): Show |
8 | HG00099.hp2 HG00741.hp1 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.-37-18934T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27378614 | |||||||
chr8:27378616 | T | C | 1 | a0002c0003t0002g0270 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-37-18932T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27378616 | |||||||
chr8:27378618 | T | C | 1 | a0002c0003t0002g0239 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-37-18930T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27378618 | |||||||
chr8:27378702 | G | A | 4 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-37-18846G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27378702 | |||||||
chr8:27378711 | G | A | 1 | a0001c0002t0001g0130 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-37-18837G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27378711 | |||||||
chr8:27379188 | T | C | 1 | a0002c0004t0002g0209 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-37-18360T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27379188 | |||||||
chr8:27379380 | C | A | 8 | a0001c0009t0002g0312 a0001c0009t0002g0313 a0002c0003t0002g0012 others(5): Show |
10 | NA18943.hp2 NA18949.hp2 NA18968.hp2 others(7): Show |
intron_variant | MODIFIER | c.-37-18168C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27379380 | |||||||
chr8:27379519 | C | T | 3 | a0002c0006t0001g0234 a0002c0006t0001g0290 a0002c0006t0001g0291 |
3 | HG02630.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-37-18029C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27379519 | |||||||
chr8:27379524 | A | G | 314 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(311): Show |
319 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(316): Show |
intron_variant | MODIFIER | c.-37-18024A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27379524 | |||||||
chr8:27379689 | A | G | 93 | a0001c0001t0003g0056 a0001c0009t0002g0018 a0001c0009t0002g0087 others(90): Show |
95 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.-37-17859A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27379689 | |||||||
chr8:27379690 | T | C | 244 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(241): Show |
249 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(246): Show |
intron_variant | MODIFIER | c.-37-17858T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27379690 | |||||||
chr8:27379691 | G | A | 1 | a0011c0019t0002g0102 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-37-17857G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27379691 | |||||||
chr8:27379741 | A | G | 3 | a0001c0008t0003g0314 a0001c0008t0003g0315 a0001c0008t0003g0316 |
3 | HG02258.hp1 HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-37-17807A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27379741 | |||||||
chr8:27380141 | G | A | 1 | a0001c0002t0001g0235 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-37-17407G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27380141 | |||||||
chr8:27380191 | G | A | 96 | a0001c0001t0003g0056 a0001c0008t0003g0314 a0001c0008t0003g0315 others(93): Show |
98 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.-37-17357G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27380191 | |||||||
chr8:27380535 | AT | A | 114 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(111): Show |
115 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.-37-17003delT | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27380535 | ||||||
chr8:27380598 | G | C | 93 | a0001c0001t0003g0056 a0001c0009t0002g0018 a0001c0009t0002g0087 others(90): Show |
95 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.-37-16950G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27380598 | |||||||
chr8:27380768 | C | T | 1 | a0002c0006t0001g0213 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-37-16780C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27380768 | |||||||
chr8:27380771 | A | G | 5 | a0001c0002t0001g0295 a0001c0008t0003g0243 a0001c0008t0003g0296 others(2): Show |
5 | HG02109.hp2 HG03139.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-37-16777A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27380771 | |||||||
chr8:27381124 | C | A | 3 | a0001c0001t0003g0088 a0001c0001t0003g0113 a0001c0001t0003g0115 |
3 | HG02572.hp1 HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-37-16424C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27381124 | |||||||
chr8:27381243 | A | C | 3 | a0001c0001t0003g0088 a0001c0001t0003g0113 a0001c0001t0003g0115 |
3 | HG02572.hp1 HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-37-16305A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27381243 | |||||||
chr8:27381253 | C | G | 1 | a0001c0002t0001g0235 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-37-16295C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27381253 | |||||||
chr8:27381309 | A | G | 93 | a0001c0001t0003g0056 a0001c0009t0002g0018 a0001c0009t0002g0087 others(90): Show |
95 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.-37-16239A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27381309 | |||||||
chr8:27381335 | A | G | 3 | a0001c0008t0003g0314 a0001c0008t0003g0315 a0001c0008t0003g0316 |
3 | HG02258.hp1 HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-37-16213A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27381335 | |||||||
chr8:27381383 | C | T | 8 | a0001c0001t0003g0022 a0001c0001t0003g0175 a0001c0001t0003g0294 others(5): Show |
8 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-37-16165C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27381383 | |||||||
chr8:27381384 | T | C | 2 | a0002c0003t0002g0239 a0002c0003t0002g0241 |
2 | HG00408.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.-37-16164T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27381384 | |||||||
chr8:27381741 | C | T | 113 | a0001c0001t0003g0056 a0001c0002t0001g0295 a0001c0008t0003g0114 others(110): Show |
117 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.-37-15807C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27381741 | |||||||
chr8:27381777 | A | G | 4 | a0001c0008t0003g0114 a0001c0030t0002g0007 a0002c0006t0001g0010 others(1): Show |
4 | HG00738.hp1 HG02615.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37-15771A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27381777 | |||||||
chr8:27381902 | T | C | 1 | a0002c0003t0002g0207 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-37-15646T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27381902 | |||||||
chr8:27381930 | T | G | 1 | a0002c0006t0001g0006 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-37-15618T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27381930 | |||||||
chr8:27382015 | T | A | 1 | a0002c0006t0001g0127 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-37-15533T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27382015 | |||||||
chr8:27382105 | G | C | 2 | a0002c0004t0002g0109 a0002c0004t0002g0110 |
2 | HG03490.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.-37-15443G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27382105 | |||||||
chr8:27382412 | T | A | 2 | a0001c0021t0004g0009 a0001c0022t0002g0008 |
2 | NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-37-15136T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27382412 | |||||||
chr8:27382556 | GT | G | 8 | a0001c0001t0003g0022 a0001c0001t0003g0175 a0001c0001t0003g0294 others(5): Show |
8 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-37-14981delT | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27382556 | ||||||
chr8:27382582 | A | G | 2 | a0001c0021t0004g0009 a0001c0022t0002g0008 |
2 | NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-37-14966A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27382582 | |||||||
chr8:27382582 | A | T | 1 | a0002c0006t0001g0006 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-37-14966A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27382582 | |||||||
chr8:27382649 | G | A | 3 | a0001c0001t0003g0081 a0001c0001t0003g0082 a0001c0001t0003g0205 |
3 | HG00738.hp2 HG01346.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.-37-14899G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27382649 | |||||||
chr8:27382728 | T | C | 1 | a0001c0022t0002g0008 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-37-14820T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27382728 | |||||||
chr8:27383022 | T | C | 1 | a0010c0033t0001g0154 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-37-14526T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27383022 | |||||||
chr8:27383038 | A | C | 113 | a0001c0001t0003g0056 a0001c0002t0001g0295 a0001c0008t0003g0114 others(110): Show |
117 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.-37-14510A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27383038 | |||||||
chr8:27383104 | GTC | G | 3 | a0001c0008t0003g0292 a0001c0008t0003g0319 a0001c0008t0003g0320 |
3 | HG02723.hp2 HG02896.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-37-14442_-37-1444 others(6): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27383104 | ||||||
chr8:27383181 | A | G | 105 | a0001c0001t0003g0056 a0001c0008t0003g0114 a0001c0009t0002g0018 others(102): Show |
109 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.-37-14367A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27383181 | |||||||
chr8:27383240 | C | A | 4 | a0001c0001t0003g0276 a0001c0007t0003g0279 a0001c0007t0003g0280 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37-14308C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27383240 | |||||||
chr8:27383365 | C | T | 1 | a0002c0006t0002g0317 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-37-14183C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27383365 | |||||||
chr8:27383373 | G | A | 2 | a0001c0002t0001g0171 a0001c0002t0001g0172 |
2 | NA18981.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.-37-14175G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27383373 | |||||||
chr8:27383551 | G | A | 3 | a0001c0001t0003g0036 a0001c0002t0001g0134 a0002c0006t0001g0323 |
3 | HG01433.hp2 HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-37-13997G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27383551 | |||||||
chr8:27383565 | G | A | 111 | a0001c0002t0001g0295 a0001c0008t0003g0114 a0001c0008t0003g0243 others(108): Show |
115 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.-37-13983G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27383565 | |||||||
chr8:27383573 | C | T | 1 | a0002c0006t0001g0006 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-37-13975C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27383573 | |||||||
chr8:27383836 | C | T | 243 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(240): Show |
248 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.-37-13712C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27383836 | |||||||
chr8:27383852 | A | ATTTTTTT others(6): Show |
3 | a0001c0008t0003g0114 a0001c0030t0002g0007 a0002c0006t0001g0010 |
3 | HG00738.hp1 HG02615.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-37-13695_-37-1368 others(17): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27383852 | ||||||
chr8:27383852 | A | ATTTTTTT others(7): Show |
7 | a0001c0002t0001g0295 a0001c0008t0003g0243 a0001c0008t0003g0296 others(4): Show |
7 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.-37-13683_-37-1368 others(18): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27383852 | ||||||
chr8:27383852 | A | ATTTTTTT others(8): Show |
6 | a0001c0012t0004g0053 a0001c0021t0004g0009 a0002c0003t0002g0216 others(3): Show |
6 | HG01081.hp1 HG01168.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.-37-13683_-37-1368 others(19): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27383852 | ||||||
chr8:27383852 | A | ATTTTTTT others(9): Show |
78 | a0001c0009t0002g0018 a0001c0009t0002g0087 a0001c0009t0002g0103 others(75): Show |
82 | HG00099.hp2 HG00423.hp1 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.-37-13683_-37-1368 others(20): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27383852 | ||||||
chr8:27383852 | A | ATTTTTTT others(10): Show |
19 | a0001c0009t0002g0107 a0001c0009t0002g0313 a0001c0012t0004g0055 others(16): Show |
19 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(16): Show |
intron_variant | MODIFIER | c.-37-13683_-37-1368 others(21): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27383852 | ||||||
chr8:27383951 | C | T | 4 | a0002c0006t0001g0006 a0002c0006t0001g0234 a0002c0006t0001g0290 others(1): Show |
4 | HG02630.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-37-13597C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27383951 | |||||||
chr8:27383961 | G | A | 6 | a0001c0002t0001g0295 a0001c0008t0003g0243 a0001c0008t0003g0296 others(3): Show |
6 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-37-13587G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27383961 | |||||||
chr8:27383993 | C | T | 2 | a0002c0003t0002g0249 a0002c0017t0002g0252 |
2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-37-13555C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27383993 | |||||||
chr8:27384000 | C | T | 1 | a0001c0001t0003g0074 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-37-13548C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27384000 | |||||||
chr8:27384069 | C | T | 2 | a0001c0030t0002g0007 a0002c0006t0002g0317 |
2 | HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-37-13479C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27384069 | |||||||
chr8:27384177 | T | C | 9 | a0001c0009t0002g0125 a0001c0009t0002g0312 a0001c0009t0002g0313 others(6): Show |
11 | HG00609.hp2 NA18943.hp2 NA18949.hp2 others(8): Show |
intron_variant | MODIFIER | c.-37-13371T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27384177 | |||||||
chr8:27384226 | A | G | 2 | a0002c0003t0002g0249 a0002c0017t0002g0252 |
2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-37-13322A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27384226 | |||||||
chr8:27384315 | A | C | 111 | a0001c0002t0001g0295 a0001c0008t0003g0243 a0001c0008t0003g0296 others(108): Show |
115 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.-37-13233A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27384315 | |||||||
chr8:27384339 | T | C | 9 | a0001c0009t0002g0125 a0001c0009t0002g0312 a0001c0009t0002g0313 others(6): Show |
11 | HG00609.hp2 NA18943.hp2 NA18949.hp2 others(8): Show |
intron_variant | MODIFIER | c.-37-13209T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27384339 | |||||||
chr8:27384388 | AAATTTGT others(5): Show |
A | 1 | a0002c0004t0002g0151 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-37-13157_-37-1314 others(16): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27384388 | ||||||
chr8:27384589 | A | G | 4 | a0001c0001t0003g0088 a0001c0001t0003g0113 a0001c0001t0003g0115 others(1): Show |
4 | HG02572.hp1 HG02818.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-37-12959A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27384589 | |||||||
chr8:27384660 | A | G | 1 | a0001c0011t0001g0149 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-37-12888A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27384660 | |||||||
chr8:27384746 | G | A | 4 | a0001c0001t0003g0088 a0001c0001t0003g0113 a0001c0001t0003g0115 others(1): Show |
4 | HG02572.hp1 HG02818.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-37-12802G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27384746 | |||||||
chr8:27384761 | G | A | 1 | a0002c0006t0001g0092 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-37-12787G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27384761 | |||||||
chr8:27385076 | G | C | 18 | a0001c0002t0001g0005 a0001c0002t0001g0077 a0001c0002t0001g0119 others(15): Show |
18 | HG01496.hp1 HG01943.hp1 HG02071.hp2 others(15): Show |
intron_variant | MODIFIER | c.-37-12472G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27385076 | |||||||
chr8:27385088 | G | A | 1 | a0002c0004t0002g0105 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-37-12460G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27385088 | |||||||
chr8:27385105 | T | A | 113 | a0001c0002t0001g0295 a0001c0008t0003g0114 a0001c0008t0003g0243 others(110): Show |
117 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.-37-12443T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27385105 | |||||||
chr8:27385136 | T | G | 2 | a0001c0001t0003g0028 a0001c0001t0003g0034 |
2 | HG01934.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.-37-12412T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27385136 | |||||||
chr8:27385363 | A | G | 1 | a0002c0003t0002g0299 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-37-12185A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27385363 | |||||||
chr8:27385391 | G | C | 1 | a0002c0005t0001g0204 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-37-12157G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27385391 | |||||||
chr8:27385452 | A | G | 1 | a0001c0001t0003g0185 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-37-12096A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27385452 | |||||||
chr8:27385482 | T | C | 1 | a0001c0009t0002g0312 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.-37-12066T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27385482 | |||||||
chr8:27385533 | C | G | 2 | a0001c0008t0003g0114 a0002c0006t0001g0010 |
2 | HG00738.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-37-12015C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27385533 | |||||||
chr8:27385557 | C | T | 30 | a0001c0001t0003g0021 a0001c0001t0003g0035 a0001c0001t0003g0037 others(27): Show |
30 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(27): Show |
intron_variant | MODIFIER | c.-37-11991C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27385557 | |||||||
chr8:27385578 | A | G | 1 | a0001c0002t0001g0235 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-37-11970A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27385578 | |||||||
chr8:27385579 | T | C | 1 | a0002c0006t0001g0020 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-37-11969T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27385579 | |||||||
chr8:27385621 | G | T | 6 | a0001c0001t0003g0276 a0001c0007t0003g0277 a0001c0007t0003g0278 others(3): Show |
6 | HG01070.hp2 HG01071.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-37-11927G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27385621 | |||||||
chr8:27385669 | G | A | 1 | a0001c0030t0002g0007 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-37-11879G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27385669 | |||||||
chr8:27385730 | TAA | T | 6 | a0001c0001t0003g0276 a0001c0007t0003g0277 a0001c0007t0003g0278 others(3): Show |
6 | HG01070.hp2 HG01071.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-37-11814_-37-1181 others(6): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27385730 | ||||||
chr8:27385892 | C | CA | 214 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(211): Show |
219 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.-37-11637dupA | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27385892 | ||||||
chr8:27385892 | CA | C | 8 | a0001c0011t0001g0079 a0001c0011t0001g0098 a0001c0011t0001g0140 others(5): Show |
8 | HG01192.hp1 HG01361.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.-37-11637delA | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27385892 | ||||||
chr8:27385918 | A | G | 2 | a0001c0021t0004g0009 a0001c0022t0002g0008 |
2 | NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-37-11630A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27385918 | |||||||
chr8:27385919 | T | C | 1 | a0001c0007t0003g0135 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-37-11629T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27385919 | |||||||
chr8:27385920 | C | T | 1 | a0001c0007t0003g0135 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-37-11628C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27385920 | |||||||
chr8:27386078 | G | A | 6 | a0001c0001t0003g0276 a0001c0007t0003g0277 a0001c0007t0003g0278 others(3): Show |
6 | HG01070.hp2 HG01071.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-37-11470G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27386078 | |||||||
chr8:27386085 | T | C | 6 | a0001c0002t0001g0295 a0001c0008t0003g0243 a0001c0008t0003g0296 others(3): Show |
6 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-37-11463T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27386085 | |||||||
chr8:27386199 | C | T | 107 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(104): Show |
108 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.-37-11349C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27386199 | |||||||
chr8:27386419 | A | C | 3 | a0002c0003t0002g0236 a0002c0003t0002g0255 a0002c0003t0002g0321 |
3 | HG02258.hp2 HG02809.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-37-11129A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27386419 | |||||||
chr8:27386440 | G | C | 1 | a0002c0003t0002g0283 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-37-11108G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27386440 | |||||||
chr8:27386565 | C | G | 1 | a0002c0023t0001g0123 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-37-10983C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27386565 | |||||||
chr8:27386783 | A | G | 113 | a0001c0002t0001g0295 a0001c0008t0003g0114 a0001c0008t0003g0243 others(110): Show |
117 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.-37-10765A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27386783 | |||||||
chr8:27386795 | G | A | 1 | a0002c0006t0001g0066 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-37-10753G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27386795 | |||||||
chr8:27386879 | GT | G | 6 | a0001c0007t0003g0277 a0001c0007t0003g0278 a0001c0021t0004g0009 others(3): Show |
6 | HG01070.hp2 HG01071.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-37-10656delT | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27386879 | ||||||
chr8:27386956 | A | G | 1 | a0001c0002t0001g0174 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-37-10592A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27386956 | |||||||
chr8:27387117 | C | T | 5 | a0002c0006t0001g0006 a0002c0006t0001g0234 a0002c0006t0001g0282 others(2): Show |
5 | HG02630.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-37-10431C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27387117 | |||||||
chr8:27387156 | C | T | 1 | a0002c0006t0001g0286 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-37-10392C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27387156 | |||||||
chr8:27387205 | A | G | 113 | a0001c0002t0001g0295 a0001c0008t0003g0114 a0001c0008t0003g0243 others(110): Show |
117 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.-37-10343A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27387205 | |||||||
chr8:27387273 | C | T | 3 | a0001c0002t0001g0178 a0001c0007t0003g0179 a0006c0028t0001g0177 |
3 | HG02647.hp2 HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-37-10275C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27387273 | |||||||
chr8:27387402 | C | T | 101 | a0001c0009t0002g0018 a0001c0009t0002g0087 a0001c0009t0002g0103 others(98): Show |
105 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.-37-10146C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27387402 | |||||||
chr8:27387458 | G | A | 4 | a0001c0001t0003g0276 a0001c0007t0003g0279 a0001c0007t0003g0280 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37-10090G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27387458 | |||||||
chr8:27387566 | C | T | 2 | a0001c0030t0002g0007 a0002c0006t0002g0317 |
2 | HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-37-9982C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27387566 | |||||||
chr8:27387739 | A | T | 2 | a0001c0021t0004g0009 a0001c0022t0002g0008 |
2 | NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-37-9809A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27387739 | |||||||
chr8:27387817 | CT | C | 123 | a0001c0002t0001g0146 a0001c0002t0001g0158 a0001c0002t0001g0171 others(120): Show |
127 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.-37-9716delT | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27387817 | ||||||
chr8:27387901 | T | C | 1 | a0002c0006t0001g0092 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-37-9647T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27387901 | |||||||
chr8:27388029 | C | T | 1 | a0001c0010t0003g0232 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-37-9519C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27388029 | |||||||
chr8:27388204 | A | C | 92 | a0001c0009t0002g0018 a0001c0009t0002g0087 a0001c0009t0002g0103 others(89): Show |
94 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.-37-9344A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27388204 | |||||||
chr8:27388263 | A | G | 1 | a0002c0006t0001g0286 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-37-9285A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27388263 | |||||||
chr8:27388273 | C | T | 92 | a0001c0009t0002g0018 a0001c0009t0002g0087 a0001c0009t0002g0103 others(89): Show |
94 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.-37-9275C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27388273 | |||||||
chr8:27388300 | A | G | 6 | a0001c0002t0001g0173 a0001c0002t0001g0174 a0001c0002t0001g0176 others(3): Show |
6 | HG01884.hp2 HG02647.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-37-9248A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27388300 | |||||||
chr8:27388625 | A | G | 1 | a0001c0008t0003g0114 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-37-8923A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27388625 | |||||||
chr8:27388788 | C | G | 4 | a0001c0007t0003g0135 a0001c0007t0003g0136 a0001c0007t0003g0137 others(1): Show |
4 | HG00735.hp2 HG01993.hp1 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.-37-8760C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27388788 | |||||||
chr8:27388820 | T | C | 235 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(232): Show |
240 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.-37-8728T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27388820 | |||||||
chr8:27388916 | A | G | 8 | a0001c0002t0001g0295 a0001c0008t0003g0243 a0001c0008t0003g0296 others(5): Show |
8 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-37-8632A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27388916 | |||||||
chr8:27389028 | A | T | 1 | a0001c0001t0003g0022 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-37-8520A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27389028 | |||||||
chr8:27389099 | G | A | 6 | a0001c0002t0001g0295 a0001c0008t0003g0243 a0001c0008t0003g0296 others(3): Show |
6 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-37-8449G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27389099 | |||||||
chr8:27389123 | G | A | 1 | a0002c0003t0002g0069 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-37-8425G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27389123 | |||||||
chr8:27389149 | C | CTT | 5 | a0002c0006t0001g0006 a0002c0006t0001g0234 a0002c0006t0001g0282 others(2): Show |
5 | HG02630.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-37-8395_-37-8394d others(4): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27389149 | ||||||
chr8:27389177 | G | C | 3 | a0001c0001t0003g0088 a0001c0001t0003g0113 a0001c0001t0003g0115 |
3 | HG02572.hp1 HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-37-8371G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27389177 | |||||||
chr8:27389179 | G | A | 1 | a0001c0010t0003g0289 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-37-8369G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27389179 | |||||||
chr8:27389232 | C | T | 1 | a0001c0001t0003g0071 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-37-8316C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27389232 | |||||||
chr8:27389261 | G | A | 4 | a0001c0001t0003g0025 a0001c0001t0003g0029 a0001c0001t0003g0030 others(1): Show |
4 | HG01109.hp2 HG01255.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37-8287G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27389261 | |||||||
chr8:27389311 | AGGAAGAC others(5): Show |
A | 1 | a0002c0004t0002g0112 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-37-8225_-37-8214d others(14): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27389311 | ||||||
chr8:27389313 | G | A | 2 | a0001c0030t0002g0007 a0002c0006t0002g0317 |
2 | HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-37-8235G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27389313 | |||||||
chr8:27389331 | A | C | 106 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(103): Show |
107 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.-37-8217A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27389331 | |||||||
chr8:27389492 | G | T | 1 | a0002c0003t0002g0256 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-37-8056G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27389492 | |||||||
chr8:27389547 | C | T | 20 | a0001c0001t0003g0181 a0001c0001t0003g0182 a0001c0001t0003g0183 others(17): Show |
20 | HG02055.hp1 HG02257.hp1 HG02486.hp1 others(17): Show |
intron_variant | MODIFIER | c.-37-8001C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27389547 | |||||||
chr8:27389559 | C | G | 1 | a0002c0004t0002g0208 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-37-7989C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27389559 | |||||||
chr8:27389613 | G | A | 1 | a0002c0004t0002g0250 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-37-7935G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27389613 | |||||||
chr8:27389781 | T | C | 6 | a0001c0001t0003g0276 a0001c0007t0003g0277 a0001c0007t0003g0278 others(3): Show |
6 | HG01070.hp2 HG01071.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-37-7767T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27389781 | |||||||
chr8:27389822 | G | A | 92 | a0001c0009t0002g0018 a0001c0009t0002g0087 a0001c0009t0002g0103 others(89): Show |
94 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.-37-7726G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27389822 | |||||||
chr8:27390069 | T | C | 6 | a0001c0002t0001g0295 a0001c0008t0003g0243 a0001c0008t0003g0296 others(3): Show |
6 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-37-7479T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27390069 | |||||||
chr8:27390130 | T | C | 113 | a0001c0002t0001g0295 a0001c0008t0003g0114 a0001c0008t0003g0243 others(110): Show |
117 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.-37-7418T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27390130 | |||||||
chr8:27390138 | C | T | 1 | a0002c0006t0002g0317 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-37-7410C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27390138 | |||||||
chr8:27390145 | G | C | 92 | a0001c0009t0002g0018 a0001c0009t0002g0087 a0001c0009t0002g0103 others(89): Show |
94 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.-37-7403G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27390145 | |||||||
chr8:27390168 | G | T | 1 | a0002c0004t0002g0099 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-37-7380G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27390168 | |||||||
chr8:27390263 | C | T | 2 | a0001c0021t0004g0009 a0001c0022t0002g0008 |
2 | NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-37-7285C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27390263 | |||||||
chr8:27390265 | C | T | 9 | a0001c0009t0002g0125 a0001c0009t0002g0312 a0001c0009t0002g0313 others(6): Show |
11 | HG00609.hp2 NA18943.hp2 NA18949.hp2 others(8): Show |
intron_variant | MODIFIER | c.-37-7283C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27390265 | |||||||
chr8:27390303 | G | T | 106 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(103): Show |
107 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.-37-7245G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27390303 | |||||||
chr8:27390343 | C | A | 12 | a0001c0002t0001g0295 a0001c0008t0003g0114 a0001c0008t0003g0243 others(9): Show |
12 | HG00738.hp1 HG02109.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.-37-7205C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27390343 | |||||||
chr8:27390438 | C | G | 1 | a0002c0006t0002g0317 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-37-7110C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27390438 | |||||||
chr8:27390502 | A | T | 92 | a0001c0009t0002g0018 a0001c0009t0002g0087 a0001c0009t0002g0103 others(89): Show |
94 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.-37-7046A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27390502 | |||||||
chr8:27390510 | A | C | 2 | a0001c0030t0002g0007 a0002c0006t0002g0317 |
2 | HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-37-7038A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27390510 | |||||||
chr8:27390515 | C | A | 1 | a0002c0004t0002g0151 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-37-7033C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27390515 | |||||||
chr8:27390647 | T | A | 113 | a0001c0002t0001g0295 a0001c0008t0003g0114 a0001c0008t0003g0243 others(110): Show |
117 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.-37-6901T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27390647 | |||||||
chr8:27390743 | T | C | 2 | a0001c0021t0004g0009 a0001c0022t0002g0008 |
2 | NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-37-6805T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27390743 | |||||||
chr8:27390879 | ACAACGGG others(7): Show |
A | 3 | a0001c0001t0003g0088 a0001c0001t0003g0113 a0001c0001t0003g0115 |
3 | HG02572.hp1 HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-37-6666_-37-6653d others(16): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27390879 | ||||||
chr8:27390918 | T | C | 244 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(241): Show |
249 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(246): Show |
intron_variant | MODIFIER | c.-37-6630T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27390918 | |||||||
chr8:27391044 | G | T | 243 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(240): Show |
248 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.-37-6504G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27391044 | |||||||
chr8:27391056 | T | A | 107 | a0001c0008t0003g0114 a0001c0009t0002g0018 a0001c0009t0002g0087 others(104): Show |
111 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.-37-6492T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27391056 | |||||||
chr8:27391080 | C | CT | 19 | a0001c0002t0001g0080 a0001c0002t0001g0117 a0001c0002t0001g0118 others(16): Show |
19 | HG00544.hp2 HG01928.hp2 HG02015.hp2 others(16): Show |
intron_variant | MODIFIER | c.-37-6454dupT | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27391080 | ||||||
chr8:27391080 | CT | C | 240 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(237): Show |
245 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(242): Show |
intron_variant | MODIFIER | c.-37-6454delT | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27391080 | ||||||
chr8:27391124 | A | G | 4 | a0001c0008t0003g0114 a0001c0030t0002g0007 a0002c0006t0001g0010 others(1): Show |
4 | HG00738.hp1 HG02615.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37-6424A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27391124 | |||||||
chr8:27391138 | TGGTGCAA others(9): Show |
T | 5 | a0002c0006t0001g0006 a0002c0006t0001g0234 a0002c0006t0001g0282 others(2): Show |
5 | HG02630.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-37-6393_-37-6378d others(18): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27391138 | ||||||
chr8:27391150 | G | A | 101 | a0001c0009t0002g0018 a0001c0009t0002g0087 a0001c0009t0002g0103 others(98): Show |
105 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.-37-6398G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27391150 | |||||||
chr8:27391154 | C | T | 23 | a0001c0001t0003g0181 a0001c0001t0003g0182 a0001c0001t0003g0183 others(20): Show |
23 | HG02055.hp1 HG02257.hp1 HG02486.hp1 others(20): Show |
intron_variant | MODIFIER | c.-37-6394C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27391154 | |||||||
chr8:27391189 | C | T | 2 | a0001c0021t0004g0009 a0001c0022t0002g0008 |
2 | NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-37-6359C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27391189 | |||||||
chr8:27391221 | C | T | 2 | a0001c0021t0004g0009 a0001c0022t0002g0008 |
2 | NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-37-6327C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27391221 | |||||||
chr8:27391245 | T | C | 111 | a0001c0002t0001g0295 a0001c0008t0003g0114 a0001c0008t0003g0243 others(108): Show |
115 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.-37-6303T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27391245 | |||||||
chr8:27391292 | T | C | 20 | a0001c0001t0003g0181 a0001c0001t0003g0182 a0001c0001t0003g0183 others(17): Show |
20 | HG02055.hp1 HG02257.hp1 HG02486.hp1 others(17): Show |
intron_variant | MODIFIER | c.-37-6256T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27391292 | |||||||
chr8:27391377 | G | A | 1 | a0001c0001t0003g0051 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-37-6171G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27391377 | |||||||
chr8:27391468 | G | C | 11 | a0001c0001t0003g0024 a0001c0001t0003g0025 a0001c0001t0003g0028 others(8): Show |
11 | HG01074.hp1 HG01109.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.-37-6080G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27391468 | |||||||
chr8:27391560 | T | C | 6 | a0001c0001t0003g0276 a0001c0007t0003g0277 a0001c0007t0003g0278 others(3): Show |
6 | HG01070.hp2 HG01071.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-37-5988T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27391560 | |||||||
chr8:27391605 | G | C | 9 | a0001c0009t0002g0125 a0001c0009t0002g0312 a0001c0009t0002g0313 others(6): Show |
11 | HG00609.hp2 NA18943.hp2 NA18949.hp2 others(8): Show |
intron_variant | MODIFIER | c.-37-5943G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27391605 | |||||||
chr8:27391811 | G | C | 105 | a0001c0009t0002g0018 a0001c0009t0002g0087 a0001c0009t0002g0103 others(102): Show |
109 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.-37-5737G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27391811 | |||||||
chr8:27391941 | A | G | 235 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(232): Show |
240 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.-37-5607A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27391941 | |||||||
chr8:27392009 | C | T | 1 | a0002c0006t0001g0287 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-37-5539C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27392009 | |||||||
chr8:27392119 | G | A | 2 | a0001c0021t0004g0009 a0001c0022t0002g0008 |
2 | NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-37-5429G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27392119 | |||||||
chr8:27392310 | C | CT | 37 | a0001c0001t0003g0039 a0001c0001t0003g0056 a0001c0001t0003g0081 others(34): Show |
39 | HG00408.hp1 HG00408.hp2 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.-37-5222dupT | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27392310 | ||||||
chr8:27392310 | CT | C | 11 | a0001c0002t0001g0080 a0001c0002t0001g0295 a0001c0008t0003g0243 others(8): Show |
11 | HG01070.hp1 HG01099.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.-37-5222delT | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27392310 | ||||||
chr8:27392312 | T | G | 1 | a0001c0002t0001g0206 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-37-5236T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27392312 | |||||||
chr8:27392472 | T | C | 4 | a0001c0008t0003g0114 a0001c0030t0002g0007 a0002c0006t0001g0010 others(1): Show |
4 | HG00738.hp1 HG02615.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37-5076T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27392472 | |||||||
chr8:27392592 | G | C | 4 | a0001c0008t0003g0114 a0001c0030t0002g0007 a0002c0006t0001g0010 others(1): Show |
4 | HG00738.hp1 HG02615.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37-4956G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27392592 | |||||||
chr8:27392889 | C | T | 4 | a0001c0001t0003g0088 a0001c0001t0003g0113 a0001c0001t0003g0115 others(1): Show |
4 | HG02572.hp1 HG02818.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-37-4659C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27392889 | |||||||
chr8:27393023 | C | T | 7 | a0001c0001t0003g0022 a0001c0001t0003g0175 a0001c0001t0003g0294 others(4): Show |
7 | HG00639.hp1 HG00733.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.-37-4525C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27393023 | |||||||
chr8:27393024 | G | A | 4 | a0001c0008t0003g0114 a0001c0030t0002g0007 a0002c0006t0001g0010 others(1): Show |
4 | HG00738.hp1 HG02615.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37-4524G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27393024 | |||||||
chr8:27393188 | C | T | 1 | a0001c0002t0001g0226 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-37-4360C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27393188 | |||||||
chr8:27393304 | T | C | 113 | a0001c0002t0001g0295 a0001c0008t0003g0114 a0001c0008t0003g0243 others(110): Show |
117 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.-37-4244T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27393304 | |||||||
chr8:27393314 | G | A | 1 | a0002c0017t0002g0252 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-37-4234G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27393314 | |||||||
chr8:27393338 | G | C | 7 | a0001c0002t0001g0173 a0001c0002t0001g0174 a0001c0002t0001g0176 others(4): Show |
7 | HG01884.hp2 HG02647.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.-37-4210G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27393338 | |||||||
chr8:27393416 | G | A | 103 | a0001c0009t0002g0018 a0001c0009t0002g0087 a0001c0009t0002g0103 others(100): Show |
107 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.-37-4132G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27393416 | |||||||
chr8:27393534 | T | C | 92 | a0001c0009t0002g0018 a0001c0009t0002g0087 a0001c0009t0002g0103 others(89): Show |
94 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.-37-4014T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27393534 | |||||||
chr8:27393545 | A | G | 2 | a0002c0003t0002g0266 a0002c0003t0002g0269 |
2 | HG02559.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-37-4003A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27393545 | |||||||
chr8:27393728 | G | C | 4 | a0001c0008t0003g0114 a0001c0030t0002g0007 a0002c0006t0001g0010 others(1): Show |
4 | HG00738.hp1 HG02615.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37-3820G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27393728 | |||||||
chr8:27393808 | A | G | 115 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(112): Show |
116 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.-37-3740A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27393808 | |||||||
chr8:27394029 | G | C | 105 | a0001c0009t0002g0018 a0001c0009t0002g0087 a0001c0009t0002g0103 others(102): Show |
109 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.-37-3519G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27394029 | |||||||
chr8:27394112 | G | A | 3 | a0001c0001t0003g0088 a0001c0001t0003g0113 a0001c0001t0003g0115 |
3 | HG02572.hp1 HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-37-3436G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27394112 | |||||||
chr8:27394208 | G | A | 2 | a0001c0021t0004g0009 a0001c0022t0002g0008 |
2 | NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-37-3340G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27394208 | |||||||
chr8:27394259 | T | C | 1 | a0001c0002t0001g0131 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-37-3289T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27394259 | |||||||
chr8:27394340 | A | G | 7 | a0001c0002t0001g0173 a0001c0002t0001g0174 a0001c0002t0001g0176 others(4): Show |
7 | HG01884.hp2 HG02647.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.-37-3208A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27394340 | |||||||
chr8:27394352 | A | G | 9 | a0001c0002t0001g0143 a0001c0002t0001g0155 a0001c0002t0001g0158 others(6): Show |
9 | HG00544.hp2 HG02015.hp2 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.-37-3196A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27394352 | |||||||
chr8:27394516 | G | A | 8 | a0001c0002t0001g0295 a0001c0008t0003g0243 a0001c0008t0003g0296 others(5): Show |
8 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-37-3032G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27394516 | |||||||
chr8:27394529 | G | A | 1 | a0001c0002t0001g0235 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-37-3019G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27394529 | |||||||
chr8:27394550 | G | A | 2 | a0001c0021t0004g0009 a0001c0022t0002g0008 |
2 | NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-37-2998G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27394550 | |||||||
chr8:27394551 | T | C | 1 | a0001c0030t0002g0007 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-37-2997T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27394551 | |||||||
chr8:27394603 | C | T | 2 | a0001c0021t0004g0009 a0001c0022t0002g0008 |
2 | NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-37-2945C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27394603 | |||||||
chr8:27394678 | T | G | 1 | a0002c0004t0002g0094 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-37-2870T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27394678 | |||||||
chr8:27394926 | C | T | 1 | a0001c0001t0003g0028 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-37-2622C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27394926 | |||||||
chr8:27395001 | G | A | 2 | a0001c0030t0002g0007 a0002c0006t0002g0317 |
2 | HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-37-2547G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27395001 | |||||||
chr8:27395031 | C | T | 111 | a0001c0002t0001g0295 a0001c0008t0003g0243 a0001c0008t0003g0296 others(108): Show |
115 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.-37-2517C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27395031 | |||||||
chr8:27395041 | C | T | 6 | a0001c0002t0001g0295 a0001c0008t0003g0243 a0001c0008t0003g0296 others(3): Show |
6 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-37-2507C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27395041 | |||||||
chr8:27395067 | C | CT | 7 | a0001c0010t0003g0289 a0001c0012t0004g0053 a0001c0012t0004g0055 others(4): Show |
7 | HG00735.hp1 HG01081.hp1 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.-37-2471dupT | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr8 | 27395067 | ||||||
chr8:27395089 | G | A | 2 | a0001c0030t0002g0007 a0002c0006t0002g0317 |
2 | HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-37-2459G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27395089 | |||||||
chr8:27395116 | T | C | 105 | a0001c0009t0002g0018 a0001c0009t0002g0087 a0001c0009t0002g0103 others(102): Show |
109 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.-37-2432T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27395116 | |||||||
chr8:27395229 | G | C | 101 | a0001c0009t0002g0018 a0001c0009t0002g0087 a0001c0009t0002g0103 others(98): Show |
105 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.-37-2319G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27395229 | |||||||
chr8:27395234 | G | A | 1 | a0001c0002t0001g0168 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-37-2314G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27395234 | |||||||
chr8:27395364 | G | A | 102 | a0001c0009t0002g0018 a0001c0009t0002g0087 a0001c0009t0002g0103 others(99): Show |
106 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.-37-2184G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27395364 | |||||||
chr8:27395446 | T | G | 2 | a0001c0002t0001g0171 a0001c0002t0001g0172 |
2 | NA18981.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.-37-2102T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27395446 | |||||||
chr8:27395475 | T | A | 1 | a0002c0006t0002g0317 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-37-2073T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27395475 | |||||||
chr8:27395492 | G | C | 9 | a0001c0009t0002g0125 a0001c0009t0002g0312 a0001c0009t0002g0313 others(6): Show |
11 | HG00609.hp2 NA18943.hp2 NA18949.hp2 others(8): Show |
intron_variant | MODIFIER | c.-37-2056G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27395492 | |||||||
chr8:27395596 | A | G | 2 | a0002c0003t0002g0223 a0002c0003t0002g0310 |
2 | NA18961.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.-37-1952A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27395596 | |||||||
chr8:27395665 | T | C | 9 | a0001c0009t0002g0125 a0001c0009t0002g0312 a0001c0009t0002g0313 others(6): Show |
11 | HG00609.hp2 NA18943.hp2 NA18949.hp2 others(8): Show |
intron_variant | MODIFIER | c.-37-1883T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27395665 | |||||||
chr8:27395699 | G | A | 1 | a0001c0010t0003g0289 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-37-1849G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27395699 | |||||||
chr8:27395838 | A | T | 1 | a0002c0006t0001g0291 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-37-1710A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27395838 | |||||||
chr8:27395880 | C | T | 2 | a0001c0021t0004g0009 a0001c0022t0002g0008 |
2 | NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-37-1668C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27395880 | |||||||
chr8:27396060 | T | C | 243 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(240): Show |
248 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.-37-1488T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27396060 | |||||||
chr8:27396156 | T | G | 2 | a0001c0021t0004g0009 a0001c0022t0002g0008 |
2 | NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-37-1392T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27396156 | |||||||
chr8:27396315 | C | A | 2 | a0001c0030t0002g0007 a0002c0006t0002g0317 |
2 | HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-37-1233C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27396315 | |||||||
chr8:27396342 | C | G | 2 | a0001c0021t0004g0009 a0001c0022t0002g0008 |
2 | NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-37-1206C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27396342 | |||||||
chr8:27396396 | A | C | 6 | a0001c0002t0001g0295 a0001c0008t0003g0243 a0001c0008t0003g0296 others(3): Show |
6 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-37-1152A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27396396 | |||||||
chr8:27396418 | A | G | 1 | a0001c0021t0004g0009 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-37-1130A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27396418 | |||||||
chr8:27396419 | T | C | 1 | a0002c0006t0002g0317 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-37-1129T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27396419 | |||||||
chr8:27396434 | G | A | 101 | a0001c0009t0002g0018 a0001c0009t0002g0087 a0001c0009t0002g0103 others(98): Show |
105 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.-37-1114G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27396434 | |||||||
chr8:27396459 | G | A | 2 | a0001c0021t0004g0009 a0001c0022t0002g0008 |
2 | NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-37-1089G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27396459 | |||||||
chr8:27396596 | T | G | 107 | a0001c0008t0003g0114 a0001c0009t0002g0018 a0001c0009t0002g0087 others(104): Show |
111 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.-37-952T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27396596 | |||||||
chr8:27396627 | T | C | 244 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(241): Show |
249 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(246): Show |
intron_variant | MODIFIER | c.-37-921T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27396627 | |||||||
chr8:27396890 | G | A | 1 | a0001c0002t0001g0142 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-37-658G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27396890 | |||||||
chr8:27397078 | C | T | 1 | a0002c0003t0002g0222 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-37-470C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27397078 | |||||||
chr8:27397079 | G | A | 9 | a0001c0009t0002g0125 a0001c0009t0002g0312 a0001c0009t0002g0313 others(6): Show |
11 | HG00609.hp2 NA18943.hp2 NA18949.hp2 others(8): Show |
intron_variant | MODIFIER | c.-37-469G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27397079 | |||||||
chr8:27397119 | C | T | 92 | a0001c0009t0002g0018 a0001c0009t0002g0087 a0001c0009t0002g0103 others(89): Show |
94 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.-37-429C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27397119 | |||||||
chr8:27397121 | C | T | 2 | a0001c0030t0002g0007 a0002c0006t0002g0317 |
2 | HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-37-427C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27397121 | |||||||
chr8:27397207 | C | T | 1 | a0001c0001t0003g0017 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-37-341C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27397207 | |||||||
chr8:27397262 | G | A | 2 | a0001c0030t0002g0007 a0002c0006t0002g0317 |
2 | HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-37-286G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27397262 | |||||||
chr8:27397443 | G | A | 1 | a0001c0002t0001g0130 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-37-105G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27397443 | |||||||
chr8:27397486 | G | A | 101 | a0001c0009t0002g0018 a0001c0009t0002g0087 a0001c0009t0002g0103 others(98): Show |
105 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.-37-62G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 1/30 | chr8 | 27397486 | |||||||
chr8:27397808 | C | T | 103 | a0001c0009t0002g0018 a0001c0009t0002g0087 a0001c0009t0002g0103 others(100): Show |
107 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.204+20C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27397808 | |||||||
chr8:27397851 | AGCAGCTC others(12): Show |
A | 92 | a0001c0009t0002g0018 a0001c0009t0002g0087 a0001c0009t0002g0103 others(89): Show |
94 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.204+74_204+92delTG others(17): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27397851 | ||||||
chr8:27397899 | G | C | 2 | a0001c0021t0004g0009 a0001c0022t0002g0008 |
2 | NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.204+111G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27397899 | |||||||
chr8:27398032 | G | T | 1 | a0001c0001t0003g0318 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.204+244G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27398032 | |||||||
chr8:27398118 | A | G | 103 | a0001c0009t0002g0018 a0001c0009t0002g0087 a0001c0009t0002g0103 others(100): Show |
107 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.204+330A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27398118 | |||||||
chr8:27398228 | T | G | 1 | a0001c0011t0001g0144 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.204+440T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27398228 | |||||||
chr8:27398363 | G | A | 2 | a0001c0030t0002g0007 a0002c0006t0002g0317 |
2 | HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.204+575G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27398363 | |||||||
chr8:27398474 | C | T | 1 | a0002c0003t0002g0256 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.204+686C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27398474 | |||||||
chr8:27398568 | A | C | 1 | a0001c0001t0003g0088 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.204+780A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27398568 | |||||||
chr8:27398746 | T | C | 105 | a0001c0009t0002g0018 a0001c0009t0002g0087 a0001c0009t0002g0103 others(102): Show |
109 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.204+958T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27398746 | |||||||
chr8:27398797 | C | G | 243 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(240): Show |
248 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.204+1009C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27398797 | |||||||
chr8:27398842 | G | A | 101 | a0001c0009t0002g0018 a0001c0009t0002g0087 a0001c0009t0002g0103 others(98): Show |
105 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.204+1054G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27398842 | |||||||
chr8:27398900 | C | T | 7 | a0001c0001t0003g0175 a0001c0001t0003g0294 a0001c0007t0003g0303 others(4): Show |
7 | HG00639.hp1 HG02630.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.204+1112C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27398900 | |||||||
chr8:27398931 | C | T | 9 | a0001c0009t0002g0125 a0001c0009t0002g0312 a0001c0009t0002g0313 others(6): Show |
11 | HG00609.hp2 NA18943.hp2 NA18949.hp2 others(8): Show |
intron_variant | MODIFIER | c.204+1143C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27398931 | |||||||
chr8:27399193 | C | T | 2 | a0001c0030t0002g0007 a0002c0006t0002g0317 |
2 | HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.204+1405C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27399193 | |||||||
chr8:27399352 | A | G | 6 | a0001c0002t0001g0295 a0001c0008t0003g0243 a0001c0008t0003g0296 others(3): Show |
6 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.204+1564A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27399352 | |||||||
chr8:27399401 | G | A | 92 | a0001c0009t0002g0018 a0001c0009t0002g0087 a0001c0009t0002g0103 others(89): Show |
94 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.204+1613G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27399401 | |||||||
chr8:27399487 | G | A | 8 | a0001c0001t0003g0022 a0001c0001t0003g0175 a0001c0001t0003g0294 others(5): Show |
8 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.204+1699G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27399487 | |||||||
chr8:27399529 | A | G | 103 | a0001c0009t0002g0018 a0001c0009t0002g0087 a0001c0009t0002g0103 others(100): Show |
107 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.204+1741A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27399529 | |||||||
chr8:27399569 | A | G | 9 | a0001c0009t0002g0125 a0001c0009t0002g0312 a0001c0009t0002g0313 others(6): Show |
11 | HG00609.hp2 NA18943.hp2 NA18949.hp2 others(8): Show |
intron_variant | MODIFIER | c.204+1781A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27399569 | |||||||
chr8:27399572 | T | G | 3 | a0001c0001t0003g0088 a0001c0001t0003g0113 a0001c0001t0003g0115 |
3 | HG02572.hp1 HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.204+1784T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27399572 | |||||||
chr8:27399576 | C | G | 6 | a0001c0002t0001g0295 a0001c0008t0003g0243 a0001c0008t0003g0296 others(3): Show |
6 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.204+1788C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27399576 | |||||||
chr8:27399628 | A | G | 2 | a0001c0021t0004g0009 a0001c0022t0002g0008 |
2 | NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.204+1840A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27399628 | |||||||
chr8:27399680 | G | C | 1 | a0001c0001t0003g0199 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.204+1892G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27399680 | |||||||
chr8:27400103 | A | G | 1 | a0001c0002t0001g0118 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.204+2315A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27400103 | |||||||
chr8:27400270 | T | G | 119 | a0001c0001t0003g0276 a0001c0002t0001g0295 a0001c0007t0003g0277 others(116): Show |
123 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.204+2482T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27400270 | |||||||
chr8:27400376 | C | T | 1 | a0002c0006t0001g0020 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.204+2588C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27400376 | |||||||
chr8:27400377 | T | C | 1 | a0002c0005t0001g0309 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.204+2589T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27400377 | |||||||
chr8:27400386 | G | A | 4 | a0002c0006t0001g0006 a0002c0006t0001g0234 a0002c0006t0001g0290 others(1): Show |
4 | HG02630.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.204+2598G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27400386 | |||||||
chr8:27400447 | TA | T | 139 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(136): Show |
142 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.204+2676delA | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27400447 | ||||||
chr8:27400448 | A | T | 1 | a0002c0004t0002g0242 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.204+2660A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27400448 | |||||||
chr8:27400569 | G | A | 112 | a0001c0002t0001g0295 a0001c0008t0003g0243 a0001c0008t0003g0296 others(109): Show |
116 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.204+2781G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27400569 | |||||||
chr8:27400581 | A | T | 3 | a0001c0010t0003g0289 a0001c0021t0004g0009 a0001c0022t0002g0008 |
3 | HG03225.hp2 NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.204+2793A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27400581 | |||||||
chr8:27400637 | G | A | 1 | a0002c0003t0002g0256 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.204+2849G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27400637 | |||||||
chr8:27400678 | G | A | 110 | a0001c0002t0001g0295 a0001c0008t0003g0243 a0001c0008t0003g0296 others(107): Show |
114 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.204+2890G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27400678 | |||||||
chr8:27400732 | A | G | 110 | a0001c0002t0001g0295 a0001c0008t0003g0243 a0001c0008t0003g0296 others(107): Show |
114 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.204+2944A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27400732 | |||||||
chr8:27400743 | T | A | 1 | a0002c0005t0001g0204 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.204+2955T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27400743 | |||||||
chr8:27400790 | G | A | 1 | a0002c0003t0002g0299 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.204+3002G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27400790 | |||||||
chr8:27400796 | G | A | 110 | a0001c0002t0001g0295 a0001c0008t0003g0243 a0001c0008t0003g0296 others(107): Show |
114 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.204+3008G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27400796 | |||||||
chr8:27400859 | A | T | 3 | a0001c0010t0003g0289 a0001c0021t0004g0009 a0001c0022t0002g0008 |
3 | HG03225.hp2 NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.204+3071A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27400859 | |||||||
chr8:27400878 | G | A | 1 | a0001c0002t0001g0176 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.204+3090G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27400878 | |||||||
chr8:27400940 | G | A | 1 | a0001c0001t0003g0031 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.204+3152G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27400940 | |||||||
chr8:27400959 | A | G | 1 | a0001c0022t0002g0008 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.204+3171A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27400959 | |||||||
chr8:27400976 | T | C | 10 | a0001c0001t0003g0022 a0001c0001t0003g0175 a0001c0001t0003g0294 others(7): Show |
10 | HG00639.hp1 HG00733.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.204+3188T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27400976 | |||||||
chr8:27400981 | A | ACCAAAAG others(1): Show |
110 | a0001c0002t0001g0295 a0001c0008t0003g0243 a0001c0008t0003g0296 others(107): Show |
114 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.204+3199_204+3200i others(10): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27400981 | ||||||
chr8:27401011 | C | A | 3 | a0001c0001t0003g0088 a0001c0001t0003g0113 a0001c0001t0003g0115 |
3 | HG02572.hp1 HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.204+3223C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27401011 | |||||||
chr8:27401117 | T | C | 130 | a0001c0001t0003g0181 a0001c0001t0003g0182 a0001c0001t0003g0183 others(127): Show |
134 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.204+3329T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27401117 | |||||||
chr8:27401141 | A | AAAAC | 110 | a0001c0002t0001g0295 a0001c0008t0003g0243 a0001c0008t0003g0296 others(107): Show |
114 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.204+3357_204+3360d others(6): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27401141 | ||||||
chr8:27401151 | G | C | 1 | a0002c0003t0002g0217 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.204+3363G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27401151 | |||||||
chr8:27401260 | AGAGAACC others(2): Show |
A | 114 | a0001c0001t0003g0051 a0001c0002t0001g0295 a0001c0008t0003g0114 others(111): Show |
118 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.204+3488_204+3496d others(11): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27401260 | ||||||
chr8:27401589 | C | T | 2 | a0001c0007t0003g0277 a0001c0007t0003g0278 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.204+3801C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27401589 | |||||||
chr8:27401634 | A | T | 110 | a0001c0002t0001g0295 a0001c0008t0003g0243 a0001c0008t0003g0296 others(107): Show |
114 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.204+3846A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27401634 | |||||||
chr8:27401645 | A | G | 20 | a0001c0001t0003g0181 a0001c0001t0003g0182 a0001c0001t0003g0183 others(17): Show |
20 | HG02055.hp1 HG02257.hp1 HG02486.hp1 others(17): Show |
intron_variant | MODIFIER | c.204+3857A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27401645 | |||||||
chr8:27401713 | A | C | 110 | a0001c0002t0001g0295 a0001c0008t0003g0243 a0001c0008t0003g0296 others(107): Show |
114 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.204+3925A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27401713 | |||||||
chr8:27401909 | A | G | 233 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(230): Show |
238 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.204+4121A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27401909 | |||||||
chr8:27402036 | T | C | 10 | a0001c0001t0003g0022 a0001c0001t0003g0175 a0001c0001t0003g0294 others(7): Show |
10 | HG00639.hp1 HG00733.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.204+4248T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27402036 | |||||||
chr8:27402157 | G | A | 9 | a0001c0009t0002g0125 a0001c0009t0002g0312 a0001c0009t0002g0313 others(6): Show |
11 | HG00609.hp2 NA18943.hp2 NA18949.hp2 others(8): Show |
intron_variant | MODIFIER | c.204+4369G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27402157 | |||||||
chr8:27402174 | G | A | 2 | a0002c0006t0001g0286 a0002c0006t0001g0287 |
2 | HG02615.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.204+4386G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27402174 | |||||||
chr8:27402232 | C | T | 6 | a0001c0001t0003g0276 a0001c0007t0003g0277 a0001c0007t0003g0278 others(3): Show |
6 | HG01070.hp2 HG01071.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.204+4444C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27402232 | |||||||
chr8:27402305 | G | A | 8 | a0001c0001t0003g0022 a0001c0001t0003g0175 a0001c0001t0003g0294 others(5): Show |
8 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.204+4517G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27402305 | |||||||
chr8:27402398 | C | T | 8 | a0001c0001t0003g0022 a0001c0001t0003g0175 a0001c0001t0003g0294 others(5): Show |
8 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.204+4610C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27402398 | |||||||
chr8:27402416 | A | T | 84 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(81): Show |
85 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.204+4628A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27402416 | |||||||
chr8:27402458 | G | A | 4 | a0001c0001t0003g0088 a0001c0001t0003g0113 a0001c0001t0003g0115 others(1): Show |
4 | HG02572.hp1 HG02818.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.204+4670G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27402458 | |||||||
chr8:27402656 | G | A | 2 | a0001c0021t0004g0009 a0001c0022t0002g0008 |
2 | NA19043.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.204+4868G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27402656 | |||||||
chr8:27402764 | A | G | 1 | a0001c0010t0003g0289 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.204+4976A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27402764 | |||||||
chr8:27402887 | T | G | 18 | a0001c0001t0003g0276 a0001c0007t0003g0277 a0001c0007t0003g0278 others(15): Show |
20 | HG00609.hp2 HG01070.hp2 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.204+5099T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27402887 | |||||||
chr8:27402889 | C | T | 1 | a0001c0002t0001g0160 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.204+5101C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27402889 | |||||||
chr8:27402967 | A | G | 107 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(104): Show |
108 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.204+5179A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27402967 | |||||||
chr8:27403055 | C | G | 6 | a0001c0001t0003g0276 a0001c0007t0003g0277 a0001c0007t0003g0278 others(3): Show |
6 | HG01070.hp2 HG01071.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.204+5267C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27403055 | |||||||
chr8:27403120 | G | A | 11 | a0001c0009t0002g0125 a0001c0009t0002g0312 a0001c0009t0002g0313 others(8): Show |
13 | HG00609.hp2 NA18943.hp2 NA18949.hp2 others(10): Show |
intron_variant | MODIFIER | c.204+5332G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27403120 | |||||||
chr8:27403265 | C | T | 1 | a0001c0001t0005g0059 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.204+5477C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27403265 | |||||||
chr8:27403294 | T | C | 5 | a0001c0001t0003g0071 a0001c0001t0003g0072 a0001c0001t0003g0074 others(2): Show |
5 | HG00544.hp1 HG00609.hp1 HG00673.hp1 others(2): Show |
intron_variant | MODIFIER | c.204+5506T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27403294 | |||||||
chr8:27403296 | G | A | 2 | a0001c0001t0003g0028 a0001c0001t0003g0034 |
2 | HG01934.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.204+5508G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27403296 | |||||||
chr8:27403310 | A | C | 9 | a0001c0001t0003g0022 a0001c0001t0003g0175 a0001c0001t0003g0294 others(6): Show |
9 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.204+5522A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27403310 | |||||||
chr8:27403318 | C | T | 1 | a0001c0010t0003g0231 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.204+5530C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27403318 | |||||||
chr8:27403329 | A | G | 3 | a0001c0001t0003g0088 a0001c0001t0003g0113 a0001c0001t0003g0115 |
3 | HG02572.hp1 HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.204+5541A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27403329 | |||||||
chr8:27403338 | ACATAGTT others(4): Show |
A | 9 | a0001c0001t0003g0022 a0001c0001t0003g0175 a0001c0001t0003g0294 others(6): Show |
9 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.204+5554_204+5564d others(13): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27403338 | ||||||
chr8:27403378 | G | T | 3 | a0001c0002t0001g0141 a0001c0002t0001g0162 a0002c0006t0001g0213 |
3 | NA18955.hp1 NA19056.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.204+5590G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27403378 | |||||||
chr8:27403408 | C | T | 9 | a0001c0009t0002g0125 a0001c0009t0002g0312 a0001c0009t0002g0313 others(6): Show |
11 | HG00609.hp2 NA18943.hp2 NA18949.hp2 others(8): Show |
intron_variant | MODIFIER | c.204+5620C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27403408 | |||||||
chr8:27403431 | T | C | 20 | a0001c0001t0003g0181 a0001c0001t0003g0182 a0001c0001t0003g0183 others(17): Show |
20 | HG02055.hp1 HG02257.hp1 HG02486.hp1 others(17): Show |
intron_variant | MODIFIER | c.204+5643T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27403431 | |||||||
chr8:27403461 | G | A | 1 | a0001c0001t0003g0150 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.204+5673G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27403461 | |||||||
chr8:27403540 | G | T | 7 | a0001c0011t0001g0079 a0001c0011t0001g0098 a0001c0011t0001g0140 others(4): Show |
7 | HG01192.hp1 HG01361.hp1 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.204+5752G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27403540 | |||||||
chr8:27403609 | G | A | 3 | a0001c0002t0001g0120 a0001c0002t0001g0121 a0001c0002t0001g0122 |
3 | NA18957.hp2 NA18969.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.204+5821G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27403609 | |||||||
chr8:27403621 | C | G | 9 | a0002c0003t0002g0247 a0002c0004t0002g0224 a0002c0004t0002g0225 others(6): Show |
9 | HG01099.hp2 HG01168.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.204+5833C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27403621 | |||||||
chr8:27403718 | C | T | 1 | a0001c0002t0001g0078 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.204+5930C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27403718 | |||||||
chr8:27403740 | CT | C | 8 | a0001c0001t0003g0022 a0001c0001t0003g0175 a0001c0001t0003g0294 others(5): Show |
8 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.204+5955delT | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27403740 | ||||||
chr8:27403748 | C | T | 6 | a0001c0002t0001g0173 a0001c0002t0001g0174 a0001c0002t0001g0176 others(3): Show |
6 | HG01884.hp2 HG02647.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.204+5960C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27403748 | |||||||
chr8:27403749 | TTGC | T | 117 | a0001c0001t0003g0022 a0001c0001t0003g0175 a0001c0001t0003g0276 others(114): Show |
119 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.204+5981_204+5983d others(5): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27403749 | ||||||
chr8:27403766 | GCTGCTC | G | 9 | a0001c0009t0002g0125 a0001c0009t0002g0312 a0001c0009t0002g0313 others(6): Show |
11 | HG00609.hp2 NA18943.hp2 NA18949.hp2 others(8): Show |
intron_variant | MODIFIER | c.204+5981_204+5986d others(8): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27403766 | ||||||
chr8:27403788 | T | C | 9 | a0001c0009t0002g0125 a0001c0009t0002g0312 a0001c0009t0002g0313 others(6): Show |
11 | HG00609.hp2 NA18943.hp2 NA18949.hp2 others(8): Show |
intron_variant | MODIFIER | c.204+6000T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27403788 | |||||||
chr8:27403801 | G | C | 1 | a0011c0019t0002g0102 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.204+6013G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27403801 | |||||||
chr8:27403904 | C | G | 1 | a0001c0002t0001g0226 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.204+6116C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27403904 | |||||||
chr8:27403974 | A | C | 5 | a0002c0006t0001g0006 a0002c0006t0001g0234 a0002c0006t0001g0282 others(2): Show |
5 | HG02630.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.204+6186A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27403974 | |||||||
chr8:27404017 | T | C | 2 | a0001c0002t0001g0235 a0001c0010t0003g0289 |
2 | HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.204+6229T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27404017 | |||||||
chr8:27404023 | C | G | 1 | a0002c0006t0002g0317 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.204+6235C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27404023 | |||||||
chr8:27404039 | CCA | C | 92 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(89): Show |
93 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.204+6252_204+6253d others(4): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27404039 | |||||||
chr8:27404180 | C | T | 3 | a0001c0008t0003g0292 a0001c0008t0003g0319 a0001c0008t0003g0320 |
3 | HG02723.hp2 HG02896.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.204+6392C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27404180 | |||||||
chr8:27404298 | A | G | 238 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(235): Show |
243 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(240): Show |
intron_variant | MODIFIER | c.204+6510A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27404298 | |||||||
chr8:27404424 | C | T | 14 | a0001c0001t0003g0175 a0001c0001t0003g0294 a0001c0002t0001g0173 others(11): Show |
14 | HG00639.hp1 HG01884.hp2 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.204+6636C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27404424 | |||||||
chr8:27404461 | C | T | 4 | a0001c0007t0003g0135 a0001c0007t0003g0136 a0001c0007t0003g0137 others(1): Show |
4 | HG00735.hp2 HG01993.hp1 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.204+6673C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27404461 | |||||||
chr8:27404620 | C | T | 1 | a0001c0002t0001g0226 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.204+6832C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27404620 | |||||||
chr8:27404670 | A | G | 1 | a0001c0007t0003g0189 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.204+6882A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27404670 | |||||||
chr8:27404678 | C | T | 155 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(152): Show |
159 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.204+6890C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27404678 | |||||||
chr8:27404782 | A | G | 7 | a0001c0001t0003g0181 a0001c0001t0003g0182 a0001c0001t0003g0183 others(4): Show |
7 | HG02055.hp1 HG02257.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.204+6994A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27404782 | |||||||
chr8:27404827 | G | C | 1 | a0001c0010t0003g0289 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.204+7039G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27404827 | |||||||
chr8:27404849 | C | G | 106 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(103): Show |
107 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.204+7061C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27404849 | |||||||
chr8:27405017 | C | CCTTCCTC others(7): Show |
1 | a0001c0009t0002g0018 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.204+7240_204+7253d others(16): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27405017 | ||||||
chr8:27405035 | C | CCT | 15 | a0001c0002t0001g0157 a0001c0002t0001g0161 a0001c0002t0001g0164 others(12): Show |
15 | HG00423.hp1 HG00609.hp2 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.204+7280_204+7281d others(4): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27405035 | ||||||
chr8:27405035 | C | CCTCT | 5 | a0001c0002t0001g0080 a0001c0002t0001g0124 a0001c0002t0001g0163 others(2): Show |
5 | HG00323.hp1 HG01884.hp2 HG02015.hp2 others(2): Show |
intron_variant | MODIFIER | c.204+7278_204+7281d others(6): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27405035 | ||||||
chr8:27405035 | C | CCTCTCT | 5 | a0001c0001t0003g0113 a0001c0001t0003g0115 a0001c0001t0003g0288 others(2): Show |
5 | HG02559.hp1 HG02818.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.204+7276_204+7281d others(8): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27405035 | ||||||
chr8:27405035 | C | CCTCTCTC others(1): Show |
3 | a0002c0005t0001g0026 a0002c0005t0001g0032 a0002c0005t0001g0033 |
3 | HG01928.hp1 HG01943.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.204+7274_204+7281d others(10): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27405035 | ||||||
chr8:27405035 | C | CCTCTCTC others(3): Show |
2 | a0001c0001t0003g0088 a0001c0002t0001g0226 |
2 | HG02572.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.204+7272_204+7281d others(12): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27405035 | ||||||
chr8:27405035 | C | CCTCTCTC others(5): Show |
5 | a0001c0001t0003g0024 a0001c0001t0003g0028 a0001c0001t0003g0065 others(2): Show |
5 | HG01934.hp1 HG02280.hp1 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.204+7270_204+7281d others(14): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27405035 | ||||||
chr8:27405035 | C | CCTCTCTC others(7): Show |
12 | a0001c0001t0003g0030 a0001c0001t0003g0035 a0001c0001t0003g0072 others(9): Show |
12 | HG00544.hp1 HG00609.hp1 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.204+7268_204+7281d others(16): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27405035 | ||||||
chr8:27405035 | C | CCTCTCTC others(9): Show |
14 | a0001c0001t0003g0034 a0001c0001t0003g0063 a0001c0001t0003g0081 others(11): Show |
14 | HG00738.hp2 HG01109.hp2 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.204+7266_204+7281d others(18): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27405035 | ||||||
chr8:27405035 | C | CCTCTCTC others(11): Show |
22 | a0001c0001t0003g0021 a0001c0001t0003g0025 a0001c0001t0003g0029 others(19): Show |
22 | HG00323.hp2 HG00621.hp1 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.204+7264_204+7281d others(20): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27405035 | ||||||
chr8:27405035 | C | CCTCTCTC others(13): Show |
12 | a0001c0001t0003g0037 a0001c0001t0003g0048 a0001c0001t0003g0051 others(9): Show |
12 | HG00673.hp1 HG01169.hp1 HG02080.hp1 others(9): Show |
intron_variant | MODIFIER | c.204+7262_204+7281d others(22): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27405035 | ||||||
chr8:27405035 | C | CCTCTCTC others(15): Show |
12 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0031 others(9): Show |
12 | HG00408.hp1 HG01074.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.204+7260_204+7281d others(24): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27405035 | ||||||
chr8:27405035 | C | CCTCTCTC others(17): Show |
6 | a0001c0001t0003g0046 a0001c0001t0003g0184 a0001c0001t0003g0185 others(3): Show |
7 | HG00438.hp1 HG00639.hp2 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.204+7258_204+7281d others(26): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27405035 | ||||||
chr8:27405035 | C | CCTCTCTC others(19): Show |
6 | a0001c0001t0003g0015 a0001c0001t0003g0090 a0001c0001t0003g0093 others(3): Show |
6 | HG01192.hp2 HG02257.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.204+7256_204+7281d others(28): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27405035 | ||||||
chr8:27405035 | C | CCTCTCTC others(21): Show |
1 | a0001c0001t0003g0183 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.204+7254_204+7281d others(30): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27405035 | ||||||
chr8:27405035 | C | CCTCTCTC others(23): Show |
2 | a0001c0001t0003g0181 a0002c0005t0001g0200 |
2 | HG01123.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.204+7252_204+7281d others(32): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27405035 | ||||||
chr8:27405035 | C | CTCTCTCT others(12): Show |
1 | a0001c0001t0003g0044 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.204+7247_204+7248i others(21): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27405035 | |||||||
chr8:27405035 | CCT | C | 4 | a0001c0002t0001g0134 a0001c0002t0001g0295 a0001c0008t0003g0296 others(1): Show |
4 | HG01433.hp2 HG02145.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.204+7280_204+7281d others(4): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27405035 | ||||||
chr8:27405035 | CCTCTCT | C | 18 | a0001c0008t0003g0243 a0001c0008t0003g0292 a0001c0008t0003g0315 others(15): Show |
18 | HG02109.hp2 HG02258.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.204+7276_204+7281d others(8): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27405035 | ||||||
chr8:27405035 | CCTCTCTC others(11): Show |
C | 100 | a0001c0001t0003g0022 a0001c0008t0003g0114 a0001c0009t0002g0103 others(97): Show |
102 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.204+7264_204+7281d others(20): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27405035 | ||||||
chr8:27405069 | T | TCTCTCTC others(20): Show |
1 | a0001c0001t0003g0187 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.204+7281_204+7282i others(29): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27405069 | |||||||
chr8:27405163 | C | A | 6 | a0001c0002t0001g0295 a0001c0008t0003g0296 a0001c0008t0003g0314 others(3): Show |
6 | HG02258.hp1 HG02486.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.204+7375C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27405163 | |||||||
chr8:27405171 | G | C | 1 | a0001c0002t0001g0155 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.204+7383G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27405171 | |||||||
chr8:27405208 | C | T | 6 | a0002c0003t0002g0012 a0002c0004t0002g0001 a0002c0004t0002g0011 others(3): Show |
8 | NA18949.hp2 NA18968.hp2 NA18980.hp2 others(5): Show |
intron_variant | MODIFIER | c.204+7420C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27405208 | |||||||
chr8:27405291 | G | A | 1 | a0001c0008t0003g0114 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.204+7503G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27405291 | |||||||
chr8:27405377 | C | G | 5 | a0001c0002t0001g0295 a0001c0008t0003g0296 a0001c0008t0003g0314 others(2): Show |
5 | HG02258.hp1 HG02486.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.204+7589C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27405377 | |||||||
chr8:27405521 | G | A | 1 | a0001c0010t0003g0289 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.204+7733G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27405521 | |||||||
chr8:27405590 | C | T | 70 | a0001c0008t0003g0243 a0001c0008t0003g0292 a0001c0008t0003g0319 others(67): Show |
71 | HG00408.hp2 HG00438.hp2 HG00621.hp2 others(68): Show |
intron_variant | MODIFIER | c.204+7802C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27405590 | |||||||
chr8:27405596 | C | T | 1 | a0001c0009t0002g0237 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.204+7808C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27405596 | |||||||
chr8:27405641 | G | A | 2 | a0001c0008t0003g0314 a0001c0008t0003g0315 |
2 | HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.204+7853G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27405641 | |||||||
chr8:27405657 | A | G | 39 | a0001c0009t0002g0107 a0001c0012t0004g0053 a0001c0012t0004g0055 others(36): Show |
40 | HG00099.hp2 HG00423.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.204+7869A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27405657 | |||||||
chr8:27405831 | G | C | 8 | a0001c0010t0003g0229 a0001c0010t0003g0230 a0001c0010t0003g0231 others(5): Show |
8 | HG02486.hp1 HG02647.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.204+8043G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27405831 | |||||||
chr8:27405842 | A | T | 62 | a0001c0009t0002g0103 a0001c0012t0004g0027 a0001c0012t0004g0211 others(59): Show |
63 | HG00408.hp2 HG00438.hp2 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.204+8054A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27405842 | |||||||
chr8:27405916 | G | T | 221 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(218): Show |
226 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.204+8128G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27405916 | |||||||
chr8:27406263 | CCTTAA | C | 124 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(121): Show |
127 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.204+8481_204+8485d others(7): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27406263 | ||||||
chr8:27406275 | T | C | 1 | a0001c0011t0001g0098 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.204+8487T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27406275 | |||||||
chr8:27406383 | C | T | 100 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(97): Show |
101 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.204+8595C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27406383 | |||||||
chr8:27406393 | A | C | 6 | a0002c0003t0002g0012 a0002c0004t0002g0001 a0002c0004t0002g0011 others(3): Show |
8 | NA18949.hp2 NA18968.hp2 NA18980.hp2 others(5): Show |
intron_variant | MODIFIER | c.204+8605A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27406393 | |||||||
chr8:27406453 | T | C | 1 | a0001c0001t0003g0036 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.204+8665T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27406453 | |||||||
chr8:27406463 | T | C | 8 | a0001c0010t0003g0229 a0001c0010t0003g0230 a0001c0010t0003g0231 others(5): Show |
8 | HG02486.hp1 HG02647.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.204+8675T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27406463 | |||||||
chr8:27406593 | T | C | 231 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(228): Show |
236 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(233): Show |
intron_variant | MODIFIER | c.204+8805T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27406593 | |||||||
chr8:27406728 | C | A | 100 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(97): Show |
101 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.204+8940C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27406728 | |||||||
chr8:27406824 | A | G | 2 | a0002c0006t0001g0234 a0002c0006t0001g0290 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.204+9036A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27406824 | |||||||
chr8:27406830 | A | G | 1 | a0002c0005t0001g0002 | 2 | HG00639.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.204+9042A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27406830 | |||||||
chr8:27407027 | C | A | 1 | a0002c0003t0002g0239 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.204+9239C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27407027 | |||||||
chr8:27407038 | G | T | 4 | a0001c0001t0003g0088 a0001c0001t0003g0113 a0001c0001t0003g0115 others(1): Show |
4 | HG02559.hp1 HG02572.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.204+9250G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27407038 | |||||||
chr8:27407150 | G | A | 318 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(315): Show |
323 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(320): Show |
intron_variant | MODIFIER | c.204+9362G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27407150 | |||||||
chr8:27407159 | G | A | 228 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(225): Show |
233 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.204+9371G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27407159 | |||||||
chr8:27407364 | A | G | 1 | a0001c0001t0003g0035 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.204+9576A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27407364 | |||||||
chr8:27407434 | C | T | 1 | a0002c0005t0001g0309 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.204+9646C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27407434 | |||||||
chr8:27407435 | G | A | 66 | a0001c0009t0002g0103 a0001c0010t0003g0289 a0001c0012t0004g0027 others(63): Show |
67 | HG00408.hp2 HG00438.hp2 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.204+9647G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27407435 | |||||||
chr8:27407694 | C | G | 4 | a0001c0001t0003g0088 a0001c0001t0003g0113 a0001c0001t0003g0115 others(1): Show |
4 | HG02559.hp1 HG02572.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.204+9906C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27407694 | |||||||
chr8:27407808 | C | T | 5 | a0001c0007t0003g0277 a0001c0007t0003g0278 a0001c0007t0003g0279 others(2): Show |
5 | HG01070.hp2 HG01071.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.204+10020C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27407808 | |||||||
chr8:27407854 | T | C | 117 | a0001c0002t0001g0295 a0001c0007t0003g0277 a0001c0007t0003g0278 others(114): Show |
119 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.204+10066T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27407854 | |||||||
chr8:27407887 | T | C | 1 | a0001c0002t0001g0118 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.204+10099T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27407887 | |||||||
chr8:27407957 | A | G | 1 | a0001c0007t0003g0303 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.204+10169A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27407957 | |||||||
chr8:27407959 | A | G | 46 | a0001c0007t0003g0277 a0001c0007t0003g0278 a0001c0007t0003g0279 others(43): Show |
47 | HG00099.hp2 HG00423.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.204+10171A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27407959 | |||||||
chr8:27408002 | C | A | 2 | a0001c0001t0003g0029 a0001c0001t0003g0030 |
2 | HG01255.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.204+10214C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27408002 | |||||||
chr8:27408008 | T | C | 1 | a0011c0019t0002g0102 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.204+10220T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27408008 | |||||||
chr8:27408152 | C | T | 1 | a0002c0003t0002g0207 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.204+10364C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27408152 | |||||||
chr8:27408163 | G | C | 16 | a0001c0002t0001g0295 a0001c0008t0003g0243 a0001c0008t0003g0296 others(13): Show |
16 | HG02109.hp2 HG02258.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.204+10375G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27408163 | |||||||
chr8:27408165 | A | G | 3 | a0001c0008t0003g0292 a0001c0008t0003g0319 a0001c0008t0003g0320 |
3 | HG02723.hp2 HG02896.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.204+10377A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27408165 | |||||||
chr8:27408190 | GA | G | 66 | a0001c0009t0002g0103 a0001c0010t0003g0289 a0001c0012t0004g0027 others(63): Show |
67 | HG00408.hp2 HG00438.hp2 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.204+10405delA | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27408190 | ||||||
chr8:27408212 | C | A | 3 | a0001c0008t0003g0292 a0001c0008t0003g0319 a0001c0008t0003g0320 |
3 | HG02723.hp2 HG02896.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.204+10424C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27408212 | |||||||
chr8:27408290 | G | A | 6 | a0002c0003t0002g0012 a0002c0004t0002g0001 a0002c0004t0002g0011 others(3): Show |
8 | NA18949.hp2 NA18968.hp2 NA18980.hp2 others(5): Show |
intron_variant | MODIFIER | c.204+10502G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27408290 | |||||||
chr8:27408370 | A | G | 41 | a0001c0008t0003g0114 a0001c0009t0002g0107 a0001c0012t0004g0053 others(38): Show |
42 | HG00099.hp2 HG00423.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.204+10582A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27408370 | |||||||
chr8:27408595 | C | T | 1 | a0002c0004t0002g0208 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.204+10807C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27408595 | |||||||
chr8:27408640 | C | T | 1 | a0002c0003t0002g0247 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.204+10852C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27408640 | |||||||
chr8:27408664 | C | G | 1 | a0002c0006t0001g0323 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.204+10876C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27408664 | |||||||
chr8:27408770 | A | T | 40 | a0001c0008t0003g0114 a0001c0009t0002g0107 a0001c0012t0004g0053 others(37): Show |
41 | HG00099.hp2 HG00423.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.204+10982A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27408770 | |||||||
chr8:27408948 | T | C | 66 | a0001c0009t0002g0103 a0001c0010t0003g0289 a0001c0012t0004g0027 others(63): Show |
67 | HG00408.hp2 HG00438.hp2 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.205-10947T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27408948 | |||||||
chr8:27408987 | G | A | 1 | a0001c0012t0004g0055 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.205-10908G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27408987 | |||||||
chr8:27409144 | C | T | 6 | a0001c0002t0001g0295 a0001c0008t0003g0243 a0001c0008t0003g0296 others(3): Show |
6 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.205-10751C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27409144 | |||||||
chr8:27409784 | C | T | 4 | a0001c0001t0003g0024 a0002c0005t0001g0026 a0002c0005t0001g0032 others(1): Show |
4 | HG01928.hp1 HG01943.hp2 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.205-10111C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27409784 | |||||||
chr8:27410023 | A | C | 4 | a0001c0001t0003g0088 a0001c0001t0003g0113 a0001c0001t0003g0115 others(1): Show |
4 | HG02559.hp1 HG02572.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.205-9872A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27410023 | |||||||
chr8:27410058 | A | T | 2 | a0002c0006t0001g0006 a0002c0006t0001g0282 |
2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.205-9837A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27410058 | |||||||
chr8:27410079 | A | G | 6 | a0001c0002t0001g0295 a0001c0008t0003g0243 a0001c0008t0003g0296 others(3): Show |
6 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.205-9816A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27410079 | |||||||
chr8:27410089 | C | G | 4 | a0001c0002t0001g0178 a0001c0002t0001g0226 a0001c0007t0003g0179 others(1): Show |
4 | HG02647.hp2 HG02965.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.205-9806C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27410089 | |||||||
chr8:27410170 | C | T | 1 | a0002c0018t0002g0089 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.205-9725C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27410170 | |||||||
chr8:27410359 | G | GC | 236 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(233): Show |
241 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.205-9534dupC | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27410359 | ||||||
chr8:27410614 | G | T | 1 | a0002c0003t0002g0263 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.205-9281G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27410614 | |||||||
chr8:27410665 | A | G | 3 | a0001c0008t0003g0292 a0001c0008t0003g0319 a0001c0008t0003g0320 |
3 | HG02723.hp2 HG02896.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.205-9230A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27410665 | |||||||
chr8:27410738 | G | T | 1 | a0002c0004t0002g0104 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.205-9157G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27410738 | |||||||
chr8:27411066 | A | G | 6 | a0002c0003t0002g0012 a0002c0004t0002g0001 a0002c0004t0002g0011 others(3): Show |
8 | NA18949.hp2 NA18968.hp2 NA18980.hp2 others(5): Show |
intron_variant | MODIFIER | c.205-8829A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27411066 | |||||||
chr8:27411099 | C | T | 74 | a0001c0002t0001g0295 a0001c0008t0003g0243 a0001c0008t0003g0296 others(71): Show |
75 | HG00408.hp2 HG00438.hp2 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.205-8796C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27411099 | |||||||
chr8:27411113 | G | A | 8 | a0001c0010t0003g0229 a0001c0010t0003g0230 a0001c0010t0003g0231 others(5): Show |
8 | HG02486.hp1 HG02647.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.205-8782G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27411113 | |||||||
chr8:27411171 | G | T | 44 | a0001c0007t0003g0277 a0001c0007t0003g0278 a0001c0007t0003g0279 others(41): Show |
45 | HG00099.hp2 HG00423.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.205-8724G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27411171 | |||||||
chr8:27411233 | T | C | 248 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(245): Show |
253 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.205-8662T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27411233 | |||||||
chr8:27411307 | G | C | 1 | a0002c0017t0002g0252 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.205-8588G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27411307 | |||||||
chr8:27411396 | A | G | 1 | a0001c0001t0003g0081 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.205-8499A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27411396 | |||||||
chr8:27411471 | T | G | 235 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(232): Show |
240 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.205-8424T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27411471 | |||||||
chr8:27411636 | C | T | 1 | a0001c0010t0003g0289 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.205-8259C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27411636 | |||||||
chr8:27411654 | A | G | 8 | a0001c0010t0003g0229 a0001c0010t0003g0230 a0001c0010t0003g0231 others(5): Show |
8 | HG02486.hp1 HG02647.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.205-8241A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27411654 | |||||||
chr8:27411899 | T | C | 111 | a0001c0002t0001g0295 a0001c0007t0003g0277 a0001c0007t0003g0278 others(108): Show |
113 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.205-7996T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27411899 | |||||||
chr8:27412046 | A | G | 1 | a0001c0001t0003g0175 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.205-7849A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27412046 | |||||||
chr8:27412055 | C | G | 226 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(223): Show |
231 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.205-7840C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27412055 | |||||||
chr8:27412090 | G | A | 5 | a0001c0007t0003g0277 a0001c0007t0003g0278 a0001c0007t0003g0279 others(2): Show |
5 | HG01070.hp2 HG01071.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.205-7805G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27412090 | |||||||
chr8:27412130 | G | A | 237 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(234): Show |
242 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(239): Show |
intron_variant | MODIFIER | c.205-7765G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27412130 | |||||||
chr8:27412161 | G | GTTGA | 117 | a0001c0002t0001g0295 a0001c0007t0003g0277 a0001c0007t0003g0278 others(114): Show |
119 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.205-7716_205-7713d others(6): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27412161 | ||||||
chr8:27412367 | G | C | 1 | a0001c0013t0003g0304 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.205-7528G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27412367 | |||||||
chr8:27412367 | G | T | 231 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(228): Show |
236 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(233): Show |
intron_variant | MODIFIER | c.205-7528G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27412367 | |||||||
chr8:27412597 | C | G | 1 | a0001c0010t0003g0229 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.205-7298C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27412597 | |||||||
chr8:27412706 | C | T | 2 | a0002c0005t0001g0196 a0002c0005t0001g0197 |
2 | NA19056.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.205-7189C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27412706 | |||||||
chr8:27412899 | G | C | 237 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(234): Show |
242 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(239): Show |
intron_variant | MODIFIER | c.205-6996G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27412899 | |||||||
chr8:27412900 | T | G | 114 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(111): Show |
117 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.205-6995T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27412900 | |||||||
chr8:27412909 | G | A | 225 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(222): Show |
230 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.205-6986G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27412909 | |||||||
chr8:27412966 | A | T | 237 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(234): Show |
242 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(239): Show |
intron_variant | MODIFIER | c.205-6929A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27412966 | |||||||
chr8:27413031 | A | T | 1 | a0002c0003t0002g0069 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.205-6864A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27413031 | |||||||
chr8:27413039 | G | GA | 6 | a0001c0007t0003g0277 a0001c0007t0003g0278 a0001c0007t0003g0279 others(3): Show |
6 | HG01070.hp2 HG01071.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.205-6844dupA | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27413039 | ||||||
chr8:27413039 | G | GAAA | 7 | a0001c0002t0001g0295 a0001c0008t0003g0243 a0001c0008t0003g0296 others(4): Show |
7 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.205-6846_205-6844d others(5): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27413039 | ||||||
chr8:27413039 | GA | G | 66 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(63): Show |
67 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.205-6844delA | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27413039 | ||||||
chr8:27413070 | TA | T | 5 | a0001c0007t0003g0277 a0001c0007t0003g0278 a0001c0007t0003g0279 others(2): Show |
5 | HG01070.hp2 HG01071.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.205-6824delA | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27413070 | |||||||
chr8:27413241 | G | A | 3 | a0002c0004t0002g0094 a0002c0004t0002g0109 a0002c0004t0002g0110 |
3 | HG00741.hp2 HG03490.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.205-6654G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27413241 | |||||||
chr8:27413324 | G | A | 1 | a0001c0001t0003g0199 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.205-6571G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27413324 | |||||||
chr8:27413330 | A | G | 4 | a0002c0005t0001g0194 a0002c0005t0001g0195 a0002c0005t0001g0200 others(1): Show |
4 | HG01081.hp2 HG01123.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.205-6565A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27413330 | |||||||
chr8:27413421 | T | C | 1 | a0001c0010t0003g0231 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.205-6474T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27413421 | |||||||
chr8:27413463 | G | A | 2 | a0001c0007t0003g0277 a0001c0007t0003g0278 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.205-6432G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27413463 | |||||||
chr8:27413553 | A | T | 1 | a0001c0030t0002g0007 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.205-6342A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27413553 | |||||||
chr8:27413562 | C | A | 3 | a0001c0002t0001g0158 a0001c0002t0001g0159 a0001c0002t0001g0160 |
3 | HG00544.hp2 NA19074.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.205-6333C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27413562 | |||||||
chr8:27413570 | T | C | 6 | a0001c0011t0001g0079 a0001c0011t0001g0098 a0001c0011t0001g0140 others(3): Show |
6 | HG01192.hp1 HG02056.hp2 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.205-6325T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27413570 | |||||||
chr8:27413668 | T | C | 1 | a0001c0010t0003g0230 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.205-6227T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27413668 | |||||||
chr8:27413717 | T | A | 3 | a0001c0013t0003g0301 a0001c0013t0003g0302 a0001c0013t0003g0304 |
3 | HG00639.hp1 HG02723.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.205-6178T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27413717 | |||||||
chr8:27413725 | G | A | 3 | a0001c0008t0003g0292 a0001c0008t0003g0319 a0001c0008t0003g0320 |
3 | HG02723.hp2 HG02896.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.205-6170G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27413725 | |||||||
chr8:27413856 | A | G | 1 | a0002c0004t0002g0112 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.205-6039A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27413856 | |||||||
chr8:27413988 | T | G | 1 | a0001c0008t0003g0114 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.205-5907T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27413988 | |||||||
chr8:27414001 | A | G | 4 | a0002c0005t0001g0194 a0002c0005t0001g0195 a0002c0005t0001g0200 others(1): Show |
4 | HG01081.hp2 HG01123.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.205-5894A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27414001 | |||||||
chr8:27414065 | A | G | 115 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(112): Show |
118 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.205-5830A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27414065 | |||||||
chr8:27414106 | G | A | 9 | a0001c0002t0001g0295 a0001c0008t0003g0243 a0001c0008t0003g0296 others(6): Show |
9 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.205-5789G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27414106 | |||||||
chr8:27414246 | GCTT | G | 3 | a0001c0008t0003g0292 a0001c0008t0003g0319 a0001c0008t0003g0320 |
3 | HG02723.hp2 HG02896.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.205-5642_205-5640d others(5): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27414246 | ||||||
chr8:27414253 | CT | C | 225 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(222): Show |
230 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(227): Show |
intron_variant | MODIFIER | c.205-5631delT | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27414253 | ||||||
chr8:27414280 | T | C | 8 | a0001c0001t0003g0022 a0001c0001t0003g0294 a0001c0007t0003g0303 others(5): Show |
8 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.205-5615T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27414280 | |||||||
chr8:27414340 | G | T | 1 | a0002c0003t0002g0271 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.205-5555G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27414340 | |||||||
chr8:27414405 | C | T | 1 | a0002c0023t0001g0123 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.205-5490C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27414405 | |||||||
chr8:27414493 | G | A | 1 | a0001c0010t0003g0289 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.205-5402G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27414493 | |||||||
chr8:27414528 | G | A | 1 | a0001c0002t0001g0155 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.205-5367G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27414528 | |||||||
chr8:27414543 | G | T | 1 | a0001c0010t0003g0232 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.205-5352G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27414543 | |||||||
chr8:27414588 | G | A | 1 | a0001c0010t0003g0229 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.205-5307G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27414588 | |||||||
chr8:27414602 | C | G | 11 | a0001c0002t0001g0295 a0001c0008t0003g0243 a0001c0008t0003g0296 others(8): Show |
12 | HG00733.hp2 HG01257.hp1 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.205-5293C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27414602 | |||||||
chr8:27414604 | C | G | 73 | a0001c0002t0001g0295 a0001c0008t0003g0243 a0001c0008t0003g0296 others(70): Show |
74 | HG00408.hp2 HG00438.hp2 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.205-5291C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27414604 | |||||||
chr8:27414606 | C | CTCTCTCT others(25): Show |
6 | a0002c0003t0002g0012 a0002c0004t0002g0001 a0002c0004t0002g0011 others(3): Show |
8 | NA18949.hp2 NA18968.hp2 NA18980.hp2 others(5): Show |
intron_variant | MODIFIER | c.205-5288_205-5287i others(34): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27414606 | ||||||
chr8:27414606 | C | CTCTCTGT others(21): Show |
3 | a0002c0006t0001g0006 a0002c0006t0001g0010 a0002c0006t0001g0282 |
3 | HG00738.hp1 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.205-5288_205-5287i others(30): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27414606 | ||||||
chr8:27414606 | C | CTCTGTGT others(21): Show |
9 | a0001c0007t0003g0303 a0001c0008t0003g0114 a0001c0010t0003g0230 others(6): Show |
9 | HG02486.hp1 HG02630.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.205-5288_205-5287i others(30): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27414606 | ||||||
chr8:27414606 | C | CTCTGTGT others(23): Show |
1 | a0002c0006t0002g0317 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.205-5288_205-5287i others(32): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27414606 | ||||||
chr8:27414606 | C | G | 89 | a0001c0001t0003g0097 a0001c0001t0003g0199 a0001c0001t0003g0227 others(86): Show |
90 | HG00408.hp2 HG00438.hp2 HG00621.hp2 others(87): Show |
intron_variant | MODIFIER | c.205-5289C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27414606 | |||||||
chr8:27414608 | G | GTGTGTGT others(19): Show |
1 | a0001c0010t0003g0229 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.205-5272_205-5271i others(28): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27414608 | ||||||
chr8:27414608 | G | GTGTGTGT others(21): Show |
143 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(140): Show |
145 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.205-5274_205-5273i others(30): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27414608 | ||||||
chr8:27414608 | G | GTGTGTGT others(23): Show |
67 | a0001c0008t0003g0314 a0001c0008t0003g0315 a0001c0009t0002g0103 others(64): Show |
68 | HG00408.hp2 HG00438.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.205-5274_205-5273i others(32): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27414608 | ||||||
chr8:27414608 | G | GTGTGTGT others(25): Show |
2 | a0001c0008t0003g0316 a0002c0006t0001g0287 |
2 | HG02258.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.205-5274_205-5273i others(34): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27414608 | ||||||
chr8:27414608 | G | GTGTGTGT others(27): Show |
1 | a0002c0023t0001g0123 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.205-5274_205-5273i others(36): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27414608 | ||||||
chr8:27414608 | G | GTGTGTGT others(23): Show |
2 | a0001c0008t0003g0243 a0001c0008t0003g0296 |
2 | HG02109.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.205-5274_205-5273i others(32): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27414608 | ||||||
chr8:27414608 | G | GTGTGTGT others(21): Show |
1 | a0001c0002t0001g0295 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.205-5274_205-5273i others(30): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27414608 | ||||||
chr8:27414608 | G | T | 19 | a0001c0007t0003g0303 a0001c0008t0003g0114 a0001c0010t0003g0230 others(16): Show |
21 | HG00738.hp1 HG02486.hp1 HG02630.hp2 others(18): Show |
intron_variant | MODIFIER | c.205-5287G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27414608 | |||||||
chr8:27414618 | G | T | 1 | a0001c0002t0001g0168 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.205-5277G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27414618 | |||||||
chr8:27414781 | C | G | 5 | a0001c0001t0003g0227 a0001c0001t0003g0228 a0001c0001t0003g0276 others(2): Show |
5 | HG02572.hp2 HG02818.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.205-5114C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27414781 | |||||||
chr8:27414843 | T | C | 235 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(232): Show |
240 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.205-5052T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27414843 | |||||||
chr8:27414884 | G | A | 1 | a0001c0030t0002g0007 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.205-5011G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27414884 | |||||||
chr8:27414890 | AC | A | 74 | a0001c0002t0001g0295 a0001c0008t0003g0243 a0001c0008t0003g0296 others(71): Show |
75 | HG00408.hp2 HG00438.hp2 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.205-5004delC | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27414890 | |||||||
chr8:27415068 | G | A | 67 | a0001c0009t0002g0103 a0001c0010t0003g0289 a0001c0012t0004g0027 others(64): Show |
68 | HG00408.hp2 HG00438.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.205-4827G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27415068 | |||||||
chr8:27415080 | TTTTG | T | 6 | a0002c0003t0002g0012 a0002c0004t0002g0001 a0002c0004t0002g0011 others(3): Show |
8 | NA18949.hp2 NA18968.hp2 NA18980.hp2 others(5): Show |
intron_variant | MODIFIER | c.205-4803_205-4800d others(6): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27415080 | ||||||
chr8:27415126 | C | T | 1 | a0001c0002t0001g0130 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.205-4769C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27415126 | |||||||
chr8:27415274 | G | C | 3 | a0001c0008t0003g0292 a0001c0008t0003g0319 a0001c0008t0003g0320 |
3 | HG02723.hp2 HG02896.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.205-4621G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27415274 | |||||||
chr8:27415646 | G | A | 10 | a0001c0010t0003g0229 a0001c0010t0003g0230 a0001c0010t0003g0231 others(7): Show |
10 | HG00738.hp1 HG02486.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.205-4249G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27415646 | |||||||
chr8:27415692 | A | G | 6 | a0001c0011t0001g0079 a0001c0011t0001g0098 a0001c0011t0001g0140 others(3): Show |
6 | HG01192.hp1 HG02056.hp2 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.205-4203A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27415692 | |||||||
chr8:27415783 | A | G | 3 | a0001c0008t0003g0292 a0001c0008t0003g0319 a0001c0008t0003g0320 |
3 | HG02723.hp2 HG02896.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.205-4112A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27415783 | |||||||
chr8:27415831 | T | C | 116 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(113): Show |
119 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.205-4064T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27415831 | |||||||
chr8:27415866 | C | T | 100 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(97): Show |
101 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.205-4029C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27415866 | |||||||
chr8:27415896 | TAGAG | T | 7 | a0001c0002t0001g0173 a0001c0002t0001g0174 a0001c0002t0001g0176 others(4): Show |
7 | HG01884.hp2 HG02647.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.205-3995_205-3992d others(6): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27415896 | ||||||
chr8:27415933 | A | G | 2 | a0002c0006t0001g0006 a0002c0006t0001g0010 |
2 | HG00738.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.205-3962A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27415933 | |||||||
chr8:27416112 | C | A | 235 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(232): Show |
240 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.205-3783C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27416112 | |||||||
chr8:27416113 | A | C | 235 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(232): Show |
240 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.205-3782A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27416113 | |||||||
chr8:27416135 | A | C | 1 | a0002c0006t0001g0282 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.205-3760A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27416135 | |||||||
chr8:27416150 | G | T | 117 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(114): Show |
120 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.205-3745G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27416150 | |||||||
chr8:27416323 | A | G | 16 | a0001c0010t0003g0229 a0001c0010t0003g0230 a0001c0010t0003g0231 others(13): Show |
18 | HG00738.hp1 HG02486.hp1 HG02647.hp1 others(15): Show |
intron_variant | MODIFIER | c.205-3572A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27416323 | |||||||
chr8:27416394 | C | T | 22 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(19): Show |
23 | HG00408.hp1 HG00639.hp2 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.205-3501C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27416394 | |||||||
chr8:27416525 | CTG | C | 112 | a0001c0002t0001g0295 a0001c0007t0003g0277 a0001c0007t0003g0278 others(109): Show |
114 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.205-3367_205-3366d others(4): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27416525 | ||||||
chr8:27416527 | G | A | 116 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(113): Show |
119 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.205-3368G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27416527 | |||||||
chr8:27416650 | A | G | 1 | a0001c0009t0002g0313 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.205-3245A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27416650 | |||||||
chr8:27416662 | A | G | 1 | a0002c0003t0002g0259 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.205-3233A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27416662 | |||||||
chr8:27416723 | C | T | 6 | a0002c0003t0002g0012 a0002c0004t0002g0001 a0002c0004t0002g0011 others(3): Show |
8 | NA18949.hp2 NA18968.hp2 NA18980.hp2 others(5): Show |
intron_variant | MODIFIER | c.205-3172C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27416723 | |||||||
chr8:27416726 | T | C | 1 | a0002c0006t0001g0050 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.205-3169T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27416726 | |||||||
chr8:27416728 | A | G | 1 | a0002c0003t0002g0300 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.205-3167A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27416728 | |||||||
chr8:27416914 | G | A | 116 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(113): Show |
119 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.205-2981G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27416914 | |||||||
chr8:27417080 | C | T | 116 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(113): Show |
119 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.205-2815C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27417080 | |||||||
chr8:27417114 | G | T | 231 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(228): Show |
236 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(233): Show |
intron_variant | MODIFIER | c.205-2781G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27417114 | |||||||
chr8:27417206 | C | T | 1 | a0002c0006t0001g0323 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.205-2689C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27417206 | |||||||
chr8:27417207 | A | G | 231 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(228): Show |
236 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(233): Show |
intron_variant | MODIFIER | c.205-2688A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27417207 | |||||||
chr8:27417258 | G | A | 228 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(225): Show |
233 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.205-2637G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27417258 | |||||||
chr8:27417281 | G | A | 1 | a0001c0007t0003g0135 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.205-2614G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27417281 | |||||||
chr8:27417396 | G | C | 8 | a0001c0010t0003g0229 a0001c0010t0003g0230 a0001c0010t0003g0231 others(5): Show |
8 | HG02486.hp1 HG02647.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.205-2499G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27417396 | |||||||
chr8:27417414 | T | C | 100 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(97): Show |
101 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.205-2481T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27417414 | |||||||
chr8:27417441 | G | A | 2 | a0001c0001t0003g0015 a0001c0001t0003g0016 |
2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.205-2454G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27417441 | |||||||
chr8:27417447 | A | AGG | 14 | a0002c0003t0002g0004 a0002c0003t0002g0067 a0002c0003t0002g0239 others(11): Show |
15 | HG00408.hp2 HG00733.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.205-2446_205-2445d others(4): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27417447 | ||||||
chr8:27417558 | T | A | 228 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(225): Show |
233 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.205-2337T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27417558 | |||||||
chr8:27417777 | A | G | 235 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(232): Show |
240 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.205-2118A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27417777 | |||||||
chr8:27417835 | G | A | 116 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(113): Show |
119 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.205-2060G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27417835 | |||||||
chr8:27417954 | G | A | 4 | a0001c0001t0003g0088 a0001c0001t0003g0113 a0001c0001t0003g0115 others(1): Show |
4 | HG02559.hp1 HG02572.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.205-1941G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27417954 | |||||||
chr8:27417968 | G | A | 8 | a0001c0010t0003g0229 a0001c0010t0003g0230 a0001c0010t0003g0231 others(5): Show |
8 | HG02486.hp1 HG02647.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.205-1927G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27417968 | |||||||
chr8:27417992 | A | G | 238 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(235): Show |
243 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(240): Show |
intron_variant | MODIFIER | c.205-1903A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27417992 | |||||||
chr8:27418001 | G | A | 116 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(113): Show |
119 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.205-1894G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27418001 | |||||||
chr8:27418132 | T | G | 100 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(97): Show |
101 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.205-1763T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27418132 | |||||||
chr8:27418209 | G | T | 112 | a0001c0002t0001g0295 a0001c0007t0003g0277 a0001c0007t0003g0278 others(109): Show |
114 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.205-1686G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27418209 | |||||||
chr8:27418251 | A | C | 1 | a0001c0001t0003g0228 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.205-1644A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27418251 | |||||||
chr8:27418277 | T | C | 106 | a0001c0002t0001g0295 a0001c0008t0003g0114 a0001c0008t0003g0243 others(103): Show |
108 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.205-1618T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27418277 | |||||||
chr8:27418283 | C | T | 8 | a0001c0010t0003g0229 a0001c0010t0003g0230 a0001c0010t0003g0231 others(5): Show |
8 | HG02486.hp1 HG02647.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.205-1612C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27418283 | |||||||
chr8:27418387 | T | C | 113 | a0001c0002t0001g0295 a0001c0008t0003g0114 a0001c0008t0003g0243 others(110): Show |
115 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.205-1508T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27418387 | |||||||
chr8:27418466 | A | T | 8 | a0001c0010t0003g0229 a0001c0010t0003g0230 a0001c0010t0003g0231 others(5): Show |
8 | HG02486.hp1 HG02647.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.205-1429A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27418466 | |||||||
chr8:27418594 | C | T | 243 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(240): Show |
248 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.205-1301C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27418594 | |||||||
chr8:27418692 | T | C | 106 | a0001c0002t0001g0295 a0001c0008t0003g0114 a0001c0008t0003g0243 others(103): Show |
108 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.205-1203T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27418692 | |||||||
chr8:27418751 | G | T | 6 | a0001c0007t0003g0277 a0001c0007t0003g0278 a0001c0007t0003g0279 others(3): Show |
6 | HG01070.hp2 HG01071.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.205-1144G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27418751 | |||||||
chr8:27418772 | A | C | 106 | a0001c0002t0001g0295 a0001c0008t0003g0114 a0001c0008t0003g0243 others(103): Show |
108 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.205-1123A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27418772 | |||||||
chr8:27419009 | C | A | 116 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(113): Show |
119 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.205-886C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27419009 | |||||||
chr8:27419030 | GA | G | 99 | a0001c0008t0003g0114 a0001c0009t0002g0103 a0001c0009t0002g0107 others(96): Show |
101 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.205-855delA | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | INFO_REALIGN_3_PRIME | chr8 | 27419030 | ||||||
chr8:27419099 | G | A | 6 | a0002c0003t0002g0012 a0002c0004t0002g0001 a0002c0004t0002g0011 others(3): Show |
8 | NA18949.hp2 NA18968.hp2 NA18980.hp2 others(5): Show |
intron_variant | MODIFIER | c.205-796G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27419099 | |||||||
chr8:27419100 | C | T | 99 | a0001c0008t0003g0114 a0001c0009t0002g0103 a0001c0009t0002g0107 others(96): Show |
101 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.205-795C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27419100 | |||||||
chr8:27419124 | A | G | 6 | a0001c0007t0003g0277 a0001c0007t0003g0278 a0001c0007t0003g0279 others(3): Show |
6 | HG01070.hp2 HG01071.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.205-771A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27419124 | |||||||
chr8:27419188 | G | A | 6 | a0002c0003t0002g0003 a0002c0003t0002g0260 a0002c0003t0002g0262 others(3): Show |
7 | HG00099.hp2 HG00741.hp1 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.205-707G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27419188 | |||||||
chr8:27419252 | T | C | 228 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(225): Show |
233 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.205-643T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27419252 | |||||||
chr8:27419487 | T | C | 6 | a0001c0001t0003g0022 a0001c0001t0003g0294 a0001c0013t0003g0301 others(3): Show |
6 | HG00639.hp1 HG00733.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.205-408T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27419487 | |||||||
chr8:27419638 | T | C | 5 | a0001c0002t0001g0080 a0001c0002t0001g0157 a0001c0002t0001g0161 others(2): Show |
5 | HG01928.hp2 NA18978.hp1 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.205-257T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 2/30 | chr8 | 27419638 | |||||||
chr8:27420111 | G | A | 3 | a0001c0008t0003g0314 a0001c0008t0003g0315 a0001c0008t0003g0316 |
3 | HG02258.hp1 HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.383+38G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 3/30 | chr8 | 27420111 | |||||||
chr8:27420125 | G | A | 6 | a0001c0007t0003g0277 a0001c0007t0003g0278 a0001c0007t0003g0279 others(3): Show |
6 | HG01070.hp2 HG01071.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.383+52G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 3/30 | chr8 | 27420125 | |||||||
chr8:27420161 | C | A | 2 | a0002c0003t0002g0003 a0002c0003t0002g0262 |
3 | HG01069.hp2 HG01071.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.383+88C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 3/30 | chr8 | 27420161 | |||||||
chr8:27420422 | G | A | 1 | a0002c0017t0002g0252 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.384-235G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 3/30 | chr8 | 27420422 | |||||||
chr8:27420514 | G | A | 1 | a0001c0001t0003g0034 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.384-143G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 3/30 | chr8 | 27420514 | |||||||
chr8:27420549 | C | A | 1 | a0001c0002t0001g0170 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.384-108C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 3/30 | chr8 | 27420549 | |||||||
chr8:27420641 | G | A | 1 | a0001c0001t0003g0071 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.384-16G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 3/30 | chr8 | 27420641 | |||||||
chr8:27420785 | C | T | 2 | a0002c0004t0002g0209 a0002c0004t0002g0210 |
2 | NA18962.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.471+41C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 4/30 | chr8 | 27420785 | |||||||
chr8:27420790 | C | T | 1 | a0002c0006t0001g0323 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.471+46C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 4/30 | chr8 | 27420790 | |||||||
chr8:27420904 | G | A | 7 | a0001c0001t0003g0181 a0001c0001t0003g0182 a0001c0001t0003g0183 others(4): Show |
7 | HG02055.hp1 HG02257.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.471+160G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 4/30 | chr8 | 27420904 | |||||||
chr8:27421029 | A | G | 1 | a0001c0002t0001g0158 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.471+285A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 4/30 | chr8 | 27421029 | |||||||
chr8:27421278 | C | CTATT | 9 | a0001c0002t0001g0078 a0001c0002t0001g0118 a0001c0002t0001g0138 others(6): Show |
9 | HG00673.hp2 HG02040.hp1 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.471+580_471+583dup others(4): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr8 | 27421278 | ||||||
chr8:27421278 | CTATT | C | 129 | a0001c0001t0003g0184 a0001c0002t0001g0005 a0001c0002t0001g0076 others(126): Show |
133 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.471+580_471+583del others(4): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr8 | 27421278 | ||||||
chr8:27421278 | CTATTTAT others(1): Show |
C | 35 | a0001c0001t0003g0022 a0001c0001t0003g0088 a0001c0001t0003g0113 others(32): Show |
35 | HG00639.hp1 HG00733.hp1 HG02258.hp2 others(32): Show |
intron_variant | MODIFIER | c.471+576_471+583del others(8): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr8 | 27421278 | ||||||
chr8:27421278 | CTATTTAT others(5): Show |
C | 2 | a0001c0007t0003g0277 a0001c0007t0003g0278 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.471+572_471+583del others(12): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr8 | 27421278 | ||||||
chr8:27421278 | CTATTTAT others(9): Show |
C | 1 | a0001c0011t0001g0140 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.471+568_471+583del others(16): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr8 | 27421278 | ||||||
chr8:27421278 | CTATTTAT others(17): Show |
C | 77 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(74): Show |
78 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.471+560_471+583del others(24): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 4/30 | INFO_REALIGN_3_PRIME | chr8 | 27421278 | ||||||
chr8:27421330 | A | G | 117 | a0001c0001t0003g0063 a0001c0001t0003g0064 a0001c0001t0003g0065 others(114): Show |
119 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.471+586A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 4/30 | chr8 | 27421330 | |||||||
chr8:27421334 | G | T | 1 | a0001c0001t0003g0318 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.471+590G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 4/30 | chr8 | 27421334 | |||||||
chr8:27421340 | T | G | 7 | a0001c0002t0001g0295 a0001c0008t0003g0243 a0001c0008t0003g0296 others(4): Show |
7 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.471+596T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 4/30 | chr8 | 27421340 | |||||||
chr8:27421467 | C | T | 1 | a0001c0001t0003g0093 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.471+723C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 4/30 | chr8 | 27421467 | |||||||
chr8:27421517 | A | C | 1 | a0001c0001t0003g0065 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.471+773A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 4/30 | chr8 | 27421517 | |||||||
chr8:27421546 | A | C | 6 | a0002c0003t0002g0012 a0002c0004t0002g0001 a0002c0004t0002g0011 others(3): Show |
8 | NA18949.hp2 NA18968.hp2 NA18980.hp2 others(5): Show |
intron_variant | MODIFIER | c.472-758A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 4/30 | chr8 | 27421546 | |||||||
chr8:27421587 | A | G | 8 | a0001c0010t0003g0229 a0001c0010t0003g0230 a0001c0010t0003g0231 others(5): Show |
8 | HG02486.hp1 HG02647.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.472-717A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 4/30 | chr8 | 27421587 | |||||||
chr8:27421590 | A | G | 8 | a0001c0010t0003g0229 a0001c0010t0003g0230 a0001c0010t0003g0231 others(5): Show |
8 | HG02486.hp1 HG02647.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.472-714A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 4/30 | chr8 | 27421590 | |||||||
chr8:27421682 | C | A | 17 | a0001c0010t0003g0229 a0001c0010t0003g0230 a0001c0010t0003g0231 others(14): Show |
19 | HG00738.hp1 HG02486.hp1 HG02647.hp1 others(16): Show |
intron_variant | MODIFIER | c.472-622C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 4/30 | chr8 | 27421682 | |||||||
chr8:27421706 | T | C | 239 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(236): Show |
244 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(241): Show |
intron_variant | MODIFIER | c.472-598T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 4/30 | chr8 | 27421706 | |||||||
chr8:27421857 | G | A | 1 | a0001c0002t0001g0188 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.472-447G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 4/30 | chr8 | 27421857 | |||||||
chr8:27421883 | A | C | 239 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(236): Show |
244 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(241): Show |
intron_variant | MODIFIER | c.472-421A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 4/30 | chr8 | 27421883 | |||||||
chr8:27422039 | C | T | 2 | a0001c0011t0001g0140 a0001c0011t0001g0166 |
2 | NA18949.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.472-265C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 4/30 | chr8 | 27422039 | |||||||
chr8:27422142 | C | A | 1 | a0002c0003t0004g0272 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.472-162C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 4/30 | chr8 | 27422142 | |||||||
chr8:27422188 | G | A | 236 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(233): Show |
241 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.472-116G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 4/30 | chr8 | 27422188 | |||||||
chr8:27422200 | G | C | 1 | a0001c0002t0001g0118 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.472-104G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 4/30 | chr8 | 27422200 | |||||||
chr8:27422600 | C | G | 99 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(96): Show |
100 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.551+217C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27422600 | |||||||
chr8:27422885 | C | T | 3 | a0002c0003t0002g0223 a0002c0003t0002g0310 a0002c0006t0002g0317 |
3 | NA18961.hp1 NA18969.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.551+502C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27422885 | |||||||
chr8:27422923 | G | A | 5 | a0001c0002t0001g0077 a0001c0002t0001g0119 a0001c0002t0001g0120 others(2): Show |
5 | NA18945.hp2 NA18957.hp2 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.551+540G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27422923 | |||||||
chr8:27422955 | G | A | 5 | a0001c0001t0003g0227 a0001c0001t0003g0228 a0001c0001t0003g0276 others(2): Show |
5 | HG02572.hp2 HG02818.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.551+572G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27422955 | |||||||
chr8:27423279 | C | G | 1 | a0004c0015t0001g0193 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.551+896C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27423279 | |||||||
chr8:27423296 | C | T | 1 | a0001c0001t0003g0031 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.551+913C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27423296 | |||||||
chr8:27423343 | C | T | 116 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(113): Show |
119 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.551+960C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27423343 | |||||||
chr8:27423426 | C | T | 1 | a0001c0009t0002g0237 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.551+1043C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27423426 | |||||||
chr8:27423427 | G | A | 1 | a0002c0004t0002g0298 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.551+1044G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27423427 | |||||||
chr8:27423479 | A | C | 1 | a0002c0006t0001g0282 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.551+1096A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27423479 | |||||||
chr8:27423519 | G | A | 3 | a0001c0013t0003g0301 a0001c0013t0003g0302 a0001c0013t0003g0304 |
3 | HG00639.hp1 HG02723.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.551+1136G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27423519 | |||||||
chr8:27423595 | G | T | 1 | a0001c0001t0003g0276 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.551+1212G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27423595 | |||||||
chr8:27423616 | G | A | 1 | a0002c0003t0002g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.551+1233G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27423616 | |||||||
chr8:27423665 | T | C | 235 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(232): Show |
240 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.551+1282T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27423665 | |||||||
chr8:27423719 | C | T | 3 | a0001c0001t0003g0081 a0001c0001t0003g0082 a0001c0001t0003g0205 |
3 | HG00738.hp2 HG01346.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.551+1336C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27423719 | |||||||
chr8:27423750 | G | A | 2 | a0001c0001t0003g0060 a0001c0001t0005g0059 |
2 | HG01069.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.551+1367G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27423750 | |||||||
chr8:27423920 | G | C | 1 | a0002c0006t0001g0282 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.551+1537G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27423920 | |||||||
chr8:27424323 | G | A | 1 | a0001c0002t0001g0167 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.551+1940G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27424323 | |||||||
chr8:27424379 | T | C | 40 | a0001c0008t0003g0114 a0001c0009t0002g0107 a0001c0012t0004g0053 others(37): Show |
41 | HG00099.hp2 HG00423.hp2 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.551+1996T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27424379 | |||||||
chr8:27424395 | G | A | 63 | a0001c0009t0002g0103 a0001c0012t0004g0027 a0001c0012t0004g0211 others(60): Show |
64 | HG00408.hp2 HG00438.hp2 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.551+2012G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27424395 | |||||||
chr8:27424546 | C | T | 116 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(113): Show |
119 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.551+2163C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27424546 | |||||||
chr8:27424692 | C | T | 1 | a0002c0003t0002g0267 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.551+2309C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27424692 | |||||||
chr8:27424871 | GA | G | 226 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(223): Show |
231 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.551+2499delA | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | INFO_REALIGN_3_PRIME | chr8 | 27424871 | ||||||
chr8:27424880 | A | T | 1 | a0002c0004t0002g0209 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.551+2497A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27424880 | |||||||
chr8:27425084 | TTA | T | 116 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(113): Show |
119 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.551+2703_551+2704d others(4): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | INFO_REALIGN_3_PRIME | chr8 | 27425084 | ||||||
chr8:27425101 | A | G | 3 | a0001c0001t0003g0039 a0001c0001t0003g0048 a0001c0001t0003g0052 |
3 | HG02080.hp1 NA18978.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.551+2718A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27425101 | |||||||
chr8:27425254 | T | G | 39 | a0001c0008t0003g0114 a0001c0009t0002g0107 a0001c0012t0004g0053 others(36): Show |
40 | HG00099.hp2 HG00423.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.551+2871T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27425254 | |||||||
chr8:27425520 | C | G | 63 | a0001c0009t0002g0103 a0001c0012t0004g0027 a0001c0012t0004g0211 others(60): Show |
64 | HG00408.hp2 HG00438.hp2 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.551+3137C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27425520 | |||||||
chr8:27425675 | A | G | 100 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(97): Show |
101 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.551+3292A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27425675 | |||||||
chr8:27425744 | C | T | 8 | a0001c0010t0003g0229 a0001c0010t0003g0230 a0001c0010t0003g0231 others(5): Show |
8 | HG02486.hp1 HG02647.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.551+3361C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27425744 | |||||||
chr8:27425961 | G | T | 1 | a0001c0002t0001g0152 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.551+3578G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27425961 | |||||||
chr8:27425987 | T | C | 1 | a0001c0030t0002g0007 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.551+3604T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27425987 | |||||||
chr8:27426071 | C | A | 1 | a0001c0030t0002g0007 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.551+3688C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27426071 | |||||||
chr8:27426107 | G | A | 1 | a0001c0009t0002g0312 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.551+3724G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27426107 | |||||||
chr8:27426121 | G | A | 1 | a0002c0003t0002g0180 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.551+3738G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27426121 | |||||||
chr8:27426156 | C | T | 4 | a0001c0009t0002g0107 a0002c0003t0002g0270 a0002c0003t0002g0274 others(1): Show |
4 | HG00423.hp2 HG02080.hp2 NA18943.hp1 others(1): Show |
intron_variant | MODIFIER | c.551+3773C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27426156 | |||||||
chr8:27426209 | A | G | 1 | a0007c0032t0003g0284 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.551+3826A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27426209 | |||||||
chr8:27426507 | A | G | 3 | a0001c0008t0003g0314 a0001c0008t0003g0315 a0001c0008t0003g0316 |
3 | HG02258.hp1 HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.552-3586A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27426507 | |||||||
chr8:27426537 | A | G | 3 | a0001c0001t0003g0063 a0001c0001t0003g0064 a0001c0001t0003g0322 |
3 | HG02055.hp2 HG02109.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.552-3556A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27426537 | |||||||
chr8:27426558 | CAGACATT others(22): Show |
C | 6 | a0002c0003t0002g0012 a0002c0004t0002g0001 a0002c0004t0002g0011 others(3): Show |
8 | NA18949.hp2 NA18968.hp2 NA18980.hp2 others(5): Show |
intron_variant | MODIFIER | c.552-3504_552-3476d others(31): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | INFO_REALIGN_3_PRIME | chr8 | 27426558 | ||||||
chr8:27426582 | G | T | 1 | a0001c0010t0003g0233 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.552-3511G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27426582 | |||||||
chr8:27426855 | T | C | 1 | a0001c0001t0003g0093 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.552-3238T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27426855 | |||||||
chr8:27426857 | A | G | 1 | a0002c0006t0001g0050 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.552-3236A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27426857 | |||||||
chr8:27426877 | G | A | 116 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(113): Show |
119 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.552-3216G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27426877 | |||||||
chr8:27426907 | T | G | 1 | a0001c0007t0003g0136 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.552-3186T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27426907 | |||||||
chr8:27426994 | A | G | 5 | a0001c0007t0003g0277 a0001c0007t0003g0278 a0001c0007t0003g0279 others(2): Show |
5 | HG01070.hp2 HG01071.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.552-3099A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27426994 | |||||||
chr8:27427005 | G | A | 1 | a0001c0022t0002g0008 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.552-3088G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27427005 | |||||||
chr8:27427070 | C | T | 3 | a0001c0007t0003g0279 a0001c0007t0003g0280 a0001c0007t0003g0281 |
3 | HG02895.hp1 HG02897.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.552-3023C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27427070 | |||||||
chr8:27427139 | T | A | 1 | a0002c0005t0001g0309 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.552-2954T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27427139 | |||||||
chr8:27427140 | C | A | 1 | a0002c0005t0001g0309 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.552-2953C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27427140 | |||||||
chr8:27427141 | T | C | 1 | a0002c0005t0001g0309 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.552-2952T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27427141 | |||||||
chr8:27427175 | C | T | 112 | a0001c0002t0001g0295 a0001c0007t0003g0277 a0001c0007t0003g0278 others(109): Show |
114 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.552-2918C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27427175 | |||||||
chr8:27427254 | A | G | 1 | a0004c0015t0001g0193 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.552-2839A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27427254 | |||||||
chr8:27427506 | C | G | 6 | a0002c0003t0002g0012 a0002c0004t0002g0001 a0002c0004t0002g0011 others(3): Show |
8 | NA18949.hp2 NA18968.hp2 NA18980.hp2 others(5): Show |
intron_variant | MODIFIER | c.552-2587C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27427506 | |||||||
chr8:27427659 | A | C | 1 | a0002c0006t0001g0127 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.552-2434A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27427659 | |||||||
chr8:27427661 | G | A | 3 | a0002c0003t0002g0004 a0002c0003t0002g0067 a0002c0006t0001g0092 |
4 | HG01257.hp1 HG01258.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.552-2432G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27427661 | |||||||
chr8:27427787 | G | C | 7 | a0001c0002t0001g0295 a0001c0008t0003g0243 a0001c0008t0003g0296 others(4): Show |
7 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.552-2306G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27427787 | |||||||
chr8:27428016 | A | G | 235 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(232): Show |
240 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.552-2077A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27428016 | |||||||
chr8:27428196 | G | T | 1 | a0002c0004t0002g0013 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.552-1897G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27428196 | |||||||
chr8:27428208 | G | C | 5 | a0001c0007t0003g0277 a0001c0007t0003g0278 a0001c0007t0003g0279 others(2): Show |
5 | HG01070.hp2 HG01071.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.552-1885G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27428208 | |||||||
chr8:27428444 | C | T | 6 | a0002c0003t0002g0012 a0002c0004t0002g0001 a0002c0004t0002g0011 others(3): Show |
8 | NA18949.hp2 NA18968.hp2 NA18980.hp2 others(5): Show |
intron_variant | MODIFIER | c.552-1649C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27428444 | |||||||
chr8:27428463 | G | T | 3 | a0001c0008t0003g0292 a0001c0008t0003g0319 a0001c0008t0003g0320 |
3 | HG02723.hp2 HG02896.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.552-1630G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27428463 | |||||||
chr8:27428591 | T | C | 1 | a0002c0003t0002g0057 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.552-1502T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27428591 | |||||||
chr8:27428737 | G | T | 1 | a0001c0002t0001g0178 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.552-1356G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27428737 | |||||||
chr8:27428862 | G | A | 116 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(113): Show |
119 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.552-1231G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27428862 | |||||||
chr8:27429094 | A | G | 116 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(113): Show |
119 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.552-999A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27429094 | |||||||
chr8:27429127 | A | G | 4 | a0001c0001t0003g0088 a0001c0001t0003g0113 a0001c0001t0003g0115 others(1): Show |
4 | HG02559.hp1 HG02572.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.552-966A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27429127 | |||||||
chr8:27429331 | C | T | 3 | a0001c0002t0001g0146 a0001c0002t0001g0169 a0001c0002t0001g0306 |
3 | NA19003.hp2 NA19005.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.552-762C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27429331 | |||||||
chr8:27429554 | A | C | 1 | a0001c0001t0003g0022 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.552-539A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27429554 | |||||||
chr8:27429615 | A | T | 8 | a0001c0010t0003g0229 a0001c0010t0003g0230 a0001c0010t0003g0231 others(5): Show |
8 | HG02486.hp1 HG02647.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.552-478A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27429615 | |||||||
chr8:27429621 | T | C | 1 | a0002c0005t0001g0309 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.552-472T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27429621 | |||||||
chr8:27429722 | A | T | 2 | a0001c0001t0003g0015 a0001c0001t0003g0016 |
2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.552-371A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27429722 | |||||||
chr8:27429810 | C | T | 73 | a0001c0002t0001g0295 a0001c0008t0003g0114 a0001c0008t0003g0243 others(70): Show |
75 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.552-283C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 5/30 | chr8 | 27429810 | |||||||
chr8:27430275 | A | G | 1 | a0001c0001t0003g0056 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.615-89A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 6/30 | chr8 | 27430275 | |||||||
chr8:27430359 | T | C | 1 | a0001c0011t0001g0144 | 1 | HG02056.hp2 | splice_region_variant&intron_variant | LOW | c.615-5T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 6/30 | chr8 | 27430359 | |||||||
chr8:27430480 | T | A | 42 | a0001c0008t0003g0114 a0001c0008t0003g0292 a0001c0008t0003g0319 others(39): Show |
43 | HG00099.hp2 HG00423.hp2 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.669+62T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 7/30 | chr8 | 27430480 | |||||||
chr8:27430516 | T | C | 118 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(115): Show |
119 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.669+98T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 7/30 | chr8 | 27430516 | |||||||
chr8:27430548 | A | G | 2 | a0002c0006t0001g0006 a0002c0006t0001g0282 |
2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.669+130A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 7/30 | chr8 | 27430548 | |||||||
chr8:27430612 | C | T | 2 | a0001c0001t0003g0186 a0001c0001t0003g0187 |
2 | HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.669+194C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 7/30 | chr8 | 27430612 | |||||||
chr8:27430748 | G | A | 1 | a0002c0004t0002g0094 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.670-128G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 7/30 | chr8 | 27430748 | |||||||
chr8:27430784 | G | A | 1 | a0001c0001t0003g0046 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.670-92G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 7/30 | chr8 | 27430784 | |||||||
chr8:27430797 | T | C | 37 | a0002c0003t0002g0004 a0002c0003t0002g0012 a0002c0003t0002g0057 others(34): Show |
38 | HG00408.hp2 HG00609.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.670-79T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 7/30 | chr8 | 27430797 | |||||||
chr8:27431294 | C | G | 1 | a0001c0001t0003g0318 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.811-104C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 8/30 | chr8 | 27431294 | |||||||
chr8:27431484 | C | T | 2 | a0002c0006t0001g0006 a0002c0006t0001g0282 |
2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.885+12C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 9/30 | chr8 | 27431484 | |||||||
chr8:27431523 | C | T | 4 | a0001c0002t0001g0078 a0001c0002t0001g0145 a0001c0002t0001g0152 others(1): Show |
4 | NA18945.hp1 NA18980.hp1 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.885+51C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 9/30 | chr8 | 27431523 | |||||||
chr8:27431609 | G | A | 109 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(106): Show |
110 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.885+137G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 9/30 | chr8 | 27431609 | |||||||
chr8:27431804 | T | C | 72 | a0001c0008t0003g0114 a0002c0003t0002g0003 a0002c0003t0002g0023 others(69): Show |
75 | HG00099.hp2 HG00438.hp2 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.885+332T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 9/30 | chr8 | 27431804 | |||||||
chr8:27431892 | G | C | 37 | a0002c0003t0002g0004 a0002c0003t0002g0012 a0002c0003t0002g0057 others(34): Show |
38 | HG00408.hp2 HG00609.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.886-368G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 9/30 | chr8 | 27431892 | |||||||
chr8:27431895 | G | C | 37 | a0002c0003t0002g0004 a0002c0003t0002g0012 a0002c0003t0002g0057 others(34): Show |
38 | HG00408.hp2 HG00609.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.886-365G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 9/30 | chr8 | 27431895 | |||||||
chr8:27431994 | A | AT | 113 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(110): Show |
114 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.886-255dupT | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 9/30 | INFO_REALIGN_3_PRIME | chr8 | 27431994 | ||||||
chr8:27431994 | A | ATT | 6 | a0001c0008t0003g0243 a0001c0008t0003g0296 a0001c0008t0003g0314 others(3): Show |
6 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.886-256_886-255dup others(2): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 9/30 | INFO_REALIGN_3_PRIME | chr8 | 27431994 | ||||||
chr8:27432064 | A | G | 5 | a0001c0008t0003g0243 a0001c0008t0003g0296 a0001c0008t0003g0314 others(2): Show |
5 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.886-196A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 9/30 | chr8 | 27432064 | |||||||
chr8:27432095 | C | T | 113 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(110): Show |
114 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.886-165C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 9/30 | chr8 | 27432095 | |||||||
chr8:27432256 | A | G | 2 | a0002c0004t0002g0244 a0002c0004t0002g0245 |
2 | HG01168.hp1 HG01169.hp2 |
splice_region_variant&intron_variant | LOW | c.886-4A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 9/30 | chr8 | 27432256 | |||||||
chr8:27432418 | T | C | 113 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(110): Show |
114 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.987+57T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 10/30 | chr8 | 27432418 | |||||||
chr8:27432446 | T | C | 113 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(110): Show |
114 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.987+85T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 10/30 | chr8 | 27432446 | |||||||
chr8:27432581 | G | A | 1 | a0001c0008t0003g0114 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.987+220G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 10/30 | chr8 | 27432581 | |||||||
chr8:27432680 | C | T | 1 | a0001c0030t0002g0007 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.987+319C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 10/30 | chr8 | 27432680 | |||||||
chr8:27432767 | G | GCAGAGCG others(2): Show |
113 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(110): Show |
114 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.987+408_987+409ins others(9): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 10/30 | INFO_REALIGN_3_PRIME | chr8 | 27432767 | ||||||
chr8:27432980 | C | T | 1 | a0002c0006t0001g0010 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.988-455C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 10/30 | chr8 | 27432980 | |||||||
chr8:27433011 | G | A | 110 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(107): Show |
111 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.988-424G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 10/30 | chr8 | 27433011 | |||||||
chr8:27433040 | T | C | 2 | a0002c0006t0001g0006 a0002c0006t0001g0282 |
2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.988-395T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 10/30 | chr8 | 27433040 | |||||||
chr8:27433154 | T | G | 1 | a0001c0009t0002g0125 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.988-281T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 10/30 | chr8 | 27433154 | |||||||
chr8:27433216 | G | A | 1 | a0001c0002t0001g0173 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.988-219G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 10/30 | chr8 | 27433216 | |||||||
chr8:27433264 | G | A | 1 | a0002c0026t0001g0238 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.988-171G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 10/30 | chr8 | 27433264 | |||||||
chr8:27433277 | C | CA | 3 | a0001c0008t0003g0292 a0001c0008t0003g0319 a0001c0008t0003g0320 |
3 | HG02723.hp2 HG02896.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.988-157dupA | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 10/30 | INFO_REALIGN_3_PRIME | chr8 | 27433277 | ||||||
chr8:27433987 | G | T | 1 | a0001c0002t0001g0131 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1106-106G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 11/30 | chr8 | 27433987 | |||||||
chr8:27434040 | T | C | 235 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(232): Show |
240 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.1106-53T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 11/30 | chr8 | 27434040 | |||||||
chr8:27434232 | C | T | 78 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(75): Show |
78 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.1145+100C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 12/30 | chr8 | 27434232 | |||||||
chr8:27434367 | C | A | 1 | a0002c0006t0001g0010 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1146-146C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 12/30 | chr8 | 27434367 | |||||||
chr8:27434603 | G | A | 2 | a0002c0003t0002g0236 a0002c0003t0002g0255 |
2 | HG02258.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1192+44G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 13/30 | chr8 | 27434603 | |||||||
chr8:27434770 | A | G | 235 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(232): Show |
240 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.1192+211A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 13/30 | chr8 | 27434770 | |||||||
chr8:27434775 | A | G | 113 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(110): Show |
114 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.1192+216A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 13/30 | chr8 | 27434775 | |||||||
chr8:27434989 | A | T | 1 | a0001c0030t0002g0007 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1192+430A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 13/30 | chr8 | 27434989 | |||||||
chr8:27435220 | C | T | 1 | a0001c0001t0003g0022 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1193-523C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 13/30 | chr8 | 27435220 | |||||||
chr8:27435639 | C | G | 2 | a0002c0006t0001g0006 a0002c0006t0001g0282 |
2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1193-104C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 13/30 | chr8 | 27435639 | |||||||
chr8:27435804 | G | A | 1 | a0001c0001t0003g0088 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1243+11G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 14/30 | chr8 | 27435804 | |||||||
chr8:27435818 | G | T | 65 | a0001c0008t0003g0114 a0002c0003t0002g0003 a0002c0003t0002g0023 others(62): Show |
68 | HG00099.hp2 HG00438.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.1243+25G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 14/30 | chr8 | 27435818 | |||||||
chr8:27436212 | G | A | 1 | a0001c0001t0005g0059 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1244-39G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 14/30 | chr8 | 27436212 | |||||||
chr8:27436364 | T | G | 1 | a0001c0025t0001g0019 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1341+16T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 15/30 | chr8 | 27436364 | |||||||
chr8:27436448 | A | C | 1 | a0002c0006t0001g0127 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1341+100A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 15/30 | chr8 | 27436448 | |||||||
chr8:27436472 | G | A | 103 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(100): Show |
103 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.1341+124G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 15/30 | chr8 | 27436472 | |||||||
chr8:27436609 | T | C | 3 | a0002c0005t0001g0026 a0002c0005t0001g0032 a0002c0005t0001g0033 |
3 | HG01928.hp1 HG01943.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1341+261T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 15/30 | chr8 | 27436609 | |||||||
chr8:27436631 | C | T | 9 | a0001c0010t0003g0229 a0001c0010t0003g0230 a0001c0010t0003g0231 others(6): Show |
9 | HG02486.hp1 HG02647.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1341+283C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 15/30 | chr8 | 27436631 | |||||||
chr8:27436667 | A | G | 1 | a0002c0003t0002g0261 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1341+319A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 15/30 | chr8 | 27436667 | |||||||
chr8:27436745 | GAAGA | G | 5 | a0001c0001t0003g0088 a0001c0001t0003g0113 a0001c0001t0003g0115 others(2): Show |
5 | HG02559.hp1 HG02572.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1342-368_1342-365d others(6): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 15/30 | INFO_REALIGN_3_PRIME | chr8 | 27436745 | ||||||
chr8:27436780 | A | G | 5 | a0001c0001t0003g0088 a0001c0001t0003g0113 a0001c0001t0003g0115 others(2): Show |
5 | HG02559.hp1 HG02572.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1342-342A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 15/30 | chr8 | 27436780 | |||||||
chr8:27436989 | G | A | 1 | a0002c0005t0001g0033 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1342-133G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 15/30 | chr8 | 27436989 | |||||||
chr8:27437015 | C | G | 235 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(232): Show |
240 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.1342-107C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 15/30 | chr8 | 27437015 | |||||||
chr8:27437089 | G | C | 90 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(87): Show |
90 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.1342-33G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 15/30 | chr8 | 27437089 | |||||||
chr8:27437250 | C | T | 1 | a0002c0003t0002g0241 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1426+44C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 16/30 | chr8 | 27437250 | |||||||
chr8:27437306 | T | C | 235 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(232): Show |
240 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.1427-90T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 16/30 | chr8 | 27437306 | |||||||
chr8:27437592 | A | G | 242 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(239): Show |
247 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.1527+96A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 17/30 | chr8 | 27437592 | |||||||
chr8:27438096 | T | A | 7 | a0001c0001t0003g0181 a0001c0001t0003g0182 a0001c0001t0003g0183 others(4): Show |
7 | HG02055.hp1 HG02257.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1643+216T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 18/30 | chr8 | 27438096 | |||||||
chr8:27438281 | G | C | 235 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(232): Show |
240 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.1643+401G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 18/30 | chr8 | 27438281 | |||||||
chr8:27438462 | C | CTGATTCT others(538): Show |
1 | a0008c0020t0002g0014 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1644-566_1644-565i others(547): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 18/30 | INFO_REALIGN_3_PRIME | chr8 | 27438462 | ||||||
chr8:27438462 | C | CTGATTCT others(535): Show |
2 | a0002c0006t0001g0006 a0002c0006t0001g0282 |
2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1644-566_1644-565i others(544): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 18/30 | INFO_REALIGN_3_PRIME | chr8 | 27438462 | ||||||
chr8:27438462 | C | CTGATTCT others(531): Show |
4 | a0001c0007t0003g0277 a0001c0007t0003g0278 a0001c0007t0003g0280 others(1): Show |
4 | HG01070.hp2 HG01071.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1644-566_1644-565i others(540): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 18/30 | INFO_REALIGN_3_PRIME | chr8 | 27438462 | ||||||
chr8:27438462 | C | CTGATTCT others(536): Show |
1 | a0002c0004t0002g0011 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1644-566_1644-565i others(545): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 18/30 | INFO_REALIGN_3_PRIME | chr8 | 27438462 | ||||||
chr8:27438462 | C | CTGATTCT others(535): Show |
160 | a0001c0001t0003g0022 a0001c0001t0003g0088 a0001c0001t0003g0093 others(157): Show |
164 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(161): Show |
intron_variant | MODIFIER | c.1644-566_1644-565i others(544): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 18/30 | INFO_REALIGN_3_PRIME | chr8 | 27438462 | ||||||
chr8:27438462 | C | CTGATTCT others(535): Show |
83 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(80): Show |
84 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.1644-566_1644-565i others(544): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 18/30 | INFO_REALIGN_3_PRIME | chr8 | 27438462 | ||||||
chr8:27438462 | C | CTGATTCT others(539): Show |
2 | a0001c0010t0003g0231 a0002c0003t0002g0310 |
2 | HG02486.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.1644-566_1644-565i others(548): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 18/30 | INFO_REALIGN_3_PRIME | chr8 | 27438462 | ||||||
chr8:27438474 | G | A | 3 | a0002c0003t0002g0270 a0002c0003t0002g0274 a0002c0006t0001g0127 |
3 | HG02080.hp2 NA18943.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.1644-557G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 18/30 | chr8 | 27438474 | |||||||
chr8:27438487 | A | G | 128 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(125): Show |
129 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.1644-544A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 18/30 | chr8 | 27438487 | |||||||
chr8:27438516 | C | T | 1 | a0004c0015t0001g0198 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1644-515C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 18/30 | chr8 | 27438516 | |||||||
chr8:27438573 | G | A | 17 | a0002c0003t0002g0223 a0002c0005t0001g0002 a0002c0005t0001g0083 others(14): Show |
18 | HG00408.hp1 HG00639.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.1644-458G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 18/30 | chr8 | 27438573 | |||||||
chr8:27438639 | C | T | 7 | a0001c0008t0003g0243 a0001c0008t0003g0296 a0001c0008t0003g0314 others(4): Show |
7 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1644-392C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 18/30 | chr8 | 27438639 | |||||||
chr8:27438682 | C | T | 2 | a0002c0006t0001g0006 a0002c0006t0001g0282 |
2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1644-349C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 18/30 | chr8 | 27438682 | |||||||
chr8:27438952 | ATCTG | A | 3 | a0001c0008t0003g0292 a0001c0008t0003g0319 a0001c0008t0003g0320 |
3 | HG02723.hp2 HG02896.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1644-72_1644-69del others(4): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 18/30 | INFO_REALIGN_3_PRIME | chr8 | 27438952 | ||||||
chr8:27438965 | T | C | 1 | a0002c0005t0001g0201 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1644-66T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 18/30 | chr8 | 27438965 | |||||||
chr8:27439147 | A | G | 1 | a0002c0006t0001g0020 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1744+16A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 19/30 | chr8 | 27439147 | |||||||
chr8:27439498 | C | T | 7 | a0001c0008t0003g0243 a0001c0008t0003g0296 a0001c0008t0003g0314 others(4): Show |
7 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1834+100C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27439498 | |||||||
chr8:27439523 | T | G | 7 | a0001c0008t0003g0243 a0001c0008t0003g0296 a0001c0008t0003g0314 others(4): Show |
7 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1834+125T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27439523 | |||||||
chr8:27439629 | A | G | 1 | a0002c0017t0002g0252 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1834+231A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27439629 | |||||||
chr8:27439685 | T | C | 90 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(87): Show |
90 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.1834+287T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27439685 | |||||||
chr8:27439710 | G | T | 1 | a0002c0003t0002g0300 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1834+312G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27439710 | |||||||
chr8:27439821 | C | T | 9 | a0001c0010t0003g0229 a0001c0010t0003g0230 a0001c0010t0003g0231 others(6): Show |
9 | HG02486.hp1 HG02647.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1835-416C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27439821 | |||||||
chr8:27439838 | C | T | 5 | a0001c0002t0001g0077 a0001c0002t0001g0119 a0001c0002t0001g0120 others(2): Show |
5 | NA18945.hp2 NA18957.hp2 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.1835-399C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27439838 | |||||||
chr8:27440058 | G | A | 8 | a0001c0001t0003g0022 a0001c0001t0003g0093 a0001c0001t0003g0294 others(5): Show |
8 | HG00639.hp1 HG00733.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1835-179G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440058 | |||||||
chr8:27440077 | G | A | 104 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(101): Show |
104 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.1835-160G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440077 | |||||||
chr8:27440108 | G | C | 67 | a0001c0008t0003g0114 a0002c0003t0002g0003 a0002c0003t0002g0023 others(64): Show |
70 | HG00099.hp2 HG00438.hp2 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.1835-129G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440108 | |||||||
chr8:27440164 | A | C | 1 | a0008c0020t0002g0014 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1835-73A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440164 | |||||||
chr8:27440165 | A | C | 1 | a0008c0020t0002g0014 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1835-72A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440165 | |||||||
chr8:27440169 | C | A | 1 | a0008c0020t0002g0014 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1835-68C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440169 | |||||||
chr8:27440173 | G | C | 1 | a0008c0020t0002g0014 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1835-64G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440173 | |||||||
chr8:27440174 | G | C | 1 | a0008c0020t0002g0014 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1835-63G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440174 | |||||||
chr8:27440178 | T | C | 1 | a0008c0020t0002g0014 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1835-59T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440178 | |||||||
chr8:27440179 | T | C | 242 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(239): Show |
247 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.1835-58T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440179 | |||||||
chr8:27440182 | G | C | 1 | a0008c0020t0002g0014 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1835-55G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440182 | |||||||
chr8:27440183 | G | T | 1 | a0008c0020t0002g0014 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1835-54G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440183 | |||||||
chr8:27440185 | T | A | 1 | a0008c0020t0002g0014 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1835-52T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440185 | |||||||
chr8:27440186 | G | A | 1 | a0008c0020t0002g0014 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1835-51G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440186 | |||||||
chr8:27440187 | G | C | 1 | a0008c0020t0002g0014 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1835-50G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440187 | |||||||
chr8:27440188 | G | A | 1 | a0008c0020t0002g0014 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1835-49G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440188 | |||||||
chr8:27440190 | G | T | 1 | a0008c0020t0002g0014 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1835-47G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440190 | |||||||
chr8:27440192 | G | T | 1 | a0008c0020t0002g0014 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1835-45G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440192 | |||||||
chr8:27440194 | C | T | 1 | a0008c0020t0002g0014 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1835-43C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440194 | |||||||
chr8:27440197 | G | C | 1 | a0008c0020t0002g0014 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1835-40G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440197 | |||||||
chr8:27440199 | C | T | 1 | a0008c0020t0002g0014 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1835-38C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440199 | |||||||
chr8:27440200 | T | A | 1 | a0008c0020t0002g0014 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1835-37T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440200 | |||||||
chr8:27440201 | C | G | 1 | a0008c0020t0002g0014 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1835-36C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440201 | |||||||
chr8:27440202 | C | G | 1 | a0008c0020t0002g0014 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1835-35C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440202 | |||||||
chr8:27440205 | C | A | 1 | a0008c0020t0002g0014 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1835-32C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440205 | |||||||
chr8:27440206 | A | C | 1 | a0001c0001t0003g0028 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1835-31A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440206 | |||||||
chr8:27440209 | C | A | 1 | a0008c0020t0002g0014 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1835-28C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440209 | |||||||
chr8:27440212 | G | A | 1 | a0008c0020t0002g0014 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1835-25G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440212 | |||||||
chr8:27440214 | C | T | 1 | a0008c0020t0002g0014 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1835-23C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440214 | |||||||
chr8:27440215 | C | A | 1 | a0008c0020t0002g0014 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1835-22C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440215 | |||||||
chr8:27440216 | T | A | 1 | a0008c0020t0002g0014 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1835-21T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440216 | |||||||
chr8:27440228 | A | G | 3 | a0001c0008t0003g0292 a0001c0008t0003g0319 a0001c0008t0003g0320 |
3 | HG02723.hp2 HG02896.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1835-9A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440228 | |||||||
chr8:27440229 | C | T | 1 | a0008c0020t0002g0014 | 1 | NA18949.hp2 | splice_region_variant&intron_variant | LOW | c.1835-8C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440229 | |||||||
chr8:27440231 | C | A | 1 | a0008c0020t0002g0014 | 1 | NA18949.hp2 | splice_region_variant&intron_variant | LOW | c.1835-6C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 20/30 | chr8 | 27440231 | |||||||
chr8:27440462 | G | T | 3 | a0002c0006t0001g0234 a0002c0006t0001g0290 a0002c0006t0001g0291 |
3 | HG02630.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2039+21G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27440462 | |||||||
chr8:27440526 | C | T | 1 | a0001c0002t0001g0192 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2039+85C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27440526 | |||||||
chr8:27440544 | G | A | 1 | a0001c0002t0001g0188 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2039+103G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27440544 | |||||||
chr8:27440561 | A | G | 243 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(240): Show |
248 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.2039+120A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27440561 | |||||||
chr8:27440862 | C | G | 1 | a0001c0030t0002g0007 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2039+421C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27440862 | |||||||
chr8:27440863 | C | T | 16 | a0001c0001t0003g0022 a0001c0001t0003g0088 a0001c0001t0003g0093 others(13): Show |
16 | HG00639.hp1 HG00733.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.2039+422C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27440863 | |||||||
chr8:27440892 | G | A | 8 | a0001c0001t0003g0031 a0001c0001t0003g0047 a0001c0001t0003g0081 others(5): Show |
8 | HG00738.hp2 HG01074.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.2039+451G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27440892 | |||||||
chr8:27440914 | C | T | 1 | a0001c0001t0003g0060 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2039+473C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27440914 | |||||||
chr8:27441039 | G | A | 1 | a0001c0002t0001g0005 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2039+598G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27441039 | |||||||
chr8:27441159 | T | C | 3 | a0001c0008t0003g0292 a0001c0008t0003g0319 a0001c0008t0003g0320 |
3 | HG02723.hp2 HG02896.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2039+718T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27441159 | |||||||
chr8:27441207 | C | T | 1 | a0002c0023t0001g0123 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2039+766C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27441207 | |||||||
chr8:27441402 | T | A | 1 | a0002c0023t0001g0123 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2039+961T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27441402 | |||||||
chr8:27441444 | A | G | 9 | a0001c0010t0003g0229 a0001c0010t0003g0230 a0001c0010t0003g0231 others(6): Show |
9 | HG02486.hp1 HG02647.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.2039+1003A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27441444 | |||||||
chr8:27441570 | C | A | 107 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(104): Show |
108 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.2039+1129C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27441570 | |||||||
chr8:27441760 | A | G | 38 | a0002c0003t0002g0004 a0002c0003t0002g0012 a0002c0003t0002g0057 others(35): Show |
39 | HG00408.hp2 HG00609.hp1 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.2040-1115A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27441760 | |||||||
chr8:27441810 | G | C | 1 | a0002c0006t0002g0317 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2040-1065G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27441810 | |||||||
chr8:27441894 | A | T | 119 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(116): Show |
120 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.2040-981A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27441894 | |||||||
chr8:27441952 | A | G | 119 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(116): Show |
120 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.2040-923A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27441952 | |||||||
chr8:27441994 | T | G | 1 | a0002c0003t0002g0259 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2040-881T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27441994 | |||||||
chr8:27442036 | C | T | 119 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(116): Show |
120 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.2040-839C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27442036 | |||||||
chr8:27442054 | G | A | 1 | a0001c0030t0002g0007 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2040-821G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27442054 | |||||||
chr8:27442136 | G | C | 73 | a0001c0008t0003g0114 a0002c0003t0002g0003 a0002c0003t0002g0023 others(70): Show |
76 | HG00099.hp2 HG00438.hp2 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.2040-739G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27442136 | |||||||
chr8:27442146 | A | G | 1 | a0001c0001t0003g0088 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2040-729A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27442146 | |||||||
chr8:27442220 | A | G | 8 | a0001c0001t0003g0088 a0001c0001t0003g0093 a0001c0001t0003g0294 others(5): Show |
8 | HG00639.hp1 HG02572.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.2040-655A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27442220 | |||||||
chr8:27442223 | T | C | 233 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(230): Show |
238 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.2040-652T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27442223 | |||||||
chr8:27442269 | A | G | 1 | a0001c0001t0003g0022 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2040-606A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27442269 | |||||||
chr8:27442418 | A | G | 119 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(116): Show |
120 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.2040-457A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27442418 | |||||||
chr8:27442452 | GGATGTTT others(14): Show |
G | 7 | a0001c0001t0003g0175 a0001c0001t0003g0227 a0001c0001t0003g0228 others(4): Show |
7 | HG02572.hp2 HG02818.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.2040-417_2040-397d others(23): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | INFO_REALIGN_3_PRIME | chr8 | 27442452 | ||||||
chr8:27442507 | C | A | 1 | a0002c0003t0002g0257 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2040-368C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27442507 | |||||||
chr8:27442525 | A | G | 8 | a0001c0002t0001g0143 a0001c0002t0001g0155 a0001c0002t0001g0159 others(5): Show |
8 | HG00423.hp2 HG00544.hp2 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.2040-350A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27442525 | |||||||
chr8:27442571 | T | C | 94 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(91): Show |
95 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.2040-304T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27442571 | |||||||
chr8:27442581 | G | T | 1 | a0002c0003t0002g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2040-294G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27442581 | |||||||
chr8:27442604 | A | G | 119 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(116): Show |
120 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.2040-271A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27442604 | |||||||
chr8:27442642 | C | T | 1 | a0001c0030t0002g0007 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2040-233C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27442642 | |||||||
chr8:27442653 | C | A | 3 | a0001c0008t0003g0292 a0001c0008t0003g0319 a0001c0008t0003g0320 |
3 | HG02723.hp2 HG02896.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2040-222C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 21/30 | chr8 | 27442653 | |||||||
chr8:27443104 | C | A | 119 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(116): Show |
120 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.2148+121C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 22/30 | chr8 | 27443104 | |||||||
chr8:27443297 | T | A | 2 | a0002c0006t0001g0006 a0002c0006t0001g0282 |
2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2148+314T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 22/30 | chr8 | 27443297 | |||||||
chr8:27443331 | A | G | 1 | a0001c0030t0002g0007 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2148+348A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 22/30 | chr8 | 27443331 | |||||||
chr8:27443643 | A | G | 119 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(116): Show |
120 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.2149-563A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 22/30 | chr8 | 27443643 | |||||||
chr8:27443681 | C | G | 3 | a0001c0008t0003g0292 a0001c0008t0003g0319 a0001c0008t0003g0320 |
3 | HG02723.hp2 HG02896.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2149-525C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 22/30 | chr8 | 27443681 | |||||||
chr8:27443934 | G | A | 46 | a0001c0008t0003g0243 a0001c0008t0003g0296 a0001c0008t0003g0314 others(43): Show |
47 | HG00408.hp2 HG00609.hp1 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.2149-272G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 22/30 | chr8 | 27443934 | |||||||
chr8:27443974 | A | G | 119 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(116): Show |
120 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.2149-232A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 22/30 | chr8 | 27443974 | |||||||
chr8:27444292 | C | T | 2 | a0002c0006t0001g0006 a0002c0006t0001g0282 |
2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2214+21C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 23/30 | chr8 | 27444292 | |||||||
chr8:27444359 | G | T | 1 | a0002c0006t0001g0066 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2214+88G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 23/30 | chr8 | 27444359 | |||||||
chr8:27444838 | C | T | 1 | a0002c0018t0002g0089 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2214+567C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 23/30 | chr8 | 27444838 | |||||||
chr8:27444886 | C | G | 1 | a0002c0004t0002g0248 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2214+615C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 23/30 | chr8 | 27444886 | |||||||
chr8:27444915 | T | C | 240 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(237): Show |
245 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(242): Show |
intron_variant | MODIFIER | c.2214+644T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 23/30 | chr8 | 27444915 | |||||||
chr8:27444916 | G | A | 112 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(109): Show |
113 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.2214+645G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 23/30 | chr8 | 27444916 | |||||||
chr8:27444932 | A | G | 1 | a0002c0017t0002g0252 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2214+661A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 23/30 | chr8 | 27444932 | |||||||
chr8:27445006 | T | G | 1 | a0002c0006t0002g0317 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2214+735T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 23/30 | chr8 | 27445006 | |||||||
chr8:27445131 | A | T | 1 | a0002c0006t0002g0317 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2215-663A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 23/30 | chr8 | 27445131 | |||||||
chr8:27445214 | T | G | 242 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(239): Show |
247 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.2215-580T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 23/30 | chr8 | 27445214 | |||||||
chr8:27445237 | A | C | 1 | a0001c0002t0001g0214 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2215-557A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 23/30 | chr8 | 27445237 | |||||||
chr8:27445327 | T | C | 242 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(239): Show |
247 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.2215-467T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 23/30 | chr8 | 27445327 | |||||||
chr8:27445367 | C | T | 5 | a0001c0001t0003g0088 a0001c0001t0003g0113 a0001c0001t0003g0115 others(2): Show |
5 | HG02559.hp1 HG02572.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2215-427C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 23/30 | chr8 | 27445367 | |||||||
chr8:27445368 | A | G | 116 | a0001c0008t0003g0114 a0002c0003t0002g0003 a0002c0003t0002g0004 others(113): Show |
120 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.2215-426A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 23/30 | chr8 | 27445368 | |||||||
chr8:27445489 | A | C | 1 | a0002c0006t0001g0020 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2215-305A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 23/30 | chr8 | 27445489 | |||||||
chr8:27445498 | T | C | 112 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(109): Show |
113 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.2215-296T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 23/30 | chr8 | 27445498 | |||||||
chr8:27445563 | T | C | 1 | a0002c0023t0001g0123 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2215-231T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 23/30 | chr8 | 27445563 | |||||||
chr8:27445609 | A | G | 242 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(239): Show |
247 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.2215-185A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 23/30 | chr8 | 27445609 | |||||||
chr8:27445683 | C | T | 1 | a0001c0022t0002g0008 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2215-111C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 23/30 | chr8 | 27445683 | |||||||
chr8:27445951 | G | A | 1 | a0001c0030t0002g0007 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2340+32G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27445951 | |||||||
chr8:27445962 | G | A | 1 | a0001c0030t0002g0007 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2340+43G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27445962 | |||||||
chr8:27446044 | C | A | 1 | a0001c0030t0002g0007 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2340+125C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27446044 | |||||||
chr8:27446224 | T | A | 2 | a0001c0002t0001g0145 a0001c0002t0001g0152 |
2 | NA18980.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.2340+305T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27446224 | |||||||
chr8:27446263 | A | T | 2 | a0002c0006t0001g0006 a0002c0006t0001g0282 |
2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2340+344A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27446263 | |||||||
chr8:27446483 | G | T | 2 | a0002c0005t0001g0083 a0002c0005t0001g0085 |
2 | NA18979.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.2340+564G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27446483 | |||||||
chr8:27446506 | G | A | 1 | a0001c0008t0003g0314 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2340+587G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27446506 | |||||||
chr8:27446564 | T | C | 19 | a0001c0002t0001g0080 a0001c0002t0001g0118 a0001c0002t0001g0141 others(16): Show |
19 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(16): Show |
intron_variant | MODIFIER | c.2340+645T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27446564 | |||||||
chr8:27446662 | A | G | 1 | a0001c0001t0003g0072 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2340+743A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27446662 | |||||||
chr8:27446753 | G | A | 1 | a0002c0003t0002g0247 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2340+834G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27446753 | |||||||
chr8:27446872 | A | G | 5 | a0001c0001t0003g0088 a0001c0001t0003g0113 a0001c0001t0003g0115 others(2): Show |
5 | HG02559.hp1 HG02572.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2340+953A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27446872 | |||||||
chr8:27446923 | T | C | 1 | a0002c0004t0002g0208 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2340+1004T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27446923 | |||||||
chr8:27447148 | C | T | 1 | a0001c0002t0001g0192 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2340+1229C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27447148 | |||||||
chr8:27447237 | A | C | 1 | a0001c0001t0003g0227 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2340+1318A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27447237 | |||||||
chr8:27447438 | C | T | 1 | a0001c0008t0003g0114 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2340+1519C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27447438 | |||||||
chr8:27447640 | C | T | 2 | a0001c0008t0003g0319 a0001c0008t0003g0320 |
2 | HG02723.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.2340+1721C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27447640 | |||||||
chr8:27448024 | G | A | 1 | a0001c0030t0002g0007 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2340+2105G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27448024 | |||||||
chr8:27448088 | A | G | 1 | a0001c0022t0002g0008 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2340+2169A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27448088 | |||||||
chr8:27448246 | T | C | 1 | a0001c0010t0003g0229 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2340+2327T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27448246 | |||||||
chr8:27448409 | C | T | 1 | a0001c0022t0002g0008 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2341-2340C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27448409 | |||||||
chr8:27448427 | A | G | 1 | a0002c0017t0002g0252 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2341-2322A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27448427 | |||||||
chr8:27448559 | A | G | 1 | a0001c0008t0003g0243 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2341-2190A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27448559 | |||||||
chr8:27448586 | C | T | 107 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(104): Show |
107 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.2341-2163C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27448586 | |||||||
chr8:27448597 | AACTTACA others(3): Show |
A | 109 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(106): Show |
109 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.2341-2137_2341-212 others(14): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | INFO_REALIGN_3_PRIME | chr8 | 27448597 | ||||||
chr8:27448642 | G | A | 126 | a0001c0008t0003g0114 a0002c0003t0002g0003 a0002c0003t0002g0004 others(123): Show |
131 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.2341-2107G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27448642 | |||||||
chr8:27448771 | C | T | 2 | a0002c0004t0002g0244 a0002c0004t0002g0245 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2341-1978C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27448771 | |||||||
chr8:27449033 | G | A | 1 | a0002c0003t0002g0256 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.2341-1716G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27449033 | |||||||
chr8:27449034 | T | A | 70 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(67): Show |
70 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.2341-1715T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27449034 | |||||||
chr8:27449083 | C | T | 3 | a0001c0008t0003g0292 a0001c0008t0003g0319 a0001c0008t0003g0320 |
3 | HG02723.hp2 HG02896.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2341-1666C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27449083 | |||||||
chr8:27449106 | C | T | 3 | a0001c0008t0003g0292 a0001c0008t0003g0319 a0001c0008t0003g0320 |
3 | HG02723.hp2 HG02896.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2341-1643C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27449106 | |||||||
chr8:27449145 | G | A | 2 | a0002c0006t0001g0006 a0002c0006t0001g0282 |
2 | NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2341-1604G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27449145 | |||||||
chr8:27449307 | A | G | 1 | a0001c0001t0003g0065 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2341-1442A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27449307 | |||||||
chr8:27449403 | T | C | 2 | a0002c0006t0001g0010 a0002c0017t0002g0252 |
2 | HG00738.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.2341-1346T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27449403 | |||||||
chr8:27449509 | G | T | 12 | a0001c0008t0003g0292 a0001c0008t0003g0319 a0001c0008t0003g0320 others(9): Show |
12 | HG02486.hp1 HG02647.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.2341-1240G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27449509 | |||||||
chr8:27449555 | G | A | 65 | a0001c0008t0003g0114 a0002c0003t0002g0003 a0002c0003t0002g0023 others(62): Show |
68 | HG00099.hp2 HG00438.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.2341-1194G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27449555 | |||||||
chr8:27449578 | A | G | 61 | a0002c0003t0002g0004 a0002c0003t0002g0012 a0002c0003t0002g0057 others(58): Show |
63 | HG00408.hp1 HG00408.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.2341-1171A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27449578 | |||||||
chr8:27449663 | C | T | 12 | a0001c0008t0003g0292 a0001c0008t0003g0319 a0001c0008t0003g0320 others(9): Show |
12 | HG02486.hp1 HG02647.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.2341-1086C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27449663 | |||||||
chr8:27449718 | G | C | 1 | a0001c0022t0002g0008 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2341-1031G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27449718 | |||||||
chr8:27449758 | G | C | 92 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(89): Show |
92 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.2341-991G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27449758 | |||||||
chr8:27449819 | A | G | 54 | a0002c0003t0002g0004 a0002c0003t0002g0012 a0002c0003t0002g0057 others(51): Show |
56 | HG00408.hp1 HG00408.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.2341-930A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27449819 | |||||||
chr8:27450005 | A | G | 91 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(88): Show |
91 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.2341-744A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27450005 | |||||||
chr8:27450200 | C | A | 12 | a0001c0008t0003g0292 a0001c0008t0003g0319 a0001c0008t0003g0320 others(9): Show |
12 | HG02486.hp1 HG02647.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.2341-549C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27450200 | |||||||
chr8:27450276 | T | C | 1 | a0002c0003t0004g0272 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2341-473T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27450276 | |||||||
chr8:27450394 | C | T | 9 | a0001c0010t0003g0229 a0001c0010t0003g0230 a0001c0010t0003g0231 others(6): Show |
9 | HG02486.hp1 HG02647.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.2341-355C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27450394 | |||||||
chr8:27450487 | G | A | 132 | a0002c0003t0002g0003 a0002c0003t0002g0004 a0002c0003t0002g0012 others(129): Show |
137 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.2341-262G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27450487 | |||||||
chr8:27450507 | C | A | 1 | a0001c0010t0003g0232 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2341-242C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27450507 | |||||||
chr8:27450508 | G | A | 25 | a0002c0004t0002g0001 a0002c0004t0002g0011 a0002c0004t0002g0013 others(22): Show |
27 | HG00438.hp2 HG00621.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.2341-241G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 24/30 | chr8 | 27450508 | |||||||
chr8:27451021 | G | A | 96 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(93): Show |
96 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.2488-22G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 25/30 | chr8 | 27451021 | |||||||
chr8:27451169 | C | G | 4 | a0001c0001t0003g0031 a0001c0001t0003g0091 a0003c0014t0003g0045 others(1): Show |
4 | HG01074.hp1 HG01099.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.2523+91C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 26/30 | chr8 | 27451169 | |||||||
chr8:27451173 | G | A | 5 | a0001c0008t0003g0243 a0001c0008t0003g0296 a0001c0008t0003g0314 others(2): Show |
5 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2523+95G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 26/30 | chr8 | 27451173 | |||||||
chr8:27451202 | C | T | 1 | a0002c0006t0001g0323 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2523+124C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 26/30 | chr8 | 27451202 | |||||||
chr8:27451255 | C | T | 1 | a0002c0006t0002g0317 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2523+177C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 26/30 | chr8 | 27451255 | |||||||
chr8:27451273 | G | A | 2 | a0002c0006t0001g0234 a0002c0006t0001g0290 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2523+195G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 26/30 | chr8 | 27451273 | |||||||
chr8:27451332 | A | G | 234 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(231): Show |
239 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.2524-153A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 26/30 | chr8 | 27451332 | |||||||
chr8:27451364 | C | G | 9 | a0001c0010t0003g0229 a0001c0010t0003g0230 a0001c0010t0003g0231 others(6): Show |
9 | HG02486.hp1 HG02647.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.2524-121C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 26/30 | chr8 | 27451364 | |||||||
chr8:27451365 | G | A | 1 | a0001c0030t0002g0007 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2524-120G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 26/30 | chr8 | 27451365 | |||||||
chr8:27451444 | C | T | 64 | a0002c0003t0002g0003 a0002c0003t0002g0023 a0002c0003t0002g0054 others(61): Show |
67 | HG00099.hp2 HG00438.hp2 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.2524-41C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 26/30 | chr8 | 27451444 | |||||||
chr8:27451581 | G | A | 1 | a0001c0001t0003g0064 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2548+72G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 27/30 | chr8 | 27451581 | |||||||
chr8:27451600 | G | A | 1 | a0001c0030t0002g0007 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2548+91G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 27/30 | chr8 | 27451600 | |||||||
chr8:27451731 | G | A | 1 | a0001c0010t0003g0297 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2548+222G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 27/30 | chr8 | 27451731 | |||||||
chr8:27451749 | C | T | 1 | a0001c0002t0001g0138 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2548+240C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 27/30 | chr8 | 27451749 | |||||||
chr8:27451760 | A | G | 1 | a0002c0006t0002g0317 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2548+251A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 27/30 | chr8 | 27451760 | |||||||
chr8:27451822 | T | C | 109 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(106): Show |
109 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.2548+313T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 27/30 | chr8 | 27451822 | |||||||
chr8:27451862 | T | C | 240 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(237): Show |
245 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(242): Show |
intron_variant | MODIFIER | c.2548+353T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 27/30 | chr8 | 27451862 | |||||||
chr8:27451927 | T | A | 5 | a0001c0008t0003g0243 a0001c0008t0003g0296 a0001c0008t0003g0314 others(2): Show |
5 | HG02109.hp2 HG02258.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.2548+418T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 27/30 | chr8 | 27451927 | |||||||
chr8:27452103 | T | G | 1 | a0001c0030t0002g0007 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2548+594T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 27/30 | chr8 | 27452103 | |||||||
chr8:27452140 | T | C | 54 | a0002c0003t0002g0004 a0002c0003t0002g0012 a0002c0003t0002g0057 others(51): Show |
56 | HG00408.hp1 HG00408.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.2548+631T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 27/30 | chr8 | 27452140 | |||||||
chr8:27452469 | G | A | 2 | a0001c0001t0003g0015 a0001c0001t0003g0016 |
2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2549-645G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 27/30 | chr8 | 27452469 | |||||||
chr8:27452559 | C | CA | 222 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(219): Show |
227 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.2549-537dupA | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 27/30 | INFO_REALIGN_3_PRIME | chr8 | 27452559 | ||||||
chr8:27452559 | C | CAA | 12 | a0001c0001t0003g0181 a0001c0001t0003g0228 a0001c0001t0003g0305 others(9): Show |
12 | HG00733.hp2 HG02055.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.2549-538_2549-537d others(4): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 27/30 | INFO_REALIGN_3_PRIME | chr8 | 27452559 | ||||||
chr8:27452632 | G | A | 2 | a0001c0001t0003g0021 a0001c0001t0003g0043 |
2 | NA18956.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.2549-482G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 27/30 | chr8 | 27452632 | |||||||
chr8:27452651 | C | T | 1 | a0001c0002t0001g0142 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2549-463C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 27/30 | chr8 | 27452651 | |||||||
chr8:27452653 | A | G | 1 | a0002c0017t0002g0252 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2549-461A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 27/30 | chr8 | 27452653 | |||||||
chr8:27452705 | A | G | 1 | a0001c0022t0002g0008 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2549-409A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 27/30 | chr8 | 27452705 | |||||||
chr8:27452744 | G | A | 1 | a0001c0002t0001g0169 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2549-370G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 27/30 | chr8 | 27452744 | |||||||
chr8:27452892 | G | C | 1 | a0002c0003t0002g0269 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2549-222G>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 27/30 | chr8 | 27452892 | |||||||
chr8:27452973 | G | A | 9 | a0001c0010t0003g0229 a0001c0010t0003g0230 a0001c0010t0003g0231 others(6): Show |
9 | HG02486.hp1 HG02647.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.2549-141G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 27/30 | chr8 | 27452973 | |||||||
chr8:27452991 | G | A | 1 | a0001c0013t0003g0304 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2549-123G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 27/30 | chr8 | 27452991 | |||||||
chr8:27453029 | A | G | 235 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(232): Show |
240 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.2549-85A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 27/30 | chr8 | 27453029 | |||||||
chr8:27453200 | G | A | 1 | a0001c0022t0002g0008 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2595+40G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 28/30 | chr8 | 27453200 | |||||||
chr8:27453291 | C | T | 3 | a0001c0008t0003g0292 a0001c0008t0003g0319 a0001c0008t0003g0320 |
3 | HG02723.hp2 HG02896.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2595+131C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 28/30 | chr8 | 27453291 | |||||||
chr8:27453389 | C | G | 1 | a0001c0001t0003g0038 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2595+229C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 28/30 | chr8 | 27453389 | |||||||
chr8:27453502 | T | A | 1 | a0001c0030t0002g0007 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2595+342T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 28/30 | chr8 | 27453502 | |||||||
chr8:27453600 | C | T | 2 | a0002c0003t0002g0263 a0002c0003t0002g0275 |
2 | HG03490.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.2595+440C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 28/30 | chr8 | 27453600 | |||||||
chr8:27453608 | C | T | 16 | a0002c0003t0002g0004 a0002c0003t0002g0012 a0002c0003t0002g0067 others(13): Show |
17 | HG00408.hp2 HG00609.hp1 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.2595+448C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 28/30 | chr8 | 27453608 | |||||||
chr8:27453727 | T | A | 33 | a0002c0003t0002g0004 a0002c0003t0002g0012 a0002c0003t0002g0057 others(30): Show |
34 | HG00408.hp2 HG00609.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.2596-427T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 28/30 | chr8 | 27453727 | |||||||
chr8:27453728 | A | T | 1 | a0002c0006t0001g0010 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2596-426A>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 28/30 | chr8 | 27453728 | |||||||
chr8:27453814 | T | C | 242 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(239): Show |
247 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.2596-340T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 28/30 | chr8 | 27453814 | |||||||
chr8:27453859 | A | G | 242 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(239): Show |
247 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.2596-295A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 28/30 | chr8 | 27453859 | |||||||
chr8:27454104 | C | T | 3 | a0001c0008t0003g0292 a0001c0008t0003g0319 a0001c0008t0003g0320 |
3 | HG02723.hp2 HG02896.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.2596-50C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 28/30 | chr8 | 27454104 | |||||||
chr8:27454523 | C | T | 109 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(106): Show |
109 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(106): Show |
splice_region_variant&intron_variant | LOW | c.2734-8C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 29/30 | chr8 | 27454523 | |||||||
chr8:27454527 | C | T | 1 | a0002c0006t0002g0317 | 1 | NA20129.hp1 | splice_region_variant&intron_variant | LOW | c.2734-4C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 29/30 | chr8 | 27454527 | |||||||
chr8:27454618 | G | A | 109 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(106): Show |
109 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(106): Show |
splice_region_variant&intron_variant | LOW | c.2814+7G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | chr8 | 27454618 | |||||||
chr8:27454715 | C | T | 1 | a0002c0005t0001g0002 | 2 | HG00639.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.2814+104C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | chr8 | 27454715 | |||||||
chr8:27454790 | G | A | 25 | a0001c0002t0001g0005 a0001c0002t0001g0077 a0001c0002t0001g0116 others(22): Show |
25 | HG00423.hp1 HG01496.hp1 HG01943.hp1 others(22): Show |
intron_variant | MODIFIER | c.2814+179G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | chr8 | 27454790 | |||||||
chr8:27454812 | G | A | 2 | a0002c0003t0002g0270 a0002c0003t0002g0274 |
2 | HG02080.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.2814+201G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | chr8 | 27454812 | |||||||
chr8:27454909 | A | G | 233 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(230): Show |
238 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.2814+298A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | chr8 | 27454909 | |||||||
chr8:27454947 | ATG | A | 65 | a0002c0003t0002g0003 a0002c0003t0002g0023 a0002c0003t0002g0054 others(62): Show |
68 | HG00099.hp2 HG00438.hp2 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.2814+340_2814+341d others(4): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr8 | 27454947 | ||||||
chr8:27455150 | CTT | C | 4 | a0001c0001t0003g0088 a0001c0001t0003g0113 a0001c0001t0003g0115 others(1): Show |
4 | HG02559.hp1 HG02572.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.2814+541_2814+542d others(4): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr8 | 27455150 | ||||||
chr8:27455170 | T | A | 97 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(94): Show |
97 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.2814+559T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | chr8 | 27455170 | |||||||
chr8:27455292 | G | A | 124 | a0002c0003t0002g0003 a0002c0003t0002g0004 a0002c0003t0002g0012 others(121): Show |
129 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.2814+681G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | chr8 | 27455292 | |||||||
chr8:27455375 | T | A | 1 | a0002c0005t0001g0002 | 2 | HG00639.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.2814+764T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | chr8 | 27455375 | |||||||
chr8:27455431 | C | T | 5 | a0001c0001t0003g0088 a0001c0001t0003g0113 a0001c0001t0003g0115 others(2): Show |
5 | HG02559.hp1 HG02572.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2814+820C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | chr8 | 27455431 | |||||||
chr8:27455568 | G | T | 109 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(106): Show |
109 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.2814+957G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | chr8 | 27455568 | |||||||
chr8:27455637 | C | G | 4 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(1): Show |
4 | HG02257.hp2 HG02622.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.2814+1026C>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | chr8 | 27455637 | |||||||
chr8:27455838 | C | A | 4 | a0001c0001t0003g0025 a0001c0001t0003g0029 a0001c0001t0003g0030 others(1): Show |
4 | HG01109.hp2 HG01255.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.2814+1227C>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | chr8 | 27455838 | |||||||
chr8:27455872 | G | A | 1 | a0007c0032t0003g0284 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2814+1261G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | chr8 | 27455872 | |||||||
chr8:27456122 | T | G | 1 | a0002c0003t0002g0300 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2814+1511T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | chr8 | 27456122 | |||||||
chr8:27456251 | C | T | 3 | a0001c0001t0003g0081 a0001c0001t0003g0082 a0001c0001t0003g0205 |
3 | HG00738.hp2 HG01346.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.2814+1640C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | chr8 | 27456251 | |||||||
chr8:27456297 | C | T | 4 | a0001c0001t0003g0088 a0001c0001t0003g0113 a0001c0001t0003g0115 others(1): Show |
4 | HG02559.hp1 HG02572.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.2814+1686C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | chr8 | 27456297 | |||||||
chr8:27456332 | T | G | 1 | a0001c0002t0001g0155 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2814+1721T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | chr8 | 27456332 | |||||||
chr8:27456338 | C | T | 4 | a0001c0001t0003g0031 a0001c0001t0003g0091 a0003c0014t0003g0045 others(1): Show |
4 | HG01074.hp1 HG01099.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.2814+1727C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | chr8 | 27456338 | |||||||
chr8:27456371 | G | A | 4 | a0001c0002t0001g0126 a0001c0002t0001g0128 a0001c0002t0001g0192 others(1): Show |
4 | NA19000.hp1 NA19057.hp2 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.2814+1760G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | chr8 | 27456371 | |||||||
chr8:27456371 | G | T | 238 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(235): Show |
243 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(240): Show |
intron_variant | MODIFIER | c.2814+1760G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | chr8 | 27456371 | |||||||
chr8:27456391 | G | A | 1 | a0001c0002t0001g0161 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2814+1780G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | chr8 | 27456391 | |||||||
chr8:27457052 | A | G | 1 | a0002c0006t0002g0317 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2815-1242A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | chr8 | 27457052 | |||||||
chr8:27457302 | A | G | 240 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(237): Show |
245 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(242): Show |
intron_variant | MODIFIER | c.2815-992A>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | chr8 | 27457302 | |||||||
chr8:27457578 | T | C | 7 | a0001c0001t0003g0175 a0001c0001t0003g0227 a0001c0001t0003g0228 others(4): Show |
7 | HG02572.hp2 HG02818.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.2815-716T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | chr8 | 27457578 | |||||||
chr8:27457841 | T | G | 240 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(237): Show |
245 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(242): Show |
intron_variant | MODIFIER | c.2815-453T>G | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | chr8 | 27457841 | |||||||
chr8:27457906 | C | T | 1 | a0001c0002t0001g0078 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.2815-388C>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | chr8 | 27457906 | |||||||
chr8:27457925 | A | C | 1 | a0001c0001t0003g0181 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2815-369A>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | chr8 | 27457925 | |||||||
chr8:27457930 | G | A | 240 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(237): Show |
245 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(242): Show |
intron_variant | MODIFIER | c.2815-364G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | chr8 | 27457930 | |||||||
chr8:27457971 | G | T | 2 | a0002c0003t0002g0258 a0002c0003t0006g0040 |
2 | NA18960.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.2815-323G>T | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | chr8 | 27457971 | |||||||
chr8:27457975 | CA | C | 6 | a0001c0002t0001g0174 a0001c0002t0001g0235 a0001c0002t0001g0295 others(3): Show |
6 | HG03041.hp2 HG03139.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.2815-296delA | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr8 | 27457975 | ||||||
chr8:27457975 | CAAAAAAA | C | 117 | a0002c0003t0002g0003 a0002c0003t0002g0004 a0002c0003t0002g0012 others(114): Show |
122 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.2815-302_2815-296d others(9): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr8 | 27457975 | ||||||
chr8:27457975 | CAAAAAAA others(3): Show |
C | 1 | a0001c0002t0001g0157 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.2815-305_2815-296d others(12): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr8 | 27457975 | ||||||
chr8:27457996 | AAAG | A | 20 | a0001c0001t0003g0024 a0001c0001t0003g0035 a0001c0001t0003g0036 others(17): Show |
20 | HG00323.hp2 HG01070.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.2815-296_2815-294d others(5): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr8 | 27457996 | ||||||
chr8:27457997 | AAG | A | 81 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0021 others(78): Show |
81 | HG00544.hp1 HG00621.hp1 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.2815-295_2815-294d others(4): Show |
PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr8 | 27457997 | ||||||
chr8:27457998 | AG | A | 9 | a0001c0001t0003g0017 a0001c0001t0003g0042 a0001c0001t0003g0046 others(6): Show |
9 | HG00438.hp1 HG01109.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.2815-295delG | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | chr8 | 27457998 | |||||||
chr8:27458140 | G | A | 1 | a0001c0030t0002g0007 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2815-154G>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | chr8 | 27458140 | |||||||
chr8:27458173 | T | A | 1 | a0001c0001t0003g0025 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2815-121T>A | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | chr8 | 27458173 | |||||||
chr8:27458209 | T | C | 235 | a0001c0001t0003g0015 a0001c0001t0003g0016 a0001c0001t0003g0017 others(232): Show |
240 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.2815-85T>C | PTK2B | ENSG00000120899.18 | transcript | ENST00000346049.10 | protein_coding | 30/30 | chr8 | 27458209 |