regionname | pos | ref | alt | annotation | impact | samples | ahapids | achapids | acthapids | actghapids | ac | an | af | len | 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 | external |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
PCGF3_chr4_700832_775089 | 758761 | C | CTCCGGAC others(46): Show |
intron_variant | MODIFIER | HG01168.hp1 HG01169.hp1 HG01257.hp2 others(30): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0009a0001c0001t0017others(4): Show | a0001c0001t0001g0007a0001c0001t0001g0051a0001c0001t0001g0156others(30): Show | 33 | 366 | 0.0902 | 53 | c.463 others(70): Show |
PCGF3 | ENSG00000185619.19 | transcript | ENST00000362003.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
PCGF3_chr4_700832_775089 | 758761 | C | CTCCGGAC others(46): Show |
intron_variant | MODIFIER | NA19080.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0219 | 1 | 366 | 0.0027 | 53 | c.463 others(70): Show |
PCGF3 | ENSG00000185619.19 | transcript | ENST00000362003.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
PCGF3_chr4_700832_775089 | 758814 | C | CTCCGGAC others(46): Show |
intron_variant | MODIFIER | HG01069.hp1 HG01255.hp1 HG02257.hp2 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0004a0001c0001t0011a0001c0001t0036 | a0001c0001t0004g0254a0001c0001t0004g0255a0001c0001t0004g0362others(6): Show | 9 | 366 | 0.0246 | 53 | c.463 others(70): Show |
PCGF3 | ENSG00000185619.19 | transcript | ENST00000362003.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
PCGF3_chr4_700832_775089 | 758814 | C | CTCCGGAC others(46): Show |
intron_variant | MODIFIER | HG00140.hp2 HG00544.hp1 HG00673.hp2 others(12): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0007a0001c0001t0030a0002c0002t0007others(1): Show | a0001c0001t0007g0002a0001c0001t0007g0300a0001c0001t0007g0304others(11): Show | 15 | 366 | 0.0410 | 53 | c.463 others(70): Show |
PCGF3 | ENSG00000185619.19 | transcript | ENST00000362003.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
PCGF3_chr4_700832_775089 | 758860 | C | CTTCTCCT others(46): Show |
intron_variant | MODIFIER | HG02735.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0232 | 1 | 366 | 0.0027 | 53 | c.463 others(70): Show |
PCGF3 | ENSG00000185619.19 | transcript | ENST00000362003.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
PCGF3_chr4_700832_775089 | 758867 | T | TTCCGGAC others(46): Show |
intron_variant | MODIFIER | HG02109.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0295 | 1 | 366 | 0.0027 | 53 | c.463 others(70): Show |
PCGF3 | ENSG00000185619.19 | transcript | ENST00000362003.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
PCGF3_chr4_700832_775089 | 758911 | T | TTCTTCTC others(46): Show |
intron_variant | MODIFIER | HG02451.hp2 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0361 | 1 | 366 | 0.0027 | 53 | c.463 others(70): Show |
PCGF3 | ENSG00000185619.19 | transcript | ENST00000362003.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
PCGF3_chr4_700832_775089 | 758973 | C | CTCCGGAC others(46): Show |
intron_variant | MODIFIER | NA18945.hp2 NA18984.hp2 NA18999.hp2 |
a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0002a0001c0001t0007g0309 | 3 | 366 | 0.0082 | 53 | c.463 others(70): Show |
PCGF3 | ENSG00000185619.19 | transcript | ENST00000362003.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
PCGF3_chr4_700832_775089 | 758973 | C | CTCCGGAC others(46): Show |
intron_variant | MODIFIER | NA19056.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0308 | 1 | 366 | 0.0027 | 53 | c.463 others(70): Show |
PCGF3 | ENSG00000185619.19 | transcript | ENST00000362003.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
PCGF3_chr4_700832_775089 | 759019 | G | GTTCTCCT others(46): Show |
intron_variant | MODIFIER | HG01168.hp1 HG01169.hp1 HG01257.hp2 others(30): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0009a0001c0001t0017others(4): Show | a0001c0001t0001g0007a0001c0001t0001g0051a0001c0001t0001g0156others(30): Show | 33 | 366 | 0.0902 | 53 | c.463 others(70): Show |
PCGF3 | ENSG00000185619.19 | transcript | ENST00000362003.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
PCGF3_chr4_700832_775089 | 759131 | C | CTTCCGGA others(46): Show |
intron_variant | MODIFIER | NA19005.hp1 | a0001 | a0001c0001 | a0001c0001t0035 | a0001c0001t0035g0046 | 1 | 366 | 0.0027 | 53 | c.463 others(70): Show |
PCGF3 | ENSG00000185619.19 | transcript | ENST00000362003.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
PCGF3_chr4_700832_775089 | 759132 | T | TTCCGGAC others(46): Show |
intron_variant | MODIFIER | HG00544.hp2 HG00609.hp1 HG00642.hp1 others(34): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0003a0001c0001t0028a0001c0001t0038others(7): Show | a0001c0001t0003g0033a0001c0001t0003g0034a0001c0001t0003g0035others(34): Show | 37 | 366 | 0.1011 | 53 | c.463 others(70): Show |
PCGF3 | ENSG00000185619.19 | transcript | ENST00000362003.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
PCGF3_chr4_700832_775089 | 759132 | T | TTCCGGAC others(46): Show |
intron_variant | MODIFIER | NA19066.hp1 | a0001 | a0001c0003 | a0001c0003t0032 | a0001c0003t0032g0109 | 1 | 366 | 0.0027 | 53 | c.463 others(70): Show |
PCGF3 | ENSG00000185619.19 | transcript | ENST00000362003.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
PCGF3_chr4_700832_775089 | 759132 | T | TTCCGGAC others(46): Show |
intron_variant | MODIFIER | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(32): Show |
a0001a0002 | a0001c0003a0002c0007 | a0001c0003t0005a0001c0003t0010a0001c0003t0015others(3): Show | a0001c0003t0005g0001a0001c0003t0005g0121a0001c0003t0005g0122others(31): Show | 35 | 366 | 0.0956 | 53 | c.463 others(70): Show |
PCGF3 | ENSG00000185619.19 | transcript | ENST00000362003.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
PCGF3_chr4_700832_775089 | 759166 | C | CTCTCCCG others(46): Show |
intron_variant | MODIFIER | HG02965.hp2 | a0001 | a0001c0001 | a0001c0001t0027 | a0001c0001t0027g0009 | 1 | 366 | 0.0027 | 53 | c.463 others(70): Show |
PCGF3 | ENSG00000185619.19 | transcript | ENST00000362003.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
PCGF3_chr4_700832_775089 | 759231 | G | GTTCTCCT others(46): Show |
intron_variant | MODIFIER | HG01071.hp1 HG02895.hp1 NA18962.hp2 others(6): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0003c0008 | a0001c0001t0001a0001c0001t0007a0001c0001t0028others(3): Show | a0001c0001t0001g0052a0001c0001t0001g0199a0001c0001t0001g0211others(6): Show | 9 | 366 | 0.0246 | 53 | c.463 others(70): Show |
PCGF3 | ENSG00000185619.19 | transcript | ENST00000362003.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
PCGF3_chr4_700832_775089 | 759332 | G | GAGTTCTT others(46): Show |
intron_variant | MODIFIER | NA18906.hp2 | a0002 | a0002c0002 | a0002c0002t0027 | a0002c0002t0027g0263 | 1 | 366 | 0.0027 | 53 | c.463 others(70): Show |
PCGF3 | ENSG00000185619.19 | transcript | ENST00000362003.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
PCGF3_chr4_700832_775089 | 759463 | G | GTCTTTCT others(46): Show |
intron_variant | MODIFIER | HG04204.hp1 | a0001 | a0001c0001 | a0001c0001t0013 | a0001c0001t0013g0152 | 1 | 366 | 0.0027 | 53 | c.463 others(70): Show |
PCGF3 | ENSG00000185619.19 | transcript | ENST00000362003.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
PCGF3_chr4_700832_775089 | 759549 | G | GTTCTCCT others(46): Show |
intron_variant | MODIFIER | HG01168.hp1 HG01169.hp1 HG01257.hp2 others(1): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0001 | a0001c0001t0001g0220a0001c0001t0001g0221a0002c0002t0001g0192others(1): Show | 4 | 366 | 0.0109 | 53 | c.463 others(70): Show |
PCGF3 | ENSG00000185619.19 | transcript | ENST00000362003.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
PCGF3_chr4_700832_775089 | 759602 | C | CTTCTCCT others(46): Show |
intron_variant | MODIFIER | NA18979.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0226 | 1 | 366 | 0.0027 | 53 | c.463 others(70): Show |
PCGF3 | ENSG00000185619.19 | transcript | ENST00000362003.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
PCGF3_chr4_700832_775089 | 759708 | C | CTTCTCCT others(46): Show |
intron_variant | MODIFIER | HG01069.hp1 HG01255.hp1 HG02257.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0011a0001c0001t0036 | a0001c0001t0011g0072a0001c0001t0011g0073a0001c0001t0011g0111others(3): Show | 6 | 366 | 0.0164 | 53 | c.463 others(70): Show |
PCGF3 | ENSG00000185619.19 | transcript | ENST00000362003.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
PCGF3_chr4_700832_775089 | 759728 | G | GTCTTTCT others(46): Show |
intron_variant | MODIFIER | HG00544.hp2 HG00609.hp1 HG00642.hp1 others(32): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0003a0001c0001t0027a0001c0001t0028others(7): Show | a0001c0001t0003g0033a0001c0001t0003g0034a0001c0001t0003g0035others(32): Show | 35 | 366 | 0.0956 | 53 | c.463 others(70): Show |
PCGF3 | ENSG00000185619.19 | transcript | ENST00000362003.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
PCGF3_chr4_700832_775089 | 759761 | C | CTTCTCCT others(46): Show |
intron_variant | MODIFIER | HG02280.hp1 HG02630.hp1 NA18963.hp1 others(2): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0007a0002c0002t0001a0002c0002t0007others(1): Show | a0001c0001t0007g0300a0001c0001t0007g0364a0002c0002t0001g0296others(2): Show | 5 | 366 | 0.0137 | 53 | c.463 others(70): Show |
PCGF3 | ENSG00000185619.19 | transcript | ENST00000362003.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
PCGF3_chr4_700832_775089 | 759781 | G | GTCTTTCT others(46): Show |
intron_variant | MODIFIER | HG02523.hp2 NA18612.hp1 NA18948.hp1 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0003a0002c0002t0048 | a0001c0001t0003g0053a0001c0001t0003g0272a0002c0002t0048g0047 | 3 | 366 | 0.0082 | 53 | c.463 others(70): Show |
PCGF3 | ENSG00000185619.19 | transcript | ENST00000362003.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
PCGF3_chr4_700832_775089 | 759867 | G | GTTCTCCT others(46): Show |
intron_variant | MODIFIER | HG02523.hp2 NA18612.hp1 NA18948.hp1 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0003a0002c0002t0048 | a0001c0001t0003g0053a0001c0001t0003g0272a0002c0002t0048g0047 | 3 | 366 | 0.0082 | 53 | c.463 others(70): Show |
PCGF3 | ENSG00000185619.19 | transcript | ENST00000362003.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
PCMT1_chr6_149744741_149816419 | 149762704 | G | GATATATA others(46): Show |
intron_variant | MODIFIER | HG02004.hp1 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0056 | 1 | 334 | 0.0030 | 53 | c.56- others(68): Show |
PCMT1 | ENSG00000120265.21 | transcript | ENST00000464889.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
PCNP_chr3_101569180_101599465 | 101586571 | T | TGTGTGTG others(46): Show |
intron_variant | MODIFIER | HG03669.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0084 | 1 | 424 | 0.0024 | 53 | c.354 others(70): Show |
PCNP | ENSG00000081154.12 | transcript | ENST00000265260.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
PCNP_chr3_101569180_101599465 | 101586572 | G | GTGTGTGT others(46): Show |
intron_variant | MODIFIER | HG01175.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0124 | 1 | 424 | 0.0024 | 53 | c.354 others(70): Show |
PCNP | ENSG00000081154.12 | transcript | ENST00000265260.8 | protein_coding | 3/4 | chr3 | TogoVar | ||||||
PCNX1_chr14_70902459_71120382 | 70917528 | T | TGGGGGGG others(46): Show |
intron_variant | MODIFIER | NA18979.hp1 | a0001 | a0001c0002 | a0001c0002t0007 | a0001c0002t0007g0106 | 1 | 352 | 0.0028 | 53 | c.153 others(70): Show |
PCNX1 | ENSG00000100731.16 | transcript | ENST00000304743.7 | protein_coding | 1/35 | chr14 | TogoVar | ||||||
PCSK2_chr20_17222040_17489578 | 17303440 | A | ATAATATA others(46): Show |
intron_variant | MODIFIER | HG01109.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0060 | 1 | 274 | 0.0037 | 53 | c.282 others(72): Show |
PCSK2 | ENSG00000125851.10 | transcript | ENST00000262545.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | |||||
PCYOX1L_chr5_149353046_149374653 | 149370033 | T | TTTTTTTT others(46): Show |
downstream_gene_variant | MODIFIER | HG02074.hp1 HG02155.hp1 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0001 | 2 | 372 | 0.0054 | 53 | c.*13 others(64): Show |
PCYOX1L | ENSG00000145882.11 | transcript | ENST00000274569.9 | protein_coding | 381 | chr5 | TogoVar | ||||||
PDCD6_chr5_266646_319974 | 299074 | G | GCTCCCCC others(46): Show |
intron_variant | MODIFIER | HG02257.hp1 HG02280.hp2 HG02647.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0019a0001c0001t0005g0270a0001c0001t0005g0271others(2): Show | 6 | 360 | 0.0167 | 53 | c.164 others(70): Show |
PDCD6 | ENSG00000249915.9 | transcript | ENST00000264933.9 | protein_coding | 2/5 | chr5 | TogoVar | ||||||
PDS5B_chr13_32581452_32783019 | 32655374 | A | ATATATAT others(46): Show |
intron_variant | MODIFIER | HG03195.hp2 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0056 | 1 | 334 | 0.0030 | 53 | c.313 others(70): Show |
PDS5B | ENSG00000083642.19 | transcript | ENST00000315596.15 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
PDS5B_chr13_32581452_32783019 | 32655374 | A | ATATATAT others(46): Show |
intron_variant | MODIFIER | NA18967.hp2 | a0001 | a0001c0006 | a0001c0006t0001 | a0001c0006t0001g0019 | 1 | 334 | 0.0030 | 53 | c.313 others(70): Show |
PDS5B | ENSG00000083642.19 | transcript | ENST00000315596.15 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
PDS5B_chr13_32581452_32783019 | 32655374 | A | ATATATAT others(46): Show |
intron_variant | MODIFIER | NA19030.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0024 | 1 | 334 | 0.0030 | 53 | c.313 others(70): Show |
PDS5B | ENSG00000083642.19 | transcript | ENST00000315596.15 | protein_coding | 3/34 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
PDZRN3_chr3_73377431_73629941 | 73580247 | A | ATGTATAC others(46): Show |
intron_variant | MODIFIER | HG03490.hp2 | a0002 | a0002c0003 | a0002c0003t0001 | a0002c0003t0001g0119 | 1 | 216 | 0.0046 | 53 | c.918 others(72): Show |
PDZRN3 | ENSG00000121440.15 | transcript | ENST00000263666.9 | protein_coding | 3/9 | chr3 | TogoVar | ||||||
PEBP1_chr12_118131124_118150584 | 118133183 | T | TATATTTT others(46): Show |
upstream_gene_variant | MODIFIER | NA19030.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0067 | 1 | 426 | 0.0024 | 53 | c.-30 others(64): Show |
PEBP1 | ENSG00000089220.5 | transcript | ENST00000261313.3 | protein_coding | 2940 | chr12 | TogoVar | ||||||
PER2_chr2_238239044_238293610 | 238269460 | C | CAACTAAC others(46): Show |
intron_variant | MODIFIER | HG01099.hp2 HG01243.hp1 HG01891.hp1 others(22): Show |
a0001a0004a0010 | a0001c0001a0004c0008a0010c0018 | a0001c0001t0006a0001c0001t0010a0001c0001t0022others(2): Show | a0001c0001t0006g0026a0001c0001t0006g0044a0001c0001t0006g0224others(21): Show | 25 | 370 | 0.0676 | 53 | c.773 others(68): Show |
PER2 | ENSG00000132326.13 | transcript | ENST00000254657.8 | protein_coding | 6/22 | chr2 | TogoVar | ||||||
PERM1_chr1_970198_987093 | 984611 | C | CTTTATTT others(46): Show |
upstream_gene_variant | MODIFIER | NA19070.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0002 | 1 | 408 | 0.0025 | 53 | c.-26 others(64): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2519 | chr1 | TogoVar | ||||||
PERM1_chr1_970198_987093 | 984611 | C | CTTTATTT others(46): Show |
upstream_gene_variant | MODIFIER | HG00597.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0136 | 1 | 408 | 0.0025 | 53 | c.-26 others(64): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2519 | chr1 | TogoVar | ||||||
PERM1_chr1_970198_987093 | 984611 | C | CTTTATTT others(46): Show |
upstream_gene_variant | MODIFIER | HG04204.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0037 | 1 | 408 | 0.0025 | 53 | c.-26 others(64): Show |
PERM1 | ENSG00000187642.10 | transcript | ENST00000433179.4 | protein_coding | 2519 | chr1 | TogoVar | ||||||
PEX1_chr7_92482025_92533520 | 92516039 | A | AAGAGAAG others(46): Show |
intron_variant | MODIFIER | NA18981.hp2 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0232 | 1 | 310 | 0.0032 | 53 | c.123 others(72): Show |
PEX1 | ENSG00000127980.16 | transcript | ENST00000248633.9 | protein_coding | 5/23 | chr7 | TogoVar | ||||||
PFKP_chr10_3062548_3141802 | 3062590 | C | CCTACTCA others(46): Show |
upstream_gene_variant | MODIFIER | NA18941.hp2 | a0001 | a0001c0005 | a0001c0005t0006 | a0001c0005t0006g0053 | 1 | 402 | 0.0025 | 53 | c.-50 others(64): Show |
PFKP | ENSG00000067057.19 | transcript | ENST00000381125.9 | protein_coding | 4957 | chr10 | TogoVar | ||||||
PGAP6_chr16_365788_386978 | 370388 | C | CCCCTACC others(46): Show |
downstream_gene_variant | MODIFIER | HG03453.hp1 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0143 | 1 | 376 | 0.0027 | 53 | c.*15 others(64): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 399 | chr16 | TogoVar | ||||||
PGAP6_chr16_365788_386978 | 370388 | C | CCCCTACC others(46): Show |
downstream_gene_variant | MODIFIER | HG01891.hp1 HG02486.hp2 |
a0002 | a0002c0002a0002c0005 | a0002c0002t0009a0002c0005t0017 | a0002c0002t0009g0011a0002c0005t0017g0051 | 2 | 376 | 0.0053 | 53 | c.*15 others(64): Show |
PGAP6 | ENSG00000129925.11 | transcript | ENST00000431232.7 | protein_coding | 399 | chr16 | TogoVar | ||||||
PGLYRP3_chr1_153292116_153317952 | 153297550 | G | GGAAGGAA others(46): Show |
3_prime_UTR_variant | MODIFIER | HG02622.hp2 | a0002 | a0002c0002 | a0002c0002t0098 | a0002c0002t0098g0071 | 1 | 434 | 0.0023 | 53 | c.*40 others(62): Show |
PGLYRP3 | ENSG00000159527.4 | transcript | ENST00000683862.1 | protein_coding | 8/8 | 405 | chr1 | TogoVar | |||||
PHF21B_chr22_44876162_45015005 | 44946161 | C | CAGAGGAG others(46): Show |
intron_variant | MODIFIER | HG01943.hp2 HG02055.hp2 HG02630.hp2 others(7): Show |
a0001 | a0001c0001a0001c0002a0001c0006 | a0001c0001t0004a0001c0002t0004a0001c0002t0006others(2): Show | a0001c0001t0004g0176a0001c0002t0004g0162a0001c0002t0006g0105others(7): Show | 10 | 300 | 0.0333 | 53 | c.121 others(72): Show |
PHF21B | ENSG00000056487.17 | transcript | ENST00000313237.10 | protein_coding | 2/12 | chr22 | TogoVar | ||||||
PHF3_chr6_63630802_63731011 | 63688224 | C | CCCCCTCC others(46): Show |
intron_variant | MODIFIER | HG02280.hp2 | a0001 | a0001c0001 | a0001c0001t0034 | a0001c0001t0034g0287 | 1 | 320 | 0.0031 | 53 | c.218 others(72): Show |
PHF3 | ENSG00000118482.12 | transcript | ENST00000262043.8 | protein_coding | 4/15 | chr6 | TogoVar | ||||||
PIH1D2_chr11_112062798_112079017 | 112067685 | A | AAAAAAAT others(46): Show |
downstream_gene_variant | MODIFIER | NA18969.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0003 | 1 | 384 | 0.0026 | 53 | c.*18 others(62): Show |
PIH1D2 | ENSG00000150773.12 | transcript | ENST00000280350.10 | protein_coding | 112 | chr11 | TogoVar | ||||||
PITPNM2_chr12_122978480_123156090 | 123031475 | A | ACCTATGG others(46): Show |
intron_variant | MODIFIER | HG01884.hp2 | a0002 | a0002c0003 | a0002c0003t0004 | a0002c0003t0004g0011 | 1 | 230 | 0.0044 | 53 | c.78+ others(68): Show |
PITPNM2 | ENSG00000090975.14 | transcript | ENST00000320201.10 | protein_coding | 3/25 | chr12 | TogoVar |