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CHROM
POS
REF
ALT
Gene
HGVS.c
HGVS.p
dbSNP142 ID
chr1
22168310
A
G
intron_variant
MODIFIER
HSPG2
c.9197-144T>C
chr1
22168216
C
T
intron_variant
MODIFIER
HSPG2
c.9197-50G>A
chr1
22167988
G
T
intron_variant
MODIFIER
HSPG2
c.9331+44C>A
chr1
22167786
G
A
splice_region_variant&intron_variant
LOW
HSPG2
c.9332-8C>T
chr1
22167785
G
A
splice_region_variant&intron_variant
LOW
HSPG2
c.9332-7C>T
chr1
22165987
G
A
missense_variant
MODERATE
HSPG2
c.9769C>T
chr1
22165901
A
G
synonymous_variant
LOW
HSPG2
c.9855T>C
chr1
22161275
G
A
synonymous_variant
LOW
HSPG2
c.10620C>T
chr1
22160148
C
T
intron_variant
MODIFIER
HSPG2
c.10834-41G>A
chr1
22160111
C
T
splice_region_variant&intron_variant
LOW
HSPG2
c.10834-4G>A
chr1
22159008
C
A
synonymous_variant
LOW
HSPG2
c.11190G>T
chr1
22158120
G
T
intron_variant
MODIFIER
HSPG2
c.11355+25C>A
chr1
22157689
G
A
intron_variant
MODIFIER
HSPG2
c.11565+19C>T
chr1
22155853
C
T
intron_variant
MODIFIER
HSPG2
c.11995+23G>A
chr1
22155841
T
C
intron_variant
MODIFIER
HSPG2
c.11995+35A>G
chr1
22155723
T
C
intron_variant
MODIFIER
HSPG2
c.11996-151A>G
chr1
22154987
G
A
intron_variant
MODIFIER
HSPG2
c.12241-68C>T
chr1
22154845
A
G
synonymous_variant
LOW
HSPG2
c.12315T>C
chr1
22150160
G
T
synonymous_variant
LOW
HSPG2
c.12955C>A
chr1
22150120
C
T
missense_variant
MODERATE
HSPG2
c.12995G>A