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CHROM
POS
REF
ALT
Gene
HGVS.c
HGVS.p
dbSNP142 ID
chr1
22205408
T
C
intron_variant
MODIFIER
HSPG2
c.2474+79A>G
chr1
22204630
G
A
intron_variant
MODIFIER
HSPG2
c.2688+49C>T
chr1
22203259
A
G
intron_variant
MODIFIER
HSPG2
c.2689-114T>C
chr1
22202109
C
T
intron_variant
MODIFIER
HSPG2
c.3305+13G>A
chr1
22201331
C
T
intron_variant
MODIFIER
HSPG2
c.3417+53G>A
chr1
22200835
C
G
intron_variant
MODIFIER
HSPG2
c.3659+64G>C
chr1
22199821
G
A
intron_variant
MODIFIER
HSPG2
c.3796+47C>T
chr1
22199081
A
T
intron_variant
MODIFIER
HSPG2
c.4032+32T>A
chr1
22191454
G
A
missense_variant
MODERATE
HSPG2
c.4511C>T
chr1
22186234
A
G
intron_variant
MODIFIER
HSPG2
c.5186-65T>C
chr1
22183739
A
G
intron_variant
MODIFIER
HSPG2
c.5397+39T>C
chr1
22183471
A
C
intron_variant
MODIFIER
HSPG2
c.5578+37T>G
chr1
22180548
T
C
intron_variant
MODIFIER
HSPG2
c.6442+138A>G
chr1
22179673
T
C
intron_variant
MODIFIER
HSPG2
c.6443-110A>G
chr1
22176542
G
A
missense_variant
MODERATE
HSPG2
c.7441C>T
chr1
22174600
A
G
intron_variant
MODIFIER
HSPG2
c.7741-14T>C
chr1
22173810
T
G
intron_variant
MODIFIER
HSPG2
c.8167+37A>C
chr1
22172911
C
T
intron_variant
MODIFIER
HSPG2
c.8319+30G>A
chr1
22168216
C
T
intron_variant
MODIFIER
HSPG2
c.9197-50G>A
chr1
22160148
C
T
intron_variant
MODIFIER
HSPG2
c.10834-41G>A