Page size
CHROM
POS
REF
ALT
Gene
HGVS.c
HGVS.p
dbSNP142 ID
chr1
228508870
G
A
intron_variant
MODIFIER
OBSCN
c.17374-175G>A
chr1
228505699
T
C
synonymous_variant
LOW
OBSCN
c.16827T>C
chr1
228505668
C
G
missense_variant
MODERATE
OBSCN
c.16796C>G
chr1
228505519
G
A
intron_variant
MODIFIER
OBSCN
c.16720+67G>A
chr1
228505204
G
A
missense_variant
MODERATE
OBSCN
c.16472G>A
chr1
228504701
G
GCTCC
intron_variant
MODIFIER
OBSCN
c.16432+16_16432+17insCTCC
chr1
228504650
G
A
missense_variant
MODERATE
OBSCN
c.16397G>A
chr1
228504472
T
C
missense_variant
MODERATE
OBSCN
c.16219T>C
chr1
228503863
C
T
intron_variant
MODIFIER
OBSCN
c.16156+43C>T
chr1
228503677
A
G
missense_variant
MODERATE
OBSCN
c.16013A>G
chr1
228497053
A
G
intron_variant
MODIFIER
OBSCN
c.15807+57A>G
chr1
228496148
C
T
intron_variant
MODIFIER
OBSCN
c.15610+64C>T
chr1
228496014
G
A
synonymous_variant
LOW
OBSCN
c.15540G>A
chr1
228495696
T
C
intron_variant
MODIFIER
OBSCN
c.15338-116T>C
chr1
228494696
G
A
synonymous_variant
LOW
OBSCN
c.14892G>A
chr1
228494438
C
T
intron_variant
MODIFIER
OBSCN
c.14797+99C>T
chr1
228494382
T
C
intron_variant
MODIFIER
OBSCN
c.14797+43T>C
chr1
228491661
A
G
intron_variant
MODIFIER
OBSCN
c.14002+22A>G
chr1
228482285
T
C
intron_variant
MODIFIER
OBSCN
c.12682+169T>C
chr1
228482028
G
C
synonymous_variant
LOW
OBSCN
c.12594G>C