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CHROM
POS
REF
ALT
Gene
HGVS.c
HGVS.p
dbSNP142 ID
chr1
228480964
A
G
intron_variant
MODIFIER
OBSCN
c.12155-90A>G
chr1
228480282
A
G
synonymous_variant
LOW
OBSCN
c.11949A>G
chr1
228475954
C
T
missense_variant
MODERATE
OBSCN
c.11291C>T
chr1
228475570
G
A
synonymous_variant
LOW
OBSCN
c.11007G>A
chr1
228468566
A
G
intron_variant
MODIFIER
OBSCN
c.9484+69A>G
chr1
228468069
G
A
missense_variant
MODERATE
OBSCN
c.9140G>A
chr1
228467087
C
T
synonymous_variant
LOW
OBSCN
c.8625C>T
chr1
228465674
C
CAAG
intron_variant
MODIFIER
OBSCN
c.8146+115_8146+116insAAG
chr1
228465370
T
G
splice_region_variant&intron_variant
LOW
OBSCN
c.8041+3T>G
chr1
228465051
A
G
intron_variant
MODIFIER
OBSCN
c.7879+37A>G
chr1
228464842
C
G
intron_variant
MODIFIER
OBSCN
c.7726-19C>G
chr1
228464316
C
G
missense_variant
MODERATE
OBSCN
c.7511C>G
chr1
228464276
T
C
missense_variant
MODERATE
OBSCN
c.7471T>C
chr1
228464248
T
G
missense_variant
MODERATE
OBSCN
c.7443T>G
chr1
228462377
G
A
missense_variant
MODERATE
OBSCN
c.6913G>A
chr1
228462332
G
A
missense_variant
MODERATE
OBSCN
c.6868G>A
chr1
228461615
G
A
missense_variant
MODERATE
OBSCN
c.6407G>A
chr1
228461408
A
AG
intron_variant
MODIFIER
OBSCN
c.6263-63_6263-62insG
chr1
228461274
C
A
intron_variant
MODIFIER
OBSCN
c.6262+26C>A
chr1
228461129
A
G
missense_variant
MODERATE
OBSCN
c.6143A>G