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CHROM
POS
REF
ALT
Gene
HGVS.c
HGVS.p
dbSNP142 ID
chr1
228459677
C
T
missense_variant
MODERATE
OBSCN
c.5741C>T
chr1
228456147
T
C
intron_variant
MODIFIER
OBSCN
c.5414-84T>C
chr1
228451836
C
T
synonymous_variant
LOW
OBSCN
c.5157C>T
chr1
228447521
G
C
intron_variant
MODIFIER
OBSCN
c.5137+44G>C
chr1
228447519
T
A
intron_variant
MODIFIER
OBSCN
c.5137+42T>A
chr1
228447513
T
G
intron_variant
MODIFIER
OBSCN
c.5137+36T>G
chr1
228444565
T
A
missense_variant
MODERATE
OBSCN
c.4799T>A
chr1
228437603
T
C
intron_variant
MODIFIER
OBSCN
c.4310-63T>C
chr1
228434467
T
C
synonymous_variant
LOW
OBSCN
c.4272T>C
chr1
228434072
C
T
intron_variant
MODIFIER
OBSCN
c.4034-157C>T
chr1
228431034
A
G
missense_variant
MODERATE
OBSCN
c.3356A>G
chr1
228412392
C
T
synonymous_variant
LOW
OBSCN
c.3162C>T
chr1
228412308
G
A
synonymous_variant
LOW
OBSCN
c.3078G>A
chr1
228412227
T
C
synonymous_variant
LOW
OBSCN
c.2997T>C
chr1
228412106
T
C
intron_variant
MODIFIER
OBSCN
c.2930-54T>C
chr1
228412068
G
C
intron_variant
MODIFIER
OBSCN
c.2930-92G>C
chr1
228402121
A
G
missense_variant
MODERATE
OBSCN
c.1505A>G
chr1
228402047
A
G
synonymous_variant
LOW
OBSCN
c.1431A>G
chr1
228399766
T
C
synonymous_variant
LOW
OBSCN
c.282T>C
chr1
228399482
C
G
5_prime_UTR_variant
MODIFIER
OBSCN
c.-3C>G