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CHROM
POS
REF
ALT
Gene
HGVS.c
HGVS.p
dbSNP142 ID
chr16
16291858
G
C
intron_variant
MODIFIER
ABCC6
c.1338+20C>G
chr16
16286614
G
C
intron_variant
MODIFIER
ABCC6
c.1431+73C>G
chr16
16286586
C
T
intron_variant
MODIFIER
ABCC6
c.1431+101G>A
chr16
16286519
G
C
intron_variant
MODIFIER
ABCC6
c.1431+168C>G
chr16
16284272
C
T
intron_variant
MODIFIER
ABCC6
c.1432-48G>A
chr16
16281154
C
A
intron_variant
MODIFIER
ABCC6
c.1780-86G>T
chr16
16281007
A
G
missense_variant
MODERATE
ABCC6
c.1841T>C
chr16
16280921
T
C
intron_variant
MODIFIER
ABCC6
c.1867+60A>G
chr16
16280895
A
G
intron_variant
MODIFIER
ABCC6
c.1867+86T>C
chr16
16280889
C
T
intron_variant
MODIFIER
ABCC6
c.1867+92G>A
chr16
16278975
GC
G
intron_variant
MODIFIER
ABCC6
c.1868-85delG
chr16
16278869
G
C
synonymous_variant
LOW
ABCC6
c.1890C>G
chr16
16278863
G
T
missense_variant
MODERATE
ABCC6
c.1896C>A
chr16
16278695
A
T
intron_variant
MODIFIER
ABCC6
c.1943+121T>A
chr16
16272670
T
C
synonymous_variant
LOW
ABCC6
c.2400A>G
chr16
16271357
T
C
missense_variant
MODERATE
ABCC6
c.2542A>G
chr16
16269962
G
A
intron_variant
MODIFIER
ABCC6
c.2591-119C>T
chr16
16269633
TG
T
intron_variant
MODIFIER
ABCC6
c.2666+134delC
chr16
16267079
A
G
intron_variant
MODIFIER
ABCC6
c.2787+62T>C
chr16
16263864
A
G
intron_variant
MODIFIER
ABCC6
c.2788-154T>C