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CHROM
POS
REF
ALT
Gene
HGVS.c
HGVS.p
dbSNP142 ID
chr12
22078838
T
G
intron_variant
MODIFIER
ABCC9
c.406+38A>C
chr12
22078571
T
A
intron_variant
MODIFIER
ABCC9
c.406+305A>T
chr12
22078556
T
C
intron_variant
MODIFIER
ABCC9
c.406+320A>G
chr12
22078245
G
C
intron_variant
MODIFIER
ABCC9
c.406+631C>G
chr12
22068849
G
T
splice_region_variant&intron_variant
LOW
ABCC9
c.574-5C>A
chr12
22065699
G
GA
intron_variant
MODIFIER
ABCC9
c.1011+106_1011+107insT
chr12
22063971
A
G
intron_variant
MODIFIER
ABCC9
c.1012-59T>C
chr12
22063749
T
C
intron_variant
MODIFIER
ABCC9
c.1164+11A>G
chr12
22063737
G
T
intron_variant
MODIFIER
ABCC9
c.1164+23C>A
chr12
22063115
A
G
synonymous_variant
LOW
ABCC9
c.1296T>C
chr12
22047174
C
T
intron_variant
MODIFIER
ABCC9
c.1660-66G>A
chr12
22047151
G
T
intron_variant
MODIFIER
ABCC9
c.1660-43C>A
chr12
22035883
T
G
intron_variant
MODIFIER
ABCC9
c.1912-76A>C
chr12
22035873
C
T
intron_variant
MODIFIER
ABCC9
c.1912-66G>A
chr12
22017486
C
G
intron_variant
MODIFIER
ABCC9
c.2199-75G>C
chr12
22017422
A
G
intron_variant
MODIFIER
ABCC9
c.2199-11T>C
chr12
22016004
GA
G
intron_variant
MODIFIER
ABCC9
c.2238-17delT
chr12
22015768
G
A
intron_variant
MODIFIER
ABCC9
c.2339+119C>T
chr12
22005510
A
G
intron_variant
MODIFIER
ABCC9
c.2506-71T>C
chr12
22005003
T
G
intron_variant
MODIFIER
ABCC9
c.2769+28A>C