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CHROM
POS
REF
ALT
Gene
HGVS.c
HGVS.p
dbSNP142 ID
chr12
31244665
C
T
missense_variant
MODERATE
DDX11
c.1102C>T
chr12
31244619
C
T
intron_variant
MODIFIER
DDX11
c.1090-34C>T
chr12
31244601
G
C
intron_variant
MODIFIER
DDX11
c.1090-52G>C
chr12
31244592
G
A
intron_variant
MODIFIER
DDX11
c.1090-61G>A
chr12
31242725
T
C
intron_variant
MODIFIER
DDX11
c.881-95T>C
chr12
31242718
T
C
intron_variant
MODIFIER
DDX11
c.881-102T>C
chr12
31242440
A
G
intron_variant
MODIFIER
DDX11
c.880+16A>G
chr12
31242399
T
C
synonymous_variant
LOW
DDX11
c.855T>C
chr12
31242314
T
C
intron_variant
MODIFIER
DDX11
c.793-23T>C
chr12
31242271
G
A
intron_variant
MODIFIER
DDX11
c.793-66G>A
chr12
31240960
G
A
intron_variant
MODIFIER
DDX11
c.684+43G>A
chr12
31240925
A
G
splice_region_variant&intron_variant
LOW
DDX11
c.684+8A>G
chr12
31240862
A
T
intron_variant
MODIFIER
DDX11
c.639-10A>T
chr12
31238946
A
G
intron_variant
MODIFIER
DDX11
c.638+886A>G
chr12
31238075
G
A
intron_variant
MODIFIER
DDX11
c.638+15G>A
chr12
31237700
G
A
intron_variant
MODIFIER
DDX11
c.480+97G>A
chr12
31237026
A
G
intron_variant
MODIFIER
DDX11
c.393+31A>G
chr12
25388290
G
T
intron_variant
MODIFIER
KRAS
c.112-7944C>A
chr12
25368462
C
T
synonymous_variant
LOW
KRAS
c.483G>A
chr12
25362217
A
G
3_prime_UTR_variant
MODIFIER
KRAS
c.*633T>C