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CHROM
POS
REF
ALT
Gene
HGVS.c
HGVS.p
dbSNP142 ID
chr3
10088266
G
T
splice_region_variant&synonymous_variant
LOW
FANCD2
c.1137G>T
chr3
10088242
G
A
intron_variant
MODIFIER
FANCD2
c.1135-22G>A
chr3
10088239
G
A
intron_variant
MODIFIER
FANCD2
c.1135-25G>A
chr3
10085624
G
T
intron_variant
MODIFIER
FANCD2
c.1134+76G>T
chr3
10085536
A
G
synonymous_variant
LOW
FANCD2
c.1122A>G
chr3
10085406
G
T
intron_variant
MODIFIER
FANCD2
c.1099-107G>T
chr3
10085130
C
G
intron_variant
MODIFIER
FANCD2
c.990-38C>G
chr3
10085035
G
T
intron_variant
MODIFIER
FANCD2
c.990-133G>T
chr3
10084224
C
T
intron_variant
MODIFIER
FANCD2
c.784-19C>T
chr3
10083169
C
T
intron_variant
MODIFIER
FANCD2
c.696-138C>T
chr3
10081631
A
G
intron_variant
MODIFIER
FANCD2
c.695+102A>G
chr3
10081545
G
C
intron_variant
MODIFIER
FANCD2
c.695+16G>C
chr3
10077955
A
G
intron_variant
MODIFIER
FANCD2
c.439-16A>G
chr3
10077023
T
C
intron_variant
MODIFIER
FANCD2
c.438+106T>C
chr3
10076975
A
C
intron_variant
MODIFIER
FANCD2
c.438+58A>C
chr3
10076842
CTT
C
intron_variant
MODIFIER
FANCD2
c.378-14_378-13delTT
chr3
10074145
G
T
intron_variant
MODIFIER
FANCD2
c.65-371G>T
chr3
10073824
G
C
intron_variant
MODIFIER
FANCD2
c.65-692G>C
chr3
9985656
C
T
synonymous_variant
LOW
CRELD1
c.1119C>T
chr3
9979660
A
G
intron_variant
MODIFIER
CRELD1
c.369-39A>G