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CHROM
POS
REF
ALT
Gene
HGVS.c
HGVS.p
dbSNP142 ID
chr16
89829196
G
C
intron_variant
MODIFIER
FANCA
c.2779-766C>G
chr16
89828484
C
T
intron_variant
MODIFIER
FANCA
c.2779-54G>A
chr16
89828437
A
G
splice_region_variant&intron_variant
LOW
FANCA
c.2779-7T>C
chr16
89825065
G
A
synonymous_variant
LOW
FANCA
c.2901C>T
chr16
89818491
T
C
intron_variant
MODIFIER
FANCA
c.3066+55A>G
chr16
89816424
G
T
intron_variant
MODIFIER
FANCA
c.3067-114C>A
chr16
89816407
A
G
intron_variant
MODIFIER
FANCA
c.3067-97T>C
chr16
89816367
T
G
intron_variant
MODIFIER
FANCA
c.3067-57A>C
chr16
89816333
C
T
intron_variant
MODIFIER
FANCA
c.3067-23G>A
chr16
89816314
A
G
splice_region_variant&intron_variant
LOW
FANCA
c.3067-4T>C
chr16
89815217
C
T
intron_variant
MODIFIER
FANCA
c.3240-42G>A
chr16
89813194
C
T
intron_variant
MODIFIER
FANCA
c.3408+45G>A
chr16
89812851
CTG
C
intron_variant
MODIFIER
FANCA
c.3513+139_3513+140delCA
chr16
89811546
A
G
intron_variant
MODIFIER
FANCA
c.3514-67T>C
chr16
89809319
T
C
synonymous_variant
LOW
FANCA
c.3654A>G
chr16
89809171
C
T
intron_variant
MODIFIER
FANCA
c.3765+37G>A
chr16
89807233
C
G
synonymous_variant
LOW
FANCA
c.3807G>C
chr16
89805914
T
C
missense_variant
MODERATE
FANCA
c.3982A>G
chr16
89804335
CT
C
3_prime_UTR_variant
MODIFIER
FANCA
c.*673delA
chr16
88505748
G
A
3_prime_UTR_variant
MODIFIER
ZNF469
c.*8G>A