http://identifiers.org/hco/7/GRCh38#140084819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#39113621-C-A

140084819-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: 3 prime UTR variant
orthologous variants: 39113621-C-G

140084843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: 3 prime UTR variant
orthologous variants: 39113645-G-A

http://identifiers.org/hco/7/GRCh38#140085088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#39113890-C-A

140085088-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 39113890-C-G

140085088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 39113890-C-T

http://identifiers.org/hco/7/GRCh38#140085099-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#39113901-A-C

140085100-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 39113902-C-G

140085100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 39113902-C-T

140085128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 39113929-T-C

http://identifiers.org/hco/7/GRCh38#140085173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#39113946-C-A

http://identifiers.org/hco/7/GRCh38#140085204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#39113974-C-A

140085204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 39113974-C-T

140086594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 39115342-G-T

140086687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 39115435-G-T

140086708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 39115456-G-A

http://identifiers.org/hco/7/GRCh38#140087080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#39115935-C-A

140087231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 39116085-A-G

140087703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 39116876-A-G

140088036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 39117243-T-C

140088145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 39117351-T-C

http://identifiers.org/hco/7/GRCh38#140088196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#39117387-C-A

140088216-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 39117407-T-G

140088219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 39117410-A-G

140088249-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 39117438-T-G

http://identifiers.org/hco/7/GRCh38#140088724-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#39117913-A-C

140088740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 39117932-A-G

140088751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 39117943-C-T

140088776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 39117967-A-G

140089069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 39118187-T-C

http://identifiers.org/hco/7/GRCh38#140089526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#39118634-C-A

140089583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 39118692-G-T

140089753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 39118842-T-C

http://identifiers.org/hco/7/GRCh38#140089990-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#39119070-A-C

140089998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 39119079-A-G

140090400-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 39119448-A-T

140090741-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 39119792-T-A

http://identifiers.org/hco/7/GRCh38#140091029-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#39120081-A-C

140091082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 39120133-A-G

140091083-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 39120134-C-G

140091083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 39120134-C-T

140091240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39120299-G-A

140091240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39120299-G-T

http://identifiers.org/hco/7/GRCh38#140091284-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#39120340-A-C

140091293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39120350-G-A

140091293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39120350-G-T

http://identifiers.org/hco/7/GRCh38#140091534-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#39120531-C-A

140091649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39120643-T-C

http://identifiers.org/hco/7/GRCh38#140094015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#39122362-C-A

http://identifiers.org/hco/7/GRCh38#140094221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#39122564-C-A

140095949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39123104-T-C

140096316-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39123417-T-A

http://identifiers.org/hco/7/GRCh38#140096440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#39123629-C-A

140096579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 39123813-G-A

140096586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 39123820-C-T

http://identifiers.org/hco/7/GRCh38#140096673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#39123907-C-A

140096673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 39123907-C-T

140096852-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39124076-T-G

140097083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39124301-A-G

140097212-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39124392-T-A

140097611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 39124704-C-T

http://identifiers.org/hco/7/GRCh38#140097641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: NMD_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#39124734-C-A

140097641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: NMD_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 39124734-C-T

http://identifiers.org/hco/7/GRCh38#140097653-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#39124746-A-C

140097711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39124770-G-A

140097711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39124770-G-T

140097712-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39124771-T-A

http://identifiers.org/hco/7/GRCh38#140097723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#39124782-C-A

140097723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39124782-C-T

140097991-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39124991-T-G

140098888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 39125885-G-A

140100046-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39126367-T-A

140100125-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39126445-T-G

http://identifiers.org/hco/7/GRCh38#140100128-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#39126452-A-C

140100128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39126452-A-G

140100204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39126530-T-C

140100628-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39126930-T-G

140110879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39129559-C-T

http://identifiers.org/hco/7/GRCh38#140110970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#39129634-C-A

140110970-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39129634-C-G

140110976-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39129640-T-A

140110976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39129640-T-C

140110976-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39129640-T-G

140110995-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39129654-T-A

140110995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39129654-T-C

140110995-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39129654-T-G

140111305-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39129938-T-A

140111305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39129938-T-C

http://identifiers.org/hco/7/GRCh38#140111309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#39129942-C-A

140111309-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39129942-C-G

140111309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39129942-C-T

140111432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39130209-G-A

140111461-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39130241-C-G

140112991-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39131998-G-C

140113291-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39134914-A-T

http://identifiers.org/hco/7/GRCh38#140113320-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#39134942-A-C

http://identifiers.org/hco/7/GRCh38#140113356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#39134967-C-A

140113356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39134967-C-T

140113754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39135348-A-G

140116743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39140226-T-C

140116895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39140368-G-A

140119091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 39142009-A-G

http://identifiers.org/hco/7/GRCh38#140119237-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#39142159-A-C

140119262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39142184-T-C

140119384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39142292-A-G

http://identifiers.org/hco/7/GRCh38#140119578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#39142619-C-A

140119578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39142619-C-T

140119782-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39142880-C-G

http://identifiers.org/hco/7/GRCh38#140119783-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#39142881-A-C

140120209-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39143269-A-T

140120362-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39143528-T-A

140120362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39143528-T-C

140120363-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39143529-T-A

http://identifiers.org/hco/7/GRCh38#140120631-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#39143781-A-C

http://identifiers.org/hco/7/GRCh38#140120647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#39143797-C-A

140120666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39143816-T-C

140120676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39143826-T-C

http://identifiers.org/hco/7/GRCh38#140124509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#39145183-C-A

140124509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39145183-C-T

140125123-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39146324-C-G

http://identifiers.org/hco/7/GRCh38#140125126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#39146327-C-A

140125154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39146340-C-T

140126219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39146614-G-T

140126230-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39146625-G-C

140126322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39146714-T-C

140126465-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39146863-A-T

140126478-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39146876-A-T

140126486-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39146884-A-T

http://identifiers.org/hco/7/GRCh38#140126490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#39146888-C-A

140126490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39146888-C-T

http://identifiers.org/hco/7/GRCh38#140126530-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#39146962-A-C

http://identifiers.org/hco/7/GRCh38#140126573-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#39147005-A-C

140126573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39147005-A-G

140126597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39147026-G-A

140126597-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39147026-G-C

140126597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39147026-G-T

140126603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39147032-G-A

140126603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39147032-G-T

http://identifiers.org/hco/7/GRCh38#140126870-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#39147293-A-C

140126883-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39147306-T-A

140126883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39147306-T-C

http://identifiers.org/hco/7/GRCh38#140126894-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#39147317-A-C

140126894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39147317-A-G

140127281-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39147547-T-G

140127291-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39147557-T-A

140127291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39147557-T-C

140127314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39147581-T-C

140127320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39147587-A-G

140127348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39147615-G-T

140127613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39147874-G-T

140127623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39147884-G-A

140127623-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39147884-G-C

140127623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39147884-G-T

140127916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39148061-T-C

http://identifiers.org/hco/7/GRCh38#140127983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#39148127-C-A

140127983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39148127-C-T

140128172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39148298-C-T

140128742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39149533-T-C

140128751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39149547-T-C

140128816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39149611-A-G

http://identifiers.org/hco/7/GRCh38#140129163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#39149914-C-A

140129419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39150147-C-T

140129437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39150164-T-C

140129480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39150199-A-G

140129480-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39150199-A-T

140129578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: synonymous variant
orthologous variants: 39150297-G-A

140129578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: synonymous variant
orthologous variants: 39150297-G-T

140129726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39150442-G-A

140129726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39150442-G-T

http://identifiers.org/hco/7/GRCh38#140129750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#39150474-C-A

140129750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39150474-C-T

140132024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39150702-T-C

140132024-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39150702-T-G

140132112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39150775-G-A

140132112-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39150775-G-C

140132465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39151106-T-C

http://identifiers.org/hco/7/GRCh38#140132510-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#39151148-A-C

140132918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39151716-G-A

140133089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39151903-T-C

140133118-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39151932-G-C

140133336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39152108-T-C

140133351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39152123-T-C

140133411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39152181-G-A

140133411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39152181-G-T

140133441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39152207-C-T

140133487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39152252-G-T

140133713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39152475-T-C

140133790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39152554-T-C

http://identifiers.org/hco/7/GRCh38#140134895-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#39153259-A-C

140134967-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39153330-G-C

140135650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39153932-C-T

140135992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39155718-C-T

140136118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39155870-A-G

140136123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39155875-G-A

140136130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39155882-G-T

140136238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39155987-A-G

http://identifiers.org/hco/7/GRCh38#140136241-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#39155990-A-C

140136268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39156017-G-A

140136452-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39156191-G-C

140136510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39156266-C-T

140137245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39156691-C-T

http://identifiers.org/hco/7/GRCh38#140137491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#39156937-C-A

140139028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39158406-G-A

140139028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39158406-G-T

140139095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39158452-T-C

140139136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: synonymous variant
orthologous variants: 39158493-G-T

140139211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39158567-A-G

140139264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39158606-A-G

140139264-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39158606-A-T

http://identifiers.org/hco/7/GRCh38#140139298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#39158640-C-A

140139445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39158778-T-C

140139460-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39158792-T-A

140139547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39158899-C-T

140146240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39162375-A-G

140146481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39162583-C-T

140146489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39162591-T-C

140146489-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39162591-T-G

140146629-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39162727-G-C

140147030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39163096-C-T

140149046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39163296-A-G

140149997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39163927-G-A

140150419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39165015-A-G

140150488-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39165091-T-G

140150541-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39165131-G-C

140150666-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39165262-T-A

140150666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39165262-T-C

http://identifiers.org/hco/7/GRCh38#140150851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#39165465-C-A

140150851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39165465-C-T

140150914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39165526-C-T

140151198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39165954-C-T

140151530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39166440-G-T

http://identifiers.org/hco/7/GRCh38#140152816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#39168407-C-A

140152816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39168407-C-T

140153201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39168867-G-A

140153229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39168907-C-T

140153298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39168977-T-C

http://identifiers.org/hco/7/GRCh38#140153526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#39169211-C-A

140153531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39169216-C-T

140153600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39169282-C-T

140153610-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39169388-T-G

140153723-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39169519-C-G

140153990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39169778-G-A

140153990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39169778-G-T

140154053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39169849-T-C

http://identifiers.org/hco/7/GRCh38#140169139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#39175126-C-A

140169139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39175126-C-T

140169346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39175459-T-C

140169487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39175573-G-A

140170120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39175879-G-A

140170120-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39175879-G-C

140171857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39179030-T-C

140171955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39179149-A-G

140172109-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39179382-G-C

140172194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39179462-T-C

140172424-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39179674-A-T

140172460-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39179731-T-G

140173132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39180292-G-A

140173257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39180438-A-G

140173266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39180448-T-C

140173321-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39180474-G-C

140173325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39180478-G-A

140173353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39180505-T-C

140173482-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39180604-A-T

140173722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39180822-T-C

140173722-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39180822-T-G

http://identifiers.org/hco/7/GRCh38#140173751-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#39180839-A-C

140173827-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39180886-C-G

140173827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39180886-C-T

140173904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39180923-C-T

140173939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39180957-G-A

140174254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39181135-C-T

140174291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39181174-T-C

140175470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39182251-G-A

140175676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron_variant, undefined
orthologous variants: 39182457-G-A

140175743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39182529-T-C

http://identifiers.org/hco/7/GRCh38#140176015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#39182749-C-A

140176023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39182755-G-T

140176036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron_variant, undefined
orthologous variants: 39182768-C-T

140176258-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39182920-C-G

140176264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39182925-C-T

140176368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39183004-C-T

140176392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39183028-G-A

140176392-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39183028-G-C

http://identifiers.org/hco/7/GRCh38#140176565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#39183202-C-A

140176566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39183203-C-T

140176607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39183244-G-A

140176607-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39183244-G-C

140176607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39183244-G-T

140176608-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39183245-G-T

140176613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39183250-G-A

140176650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39183286-G-A

140176650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39183286-G-T

140176701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39183333-T-C

140176701-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39183333-T-G

http://identifiers.org/hco/7/GRCh38#140176704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#39183336-C-A

140176704-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39183336-C-G

140176704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: intron variant
orthologous variants: 39183336-C-T

http://identifiers.org/hco/7/GRCh38#140176830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#39183461-C-A

140176830-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: synonymous variant
orthologous variants: 39183461-C-G

140176830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: synonymous variant
orthologous variants: 39183461-C-T

http://identifiers.org/hco/7/GRCh38#140176866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#39183497-C-A

140176866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22224
most severe consequence: synonymous variant
orthologous variants: 39183497-C-T