18858961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86321602-T-C

18858962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86321603-G-A

18859084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86321718-T-C

18859084-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86321718-T-G

18859142-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86321778-A-T

18859166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 86321797-G-A

18859459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86322066-C-T

18859596-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86322213-T-G

http://identifiers.org/hco/9/GRCh38#18859624-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#86322241-A-C

18859624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86322241-A-G

18859891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86322421-G-T

http://identifiers.org/hco/9/GRCh38#18860591-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#86323038-A-C

18860881-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86323394-C-G

18861181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86324052-T-C

18861275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86324139-T-C

18861342-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86324209-C-G

18861409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86324270-A-G

18861417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86324278-G-A

18861420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86324281-T-C

http://identifiers.org/hco/9/GRCh38#18861512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#86324372-C-A

http://identifiers.org/hco/9/GRCh38#18861513-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#86324373-A-C

18861531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86324391-C-T

18861794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86324637-C-T

18861889-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86324743-C-G

18862151-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86324994-T-G

18862205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86325048-T-C

18862222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86325065-G-A

18862725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86325565-G-A

18862903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86325742-G-T

18863007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86325847-T-C

18863224-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86326077-C-G

18863335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86326187-C-T

18863496-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86326349-A-T

18863616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86326472-G-A

18863658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86326514-C-T

18863697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86326552-C-T

18863842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86326697-C-T

18864198-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86327108-C-G

http://identifiers.org/hco/9/GRCh38#18864307-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#86327225-A-C

http://identifiers.org/hco/9/GRCh38#18864350-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#86327268-A-C

18864361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86327280-T-C

18864486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86327403-A-G

18864597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86327487-C-T

18864784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86327683-T-C

18865788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86328131-G-T

http://identifiers.org/hco/9/GRCh38#18865789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#86328132-C-A

18865846-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86328187-T-G

18866323-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86328674-C-G

18866323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86328674-C-T

18866388-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86328743-C-G

18867326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86330387-C-T

18867339-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86330400-T-A

18867339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86330400-T-C

18867376-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86330424-T-A

18867426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86330499-G-A

http://identifiers.org/hco/9/GRCh38#18867494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#86330552-C-A

18867500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86330558-G-A

18867500-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86330558-G-C

18867622-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86330674-T-G

18887028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86331013-A-G

18887136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86331122-A-G

18887142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86331133-T-C

18887149-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86331140-C-G

18887183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86331170-G-A

18887183-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86331170-G-C

http://identifiers.org/hco/9/GRCh38#18887765-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#86331762-A-C

18887765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86331762-A-G

18887765-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86331762-A-T

18888311-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86332187-C-G

18888624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86332587-A-G

18888660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86332622-G-A

18888700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86332683-C-T

18889007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86332959-C-T

18889057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86333008-A-G

18889066-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86333017-T-A

18889082-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86333033-T-G

18889093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86333044-G-A

18889101-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86333052-G-C

18889218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86333179-G-T

18889219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86333180-T-C

18889405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86333436-G-A

http://identifiers.org/hco/9/GRCh38#18889432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#86333497-C-A

18889432-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86333497-C-G

18889432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86333497-C-T

18889442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86333590-A-G

http://identifiers.org/hco/9/GRCh38#18889447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#86333595-C-A

18889447-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86333595-C-G

18889447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86333595-C-T

http://identifiers.org/hco/9/GRCh38#18889450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#86333598-C-A

18889450-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86333598-C-G

18889450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86333598-C-T

18889479-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86333628-T-A

18889489-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86333638-C-G

18889489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86333638-C-T

18889529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86333669-G-T

18889627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 86333767-G-A

18889627-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 86333767-G-C

18889627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 86333767-G-T

http://identifiers.org/hco/9/GRCh38#18889641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#86333781-C-A

18889641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 86333781-C-T

18889665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 86333805-G-A

http://identifiers.org/hco/9/GRCh38#18889729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#86333869-C-A

18889729-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 86333869-C-G

18889729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 86333869-C-T

18889807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86333933-G-A

18889807-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86333933-G-C

18889807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86333933-G-T

18889812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86333937-G-A

18889812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86333937-G-T

http://identifiers.org/hco/9/GRCh38#18889874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#86333978-C-A

18889874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86333978-C-T

18889882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86333986-G-A

18889882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86333986-G-T

18889896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86333993-G-A

18889896-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86333993-G-C

18889896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86333993-G-T

18890008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86334111-T-C

18890132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86334425-C-T

18890201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86334499-G-A

18890201-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86334499-G-C

18890316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86334625-C-T

18890578-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86334894-C-G

http://identifiers.org/hco/9/GRCh38#18890609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#86334925-C-A

18890609-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86334925-C-G

18890657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86334973-A-G

18890657-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86334973-A-T

18890703-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86335019-G-C

18890787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86335102-T-C

18890962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86335280-G-A

http://identifiers.org/hco/9/GRCh38#18890969-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#86335287-A-C

18890996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86335314-T-C

18891018-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86335335-T-G

18891372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86335652-A-G

18891412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86335689-G-A

http://identifiers.org/hco/9/GRCh38#18891435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#86335708-C-A

18891441-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86335714-C-G

18891441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86335714-C-T

18891446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86335719-T-C

18891560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86335819-G-A

18891599-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86335872-A-T

18891690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86335963-C-T

18891746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86336026-C-T

18891936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86336285-A-G

18892083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86336409-G-A

18892166-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86336502-G-C

18892311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86336645-G-A

18892374-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86336694-T-G

18892563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 86336883-G-A

18892563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 86336883-G-T

18892569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 86336889-G-A

18892569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 86336889-G-T

18905448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86341273-A-G

18905452-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86341277-C-G

18905452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86341277-C-T

18905480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86341305-A-G

http://identifiers.org/hco/9/GRCh38#18905575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#86341389-C-A

18905575-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 86341389-C-G

18905575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 86341389-C-T

18905640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 86341460-G-T

18905701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 86341516-G-A

18905701-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 86341516-G-C

18905701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 86341516-G-T

http://identifiers.org/hco/9/GRCh38#18905708-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#86341523-A-C

18905708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 86341523-A-G

http://identifiers.org/hco/9/GRCh38#18905732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#86341547-C-A

18905777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 86341589-T-C

18905808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 86341620-C-T

18905826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 86341638-A-G

18905909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86341721-A-G

http://identifiers.org/hco/9/GRCh38#18905938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#86341751-C-A

18905938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86341751-C-T

18905963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86341765-G-A

18905963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86341765-G-T

http://identifiers.org/hco/9/GRCh38#18906002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#86341804-C-A

18906185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86341963-T-C

18906226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86342001-A-G

18906314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86342085-C-T

18906446-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86342209-T-G

18906761-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 86342466-G-C

18906798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 86342503-C-T

18906887-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 86342592-C-G

18906929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 86342634-A-G

18906936-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 86342641-T-A

http://identifiers.org/hco/9/GRCh38#18906950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#86342655-C-A

18906950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 86342655-C-T

http://identifiers.org/hco/9/GRCh38#18906974-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#86342679-A-C

18906975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 86342680-G-T

18907035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 86342740-G-A

18907035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 86342740-G-T

18907045-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 86342750-T-A

18907045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 86342750-T-C

18907103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 86342825-G-A

18907103-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 86342825-G-C

18907103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 86342825-G-T

http://identifiers.org/hco/9/GRCh38#18907121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#86342852-C-A

18907121-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 86342852-C-G

http://identifiers.org/hco/9/GRCh38#18907126-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#86342857-A-C

18907190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 86342908-A-G

http://identifiers.org/hco/9/GRCh38#18907196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#86342914-C-A

http://identifiers.org/hco/9/GRCh38#18907272-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#86342990-A-C

18907272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 86342990-A-G

18907299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 86343019-G-A

18907301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 86343021-G-A

18907420-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 86343136-C-G

18907420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 86343136-C-T

http://identifiers.org/hco/9/GRCh38#18907438-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#86343154-A-C

http://identifiers.org/hco/9/GRCh38#18907446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#86343165-C-A

http://identifiers.org/hco/9/GRCh38#18907461-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#86343193-A-C

18907461-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 86343193-A-T

http://identifiers.org/hco/9/GRCh38#18907467-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#86343199-A-C

18907467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 86343199-A-G

18907509-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 86343241-T-A

18907540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 86343278-C-T

18907569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 86343307-A-G

http://identifiers.org/hco/9/GRCh38#18907644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#86343377-C-A

18907664-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 86343397-T-G

18907782-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 86343511-A-T

18908064-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 86343750-C-G

18908064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 86343750-C-T

http://identifiers.org/hco/9/GRCh38#18908131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#86343794-C-A

18908131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 86343794-C-T

18908201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 86343866-G-A

18908201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 86343866-G-T

18908422-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 86344059-A-T

http://identifiers.org/hco/9/GRCh38#18908573-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#86344210-A-C

18908573-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 86344210-A-T

http://identifiers.org/hco/9/GRCh38#18908574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#86344211-C-A

18908574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 86344211-C-T

http://identifiers.org/hco/9/GRCh38#18908598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#86344235-C-A

18908703-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 86344325-T-A

18908703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 86344325-T-C

18908753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 86344381-G-T

18908868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 86344484-G-A

18908868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 86344484-G-T

http://identifiers.org/hco/9/GRCh38#18908879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#86344495-C-A

18908879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 86344495-C-T

18908907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 86344515-T-C

18908907-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 86344515-T-G

18908922-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 86344530-T-A

18908922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 86344530-T-C

18909034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 86344579-A-G

18909121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 86344675-A-G

18909166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 86344724-A-G

http://identifiers.org/hco/9/GRCh38#18909183-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#86344740-A-C

18909208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 86344766-G-A

18909208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 86344766-G-T

http://identifiers.org/hco/9/GRCh38#18909237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#86344779-C-A

18909237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 86344779-C-T

http://identifiers.org/hco/9/GRCh38#18909238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#86344780-C-A

18909238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 86344780-C-T

18909241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 86344783-T-C

18909244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 86344787-T-C

18909245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 86344788-G-A

18909245-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 86344788-G-C

18909245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 86344788-G-T

18909290-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 86344842-G-C

18909290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 86344842-G-T

18909297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 86344849-G-A

http://identifiers.org/hco/9/GRCh38#18909314-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#86344866-A-C

http://identifiers.org/hco/9/GRCh38#18909356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#86344938-C-A

18909356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 86344938-C-T

18909362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 86344944-G-A

18909362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 86344944-G-T

http://identifiers.org/hco/9/GRCh38#18909454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#86345071-C-A

18909454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 86345071-C-T

18909545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 86345157-G-T

18909554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 86345166-G-A

18909554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 86345166-G-T

18909599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 86345208-G-A

http://identifiers.org/hco/9/GRCh38#18909652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#86345260-C-A

18909682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 86345281-A-G

18909741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 86345338-T-C

http://identifiers.org/hco/9/GRCh38#18909777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#86345373-C-A

18909777-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 86345373-C-G

18909777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 86345373-C-T

18909812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 86345420-T-C

http://identifiers.org/hco/9/GRCh38#18909839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#86345453-C-A

18909839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 86345453-C-T

18909867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 86345512-A-G

18909991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 86345684-G-T

18910064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 86345768-C-T

18910151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 86345852-A-G

18910356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 86346045-T-C

18910710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 86346376-G-A

http://identifiers.org/hco/9/GRCh38#18910756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86346427-C-A

18910955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86346627-G-T

18910961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86346633-T-C

18911226-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86346874-C-G

18911786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86347307-G-A

18911926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86347451-A-G

http://identifiers.org/hco/9/GRCh38#18911965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86347495-C-A

http://identifiers.org/hco/9/GRCh38#18912481-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86351813-A-C

http://identifiers.org/hco/9/GRCh38#18912484-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86351816-A-C

18912484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86351816-A-G

18912517-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86351843-A-T

18912520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86351846-G-A

18912576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86351898-G-A

18912609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86351926-G-A

18912613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86351930-T-C

18912664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86351960-G-A

18912664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86351960-G-T

18912996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86352088-A-G

http://identifiers.org/hco/9/GRCh38#18913011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86352096-C-A

http://identifiers.org/hco/9/GRCh38#18913163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86352218-C-A

18913467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86352491-A-G

18913501-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86352525-G-C

http://identifiers.org/hco/9/GRCh38#18913528-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86352554-A-C

18913679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86352682-C-T

18913714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86352709-C-T

18913773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86352762-G-A

18913921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86352919-G-A

18914098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86353101-G-A

18914098-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86353101-G-C

18914206-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86353209-G-C

18914480-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86353461-A-T

18914521-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86353502-G-C

18914521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86353502-G-T

18914967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86353717-T-C

18915002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86353751-C-T

18915296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86354030-G-A

18915316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86354053-G-A

18915374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86354107-T-C

18917829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86355415-A-G

http://identifiers.org/hco/9/GRCh38#18919536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86356155-C-A

http://identifiers.org/hco/9/GRCh38#18919837-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86356494-A-C

18919838-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86356495-C-G

18919838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86356495-C-T

18919900-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86356557-C-G

18919934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86356585-G-A

18919970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86356602-C-T

http://identifiers.org/hco/9/GRCh38#18920234-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86356855-A-C

18920251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86356872-G-A

18920251-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86356872-G-C

http://identifiers.org/hco/9/GRCh38#18920756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86357379-C-A

18920984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86357603-C-T

18921016-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86357634-A-T

18921350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86357960-T-C

18921508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86358168-C-T

18921616-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86358432-A-T

18921654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86358465-G-A

18921654-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86358465-G-C

18922024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86358882-G-A

18922024-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86358882-G-C

http://identifiers.org/hco/9/GRCh38#18922047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86358904-C-A

18922184-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86359010-C-G

18922461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86359277-G-A

18922545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86359394-C-T

18922588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86359429-G-A

18922650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86359493-G-A

18926322-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3 prime UTR variant
orthologous variants: 86361396-G-C

18926322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3 prime UTR variant
orthologous variants: 86361396-G-T

18926546-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3 prime UTR variant
orthologous variants: 86361594-G-C

http://identifiers.org/hco/9/GRCh38#18926716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86361815-C-A

18926716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3 prime UTR variant
orthologous variants: 86361815-C-T

http://identifiers.org/hco/9/GRCh38#18926936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86362016-C-A

18927191-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3 prime UTR variant
orthologous variants: 86362220-G-C

18927251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3 prime UTR variant
orthologous variants: 86362280-G-A

18927251-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3 prime UTR variant
orthologous variants: 86362280-G-C

18927259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3 prime UTR variant
orthologous variants: 86362288-C-T

http://identifiers.org/hco/9/GRCh38#18927274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86362303-C-A

18927496-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3 prime UTR variant
orthologous variants: 86362501-T-G

http://identifiers.org/hco/9/GRCh38#18927551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86362555-C-A

18927551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3 prime UTR variant
orthologous variants: 86362555-C-T

18927613-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3 prime UTR variant
orthologous variants: 86362597-T-A

http://identifiers.org/hco/9/GRCh38#18927616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86362600-C-A

http://identifiers.org/hco/9/GRCh38#18927770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86362757-C-A

18927770-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3 prime UTR variant
orthologous variants: 86362757-C-G

18927843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3 prime UTR variant
orthologous variants: 86362826-G-T

18927912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3 prime UTR variant
orthologous variants: 86362895-T-C

18927925-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3 prime UTR variant
orthologous variants: 86362908-G-C

18927925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3 prime UTR variant
orthologous variants: 86362908-G-T

18928003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3 prime UTR variant
orthologous variants: 86362996-G-A

18928003-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3 prime UTR variant
orthologous variants: 86362996-G-C

18928003-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3 prime UTR variant
orthologous variants: 86362996-G-T

18928063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 86363062-C-T

http://identifiers.org/hco/9/GRCh38#18928181-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86363180-A-C

18928204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 86363203-G-A

18928245-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 86363244-C-G

18928245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 86363244-C-T

http://identifiers.org/hco/9/GRCh38#18928273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86363272-C-A

18928273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 86363272-C-T

18928480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 86363479-G-A

18928480-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 86363479-G-C

18928480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 86363479-G-T

18928638-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 86363637-G-C

http://identifiers.org/hco/9/GRCh38#18928672-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86363671-A-C

18928680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 86363679-A-G

18928880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 86363879-G-A

18928880-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 86363879-G-C

18929110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86364106-T-C

18929117-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86364113-T-G

http://identifiers.org/hco/9/GRCh38#18929146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86364142-C-A

18929146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86364142-C-T

18929266-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86364264-C-G

18929288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86364286-T-C

18929802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86364731-G-A

18929812-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86364741-G-C

18929814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86364743-A-G

18929818-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86364747-G-C

18929819-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86364748-C-G

18929955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86364881-A-G

18929979-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86364905-T-G

18929990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86364916-T-C

18930026-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86364952-A-T

18930248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86365055-C-T

18930396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86365168-C-T

18930414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86365183-C-T

18930848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86365289-T-C

18930864-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86365305-T-A

18930879-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86365320-A-T

18931051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86365495-A-G

18935539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86382461-C-T

18935632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86382555-G-A

18935763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86382664-T-C

18936211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86383115-C-T

18937239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86384170-G-A

18937299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86384231-G-T

18937305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86384239-T-C

18937382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86384318-T-C

18937454-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86384374-T-A

18937506-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86384420-T-G

18937598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86384520-G-A

18937605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86384529-T-C

18937708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86384626-T-C

18937726-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86384639-G-C

18938716-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86384798-C-G

18938876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86384903-A-G

18938971-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86385005-A-T

18939289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86385297-A-G

18939342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86385333-C-T

18940979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86396394-T-C

18941213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86396631-G-A

18941251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86396669-G-T

18941313-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86396720-A-T

18941379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86396891-C-T

18941414-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86396926-C-G

18941484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86396979-G-A

http://identifiers.org/hco/9/GRCh38#18941487-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86396982-A-C

18941487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86396982-A-G

18941487-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86396982-A-T

18941509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86397004-A-G

18941512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86397007-T-C

18941592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86397076-G-T

18941809-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 86397285-T-G

18941826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, missense_variant
orthologous variants: 86397302-G-A

18941826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, missense_variant
orthologous variants: 86397302-G-T

18941867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86397344-G-T

http://identifiers.org/hco/9/GRCh38#18941899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86397375-C-A

18941899-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86397375-C-G

18941899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86397375-C-T

18941900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86397376-T-C

18941900-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86397376-T-G

http://identifiers.org/hco/9/GRCh38#18941909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86397385-C-A

18941909-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86397385-C-G

http://identifiers.org/hco/9/GRCh38#18942008-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86397458-A-C

18942129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86397583-G-A

18942129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86397583-G-T

18942322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86397775-G-A

18942387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86397818-C-T

18942841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86398265-C-T

http://identifiers.org/hco/9/GRCh38#18943022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86398431-C-A

18943073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86398482-C-T

18943074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86398483-G-A

18943330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86398747-C-T

18943736-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86399134-T-A

18943975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86399285-G-A

18943975-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86399285-G-C

18944090-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86399403-T-A

18944412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86399768-T-C

18944534-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86399888-C-G

18944549-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86399912-T-A

18944853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86400212-T-C

18944931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86400287-G-A

18944931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86400287-G-T

18945243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86401097-G-T

18945413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86401276-G-A

18945449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86401308-C-T

18945605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86401414-A-G

http://identifiers.org/hco/9/GRCh38#18945712-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86401505-A-C

18945712-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86401505-A-T

http://identifiers.org/hco/9/GRCh38#18945794-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86401601-A-C

18945799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86401606-G-T

18945845-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86401649-G-C

18945900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86401703-G-T

18946584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86402043-C-T

18946647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86402101-G-A

18946676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86402120-C-T

18946933-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86402481-A-T

18947116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86402648-G-A

18947250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86402763-A-G

18947251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86402764-T-C

18947413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86402950-C-T

18947444-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86402983-A-T

18947620-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 86403124-T-A

18947620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 86403124-T-C

18947632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 86403136-A-G

18947637-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 86403141-G-C

18947649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 86403152-T-C

18947678-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 86403181-C-G

18947762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86403314-T-C

18947763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86403315-C-T

18947869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86403421-A-G

18947932-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86403483-C-G

http://identifiers.org/hco/9/GRCh38#18947952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#86403504-C-A

18947952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86403504-C-T

18948205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86403688-G-A

18948333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86403842-T-C

18948334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86403843-T-C

http://identifiers.org/hco/9/GRCh38#18948400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86403968-C-A

18948692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86404231-A-G

18948712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86404251-A-G

18948765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86404304-C-T

18948944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86404498-C-T

18948976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86404524-T-C

http://identifiers.org/hco/9/GRCh38#18949038-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86404587-A-C

18949046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86404595-T-C

18949776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86405059-G-A

18949834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86405124-C-T

http://identifiers.org/hco/9/GRCh38#18949860-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86405155-A-C

18949986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86405284-G-A

18950045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86405358-T-C

http://identifiers.org/hco/9/GRCh38#18950115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86405423-C-A

18950115-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86405423-C-G

18950115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86405423-C-T

http://identifiers.org/hco/9/GRCh38#18950651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86405899-C-A

18950651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86405899-C-T

18950678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86405926-A-G

18950785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 86406004-A-G

18950792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 86406011-C-T

18950807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 86406026-G-A

18950807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 86406026-G-T

18950810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 86406029-T-C

18950871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 86406090-G-A

18950882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 86406101-A-G

18950910-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 86406129-G-C

18950934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 86406153-C-T

http://identifiers.org/hco/9/GRCh38#18951045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86406256-C-A

18951045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86406256-C-T

18951072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86406282-T-C

18951225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86406440-A-G

http://identifiers.org/hco/9/GRCh38#18951741-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86408220-A-C

18952035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86408392-C-T

18952172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86408512-C-T

18952219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86408557-C-T

18952240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86408575-C-T

18952331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86408764-G-T

18953060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86411779-T-C

18953264-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86411969-T-G

18953602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86413418-G-A

18953625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86413444-C-T

18954000-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86414001-T-G

18954109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86414120-A-G

18954331-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86414293-G-C

18954706-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86414351-T-A

18954706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86414351-T-C

http://identifiers.org/hco/9/GRCh38#18954961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86414516-C-A

18955305-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86414654-T-G

18955312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86414661-T-C

18955394-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86414733-G-C

18955430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86414769-G-A

18955430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86414769-G-T

18955437-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86414776-G-C

18955495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86414830-G-A

18955503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86414840-G-A

18955676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86415116-T-C

18955724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86415164-C-T

18955730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86415170-G-A

http://identifiers.org/hco/9/GRCh38#18956772-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86416552-A-C

18956854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86416625-G-A

18956854-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86416625-G-C

http://identifiers.org/hco/9/GRCh38#18956907-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86416684-A-C

18956909-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86416686-G-C

18957166-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86416874-C-G

http://identifiers.org/hco/9/GRCh38#18957219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86416929-C-A

18957368-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86417059-T-A

http://identifiers.org/hco/9/GRCh38#18957562-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86417270-A-C

18957562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86417270-A-G

18957679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86417387-G-A

18957780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86417474-T-C

18957834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86417519-T-C

18957883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86417561-T-C

18958706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86421631-G-A

18958788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86421701-C-T

18958939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86421874-A-G

18959002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86421944-T-C

18959076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86421997-G-A

18959076-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86421997-G-C

18968927-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86422776-G-C

18969112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86422964-G-A

18969112-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86422964-G-C

http://identifiers.org/hco/9/GRCh38#18969357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86423214-C-A

18969357-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86423214-C-G

18969358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86423215-T-C

18969427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86423283-T-C

18969432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86423288-G-T

18969653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86423733-C-T

18969785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86423862-G-A

18969866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86423949-T-C

18969866-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86423949-T-G

http://identifiers.org/hco/9/GRCh38#18969953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86424033-C-A

18970463-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86424506-T-A

18970463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86424506-T-C

18970478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86424517-G-A

http://identifiers.org/hco/9/GRCh38#18970503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86424543-C-A

18970516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86424556-G-T

18970563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86424606-T-C

http://identifiers.org/hco/9/GRCh38#18970582-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86424625-A-C

18970582-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86424625-A-T

18970587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86424630-A-G

18970597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86424640-A-G

18970647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86424689-G-A

18970647-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86424689-G-C

18970696-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86424738-C-G

18970696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86424738-C-T

18970787-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86424850-T-A

18970811-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86424875-G-C

http://identifiers.org/hco/9/GRCh38#18971043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86425267-C-A

18971185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86425483-G-A

18971235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86425534-G-A

18971354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86425660-T-C

18971442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86425747-G-A

18971587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86425889-T-C

18972116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86426487-C-T

18972206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86426557-C-T

http://identifiers.org/hco/9/GRCh38#18972378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86426718-C-A

18972671-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86427154-C-G

18972818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86427288-C-T

http://identifiers.org/hco/9/GRCh38#18972834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86427304-C-A

18972834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86427304-C-T

18973129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86427529-C-T

18973303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86427674-T-C

18973317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86427693-A-G

18973335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86427710-A-G

18973373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86427747-T-C

18973389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86427787-C-T

18973685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86428100-G-A

18973685-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86428100-G-C

18973685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86428100-G-T

http://identifiers.org/hco/9/GRCh38#18973708-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86428118-A-C

18973927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86428346-G-A

18973979-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86428587-G-C

18974205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86428788-C-T

18975136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86438243-C-T

18975171-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86438276-G-C

18975306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86438354-G-T

http://identifiers.org/hco/9/GRCh38#18975449-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86438474-A-C

18975450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86438475-G-A

18975468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86438491-C-T

18975501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86438524-T-C

18975546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86438568-G-A

18976236-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86438685-G-C

18976280-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86438740-G-C

18976305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86438765-A-G

18976410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86438857-G-T

18976456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86438903-T-C

18976472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86438919-A-G

18976844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86439278-G-A

18976982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86439403-A-G

18978203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86439451-A-G

18978296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86439534-A-G

18978317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86439552-C-T

18978322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86439557-A-G

18978543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86439752-T-C

18978626-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86439834-G-C

18978719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86439927-C-T

18978823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86440022-C-T

18979000-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86440194-C-G

18979040-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86440231-C-G

18979040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86440231-C-T

18980054-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86441469-G-C

18980074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86441492-G-T

18980093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86441511-T-C

18980492-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86442218-A-T

18980495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86442221-G-T

18980520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86442244-G-A

18980522-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86442246-T-A

18980522-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86442246-T-G

18980751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86442422-G-A

18980751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86442422-G-T

18980875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86442582-T-C

18980965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86442677-C-T

18981088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86442779-C-T

18981478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86443118-G-A

18981479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86443119-G-T

18981755-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86443379-A-T

18981941-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86443531-T-G

18982003-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86443591-C-G

18982240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86443786-A-G

18982315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86443860-T-C

18982367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86443909-G-A

18985678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86445897-C-T

18985894-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86446101-G-C

18986034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86446242-A-G

18986335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86446537-A-G

18986341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86446543-C-T

18986428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86446632-T-C

18986617-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86446913-A-T

18986621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86446917-G-A

18986969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86447255-G-A

18986990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86447276-T-C

http://identifiers.org/hco/9/GRCh38#18987003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86447289-C-A

18987003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86447289-C-T

18987065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86447375-G-A

18987086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86447394-T-C

18987145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86447435-G-A

http://identifiers.org/hco/9/GRCh38#18987178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86447467-C-A

http://identifiers.org/hco/9/GRCh38#18987193-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86447482-A-C

18987193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86447482-A-G

18987357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86447607-G-A

18987464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86447717-T-C

18987550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86447793-G-A

18988495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86448429-T-C

18988495-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86448429-T-G

http://identifiers.org/hco/9/GRCh38#18988756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86448572-C-A

18989056-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86449066-A-T

18989114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86449124-A-G

18989130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86449144-A-G

18989149-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86449163-C-G

http://identifiers.org/hco/9/GRCh38#18989220-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86449229-A-C

18989252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86449261-T-C

18989368-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86449369-T-A

18989368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86449369-T-C

http://identifiers.org/hco/9/GRCh38#18989391-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86449392-A-C

http://identifiers.org/hco/9/GRCh38#18989540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86449544-C-A

18989989-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86449878-G-C

http://identifiers.org/hco/9/GRCh38#18993417-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86450803-A-C

18993443-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 86450829-C-G

18993443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 86450829-C-T

http://identifiers.org/hco/9/GRCh38#18993487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86450868-C-A

18993543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 86450926-C-T

18993607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86451316-A-G

http://identifiers.org/hco/9/GRCh38#18993635-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86451358-A-C

18993918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86451622-G-A

18993918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86451622-G-T

18994574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86452245-G-A

18994671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86452333-G-A

18994708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86452372-T-C

18995043-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86452709-A-T

18995099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86452765-G-T

18995131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86452808-T-C

18995235-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86452897-G-C

18995267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86452929-T-C

18995361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86453024-T-C

18995444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86453084-G-A

18995628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86453618-C-T

18995657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86453634-T-C

19007651-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86455901-A-T

19008438-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86457882-C-G

19008438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86457882-C-T

19008628-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86458058-A-T

http://identifiers.org/hco/9/GRCh38#19008781-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86460120-A-C

19008826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86460161-C-T

19009046-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86460359-T-A

19009063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86460378-T-C

19009216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86460521-C-T

http://identifiers.org/hco/9/GRCh38#19009426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86460752-C-A

19009426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86460752-C-T

19009785-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86461093-T-A

19009785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86461093-T-C

19009805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86461113-G-A

19009813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86461121-T-C

19010348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86461245-G-A

19010348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86461245-G-T

19010393-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86461288-T-A

19010393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86461288-T-C

19010403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86461298-G-T

19010494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86461383-A-G

http://identifiers.org/hco/9/GRCh38#19010543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86461405-C-A

19010800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86462064-G-A

19010869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86462130-C-T

19011085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86462310-G-A

19011373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86462569-T-C

19011375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86462571-G-T

http://identifiers.org/hco/9/GRCh38#19011424-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86462617-A-C

19011484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86462674-C-T

19011501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86462691-C-T

19011595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86462797-C-T

19012912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86463654-T-C

19012952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86463703-G-A

19013058-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86463812-G-C

19013122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86463883-G-A

19013312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86464009-T-C

19013382-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86464078-G-C

19013391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86464087-A-G

19013392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86464088-G-T

19013400-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 86464096-G-C

19013468-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86464166-C-G

19013496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86464194-T-C

19013500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86464198-G-A

19013507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86464206-C-T

http://identifiers.org/hco/9/GRCh38#19013515-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86464214-A-C

19013515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86464214-A-G

19013515-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86464214-A-T

19014807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86466638-G-T

19014864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86466694-G-A

19015170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86466963-T-C

19015187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86466979-T-C

19015937-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86467137-T-G

19015952-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86467153-A-T

19016089-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86467275-G-C

19016166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86467347-T-C

19016611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86467612-G-A

http://identifiers.org/hco/9/GRCh38#19016776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86467759-C-A

19016776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86467759-C-T

19022454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86469495-G-A

19022454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86469495-G-T

19022523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86469566-G-A

19022557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86469597-A-G

19022582-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86469622-T-A

19022709-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86469749-T-G

19023031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86470041-G-A

19023219-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86470196-T-G

19023239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86470216-C-T

19023241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86470218-A-G

19023248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86470232-C-T

19023288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86470265-C-T

19023298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86470275-C-T

19023303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86470280-C-T

19023373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86470333-T-C

19023389-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86470344-C-G

19024935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86470575-C-T

19025105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86470753-G-A

19025235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86470860-T-C

19025249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86470874-C-T

19025273-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86470906-T-G

19025545-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86471181-A-T

19025642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86471265-T-C

19025718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86471344-G-A

19025719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86471345-C-T

19025736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86471366-T-C

19025774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86471404-T-C

http://identifiers.org/hco/9/GRCh38#19025802-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86471436-A-C

19025817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86471451-A-G

19025894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86471528-A-G

19025894-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86471528-A-T

19026390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86472525-A-G

19026482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86472612-G-A

19026537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86472663-T-C

19026648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86472765-T-C

19026668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86472781-G-A

19028401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86472856-C-T

19028403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86472858-G-A

19028403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86472858-G-T

19028434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86472883-G-A

19028438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86472887-A-G

19028461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86472910-T-C

19028813-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86473246-A-T

19029000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86473450-T-C

19029000-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86473450-T-G

19030999-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86474690-G-C

19031026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86474716-G-A

19031111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86474774-G-A

19031121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86474784-T-C

19031571-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86474921-A-T

http://identifiers.org/hco/9/GRCh38#19031589-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86474939-A-C

19031855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86475184-G-A

19031859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86475188-T-C

19032064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86475400-G-A

19032290-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86475615-T-A

19032510-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86475822-A-T

19032634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86475927-C-T

19032775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86476081-G-A

19032775-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86476081-G-C

19032775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 86476081-G-T

19032904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 86476245-T-C

19032952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 86476275-G-A

19032952-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 86476275-G-C

19032952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 86476275-G-T

19032961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 86476284-G-A

19032961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 86476284-G-T

19032991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 86476310-G-A

19032991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 86476310-G-T

http://identifiers.org/hco/9/GRCh38#19033006-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86476328-A-C

19033006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 86476328-A-G

http://identifiers.org/hco/9/GRCh38#19033024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86476346-C-A

19033024-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 86476346-C-G

19033024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 86476346-C-T

19033108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 86476429-A-G

http://identifiers.org/hco/9/GRCh38#19033163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86476481-C-A

19033163-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 86476481-C-G

19033163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 86476481-C-T

http://identifiers.org/hco/9/GRCh38#19033216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86476530-C-A

19033216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 86476530-C-T

19033225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 86476539-G-A

19033225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 86476539-G-T

19033263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86476573-G-A

19033263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86476573-G-T

19033306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86476618-G-A

19033344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86476657-G-A

19033344-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86476657-G-C

19033344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86476657-G-T

http://identifiers.org/hco/9/GRCh38#19033349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86476662-C-A

http://identifiers.org/hco/9/GRCh38#19033391-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86476706-A-C

19033391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86476706-A-G

19033391-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86476706-A-T

19033417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86476735-T-C

19033417-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86476735-T-G

19033465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86476789-C-T

19033474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86476798-G-A

19033537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86476859-C-T

19033544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86476866-G-A

19033830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86477110-G-A

http://identifiers.org/hco/9/GRCh38#19033914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86477198-C-A

19048959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 86493536-C-T

19049148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: intron variant
orthologous variants: 86493636-C-T

http://identifiers.org/hco/9/GRCh38#19049208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: splice donor variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86493700-C-A

19049208-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: splice donor variant
orthologous variants: 86493700-C-G

19049208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: splice donor variant
orthologous variants: 86493700-C-T

http://identifiers.org/hco/9/GRCh38#19049224-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86493713-A-C

19049224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 5 prime UTR variant
orthologous variants: 86493713-A-G

19049224-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 5 prime UTR variant
orthologous variants: 86493713-A-T

http://identifiers.org/hco/9/GRCh38#19049274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#86493765-C-A

19049274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 5 prime UTR variant
orthologous variants: 86493765-C-T

19049294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 5 prime UTR variant
orthologous variants: 86493779-G-A

19049294-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 5 prime UTR variant
orthologous variants: 86493779-G-C

19049294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 5 prime UTR variant
orthologous variants: 86493779-G-T

19049314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 5 prime UTR variant
orthologous variants: 86493800-G-A

19049314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 5 prime UTR variant
orthologous variants: 86493800-G-T

19049332-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 5 prime UTR variant
orthologous variants: 86493818-T-G

19049339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28566
most severe consequence: 5 prime UTR variant
orthologous variants: 86493825-C-T