88378775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: 5 prime UTR variant
orthologous variants: 57557846-G-T

88378806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: 5 prime UTR variant
orthologous variants: 57557923-A-G

http://identifiers.org/hco/4/GRCh38#88378814-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57557931-A-C

88378814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: 5 prime UTR variant
orthologous variants: 57557931-A-G

88378814-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: 5 prime UTR variant
orthologous variants: 57557931-A-T

http://identifiers.org/hco/4/GRCh38#88378886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57557991-C-A

88378886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: 5 prime UTR variant
orthologous variants: 57557991-C-T

http://identifiers.org/hco/4/GRCh38#88378893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57557998-C-A

88378893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: 5 prime UTR variant
orthologous variants: 57557998-C-T

http://identifiers.org/hco/4/GRCh38#88378927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: NMD_transcript_variant, stop_gained, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#57558027-C-A

88378927-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: NMD_transcript_variant, stop_gained, undefined
orthologous variants: 57558027-C-G

88378927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: NMD_transcript_variant, synonymous_variant, undefined
orthologous variants: 57558027-C-T

88378979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 57558079-A-G

http://identifiers.org/hco/4/GRCh38#88378984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57558081-C-A

88378984-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 57558081-C-G

88378984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 57558081-C-T

88379042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57558139-A-G

88379101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 57558198-G-A

88379101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 57558198-G-T

88379111-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 57558208-G-C

88379111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, stop_gained, undefined
orthologous variants: 57558208-G-T

88379163-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57558256-C-G

88379163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57558256-C-T

http://identifiers.org/hco/4/GRCh38#88383243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57560180-C-A

88383243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 57560180-C-T

http://identifiers.org/hco/4/GRCh38#88383244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57560181-C-A

88383244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 57560181-C-T

http://identifiers.org/hco/4/GRCh38#88383340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57560277-C-A

88383340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 57560277-C-T

88383361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57560298-G-A

88383361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 57560298-G-T

http://identifiers.org/hco/4/GRCh38#88383452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57560373-C-A

88383452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57560373-C-T

88383976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57560566-G-A

88383980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57560570-A-G

88384120-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57560716-A-T

88385468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57561501-A-G

http://identifiers.org/hco/4/GRCh38#88385565-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57561601-A-C

88385565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 57561601-A-G

88385565-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 57561601-A-T

88385580-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57561616-G-C

88389360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57574365-T-C

88389417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57574423-T-C

88389679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57574645-G-A

88390206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57574844-G-A

88390206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57574844-G-T

88390252-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57574888-T-G

88390262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57574898-G-A

88390345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57574981-A-G

88390349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57574983-T-C

88390470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57575200-C-T

88390548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57575275-A-G

http://identifiers.org/hco/4/GRCh38#88390552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57575279-C-A

88390552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57575279-C-T

88390556-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 57575283-T-A

88390659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 57575421-A-G

88390707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57575469-G-T

88390719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 57575481-C-T

http://identifiers.org/hco/4/GRCh38#88390728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57575490-C-A

88390811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57575573-G-A

88390844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57575606-C-T

88390848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 57575610-G-A

88390872-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57575634-T-A

http://identifiers.org/hco/4/GRCh38#88390936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57575698-C-A

88390936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57575698-C-T

88391812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57576473-C-T

88391823-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57576485-C-G

http://identifiers.org/hco/4/GRCh38#88393482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57576944-C-A

88393482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 57576944-C-T

88393515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57576977-G-A

88393538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57577000-G-A

88393538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57577000-G-T

http://identifiers.org/hco/4/GRCh38#88393594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57577056-C-A

88393594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57577056-C-T

88393608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57577070-T-C

88393671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57577134-A-G

88393674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57577137-A-G

http://identifiers.org/hco/4/GRCh38#88393677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57577140-C-A

http://identifiers.org/hco/4/GRCh38#88393689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57577152-C-A

88393691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57577154-A-G

88393731-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57577194-A-T

http://identifiers.org/hco/4/GRCh38#88393862-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57577318-A-C

88393862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57577318-A-G

88393868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57577326-G-A

88393930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57577388-G-A

88393930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57577388-G-T

88393950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57577408-G-A

88394935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57578733-C-T

88395139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

88396082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57581125-A-G

88396118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 57581161-T-C

88396134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 57581177-T-C

88396768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57583943-G-T

88396887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 57584063-G-A

http://identifiers.org/hco/4/GRCh38#88396934-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57584110-A-C

88396963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57584139-A-G

88396984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57584160-G-A

88397077-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57584244-A-T

88397094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57584265-A-G

88397871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57584401-C-T

http://identifiers.org/hco/4/GRCh38#88397920-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57584451-A-C

http://identifiers.org/hco/4/GRCh38#88398013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57584499-C-A

88398013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57584499-C-T

88398132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57584611-T-C

88398208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 57584685-A-G

88398208-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 57584685-A-T

http://identifiers.org/hco/4/GRCh38#88404708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57587632-C-A

http://identifiers.org/hco/4/GRCh38#88404734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57587653-C-A

88404736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57587655-G-A

88404736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57587655-G-T

http://identifiers.org/hco/4/GRCh38#88404778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57587695-C-A

88404829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57587734-G-T

88404835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57587740-G-A

88404835-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57587740-G-C

88404835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57587740-G-T

88404877-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 57587789-A-T

88405101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron variant
orthologous variants: 57588012-T-C

88405150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron variant
orthologous variants: 57588060-G-T

88405188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron variant
orthologous variants: 57588117-C-T

88405370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron variant
orthologous variants: 57588285-G-A

88405447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron variant
orthologous variants: 57588562-A-G

http://identifiers.org/hco/4/GRCh38#88405461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57588576-C-A

88405461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron variant
orthologous variants: 57588576-C-T

http://identifiers.org/hco/4/GRCh38#88405532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57588733-C-A

88405532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron variant
orthologous variants: 57588733-C-T

http://identifiers.org/hco/4/GRCh38#88405588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57588794-C-A

88405588-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: missense variant
orthologous variants: 57588794-C-G

88405588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: synonymous variant
orthologous variants: 57588794-C-T

88405590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: synonymous variant
orthologous variants: 57588796-G-A

88405590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: synonymous variant
orthologous variants: 57588796-G-T

88405596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: synonymous variant
orthologous variants: 57588802-A-G

88405911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron variant
orthologous variants: 57589060-C-T

88405924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron variant
orthologous variants: 57589073-A-G

88408528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: missense variant
orthologous variants: 57595602-A-G

88408543-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: missense variant
orthologous variants: 57595617-T-A

http://identifiers.org/hco/4/GRCh38#88408614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57595688-C-A

88408614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: synonymous variant
orthologous variants: 57595688-C-T

88408667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron variant
orthologous variants: 57595772-A-G

88409431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron variant
orthologous variants: 57595823-G-A

88409479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron variant
orthologous variants: 57595873-T-C

88409648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron variant
orthologous variants: 57596038-C-T

88413101-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 57596454-C-G

88413367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57596710-A-G

88416978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57602314-A-G

88417022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57602355-A-G

http://identifiers.org/hco/4/GRCh38#88417359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57602813-C-A

88417359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57602813-C-T

http://identifiers.org/hco/4/GRCh38#88417418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57602874-C-A

88417418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 57602874-C-T

88417493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 57602949-A-G

88417523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 57602979-G-A

88417523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 57602979-G-T

88417573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 57603029-G-A

http://identifiers.org/hco/4/GRCh38#88417641-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57603118-A-C

http://identifiers.org/hco/4/GRCh38#88423870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57623113-C-A

88424084-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57623303-T-G

88424248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57623520-A-G

88424258-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57623530-G-C

88424485-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57623892-A-T

http://identifiers.org/hco/4/GRCh38#88424502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57623941-C-A

88424502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57623941-C-T

http://identifiers.org/hco/4/GRCh38#88424518-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57623970-A-C

88424518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57623970-A-G

88424518-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57623970-A-T

88424522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57623974-G-A

88424522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57623974-G-T

88424528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57623980-G-A

88424528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57623980-G-T

88424620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 57624075-T-C

88424688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 57624143-C-T

88427044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57627191-A-G

88427053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57627200-G-T

88427062-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57627209-C-G

88427141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57627274-A-G

88427160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57627293-C-T

88427267-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57627423-G-C

88427373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57627517-G-A

88427609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57627681-T-C

88427652-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57627716-T-G

http://identifiers.org/hco/4/GRCh38#88427700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57627758-C-A

88427776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57627820-G-A

88427815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57627861-C-T

88427917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57627964-A-G

88428007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57628014-A-G

88428288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57628271-T-C

88428306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57628289-T-C

http://identifiers.org/hco/4/GRCh38#88428361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57628342-C-A

88428466-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57628430-G-C

88428490-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57628443-T-A

88428490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57628443-T-C

88428590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 57629024-A-G

88428620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 57629033-T-C

88428639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 57629048-A-G

88428704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 57629108-G-A

88428704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 57629108-G-T

http://identifiers.org/hco/4/GRCh38#88428719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57629123-C-A

88428719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 57629123-C-T

88428749-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 57629153-T-A

88428749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 57629153-T-C

88428868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57629275-G-T

http://identifiers.org/hco/4/GRCh38#88428894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57629301-C-A

88428894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57629301-C-T

88428978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57629364-T-C

88429110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57629575-A-G

88429191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57629657-C-T

88429200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57629666-C-T

88429323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57629789-C-T

88429662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57630101-G-A

88430240-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57630644-G-C

88430842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57631078-C-T

88430880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57631116-C-T

88430953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57631154-G-A

88431028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57631237-G-A

88431028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57631237-G-T

88431063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57631273-T-C

88431089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57631298-G-T

88431152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57631364-C-T

88431165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 57631377-G-A

88431165-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 57631377-G-C

88431195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 57631407-G-A

88431229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 57631441-T-C

88431286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 57631498-G-T

88431347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57631541-G-A

http://identifiers.org/hco/4/GRCh38#88431348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57631542-C-A

88431348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57631542-C-T

88431385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57631574-G-A

88431385-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57631574-G-C

88431401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57631589-T-C

88431422-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57631609-T-A

http://identifiers.org/hco/4/GRCh38#88434739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57631975-C-A

88434811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57632055-C-T

88435111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57632321-T-C

88435239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57632498-G-A

88435263-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57632544-T-A

88435887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 57635156-G-A

88435982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57635230-G-A

88435982-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57635230-G-C

88435982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57635230-G-T

88436002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57635250-A-G

88436361-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57636091-G-C

88436405-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57636140-T-G

http://identifiers.org/hco/4/GRCh38#88436671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57636444-C-A

88436737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57636499-T-C

88436782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57636542-G-T

http://identifiers.org/hco/4/GRCh38#88436829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57636587-C-A

88436829-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57636587-C-G

88436897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 57636653-T-C

88436960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 57636713-A-G

88436986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57636738-A-G

88436999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57636751-G-A

88436999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57636751-G-T

88437685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57637050-G-A

88437685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57637050-G-T

88437686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 57637051-G-A

http://identifiers.org/hco/4/GRCh38#88437770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57637135-C-A

88437770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 57637135-C-T

http://identifiers.org/hco/4/GRCh38#88439719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57638905-C-A

88439719-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57638905-C-G

88439719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57638905-C-T

88439823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57639009-T-C

88439823-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57639009-T-G

88440077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57639254-C-T

88440090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57639269-G-A

88440090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57639269-G-T

88440101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57639280-A-G

http://identifiers.org/hco/4/GRCh38#88442125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57639575-C-A

88442192-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57639643-T-A

88442192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 57639643-T-C

88442426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 57639877-G-A

http://identifiers.org/hco/4/GRCh38#88442441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57639891-C-A

http://identifiers.org/hco/4/GRCh38#88442522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#57639980-C-A

88442522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26072
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 57639980-C-T