http://identifiers.org/hco/3/GRCh38#57293857-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26613513-A-C

57293878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26613492-G-A

57293878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26613492-G-T

http://identifiers.org/hco/3/GRCh38#57293945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26613425-C-A

57293945-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26613425-C-G

57294009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26613356-G-A

57294009-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26613356-G-C

57294009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26613356-G-T

57294011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26613354-A-G

http://identifiers.org/hco/3/GRCh38#57294037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26613328-C-A

57294427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26612909-A-G

57294444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26612863-G-A

57294619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26612654-C-T

57294809-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26612393-A-T

http://identifiers.org/hco/3/GRCh38#57295334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26611216-C-A

57295386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26611180-G-T

57295387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26611179-T-C

57295397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26611169-A-G

57295470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26611098-T-C

57295498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26611070-A-G

http://identifiers.org/hco/3/GRCh38#57295660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26610912-C-A

57295660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26610912-C-T

57295666-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26610906-T-G

http://identifiers.org/hco/3/GRCh38#57295992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26609102-C-A

57296147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26608971-A-G

57296260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26608857-G-A

57296260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26608857-G-T

57296517-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26608648-A-T

57296593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26608512-T-C

57296598-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26608507-G-C

57296638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26608233-T-C

57296806-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26608039-T-G

57296916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_retained_variant, synonymous_variant
orthologous variants: 26607929-T-C

57297034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26607797-G-A

http://identifiers.org/hco/3/GRCh38#57297138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26607715-C-A

57297138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26607715-C-T

http://identifiers.org/hco/3/GRCh38#57297144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26607709-C-A

57297150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26607703-T-C

57297169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26607684-T-C

57297222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26607632-G-A

57297222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26607632-G-T

57298231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 26607023-A-G

57301637-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26606348-T-G

57301681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26606265-C-T

57301691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26606255-C-T

57301862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 26606085-A-G

57301907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 26606040-T-C

57301977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26605970-G-T

57302087-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26605856-T-A

57302087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26605856-T-C

57302509-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26603039-A-T

http://identifiers.org/hco/3/GRCh38#57303006-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26602130-A-C

57303072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26602065-G-A

57303142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26602001-A-G

57309081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26601818-A-G

57309081-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26601818-A-T

57309089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26601810-A-G

57309089-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26601810-A-T

57309098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26601798-A-G

57309111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26601766-G-A

57309111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26601766-G-T

57309136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 26601741-G-T

57309385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26600321-T-C

57309594-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26600108-G-C

57309594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26600108-G-T

57309658-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 26600052-A-T

57309919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26599831-A-G

57309960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26599794-G-T

57310191-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26599600-A-T

57310278-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26599527-T-A

57310279-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26599526-C-G

57310304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26599498-G-A

57310739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: missense variant
orthologous variants: 26598935-T-C

57310758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: missense variant
orthologous variants: 26598916-G-A

57311060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26598585-G-T

http://identifiers.org/hco/3/GRCh38#57311078-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26598570-A-C

57311078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26598570-A-G

57311078-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26598570-A-T

57311079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26598569-G-T

57311087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26598561-G-A

57311087-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26598561-G-C

57311087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26598561-G-T

57311107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26598539-G-A

57312148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26598240-A-G

57312489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26597928-T-C

57312520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26597894-A-G

57314506-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, missense_variant
orthologous variants: 26597290-G-C

57314540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, missense_variant
orthologous variants: 26597256-T-C

http://identifiers.org/hco/3/GRCh38#57314778-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26597023-A-C

57314778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26597023-A-G

http://identifiers.org/hco/3/GRCh38#57314966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26596845-C-A

57315163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26596659-G-A

57315203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26596621-C-T

57321926-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26595112-T-G

57321968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26595075-T-C

57321970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26595073-C-T

57322002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26595043-G-A

57322206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26594867-T-C

http://identifiers.org/hco/3/GRCh38#57322224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26594849-C-A

57322224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26594849-C-T

57322437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: missense variant
orthologous variants: 26594659-G-T

57322633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26594559-G-A

57322633-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26594559-G-C

57322633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26594559-G-T

57322914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26594484-A-G

57322988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26594451-T-C

57322989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26594450-A-G

57323062-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: missense variant
orthologous variants: 26594375-G-C

57323062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: missense variant
orthologous variants: 26594375-G-T

57323369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26594072-A-G

57323457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26593987-A-G

57323492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: missense variant
orthologous variants: 26593801-G-A

57323492-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: missense variant
orthologous variants: 26593801-G-C

http://identifiers.org/hco/3/GRCh38#57323732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26593569-C-A

57323732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26593569-C-T

http://identifiers.org/hco/3/GRCh38#57323739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26593562-C-A

57323739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26593562-C-T

57323794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26593504-G-A

57334550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: missense variant
orthologous variants: 26590788-T-C

57334651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26590693-A-G

57334655-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26590690-T-G

57334860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: missense variant
orthologous variants: 26587061-G-A

57334964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26586958-T-C

57334978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26586945-A-G

57334978-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26586945-A-T

57357090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26581399-T-C

57357125-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26581355-G-C

57357164-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26581315-G-C

57357278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, stop_gained
orthologous variants: 26581200-G-T

http://identifiers.org/hco/3/GRCh38#57357311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26581167-C-A

57357311-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, missense_variant
orthologous variants: 26581167-C-G

57357311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, missense_variant
orthologous variants: 26581167-C-T

http://identifiers.org/hco/3/GRCh38#57357443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26581035-C-A

57357443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26581035-C-T

57357596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26580891-A-G

57360317-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26580198-T-A

57360366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26580150-A-G

57361476-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26579129-T-A

57361476-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26579129-T-G

57361477-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26579128-T-A

57363513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26578658-G-T

57363871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26578328-C-T

57364271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26577683-T-C

57366596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26577053-G-T

57366670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26576977-T-C

http://identifiers.org/hco/3/GRCh38#57366768-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26576877-A-C

57366924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 26576721-A-G

http://identifiers.org/hco/3/GRCh38#57366994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26576649-C-A

57366994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26576649-C-T

http://identifiers.org/hco/3/GRCh38#57367988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26575899-C-A

57368003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26575884-A-G

http://identifiers.org/hco/3/GRCh38#57368063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26575848-C-A

57374742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26573666-A-G

57374785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26573624-T-C

57374808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26573570-G-A

57374808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26573570-G-T

57374827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26573556-C-T

57374877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26573476-G-A

57375255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26573116-G-T

57375330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26573042-A-G

57375395-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, missense_variant
orthologous variants: 26572983-A-T

57375500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, missense_variant
orthologous variants: 26572878-C-T

57376103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26572048-G-A

57376363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26571836-A-G

57376364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26571835-T-C

57376858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26571471-T-C

57376939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26571387-G-T

http://identifiers.org/hco/3/GRCh38#57376996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26571340-C-A

57376996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, missense_variant
orthologous variants: 26571340-C-T

57377193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 26571143-T-C

57377256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26571087-T-C

57377341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26571029-T-C

57377448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26570937-T-C

57379100-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26558778-A-T

57379143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26558735-T-C

57379243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 26558635-G-A

57379243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 26558635-G-T

57379354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26558525-A-G

57379949-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26556093-T-A

57380087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26555971-A-G

57380087-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26555971-A-T

http://identifiers.org/hco/3/GRCh38#57381649-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26554074-A-C

57382182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26553465-C-T

57382208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26553434-C-T

57382284-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, missense_variant
orthologous variants: 26553365-T-A

57382514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26553078-G-T

57382606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26552963-G-A

57384899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, missense_variant
orthologous variants: 26552503-T-C

57384914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, missense_variant
orthologous variants: 26552488-T-C

57385024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26552370-A-G

57385045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26552349-T-C

57385110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26552284-A-G

http://identifiers.org/hco/3/GRCh38#57385317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26551371-C-A

57385372-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, missense_variant
orthologous variants: 26551317-T-G

57385579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, undefined
orthologous variants: 26551127-A-G

57385582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, undefined
orthologous variants: 26551124-T-C

57385914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26551095-A-G

57386019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26550969-G-T

57386103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26550891-A-G

57386574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, missense_variant
orthologous variants: 26549869-T-C

57386865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26549621-G-A

57387003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26549485-A-G

57387175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 26548893-T-C

http://identifiers.org/hco/3/GRCh38#57387215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26548853-C-A

http://identifiers.org/hco/3/GRCh38#57387220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, splice_acceptor_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26548848-C-A

57387220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, splice_acceptor_variant
orthologous variants: 26548848-C-T

http://identifiers.org/hco/3/GRCh38#57387281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26548798-C-A

57387337-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26548759-T-A

57387368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26548735-G-T

57387972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26548497-G-A

57388125-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26548335-T-A

57388215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26548246-G-A

57388408-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26547917-T-G

http://identifiers.org/hco/3/GRCh38#57388451-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26547878-A-C

57388453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26547876-A-G

57388453-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26547876-A-T

http://identifiers.org/hco/3/GRCh38#57391825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26546578-C-A

57391930-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, missense_variant
orthologous variants: 26546456-C-G

57391930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, missense_variant
orthologous variants: 26546456-C-T

57392166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26546229-G-A

57392166-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26546229-G-C

57392171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26546224-T-C

57392325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26546066-G-A

57392726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26543881-A-G

57393039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26543589-T-C

57393049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26543579-T-C

57393094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26543534-C-T

57394128-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26541119-A-T

http://identifiers.org/hco/3/GRCh38#57394151-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26541094-A-C

57394163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 26541081-G-T

http://identifiers.org/hco/3/GRCh38#57394255-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26540989-A-C

57394347-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26540897-G-C

http://identifiers.org/hco/3/GRCh38#57394403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26540841-C-A

http://identifiers.org/hco/3/GRCh38#57394407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26540837-C-A

57394584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26540690-C-T

57402515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26538638-C-T

57402516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26538637-A-G

57402516-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26538637-A-T

57403107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26538460-G-A

57403172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26538416-G-A

57403172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26538416-G-T

57403442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: missense variant
orthologous variants: 26538156-G-T

http://identifiers.org/hco/3/GRCh38#57403493-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26538105-A-C

57403546-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26538056-T-A

57404876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26537596-G-A

57404876-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26537596-G-C

57404876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26537596-G-T

57404936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26537544-G-A

57404962-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 26537512-T-A

57404962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 26537512-T-C

http://identifiers.org/hco/3/GRCh38#57405202-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26537292-A-C

57405202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26537292-A-G

57405202-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26537292-A-T

57405374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26536972-G-A

http://identifiers.org/hco/3/GRCh38#57405504-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26536815-A-C

57405504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26536815-A-G

57405504-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26536815-A-T

57405594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26536720-T-C

57405675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: missense variant
orthologous variants: 26536637-T-C

57405675-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: missense variant
orthologous variants: 26536637-T-G

57405862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: missense variant
orthologous variants: 26536450-C-T

http://identifiers.org/hco/3/GRCh38#57405995-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26536316-A-C

57405995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26536316-A-G

57406042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26536277-T-C

57406042-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26536277-T-G

57406696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26536015-C-T

http://identifiers.org/hco/3/GRCh38#57406885-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26535827-A-C

57407375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26535690-T-C

http://identifiers.org/hco/3/GRCh38#57407590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26535431-C-A

57407591-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26535430-T-G

57407847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26535202-A-G

57407920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26535080-G-A

57407928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26535072-C-T

http://identifiers.org/hco/3/GRCh38#57407939-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26535062-A-C

57407955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26535042-C-T

http://identifiers.org/hco/3/GRCh38#57408157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26534855-C-A

57408157-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26534855-C-G

http://identifiers.org/hco/3/GRCh38#57408176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26534836-C-A

57408574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26534486-T-C

57408574-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26534486-T-G

57408606-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26534455-T-A

57408618-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26534443-T-A

57408669-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26534425-T-A

57408669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26534425-T-C

http://identifiers.org/hco/3/GRCh38#57408677-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26534417-A-C

57408677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26534417-A-G

57408677-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26534417-A-T

57408743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26534371-T-C

57408757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26534364-C-T

57408824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26534297-T-C

57408937-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26534187-G-C

57408937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26534187-G-T

57408942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26534182-G-A

http://identifiers.org/hco/3/GRCh38#57413330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26523954-C-A

57413772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: synonymous variant
orthologous variants: 26523504-T-C

57413928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26523347-A-G

http://identifiers.org/hco/3/GRCh38#57414101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26523203-C-A

57414101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26523203-C-T

57414267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26522879-A-G

http://identifiers.org/hco/3/GRCh38#57414713-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26522507-A-C

57415198-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26522216-C-G

57415326-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26522147-A-T

57415343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26522130-C-T

http://identifiers.org/hco/3/GRCh38#57415366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26522107-C-A

57415366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26522107-C-T

http://identifiers.org/hco/3/GRCh38#57419154-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26521107-A-C

57419204-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26521058-A-T

57419233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26521029-T-C

http://identifiers.org/hco/3/GRCh38#57419326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26520930-C-A

57419326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26520930-C-T

57419348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26520908-T-C

57419348-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26520908-T-G

http://identifiers.org/hco/3/GRCh38#57419506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26520755-C-A

57419544-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26520719-T-G

57419555-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26520708-T-A

57419555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26520708-T-C

57419555-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26520708-T-G

http://identifiers.org/hco/3/GRCh38#57419723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26520026-C-A

57419889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26519750-T-C

57420088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26519561-T-C

57420121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26519529-G-A

57420338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26519365-A-G

57420632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26519117-G-A

57420647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26519105-C-T

57421378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26518504-G-A

57421378-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26518504-G-C

57421378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26518504-G-T

57421381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26518501-A-G

57421463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26518371-T-C

57421463-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26518371-T-G

57421519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 26518313-T-C

57421648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: missense variant
orthologous variants: 26518184-C-T

57421755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26518079-T-C

57421841-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26518003-T-A

57421841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26518003-T-C

57421842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26518002-G-A

57421842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26518002-G-T

57421843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26518001-G-A

57421843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26518001-G-T

57421863-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26517977-G-C

57421863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26517977-G-T

57422986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26517671-G-A

57423028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26517629-G-A

57423057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26517603-G-A

57423290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26517389-T-C

57423294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26517384-T-C

57423513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26517190-G-A

57424041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26514567-C-T

57424113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26514497-C-T

57424136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26514476-A-G

57424149-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26514463-A-T

57424808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26514424-G-A

57424893-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26514340-C-G

http://identifiers.org/hco/3/GRCh38#57424913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26514321-C-A

57424960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26514276-A-G

57424960-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26514276-A-T

57425237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26513987-G-A

57425237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26513987-G-T

57425666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26513880-A-G

57426003-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26513553-G-C

57426019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26513537-T-C

57426019-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26513537-T-G

57426176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26513397-C-T

57426290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26513346-A-G

http://identifiers.org/hco/3/GRCh38#57426442-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26513206-A-C

http://identifiers.org/hco/3/GRCh38#57426554-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26513118-A-C

57426557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26513115-A-G

57426876-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26513070-G-C

57426940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26513007-T-C

57427101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26512844-C-T

57428372-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, missense_variant
orthologous variants: 26508392-T-G

http://identifiers.org/hco/3/GRCh38#57428504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26508274-C-A

57428504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26508274-C-T

57428739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: missense variant
orthologous variants: 26507895-T-C

57428739-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: missense variant
orthologous variants: 26507895-T-G

57428963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26507678-G-A

57428963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26507678-G-T

57429008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26507634-T-C

57429089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26507554-C-T

57429325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26507440-C-T

57429606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26507367-C-T

57429639-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26507347-T-A

57429661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26507325-A-G

http://identifiers.org/hco/3/GRCh38#57429665-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26507321-A-C

57429665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26507321-A-G

57430538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26507026-T-C

57430538-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26507026-T-G

57430864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26506709-G-T

57431014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26506471-C-T

57431044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26506441-G-T

57431134-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26506354-C-G

57431153-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26506336-C-G

57431197-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26506290-T-A

57431202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26506285-C-T

57431857-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26505494-T-A

57431857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26505494-T-C

57432144-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26505252-C-G

57432144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26505252-C-T

57432164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26505232-A-G

57432164-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26505232-A-T

57432700-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26504918-C-G

57432808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26504822-T-C

57433020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26504633-T-C

57433070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26504582-A-G

http://identifiers.org/hco/3/GRCh38#57433174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26503906-C-A

57433206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26503892-C-T

http://identifiers.org/hco/3/GRCh38#57433219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26503877-C-A

57433219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26503877-C-T

57433277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26503836-T-C

57433279-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26503834-T-A

57433341-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26503790-C-G

57433513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 26503615-G-A

57433558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26503566-A-G

57433601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26503523-G-A

57433769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: missense variant
orthologous variants: 26503360-T-C

57433781-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: missense variant
orthologous variants: 26503348-T-A

57433781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: missense variant
orthologous variants: 26503348-T-C

http://identifiers.org/hco/3/GRCh38#57433829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: splice acceptor variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26503300-C-A

57433842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26503292-G-A

57433842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26503292-G-T

57433851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26503283-A-G

57433888-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26503240-T-A

57433888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26503240-T-C

57433896-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26503232-T-A

57433896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26503232-T-C

57433926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26503202-A-G

http://identifiers.org/hco/3/GRCh38#57433953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26503175-C-A

57433976-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26503153-T-A

57434126-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26503013-G-C

57434156-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26502997-T-A

57434384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26502804-G-A

57434835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26502466-C-T

57434864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26502441-G-A

57435067-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26502258-T-G

57435479-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26501839-T-A

57435488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26501830-G-A

57435626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26501717-G-A

57435626-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26501717-G-C

57435692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26501701-C-T

57435845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26501671-G-A

57435845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26501671-G-T

57435863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26501654-C-T

57436082-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26501441-A-T

57436329-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26501236-C-G

57436329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26501236-C-T

57436411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26501154-C-T

http://identifiers.org/hco/3/GRCh38#57436823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26500979-C-A

57436823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26500979-C-T

57436827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26500975-G-T

57436893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26500926-G-A

57436893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26500926-G-T

http://identifiers.org/hco/3/GRCh38#57436922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26500899-C-A

57436922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26500899-C-T

http://identifiers.org/hco/3/GRCh38#57436925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26500896-C-A

57436942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26500875-T-C

57436993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: missense variant
orthologous variants: 26500824-T-C

57437085-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26500729-T-A

57437085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26500729-T-C

57437085-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26500729-T-G

57444612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26496372-T-C

http://identifiers.org/hco/3/GRCh38#57444839-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26496153-A-C

57445102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26495871-T-C

http://identifiers.org/hco/3/GRCh38#57445138-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26495836-A-C

http://identifiers.org/hco/3/GRCh38#57445191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: stop gained
orthologous variants: http://identifiers.org/mco/14/GRCm39#26495779-C-A

57445191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: missense variant
orthologous variants: 26495779-C-T

http://identifiers.org/hco/3/GRCh38#57445232-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26495738-A-C

57445232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: missense variant
orthologous variants: 26495738-A-G

57445246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: synonymous variant
orthologous variants: 26495724-T-C

57445373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: missense variant
orthologous variants: 26495597-A-G

57445425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 26495545-G-A

57445425-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 26495545-G-C

57445427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 26495543-A-G

57445427-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 26495543-A-T

57445454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26495516-A-G

57445499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26495467-G-A

57445499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26495467-G-T

57446011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26495140-A-G

http://identifiers.org/hco/3/GRCh38#57446012-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26495139-A-C

57446080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: missense variant
orthologous variants: 26495071-G-T

57446160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: synonymous variant
orthologous variants: 26494991-T-C

57446272-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: splice acceptor variant
orthologous variants: 26494879-T-A

57446317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26494839-A-G

57446382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26494777-C-T

http://identifiers.org/hco/3/GRCh38#57446685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26494492-C-A

57446685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: missense variant
orthologous variants: 26494492-C-T

57446763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26494391-T-C

57446786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26494368-T-C

57446867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26494297-C-T

57447020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26494136-A-G

57447139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26494036-T-C

57447235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26493942-T-C

57447243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26493934-A-G

57447258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26493922-G-A

http://identifiers.org/hco/3/GRCh38#57452793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26493073-C-A

57452793-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26493073-C-G

57452922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: missense variant
orthologous variants: 26492945-A-G

57453143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26492725-G-A

http://identifiers.org/hco/3/GRCh38#57453407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26492312-C-A

57453407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 26492312-C-T

57455167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26491680-G-A

57455422-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26491481-T-A

57455422-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26491481-T-G

57455556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26491373-T-C

57455839-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26491091-T-G

57455965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26490968-T-C

57455981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26490952-A-G

57456166-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26490798-A-T

57456193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26490772-G-A

57456636-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26490115-C-G

57456636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26490115-C-T

57456661-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26490090-G-C

57457215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26489252-T-C

57458018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26488229-G-T

http://identifiers.org/hco/3/GRCh38#57458077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26488170-C-A

57458077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26488170-C-T

57458159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 26488088-A-G

57458305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26487946-A-G

57459248-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26460869-T-A

57459248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26460869-T-C

57459269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26460845-C-T

57459399-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26460705-C-G

57459524-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26460570-T-A

http://identifiers.org/hco/3/GRCh38#57459808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26460288-C-A

57459808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26460288-C-T

57459887-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26460212-G-C

http://identifiers.org/hco/3/GRCh38#57459904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26460194-C-A

57459904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26460194-C-T

57460216-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26459879-T-G

57460326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26459644-C-T

57460642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26459110-A-G

57460648-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26459104-T-A

57460909-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26458764-G-C

57460909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26458764-G-T

http://identifiers.org/hco/3/GRCh38#57461076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26457794-C-A

57461362-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26457086-T-A

57461362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26457086-T-C

57461443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26457011-G-A

57461607-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: missense variant
orthologous variants: 26456851-G-C

57461722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26456698-G-A

57461722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26456698-G-T

57461837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26456547-G-T

57461865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26456520-T-C

57462042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26456174-A-G

57462934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26455575-T-C

57462934-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26455575-T-G

57462936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26455573-C-T

57468727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 26445796-T-C

57468965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: missense variant
orthologous variants: 26445558-C-T

57468981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: splice acceptor variant
orthologous variants: 26445542-T-C

57468991-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26445532-G-C

57468991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26445532-G-T

57468994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26445529-A-G

57469174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26445373-C-T

57470590-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: missense variant
orthologous variants: 26445054-T-A

57470611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: missense variant
orthologous variants: 26445033-T-C

http://identifiers.org/hco/3/GRCh38#57471419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26444834-C-A

57471419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26444834-C-T

57471448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26444806-T-C

http://identifiers.org/hco/3/GRCh38#57471467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26444789-C-A

57471467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26444789-C-T

57471493-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: synonymous variant
orthologous variants: 26444763-T-G

57471500-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: missense variant
orthologous variants: 26444756-T-G

57471633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26444622-T-C

57472296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26444038-G-A

57472515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26443396-T-C

http://identifiers.org/hco/3/GRCh38#57472748-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26443188-A-C

57472748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26443188-A-G

57483206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26439314-T-C

57483252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26439275-G-A

57483252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26439275-G-T

57483278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26439254-A-G

57483407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: missense variant
orthologous variants: 26439166-A-G

57483431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: missense variant
orthologous variants: 26439142-G-A

57483521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26439052-T-C

57483556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26439018-A-G

57484246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26438197-G-A

57484326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26438128-T-C

57486463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26438022-A-G

http://identifiers.org/hco/3/GRCh38#57486481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26438004-C-A

57489419-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26437974-T-A

http://identifiers.org/hco/3/GRCh38#57489424-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26437968-A-C

57489469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26437924-T-C

57489471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26437922-G-T

http://identifiers.org/hco/3/GRCh38#57489472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26437921-C-A

57489472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26437921-C-T

57489492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26437901-G-T

http://identifiers.org/hco/3/GRCh38#57489725-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26437678-A-C

57489725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26437678-A-G

57489808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26437601-G-T

57489880-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26437463-C-G

57489911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26437440-G-A

http://identifiers.org/hco/3/GRCh38#57489974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26437399-C-A

57490402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26437185-A-G

57490404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26437183-G-A

57490432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26437158-G-A

57490486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26437107-A-G

57490534-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26437061-C-G

57490598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26436998-T-C

57490671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron variant
orthologous variants: 26436930-C-T

57501181-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26433364-T-G

57501191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26433354-G-T

http://identifiers.org/hco/3/GRCh38#57501287-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26432263-A-C

57501287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26432263-A-G

57501322-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 26432221-T-A

57501322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 26432221-T-C

57501478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26432071-A-G

57502196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26431523-T-C

57502532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26431221-A-G

57502540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26431213-A-G

57503019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26431200-C-T

57503031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26431188-G-A

http://identifiers.org/hco/3/GRCh38#57503285-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26430957-A-C

57503870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26430623-T-C

57503876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26430617-A-G

57503876-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26430617-A-T

57503905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26430588-T-C

57503905-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26430588-T-G

57503961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26430539-A-G

57503984-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26430518-A-T

57504005-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26430488-A-T

http://identifiers.org/hco/3/GRCh38#57504218-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26430272-A-C

57504218-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26430272-A-T

57506176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26429804-G-A

57506268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26429740-C-T

57506805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26429556-A-G

57506853-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26429511-G-C

57506983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26429388-G-A

57507016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26429351-C-T

57507890-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26428232-T-G

57507908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26428214-G-T

57507931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26428202-G-A

57507931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26428202-G-T

http://identifiers.org/hco/3/GRCh38#57508079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26428177-C-A

57508079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26428177-C-T

57508624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26427852-G-A

57508624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26427852-G-T

57508642-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26427835-T-G

57508644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26427833-G-A

57508644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26427833-G-T

57508663-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26427814-T-A

57508664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26427813-G-A

57508664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26427813-G-T

57508840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26427657-T-C

57508936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26427426-A-G

57508997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26427367-A-G

57509050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26427338-T-C

57509050-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26427338-T-G

57509330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26427069-G-A

http://identifiers.org/hco/3/GRCh38#57509364-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26427036-C-A

57509377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26427023-T-C

57509461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26426941-T-C

57510267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26419128-G-A

57511055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26418313-A-G

57511055-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26418313-A-T

57522909-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26417879-G-C

57522990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26417803-A-G

57522990-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26417803-A-T

57523449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26417662-G-A

57523449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26417662-G-T

57523485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26417635-T-C

57523493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26417627-A-G

57523503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26417617-G-T

57523617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 26417511-A-G

57523653-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26417458-T-G

57523663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26417438-T-C

57523805-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 26417182-T-A

57523805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 26417182-T-C

57523843-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26417144-T-A

57523863-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26417124-A-T

http://identifiers.org/hco/3/GRCh38#57523928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26417063-C-A

57523928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26417063-C-T

http://identifiers.org/hco/3/GRCh38#57523989-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26416990-A-C

57523989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26416990-A-G

http://identifiers.org/hco/3/GRCh38#57524177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26416679-C-A

57524186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26416670-A-G

57542585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26414881-G-T

57542880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 26414589-C-T

http://identifiers.org/hco/3/GRCh38#57542964-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#26414505-A-C

57542964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26414505-A-G

57543313-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26414203-T-G

57544436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2943
most severe consequence: 5 prime UTR variant
orthologous variants: 26412709-T-C