http://identifiers.org/hco/3/GRCh38#123282620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35125813-C-A

123282620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 3 prime UTR variant
orthologous variants: 35125813-C-T

123282714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 3 prime UTR variant
orthologous variants: 35125731-G-T

123282720-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 3 prime UTR variant
orthologous variants: 35125725-T-A

123282854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 3 prime UTR variant
orthologous variants: 35125657-G-A

123282856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 3 prime UTR variant
orthologous variants: 35125655-C-T

123282862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 3 prime UTR variant
orthologous variants: 35125649-A-G

123282872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 3 prime UTR variant
orthologous variants: 35125639-T-C

123283139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 3 prime UTR variant
orthologous variants: 35125415-T-C

123283226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 3 prime UTR variant
orthologous variants: 35125329-G-A

http://identifiers.org/hco/3/GRCh38#123283301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35125269-C-A

123283301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 3 prime UTR variant
orthologous variants: 35125269-C-T

123283480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 3 prime UTR variant
orthologous variants: 35125112-A-G

123283480-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 3 prime UTR variant
orthologous variants: 35125112-A-T

123283489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 3 prime UTR variant
orthologous variants: 35125103-T-C

http://identifiers.org/hco/3/GRCh38#123283671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35125017-C-A

123283671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 35125017-C-T

123283888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 35124804-G-A

123283888-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 35124804-G-T

http://identifiers.org/hco/3/GRCh38#123283894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35124798-C-A

123283894-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 35124798-C-G

http://identifiers.org/hco/3/GRCh38#123284126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35124573-C-A

123284126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 35124573-C-T

http://identifiers.org/hco/3/GRCh38#123284287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35124429-C-A

123284287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 35124429-C-T

123284312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 35124399-C-T

http://identifiers.org/hco/3/GRCh38#123284351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35124358-C-A

http://identifiers.org/hco/3/GRCh38#123284494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35124217-C-A

123284494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 35124217-C-T

123284615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35124102-A-G

123284615-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35124102-A-T

123284792-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35123925-G-C

123284792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35123925-G-T

http://identifiers.org/hco/3/GRCh38#123284842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35123876-C-A

123286147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35123208-C-T

123286293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35123116-G-A

123286548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35122898-G-A

123286548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35122898-G-T

123286562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35122884-C-T

123286603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35122845-A-G

123286606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35122842-T-C

123286619-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35122829-A-T

http://identifiers.org/hco/3/GRCh38#123286625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#35122823-C-A

123286625-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35122823-C-G

123286655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35122789-G-A

123286655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35122789-G-T

123286662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35122782-G-T

123286841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 35122588-A-G

http://identifiers.org/hco/3/GRCh38#123286874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#35122555-C-A

123286874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 35122555-C-T

123286944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35122507-T-C

123286969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35122484-T-C

123286969-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35122484-T-G

http://identifiers.org/hco/3/GRCh38#123287001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35122457-C-A

123287001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35122457-C-T

http://identifiers.org/hco/3/GRCh38#123287035-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35122397-A-C

http://identifiers.org/hco/3/GRCh38#123287036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35122396-C-A

123287036-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35122396-C-G

123287036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35122396-C-T

123287048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35122384-T-C

123287472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35122189-T-C

123287527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35122149-G-A

123287674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35122033-T-C

123288095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35121723-G-A

123288307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35121529-C-T

123289182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35120224-A-G

123289677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35120071-G-A

123289677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35120071-G-T

123289930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35119845-G-T

123290026-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35119750-T-A

123290026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35119750-T-C

123290028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35119748-T-C

http://identifiers.org/hco/3/GRCh38#123290064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35119714-C-A

123290064-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35119714-C-G

123290064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35119714-C-T

123290067-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35119711-T-A

123290067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35119711-T-C

123290118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35119668-G-A

123290131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35119654-C-T

123290308-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35119499-T-A

123290309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35119498-C-T

123291503-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35118659-T-A

123291503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35118659-T-C

123291503-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35118659-T-G

123291507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35118655-G-T

123291585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35118585-C-T

123291678-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35118511-G-C

123291774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35118435-G-A

123291814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35118400-A-G

123291967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35118251-G-T

123292028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35118193-T-C

123292089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35118147-G-A

123292129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35118120-G-A

123292574-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35117704-G-C

123292666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35117626-G-A

123292718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35117572-G-T

123292719-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35117571-T-G

123294941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35115036-G-A

123294941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35115036-G-T

123295068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35114886-G-A

123295182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35114789-G-A

123295298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35114696-A-G

123295326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35114665-G-A

123295357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35114639-T-C

123296202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35114344-G-A

123296236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35114310-A-G

http://identifiers.org/hco/3/GRCh38#123296278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35114271-C-A

123296278-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35114271-C-G

123296278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35114271-C-T

123296336-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35114235-C-G

123296336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35114235-C-T

http://identifiers.org/hco/3/GRCh38#123296340-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35114231-A-C

123296340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35114231-A-G

http://identifiers.org/hco/3/GRCh38#123296343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35114228-C-A

123296343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35114228-C-T

http://identifiers.org/hco/3/GRCh38#123296367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35114208-C-A

123296367-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35114208-C-G

123296367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35114208-C-T

123296814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35113893-C-T

123296818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35113889-T-C

123296834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35113873-A-G

http://identifiers.org/hco/3/GRCh38#123296840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35113867-C-A

123296840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35113867-C-T

http://identifiers.org/hco/3/GRCh38#123296847-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35113860-A-C

http://identifiers.org/hco/3/GRCh38#123297014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35113738-C-A

123297014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 35113738-C-T

123297071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35113686-G-T

123297080-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35113677-C-G

123297080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35113677-C-T

123297092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35113665-G-T

123297096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35113661-A-G

123297163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35113593-A-G

123297199-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35113562-T-G

123297216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35113545-G-A

123297216-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35113545-G-C

123297228-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35113532-T-A

http://identifiers.org/hco/3/GRCh38#123297249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35113518-C-A

123297249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35113518-C-T

http://identifiers.org/hco/3/GRCh38#123297479-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35113313-A-C

123297558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35113234-G-T

http://identifiers.org/hco/3/GRCh38#123297583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35113210-C-A

http://identifiers.org/hco/3/GRCh38#123297791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35113038-C-A

123300022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35112149-C-T

123300027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35112144-T-C

123300027-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35112144-T-G

123300037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35112134-G-A

123300037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35112134-G-T

http://identifiers.org/hco/3/GRCh38#123300089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35112076-C-A

123300090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35112075-A-G

123300363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35111806-T-C

123300386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35111785-G-A

http://identifiers.org/hco/3/GRCh38#123300413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35111738-C-A

123300413-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35111738-C-G

123300413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35111738-C-T

123300417-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35111734-T-A

123300417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35111734-T-C

123300440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35111711-T-C

123300454-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35111697-C-G

123300494-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35111655-G-C

123300713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35111497-C-T

123301179-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35111070-T-G

123301206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35111052-C-T

123301207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35111051-C-T

123301251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35111011-G-A

123301285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35110967-A-G

123301415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35110834-G-A

http://identifiers.org/hco/3/GRCh38#123301445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35110803-C-A

123301469-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35110785-G-C

123302910-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35110689-T-A

123302910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35110689-T-C

123303261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35110356-T-C

123303296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35110320-G-A

123303296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35110320-G-T

http://identifiers.org/hco/3/GRCh38#123303335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35110279-C-A

123303335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35110279-C-T

123303362-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35110257-T-A

123303362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35110257-T-C

123303944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35110092-G-T

123303969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35110071-G-T

123304058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35109998-G-T

123304080-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35109976-G-C

123304094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 35109962-C-T

123304226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35109854-G-A

123304226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35109854-G-T

http://identifiers.org/hco/3/GRCh38#123304258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35109822-C-A

123304258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35109822-C-T

123304364-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35109724-T-G

123304526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35109584-C-T

123304631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35109516-G-A

123304842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35109317-T-C

123304911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35109246-A-G

123304989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35109177-C-T

123304990-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35109176-C-G

123305140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35108956-C-T

123309333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

http://identifiers.org/hco/3/GRCh38#123310302-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35106956-A-C

123310329-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35106936-C-G

123310472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35106810-C-T

http://identifiers.org/hco/3/GRCh38#123310546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35106737-C-A

123310546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35106737-C-T

123310773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35106567-C-T

123310780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35106561-G-A

123310799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35106540-G-T

123310990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35106398-C-T

123311087-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35106305-G-C

123311133-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35106259-T-A

123311133-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35106259-T-G

123311299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35106089-G-A

123311446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35105834-C-T

123311507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35105753-G-A

123311523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35105737-G-T

123311667-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35105608-C-G

http://identifiers.org/hco/3/GRCh38#123311679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35105597-C-A

123313928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35104186-C-T

123313953-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35104164-A-T

http://identifiers.org/hco/3/GRCh38#123314126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35104055-C-A

123314126-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35104055-C-G

123314175-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35104007-C-G

123314180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35104006-G-A

123314342-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35103870-G-C

123314374-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35103832-C-G

http://identifiers.org/hco/3/GRCh38#123314397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35103803-C-A

123314399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35103801-A-G

123314686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35103570-C-T

123315101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35103253-G-A

123315114-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35103240-C-G

123315157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35103213-G-A

123315251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35103127-C-T

123315267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35103111-C-T

123315283-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35103097-T-G

123315396-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35102995-T-G

123316331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35102127-A-G

123316509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35101945-G-A

123316546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35101909-G-A

123316608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35101847-G-A

123316715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35101752-G-A

123316739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35101729-G-A

123317897-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35100905-T-A

123317897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35100905-T-C

http://identifiers.org/hco/3/GRCh38#123317900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35100902-C-A

123317924-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35100881-G-T

123318000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35100823-A-G

123318145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35100679-G-A

http://identifiers.org/hco/3/GRCh38#123318188-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35100638-A-C

123318188-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35100638-A-T

123318262-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35100591-G-C

123318262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35100591-G-T

123318267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35100586-A-G

123318352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35100489-C-T

123318714-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35100221-C-G

123318714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35100221-C-T

123318716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35100219-T-C

123318914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35100113-G-A

123318914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35100113-G-T

123319523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35099837-T-C

123319535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35099822-G-T

123319632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35099744-T-C

http://identifiers.org/hco/3/GRCh38#123319937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35099444-C-A

123319937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35099444-C-T

123319953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35099428-G-A

123320358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35099118-G-T

123320622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35098941-T-C

123320825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35098814-G-A

123320949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35098707-G-A

123320994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35098660-C-T

123321153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35098558-T-C

123321298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35098407-G-A

http://identifiers.org/hco/3/GRCh38#123321443-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35098242-A-C

123321686-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35098036-T-A

123321711-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35098010-C-G

123321918-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35097865-T-A

123322079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35097715-C-T

123322097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35097697-G-A

123322097-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35097697-G-C

123322097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35097697-G-T

123322159-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35097636-G-C

123322191-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35097606-C-G

123322195-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35097601-C-G

123322313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35097489-G-A

http://identifiers.org/hco/3/GRCh38#123322517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35097319-C-A

123322653-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35097127-C-G

123322741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35097021-T-C

123322846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35096910-G-A

123322880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35096875-A-G

http://identifiers.org/hco/3/GRCh38#123322907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35096855-C-A

123322922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35096841-G-A

123323082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35096641-G-A

123323102-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35096621-C-G

123323210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35096536-T-C

http://identifiers.org/hco/3/GRCh38#123323234-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35096515-A-C

123323234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35096515-A-G

123323247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35096502-G-A

123323323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35096427-A-G

123323401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35096361-T-C

123323401-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35096361-T-G

123324283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35095782-T-C

123324542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35095631-G-A

123324542-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35095631-G-C

123324839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35095345-C-T

123324976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35095210-A-G

123325338-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35094917-T-A

123325353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35094902-C-T

123325395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35094860-G-A

123325395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35094860-G-T

123325410-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35094845-A-T

123325467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 35094788-A-G

123325541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35094699-T-C

123325555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35094685-G-A

123325555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35094685-G-T

123325702-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35094623-G-C

123325761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35094564-C-T

123325873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35094426-T-C

123326067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35094234-G-A

123326161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35094159-G-A

123326429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35093967-G-A

123326687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35093720-A-G

123327014-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35093435-G-C

123327462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35092747-G-A

http://identifiers.org/hco/3/GRCh38#123327594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35092618-C-A

123327594-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35092618-C-G

123327594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35092618-C-T

123327700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35092506-G-T

123327751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35092455-T-C

123327813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35092392-G-A

123327813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35092392-G-T

http://identifiers.org/hco/3/GRCh38#123327886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35092362-C-A

123327886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35092362-C-T

123327928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35092311-A-G

123327948-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35092297-C-G

123327968-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35092277-A-T

123328331-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35091794-G-C

123328361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35091764-A-G

123328514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35091517-C-T

123328552-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35091453-T-A

123328552-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35091453-T-G

123328563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35091436-G-A

123328563-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35091436-G-C

123328563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35091436-G-T

123328926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, undefined
orthologous variants: 35091068-A-G

http://identifiers.org/hco/3/GRCh38#123328943-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35091051-A-C

123329057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, undefined
orthologous variants: 35090930-T-C

123329191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35090788-T-C

123329387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35090577-G-T

123329783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35090293-A-G

123329783-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35090293-A-T

123330200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35089997-A-G

123330209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35089988-C-T

123330281-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35089922-G-C

123330781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35089538-C-T

123330788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35089531-C-T

123330798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35089521-G-A

123330798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35089521-G-T

http://identifiers.org/hco/3/GRCh38#123330799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35089520-C-A

123330799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35089520-C-T

http://identifiers.org/hco/3/GRCh38#123330831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35089493-C-A

123330831-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35089493-C-G

123330831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35089493-C-T

123330858-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35089475-G-C

123330858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35089475-G-T

123331039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35089301-A-G

123331204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35089147-G-A

123331247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35089104-T-C

123331393-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35088759-C-G

123331433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35088722-G-T

123331573-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35088581-T-A

123331801-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35088323-A-T

123332254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35087893-G-A

http://identifiers.org/hco/3/GRCh38#123332460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35087720-C-A

123332460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35087720-C-T

123332696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35087527-G-A

123332696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35087527-G-T

123332953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35087443-C-T

123333172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35087370-G-A

123333263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35087299-T-C

http://identifiers.org/hco/3/GRCh38#123333306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35087256-C-A

123333376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35087197-A-G

123333376-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35087197-A-T

123333399-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35087177-A-T

123333481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35087081-G-A

123333481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35087081-G-T

123333650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35086708-G-A

123333800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35086484-C-T

http://identifiers.org/hco/3/GRCh38#123333929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35086369-C-A

123333956-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35086341-T-G

123333983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35086288-C-T

123334158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35086112-G-A

123334195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35086088-C-T

123334227-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35086060-T-G

123334294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35086011-G-A

123335452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35084826-G-A

123335452-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35084826-G-C

http://identifiers.org/hco/3/GRCh38#123336022-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35084380-A-C

123336152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35084275-G-T

123336361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35084120-G-A

123336465-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35084021-G-C

123336468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35084018-G-T

123336513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35083996-G-T

123337118-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35083499-T-A

123337118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35083499-T-C

123338227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35081597-C-T

123338397-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35081401-G-C

123338481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35081319-G-A

123338481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35081319-G-T

123338871-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35081001-T-G

123338891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35080982-G-A

123338994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35080889-T-C

123339277-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35080665-T-G

123339332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35080614-G-A

123339332-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35080614-G-C

123339599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35080464-C-T

123339689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35080395-G-A

123339689-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35080395-G-C

123339699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35080371-C-T

123342153-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35078498-T-A

123342266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35078395-G-A

123342309-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35078347-C-G

123342309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35078347-C-T

123342312-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35078344-G-C

123342529-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35078130-T-G

123342531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35078128-G-A

123342533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35078124-G-A

123342600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35078053-C-T

123342655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35077965-G-A

123342804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35077836-C-T

123342888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35077761-C-T

123342938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35077717-G-A

123342945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35077710-G-T

123343152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35077324-G-A

123343186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35077280-T-C

123343248-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35077219-C-G

123343342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35077128-T-C

123343454-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35077040-C-G

123343812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35076712-G-A

123343816-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35076708-T-A

123343886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35076643-C-T

123344501-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35076188-T-A

123344503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35076186-C-T

123344556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35076131-G-T

http://identifiers.org/hco/3/GRCh38#123345139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35075609-C-A

123345150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35075595-G-T

123345495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35075387-G-A

123345735-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35075147-G-C

123345736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35075146-A-G

123345795-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35075098-C-G

123346393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35074624-G-A

123346682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35074384-T-C

123346774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35074300-G-A

123346774-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35074300-G-C

123346992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35074096-G-A

123347733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35073663-G-A

123347733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35073663-G-T

123347788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 35073624-T-C

123347941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35073471-C-T

123347954-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35073458-A-T

123348082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35073373-T-C

123348082-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35073373-T-G

123348098-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35073357-C-G

123348134-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35073319-T-A

123348235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35073216-C-T

123348481-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35073061-G-C

123348691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35072850-G-A

123348722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35072819-G-A

123348887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35072653-C-T

http://identifiers.org/hco/3/GRCh38#123349164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35072400-C-A

123349271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35072319-T-C

123349461-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35072150-C-G

123349461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35072150-C-T

http://identifiers.org/hco/3/GRCh38#123349468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35072143-C-A

http://identifiers.org/hco/3/GRCh38#123349547-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35072066-A-C

123349665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35071971-G-T

http://identifiers.org/hco/3/GRCh38#123349948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35071908-C-A

123349963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35071894-G-A

123350477-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35071357-C-G

123350477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35071357-C-T

123350531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35071306-C-T

123350570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35071280-G-A

123350647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35071205-G-A

123350971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35070777-G-A

123351070-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35070683-G-C

123351111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35070389-G-A

123351193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35070314-G-A

123351319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35070217-C-T

123351662-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35069954-C-G

123352197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35069529-C-T

123352225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35069505-G-A

http://identifiers.org/hco/3/GRCh38#123352314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35069417-C-A

123352321-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35069410-G-C

123352368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35069357-T-C

http://identifiers.org/hco/3/GRCh38#123352395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35069333-C-A

123352395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35069333-C-T

123352594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35069156-A-G

123352608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35069130-A-G

123352609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35069129-G-T

123352671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35069062-C-T

http://identifiers.org/hco/3/GRCh38#123352686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35069046-C-A

123352686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35069046-C-T

123352806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35068933-C-T

http://identifiers.org/hco/3/GRCh38#123353187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35068604-C-A

123353284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35068500-G-A

123353753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35068060-A-G

123353833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35067978-T-C

123354005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35067786-A-G

123354219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35067588-T-C

123354376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35067299-T-C

123354376-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35067299-T-G

123354476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35067073-G-T

123354565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35066921-G-A

http://identifiers.org/hco/3/GRCh38#123354569-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35066917-A-C

123354817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35066622-G-A

123354888-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35066551-T-G

123354983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 35066454-T-C

123355688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35065858-C-T

123356574-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35062801-T-G

123356646-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35062737-G-C

123356812-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35062581-C-G

123357022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35062279-A-G

123357253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35062040-A-G

123357291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35062008-G-T

123357399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35061897-C-T

http://identifiers.org/hco/3/GRCh38#123357495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35061787-C-A

123357571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35061722-T-C

123358870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35060932-G-A

123359384-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35060368-A-T

http://identifiers.org/hco/3/GRCh38#123359728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35060045-C-A

123359756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35060016-C-T

123360275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35059394-A-G

123360315-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35059376-T-A

123360315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35059376-T-C

123360315-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35059376-T-G

123360467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35059236-G-A

http://identifiers.org/hco/3/GRCh38#123360524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35059195-C-A

http://identifiers.org/hco/3/GRCh38#123360775-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35058534-A-C

123361216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35058106-C-T

123361220-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35058102-C-G

123361220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35058102-C-T

123361599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35057756-G-A

123362347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35057365-A-G

http://identifiers.org/hco/3/GRCh38#123362515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35057228-C-A

123362516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35057227-T-C

123363168-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35056661-T-A

123363168-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35056661-T-G

123363172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35056657-G-A

123363172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35056657-G-T

123363174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35056655-A-G

http://identifiers.org/hco/3/GRCh38#123363178-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35056651-A-C

http://identifiers.org/hco/3/GRCh38#123363184-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35056645-A-C

123363186-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35056643-A-T

123363201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35056639-G-A

123363201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35056639-G-T

123364005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35055988-T-C

123364268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35055752-A-G

123364317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35055702-T-C

123364507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35055570-G-A

123364507-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35055570-G-C

123364712-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35055341-G-C

123364740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35055313-T-C

123365426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35054551-C-T

123365664-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35054283-T-G

123366329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35053835-A-G

123367035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35053166-G-A

123367054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35053156-C-T

123367154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35053093-G-A

123367368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35052899-C-T

123367564-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35052718-G-C

123367690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35052614-G-T

123367899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant, splice_donor_variant
orthologous variants: 35052319-C-T

123367945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 35052257-G-A

123367945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 35052257-G-T

123368051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 35052030-G-A

123368051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 35052030-G-T

123368100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35051989-G-A

123368100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35051989-G-T

http://identifiers.org/hco/3/GRCh38#123368138-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35051952-A-C

123368138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35051952-A-G

123368138-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35051952-A-T

123368172-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35051913-T-A

123368906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35051659-T-C

http://identifiers.org/hco/3/GRCh38#123369884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35051171-C-A

http://identifiers.org/hco/3/GRCh38#123370142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35050935-C-A

123370410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35050676-T-C

123370422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35050663-G-A

123370506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35050574-T-C

123370824-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35050227-T-A

123370824-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35050227-T-G

123370862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35050193-G-A

123370909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35050172-C-T

123371082-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35050019-G-C

123371394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35049741-T-C

123371408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35049719-A-G

123371559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35049603-G-A

123371721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35049347-G-A

123371893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35049117-G-A

123373593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35047073-G-T

http://identifiers.org/hco/3/GRCh38#123373746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35046936-C-A

http://identifiers.org/hco/3/GRCh38#123373773-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35046930-A-C

123373773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35046930-A-G

123373773-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35046930-A-T

http://identifiers.org/hco/3/GRCh38#123373775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35046928-C-A

123373794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35046914-G-T

http://identifiers.org/hco/3/GRCh38#123374275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35046201-C-A

123374275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35046201-C-T

123374382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35046093-C-T

123374783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35045718-T-C

123374806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35045696-G-A

123374806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35045696-G-T

123374935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35045567-G-A

123374940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35045562-G-A

123375098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35045410-G-A

123375238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35045274-T-C

123375252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35045260-T-C

123375429-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35045080-G-C

123375511-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 35044996-C-G

123375511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 35044996-C-T

123375684-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 35044819-T-A

123375771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35044731-G-A

123375771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35044731-G-T

123376200-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35044303-T-A

http://identifiers.org/hco/3/GRCh38#123376745-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35044058-A-C

123376931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35043872-T-C

123377207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35043631-G-A

http://identifiers.org/hco/3/GRCh38#123378536-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35042188-A-C

123378772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35041981-G-A

123378772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35041981-G-T

123378791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35041962-A-G

123378805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35041949-T-C

123379206-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35041434-T-A

123379237-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35041404-C-G

123379303-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35041344-T-G

http://identifiers.org/hco/3/GRCh38#123379342-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35041304-A-C

123379683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35040976-G-T

123379995-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35040673-G-C

123379995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35040673-G-T

http://identifiers.org/hco/3/GRCh38#123380751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35040064-C-A

123381336-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35039598-T-G

123381345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35039589-C-T

123381370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35039562-T-C

123381760-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35039195-C-G

http://identifiers.org/hco/3/GRCh38#123382242-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35038724-A-C

123382309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35038611-C-T

123382446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35038510-G-A

123382669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35038302-C-T

123382756-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35038237-A-T

123383352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35037351-G-A

123383384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35037318-C-T

123383401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35037302-G-A

http://identifiers.org/hco/3/GRCh38#123383406-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35037297-A-C

123383406-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35037297-A-T

123383684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35037132-C-T

123383737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35037074-G-A

123383998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35036987-T-C

123383998-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35036987-T-G

123384325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35036704-G-A

123384803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35036375-T-C

123384880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35036306-G-A

123385214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35035981-A-G

123385601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35035475-C-T

123385718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35035361-G-A

123386006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35035071-C-T

123386257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35034879-G-A

123386328-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35034794-A-T

123386779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35034424-C-T

123387025-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35034200-C-G

123387427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35033828-A-G

123388272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35033085-T-C

123388574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35032864-G-T

123388701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35032739-A-G

123388999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35032475-C-T

123389170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35032106-C-T

123389209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35031981-A-G

123389286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35031903-A-G

123389410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35031726-A-G

123389672-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35031532-G-C

123389681-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35031523-C-G

123389752-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35031452-G-C

http://identifiers.org/hco/3/GRCh38#123389870-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35031334-A-C

123389908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35031295-T-C

123389978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35031236-A-G

123389984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35031230-A-G

http://identifiers.org/hco/3/GRCh38#123390305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35030963-C-A

123390632-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35030703-G-C

123390632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35030703-G-T

123390995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35030362-T-C

123391173-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35030180-G-C

123391173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35030180-G-T

123391500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35029806-C-T

http://identifiers.org/hco/3/GRCh38#123391981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35029342-C-A

123392051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35029264-G-A

123392051-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35029264-G-C

123392051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35029264-G-T

123392896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35028649-C-T

http://identifiers.org/hco/3/GRCh38#123393004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35028591-C-A

123393004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35028591-C-T

123394144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35028293-A-G

123394606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35027848-G-A

123397930-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35026482-G-C

123398228-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35026182-G-C

123398228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35026182-G-T

123398489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35025955-G-A

123398774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35025747-T-C

123398850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35025680-G-A

123398987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35025528-C-T

123399219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35025309-G-A

123399370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35024894-T-C

123399782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35024467-C-T

123399874-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35024378-G-C

123400755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35023523-A-G

123401060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35023289-G-A

123401270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35022979-G-A

123401295-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35022955-A-T

123401358-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35022876-C-G

123401374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35022859-T-C

http://identifiers.org/hco/3/GRCh38#123401421-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35022808-A-C

123401444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35022777-C-T

123401473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35022744-T-C

123401636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35022385-C-T

123402071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35022089-T-C

123402164-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35021984-C-G

123402219-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35021934-T-A

123402219-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35021934-T-G

123402248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35021912-C-T

123402402-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35021762-C-G

123402426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35021737-T-C

123402432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35021731-T-C

123402874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35021671-G-A

123402979-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35021553-C-G

123403014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35021516-G-A

123403823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35021008-G-T

123403842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35020989-T-C

http://identifiers.org/hco/3/GRCh38#123404118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35020759-C-A

123404129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35020748-G-T

123404148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 35020737-A-G

http://identifiers.org/hco/3/GRCh38#123404303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35020565-C-A

http://identifiers.org/hco/3/GRCh38#123404315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35020554-C-A

http://identifiers.org/hco/3/GRCh38#123404320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35020549-C-A

123404320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35020549-C-T

123404360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35020514-G-T

123404385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35020490-G-A

123404422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35020453-G-A

123404481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35020405-G-A

123404481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35020405-G-T

123404545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35020344-G-A

123404545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35020344-G-T

123404583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35020308-G-A

123404583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35020308-G-T

123405482-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35019371-C-G

123405482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35019371-C-T

123405493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35019360-G-A

123405499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35019354-G-A

http://identifiers.org/hco/3/GRCh38#123406220-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35017828-A-C

http://identifiers.org/hco/3/GRCh38#123406342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35017703-C-A

123406342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35017703-C-T

123406360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35017686-C-T

123406371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35017675-A-G

123406437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35017621-G-A

123406565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35017510-T-C

123406879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35017308-G-A

123406953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35017242-C-T

123407012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35017208-C-T

123407040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35017180-G-A

123407097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35017130-C-T

http://identifiers.org/hco/3/GRCh38#123407208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35016998-C-A

123407208-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35016998-C-G

123407378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35016746-G-A

123408125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35015543-G-A

123408125-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35015543-G-C

123408125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35015543-G-T

123408227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35015440-G-A

123408227-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35015440-G-C

http://identifiers.org/hco/3/GRCh38#123409575-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35014713-A-C

123409575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35014713-A-G

123410114-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35014198-C-G

123410157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, undefined
orthologous variants: 35014155-C-T

123410259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35014038-G-T

123411147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35013588-C-T

123411927-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35012888-C-G

123411927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35012888-C-T

123411980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35012836-G-T

123412177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, undefined
orthologous variants: 35012644-G-A

123412874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35011916-C-T

123412978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35011798-A-G

123413021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35011764-C-T

123413151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35011644-A-G

123413294-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35011535-A-T

123413751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35011237-C-T

123413831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35011171-A-G

http://identifiers.org/hco/3/GRCh38#123413969-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35011016-A-C

123414068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35010912-C-T

123414479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35010620-A-G

123414997-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35010424-A-T

http://identifiers.org/hco/3/GRCh38#123415109-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35010314-A-C

123415306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35010116-G-A

123415306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35010116-G-T

123415597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35009818-T-C

123415648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35009767-G-A

123415648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35009767-G-T

123415756-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35009684-G-C

123415785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35009652-A-G

123415988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35009439-G-A

123416034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35009394-A-G

http://identifiers.org/hco/3/GRCh38#123416055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35009375-C-A

123416055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35009375-C-T

123416061-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35009369-G-C

123416061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35009369-G-T

http://identifiers.org/hco/3/GRCh38#123416074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35009356-C-A

123416074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35009356-C-T

123416144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35009325-A-G

http://identifiers.org/hco/3/GRCh38#123416177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35009304-C-A

123416177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 35009304-C-T

123416192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, missense_variant
orthologous variants: 35009288-G-A

123416192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, missense_variant
orthologous variants: 35009288-G-T

123416194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, missense_variant
orthologous variants: 35009286-G-A

123416258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, stop_gained
orthologous variants: 35009252-G-A

123416314-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35009199-C-G

123416314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35009199-C-T

123416873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35006383-C-T

http://identifiers.org/hco/3/GRCh38#123416997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35006281-C-A

123417017-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35006260-A-T

123417170-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35006035-C-G

123417248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35005982-T-C

123417510-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35005701-C-G

123417523-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35005688-G-C

123417673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35005537-G-A

123417743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35005486-C-T

123417924-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35005312-A-T

123418162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35005089-T-C

123418183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35005067-C-T

http://identifiers.org/hco/3/GRCh38#123418240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35005011-C-A

123418888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35004819-G-A

123418906-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35004805-C-G

123418906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35004805-C-T

123418916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35004795-A-G

http://identifiers.org/hco/3/GRCh38#123418942-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35004766-C-A

123418942-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35004766-C-G

123418942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35004766-C-T

123419133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35004536-C-T

123419234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35004463-T-C

123419255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35004442-G-A

123419255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35004442-G-T

http://identifiers.org/hco/3/GRCh38#123419286-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35004409-C-A

123419305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35004390-G-T

http://identifiers.org/hco/3/GRCh38#123419323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35004372-C-A

123419323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35004372-C-T

http://identifiers.org/hco/3/GRCh38#123419421-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35004281-A-C

123419440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35004270-C-T

123419783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35003980-T-C

123419853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35003933-C-T

http://identifiers.org/hco/3/GRCh38#123420029-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35003789-A-C

123420029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35003789-A-G

123420029-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35003789-A-T

123420061-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35003758-C-G

123420090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35003727-G-A

123420090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35003727-G-T

123420146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35003671-T-C

123420232-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35003582-G-C

123420366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35003483-T-C

123420373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35003476-G-A

123420373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35003476-G-T

123420404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35003446-G-A

123420542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35003312-A-G

123420542-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35003312-A-T

http://identifiers.org/hco/3/GRCh38#123420722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35003264-C-A

http://identifiers.org/hco/3/GRCh38#123420891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35003144-C-A

123420893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35003142-T-C

123420992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35003080-T-C

123421016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35003056-G-A

123421109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35002961-T-C

123421364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35002697-A-G

http://identifiers.org/hco/3/GRCh38#123421448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35002611-C-A

123421478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35002577-A-G

123421821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35002318-T-C

123421826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35002313-G-A

123421843-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35002299-G-C

123421991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35002135-T-C

http://identifiers.org/hco/3/GRCh38#123422572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35001586-C-A

123422660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35001522-C-T

123422946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35001242-G-A

123422959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35001229-T-C

123423222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35001050-G-A

http://identifiers.org/hco/3/GRCh38#123423319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35000968-C-A

123423319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35000968-C-T

123423350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35000933-G-A

123423395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35000916-C-T

123423659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35000672-C-T

123423663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35000668-A-G

123423811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35000497-G-A

123423842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35000464-G-T

123423886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35000403-G-A

http://identifiers.org/hco/3/GRCh38#123424153-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#35000178-A-C

123424153-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 35000178-A-T

123424597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34999975-G-A

123424626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34999947-C-T

123424782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron_variant, missense_variant
orthologous variants: 34999834-G-A

123424897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 34999724-C-T

123424957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 34999664-G-A

123425106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 34999521-G-A

123425106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 34999521-G-T

http://identifiers.org/hco/3/GRCh38#123425217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#34999411-C-A

http://identifiers.org/hco/3/GRCh38#123425603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#34998466-C-A

http://identifiers.org/hco/3/GRCh38#123425637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#34998496-C-A

123425637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 34998496-C-T

123426825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34998113-C-T

123427254-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34997378-C-G

123427254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34997378-C-T

http://identifiers.org/hco/3/GRCh38#123427262-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#34997366-A-C

123427326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34997305-C-T

123427658-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34996912-G-C

123427664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34996906-G-A

123427735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34996846-T-C

123427822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34996778-T-C

http://identifiers.org/hco/3/GRCh38#123428107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#34996527-C-A

123428344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34996328-T-C

123428399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34996276-T-C

123428454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34996220-T-C

123428513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34996160-G-A

123428513-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34996160-G-C

123428635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34995951-G-T

123429467-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34994368-T-A

http://identifiers.org/hco/3/GRCh38#123429470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#34994365-C-A

http://identifiers.org/hco/3/GRCh38#123429529-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#34994280-A-C

123429708-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34993874-A-T

123429749-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34993833-C-G

123429749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34993833-C-T

123430019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34993636-C-T

123430151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34993545-T-C

123430256-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34993275-T-G

123430288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34993209-G-A

123430288-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34993209-G-C

123430739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34992574-T-C

123430954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34992412-G-A

123430954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34992412-G-T

http://identifiers.org/hco/3/GRCh38#123430991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#34992380-C-A

123431041-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34992333-T-A

123431041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34992333-T-C

123431190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34992182-A-G

123431544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34992014-T-C

123431544-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34992014-T-G

123431680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34991906-T-C

123431774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34991810-T-C

123432077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34991421-C-T

http://identifiers.org/hco/3/GRCh38#123432082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#34991416-C-A

123432152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34991347-A-G

123432213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34991286-C-T

123433239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34990118-C-T

123433490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34989878-G-A

123433506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34989860-G-A

123433614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34989592-G-A

123433707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34989434-A-G

123433898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34989260-G-A

123434163-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34989017-T-A

123434272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34988908-C-T

123434326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34988863-T-C

123434326-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34988863-T-G

http://identifiers.org/hco/3/GRCh38#123434634-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#34988655-A-C

123434656-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34988633-C-G

123434656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34988633-C-T

http://identifiers.org/hco/3/GRCh38#123434847-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#34988473-A-C

123434894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34988223-G-A

123436993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34987399-C-T

123437006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34987386-T-C

123437018-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34987374-T-A

123437124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34987280-A-G

123437160-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34987242-T-A

123437400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34987079-G-T

123437717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34986659-G-T

http://identifiers.org/hco/3/GRCh38#123438253-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#34986162-A-C

123438282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34986133-T-C

http://identifiers.org/hco/3/GRCh38#123438323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#34986092-C-A

123439765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34985628-G-A

123439782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34985612-A-G

123439945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34985495-C-T

123440305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34985142-G-T

123440402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34985062-C-T

123440759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34984796-C-T

123440954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34984596-C-T

123440969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34984582-A-G

123440978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34984573-C-T

123441274-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34983512-C-G

123441622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34983216-C-T

123441895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34982982-G-A

123441961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34982921-G-T

123441971-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34982911-T-A

123442539-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34982124-T-G

123442631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34982052-G-A

123442631-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34982052-G-C

123443132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34981548-G-A

123443198-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34981484-G-C

123443278-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34981388-G-C

123443485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34981201-T-C

123443752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34980938-G-A

123443813-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34980869-A-T

123444322-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34980362-C-G

123445031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34979692-G-A

123445244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34979472-A-G

123445253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34979463-G-A

123445791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34978998-G-A

123446178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34978687-A-G

123446648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34978299-T-C

123446803-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34978160-A-T

123447128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34977864-C-T

123447252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34977741-A-G

123447358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34977653-A-G

123447358-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34977653-A-T

123447391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34977624-G-A

123447391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34977624-G-T

123447403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34977612-G-A

123447403-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34977612-G-C

123447403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: intron variant
orthologous variants: 34977612-G-T

123448010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: missense variant
orthologous variants: 34977011-T-C

123448097-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: missense variant
orthologous variants: 34976918-T-A

123448097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: missense variant
orthologous variants: 34976918-T-C

123448097-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: missense variant
orthologous variants: 34976918-T-G

123448256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: missense_variant, undefined
orthologous variants: 34976759-A-G

123448256-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: missense_variant, undefined
orthologous variants: 34976759-A-T

123448397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: missense_variant, undefined
orthologous variants: 34976615-G-A

123448397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: missense_variant, undefined
orthologous variants: 34976615-G-T

123448409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: missense_variant, undefined
orthologous variants: 34976603-G-A

123448409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: missense_variant, undefined
orthologous variants: 34976603-G-T

123448484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: missense variant
orthologous variants: 34976528-G-A

123448484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: missense variant
orthologous variants: 34976528-G-T

http://identifiers.org/hco/3/GRCh38#123448962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#34976035-C-A

123448962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 5 prime UTR variant
orthologous variants: 34976035-C-T

123449015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 5 prime UTR variant
orthologous variants: 34975982-G-A

http://identifiers.org/hco/3/GRCh38#123449016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#34975981-C-A

123449016-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 5 prime UTR variant
orthologous variants: 34975981-C-G

123449016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 5 prime UTR variant
orthologous variants: 34975981-C-T

123449044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 5 prime UTR variant
orthologous variants: 34975953-A-G

123449044-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 236
most severe consequence: 5 prime UTR variant
orthologous variants: 34975953-A-T