http://identifiers.org/hco/8/GRCh38#119873720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54975765-C-A

119873770-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54975815-T-A

119873772-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54975817-T-G

119873815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54975862-G-A

119873815-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54975862-G-C

119873815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54975862-G-T

119873845-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54975892-C-G

119873845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54975892-C-T

119873866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54975913-C-T

119873911-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54975958-C-G

119873911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54975958-C-T

119874032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54976071-C-T

119874099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54976138-G-A

119874102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54976141-G-A

119874117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54976161-G-A

119874117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54976161-G-T

119874148-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54976184-T-A

119874148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54976184-T-C

119874148-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54976184-T-G

http://identifiers.org/hco/8/GRCh38#119874190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54976226-C-A

119874190-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54976226-C-G

119874191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54976227-G-A

119874191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54976227-G-T

119874242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54976278-G-A

119874242-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54976278-G-C

119874242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54976278-G-T

http://identifiers.org/hco/8/GRCh38#119874285-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54976308-A-C

119874285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 54976308-A-G

119874285-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 54976308-A-T

http://identifiers.org/hco/8/GRCh38#119874303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54976323-C-A

119874303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54976323-C-T

http://identifiers.org/hco/8/GRCh38#119874324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54976344-C-A

119874324-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54976344-C-G

119874324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54976344-C-T

119874380-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54976386-C-G

http://identifiers.org/hco/8/GRCh38#119874385-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54976391-A-C

119874385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54976391-A-G

119874406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54976413-G-A

119874406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54976413-G-T

119874490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 54976498-A-G

119874496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 54976506-G-A

119874496-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 54976506-G-C

119874496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 54976506-G-T

119874672-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, undefined
orthologous variants: 54976659-C-G

119874672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, undefined
orthologous variants: 54976659-C-T

119874978-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 54976968-T-A

119874978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 54976968-T-C

119874989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 54976977-C-T

119876042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 54977294-G-A

119876262-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 54977461-G-C

119876923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 54977825-T-C

119877002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 54977906-G-T

119877017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 54977921-C-T

119878629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 54979261-T-C

119889925-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 54981455-G-C

http://identifiers.org/hco/8/GRCh38#119891939-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54983865-A-C

119892716-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, undefined
orthologous variants: 54984319-T-A

http://identifiers.org/hco/8/GRCh38#119893070-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54984586-A-C

http://identifiers.org/hco/8/GRCh38#119893258-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54984686-A-C

119893921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 54985265-C-T

119893938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 54985285-A-G

119893945-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 54985295-T-A

119894009-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 54985362-T-A

119894020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 54985372-T-C

119894080-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 54985432-G-C

119894080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 54985432-G-T

119900687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 54985808-A-G

119900687-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 54985808-A-T

119900715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 54985846-G-A

119901210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 54986295-T-C

119902075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 54986713-C-T

http://identifiers.org/hco/8/GRCh38#119906983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#54989120-C-A

119907141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 54989272-T-C

119907141-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 54989272-T-G

119908821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 54991764-G-A

119909246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 54992214-G-A

119909422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 54992387-A-G

119909551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 54992539-G-A

119912197-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 54994971-T-A

119912509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 54995583-G-A

119912511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 54995585-G-A

119915820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 54997500-T-C

119919314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55002138-A-G

119919326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55002150-C-T

119919534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55002457-G-A

119919933-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, undefined
orthologous variants: 55002859-G-C

119920031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, undefined
orthologous variants: 55002957-C-T

119920320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55003226-T-C

119920416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55003316-T-C

119920672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55003511-C-T

119920685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, undefined
orthologous variants: 55003524-G-A

119920715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, undefined
orthologous variants: 55003554-G-A

119920858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55003801-C-T

119921008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55003961-G-T

119921428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55005188-A-G

http://identifiers.org/hco/8/GRCh38#119921747-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#55005583-A-C

119921747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55005583-A-G

119921747-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55005583-A-T

119921749-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55005585-T-G

119921756-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55005592-T-G

119921885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55005712-C-T

119922203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55006040-C-T

119922233-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55006085-G-C

119922432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55006288-C-T

119922664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55006512-T-C

119926143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55009211-T-C

119926411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55009421-C-T

119926480-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55009488-T-A

119926534-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55009537-A-T

119926552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55009554-G-A

119926628-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55009634-A-T

119926642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55009648-T-C

119926746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55009946-G-T

119926825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55010018-A-G

119927149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55010816-G-A

119927340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55011002-C-T

119927344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55011006-G-A

http://identifiers.org/hco/8/GRCh38#119927388-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#55011054-A-C

119927393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55011059-C-T

119927450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55011120-G-A

119928505-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, missense_variant
orthologous variants: 55012842-C-G

119928505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 55012842-C-T

119928556-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 55012893-A-T

119928624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55012962-C-T

http://identifiers.org/hco/8/GRCh38#119928706-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#55013233-A-C

119928706-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55013233-A-T

119928725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55013246-G-A

119928725-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55013246-G-C

119928725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55013246-G-T

119928736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55013257-G-T

119929270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55014751-G-A

119929326-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55014806-C-G

119929399-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55014844-C-G

119929418-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55014864-C-G

119929483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55014904-G-T

119929492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55014913-G-A

119929563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55014985-T-C

119929563-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55014985-T-G

119929607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55015026-G-A

119929673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55015074-G-A

119929673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55015074-G-T

119929681-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55015082-T-A

119929681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55015082-T-C

http://identifiers.org/hco/8/GRCh38#119929682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#55015083-C-A

119929715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55015115-G-T

119929720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55015120-T-C

http://identifiers.org/hco/8/GRCh38#119929749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#55015139-C-A

119929749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55015139-C-T

119929750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55015140-G-A

119929750-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55015140-G-C

119929750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55015140-G-T

119929788-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55015157-T-G

119929803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55015172-A-G

119929886-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, missense_variant
orthologous variants: 55015255-C-G

119929896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, missense_variant
orthologous variants: 55015265-A-G

119929896-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, missense_variant
orthologous variants: 55015265-A-T

http://identifiers.org/hco/8/GRCh38#119930022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#55015595-C-A

119930022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55015595-C-T

119930034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55015606-A-G

119930034-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55015606-A-T

119930046-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55015618-T-G

119930066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55015638-T-C

119930072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55015644-A-G

http://identifiers.org/hco/8/GRCh38#119935955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#55018707-C-A

119935976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55018728-T-C

119936138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55018875-C-T

119936156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55018890-T-C

119936551-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55019263-A-T

119942138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55026303-T-C

119945099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55027629-G-A

119945251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55027764-A-G

119945315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55027823-G-A

119945403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55027910-A-G

119945522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55028099-A-G

119945576-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55028293-C-G

119945657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55028706-C-T

119945794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55028841-T-C

119945817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55028860-G-A

119945936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55028962-G-T

119945992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55029005-C-T

119947193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55030810-C-T

http://identifiers.org/hco/8/GRCh38#119947489-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#55031055-A-C

119947600-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55031169-T-A

119947600-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55031169-T-G

119947672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55031235-G-A

119947718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55031266-C-T

119951263-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55033814-C-G

119951511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55034051-T-C

119951892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55035416-C-T

119951962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55035480-C-T

http://identifiers.org/hco/8/GRCh38#119952022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#55035550-C-A

119952332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55035869-T-C

119952343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55035880-T-C

119952918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55036490-G-T

119955845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55040610-A-G

119955965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55040722-G-A

119955969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55040725-A-G

119955996-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55040752-T-A

119956017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55040773-A-G

119956069-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55040826-G-C

119956228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55041205-C-T

119956270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55041247-G-A

119956369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55041346-G-A

119956441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55041409-G-A

119956652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55041617-A-G

119957307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55042161-C-T

119964734-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55044044-T-G

119965099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55044114-T-C

119965099-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55044114-T-G

119965102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55044117-G-A

119965102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55044117-G-T

119965111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55044126-T-C

119965122-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55044137-T-G

119965125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55044140-G-A

119965125-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55044140-G-C

119965125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55044140-G-T

119965145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55044160-G-A

119965145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55044160-G-T

119965182-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55044204-G-C

119965193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55044215-G-A

119965193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55044215-G-T

119965229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 55044258-C-T

http://identifiers.org/hco/8/GRCh38#119965252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#55044281-C-A

119965281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: missense variant
orthologous variants: 55044310-G-A

119965281-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: missense variant
orthologous variants: 55044310-G-T

119965293-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: missense variant
orthologous variants: 55044322-C-G

119965293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: missense variant
orthologous variants: 55044322-C-T

119965439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55044468-G-A

119965503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55044529-A-G

http://identifiers.org/hco/8/GRCh38#119965521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#55044545-C-A

119965544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55044567-T-C

119965551-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55044574-T-A

119967669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55047987-G-A

119967906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55048256-G-A

119968005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55048354-G-T

http://identifiers.org/hco/8/GRCh38#119968014-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#55048363-A-C

119969118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55049945-C-T

119969152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron variant
orthologous variants: 55049979-T-C

119969917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55050438-G-A

119969917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55050438-G-T

119969984-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55050505-T-G

119970157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55050670-G-A

119973607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55052739-C-T

119973693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55052824-C-T

119973708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55052842-G-A

119973708-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55052842-G-C

119973965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55053066-G-A

119973994-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55053088-T-A

119978080-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55056999-A-T

119990374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55059592-G-A

119990467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55059677-C-T

119990603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55059759-C-T

119990607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55059763-A-G

119991013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55060159-G-A

119993210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55062348-C-T

119995764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55065314-A-G

119995938-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55065469-A-T

http://identifiers.org/hco/8/GRCh38#119996022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#55065854-C-A

119996055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55065898-G-A

119996055-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55065898-G-C

http://identifiers.org/hco/8/GRCh38#119996067-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#55065907-A-C

119996067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55065907-A-G

119996749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55066737-G-A

119996982-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55066925-C-G

119997005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55066948-G-A

119997005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55066948-G-T

119997059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55067003-G-A

119997374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55067180-A-G

119997388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55067194-C-T

http://identifiers.org/hco/8/GRCh38#120001058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#55071709-C-A

120001073-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55071721-T-A

120001283-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55071904-C-G

120001378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55071983-G-A

120001378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55071983-G-T

http://identifiers.org/hco/8/GRCh38#120001379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#55071984-C-A

120001379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55071984-C-T

120001449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55072056-G-T

http://identifiers.org/hco/8/GRCh38#120001450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#55072057-C-A

120001450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55072057-C-T

http://identifiers.org/hco/8/GRCh38#120001465-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#55072072-A-C

120001465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55072072-A-G

http://identifiers.org/hco/8/GRCh38#120001477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#55072084-C-A

120001477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55072084-C-T

120001501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55072108-G-A

120001501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55072108-G-T

120001595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55072197-A-G

120001628-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55072230-C-G

120001770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55072366-C-T

120001771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55072367-A-G

120002917-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55075532-G-C

120002919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55075534-G-A

120002919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55075534-G-T

http://identifiers.org/hco/8/GRCh38#120002930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#55075544-C-A

120002930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55075544-C-T

http://identifiers.org/hco/8/GRCh38#120002931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#55075545-C-A

120002931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55075545-C-T

120002932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55075546-G-A

120002932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55075546-G-T

120002933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55075547-A-G

120002973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 55075584-A-G

120003002-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55075613-C-G

120003002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55075613-C-T

120003014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55075625-G-A

120003169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55075795-G-T

120003206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55075818-G-A

120003206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55075818-G-T

120003222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55075830-G-A

120003237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55075844-G-A

120003237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55075844-G-T

120003248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55075855-T-C

120003248-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55075855-T-G

120003256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55075863-A-G

120003593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55076162-G-A

120003605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55076221-C-T

120003654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55076315-A-G

120005102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55076906-G-A

120005154-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55076943-G-C

120005219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55077001-C-T

120005345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55077114-T-C

http://identifiers.org/hco/8/GRCh38#120005402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#55077170-C-A

120005936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55077662-A-G

120005956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55077682-G-T

120006244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55077938-T-C

http://identifiers.org/hco/8/GRCh38#120006263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#55077953-C-A

120006263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55077953-C-T

120006283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55077970-G-A

120006610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55078706-G-A

120006610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55078706-G-T

120006652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55078741-G-A

120006652-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55078741-G-C

http://identifiers.org/hco/8/GRCh38#120006656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#55078745-C-A

120006672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55078759-T-C

http://identifiers.org/hco/8/GRCh38#120006705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#55078791-C-A

120006705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55078791-C-T

120006711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55078797-G-T

http://identifiers.org/hco/8/GRCh38#120006777-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#55078856-A-C

120006777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55078856-A-G

120006796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55078875-G-A

120006845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55078924-C-T

120007007-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55079199-T-G

120007077-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55079269-C-G

120007108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55079303-T-C

120007379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55079613-G-A

120007381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55079615-A-G

120007382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55079616-G-A

120007399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55079622-A-G

120007446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55079675-G-A

120007446-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55079675-G-T

120008180-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55081098-C-G

http://identifiers.org/hco/8/GRCh38#120008555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#55081151-C-A

120008606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55081182-G-A

120008640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55081214-G-A

120008640-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55081214-G-C

120008655-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55081229-T-A

120008741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55081317-A-G

120008742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55081318-T-C

120008785-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55081361-C-G

120008785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55081361-C-T

120008830-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55081402-T-A

http://identifiers.org/hco/8/GRCh38#120008945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#55081484-C-A

120008955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55081494-T-C

120008984-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55081521-G-C

120008989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55081526-A-G

120008990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55081527-G-A

120008992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55081529-C-T

120009062-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55081598-G-C

120009124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55081660-A-G

http://identifiers.org/hco/8/GRCh38#120009153-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#55081697-A-C

120009153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55081697-A-G

120009153-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55081697-A-T

http://identifiers.org/hco/8/GRCh38#120009156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#55081700-C-A

120009156-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55081700-C-G

120009163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55081707-A-G

120009176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55081720-G-A

120009360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55081852-T-C

120011521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55083004-A-G

120011859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55083258-A-G

120012025-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55083405-A-T

120012115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55083499-T-C

120013296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55084157-A-G

120016934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55086308-T-C

120016958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55086332-C-T

http://identifiers.org/hco/8/GRCh38#120017104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#55086464-C-A

120017455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55086938-C-T

120017608-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55087374-G-C

http://identifiers.org/hco/8/GRCh38#120017817-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#55087637-A-C

120017895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55087715-G-T

120018969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55088082-A-G

120018969-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55088082-A-T

120024781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55089964-G-A

120024987-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55090110-T-A

120025040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55090165-T-C

120025092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55090216-A-G

120025121-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55090245-T-A

120025129-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55090334-C-G

120025129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55090334-C-T

120025137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55090363-G-A

http://identifiers.org/hco/8/GRCh38#120025149-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#55090375-A-C

120025256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55090502-G-A

120027468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55094408-G-A

120027512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55094441-C-T

120027592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55094472-C-T

120027642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55094519-T-C

120027929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55094775-G-A

120028057-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55094882-G-C

120029259-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55095430-C-G

120029259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55095430-C-T

120030181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55096034-T-C

120030182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55096035-C-T

120033522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55099998-C-T

120033696-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55100172-T-A

120033848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55100324-C-T

120033879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55100397-A-G

120037517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55105582-G-A

120037565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55105633-A-G

120037573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55105641-G-A

120037574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55105642-T-C

120040541-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55106781-T-A

120041185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55108286-T-C

120041240-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55108358-C-G

120041240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55108358-C-T

http://identifiers.org/hco/8/GRCh38#120041289-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#55108420-A-C

120041289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55108420-A-G

120041309-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55108440-G-C

120041333-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55108464-T-G

120041432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55108554-G-A

120041613-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55108695-C-G

120042093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55109333-G-A

120042226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55109450-G-A

120042228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55109452-G-A

http://identifiers.org/hco/8/GRCh38#120042342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#55109568-C-A

120043446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55111842-A-G

120048241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55112644-G-A

120048493-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55112915-C-G

120048515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55112936-C-T

120048565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55112980-T-C

120048671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55113094-T-C

120048676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55113099-C-T

120048957-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55113604-A-T

120049088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55113743-A-G

120049689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: synonymous variant
orthologous variants: 55115516-G-A

120049774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: 3 prime UTR variant
orthologous variants: 55115584-A-G

120049826-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: 3 prime UTR variant
orthologous variants: 55115638-A-T

http://identifiers.org/hco/8/GRCh38#120049947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#55115900-C-A

120049968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: 3 prime UTR variant
orthologous variants: 55115921-A-G

120049997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: 3 prime UTR variant
orthologous variants: 55115946-T-C

120049997-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: 3 prime UTR variant
orthologous variants: 55115946-T-G

http://identifiers.org/hco/8/GRCh38#120050001-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#55115950-A-C

120050184-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: 3 prime UTR variant
orthologous variants: 55116283-A-T

120050185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: 3 prime UTR variant
orthologous variants: 55116284-C-T

120050209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: 3 prime UTR variant
orthologous variants: 55116308-G-T

120050291-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: 3 prime UTR variant
orthologous variants: 55116488-C-G

120050366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: 3 prime UTR variant
orthologous variants: 55116569-A-G

http://identifiers.org/hco/8/GRCh38#120050431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#55116636-C-A

120050465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: 3 prime UTR variant
orthologous variants: 55116670-G-A

120050465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 22953
most severe consequence: 3 prime UTR variant
orthologous variants: 55116670-G-T