http://identifiers.org/hco/2/GRCh38#87454940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128271665-C-A

87455250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 128271419-G-A

87455250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 128271419-G-T

87455446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 128271232-G-A

87455694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 128270979-G-T

87455907-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128270779-G-C

87456184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128270512-T-C

87456284-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128270420-G-C

87456529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128270258-C-T

http://identifiers.org/hco/2/GRCh38#87456804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128270011-C-A

87456804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128270011-C-T

87456988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128269851-C-T

http://identifiers.org/hco/2/GRCh38#87457045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128269806-C-A

87457136-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128269724-T-A

87457339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128269545-T-C

87457356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128269529-G-A

87457681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128269223-G-A

http://identifiers.org/hco/2/GRCh38#87457736-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#128269189-C-A

87457736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128269189-C-T

http://identifiers.org/hco/2/GRCh38#87457772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128269170-C-A

87457772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128269170-C-T

87457800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128269142-A-G

87457859-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128269086-T-A

http://identifiers.org/hco/2/GRCh38#87457916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128269015-C-A

87457920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128269011-G-T

87457939-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128268994-T-A

87458398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128268436-T-C

87458441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128268390-G-A

http://identifiers.org/hco/2/GRCh38#87458459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128268370-C-A

87458459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128268370-C-T

87458460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128268369-G-A

http://identifiers.org/hco/2/GRCh38#87458753-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128268000-C-A

87458753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128268000-C-T

87458755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128267998-G-A

87458807-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128267943-C-G

87458807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128267943-C-T

87458927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 128267771-G-A

87458927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 128267771-G-T

87458933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 128267765-C-T

87458997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128267701-C-T

87459067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 128267631-A-G

87459124-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128267573-A-T

87459246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128267463-A-G

87459959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128266591-T-C

87460045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128266513-G-A

http://identifiers.org/hco/2/GRCh38#87460055-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128266504-A-C

87460073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128266490-A-G

87460116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128266447-G-T

87460140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128266423-T-C

87460202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128266361-G-A

87460202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128266361-G-T

87460252-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128266312-C-G

87460383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128266190-C-T

87460558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128266033-G-T

87460613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128266009-C-T

87461161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128265358-C-T

87461699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128264643-A-G

87461850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128264457-A-G

87461851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128264456-T-C

87461852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128264455-G-A

87462671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128263293-T-C

87462744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128263235-A-G

87462766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128263221-T-C

87462818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128263172-C-T

87462824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128263166-C-T

87463185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128262889-G-A

87463452-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128262673-A-T

87466851-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 128260227-A-T

87466868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 128260209-C-T

87466895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 128260182-T-C

87466906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 128260171-G-A

87466934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 128260146-G-T

87467030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 128260081-C-T

87467091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 128260016-T-C

87467096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 128260011-A-G

87467157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 128259951-G-A

http://identifiers.org/hco/2/GRCh38#87467168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#128259940-C-A

87467168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 128259940-C-T

87467755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128259299-A-G

87467757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128259297-C-T

87467849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128259204-G-T

87467905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128259105-T-C

87469664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128258269-C-T

87469886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128258085-G-A

87469950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128257918-A-G

87469950-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128257918-A-T

87470047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128257748-C-T

87470174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128257629-G-A

http://identifiers.org/hco/2/GRCh38#87470232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128257568-C-A

87470245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128257555-G-A

http://identifiers.org/hco/2/GRCh38#87470287-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128257511-A-C

87470287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128257511-A-G

87470400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128257262-C-T

87470627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128257096-T-C

87470643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128257080-T-C

87471188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128256520-G-A

87471311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128256439-G-A

http://identifiers.org/hco/2/GRCh38#87471426-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128256331-A-C

87471440-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128256325-T-A

87472956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128256144-G-T

http://identifiers.org/hco/2/GRCh38#87473009-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128256075-A-C

87473052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128256039-A-G

87473117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128255967-A-G

87473412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128255736-G-T

87473766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128255229-G-A

87474044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128255008-G-A

87474169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128254909-G-T

87474449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128254644-C-T

87474707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128254474-T-C

87475015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128254190-A-G

87475704-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128252834-T-A

87475783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128252756-G-T

http://identifiers.org/hco/2/GRCh38#87475900-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128252641-A-C

87476004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128252539-A-G

87476317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128252034-G-A

87476485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128251511-C-T

http://identifiers.org/hco/2/GRCh38#87476794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128251070-C-A

87477487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128250707-C-T

87477496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128250698-T-C

87477546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128250648-T-C

87477666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128250217-A-G

87477769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128250134-G-A

87477769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128250134-G-T

http://identifiers.org/hco/2/GRCh38#87477787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128250116-C-A

87477787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128250116-C-T

http://identifiers.org/hco/2/GRCh38#87477818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128250084-C-A

87477818-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128250084-C-G

87482297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128247858-C-T

87482343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128247804-G-A

87482343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128247804-G-T

87482483-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128247728-A-T

87482545-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128247666-A-T

87482743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128247463-G-T

87484992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128246262-A-G

87485102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128246193-T-C

87485519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128245837-C-T

87485592-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128245772-A-T

87485649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128245725-G-T

87486155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128245234-C-T

87486203-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128245187-T-G

87486246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128245144-C-T

87486280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128245102-G-A

87486286-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128245096-T-A

87486320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128245059-C-T

87486787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128244921-G-A

87486947-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128244798-C-G

http://identifiers.org/hco/2/GRCh38#87487095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128244652-C-A

http://identifiers.org/hco/2/GRCh38#87487196-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128244551-A-C

87487223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128244520-C-T

87487300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128244430-A-G

http://identifiers.org/hco/2/GRCh38#87487479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128244248-C-A

http://identifiers.org/hco/2/GRCh38#87487506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128244222-C-A

87487506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128244222-C-T

87487542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128244185-C-T

87487627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128244117-C-T

87487707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128243924-T-C

87488028-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128243619-A-T

87488060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128243605-T-C

87488106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128243551-T-C

http://identifiers.org/hco/2/GRCh38#87488142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128243515-C-A

87488142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128243515-C-T

87489073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128243249-T-C

87489088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128243235-G-A

87489144-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128243188-A-T

http://identifiers.org/hco/2/GRCh38#87489576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128242793-C-A

87489650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128242717-C-T

87490529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128241975-T-C

87490584-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128241937-G-C

87490663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128241859-G-A

87490746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128241776-A-G

87491269-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128241321-A-T

87491417-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128241179-G-C

87491534-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128241055-T-A

87491581-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128241010-C-G

http://identifiers.org/hco/2/GRCh38#87491703-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128240902-A-C

87491703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128240902-A-G

87491726-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128240879-A-T

87495670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128239156-G-A

87495670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128239156-G-T

87495672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128239154-G-A

87495720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128239116-C-T

http://identifiers.org/hco/2/GRCh38#87495903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128238952-C-A

http://identifiers.org/hco/2/GRCh38#87495970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128238320-C-A

87495994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128238300-C-T

87496211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128238095-C-T

87496328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128237992-C-T

87496397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128237925-T-C

http://identifiers.org/hco/2/GRCh38#87496581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128237730-C-A

87496581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128237730-C-T

87496701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128237610-T-C

87496856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128237480-T-C

87496875-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128237454-C-G

87497305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128237147-C-T

87497440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128237048-T-C

87498296-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128236076-C-G

87498612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128235727-G-A

87498612-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128235727-G-C

87498612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128235727-G-T

87498744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128235601-A-G

87499212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128235267-T-C

87499241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128235238-A-G

http://identifiers.org/hco/2/GRCh38#87499268-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128235205-A-C

87499268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128235205-A-G

87499303-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128235170-A-T

87499421-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128235044-G-C

87499452-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128235009-G-C

87499756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128234798-T-C

http://identifiers.org/hco/2/GRCh38#87499852-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128234707-A-C

87499852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128234707-A-G

87499932-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128234642-C-G

87499934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128234640-C-T

87499966-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128234605-T-G

87500011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128234552-T-C

87500039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128234526-C-T

87500268-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128234270-T-G

87500305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128234226-C-T

87500523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128234034-G-T

http://identifiers.org/hco/2/GRCh38#87500580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128233972-C-A

87500580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128233972-C-T

87500586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128233966-G-A

87500586-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128233966-G-C

87500586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128233966-G-T

87500672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128233887-A-G

http://identifiers.org/hco/2/GRCh38#87500703-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128233855-A-C

http://identifiers.org/hco/2/GRCh38#87500823-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128233739-A-C

87500848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128233714-A-G

87501161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128233271-C-T

87501235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128233202-G-A

87501256-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128233181-T-G

87501366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128233080-G-T

87501532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128232493-T-C

87501559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128232467-T-C

87501587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128232437-A-G

87501591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128232433-T-C

87501639-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128232385-A-T

87501734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128232286-G-T

http://identifiers.org/hco/2/GRCh38#87501829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128232192-C-A

87502041-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128231978-A-T

http://identifiers.org/hco/2/GRCh38#87502251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128231770-C-A

87503211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128230861-T-C

87503248-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128230825-G-C

87503658-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128230744-T-A

87503719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128230699-G-A

87503808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128230610-T-C

87504012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128230477-G-T

http://identifiers.org/hco/2/GRCh38#87504540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128230128-C-A

87504540-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128230128-C-G

87504540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128230128-C-T

87504850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128229298-G-A

87504855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128229293-G-A

http://identifiers.org/hco/2/GRCh38#87505336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128228403-C-A

87505414-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128228329-A-T

87505623-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128228172-A-T

87505774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128227987-A-G

87506120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128227638-C-T

87506341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128227403-G-T

87506885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128227205-A-G

87506959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128227143-C-T

87507154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128226959-C-T

87507176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128226954-A-G

87507291-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128226843-T-G

87507840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128226313-T-C

87508203-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128225994-G-C

87508224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128225973-A-G

87508232-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128225966-T-G

87508274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128225927-G-A

87508274-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128225927-G-C

87508306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128225901-A-G

87508356-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128225865-A-T

87508618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128225652-G-A

87508618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128225652-G-T

87508713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128224977-A-G

87508864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128224822-A-G

87508931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128224795-G-A

87508941-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128224785-T-A

87508970-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128224757-C-G

87509069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128224661-G-T

http://identifiers.org/hco/2/GRCh38#87509215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128224521-C-A

87509335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 128224394-G-A

87509538-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128224208-C-G

87509598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128224150-C-T

87510427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128223638-A-G

87510928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128223141-G-A

87510993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128223077-G-A

87510993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128223077-G-T

87511098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128222969-C-T

87511118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128222951-C-T

87511216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128222843-T-C

87511452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128222623-T-C

87511509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128222568-A-G

87511515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128222562-T-C

87511612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128222469-A-G

87512022-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128222117-G-C

87512287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128221850-C-T

87512585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128221567-G-A

http://identifiers.org/hco/2/GRCh38#87512591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128221561-C-A

87513160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128220927-T-C

http://identifiers.org/hco/2/GRCh38#87513426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128220656-C-A

http://identifiers.org/hco/2/GRCh38#87513492-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128220588-A-C

87513508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128220567-G-A

87513508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128220567-G-T

87513935-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128220157-A-T

87513955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128220136-G-T

87514116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128219890-A-G

87514471-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128219563-A-T

http://identifiers.org/hco/2/GRCh38#87514569-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128219477-A-C

87514569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128219477-A-G

87514569-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128219477-A-T

87514581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128219465-A-G

87514831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128219231-C-T

87514842-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128219220-G-C

87515020-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128219072-C-G

87515020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128219072-C-T

87515142-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128218968-T-A

87515142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128218968-T-C

87515308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128218748-A-G

87515308-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128218748-A-T

87515355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128218705-C-T

87515539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128218523-G-A

87515539-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128218523-G-C

http://identifiers.org/hco/2/GRCh38#87515556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128218507-C-A

87515696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128218380-A-G

87515795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128218164-G-T

http://identifiers.org/hco/2/GRCh38#87515812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128218147-C-A

87515812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128218147-C-T

87515813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128218146-C-T

87516110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128217804-G-T

http://identifiers.org/hco/2/GRCh38#87516264-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128217656-A-C

87517452-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128217214-A-T

87517501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128217167-G-A

87517501-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128217167-G-C

87517501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128217167-G-T

87517522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128217141-G-T

http://identifiers.org/hco/2/GRCh38#87517529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128217134-C-A

87517529-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128217134-C-G

87517529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128217134-C-T

http://identifiers.org/hco/2/GRCh38#87517553-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128217114-A-C

http://identifiers.org/hco/2/GRCh38#87517562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128217108-C-A

87517608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128217055-A-G

http://identifiers.org/hco/2/GRCh38#87517700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128216991-C-A

http://identifiers.org/hco/2/GRCh38#87517713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128216976-C-A

87517713-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128216976-C-G

87517723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128216970-G-T

87518510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128216831-G-T

87518554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128216787-A-G

87518555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128216786-G-T

http://identifiers.org/hco/2/GRCh38#87518594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128216747-C-A

87518594-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128216747-C-G

87518605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128216736-A-G

87518771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128216573-A-G

87518776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128216568-G-T

http://identifiers.org/hco/2/GRCh38#87518793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128216551-C-A

87518793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128216551-C-T

http://identifiers.org/hco/2/GRCh38#87518794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128216550-C-A

87518794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128216550-C-T

87518874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128216469-A-G

87518877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128216466-G-T

87519517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128215835-C-T

87520033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128215492-C-T

87520034-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128215491-T-A

87520154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128215388-G-A

87520225-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128215317-T-A

87520297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128215246-G-T

87520316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128215233-C-T

87520363-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128215152-G-C

87520363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128215152-G-T

87520511-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128215002-C-G

87520511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128215002-C-T

87520604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128214899-T-C

87520610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128214893-T-C

87520610-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128214893-T-G

87520648-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128214853-A-T

87520664-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128214828-T-G

87520747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128214749-C-T

87520987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128214552-C-T

87521050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128214502-G-T

87521114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128214438-G-T

http://identifiers.org/hco/2/GRCh38#87521317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128214233-C-A

87521317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128214233-C-T

http://identifiers.org/hco/2/GRCh38#87521359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128214187-C-A

87521359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128214187-C-T

87521371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128214171-G-A

87521371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128214171-G-T

http://identifiers.org/hco/2/GRCh38#87521404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128214137-C-A

http://identifiers.org/hco/2/GRCh38#87521547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128213989-C-A

http://identifiers.org/hco/2/GRCh38#87521642-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128213878-C-A

87521642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128213878-C-T

87521643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128213877-A-G

87521894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128213631-A-G

87522033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128213525-C-T

87522121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128213448-G-A

87522326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128213247-T-C

87522362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128213211-T-C

87522523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128213056-G-A

87522528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128213051-T-C

87522528-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128213051-T-G

87522564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128213026-C-T

87523388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128212338-C-T

http://identifiers.org/hco/2/GRCh38#87523677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128212012-C-A

87523789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128211605-A-G

http://identifiers.org/hco/2/GRCh38#87523816-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128211589-A-C

http://identifiers.org/hco/2/GRCh38#87523824-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128211581-A-C

87523824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128211581-A-G

87524754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128210843-G-T

87526106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128209703-G-A

http://identifiers.org/hco/2/GRCh38#87526437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128209398-C-A

87526515-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128209327-T-A

87526722-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128209151-G-C

http://identifiers.org/hco/2/GRCh38#87526863-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128208994-A-C

87526888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128208984-C-T

87528073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128208423-C-T

87528138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128208352-A-G

87528381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128208161-G-A

87528596-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128207940-C-G

87528901-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128207674-G-C

http://identifiers.org/hco/2/GRCh38#87529199-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128207363-A-C

87529199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128207363-A-G

87531989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128207216-G-A

87534210-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128206278-G-C

87534210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128206278-G-T

87534630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128205887-G-A

87534937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128205635-G-A

87534981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128205602-A-G

87535223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128205359-A-G

87535238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128205345-A-G

87535503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128204644-T-C

87535724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128204452-G-A

87535741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128204423-G-T

http://identifiers.org/hco/2/GRCh38#87538911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128203302-C-A

87539161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128203159-T-C

87539224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128203109-C-T

87539225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128203108-G-A

http://identifiers.org/hco/2/GRCh38#87539268-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128203073-C-A

87539299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128203043-G-A

87539329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128203018-C-T

87539558-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128202902-G-C

87539709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128202754-C-T

87540577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128201931-C-T

87540645-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128201874-T-A

87540673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128201860-G-A

87540985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128201583-T-C

87540991-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128201578-G-C

87540991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128201578-G-T

http://identifiers.org/hco/2/GRCh38#87541124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128201438-C-A

87541124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128201438-C-T

87542995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128200050-A-G

87543144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128199910-G-T

87543146-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128199908-T-G

87543149-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128199904-T-A

87543149-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128199904-T-G

87543151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128199902-A-G

87543151-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128199902-A-T

87543165-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128199888-G-T

87547290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128196449-G-A

http://identifiers.org/hco/2/GRCh38#87547292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128196447-C-A

87547448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128196306-G-T

87547449-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128196305-A-T

87547489-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128196259-A-T

87547546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128196190-C-T

87547600-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128196136-C-G

87547668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128196067-C-T

87547907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128195813-A-G

87550764-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128194714-A-T

87553773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128193599-G-A

http://identifiers.org/hco/2/GRCh38#87553859-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128193492-A-C

87553859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128193492-A-G

87554563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128193132-A-G

87554563-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128193132-A-T

87554768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128192949-G-T

87554897-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128192771-C-G

87555006-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128192674-T-G

87555212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128192461-A-G

87555232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128192422-G-A

87555387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128192290-T-C

87569672-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128187849-T-G

http://identifiers.org/hco/2/GRCh38#87569752-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128187764-A-C

87569752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128187764-A-G

87569958-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128187588-T-G

87570111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128187430-C-T

87570167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128187404-G-A

http://identifiers.org/hco/2/GRCh38#87570176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128187395-C-A

87570176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128187395-C-T

87570313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128187266-C-T

87570693-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128186532-T-A

87570693-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128186532-T-G

87570724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128186502-G-A

87570724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128186502-G-T

87570871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128184926-G-T

87570894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128184900-G-A

87570953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128184849-A-G

87571176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128184671-C-T

87571187-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128184660-G-C

87571198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128184649-C-T

87571213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128184635-A-G

87571234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128184616-G-A

87571475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128184385-A-G

87571854-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128184053-T-G

87572013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128183939-T-C

87572402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128183168-G-A

87572456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128183131-A-G

87572791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128182605-A-G

87572851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128182549-C-T

87572868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128182532-A-G

87573110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128182329-A-G

http://identifiers.org/hco/2/GRCh38#87573113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128182326-C-A

87573158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 128182285-T-C

87573196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128182255-G-A

87573213-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128182238-T-A

87573213-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128182238-T-G

87573232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128182218-G-A

87573232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128182218-G-T

87573428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128182024-G-A

http://identifiers.org/hco/2/GRCh38#87573613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128181835-C-A

87573613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128181835-C-T

87573638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128181810-G-A

87573865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128181568-G-T

http://identifiers.org/hco/2/GRCh38#87573942-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128181464-C-A

http://identifiers.org/hco/2/GRCh38#87574287-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128181084-A-C

87574287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128181084-A-G

87574293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128181078-A-G

87574578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128180779-G-A

87574782-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128180557-C-G

87574950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128180452-G-A

87575211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128180268-G-A

87575654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128179869-G-A

http://identifiers.org/hco/2/GRCh38#87575789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128179783-C-A

87575789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128179783-C-T

http://identifiers.org/hco/2/GRCh38#87575796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128179776-C-A

87575906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128179638-C-T

87576101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128179466-G-A

http://identifiers.org/hco/2/GRCh38#87576669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128178913-C-A

87576669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128178913-C-T

87576821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128178768-C-T

87576909-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128178555-C-G

87577318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128178123-G-T

87577610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128177848-C-T

87577765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128177700-G-A

87578800-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128176640-C-G

87578820-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128176620-A-T

87578888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128176552-C-T

87580350-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128175678-G-C

87580696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128175372-T-C

87580723-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128175345-A-T

87580728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128175340-G-A

http://identifiers.org/hco/2/GRCh38#87580739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128175329-C-A

87580869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128175216-T-C

87580869-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128175216-T-G

87580925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128175072-A-G

87580982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128174945-A-G

87581077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128174871-G-A

87581097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128174851-C-T

87581317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128174633-G-A

87581426-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128174518-T-A

87581426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128174518-T-C

87581522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128174449-C-T

http://identifiers.org/hco/2/GRCh38#87581524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128174447-C-A

87581606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128174361-A-G

87581704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128174207-G-T

87581705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128174206-G-T

87581965-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128173716-T-G

87582610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128173081-T-C

87582652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128173040-C-T

87582920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128172783-G-A

87582980-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128172748-T-G

87583199-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128172594-T-A

87583199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128172594-T-C

87583256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 128172536-A-G

87583291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: non coding transcript exon variant
orthologous variants: 128172501-C-T

87583390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128172400-G-A

87583615-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128172238-T-A

http://identifiers.org/hco/2/GRCh38#87584009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128171859-C-A

87584009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128171859-C-T

87584041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128171827-G-A

87584045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128171823-G-T

87592580-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128167863-G-T

87592614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128167830-G-T

87592713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128167717-A-G

87592714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128167716-T-C

http://identifiers.org/hco/2/GRCh38#87592749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128167681-C-A

87592749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128167681-C-T

87592800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128167652-G-A

http://identifiers.org/hco/2/GRCh38#87593212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128167509-C-A

87593256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128167469-T-C

87593284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128167441-G-A

87593334-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128167391-C-G

87593413-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128167295-A-T

87593463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128167253-A-G

87593563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128167171-A-G

87593673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128167058-A-G

87594018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128166774-T-C

87594030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128166762-T-C

87594094-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128166698-G-C

87594125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128166667-C-T

87594170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128166622-C-T

87594180-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128166612-T-A

87594180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128166612-T-C

http://identifiers.org/hco/2/GRCh38#87594281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128166517-C-A

87594297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128166501-G-T

87594529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128166310-T-C

87594640-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128166232-C-G

87595217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128163807-C-T

87595492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128163511-C-T

87595543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128163473-A-G

87595594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128163423-C-T

87595628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128163383-A-G

87595645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128163363-C-T

87595702-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128163311-G-C

87595756-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128163259-G-C

87595803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128163211-C-T

87595810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128163206-C-T

87598173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128160041-G-T

87598232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128159983-A-G

http://identifiers.org/hco/2/GRCh38#87598847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128159562-C-A

87599001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128159504-A-G

87599033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128159472-T-C

87599063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128159439-C-T

87599266-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128159295-T-G

87599278-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128159283-G-C

87599456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128159144-A-G

87599753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128158888-T-C

87599764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128158877-C-T

87599808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128158820-A-G

87600095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128158702-G-A

87600183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128158605-G-A

87602023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128156183-C-T

87602512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128155751-G-T

87602687-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128155629-T-A

87602687-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128155629-T-G

http://identifiers.org/hco/2/GRCh38#87602826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#128155509-C-A

87602826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128155509-C-T

87603208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128155149-T-C

87603515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128154882-T-C

http://identifiers.org/hco/2/GRCh38#87604174-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128154699-A-C

87604174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128154699-A-G

87604217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128154658-G-A

87604217-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128154658-G-C

87604292-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128154612-C-G

87604524-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128154371-A-T

http://identifiers.org/hco/2/GRCh38#87604674-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128154231-A-C

87604719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128154175-C-T

87604861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128154073-C-T

http://identifiers.org/hco/2/GRCh38#87604877-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128154059-A-C

http://identifiers.org/hco/2/GRCh38#87604931-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128154018-A-C

87605222-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128153672-A-T

87605236-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128153658-T-A

87605236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128153658-T-C

87605436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128153441-T-C

87605506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128153371-T-C

87605835-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128152415-G-C

http://identifiers.org/hco/2/GRCh38#87605969-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128152294-A-C

87606465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128151860-A-G

87606631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128151703-C-T

http://identifiers.org/hco/2/GRCh38#87606715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128151625-C-A

87606715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: non coding transcript exon variant
orthologous variants: 128151625-C-T

87606761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: non coding transcript exon variant
orthologous variants: 128151576-A-G

87606794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128151539-G-A

87607015-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128151324-G-C

87607212-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128151164-T-A

http://identifiers.org/hco/2/GRCh38#87607412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128150990-C-A

87607438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128150964-C-T

87607552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128150850-G-T

87607648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128150807-T-C

87607649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128150806-A-G

87608807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128152328-G-A

87608807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128152328-G-T

87608857-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128152276-C-G

http://identifiers.org/hco/2/GRCh38#87608937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128152196-C-A

87608937-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128152196-C-G

87622157-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128143572-T-G

87622165-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128143564-T-A

87622234-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128143482-G-C

87622380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128143336-G-A

87622384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128143332-G-A

http://identifiers.org/hco/2/GRCh38#87622698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128143056-C-A

87622937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128142817-A-G

87622944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128142809-C-T

87625385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128141451-G-T

87625691-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128141197-T-A

87625717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128141189-C-T

http://identifiers.org/hco/2/GRCh38#87626534-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128140078-C-A

87626535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128140077-T-C

87626627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128139981-C-T

http://identifiers.org/hco/2/GRCh38#87626628-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128139980-A-C

87627133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128139661-T-C

87627253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128139527-G-A

87627253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128139527-G-T

87627406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128139270-C-T

87627529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128139158-T-C

87627709-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128138966-A-T

87627829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128138883-C-T

http://identifiers.org/hco/2/GRCh38#87628801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128138295-C-A

87629258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128137743-G-T

87629418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128137601-T-C

87629529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128137364-A-G

http://identifiers.org/hco/2/GRCh38#87629583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#128137323-C-A

87629583-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 128137323-C-G

87629583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 128137323-C-T

http://identifiers.org/hco/2/GRCh38#87629906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128137008-C-A

87629906-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128137008-C-G

87629906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128137008-C-T

87629912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128137002-T-C

87629996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 128136908-G-A

87632177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128135100-C-T

87632321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128134934-T-C

87634002-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128131494-T-A

87634002-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128131494-T-G

87634011-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128131485-T-A

http://identifiers.org/hco/2/GRCh38#87634128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128131382-C-A

87634223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128131279-G-T

87634341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128131178-A-G

http://identifiers.org/hco/2/GRCh38#87634344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128131175-C-A

87634363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128131154-G-A

http://identifiers.org/hco/2/GRCh38#87634423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128131086-C-A

87634423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128131086-C-T

87634441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128131064-T-C

87634605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128130901-A-G

87634607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128130899-G-A

87634620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128130884-G-A

87634626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128130878-G-A

87634633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128130869-G-A

87635101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128130421-G-A

87635132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 128130390-C-T

87635232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128130327-C-T

87635575-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128129992-T-A

87635585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 128129982-T-C

http://identifiers.org/hco/2/GRCh38#87636415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#128129136-C-A

87636435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: non coding transcript exon variant
orthologous variants: 128129117-T-C

87636546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: non coding transcript exon variant
orthologous variants: 128129022-A-G

87636635-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28717
most severe consequence: non coding transcript exon variant
orthologous variants: 128128935-T-A