63159272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 99414436-T-C

63159287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99414451-G-A

63159303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99414467-A-G

63159428-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99414566-G-C

http://identifiers.org/hco/1/GRCh38#63159517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#99414645-C-A

63159517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99414645-C-T

63159554-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99414686-C-G

63159641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99414769-A-G

63160338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99416883-T-C

http://identifiers.org/hco/1/GRCh38#63160374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#99416918-C-A

63160402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99416932-T-C

63160536-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99417050-T-A

http://identifiers.org/hco/1/GRCh38#63160913-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#99417370-A-C

63160925-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99417382-C-G

63161065-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99417528-T-A

http://identifiers.org/hco/1/GRCh38#63161256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#99417692-C-A

63161285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99417719-C-T

63161308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99417740-G-T

63161422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99417749-A-G

63161665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99417858-G-T

63161801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99417962-T-C

63162242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99418332-T-C

http://identifiers.org/hco/1/GRCh38#63162306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#99418349-C-A

63162492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99418376-A-G

63162492-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99418376-A-T

63162555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99418389-A-G

63162558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99418392-T-C

63162625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99418450-T-C

63162781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99418544-C-T

http://identifiers.org/hco/1/GRCh38#63162787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#99418550-C-A

63162787-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99418550-C-G

63162832-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99418593-C-G

63162872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99418627-A-G

http://identifiers.org/hco/1/GRCh38#63162921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#99418671-C-A

http://identifiers.org/hco/1/GRCh38#63162950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#99418699-C-A

63162950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99418699-C-T

63162974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99418722-G-A

63162974-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99418722-G-C

63162974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99418722-G-T

63162977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99418725-T-C

63162988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99418736-A-G

63163154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99418901-G-A

63163154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99418901-G-T

63163378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99419125-A-G

63163568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99419303-A-G

63163573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99419308-C-T

63163733-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99419369-T-G

63163773-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99419416-T-A

63163779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99419422-T-C

63164637-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99421458-T-G

63164643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99421464-C-T

63164666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99421487-C-T

63164891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99421700-A-G

63164918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99421716-A-G

63164972-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99421770-T-A

63164977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99421775-C-T

63165037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99421826-C-T

63165038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99421827-C-T

63165755-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99422101-T-A

63165755-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99422101-T-G

63165880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99422215-C-T

63165974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99422317-A-G

63166353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99422683-T-C

63166354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99422684-A-G

63166939-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99422841-T-G

http://identifiers.org/hco/1/GRCh38#63167105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#99423037-C-A

63167414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99423461-G-A

63169639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99430551-A-G

http://identifiers.org/hco/1/GRCh38#63169778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#99430683-C-A

63169778-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99430683-C-G

63169988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99431228-A-G

63169988-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99431228-A-T

63170027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99431261-T-C

http://identifiers.org/hco/1/GRCh38#63170117-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#99431349-A-C

63171064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99431778-T-C

63171065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99431779-A-G

63171131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99431840-T-C

63171734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99432117-A-G

63171987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99432401-T-C

63171989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99432403-G-T

63172329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99432739-T-C

63172736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99433447-G-A

63172817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99433524-G-A

63173089-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99433907-T-G

63173158-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99433973-A-T

63173460-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99434260-G-C

http://identifiers.org/hco/1/GRCh38#63173497-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#99434297-A-C

63173497-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99434297-A-T

63173697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99434484-C-T

63176923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99435791-A-G

63176966-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99435832-T-G

63176983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99435842-T-C

http://identifiers.org/hco/1/GRCh38#63177580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#99436224-C-A

63177713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99436349-C-T

63178071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99436784-A-G

http://identifiers.org/hco/1/GRCh38#63178097-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#99436804-A-C

63178097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99436804-A-G

63178139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99436834-A-G

63178139-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99436834-A-T

63178309-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99437014-G-C

63181495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99441200-C-T

63181715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99441561-A-G

63181722-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99441568-C-G

63181775-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99441617-G-C

63181836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99441678-T-C

63181887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99441728-C-T

63182552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99442827-G-A

63183051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99443317-T-C

63183232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99443523-C-T

63183386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99443675-G-A

63183386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99443675-G-T

63183504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99443788-C-T

63183537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99443821-A-G

63183692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99443949-G-T

http://identifiers.org/hco/1/GRCh38#63183693-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#99443950-A-C

63188417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99448727-A-G

63188507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99448843-G-A

63188522-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99448867-C-G

63188522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99448867-C-T

63188830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99449084-T-C

63188836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99449090-A-G

63188837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99449091-T-C

63188842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99449096-T-C

63188852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99449106-A-G

63188852-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99449106-A-T

63189110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99449258-T-C

63189138-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99449283-G-C

63189186-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99449358-G-C

63189329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99449554-A-G

63189844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99449991-T-C

63189853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99450000-A-G

63189864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99450011-T-C

http://identifiers.org/hco/1/GRCh38#63189892-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#99450040-A-C

63190101-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99450243-A-T

63190160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99450302-T-C

63190256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99450442-C-T

63190286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99450470-T-C

63190288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99450472-A-G

63190348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99450531-A-G

63190348-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99450531-A-T

63190392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99450575-G-A

63190392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99450575-G-T

http://identifiers.org/hco/1/GRCh38#63190528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#99450701-C-A

63190540-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99450713-T-G

63190936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99453197-T-C

63190949-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99453210-A-T

63190983-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99453249-T-G

63191119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99453374-G-T

63191322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99453529-C-T

63191399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99453613-T-C

63191497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99453706-A-G

63191497-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99453706-A-T

http://identifiers.org/hco/1/GRCh38#63191779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#99453950-C-A

http://identifiers.org/hco/1/GRCh38#63191905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#99454049-C-A

63191947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99454079-T-C

63192147-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99454271-A-T

63192191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99454315-A-G

63192374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99454497-G-A

http://identifiers.org/hco/1/GRCh38#63192471-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#99454584-A-C

63192583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99454709-C-T

63192714-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99455510-G-C

63192795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99455597-T-C

63192862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99455657-G-T

63193089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99455779-T-C

63193170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99455842-C-T

63193171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99455843-G-A

63193233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99455901-A-G

63193571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99456220-G-A

63193571-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99456220-G-C

63194340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99456657-C-T

63195215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99457859-T-C

63195257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99457901-A-G

63195326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99457968-A-G

63195485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99458128-G-A

63195626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99458261-T-C

63195929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99458630-T-C

63195934-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99458635-C-G

63195934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99458635-C-T

63196363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99459226-T-C

63196498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99459320-A-G

63196533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99459358-T-C

63196640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99459441-G-A

63196764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99459585-G-A

63196764-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99459585-G-C

63197254-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99460080-A-T

63197316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99460142-C-T

http://identifiers.org/hco/1/GRCh38#63197411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#99460232-C-A

63197435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99460256-G-A

63197538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99460354-T-C

63197723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99460444-C-T

63197801-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99460500-A-T

63197854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99460537-T-C

63197919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99460590-A-G

63198125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99460761-A-G

63198422-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99461024-C-G

63198633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99461230-G-A

63198633-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99461230-G-C

63198776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99461369-G-T

63198824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99461404-T-C

63198880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99461457-A-G

63198892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99461469-C-T

63198967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99461530-A-G

63198987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99461550-A-G

63199050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99461613-G-T

63199285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99461842-T-C

63199394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99461966-A-G

63199547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99462118-T-C

63200570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99463116-G-A

63200683-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99463237-G-C

63201347-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99463892-G-C

63201480-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99464025-C-G

63201735-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99464281-T-G

http://identifiers.org/hco/1/GRCh38#63201784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#99464331-C-A

63201784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99464331-C-T

63202172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99464839-C-T

63202469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99465074-T-C

63202552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99465130-A-G

63202739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99465332-G-A

63206817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99468177-G-T

63207033-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99468775-T-A

63207033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99468775-T-C

63207034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99468776-G-A

63207034-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99468776-G-C

63207034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99468776-G-T

63208760-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99469102-T-G

63208788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99469130-T-C

63208814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99469154-C-T

63208884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99469206-G-A

63209049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99469339-G-A

63209085-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99469375-T-G

63209278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99469595-G-A

63209345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99469752-C-T

63209383-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99469792-G-C

63209400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99469809-C-T

63209439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99469847-T-C

63209507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99469904-C-T

63209554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99469958-C-T

http://identifiers.org/hco/1/GRCh38#63209888-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#99470289-A-C

63210039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99470440-A-G

http://identifiers.org/hco/1/GRCh38#63210199-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#99470592-A-C

63210267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99470641-C-T

63218301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99473949-C-T

63218342-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99473987-A-T

63218593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99474416-G-T

63218611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99474436-C-T

http://identifiers.org/hco/1/GRCh38#63218676-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#99474493-A-C

63218676-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99474493-A-T

63218730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99474688-C-T

63218774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99474736-G-T

63218797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99474757-T-C

63218801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99474761-G-A

63218843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99474799-A-G

63218950-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99475048-G-C

63219154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99475231-C-T

63219404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99477297-A-G

63219558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99477586-G-T

http://identifiers.org/hco/1/GRCh38#63219617-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#99477645-A-C

http://identifiers.org/hco/1/GRCh38#63221595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#99479743-C-A

63221622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99479764-G-A

63221736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99479849-T-C

63221925-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99480014-G-C

63221934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99480023-G-A

63221948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99480038-G-T

63222127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99480154-T-C

63222499-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99480518-A-T

63222520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99480539-G-A

63222653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99480642-G-T

63222768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99480749-G-T

63222879-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99480816-G-C

63222931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99480870-T-C

63223684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99481757-G-A

63223688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99481761-C-T

63238479-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99483198-G-C

63238520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99483239-A-G

63239018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99483707-T-C

63239027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99483716-G-T

63239108-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99483816-T-A

63239121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99483829-C-T

63239366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99484034-C-T

63239384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99484052-G-A

63239384-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99484052-G-C

63239430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99484100-A-G

63239433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99484103-G-A

63239485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99484150-T-C

63239486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99484151-G-A

63239554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99484203-C-T

http://identifiers.org/hco/1/GRCh38#63239644-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#99484296-A-C

63242539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99484540-T-C

63242603-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99484600-T-A

63242747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99484752-A-G

63242793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99484797-G-A

63242874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99484872-G-T

63243094-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99485064-A-T

63243107-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99485075-T-A

63243111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99485079-G-A

63243483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99485636-C-T

63243700-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99485850-T-A

63243885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99486093-G-A

63243933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99486139-C-T

63244600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99486178-G-A

63244600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99486178-G-T

63244834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99486408-G-A

63244852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99486427-G-A

63244852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99486427-G-T

63245089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99486669-A-G

63245300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99486874-G-A

63246565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99488460-G-A

63246597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99488493-A-G

63247122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99489019-C-T

63247241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99489147-G-A

63247252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99489158-T-C

63247320-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99489221-A-T

63247348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99489245-G-A

63247862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99489418-A-G

63248036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99489590-A-G

63248293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99489831-G-A

63248646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99490183-A-G

63248689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99490226-T-C

63248738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99490275-C-T

63248927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99490441-G-T

http://identifiers.org/hco/1/GRCh38#63248964-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#99490481-A-C

http://identifiers.org/hco/1/GRCh38#63248965-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#99490482-A-C

63251608-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99490661-T-G

http://identifiers.org/hco/1/GRCh38#63254663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#99492758-C-A

63254983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99493002-G-A

63255125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99493066-A-G

63255126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99493067-A-G

63255160-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99493087-G-T

63255407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99493251-C-T

63255409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99493253-C-T

63255645-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99494560-A-T

http://identifiers.org/hco/1/GRCh38#63255716-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#99494628-A-C

63256051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99494946-G-A

http://identifiers.org/hco/1/GRCh38#63256158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#99494992-C-A

63256192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99495024-T-C

63256257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99495080-A-G

63256384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99495668-A-G

63256409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99495700-T-C

63256599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99495857-G-A

63256689-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99496023-T-G

63256853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99496174-G-T

http://identifiers.org/hco/1/GRCh38#63256936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#99496244-C-A

63256936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99496244-C-T

63257086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99496393-G-T

63257533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99496837-T-C

63257857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99497154-G-A

63257949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99497252-G-A

63257949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99497252-G-T

63258049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 99498342-G-T

http://identifiers.org/hco/1/GRCh38#63258118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#99498384-C-A

63258118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99498384-C-T

http://identifiers.org/hco/1/GRCh38#63258193-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#99498463-A-C

63258193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99498463-A-G

63258257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99498488-G-A

63258413-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99498632-G-C

http://identifiers.org/hco/1/GRCh38#63258417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#99498636-C-A

63258417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99498636-C-T

63261335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99500553-C-T

63261344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99500562-C-T

63261384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99500593-C-T

63261524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99500731-G-A

63261524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99500731-G-T

63261815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 99501024-T-C

63261815-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 99501024-T-G

63261824-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_acceptor_variant, undefined
orthologous variants: 99501036-T-A

63261847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 99501059-T-C

63261847-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 99501059-T-G

http://identifiers.org/hco/1/GRCh38#63261858-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#99501070-A-C

63261858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 99501070-A-G

63261901-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99501111-G-C

63261901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99501111-G-T

63261918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99501128-T-C

63261940-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99501150-T-G

http://identifiers.org/hco/1/GRCh38#63261941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#99501151-C-A

63261983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 99501192-G-A

63261983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 99501192-G-T

63262018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99501227-G-A

63262018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99501227-G-T

63262041-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99501259-T-G

http://identifiers.org/hco/1/GRCh38#63262132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#99501362-C-A

63262132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99501362-C-T

http://identifiers.org/hco/1/GRCh38#63262170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#99501396-C-A

63262170-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 99501396-C-G

63262170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 99501396-C-T

63262191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 99501417-G-A

63262191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 99501417-G-T

http://identifiers.org/hco/1/GRCh38#63262260-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#99501486-A-C

63262260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99501486-A-G

63262308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99501567-A-G

http://identifiers.org/hco/1/GRCh38#63262319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#99501578-C-A

http://identifiers.org/hco/1/GRCh38#63262338-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#99501597-A-C

63262338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 99501597-A-G

http://identifiers.org/hco/1/GRCh38#63262344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#99501602-C-A

63262344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 99501602-C-T

http://identifiers.org/hco/1/GRCh38#63262397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#99501730-C-A

63262397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99501730-C-T

http://identifiers.org/hco/1/GRCh38#63262399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#99501732-C-A

63262399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99501732-C-T

63262405-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99501738-T-A

63262446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99501779-G-A

63262446-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99501779-G-T

63262475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99501807-G-A

63262475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99501807-G-T

http://identifiers.org/hco/1/GRCh38#63262485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#99501817-C-A

63262485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99501817-C-T

63262551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99501880-T-C

63262638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99501966-T-C

63262651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99501979-G-A

63262651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99501979-G-T

http://identifiers.org/hco/1/GRCh38#63262656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#99501983-C-A

63262656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99501983-C-T

63262684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99502010-A-G

63262684-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99502010-A-T

63262685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99502011-T-C

63262708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 99502034-G-A

63262708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 99502034-G-T

63262723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99502046-A-G

63262729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99502052-G-A

63262729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99502052-G-T

63265061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99506319-T-C

63267442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

63267466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

63267496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

63267574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

http://identifiers.org/hco/1/GRCh38#63267580-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-C

http://identifiers.org/hco/1/GRCh38#63268629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#99509385-C-A

http://identifiers.org/hco/1/GRCh38#63268716-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#99509468-A-C

63269007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99509755-C-T

63269109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99509868-T-C

63269133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99509892-C-T

63269156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99509968-C-T

http://identifiers.org/hco/1/GRCh38#63269289-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#99510098-A-C

63269366-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99510335-C-G

63269678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99510799-T-C

63269680-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99510801-G-C

63270097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99511164-A-G

63274247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99512288-C-T

63274376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99512417-G-T

http://identifiers.org/hco/1/GRCh38#63274501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#99512543-C-A

63275087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99513129-T-C

63275568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99513586-C-T

63276310-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99514267-C-G

63276312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99514269-G-T

63276475-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99514424-T-A

63276671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99514609-G-A

63276671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99514609-G-T

63276712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99514649-C-T

http://identifiers.org/hco/1/GRCh38#63276713-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#99514650-A-C

63276801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99514764-G-A

63276809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99514772-C-T

63276972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99514926-A-G

63277015-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99514967-T-A

63277147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99515099-G-T

63277229-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99515181-A-T

63277457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99515390-T-C

63277558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99515477-T-C

63294748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99525033-G-A

63294791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99525084-A-G

63294842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99525135-T-C

63294952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99525274-G-A

63303242-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99527377-A-T

http://identifiers.org/hco/1/GRCh38#63303332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#99527466-C-A

63303332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99527466-C-T

63303347-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99527481-A-T

63304699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: non coding transcript exon variant
orthologous variants: 99529672-A-G

63304700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: non coding transcript exon variant
orthologous variants: 99529673-T-C

63305169-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99530135-C-G

63305435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99530417-T-C

63305455-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99530437-T-A

63305455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99530437-T-C

http://identifiers.org/hco/1/GRCh38#63305457-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#99530439-A-C

63305520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99530498-T-C

63305785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99530806-T-C

63305920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99530944-C-T

63305926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99530950-T-C

63310460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99532782-A-G

63310513-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99532832-T-A

63316212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99538135-G-T

63316639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99538559-G-A

63316639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99538559-G-T

63316656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99538571-G-T

63316785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99538735-G-A

63316997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99538939-G-T

http://identifiers.org/hco/1/GRCh38#63317073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#99539023-C-A

63317073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 99539023-C-T

http://identifiers.org/hco/1/GRCh38#63317095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#99539045-C-A

63317095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: non coding transcript exon variant
orthologous variants: 99539045-C-T

63317233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27294
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 99539165-G-A