63316589-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41033691-G-C

63316589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41033691-G-T

63316674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41033762-G-T

63316989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41034173-C-T

http://identifiers.org/hco/9/GRCh38#63317020-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41034200-A-C

63317273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41034381-G-T

63317288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41034396-G-A

63317383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41034492-G-A

63317383-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41034492-G-C

63317383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41034492-G-T

63317387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41034496-G-A

63317387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41034496-G-T

63317400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41034509-G-A

63317400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41034509-G-T

63317437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41034535-G-A

http://identifiers.org/hco/9/GRCh38#63317473-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41034547-C-A

63317473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41034547-C-T

http://identifiers.org/hco/9/GRCh38#63317501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41034575-C-A

63317501-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41034575-C-G

63317501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41034575-C-T

63317514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41034587-G-T

63317593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41034649-G-A

63317593-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41034649-G-C

63317593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41034649-G-T

http://identifiers.org/hco/9/GRCh38#63317598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41034654-C-A

63317598-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41034654-C-G

63317657-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41034704-C-G

http://identifiers.org/hco/9/GRCh38#63317658-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41034705-A-C

63317658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41034705-A-G

63317664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41034711-G-A

63317664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41034711-G-T

http://identifiers.org/hco/9/GRCh38#63317682-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41034726-A-C

63317682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41034726-A-G

63317685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41034729-G-A

63317695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41034739-G-T

63317701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41034745-G-A

63317701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41034745-G-T

63317702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 41034746-G-A

63317702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 41034746-G-T

63317723-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41034767-T-A

63317723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41034767-T-C

63317723-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41034767-T-G

63317790-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41034829-T-A

63317790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41034829-T-C

63317790-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41034829-T-G

63317897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41034936-G-A

63317897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41034936-G-T

63317984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41035016-G-A

63317984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41035016-G-T

63318011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41035039-C-T

http://identifiers.org/hco/9/GRCh38#63318024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41035052-C-A

63318024-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41035052-C-G

63318024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41035052-C-T

63318037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41035065-A-G

63318037-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41035065-A-T

http://identifiers.org/hco/9/GRCh38#63318233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41035225-C-A

63318233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41035225-C-T

63318248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41035240-G-A

63318248-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41035240-G-C

63318248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41035240-G-T

http://identifiers.org/hco/9/GRCh38#63318260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41035252-C-A

63318260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 41035252-C-T

63318325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41035298-T-C

63318325-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41035298-T-G

63318351-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41035356-A-T

63318354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41035359-T-C

http://identifiers.org/hco/9/GRCh38#63318356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41035361-C-A

63318356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41035361-C-T

http://identifiers.org/hco/9/GRCh38#63318375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41035403-C-A

63318375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41035403-C-T

63318381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41035409-T-C

63318389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41035417-T-C

http://identifiers.org/hco/9/GRCh38#63318439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41035461-C-A

63318439-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41035461-C-G

63318439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41035461-C-T

http://identifiers.org/hco/9/GRCh38#63318530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41035553-C-A

63318530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41035553-C-T

63318591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41035614-T-C

63318594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41035617-G-A

63318628-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41035640-T-A

63318628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41035640-T-C

63318628-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41035640-T-G

63318629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41035641-G-A

63318632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41035644-A-G

63318632-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41035644-A-T

63318642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41035654-A-G

63318674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41035676-G-A

63318674-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41035676-G-C

63318674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41035676-G-T

63318691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41035693-G-A

63318691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41035693-G-T

http://identifiers.org/hco/9/GRCh38#63318745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41035731-C-A

63318745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41035731-C-T

http://identifiers.org/hco/9/GRCh38#63318747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41035733-C-A

63318747-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41035733-C-G

63318747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41035733-C-T

63318793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41035775-G-A

63318841-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41035824-G-C

63318865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41035848-A-G

63318912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41035895-C-T

63318914-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41035897-C-G

63318914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41035897-C-T

63318989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41035970-G-A

63319075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41036054-G-A

63319075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41036054-G-T

63319118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41036097-T-C

63319150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41036129-G-T

63319167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41036146-G-A

http://identifiers.org/hco/9/GRCh38#63319187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41036166-C-A

63319187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41036166-C-T

63319256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41036212-G-A

63319264-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41036220-T-A

63319264-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41036220-T-G

63319265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41036222-G-A

63319266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41036223-G-A

63319266-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41036223-G-C

63319269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41036226-T-C

63319269-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41036226-T-G

http://identifiers.org/hco/9/GRCh38#63319301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41036255-C-A

http://identifiers.org/hco/9/GRCh38#63319303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41036257-C-A

63319406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41036355-C-T

63319474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41036428-G-A

63319474-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41036428-G-C

http://identifiers.org/hco/9/GRCh38#63319497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41036451-C-A

63319497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41036451-C-T

63319522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41036479-G-T

63322912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41040889-T-C

63323002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41040971-G-T

63323031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41040998-T-C

63323062-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41041017-C-G

63323083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41041030-T-C

63323135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41041051-G-A

63323135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41041051-G-T

http://identifiers.org/hco/9/GRCh38#63323166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41041082-C-A

63323166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41041082-C-T

63323168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41041084-C-T

63323196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41041113-A-G

http://identifiers.org/hco/9/GRCh38#63323330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41041215-C-A

63323411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41041281-G-A

63323467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41041337-T-C

63323473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41041343-C-T

http://identifiers.org/hco/9/GRCh38#63323503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41041373-C-A

63323503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41041373-C-T

http://identifiers.org/hco/9/GRCh38#63323681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41041555-C-A

63324072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41041798-G-A

63324164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41041874-A-G

63324306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41043065-G-A

63324423-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41043176-T-G

63325655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41044142-G-A

http://identifiers.org/hco/9/GRCh38#63325748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41044229-C-A

http://identifiers.org/hco/9/GRCh38#63325816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41044309-C-A

63325816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41044309-C-T

63325819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41044312-C-T

63325850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41044342-C-T

63325902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41044388-A-G

63326047-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41044503-C-G

63326047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41044503-C-T

63326052-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41044508-T-A

63326052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41044508-T-C

http://identifiers.org/hco/9/GRCh38#63326069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41044540-C-A

63326105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41044618-T-C

63326113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41044632-T-C

http://identifiers.org/hco/9/GRCh38#63326266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41044827-C-A

63326338-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41044925-G-C

63326349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41044936-A-G

63326392-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41045001-T-A

63326490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41045098-T-C

63326622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41045170-C-T

http://identifiers.org/hco/9/GRCh38#63326625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41045173-C-A

63326625-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41045173-C-G

63326625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41045173-C-T

63326643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41045192-A-G

63326655-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41045204-A-T

http://identifiers.org/hco/9/GRCh38#63326706-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41045256-A-C

63326716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41045266-G-T

http://identifiers.org/hco/9/GRCh38#63326754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41045304-C-A

63326754-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41045304-C-G

63326754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41045304-C-T

63326794-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41045337-T-G

63326808-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41045346-C-G

63326808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41045346-C-T

63326811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41045349-G-A

63326811-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41045349-G-C

63326811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41045349-G-T

63326828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41045366-A-G

http://identifiers.org/hco/9/GRCh38#63326858-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41045396-A-C

63326858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 41045396-A-G

http://identifiers.org/hco/9/GRCh38#63326873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41045411-C-A

63326873-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41045411-C-G

63326873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41045411-C-T

http://identifiers.org/hco/9/GRCh38#63326970-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41045508-A-C

63326970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41045508-A-G

63326989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41045527-G-A

63326989-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41045527-G-C

63326989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41045527-G-T

63327008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41045546-A-G

http://identifiers.org/hco/9/GRCh38#63327094-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41045630-A-C

63327096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41045632-T-C

63327101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41045637-A-G

63327101-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41045637-A-T

63327103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41045639-G-A

63327130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41045667-C-T

63327153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41045690-G-A

63327244-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41045760-T-G

63327421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41045899-T-C

63327466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41045943-G-A

63327467-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41045944-A-T

http://identifiers.org/hco/9/GRCh38#63327584-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#41046034-A-C

63327593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41046043-T-C

63327662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41046122-G-A

63327662-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41046122-G-C

63327675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32048
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41046135-A-G