123984213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58438881-G-T

123984249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58438917-T-C

123984275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58438943-G-T

123984303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58438970-A-G

123984545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58439019-G-A

123984545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58439019-G-T

http://identifiers.org/hco/8/GRCh38#123984686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58439122-C-A

123984796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58439216-G-A

123984796-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58439216-G-C

123984802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58439222-G-A

123984802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58439222-G-T

123984804-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58439224-T-A

123984804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58439224-T-C

123984823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58439243-A-G

123984925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58439360-G-T

http://identifiers.org/hco/8/GRCh38#123985084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58439666-C-A

123985086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58439668-T-C

http://identifiers.org/hco/8/GRCh38#123985125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58439711-C-A

http://identifiers.org/hco/8/GRCh38#123985139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58439725-C-A

123985154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58439740-G-T

123985155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58439741-C-T

http://identifiers.org/hco/8/GRCh38#123985156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58439742-C-A

123985174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58439760-T-C

123985211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58439794-A-G

123985235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58439818-G-T

http://identifiers.org/hco/8/GRCh38#123985324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58439905-C-A

123985361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58439938-A-G

123985376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58439953-T-C

http://identifiers.org/hco/8/GRCh38#123985388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58439964-C-A

123985388-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58439964-C-G

123985578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58440458-G-T

http://identifiers.org/hco/8/GRCh38#123985728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58440603-C-A

123985731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58440606-T-C

http://identifiers.org/hco/8/GRCh38#123985738-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58440613-A-C

http://identifiers.org/hco/8/GRCh38#123985763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58440630-C-A

http://identifiers.org/hco/8/GRCh38#123985856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58440738-C-A

123985905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58440794-G-T

123985975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58440860-T-C

123985979-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58440864-T-A

123985981-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58440866-A-T

http://identifiers.org/hco/8/GRCh38#123986199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58441086-C-A

123986199-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58441086-C-G

123986199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58441086-C-T

123986240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58441113-A-G

123986246-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58441119-T-G

http://identifiers.org/hco/8/GRCh38#123986288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58441166-C-A

123986344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58441220-T-C

124000505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58441282-G-A

124000510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58441287-T-C

http://identifiers.org/hco/8/GRCh38#124000526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58441301-C-A

124000651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58441432-G-A

124000669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58441450-G-T

124000865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58441635-A-G

http://identifiers.org/hco/8/GRCh38#124002663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58442491-C-A

124002770-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58442594-T-A

http://identifiers.org/hco/8/GRCh38#124003106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58443167-C-A

124003106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58443167-C-T

124003107-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58443168-A-T

http://identifiers.org/hco/8/GRCh38#124003133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58443187-C-A

124003133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58443187-C-T

http://identifiers.org/hco/8/GRCh38#124003140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58443194-C-A

124003140-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58443194-C-G

124003140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58443194-C-T

124003180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58443234-C-T

124003207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58443261-G-T

124003410-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58443468-A-T

124003853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58443581-A-G

124007748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58444779-T-C

124007755-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58444786-T-A

124007927-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58444910-T-A

124010413-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58445269-T-A

http://identifiers.org/hco/8/GRCh38#124010424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58445276-C-A

124010472-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58445324-T-G

124010522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58445367-A-G

124010523-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58445368-T-A

124010539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58445381-G-A

124010539-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58445381-G-C

124010556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58445398-G-T

124010663-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58445507-G-C

124010743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58445576-G-A

124010743-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58445576-G-C

124010749-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58445581-T-A

124010755-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58445587-G-C

124010769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58445600-G-A

124010769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58445600-G-T

124010825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58445652-T-C

124010864-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58445684-T-A

124010864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58445684-T-C

124010864-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58445684-T-G

124010900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58445718-T-C

124012203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58446042-T-C

124012267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58446098-T-C

124012295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58446127-G-T

124012564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58446291-C-T

124012677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58446403-A-G

http://identifiers.org/hco/8/GRCh38#124012923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58446629-C-A

http://identifiers.org/hco/8/GRCh38#124012943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58446645-C-A

124012945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58446647-A-G

124012970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58446673-C-T

124013172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58446864-G-A

http://identifiers.org/hco/8/GRCh38#124013353-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58447040-A-C

124013353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58447040-A-G

124013370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58447058-A-G

http://identifiers.org/hco/8/GRCh38#124013461-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#58447128-A-C

124013461-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58447128-A-T

124013504-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58447171-T-A

124013505-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58447172-G-C

124013515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58447182-T-C

124013522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58447189-G-T

124013566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58447221-A-G

124015251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58447444-G-A

124015268-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58447461-T-A

124015283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58447473-A-G

124015588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58447762-T-C

124015595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58447769-A-G

124015597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58447771-A-G

124015741-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58447991-A-T

http://identifiers.org/hco/8/GRCh38#124015881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58448131-C-A

124015881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58448131-C-T

124015891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58448139-G-A

124015891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58448139-G-T

124015908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58448156-C-T

124015922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58448175-G-A

124015922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58448175-G-T

124016006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58448238-T-C

124016012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58448243-A-G

124016012-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58448243-A-T

124016087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58448316-C-T

124016242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58448477-C-T

124016277-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58448511-T-A

124016548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58448762-T-C

124016629-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58448848-A-T

124016745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58448926-A-G

124016849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58449004-G-A

124016849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58449004-G-T

124017319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58449428-A-G

124017396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58449499-G-A

124017501-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58449592-A-T

http://identifiers.org/hco/8/GRCh38#124017529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58449620-C-A

124017529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58449620-C-T

124017581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58449680-T-C

http://identifiers.org/hco/8/GRCh38#124017630-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#58449726-C-A

124017630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 58449726-C-T

124017631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58449727-C-T

124017715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58449811-G-A

124017715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58449811-G-T

124017777-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58449885-G-C

124017867-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58449974-G-C

124017867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58449974-G-T

124017933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58450033-C-T

124017957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58450051-C-T

124017989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58450087-G-A

124017989-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58450087-G-C

124017989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58450087-G-T

124018087-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58450349-T-G

124018149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58450420-G-A

124018193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58450467-T-C

124018488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58450744-C-T

124018687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58450947-C-T

124019047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58451633-G-A

http://identifiers.org/hco/8/GRCh38#124019332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58451907-C-A

124019367-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58451942-C-G

124019367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58451942-C-T

124019827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58452369-T-C

124019874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58452418-G-A

124019933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58452454-G-A

124021405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58453566-G-A

124021405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58453566-G-T

http://identifiers.org/hco/8/GRCh38#124021406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58453567-C-A

124021406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58453567-C-T

124021416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58453577-G-A

124021416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58453577-G-T

124021479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58453641-C-T

http://identifiers.org/hco/8/GRCh38#124021485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58453647-C-A

124021494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58453655-G-A

http://identifiers.org/hco/8/GRCh38#124021516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58453677-C-A

124021516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58453677-C-T

124021585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58453748-G-A

124021585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58453748-G-T

124021688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58453851-A-G

124021747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58453910-G-A

124021824-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58453929-T-A

124021855-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58453951-A-T

124021865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58453961-C-T

124021876-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58453972-A-T

124021948-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58454049-T-A

124022025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58454124-A-G

124022096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58454191-C-T

124022363-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58454553-C-G

124022363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58454553-C-T

124022461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58454621-C-T

124022474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58454630-A-G

124023303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58455075-T-C

124023303-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58455075-T-G

http://identifiers.org/hco/8/GRCh38#124023400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58455156-C-A

124023402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58455158-A-G

http://identifiers.org/hco/8/GRCh38#124023405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58455161-C-A

124023405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58455161-C-T

124023408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58455164-A-G

http://identifiers.org/hco/8/GRCh38#124023414-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58455170-A-C

124023455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58455192-T-C

124023464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58455201-C-T

124023506-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58455243-T-G

124023507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58455244-G-A

124023507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58455244-G-T

124023510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58455247-C-T

http://identifiers.org/hco/8/GRCh38#124023652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58455385-C-A

124023666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58455399-T-C

http://identifiers.org/hco/8/GRCh38#124023685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58455418-C-A

124023685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58455418-C-T

124023699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58455431-T-C

http://identifiers.org/hco/8/GRCh38#124023735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58455466-C-A

124023735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58455466-C-T

124027284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58456293-G-A

124027289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58456298-A-G

124027934-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58457085-A-T

124028146-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58457296-T-A

124028146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58457296-T-C

124028310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58457450-T-C

124028640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58457765-T-C

124028766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58457887-C-T

124033276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58459405-C-T

124033439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58459707-G-A

124033510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58459780-C-T

124033526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58459796-A-G

124033589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58459861-A-G

124033667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58459918-C-T

124034076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58461141-T-C

124034263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58461311-C-T

124034298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58461338-A-G

124034459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58461496-G-A

124034486-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58461515-C-G

124034486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58461515-C-T

124035047-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58462014-C-G

124035047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58462014-C-T

124035161-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58462121-A-T

124035164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58462129-G-A

124035164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58462129-G-T

124035294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58462256-G-A

124035294-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58462256-G-C

http://identifiers.org/hco/8/GRCh38#124035352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#58462314-C-A

124035352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58462314-C-T

http://identifiers.org/hco/8/GRCh38#124035437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#58462399-C-A

124035515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58462479-A-G

http://identifiers.org/hco/8/GRCh38#124035516-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58462480-A-C

124035524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58462488-G-A

124035593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58462549-T-C

http://identifiers.org/hco/8/GRCh38#124035668-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58462614-A-C

124035741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58462690-C-T

124035742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58462691-G-A

124035742-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58462691-G-C

124035891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58462814-G-A

124035955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58462883-G-T

124036049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58462978-T-C

http://identifiers.org/hco/8/GRCh38#124036265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58463171-C-A

124036265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58463171-C-T

124036320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58463226-A-G

http://identifiers.org/hco/8/GRCh38#124036370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58463264-C-A

124036370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58463264-C-T

124036416-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58463310-T-G

http://identifiers.org/hco/8/GRCh38#124036438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58463332-C-A

http://identifiers.org/hco/8/GRCh38#124037530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58464339-C-A

124037530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58464339-C-T

124037700-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58464516-C-G

124038048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58464866-A-G

124038105-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58464924-G-C

124038354-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58465184-T-A

124038431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58465283-C-T

124038767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58465557-G-A

124038826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58465637-A-G

124038862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58465673-A-G

124038946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58465754-A-G

124039143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58465934-C-T

124039208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58465999-A-G

124039244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58466035-C-T

124039326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58466132-G-A

http://identifiers.org/hco/8/GRCh38#124039402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58466226-C-A

124039402-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58466226-C-G

124039450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58466274-C-T

124039478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58466324-A-G

124039547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58466385-C-T

124039740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58466567-T-C

http://identifiers.org/hco/8/GRCh38#124039741-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58466568-C-A

124039741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58466568-C-T

124039742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58466569-A-G

124039742-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58466569-A-T

124039795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58466615-G-T

http://identifiers.org/hco/8/GRCh38#124039806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58466626-C-A

124039830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58466650-C-T

124039860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58466678-C-T

124039878-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 58466696-A-T

124040031-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58466841-T-A

124040039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58466850-T-C

124040094-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58466907-T-A

124040094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58466907-T-C

http://identifiers.org/hco/8/GRCh38#124040154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#58466988-C-A

124040154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58466988-C-T

124040250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58467076-G-A

124040271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58467097-G-A

124040280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58467106-A-G

124040292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58467118-G-A

124040292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58467118-G-T

http://identifiers.org/hco/8/GRCh38#124040303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#58467137-C-A

124040303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58467137-C-T

124040383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58467214-A-G

124040500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26652
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58467316-A-G