http://identifiers.org/hco/1/GRCh38#15112383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#141834278-C-A

15112383-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 141834278-C-G

15112383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 141834278-C-T

15112419-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: 141834244-C-G

15112419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: 141834244-C-T

15112440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 141834222-C-T

15112479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 141834183-T-C

15112567-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 141834100-T-A

15112584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 141834097-G-T

http://identifiers.org/hco/1/GRCh38#15112655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#141834034-C-A

15112655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 141834034-C-T

http://identifiers.org/hco/1/GRCh38#15112694-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#141833999-A-C

15112748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 141833987-G-A

15112748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 141833987-G-T

15112766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 141833969-A-G

15112774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 141833961-G-A

http://identifiers.org/hco/1/GRCh38#15112896-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#141833851-C-A

15112896-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 141833851-C-G

15112896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 141833851-C-T

15112909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 141833839-A-G

15112909-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 141833839-A-T

http://identifiers.org/hco/1/GRCh38#15112927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#141833823-C-A

15112927-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 141833823-C-G

15112927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 141833823-C-T

http://identifiers.org/hco/1/GRCh38#15112933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#141833817-C-A

15112933-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 141833817-C-G

15112933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 141833817-C-T

http://identifiers.org/hco/1/GRCh38#15113006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#141833761-C-A

15113006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 141833761-C-T

15113007-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 141833760-T-A

15113007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 141833760-T-C

15113007-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 141833760-T-G

15113941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 141832754-G-T

http://identifiers.org/hco/1/GRCh38#15113977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#141832718-C-A

15113979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 141832716-G-A

15113979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 141832716-G-T

http://identifiers.org/hco/1/GRCh38#15113980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#141832715-C-A

15113980-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 141832715-C-G

15113980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 141832715-C-T

15113998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 141832699-G-T

15114012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 141832684-G-A

15114012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 141832684-G-T

15114064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 141832641-A-G

15114064-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 141832641-A-T

15114096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 141832606-A-G

http://identifiers.org/hco/1/GRCh38#15114165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#141832538-C-A

15114165-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 141832538-C-G

http://identifiers.org/hco/1/GRCh38#15114248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#141832474-C-A

15114276-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 141832448-C-G

http://identifiers.org/hco/1/GRCh38#15114313-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#141832412-C-A

15114315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 141832410-T-C

15114426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 141832304-T-C

http://identifiers.org/hco/1/GRCh38#15114433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#141832297-C-A

http://identifiers.org/hco/1/GRCh38#15114461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#141832273-C-A

15114461-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 141832273-C-G

15114582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 141832152-C-T

15114627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 141832107-A-G

15114644-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 141832093-T-A

15114645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 141832092-G-T

15114667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 141832070-G-A

15114667-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 141832070-G-C

15114667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 141832070-G-T

15114768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 141831970-G-A

15114768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 141831970-G-T

http://identifiers.org/hco/1/GRCh38#15114769-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#141831969-A-C

15114769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 141831969-A-G

15114769-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 141831969-A-T

15114813-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 141831928-A-T

http://identifiers.org/hco/1/GRCh38#15114814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#141831927-C-A

15114814-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 141831927-C-G

15114814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 141831927-C-T

http://identifiers.org/hco/1/GRCh38#15114879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#141831882-C-A

http://identifiers.org/hco/1/GRCh38#15114977-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#141831817-A-C

15114977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 141831817-A-G

http://identifiers.org/hco/1/GRCh38#15115008-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#141831795-A-C

15115008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 141831795-A-G

15115008-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 141831795-A-T

http://identifiers.org/hco/1/GRCh38#15115047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#141831751-C-A

15115047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 141831751-C-T

http://identifiers.org/hco/1/GRCh38#15115086-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#141831730-C-A

15115086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 141831730-C-T

15115125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 141831694-A-G

15115128-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 141831685-G-T

http://identifiers.org/hco/1/GRCh38#15115150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#141831664-C-A

15115150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 141831664-C-T

http://identifiers.org/hco/1/GRCh38#15115196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#141831629-C-A

15115196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 141831629-C-T

15115209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 141831625-T-C

http://identifiers.org/hco/1/GRCh38#15115292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#141831566-C-A

http://identifiers.org/hco/1/GRCh38#15115293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#141831565-C-A

15115293-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 141831565-C-G

15115293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 141831565-C-T

15115343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 141831538-G-T

15115391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 141831490-A-G

http://identifiers.org/hco/1/GRCh38#15115569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#141831389-C-A

15115569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 141831389-C-T

15115626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 141831338-C-T

http://identifiers.org/hco/1/GRCh38#15115737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#141831223-C-A

http://identifiers.org/hco/1/GRCh38#15115792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#141831170-C-A

15115833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 141831129-T-C

15115843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 141831119-T-C

15115942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 141831013-G-T

15115950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 141831005-G-A

15115990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 141830965-C-T

15116069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 141830903-G-A

15116069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 141830903-G-T

http://identifiers.org/hco/1/GRCh38#15116119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#141830859-C-A

15116119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 141830859-C-T

15116125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 141830853-C-T

15116282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 141830738-C-T

15116301-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 141830719-T-A

15116330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 141830696-T-C

15116461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 141830574-T-C

http://identifiers.org/hco/1/GRCh38#15116537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#141830498-C-A

15116573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 141830460-G-A

15116573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 141830460-G-T

15117454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 141830139-T-C

15117549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 141830069-T-C

http://identifiers.org/hco/1/GRCh38#15117558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#141830060-C-A

15117558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 141830060-C-T

15117560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 141830058-G-A

15117588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 141830031-C-T

http://identifiers.org/hco/1/GRCh38#15117590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#141830029-C-A

15117590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 141830029-C-T

15117646-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 141829972-C-G

http://identifiers.org/hco/1/GRCh38#15117656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#141829963-C-A

15117656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 141829963-C-T

15117668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 141829950-T-C

http://identifiers.org/hco/1/GRCh38#15117670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#141829948-C-A

15117670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 141829948-C-T

http://identifiers.org/hco/1/GRCh38#15117684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#141829934-C-A

15117684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 141829934-C-T

15117738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 141829906-A-G

15117738-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 141829906-A-T

http://identifiers.org/hco/1/GRCh38#15117740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#141829904-C-A

15117740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 141829904-C-T

15117876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141829833-G-A

15117876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141829833-G-T

http://identifiers.org/hco/1/GRCh38#15117995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#141829748-C-A

15118132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141829615-G-T

http://identifiers.org/hco/1/GRCh38#15118267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141829520-C-A

http://identifiers.org/hco/1/GRCh38#15118275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141829512-C-A

15118275-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141829512-C-G

15118275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141829512-C-T

http://identifiers.org/hco/1/GRCh38#15118313-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141829471-A-C

15118313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141829471-A-G

http://identifiers.org/hco/1/GRCh38#15118340-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141829431-A-C

15118340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141829431-A-G

http://identifiers.org/hco/1/GRCh38#15118343-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141829417-A-C

15118343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141829417-A-G

15118365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141829395-A-G

http://identifiers.org/hco/1/GRCh38#15118366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141829394-C-A

http://identifiers.org/hco/1/GRCh38#15118411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141829355-C-A

15118411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141829355-C-T

http://identifiers.org/hco/1/GRCh38#15118544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141829307-C-A

15118544-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141829307-C-G

15118547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141829304-C-T

http://identifiers.org/hco/1/GRCh38#15118569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141829282-C-A

15118569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141829282-C-T

15118608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141829246-T-C

15118666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141829223-T-C

15118670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141829219-A-G

15118672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141829217-G-T

http://identifiers.org/hco/1/GRCh38#15118675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141829214-C-A

15118676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141829213-T-C

http://identifiers.org/hco/1/GRCh38#15118698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141829196-C-A

15118698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141829196-C-T

15118712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141829185-G-T

15137969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141825337-T-C

15138019-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141825284-C-G

15138514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141824935-A-G

15139716-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141823446-G-C

15139761-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141823419-T-A

15139778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141823396-C-T

15139802-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141823376-A-T

15139814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141823364-T-C

15139814-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141823364-T-G

15140126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141823138-C-T

15140129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141823135-G-A

15140163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141823101-G-A

15140456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141822845-T-C

15140471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141822828-C-T

15148639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141816225-T-C

http://identifiers.org/hco/1/GRCh38#15148662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141816202-C-A

15148662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141816202-C-T

15148771-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141816097-C-G

15150648-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141814163-T-G

15150800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141814034-G-A

15150831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141814000-T-C

15152206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141812602-G-A

15152226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141812583-A-G

15152357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_acceptor_variant, undefined
orthologous variants: 141812486-T-C

15152379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 141812471-T-C

15152414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 141812439-A-G

http://identifiers.org/hco/1/GRCh38#15152509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#141812260-C-A

15152510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 141812259-G-A

15152510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 141812259-G-T

15152589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 141812183-A-G

15152715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 141812148-A-G

15152909-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 141812045-C-G

15152909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 141812045-C-T

15153160-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 141811854-C-G

15153160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 141811854-C-T

15153438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26301
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 141811706-G-A