202075670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59566552-A-G

http://identifiers.org/hco/2/GRCh38#202075694-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#59566571-A-C

202075744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59566620-A-G

202075818-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59566680-G-C

202075984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59566826-G-A

202075984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59566826-G-T

202076132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59566950-C-T

202076492-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59567206-C-G

202076518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59567235-G-T

202076768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59567564-T-C

http://identifiers.org/hco/2/GRCh38#202076819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#59567600-C-A

202076819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59567600-C-T

202076838-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59567610-C-G

202076886-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59567654-C-G

202077020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59567764-C-T

202077065-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59567809-A-T

202079361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59568306-G-A

202079377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59568322-G-A

202079436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59568372-A-G

202079443-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59568379-T-A

202079464-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59568399-C-G

202079536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59568473-T-C

202079697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59568580-T-C

202079729-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59568606-T-G

202079785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59568635-G-A

202079868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59568718-T-C

http://identifiers.org/hco/2/GRCh38#202079871-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#59568721-A-C

202080368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59570313-T-C

202083739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59571227-G-T

202083763-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59571241-C-G

202083763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59571241-C-T

202084140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59574408-G-A

202084201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59574468-G-A

202084316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59574578-G-A

202084553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59574783-T-C

202085077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59575294-C-T

202085176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59575377-T-C

202085197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59575399-T-C

202085493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59576297-G-A

202085514-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59576276-G-C

202085734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59576050-G-A

202088954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59577621-C-T

http://identifiers.org/hco/2/GRCh38#202089556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#59578707-C-A

http://identifiers.org/hco/2/GRCh38#202090261-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#59579785-A-C

http://identifiers.org/hco/2/GRCh38#202090300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#59579824-C-A

202090505-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59579989-C-G

202090625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59580108-A-G

202090625-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59580108-A-T

http://identifiers.org/hco/2/GRCh38#202090631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#59580114-C-A

202090631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59580114-C-T

http://identifiers.org/hco/2/GRCh38#202090652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#59580135-C-A

http://identifiers.org/hco/2/GRCh38#202090715-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#59580197-A-C

202090715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59580197-A-G

http://identifiers.org/hco/2/GRCh38#202090755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#59580458-C-A

202090755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59580458-C-T

http://identifiers.org/hco/2/GRCh38#202090764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#59580467-C-A

202090817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 59580520-G-A

http://identifiers.org/hco/2/GRCh38#202091035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#59580735-C-A

202091035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59580735-C-T

202091594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59581221-T-C

202091626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59581248-G-A

202091661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59581283-T-C

202091736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59581356-G-A

202091768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59581385-C-T

202091907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59581513-C-T

http://identifiers.org/hco/2/GRCh38#202092153-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#59581760-A-C

202092153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59581760-A-G

202092173-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59581780-T-G

202092688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59583343-T-C

202092810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59583524-T-C

202092844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59583551-C-T

202092872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59583579-C-T

http://identifiers.org/hco/2/GRCh38#202092934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#59583639-C-A

202092934-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59583639-C-G

202092973-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59583676-A-T

202093155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 59583858-T-C

202093155-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 59583858-T-G

202093293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59584492-A-G

202093293-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59584492-A-T

202093482-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59584647-T-G

http://identifiers.org/hco/2/GRCh38#202093904-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#59585158-A-C

http://identifiers.org/hco/2/GRCh38#202094510-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#59585449-A-C

202094510-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59585449-A-T

202094511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59585450-T-C

202094779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59585698-A-G

202094863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59585785-G-A

202094889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59585806-C-T

202094971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59585863-C-T

http://identifiers.org/hco/2/GRCh38#202095521-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#59587615-A-C

202095696-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59587773-T-A

202095762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59587841-G-A

202096314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59588044-G-A

202096364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59588072-G-A

202096512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59588197-C-T

202096837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59588506-G-T

202096942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59588610-G-A

202096972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59588639-G-A

202097047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59588713-G-A

202097523-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 59589144-T-G

202097551-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 59589172-T-G

202097562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 59589183-T-C

202097562-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 59589183-T-G

202097617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59589247-T-C

202097617-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59589247-T-G

http://identifiers.org/hco/2/GRCh38#202097620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#59589250-C-A

202097620-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59589250-C-G

202097620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59589250-C-T

202098459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59589491-G-A

202098776-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59589698-T-G

202098958-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59589985-T-A

202098958-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59589985-T-G

202099784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 59590464-G-A

202099784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 59590464-G-T

202099809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59590489-A-G

http://identifiers.org/hco/2/GRCh38#202099902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#59590565-C-A

http://identifiers.org/hco/2/GRCh38#202099906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#59590569-C-A

202099906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59590569-C-T

202099927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59590585-G-A

202100345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 59591617-A-G

202100398-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 59591670-A-T

202100405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 59591677-A-G

202100518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59592002-T-C

202100590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59592047-G-T

202100591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59592048-G-A

202100591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59592048-G-T

202101156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59592780-T-C

202101506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59593089-G-A

202101781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59593352-C-T

202102337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59594079-C-T

202102712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59595065-G-A

202102813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59595177-C-T

http://identifiers.org/hco/2/GRCh38#202102830-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#59595194-A-C

202102830-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59595194-A-T

http://identifiers.org/hco/2/GRCh38#202102855-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#59595220-A-C

202102855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59595220-A-G

202102879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59595247-G-A

202102879-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59595247-G-C

202102879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59595247-G-T

http://identifiers.org/hco/2/GRCh38#202103179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#59595565-C-A

202103179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59595565-C-T

http://identifiers.org/hco/2/GRCh38#202103554-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#59596353-A-C

http://identifiers.org/hco/2/GRCh38#202105644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#59597143-C-A

202105645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59597144-A-G

202105713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59597213-A-G

202105720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59597220-A-G

http://identifiers.org/hco/2/GRCh38#202105864-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#59597339-A-C

http://identifiers.org/hco/2/GRCh38#202105904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#59597379-C-A

202105904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 59597379-C-T

202106079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59597527-T-C

202106100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59597549-G-A

202106373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59597706-T-C

202106743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59597965-C-T

202107094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59600150-A-G

202107097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59600153-T-C

http://identifiers.org/hco/2/GRCh38#202107280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#59600250-C-A

202107589-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59600507-G-C

http://identifiers.org/hco/2/GRCh38#202107987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#59600694-C-A

202107987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59600694-C-T

202108343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59600983-A-G

202108408-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59601048-C-G

202108408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59601048-C-T

http://identifiers.org/hco/2/GRCh38#202109549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#59601742-C-A

202109549-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59601742-C-G

http://identifiers.org/hco/2/GRCh38#202109666-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#59601858-A-C

202109667-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 59601859-T-A

202109667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 59601859-T-C

202109704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 59601896-G-A

202109731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 59601923-C-T

202109894-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59602066-T-A

202109901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59602073-G-T

202109903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59602075-G-T

202110044-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59602186-G-C

202110358-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59602470-G-C

202110459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59602549-G-A

202110572-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59602911-T-G

202110676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59602990-G-A

202110746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59603056-C-T

202110945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59603243-A-G

202111145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59603371-G-A

202111598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59603493-T-C

202111700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59603615-T-C

202111908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59603885-C-T

202112724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59605225-G-A

202112829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59605315-G-A

http://identifiers.org/hco/2/GRCh38#202113219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#59605636-C-A

202113449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59605866-A-G

202113513-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59605922-T-A

202113513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59605922-T-C

202113729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 59606140-G-T

202113750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59606161-G-A

202113750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59606161-G-T

http://identifiers.org/hco/2/GRCh38#202114021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#59606438-C-A

202114021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59606438-C-T

202114046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59606464-G-T

202114065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59606483-T-C

202114065-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59606483-T-G

202114298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59606720-C-T

202114577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59606988-G-A

http://identifiers.org/hco/2/GRCh38#202114777-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#59607210-A-C

202114779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59607242-G-A

202114783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59607246-A-G

http://identifiers.org/hco/2/GRCh38#202114806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#59607270-C-A

202115326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59608044-C-T

202115356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59608084-G-A

202115356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59608084-G-T

202115381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59608099-T-C

202115538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59608242-T-C

202115965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 59608660-T-C

202115965-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 59608660-T-G

202116019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 59608715-C-T

202116156-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59608847-T-A

202116156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59608847-T-C

http://identifiers.org/hco/2/GRCh38#202116273-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#59608964-A-C

202116276-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59608967-T-A

http://identifiers.org/hco/2/GRCh38#202116294-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41164
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#59608983-A-C