99355435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: non coding transcript exon variant
orthologous variants: 47591183-A-G

99355465-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: non coding transcript exon variant
orthologous variants: 47591213-T-A

99355465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: non coding transcript exon variant
orthologous variants: 47591213-T-C

99355529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: non coding transcript exon variant
orthologous variants: 47591279-G-T

99355561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: non coding transcript exon variant
orthologous variants: 47591324-G-A

99355608-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 47591393-G-T

99355652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47591427-T-C

http://identifiers.org/hco/9/GRCh38#99355705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47591462-C-A

99355705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47591462-C-T

99355748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47591499-G-T

99355824-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47591564-T-A

99355824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47591564-T-C

http://identifiers.org/hco/9/GRCh38#99356021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47591759-C-A

99356021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47591759-C-T

99356025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47591763-T-C

99356053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47591792-G-A

99356053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47591792-G-T

99356063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47591802-T-C

http://identifiers.org/hco/9/GRCh38#99356248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47591945-C-A

99356248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47591945-C-T

99356301-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47591996-T-A

99356301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47591996-T-C

http://identifiers.org/hco/9/GRCh38#99356354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47592091-C-A

99356354-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47592091-C-G

99356644-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47592388-G-C

99356679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47592416-A-G

99356920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47592669-T-C

99357046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47592793-C-T

http://identifiers.org/hco/9/GRCh38#99357307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47592990-C-A

99357307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47592990-C-T

99358270-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47593782-C-G

http://identifiers.org/hco/9/GRCh38#99358401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47593902-C-A

99358401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47593902-C-T

99358421-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47593923-G-C

99358421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47593923-G-T

99358662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47594135-G-A

99358701-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47594170-A-T

99359238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47594699-G-T

99359239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47594700-G-A

99359239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47594700-G-T

99359242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47594703-G-A

http://identifiers.org/hco/9/GRCh38#99359418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47595320-C-A

99359418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47595320-C-T

99359435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47595333-C-T

99359439-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47595337-T-A

http://identifiers.org/hco/9/GRCh38#99359495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47595393-C-A

99359495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47595393-C-T

http://identifiers.org/hco/9/GRCh38#99359581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47595480-C-A

99359581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47595480-C-T

99359593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47595492-G-A

99359593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47595492-G-T

99359611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47595509-G-A

99359611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47595509-G-T

99359642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47595536-G-A

99359855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47595704-A-G

99359874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47595723-A-G

http://identifiers.org/hco/9/GRCh38#99359898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47595747-C-A

99359988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47595834-G-A

99360000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47595846-G-T

99360071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47595910-A-G

99360223-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47596069-G-C

99360226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47596072-C-T

99360289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47596140-A-G

99360407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47596265-G-A

99360412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47596270-A-G

http://identifiers.org/hco/9/GRCh38#99360448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47596309-C-A

http://identifiers.org/hco/9/GRCh38#99360485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47596328-C-A

99360597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47596417-T-C

99360659-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47596465-T-A

99361146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47596864-G-T

99361160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47596878-C-T

99361217-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47596932-A-T

99361384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47597088-T-C

99361411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47597112-G-T

99361429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47597130-C-T

99361557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47597256-C-T

99361680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47597431-G-A

99362013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47597761-G-A

99362049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47597796-C-T

http://identifiers.org/hco/9/GRCh38#99362266-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47598005-A-C

99362276-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47598007-G-C

http://identifiers.org/hco/9/GRCh38#99362404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47598142-C-A

99362404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47598142-C-T

http://identifiers.org/hco/9/GRCh38#99362629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47598403-C-A

99362785-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47598562-A-T

99362825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47598600-C-T

99362837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47598612-A-G

99362844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47598619-G-A

99363057-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47598806-C-G

99363132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47598872-G-A

99363349-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47599042-A-T

99363477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47599155-G-A

99363717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47599374-A-G

99364130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47599751-C-T

99364910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47600161-G-A

99364928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47600180-G-A

99364996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47600248-G-A

99364997-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47600249-C-G

99365324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47600568-A-G

99365341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47600585-G-T

99365348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47600592-C-T

99365596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47600792-A-G

99365900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47601054-G-A

99366060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47601171-T-C

99366140-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47601234-T-G

99366377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47601476-G-T

99366643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47601739-G-T

99367303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47602782-G-A

99367444-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47602912-T-A

99367444-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47602912-T-G

99367537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47602952-G-T

99367565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47602980-A-G

99367566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47602981-G-T

99367602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47603011-A-G

http://identifiers.org/hco/9/GRCh38#99367611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47603022-C-A

99367611-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 47603022-C-G

http://identifiers.org/hco/9/GRCh38#99367740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47603152-C-A

99367818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47603212-A-G

99367876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47603276-T-C

99368042-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47603457-C-G

99368239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47603657-C-T

99368304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47603733-T-C

99368311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47603740-A-G

99368335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47603767-T-C

99368340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47603772-G-T

99368588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47604047-A-G

http://identifiers.org/hco/9/GRCh38#99368663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47604135-C-A

99368663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47604135-C-T

99368721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47604198-T-C

99368811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47604288-G-A

99368823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47604300-C-T

http://identifiers.org/hco/9/GRCh38#99368865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47604339-C-A

99368865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47604339-C-T

99368942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47604437-T-C

http://identifiers.org/hco/9/GRCh38#99368948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47604443-C-A

99368949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47604444-T-C

99368967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47604456-G-T

http://identifiers.org/hco/9/GRCh38#99368978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47604465-C-A

99368978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47604465-C-T

99369206-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47605257-T-G

99369297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47605347-G-A

99369371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47605422-G-A

99369405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47605480-C-T

99369434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47605510-C-T

99369441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47605518-T-C

99369502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47605575-G-A

99369550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47605621-C-T

99369622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47605698-G-A

99369622-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47605698-G-T

http://identifiers.org/hco/9/GRCh38#99369706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47605773-C-A

99371733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47606346-G-A

99371733-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47606346-G-C

99371733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47606346-G-T

99371736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47606349-C-T

99371739-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47606353-T-G

99371778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47606384-T-C

99371845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47606443-T-C

99371847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47606445-G-T

99371959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47606555-G-A

99371959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47606555-G-T

99372121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47606766-G-T

99372209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47606854-A-G

http://identifiers.org/hco/9/GRCh38#99372347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47606986-C-A

99372380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47607010-G-A

99372380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47607010-G-T

http://identifiers.org/hco/9/GRCh38#99372426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47607038-C-A

99372464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47607076-G-A

99372470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47607082-C-T

99372531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47607143-T-C

99372566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47607188-T-C

99372621-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47607236-C-G

99372658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47607272-T-C

99372785-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47607385-G-C

http://identifiers.org/hco/9/GRCh38#99372816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47607413-C-A

99372859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47607455-G-A

99372869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47607465-G-A

99372919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 47607514-A-G

99373391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47607949-T-C

99373683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47608525-C-T

99373917-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47608698-C-G

http://identifiers.org/hco/9/GRCh38#99373918-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47608699-A-C

99373918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47608699-A-G

99373918-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47608699-A-T

http://identifiers.org/hco/9/GRCh38#99373950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47608732-C-A

99373950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47608732-C-T

99373960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47608742-G-T

99374229-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: non coding transcript exon variant
orthologous variants: 47609003-C-G

99374271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: non coding transcript exon variant
orthologous variants: 47609045-T-C

99374501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47609328-A-G

99374507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47609334-A-G

99374793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47609622-A-G

99374818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47609640-A-G

99374940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47609756-G-A

99374985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47609819-G-A

99375046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47609912-G-T

99375086-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47609945-T-A

99375130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 47609984-T-C

http://identifiers.org/hco/9/GRCh38#99375138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47609992-C-A

99375183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47610037-A-G

http://identifiers.org/hco/9/GRCh38#99375202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47610055-C-A

99375246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47610100-G-A

99375246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47610100-G-T

http://identifiers.org/hco/9/GRCh38#99375265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47610116-C-A

http://identifiers.org/hco/9/GRCh38#99375291-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47610137-A-C

99375394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47610233-G-T

99375557-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47610910-T-A

99375615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47610972-C-T

http://identifiers.org/hco/9/GRCh38#99375619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47610976-C-A

99375619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47610976-C-T

http://identifiers.org/hco/9/GRCh38#99375735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47611092-C-A

http://identifiers.org/hco/9/GRCh38#99375893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47611250-C-A

99376120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47611487-G-A

99377061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42408
most severe consequence: non coding transcript exon variant
orthologous variants: 47613403-A-G