35558774-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155861094-G-C

http://identifiers.org/hco/20/GRCh38#35558862-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155861177-A-C

35558877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155861194-G-T

35558878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155861195-G-A

http://identifiers.org/hco/20/GRCh38#35558908-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155861225-A-C

35558908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155861225-A-G

35558917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155861234-G-A

35558917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155861234-G-T

35558935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155861252-G-A

35558944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155861261-G-A

35558962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155861279-C-T

35559097-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155861413-G-C

35559130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155861441-G-A

35559158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 155861453-G-A

35559158-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 155861453-G-C

http://identifiers.org/hco/20/GRCh38#35559173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155861468-C-A

35559395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155861679-G-A

35559395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155861679-G-T

http://identifiers.org/hco/20/GRCh38#35559647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155861925-C-A

35559721-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155861973-A-T

35559748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155861994-G-A

http://identifiers.org/hco/20/GRCh38#35559751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155861997-C-A

35559751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155861997-C-T

35559761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155862007-G-T

35559840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155862027-C-T

35559873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155862043-T-C

35559873-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155862043-T-G

35559904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155862072-A-G

35560062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155862218-G-A

http://identifiers.org/hco/20/GRCh38#35560250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155862389-C-A

35560250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155862389-C-T

http://identifiers.org/hco/20/GRCh38#35560429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155862574-C-A

35560429-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155862574-C-G

35560454-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155862598-C-G

35560454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155862598-C-T

35560490-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155862610-T-A

35560605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155862726-C-T

35560680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155862793-G-A

35560680-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155862793-G-T

http://identifiers.org/hco/20/GRCh38#35560682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155862795-C-A

http://identifiers.org/hco/20/GRCh38#35560689-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155862845-A-C

35560689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155862845-A-G

http://identifiers.org/hco/20/GRCh38#35560694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155862850-C-A

35560729-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155863045-T-A

35560858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155863303-C-T

35561052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155863468-A-G

35561103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155863514-C-T

35561230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155863728-A-G

35561231-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155863729-T-A

35561231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155863729-T-C

35561248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155863746-G-A

35561378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155863856-C-T

35561713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155864343-G-A

35561713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155864343-G-T

35561854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 155864446-G-A

35561893-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155864485-A-T

35561904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155864496-G-A

35561904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155864496-G-T

35561905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155864497-A-G

35561945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 155864537-G-A

35561945-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 155864537-G-C

35561945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 155864537-G-T

http://identifiers.org/hco/20/GRCh38#35561978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155864570-C-A

35561978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155864570-C-T

35561980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155864572-A-G

35562076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155864657-G-A

35562680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155864926-T-C

35562703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155864949-T-C

35562747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155864975-T-C

35562795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155865003-G-T

35562797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155865005-G-T

http://identifiers.org/hco/20/GRCh38#35562818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155865026-C-A

http://identifiers.org/hco/20/GRCh38#35562869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155865077-C-A

35562957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155865165-G-A

35562957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155865165-G-T

35562958-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155865166-G-C

35563014-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155865211-T-A

35563014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155865211-T-C

35563014-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155865211-T-G

35563021-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155865218-T-A

35563021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155865218-T-C

35563021-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155865218-T-G

http://identifiers.org/hco/20/GRCh38#35563032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155865227-C-A

35563032-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155865227-C-G

http://identifiers.org/hco/20/GRCh38#35563036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155865231-C-A

35563036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155865231-C-T

35563039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155865234-C-T

http://identifiers.org/hco/20/GRCh38#35563063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155865256-C-A

35563372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155865443-A-G

35563419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155865465-G-A

35563494-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155865535-A-T

35563569-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155865603-C-G

35563667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155865685-C-T

35563722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155865706-A-G

http://identifiers.org/hco/20/GRCh38#35563742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155865726-C-A

35563751-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155865735-C-G

35563765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155865757-A-G

35563800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155865790-G-A

35563800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155865790-G-T

35563823-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155865821-A-T

http://identifiers.org/hco/20/GRCh38#35563847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155865858-C-A

35563847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 155865858-C-T

35563954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155865965-C-T

http://identifiers.org/hco/20/GRCh38#35564013-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155866024-A-C

35564013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 155866024-A-G

35564307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155866257-G-A

35564307-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155866257-G-C

35564307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155866257-G-T

35564309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155866259-G-A

35564336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155866283-C-T

35564354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155866290-T-C

http://identifiers.org/hco/20/GRCh38#35564403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155866347-C-A

35564403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155866347-C-T

35564521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155866429-G-A

35564530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155866443-T-C

http://identifiers.org/hco/20/GRCh38#35564675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155866481-C-A

http://identifiers.org/hco/20/GRCh38#35564723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155866524-C-A

35564738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155866539-C-T

35564762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155866567-G-A

35564828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155866633-G-A

35564849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155866654-G-A

35564866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155866671-C-T

35564935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155866741-G-T

35564960-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155866766-A-T

35564976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155866782-A-G

35564976-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155866782-A-T

35565013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155866798-T-C

http://identifiers.org/hco/20/GRCh38#35565015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155866800-C-A

35565015-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155866800-C-G

35565051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155866832-G-A

35565056-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155866837-C-G

35565087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155866858-G-A

35565141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155866912-C-T

35565211-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155866982-G-C

http://identifiers.org/hco/20/GRCh38#35565215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155866986-C-A

35565215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155866986-C-T

35565233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 155867009-G-A

35576083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155871006-T-C

35576083-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155871006-T-G

http://identifiers.org/hco/20/GRCh38#35576088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155871011-C-A

35576131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155871053-T-C

http://identifiers.org/hco/20/GRCh38#35576143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155871063-C-A

35576143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155871063-C-T

http://identifiers.org/hco/20/GRCh38#35576262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155871177-C-A

35576262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155871177-C-T

http://identifiers.org/hco/20/GRCh38#35576555-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155871700-A-C

http://identifiers.org/hco/20/GRCh38#35576590-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155871733-A-C

http://identifiers.org/hco/20/GRCh38#35576766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155871908-C-A

http://identifiers.org/hco/20/GRCh38#35576887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155872026-C-A

35578810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155873081-T-C

35578923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155873191-G-A

http://identifiers.org/hco/20/GRCh38#35579050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155873313-C-A

35579183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155873430-G-A

http://identifiers.org/hco/20/GRCh38#35579186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155873433-C-A

35579186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155873433-C-T

35579433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155873680-C-T

http://identifiers.org/hco/20/GRCh38#35579592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155873824-C-A

http://identifiers.org/hco/20/GRCh38#35579641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155873863-C-A

35579641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155873863-C-T

35581905-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155876678-A-T

35581938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155876707-T-C

35581952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155876720-A-G

http://identifiers.org/hco/20/GRCh38#35581991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155876751-C-A

35582225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155877029-A-G

35582444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155877247-G-T

35582472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155877276-G-T

http://identifiers.org/hco/20/GRCh38#35582809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155877324-C-A

35582810-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155877325-C-G

http://identifiers.org/hco/20/GRCh38#35582959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155877475-C-A

35583016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 155877532-G-T

35583049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155877640-G-A

35583049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155877640-G-T

35583271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155877944-C-T

http://identifiers.org/hco/20/GRCh38#35583294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155877967-C-A

35583294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155877967-C-T

35583346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155878010-T-C

35583548-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155878154-T-G

35583574-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155878174-T-A

35583574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155878174-T-C

35583657-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155878250-T-A

35583657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155878250-T-C

35583660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155878253-C-T

35583886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155878479-T-C

http://identifiers.org/hco/20/GRCh38#35583937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155878518-C-A

35583993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155878574-G-A

35583993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155878574-G-T

35584174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155878753-G-A

35584174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155878753-G-T

35584431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155878937-C-T

35584552-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155879033-T-G

35584862-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155879151-C-G

35584862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155879151-C-T

35585033-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155879181-G-C

35585075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155879219-A-G

35585075-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155879219-A-T

http://identifiers.org/hco/20/GRCh38#35585087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155879231-C-A

http://identifiers.org/hco/20/GRCh38#35585116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155879261-C-A

35585116-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 155879261-C-G

35585117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 155879262-C-T

http://identifiers.org/hco/20/GRCh38#35585232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155879377-C-A

35585232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155879377-C-T

35585255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155879400-C-T

35585285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155879430-G-A

35585285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155879430-G-T

35585294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155879440-G-T

35595226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155880801-G-A

35595268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155880841-C-T

35595271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155880844-G-T

http://identifiers.org/hco/20/GRCh38#35595393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155880920-C-A

35595393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155880920-C-T

35595494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155881002-G-A

http://identifiers.org/hco/20/GRCh38#35595537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155881045-C-A

35595537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155881045-C-T

http://identifiers.org/hco/20/GRCh38#35595568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155881076-C-A

35595628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155881136-C-T

35595682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155881205-G-T

35595857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155881312-T-C

35595997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155881409-A-G

35596233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155881827-C-T

35598878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155885806-T-C

35598902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155885829-G-T

35598922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155885848-A-G

35598995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155885921-G-T

35599004-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155885930-C-G

35599007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 155885933-A-G

35599060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155885986-A-G

35599060-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155885986-A-T

35599067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155885993-A-G

35599213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155886108-C-T

http://identifiers.org/hco/20/GRCh38#35599420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155886229-C-A

35599420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155886229-C-T

http://identifiers.org/hco/20/GRCh38#35599440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155886248-C-A

35599440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155886248-C-T

35599468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155886268-G-T

35599520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155886319-T-C

http://identifiers.org/hco/20/GRCh38#35599564-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155886360-A-C

35599631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155886427-A-G

35599661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155886457-G-T

35599662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155886458-A-G

35599692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 155886489-A-G

35599692-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 155886489-A-T

http://identifiers.org/hco/20/GRCh38#35599796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155886598-C-A

35599796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155886598-C-T

35599818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155886623-T-C

http://identifiers.org/hco/20/GRCh38#35599835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155886642-C-A

35599835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155886642-C-T

35599837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155886644-C-T

http://identifiers.org/hco/20/GRCh38#35599902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155886710-C-A

35599902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155886710-C-T

http://identifiers.org/hco/20/GRCh38#35599915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155886723-C-A

35599915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155886723-C-T

http://identifiers.org/hco/20/GRCh38#35599922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155886730-C-A

35599922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155886730-C-T

http://identifiers.org/hco/20/GRCh38#35600004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155886807-C-A

35600004-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155886807-C-G

35600004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155886807-C-T

35600092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155886915-G-A

35600105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 155886928-C-T

http://identifiers.org/hco/20/GRCh38#35600213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155887036-C-A

35600213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155887036-C-T

http://identifiers.org/hco/20/GRCh38#35600244-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155887067-A-C

35600244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155887067-A-G

35600287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155887108-G-A

35600287-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155887108-G-C

35600287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155887108-G-T

http://identifiers.org/hco/20/GRCh38#35600581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155887347-C-A

35600581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155887347-C-T

35600636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155887402-C-T

http://identifiers.org/hco/20/GRCh38#35600711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155887486-C-A

35600711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155887486-C-T

35600745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155887520-G-A

35600745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155887520-G-T

35600768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155887543-A-G

http://identifiers.org/hco/20/GRCh38#35600875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155887650-C-A

35600875-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155887650-C-G

35600875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155887650-C-T

35600905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155887680-G-A

35600905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155887680-G-T

35600952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155887726-A-G

35600971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 155887745-G-A

35600971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 155887745-G-T

http://identifiers.org/hco/20/GRCh38#35601011-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155887781-A-C

http://identifiers.org/hco/20/GRCh38#35601018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155887788-C-A

35601018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155887788-C-T

35601019-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155887789-G-C

35601019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155887789-G-T

35601022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155887792-G-A

35601083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155887848-G-A

35601515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155887971-C-T

35601524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 155887981-G-A

35601535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 155887992-C-T

35601542-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 155887999-C-G

35601542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 155887999-C-T

35601587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 155888044-C-T

35601623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155888080-G-T

35601632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155888089-G-T

http://identifiers.org/hco/20/GRCh38#35601641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#155888098-C-A

35601641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 155888098-C-T

35601674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 155888131-G-A

35601698-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155888155-G-C

35601702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155888159-C-T

35601746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 155888198-G-A

35601746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 155888198-G-T

35601751-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 155888201-A-T

35601780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155888840-G-T

35601789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155888847-G-A

35601789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155888847-G-T

http://identifiers.org/hco/20/GRCh38#35601809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#155888867-C-A

35601809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 155888867-C-T

35601829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155888887-G-A

35601829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155888887-G-T

35601907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155888965-G-A

http://identifiers.org/hco/20/GRCh38#35602024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155889076-C-A

35602024-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155889076-C-G

35602027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155889079-G-A

35602051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 155889107-G-A

35602051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 155889107-G-T

http://identifiers.org/hco/20/GRCh38#35602091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#155889145-C-A

35602145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155889199-C-T

35602183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155889237-A-G

http://identifiers.org/hco/20/GRCh38#35602243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155889297-C-A

35602243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155889297-C-T

35602262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155889316-G-A

35602262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155889316-G-T

35602299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155889354-G-A

35602299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155889354-G-T

35602343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155889382-A-G

35602343-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155889382-A-T

http://identifiers.org/hco/20/GRCh38#35602374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155889405-C-A

35602374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155889405-C-T

35602428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155889459-G-A

35602428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155889459-G-T

35602431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155889462-G-A

35602435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155889466-G-T

35602466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155889484-G-A

35602587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155889589-G-T

35602610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 155889612-T-C

35602621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155889623-G-A

35602621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155889623-G-T

http://identifiers.org/hco/20/GRCh38#35602634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155889635-C-A

35602634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155889635-C-T

35602657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155889689-T-C

35602760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155889868-A-G

35602760-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155889868-A-T

http://identifiers.org/hco/20/GRCh38#35602790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155889898-C-A

35602790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155889898-C-T

http://identifiers.org/hco/20/GRCh38#35602800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155889907-C-A

35602800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155889907-C-T

35602807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155889914-A-G

http://identifiers.org/hco/20/GRCh38#35602851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155889960-C-A

35602888-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155889994-C-G

35602909-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155890015-T-A

35602955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155890053-T-C

http://identifiers.org/hco/20/GRCh38#35602985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155890082-C-A

35602985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155890082-C-T

http://identifiers.org/hco/20/GRCh38#35603003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155890100-C-A

35603003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 155890100-C-T

http://identifiers.org/hco/20/GRCh38#35603028-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155890126-A-C

35603042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155890140-G-T

35603043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155890141-T-C

35603080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155890178-G-A

35603080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155890178-G-T

35603214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155890313-A-G

35603247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155890337-A-G

http://identifiers.org/hco/20/GRCh38#35603294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155890384-C-A

35603294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155890384-C-T

35603384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155890455-C-T

http://identifiers.org/hco/20/GRCh38#35603392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155890463-C-A

35603392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155890463-C-T

35603402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155890473-T-C

35603406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155890477-G-T

35603433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155890485-G-A

35603433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155890485-G-T

35603437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155890489-T-C

35603474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155890510-C-T

35603769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155890769-G-A

http://identifiers.org/hco/20/GRCh38#35603911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155890902-C-A

35603911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155890902-C-T

35603994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155890973-T-C

35603999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155890978-G-A

35603999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155890978-G-T

35604107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155891085-G-T

http://identifiers.org/hco/20/GRCh38#35604254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155891305-C-A

35604254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155891305-C-T

35604268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155891319-T-C

http://identifiers.org/hco/20/GRCh38#35604292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155891343-C-A

35604385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155891426-T-C

35604435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155891457-G-A

35604435-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155891457-G-C

35604435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155891457-G-T

35604438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155891460-G-T

35604524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155891539-G-T

35604535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155891550-C-T

http://identifiers.org/hco/20/GRCh38#35604634-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155891649-A-C

http://identifiers.org/hco/20/GRCh38#35604644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155891659-C-A

35604665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155891676-C-T

35604702-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155891700-C-G

35604702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155891700-C-T

35604744-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155891745-T-A

35604751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155891752-T-C

35604755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155891753-G-T

35604766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155891764-G-T

35604780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155891777-T-C

35605875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155893560-C-T

35605876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155893561-G-A

35605922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155893603-G-T

35605962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155893643-G-A

35606009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155893759-G-T

35606016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155893766-G-T

35606058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155893835-G-A

35606064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155893841-T-C

http://identifiers.org/hco/20/GRCh38#35606069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155893846-C-A

http://identifiers.org/hco/20/GRCh38#35606188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155893962-C-A

35606197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155893971-G-A

35606233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155894007-G-A

35606233-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155894007-G-T

35606238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155894012-G-A

35606238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155894012-G-T

http://identifiers.org/hco/20/GRCh38#35606333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155894093-C-A

35606333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155894093-C-T

35606335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155894095-G-A

35606335-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155894095-G-C

35606335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155894095-G-T

http://identifiers.org/hco/20/GRCh38#35606424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155894184-C-A

35606424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155894184-C-T

http://identifiers.org/hco/20/GRCh38#35606448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155894213-C-A

35606448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 155894213-C-T

35606979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155894390-G-A

35606979-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155894390-G-C

http://identifiers.org/hco/20/GRCh38#35606982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155894393-C-A

35607031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155894423-C-T

35607066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155894458-G-T

35607183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155894563-A-G

http://identifiers.org/hco/20/GRCh38#35607202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#155894582-C-A

35607202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 155894582-C-T

35607221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155894596-T-C

http://identifiers.org/hco/20/GRCh38#35607224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155894599-C-A

35607229-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155894604-T-A

http://identifiers.org/hco/20/GRCh38#35607230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155894605-C-A

35607230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155894605-C-T

http://identifiers.org/hco/20/GRCh38#35607237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155894612-C-A

35607237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155894612-C-T

35607295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 155894668-A-G

http://identifiers.org/hco/20/GRCh38#35607366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155894743-C-A

35607366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155894743-C-T

http://identifiers.org/hco/20/GRCh38#35607375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155894752-C-A

35607388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155894765-T-C

35607404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155894778-G-A

35607404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 155894778-G-T

http://identifiers.org/hco/20/GRCh38#35607410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#155894784-C-A

35607418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155894792-G-A

35607418-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non coding transcript exon variant
orthologous variants: 155894792-G-C

35607429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 155894803-T-C

35607449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 155894823-G-A

http://identifiers.org/hco/20/GRCh38#35607500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#155894873-C-A

35607502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15801
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 155894875-G-A