45092810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: 3 prime UTR variant
orthologous variants: 122109877-T-C

45092953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: 3 prime UTR variant
orthologous variants: 122110001-A-G

45092953-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: 3 prime UTR variant
orthologous variants: 122110001-A-T

45093044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: 3 prime UTR variant
orthologous variants: 122110098-C-T

45093120-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: 3 prime UTR variant
orthologous variants: 122110166-G-C

45093165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: 3 prime UTR variant
orthologous variants: 122110198-C-T

http://identifiers.org/hco/15/GRCh38#45093260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122110265-C-A

http://identifiers.org/hco/15/GRCh38#45093327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122110327-C-A

45093336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: 3 prime UTR variant
orthologous variants: 122110336-C-T

http://identifiers.org/hco/15/GRCh38#45093354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122110352-C-A

45093354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: 3 prime UTR variant
orthologous variants: 122110352-C-T

45093362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: 3 prime UTR variant
orthologous variants: 122110360-T-C

45093362-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: 3 prime UTR variant
orthologous variants: 122110360-T-G

45093568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: 3 prime UTR variant
orthologous variants: 122110549-A-G

45093581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: 3 prime UTR variant
orthologous variants: 122110562-C-T

http://identifiers.org/hco/15/GRCh38#45093614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122110597-C-A

45093614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: 3 prime UTR variant
orthologous variants: 122110597-C-T

45093647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: 3 prime UTR variant
orthologous variants: 122110611-A-G

45093647-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: 3 prime UTR variant
orthologous variants: 122110611-A-T

http://identifiers.org/hco/15/GRCh38#45093700-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122110661-A-C

45093700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: 3 prime UTR variant
orthologous variants: 122110661-A-G

45093700-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: 3 prime UTR variant
orthologous variants: 122110661-A-T

45093715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: 3 prime UTR variant
orthologous variants: 122110674-T-C

45093715-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: 3 prime UTR variant
orthologous variants: 122110674-T-G

45093807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: 3 prime UTR variant
orthologous variants: 122110766-G-A

45093807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: 3 prime UTR variant
orthologous variants: 122110766-G-T

45094039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: 3 prime UTR variant
orthologous variants: 122110844-C-T

45094148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: 3 prime UTR variant
orthologous variants: 122110916-G-A

http://identifiers.org/hco/15/GRCh38#45094149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122110917-C-A

45094184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: missense variant
orthologous variants: 122110952-C-T

45094390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron variant
orthologous variants: 122111128-G-A

45094404-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron variant
orthologous variants: 122111142-T-G

45094820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron variant
orthologous variants: 122111343-C-T

45094822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron variant
orthologous variants: 122111345-C-T

45094849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron variant
orthologous variants: 122111363-C-T

http://identifiers.org/hco/15/GRCh38#45094916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122111375-C-A

45094957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: synonymous variant
orthologous variants: 122111416-G-A

45095010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: missense variant
orthologous variants: 122111469-G-A

45095129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron variant
orthologous variants: 122111586-T-C

http://identifiers.org/hco/15/GRCh38#45095157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122111604-C-A

45095467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: synonymous variant
orthologous variants: 122111883-T-C

45095467-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: synonymous variant
orthologous variants: 122111883-T-G

45095674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron variant
orthologous variants: 122112090-G-A

45095705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron variant
orthologous variants: 122112101-G-T

45095733-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron variant
orthologous variants: 122112129-T-A

45095746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron variant
orthologous variants: 122112148-G-A

45095746-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron variant
orthologous variants: 122112148-G-C

45095746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron variant
orthologous variants: 122112148-G-T

45095803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron variant
orthologous variants: 122112170-A-G

45095883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: missense variant
orthologous variants: 122112253-C-T

http://identifiers.org/hco/15/GRCh38#45095966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122112336-C-A

45096026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: synonymous variant
orthologous variants: 122112396-G-A

45096026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: synonymous variant
orthologous variants: 122112396-G-T

45096111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron variant
orthologous variants: 122112472-A-G

45096710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron variant
orthologous variants: 122112911-T-C

45096827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron variant
orthologous variants: 122113027-T-C

45096944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron variant
orthologous variants: 122113150-C-T

45097065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron variant
orthologous variants: 122113404-T-C

45097131-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron variant
orthologous variants: 122113449-A-T

http://identifiers.org/hco/15/GRCh38#45097138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122113454-C-A

45097138-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron variant
orthologous variants: 122113454-C-G

45097229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron variant
orthologous variants: 122113534-G-A

45097254-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: synonymous variant
orthologous variants: 122113558-C-G

45097254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: synonymous variant
orthologous variants: 122113558-C-T

45097266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: synonymous variant
orthologous variants: 122113570-G-A

45097266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: missense variant
orthologous variants: 122113570-G-T

45097698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: synonymous variant
orthologous variants: 122114015-A-G

http://identifiers.org/hco/15/GRCh38#45097749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122114066-C-A

45097749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 122114066-C-T

45097855-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron variant
orthologous variants: 122114175-C-G

45097929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron variant
orthologous variants: 122114243-T-C

45097981-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron variant
orthologous variants: 122114292-C-G

45097981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron variant
orthologous variants: 122114292-C-T

45097999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron variant
orthologous variants: 122114320-C-T

45098062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 122114383-G-A

45098063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 122114384-G-A

45098190-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron variant
orthologous variants: 122114503-A-T

45098268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron variant
orthologous variants: 122114579-T-C

http://identifiers.org/hco/15/GRCh38#45098394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122114689-C-A

45098465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron variant
orthologous variants: 122114751-G-T

45098473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron variant
orthologous variants: 122114760-A-G

45098481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron variant
orthologous variants: 122114768-T-C

45098482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron variant
orthologous variants: 122114769-G-A

45098556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron variant
orthologous variants: 122114837-G-A

45099375-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 122115046-G-C

45099375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 122115046-G-T

45099427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 122115098-G-A

45100219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 122115811-C-T

http://identifiers.org/hco/15/GRCh38#45100384-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122115959-A-C

45100384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122115959-A-G

45100402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122115976-T-C

http://identifiers.org/hco/15/GRCh38#45100411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122115985-C-A

http://identifiers.org/hco/15/GRCh38#45100420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122115995-C-A

45100420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122115995-C-T

45100534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122116130-C-T

http://identifiers.org/hco/15/GRCh38#45100558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122116162-C-A

45100558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122116162-C-T

45100633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122116236-A-G

45100744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122116495-G-A

http://identifiers.org/hco/15/GRCh38#45100801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122116552-C-A

45100983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 122116745-A-G

45100983-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 122116745-A-T

45100999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 122116760-G-T

http://identifiers.org/hco/15/GRCh38#45101007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122116768-C-A

45101007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 122116768-C-T

45101043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 122116805-G-A

45101131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 122116886-G-A

45101131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 122116886-G-T

45101139-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 122116894-T-A

45101139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 122116894-T-C

http://identifiers.org/hco/15/GRCh38#45101158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122116917-C-A

45101167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: -C-T

45101194-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 122116953-T-G

45101327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122117085-A-G

45101437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122117202-A-G

45101484-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122117242-T-A

45101484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122117242-T-C

45101613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122117342-G-A

45101613-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122117342-G-C

45101613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122117342-G-T

45101619-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122117348-T-A

45101619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122117348-T-C

45101744-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122117460-T-G

45101859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 122117548-G-A

45101859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 122117548-G-T

45101887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 122117576-C-T

45101911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 122117600-C-T

45101980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 122117669-G-A

45102027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122117712-G-A

45102027-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122117712-G-C

45102080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122117750-G-A

http://identifiers.org/hco/15/GRCh38#45102135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122117803-C-A

45102152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122117820-G-A

45102393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122118065-G-A

45102855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122118675-G-A

45103351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122119252-T-C

45103745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122119564-G-A

45103781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122119600-A-G

45103953-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 122119766-C-G

45104104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122119915-G-T

http://identifiers.org/hco/15/GRCh38#45104135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122119944-C-A

45104135-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122119944-C-G

45104243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 122120052-G-A

45104392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122120200-G-A

45104492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122120291-G-A

45104492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122120291-G-T

45104497-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122120296-T-A

45104644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122120447-G-A

45104664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122120467-G-A

45104671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122120474-C-T

45104732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122120523-C-T

http://identifiers.org/hco/15/GRCh38#45105218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122120696-C-A

45105373-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122120860-T-A

45105443-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122120926-C-G

45105526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122120978-A-G

http://identifiers.org/hco/15/GRCh38#45105539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122120991-C-A

45105539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122120991-C-T

45105564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122121016-C-T

http://identifiers.org/hco/15/GRCh38#45105576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122121025-C-A

45105579-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122121028-T-A

http://identifiers.org/hco/15/GRCh38#45105765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122121199-C-A

45105765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 122121199-C-T

45105790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 122121224-A-G

45105850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122121284-C-T

45105991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122121419-G-A

45105991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122121419-G-T

http://identifiers.org/hco/15/GRCh38#45106014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122121442-C-A

45106045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122121473-G-A

45106045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122121473-G-T

45106050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122121478-G-T

45106083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122121504-G-A

45106106-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122121526-G-C

45106116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122121536-G-A

45106116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122121536-G-T

45106332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 122121752-G-A

45106343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122121763-T-C

45106343-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122121763-T-G

45106433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122121841-G-A

45106433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122121841-G-T

45106456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122121864-G-A

45106456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122121864-G-T

45106577-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 122121971-C-G

45106577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 122121971-C-T

45106593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 122121987-T-C

45106704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122122105-A-G

45106739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122122141-C-T

45106744-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122122145-T-A

http://identifiers.org/hco/15/GRCh38#45106777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122122177-C-A

45106777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122122177-C-T

45106850-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 122122311-G-C

45106850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 122122311-G-T

45106917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 122122378-A-G

http://identifiers.org/hco/15/GRCh38#45106930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122122391-C-A

45106930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 122122391-C-T

45106992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122122454-C-T

http://identifiers.org/hco/15/GRCh38#45107026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122122486-C-A

45107026-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122122486-C-G

45107034-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122122494-C-G

45107034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122122494-C-T

http://identifiers.org/hco/15/GRCh38#45107083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122122542-C-A

45107083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122122542-C-T

45107105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122122565-A-G

45107169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122122615-G-T

45107205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122122645-G-A

45107235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122122664-A-G

45107278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122122696-C-T

45107294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122122708-T-C

45107305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122122719-T-C

45107339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122122734-A-G

45107339-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122122734-A-T

45107381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 122122776-T-C

45107436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 122122831-G-A

45107436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 122122831-G-T

45107507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122122901-C-T

45107981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122123007-G-T

45108005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122123032-G-A

45108094-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 122123120-T-A

45108094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 122123120-T-C

45108094-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 122123120-T-G

45108145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 122123171-G-A

45108244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 122123270-G-A

45108244-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 122123270-G-C

45108245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 122123271-G-A

45108756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 122123738-T-C

45108909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 122123905-C-T

45109002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 122123986-T-C

http://identifiers.org/hco/15/GRCh38#45109189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122124143-C-A

http://identifiers.org/hco/15/GRCh38#45109305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122124268-C-A

45109310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 122124273-A-G

45109311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 122124274-T-C

45109349-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 122124303-T-A

45109367-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 122124321-A-T

45109404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 122124358-G-A

45109404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 122124358-G-T

45109406-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 122124360-C-G

45109503-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 122124459-C-G

45109503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 122124459-C-T

45109542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 122124490-C-T

45109546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 122124494-G-A

45109590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 122124538-G-A

45109619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 122124567-T-C

http://identifiers.org/hco/15/GRCh38#45109649-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122124597-A-C

45109692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 122124853-A-G

45109697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 122124858-A-G

45109710-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 122124892-A-T

45109722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 122124905-G-A

45109819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 122124997-G-T

http://identifiers.org/hco/15/GRCh38#45109847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122125023-C-A

45109867-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 122125047-C-G

45109876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 122125056-G-A

45110052-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122125230-G-C

http://identifiers.org/hco/15/GRCh38#45110362-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122125499-C-A

http://identifiers.org/hco/15/GRCh38#45110416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122125554-C-A

45110416-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122125554-C-G

45110416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122125554-C-T

45110423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122125561-C-T

45110574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122125690-A-G

45110575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122125691-T-C

45110579-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122125695-C-G

45110586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122125702-C-T

45110717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 122125842-G-A

45110733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122125858-G-A

45110940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122126284-A-G

45111013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122126378-G-A

45111019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122126386-G-A

45111019-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122126386-G-C

45111019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122126386-G-T

45111037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122126405-G-A

45111037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122126405-G-T

45111094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 122126459-G-A

45111147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 122126512-G-T

45111273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 122126638-G-T

45111298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 122126662-C-T

45111350-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 122126741-C-G

http://identifiers.org/hco/15/GRCh38#45111366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122126757-C-A

45111412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 122126827-G-A

45111412-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 122126827-G-C

45111412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 122126827-G-T

http://identifiers.org/hco/15/GRCh38#45111427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#122126842-C-A

45111427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 122126842-C-T

45111591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: 122127006-G-A

45111591-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: 122127006-G-C

45111591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: 122127006-G-T

45111672-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 122127051-G-C

45111672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 122127051-G-T

http://identifiers.org/hco/15/GRCh38#45111686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122127061-C-A

http://identifiers.org/hco/15/GRCh38#45111713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122127086-C-A

45111713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 122127086-C-T

45111714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 122127087-C-T

45111748-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 122127124-C-G

45111748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 122127124-C-T

45111749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 122127125-G-A

45111749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 122127125-G-T

http://identifiers.org/hco/15/GRCh38#45111754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122127130-C-A

45111801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 122127196-C-T

45111805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 122127200-G-A

45111805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 122127200-G-T

45111900-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 122127295-C-G

45111900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 122127295-C-T

45111936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 122127331-G-A

45111936-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 122127331-G-C

45111936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 122127331-G-T

45112054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122127432-G-A

45112054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122127432-G-T

45112056-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122127434-T-G

45112117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122127502-T-C

45112117-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122127502-T-G

45112272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122127633-G-A

45112307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122127667-T-C

45112311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122127671-G-A

http://identifiers.org/hco/15/GRCh38#45112538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122127840-C-A

45112538-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122127840-C-G

45112561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 122127864-G-A

45112867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122128119-C-T

http://identifiers.org/hco/15/GRCh38#45112907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122128138-C-A

http://identifiers.org/hco/15/GRCh38#45112937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122128148-C-A

45112937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122128148-C-T

45113033-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 122128250-A-T

http://identifiers.org/hco/15/GRCh38#45113122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122128339-C-A

45113122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122128339-C-T

45113192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122128413-T-C

45113228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122128459-G-T

http://identifiers.org/hco/15/GRCh38#45113234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122128464-C-A

45113234-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122128464-C-G

45113234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122128464-C-T

http://identifiers.org/hco/15/GRCh38#45113264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122128500-C-A

45113264-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122128500-C-G

45113264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122128500-C-T

45113461-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron variant
orthologous variants: 122128682-G-C

45113461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron variant
orthologous variants: 122128682-G-T

http://identifiers.org/hco/15/GRCh38#45113507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122128700-C-A

45113507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron variant
orthologous variants: 122128700-C-T

45113693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron variant
orthologous variants: 122128831-G-A

45113726-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron variant
orthologous variants: 122128844-A-T

45113848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron variant
orthologous variants: 122128949-G-A

45113848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron variant
orthologous variants: 122128949-G-T

http://identifiers.org/hco/15/GRCh38#45113860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122128962-C-A

http://identifiers.org/hco/15/GRCh38#45113877-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122128970-A-C

45113877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron variant
orthologous variants: 122128970-A-G

http://identifiers.org/hco/15/GRCh38#45113922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122128996-C-A

45113922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron variant
orthologous variants: 122128996-C-T

http://identifiers.org/hco/15/GRCh38#45113929-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122129003-A-C

45113929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron variant
orthologous variants: 122129003-A-G

45113929-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron variant
orthologous variants: 122129003-A-T

45113938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron variant
orthologous variants: 122129012-G-A

45113938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron variant
orthologous variants: 122129012-G-T

45113942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron variant
orthologous variants: 122129017-G-A

45113942-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron variant
orthologous variants: 122129017-G-C

45113942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: intron variant
orthologous variants: 122129017-G-T

45113989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: 5 prime UTR variant
orthologous variants: 122129050-T-C

45113989-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: 5 prime UTR variant
orthologous variants: 122129050-T-G

45113994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: 5 prime UTR variant
orthologous variants: 122129055-G-T

45114003-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: 5 prime UTR variant
orthologous variants: 122129064-G-T

http://identifiers.org/hco/15/GRCh38#45114036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122129096-C-A

45114036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: 5 prime UTR variant
orthologous variants: 122129096-C-T

http://identifiers.org/hco/15/GRCh38#45114049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#122129109-C-A

45114146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13273
most severe consequence: 5 prime UTR variant
orthologous variants: 122129181-C-T