37820501-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: non coding transcript exon variant
orthologous variants: 79809474-G-C

37820501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: non coding transcript exon variant
orthologous variants: 79809474-G-T

37820568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: non coding transcript exon variant
orthologous variants: 79809542-C-T

37821005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79809890-A-G

37821605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79810456-T-C

http://identifiers.org/hco/2/GRCh38#37821860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79810715-C-A

37821860-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79810715-C-G

37821864-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79810719-C-G

37821926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79810751-A-G

37821973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79810793-T-C

37822151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79810976-T-C

37822492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79811315-T-C

37822618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79811444-G-A

http://identifiers.org/hco/2/GRCh38#37822778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79811600-C-A

37822778-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79811600-C-G

37822778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79811600-C-T

37822779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79811601-G-A

37822792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79811615-A-G

37822834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79811653-C-T

37823670-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79811981-T-A

37823769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79812077-G-A

37823769-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79812077-G-C

37823857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79812172-G-T

37824334-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79813156-G-C

37824584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79813379-C-T

37824789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79813580-C-T

37824820-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79813610-G-C

37824820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79813610-G-T

37824831-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79813623-T-G

37824842-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79813634-A-T

http://identifiers.org/hco/2/GRCh38#37825370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79814094-C-A

37825469-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79814192-G-C

37825494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79814217-C-T

37825722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79814383-C-T

37825991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79815684-A-G

http://identifiers.org/hco/2/GRCh38#37826106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79815745-C-A

37826106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79815745-C-T

http://identifiers.org/hco/2/GRCh38#37826117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79815756-C-A

37826134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79815773-G-A

37826151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79815788-A-G

37826187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79815825-G-A

37826187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79815825-G-T

37826203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79815836-A-G

37826255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79815886-A-G

37826406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79816016-A-G

http://identifiers.org/hco/2/GRCh38#37826431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79816041-C-A

37826432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79816042-T-C

37826441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79816051-C-T

37826447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79816057-G-A

37826447-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79816057-G-C

37827171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79816628-G-A

37827171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79816628-G-T

37827303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79816759-T-C

37827342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79816796-G-T

37827434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79816888-C-T

37827562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79817021-G-T

http://identifiers.org/hco/2/GRCh38#37827596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79817050-C-A

37827711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79817164-G-A

37827748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79817200-T-C

http://identifiers.org/hco/2/GRCh38#37827852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79817309-C-A

37827852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79817309-C-T

37827892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79817349-A-G

http://identifiers.org/hco/2/GRCh38#37827951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79817393-C-A

37827951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79817393-C-T

37828011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79817452-A-G

37828829-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79818293-A-T

37828838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79818302-T-C

37829264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79818461-A-G

37829272-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79818468-T-G

37829278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79818473-G-A

37829278-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79818473-G-C

37829278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79818473-G-T

37829300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79818495-G-T

37829356-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79818555-C-G

37829411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79818565-G-A

http://identifiers.org/hco/2/GRCh38#37829502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79818658-C-A

37829502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79818658-C-T

37829503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 79818659-C-T

37829545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79818705-G-A

37829545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79818705-G-T

37829599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79818757-C-T

37830026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79819153-G-A

37830034-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79819161-T-A

37830105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79819255-G-A

37830263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79819414-C-T

37831023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79820723-A-G

37831168-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79820869-C-G

37831168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79820869-C-T

37831198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79820901-A-G

37831342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79821023-G-A

37831386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79821067-G-A

37831386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79821067-G-T

37831392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79821073-G-A

37831399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79821080-G-A

37831438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79821119-G-T

37831520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79821198-G-A

37831541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79821219-A-G

http://identifiers.org/hco/2/GRCh38#37831733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79821400-C-A

37831807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79821467-G-T

37831904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79821568-A-G

http://identifiers.org/hco/2/GRCh38#37831989-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79821652-A-C

37831989-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79821652-A-T

37832149-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79821798-A-T

37832233-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79821844-G-T

37832587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79822173-T-C

http://identifiers.org/hco/2/GRCh38#37832644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#79822227-C-A

37832644-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79822227-C-G

37832645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79822228-C-T

37832992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79823131-A-G

37832993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79823132-C-T

37833060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79823199-G-A

37833067-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79823206-G-C

37833089-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79823230-C-G

37833105-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79823246-G-C

37833298-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79823402-T-A

37833299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79823403-A-G

37833299-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79823403-A-T

37833451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79823823-A-G

http://identifiers.org/hco/2/GRCh38#37833481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79823848-C-A

37833483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79823850-C-T

37833697-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79824005-G-C

37833738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79824036-G-A

37833852-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79824152-T-A

37833852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79824152-T-C

37833852-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79824152-T-G

http://identifiers.org/hco/2/GRCh38#37834293-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79824303-A-C

37834300-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79824310-T-G

37834324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79824334-C-T

http://identifiers.org/hco/2/GRCh38#37834401-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79824386-A-C

37834484-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79824462-T-A

37835494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79824832-T-C

http://identifiers.org/hco/2/GRCh38#37835550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79824889-C-A

37835550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79824889-C-T

37835719-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79825042-A-T

37835724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79825047-T-C

http://identifiers.org/hco/2/GRCh38#37835881-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79825191-A-C

37835889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79825196-T-C

37835954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79825313-C-T

37836032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79825410-C-T

http://identifiers.org/hco/2/GRCh38#37836622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79825689-C-A

37836622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79825689-C-T

37836672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79825739-G-A

37836710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79825777-A-G

37836769-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79825831-G-C

http://identifiers.org/hco/2/GRCh38#37836939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79825960-C-A

37836939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79825960-C-T

37836959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79825979-A-G

37837456-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79828646-G-C

http://identifiers.org/hco/2/GRCh38#37837557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79828751-C-A

37837689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79828879-C-T

37837738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79828937-T-C

37838065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79829272-G-T

37838080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79829287-G-A

37838091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79829298-G-A

37838091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79829298-G-T

37838101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79829308-T-C

37838220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79829416-T-C

http://identifiers.org/hco/2/GRCh38#37838458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79829574-C-A

37838467-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79829582-C-G

37838597-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79829702-T-A

37839009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79830139-C-T

37839090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79830209-C-T

http://identifiers.org/hco/2/GRCh38#37839629-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79831105-A-C

37839637-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79831113-T-A

37839732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79831169-A-G

37839793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79831227-C-T

37839800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79831234-G-A

37840058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79832185-G-A

http://identifiers.org/hco/2/GRCh38#37840068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79832196-C-A

http://identifiers.org/hco/2/GRCh38#37840151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79832239-C-A

37840151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79832239-C-T

37840162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79832250-C-T

37840170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79832258-C-T

37840190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79832280-T-C

37840325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79832420-C-T

http://identifiers.org/hco/2/GRCh38#37840378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79832473-C-A

37840413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79832507-G-A

37840497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79832616-A-G

37840518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79832640-T-C

http://identifiers.org/hco/2/GRCh38#37840593-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79832703-A-C

37840593-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79832703-A-T

37840687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79832797-G-A

37840749-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79832859-G-C

37840875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79832976-G-A

http://identifiers.org/hco/2/GRCh38#37840927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79833029-C-A

37840927-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79833029-C-G

37841078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79833176-G-A

37841301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79833451-G-A

37841301-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79833451-G-C

37841350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79833500-T-C

37841360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79833510-T-C

37841394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79833549-C-T

37841494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79833650-A-G

37841520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79833674-C-T

37841613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79833761-C-T

http://identifiers.org/hco/2/GRCh38#37841665-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79833817-A-C

37841665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79833817-A-G

37841755-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79833880-T-A

37841861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79833962-G-A

37841953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79834060-G-A

37841953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79834060-G-T

http://identifiers.org/hco/2/GRCh38#37842710-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79834620-A-C

37843094-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79834871-T-A

37843532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79835318-A-G

37843532-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79835318-A-T

37843638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79835424-T-C

37843912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79835743-A-G

37843954-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79835906-T-G

37843987-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79835977-T-A

37843987-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79835977-T-G

37844259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79836202-T-C

37844381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79836460-G-A

37844402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79836515-G-T

37844499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79836610-T-C

37844570-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79836682-T-G

37844576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79836688-C-T

37844589-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79836703-G-C

37844589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79836703-G-T

http://identifiers.org/hco/2/GRCh38#37844827-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79836885-A-C

37845012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79837077-T-C

37845025-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79837090-T-G

37845095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79837153-T-C

37845189-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79837270-G-C

37845211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79837491-G-T

37845264-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79837544-T-A

37845264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79837544-T-C

37847103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79842435-A-G

37847166-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79842498-C-G

37847216-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79842548-A-T

37847220-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79842552-T-G

37848197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79843193-G-A

37848403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79843381-C-T

37848426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79843404-C-T

37848826-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79844352-A-T

37849089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79844626-C-T

37849129-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79844658-G-C

37849190-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79844726-C-G

37849892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79845031-A-G

37849915-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79845054-A-T

37850438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79845688-T-C

37850438-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79845688-T-G

37850655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79845898-C-T

37850664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79845905-T-C

37850740-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79845950-T-G

37850741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79845951-G-A

37850769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79845979-G-A

37850771-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79845981-G-C

37851341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79846234-G-A

37851425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79846316-G-T

37851429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79846320-T-C

37851462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79846354-T-C

37851483-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79846375-G-C

37851706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79846949-C-T

37851723-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79846957-C-G

37851723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79846957-C-T

37851858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79847066-T-C

37852049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79847242-A-G

37852155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79847348-T-C

37852253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79847446-C-T

37852526-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79847718-C-G

37852526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79847718-C-T

37852656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79847847-C-T

37852695-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79847877-G-C

37852737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79847915-T-C

37853203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79848029-G-A

http://identifiers.org/hco/2/GRCh38#37853323-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79848144-A-C

37853824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79848335-T-C

37854611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79850548-A-G

37854770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79850697-A-G

37854805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79850733-G-A

37854805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79850733-G-T

37854811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79850739-G-T

37855061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79850982-C-T

37855137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79851034-C-T

37855196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79851090-T-C

37855215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79851109-T-C

http://identifiers.org/hco/2/GRCh38#37855319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79851206-C-A

37855328-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79851215-T-A

37855578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79851472-C-T

37855700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79851620-G-T

37855814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79851734-C-T

37855883-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79851801-C-G

37855883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79851801-C-T

37856071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79851966-G-T

37856087-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79851982-C-G

37856162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79852055-T-C

37856166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79852059-C-T

37856232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79852114-G-A

37856308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79852190-G-T

37856447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79852331-C-T

37856465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79852349-A-G

37856465-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79852349-A-T

37856481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79852366-G-A

37856581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79852647-G-A

37856581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79852647-G-T

37856666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79852755-C-T

37856697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79852786-G-A

37856726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 79852817-C-T

37856763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79852849-C-T

37856790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79852877-C-T

37856813-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79852899-T-A

37856813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79852899-T-C

37856901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79852977-C-T

37856960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79853040-A-G

37856988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79853067-T-C

37857509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79853217-C-T

37857545-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79853254-G-C

37857830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79853519-C-T

37857902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79853584-C-T

37858309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79854969-T-C

37858335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79854995-G-A

37858486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79855155-G-A

37858486-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79855155-G-C

37858670-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79855316-C-G

37859008-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79855617-T-G

37859816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79855861-A-G

http://identifiers.org/hco/2/GRCh38#37859946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79855989-C-A

37860030-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79856411-A-T

http://identifiers.org/hco/2/GRCh38#37860038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79856419-C-A

37860038-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79856419-C-G

37860038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79856419-C-T

37860139-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79856501-C-G

37860139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79856501-C-T

http://identifiers.org/hco/2/GRCh38#37860184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79856546-C-A

37860184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79856546-C-T

http://identifiers.org/hco/2/GRCh38#37860198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79856560-C-A

37860644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79857211-A-G

37860866-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79858135-T-A

37860944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79858218-G-A

37860994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79858266-G-A

37860994-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79858266-G-C

http://identifiers.org/hco/2/GRCh38#37861139-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79858406-A-C

37861281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79858548-T-C

37861395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79858655-G-A

37861416-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79858676-A-T

http://identifiers.org/hco/2/GRCh38#37861691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79858916-C-A

http://identifiers.org/hco/2/GRCh38#37861922-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79859114-C-A

37861922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79859114-C-T

37861939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79859130-C-T

http://identifiers.org/hco/2/GRCh38#37861970-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79859160-A-C

37862168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79859319-A-G

37862168-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79859319-A-T

37862169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79859320-G-A

37862169-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79859320-G-C

37862169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79859320-G-T

37862170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79859321-G-A

37862170-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79859321-G-C

37862170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79859321-G-T

http://identifiers.org/hco/2/GRCh38#37862176-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79859327-A-C

37862176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79859327-A-G

37862176-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79859327-A-T

37862388-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79859522-T-G

37864501-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79860198-T-G

37864647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79860345-C-T

37864714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79860418-C-T

37864866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79860561-C-T

37864886-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79860582-C-G

http://identifiers.org/hco/2/GRCh38#37864898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79860594-C-A

37865055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79860734-T-C

37865211-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: non coding transcript exon variant
orthologous variants: 79860876-G-C

37865211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: non coding transcript exon variant
orthologous variants: 79860876-G-T

37865289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79860962-G-A

http://identifiers.org/hco/2/GRCh38#37865718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79861324-C-A

37865983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79861587-C-T

37865996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79861599-C-T

37866260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79861849-A-G

37866588-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79862080-T-A

37866732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79862224-T-C

37866887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79862370-T-C

37867138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79862611-T-C

37867222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79862695-G-A

37867222-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79862695-G-C

37867240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79862715-C-T

37867648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79863129-T-C

37867650-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79863131-C-G

37867682-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79863163-C-G

37867767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79863234-G-A

http://identifiers.org/hco/2/GRCh38#37867769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79863236-C-A

37867769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79863236-C-T

37871352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79869998-A-G

37871466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79870216-G-A

37871531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79870254-A-G

37871531-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79870254-A-T

37871705-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79870518-C-G

37871711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79870524-G-A

37871755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79870565-C-T

37871805-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79870616-T-G

37871859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79870672-T-C

http://identifiers.org/hco/2/GRCh38#37872252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79871040-C-A

37872422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79871180-A-G

37872536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79871298-G-A

37872735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79871510-T-C

37872983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79871696-A-G

37873551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79872216-G-A

http://identifiers.org/hco/2/GRCh38#37873668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79872333-C-A

37875159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79872872-A-G

37875436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79873053-C-T

http://identifiers.org/hco/2/GRCh38#37875510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79873112-C-A

37875510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79873112-C-T

37875535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79873136-G-A

37875678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79873272-G-T

http://identifiers.org/hco/2/GRCh38#37875742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79873328-C-A

37875742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 79873328-C-T

37875755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79873334-G-T

37875759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79873338-C-T

http://identifiers.org/hco/2/GRCh38#37875772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79873351-C-A

37875772-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79873351-C-G

http://identifiers.org/hco/2/GRCh38#37875803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79873380-C-A

37875831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79873433-A-G

37875849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79873451-G-A

37875849-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79873451-G-C

37875849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79873451-G-T

http://identifiers.org/hco/2/GRCh38#37875850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#79873458-C-A

37875850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 79873458-C-T

37875888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 79873495-G-A

37875888-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 79873495-G-T

37875891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 79873498-A-G

37876000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79873579-T-C

37876080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 79873642-A-G

37876219-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: non coding transcript exon variant
orthologous variants: 79873757-C-G

37876223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37459
most severe consequence: non coding transcript exon variant
orthologous variants: 79873760-G-A