9418461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66457984-A-G

9418544-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66457903-T-A

9418544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66457903-T-C

http://identifiers.org/hco/12/GRCh38#9418652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#66457821-C-A

9418652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 66457821-C-T

9418703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 66457792-G-A

9418745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66457749-G-A

http://identifiers.org/hco/12/GRCh38#9418770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#66457726-C-A

9418770-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66457726-C-G

9418813-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66457683-T-G

9418842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66457654-G-A

9418931-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 66457565-T-A

9418931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 66457565-T-C

9418931-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 66457565-T-G

9418935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 66457561-T-C

http://identifiers.org/hco/12/GRCh38#9419087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#66457425-C-A

9419087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66457425-C-T

9419117-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66457397-G-C

9419117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66457397-G-T

9419154-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66457360-G-C

9419154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66457360-G-T

9419221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66457286-T-C

9419276-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66457251-A-T

9419297-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66457235-T-A

9419297-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66457235-T-G

9419349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66457181-A-G

9419450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66457081-C-T

9419456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66457075-T-C

http://identifiers.org/hco/12/GRCh38#9419464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#66457070-C-A

9419464-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66457070-C-G

9419464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66457070-C-T

9419918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66456368-G-A

http://identifiers.org/hco/12/GRCh38#9419965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#66456323-C-A

9420010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66456277-T-C

9420021-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66456266-T-G

9420053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66456234-G-A

9420053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66456234-G-T

9420072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66456215-G-A

9420072-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66456215-G-C

9420227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66456052-T-C

9420227-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66456052-T-G

9420245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66456034-T-C

9420271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66456008-G-A

9420271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66456008-G-T

9420329-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66455956-T-A

9420329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66455956-T-C

9420397-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66455889-T-A

9420397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66455889-T-C

9420397-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66455889-T-G

9420442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66455864-G-A

9420442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66455864-G-T

9420519-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66455792-T-A

9420519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66455792-T-C

9420532-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66455779-G-C

9420586-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66455725-C-G

9420586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66455725-C-T

9420795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66455597-A-G

9420961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66455440-G-A

9420961-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66455440-G-C

9421019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66455394-C-T

9421045-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66455368-C-G

9421100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66455325-G-A

9421100-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66455325-G-C

9421134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66455296-G-T

9421227-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66455210-T-G

9421255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66455182-G-A

9421255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66455182-G-T

http://identifiers.org/hco/12/GRCh38#9421261-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#66455176-A-C

9421261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66455176-A-G

9421263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66455174-T-C

9421263-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66455174-T-G

http://identifiers.org/hco/12/GRCh38#9421286-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#66455153-C-A

9421286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66455153-C-T

9421300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66455140-A-G

9421360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66455116-G-A

9421360-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66455116-G-C

9421360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66455116-G-T

9421374-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66455102-T-G

9421476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66455000-G-A

9421476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66455000-G-T

http://identifiers.org/hco/12/GRCh38#9421504-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#66454972-A-C

9421504-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66454972-A-T

9421511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66454966-G-T

9421659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66454827-A-G

9421681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66454805-G-A

9421681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66454805-G-T

9421810-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 66454742-C-G

9421844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66454707-G-A

9421844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66454707-G-T

9421980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66454569-G-A

9421980-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66454569-G-C

9421980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66454569-G-T

9422032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66454528-A-G

9422059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66454505-G-A

9422064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66454500-G-A

9424256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66451511-G-A

9424256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66451511-G-T

http://identifiers.org/hco/12/GRCh38#9424394-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#66451375-A-C

9424394-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66451375-A-T

9424421-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66451348-T-A

9424421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66451348-T-C

9424421-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66451348-T-G

9424422-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66451347-T-A

9424422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66451347-T-C

9424422-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66451347-T-G

http://identifiers.org/hco/12/GRCh38#9424441-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#66451328-A-C

9424441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66451328-A-G

9424441-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66451328-A-T

http://identifiers.org/hco/12/GRCh38#9424527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#66451284-C-A

9424527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 66451284-C-T

http://identifiers.org/hco/12/GRCh38#9424577-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#66451234-A-C

9424577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66451234-A-G

9424602-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66451209-T-A

9425291-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66450890-T-A

http://identifiers.org/hco/12/GRCh38#9425363-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#66450825-C-A

9425391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66450809-G-T

9425397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66450803-T-C

9425459-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66450777-C-G

9425459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66450777-C-T

9425518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66450718-G-A

9425536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66450700-A-G

9425536-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66450700-A-T

http://identifiers.org/hco/12/GRCh38#9425573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#66450663-C-A

9425686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66450569-C-T

9425715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 66450540-C-T

9425778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66450477-T-C

http://identifiers.org/hco/12/GRCh38#9425977-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#66450295-A-C

9425977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66450295-A-G

9425977-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66450295-A-T

9426005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66450274-G-A

9426005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66450274-G-T

http://identifiers.org/hco/12/GRCh38#9426172-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#66450140-A-C

9427114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66447994-G-A

9427114-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66447994-G-C

9427298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66447833-T-C

9427655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66447389-A-G

9427680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66447364-T-C

9427681-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66447363-G-C

9427688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66447356-T-C

9427740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66447305-T-C

9427755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66447290-A-G

http://identifiers.org/hco/12/GRCh38#9427793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#66447252-C-A

9427793-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66447252-C-G

9427874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66447173-G-A

9427874-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66447173-G-C

9427886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66447161-A-G

9427921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66447119-T-C

9429028-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66446560-T-A

9429028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66446560-T-C

9429031-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66446557-T-A

9429031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66446557-T-C

http://identifiers.org/hco/12/GRCh38#9429040-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#66446548-A-C

9429040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66446548-A-G

9429061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66446527-G-T

9429071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66446517-G-A

9429100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66446503-C-T

9429121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66446481-G-A

9429121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66446481-G-T

http://identifiers.org/hco/12/GRCh38#9429139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#66446463-C-A

9429139-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66446463-C-G

9429171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66446431-T-C

9429174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66446428-G-A

9429179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66446423-A-G

9429180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66446422-G-A

9429191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66446411-T-C

9429200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66446402-T-C

9429212-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 66446390-C-G

http://identifiers.org/hco/12/GRCh38#9429220-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#66446382-A-C

http://identifiers.org/hco/12/GRCh38#9429235-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#66446368-A-C

9429242-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66446361-G-C

9429259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66446345-T-C

9429259-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66446345-T-G

9429271-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66446332-C-G

9429271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66446332-C-T

9429272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66446331-C-T

http://identifiers.org/hco/12/GRCh38#9429275-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#66446328-A-C

9429275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66446328-A-G

9429275-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66446328-A-T

9429295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66446310-G-A

9429295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66446310-G-T

9429296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66446309-T-C

9429342-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66446263-A-T

9429383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66446236-C-T

9429410-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66446210-C-G

http://identifiers.org/hco/12/GRCh38#9429454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#66446181-C-A

9429454-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66446181-C-G

9429454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66446181-C-T

9429456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66446179-G-A

9429456-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66446179-G-C

9429456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66446179-G-T

9429589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66446038-G-A

9429589-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66446038-G-C

9429669-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66445961-A-T

9429722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66445911-G-A

9429722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66445911-G-T

9429735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66445897-G-A

9429752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66445854-T-C

9429802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66445817-G-A

9430176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66445575-C-T

9430237-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66445507-T-G

9430415-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66445375-C-G

9430451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66445348-G-T

9430494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66445309-T-C

9430515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66445288-G-A

9430515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66445288-G-T

http://identifiers.org/hco/12/GRCh38#9430541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#66445262-C-A

9430576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66445244-A-G

9430576-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66445244-A-T

9430627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66445193-G-A

9430627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66445193-G-T

9430635-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66445185-T-A

9430635-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66445185-T-G

9430669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66445151-G-A

9430669-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66445151-G-C

9430669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66445151-G-T

9430715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66445105-A-G

9430733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66445087-A-G

9430733-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66445087-A-T

http://identifiers.org/hco/12/GRCh38#9430831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#66444971-C-A

9430831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66444971-C-T

9430856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66444938-G-A

9430856-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66444938-G-C

9430856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66444938-G-T

9431134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66444693-A-G

9431204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66444631-G-A

9431204-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66444631-G-C

9431207-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66444628-A-T

9431531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66444240-C-T

http://identifiers.org/hco/12/GRCh38#9431570-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#66444145-A-C

9431659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66444061-A-G

9431977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66443839-G-A

http://identifiers.org/hco/12/GRCh38#9432157-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#66443712-A-C

9432205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66443668-C-T

9432222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66443651-G-A

9432222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66443651-G-T

9432233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66443640-G-A

9432233-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66443640-G-T

9432344-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66443509-T-A

9432376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66443477-G-A

9432376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66443477-G-T

http://identifiers.org/hco/12/GRCh38#9432391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#66443462-C-A

9432391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66443462-C-T

http://identifiers.org/hco/12/GRCh38#9432399-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#66443454-A-C

9432402-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66443451-G-C

9432402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66443451-G-T

9432453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66443400-C-T

9432482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66443371-G-A

9432482-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66443371-G-C

http://identifiers.org/hco/12/GRCh38#9432485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#66443368-C-A

9432485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66443368-C-T

http://identifiers.org/hco/12/GRCh38#9432527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#66443326-C-A

9432534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66443319-C-T

9432550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66443303-T-C

http://identifiers.org/hco/12/GRCh38#9432555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#66443298-C-A

9432586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66443269-A-G

9432586-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66443269-A-T

http://identifiers.org/hco/12/GRCh38#9432611-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#66443244-A-C

9432629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66443226-G-A

9432629-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66443226-G-C

9432699-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66443169-T-A

http://identifiers.org/hco/12/GRCh38#9432704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#66443164-C-A

9432704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66443164-C-T

9432753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66443128-A-G

http://identifiers.org/hco/12/GRCh38#9432848-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#66443040-A-C

9432902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66442975-A-G

9432902-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66442975-A-T

9432992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66442879-A-G

9432992-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66442879-A-T

http://identifiers.org/hco/12/GRCh38#9433142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#66441336-C-A

9433142-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66441336-C-G

9433142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66441336-C-T

9433172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66441306-C-T

http://identifiers.org/hco/12/GRCh38#9433182-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#66441297-A-C

9433182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66441297-A-G

9433256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66441231-T-C

9433356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66441137-C-T

http://identifiers.org/hco/12/GRCh38#9433375-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#66441118-A-C

9433449-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66441044-G-C

http://identifiers.org/hco/12/GRCh38#9433513-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#66441002-A-C

9433515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66441000-G-A

9433522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66440993-G-A

9433522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66440993-G-T

9433620-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66440890-T-G

9434115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66440235-C-T

9434119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66440231-G-A

9434119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66440231-G-T

9434127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66440223-C-T

9434132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66440218-T-C

http://identifiers.org/hco/12/GRCh38#9436942-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#66437832-C-A

9436942-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 66437832-C-G

9436942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 66437832-C-T

http://identifiers.org/hco/12/GRCh38#9436947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#66437827-C-A

9436947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 66437827-C-T

http://identifiers.org/hco/12/GRCh38#9437003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#66437774-C-A

9437003-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66437774-C-G

9437003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66437774-C-T

9437013-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66437764-T-A

9437013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66437764-T-C

9437013-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66437764-T-G

http://identifiers.org/hco/12/GRCh38#9437018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#66437759-C-A

9437018-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66437759-C-G

9437018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66437759-C-T

9437019-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66437758-T-A

9437019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66437758-T-C

9437019-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66437758-T-G

9437037-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66437740-T-A

9437037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66437740-T-C

http://identifiers.org/hco/12/GRCh38#9437050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#66437727-C-A

9437050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66437727-C-T

http://identifiers.org/hco/12/GRCh38#9437070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#66437707-C-A

9437070-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66437707-C-G

9437070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66437707-C-T

9437132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66437654-G-A

9437132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66437654-G-T

9437143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66437643-T-C

9437163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66437624-T-C

9437163-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66437624-T-G

9437190-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66437616-C-G

9437211-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66437604-G-C

9437306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66437583-T-C

9437306-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66437583-T-G

http://identifiers.org/hco/12/GRCh38#9437365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#66437572-C-A

9437365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66437572-C-T

9437394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66437548-G-A

9437425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66437517-A-G

9437463-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66437479-T-A

9437463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66437479-T-C

http://identifiers.org/hco/12/GRCh38#9437533-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#66437422-A-C

9437533-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66437422-A-T

http://identifiers.org/hco/12/GRCh38#9437596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#66437386-C-A

9437596-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66437386-C-G

9437596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66437386-C-T

9437678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66437356-G-A

9437678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66437356-G-T

9437686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66437347-G-T

http://identifiers.org/hco/12/GRCh38#9437912-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#66437202-A-C

9437912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66437202-A-G

9437912-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66437202-A-T

http://identifiers.org/hco/12/GRCh38#9437917-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#66437197-A-C

9437917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66437197-A-G

9437917-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66437197-A-T

9437926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66437188-T-C

9437927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66437187-G-A

9437927-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66437187-G-C

9437927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66437187-G-T

http://identifiers.org/hco/12/GRCh38#9437929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#66437174-C-A

9437929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66437174-C-T

http://identifiers.org/hco/12/GRCh38#9437941-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#66437162-A-C

http://identifiers.org/hco/12/GRCh38#9437999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#66437107-C-A

9437999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66437107-C-T

9438001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66437105-C-T

9438017-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66437089-T-G

9438020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66437086-G-A

9438042-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66437064-T-G

9438049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66437057-G-A

9438093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66437013-G-A

9438093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66437013-G-T

9438131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66436978-G-A

9438149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66436960-A-G

9438158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66436951-G-A

9438158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66436951-G-T

9438159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66436950-C-T

9438166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66436943-C-T

9438177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66436932-A-G

9438177-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66436932-A-T

9438178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66436931-G-A

http://identifiers.org/hco/12/GRCh38#9438184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#66436925-C-A

9438184-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66436925-C-G

9438184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66436925-C-T

9438190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66436919-C-T

9438195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66436914-C-T

http://identifiers.org/hco/12/GRCh38#9438258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#66436851-C-A

http://identifiers.org/hco/12/GRCh38#9438263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#66436846-C-A

9438263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 66436846-C-T

9438333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66436779-A-G

9438349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66436763-G-A

9438364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66436750-G-A

9438364-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66436750-G-C

9438364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66436750-G-T

9438375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66436739-T-C

9438402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66436719-A-G

9438402-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66436719-A-T

9438453-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66436677-G-C

9438634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66436504-C-T

9443388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66433463-G-A

9443388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66433463-G-T

9443409-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66433442-G-C

9443409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66433442-G-T

9443450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66433402-A-G

http://identifiers.org/hco/12/GRCh38#9443485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#66433363-C-A

9443485-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66433363-C-G

9443485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66433363-C-T

http://identifiers.org/hco/12/GRCh38#9443529-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#66433319-A-C

9443542-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66433306-G-C

9443543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66433305-T-C

9443543-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66433305-T-G

9443547-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66433301-A-T

9443568-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66433280-G-C

9443597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: non coding transcript exon variant
orthologous variants: 66433251-C-T

9443898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66432714-G-A

http://identifiers.org/hco/12/GRCh38#9443954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#66432671-C-A

9443954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66432671-C-T

9443974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66432658-C-T

9444035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66432600-C-T

9444180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66432457-C-T

9444600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66432387-C-T

http://identifiers.org/hco/12/GRCh38#9444713-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#66432200-A-C

9444737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66432167-G-A

9444863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66432078-T-C

9444989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66431979-A-G

http://identifiers.org/hco/12/GRCh38#9445013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#66431954-C-A

9445013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 66431954-C-T

9445085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 66431879-A-G

http://identifiers.org/hco/12/GRCh38#9445486-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2737
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#66431396-A-C