93727086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72412335-A-G

93742337-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72410759-C-G

93742602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72410482-A-G

http://identifiers.org/hco/15/GRCh38#93742620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72410464-C-A

http://identifiers.org/hco/15/GRCh38#93742638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72410446-C-A

93742638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72410446-C-T

93742721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72410365-C-T

93742757-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72410329-T-A

93742811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72410279-A-G

93742865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72410225-G-A

93742883-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72410213-C-G

93742883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72410213-C-T

93742908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72410188-G-A

93743013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72410086-T-C

93743042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72410046-T-C

http://identifiers.org/hco/15/GRCh38#93744039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72409003-C-A

93744086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72408971-A-G

93744101-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72408956-C-G

93744101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72408956-C-T

http://identifiers.org/hco/15/GRCh38#93744179-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72408867-A-C

93744366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72408694-G-T

93744655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72408452-T-C

93759294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72405564-A-G

93759536-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72405325-C-G

93759654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72405208-C-T

93759656-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72405206-C-G

93759656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72405206-C-T

93759663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72405178-G-T

93759664-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72405177-C-G

93759768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72405073-A-G

93759928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72404795-A-G

93760139-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72404607-C-G

93760322-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72404430-C-G

93760470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72404285-T-C

93760470-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72404285-T-G

http://identifiers.org/hco/15/GRCh38#93760482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72404273-C-A

93760482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72404273-C-T

93760483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72404272-G-A

93760483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72404272-G-T

http://identifiers.org/hco/15/GRCh38#93760495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72404260-C-A

93760495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72404260-C-T

93760512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72404243-A-G

http://identifiers.org/hco/15/GRCh38#93760517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72404237-C-A

93760517-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72404237-C-G

93760517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72404237-C-T

http://identifiers.org/hco/15/GRCh38#93760527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72404227-C-A

93760527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72404227-C-T

http://identifiers.org/hco/15/GRCh38#93760581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72403534-C-A

93760587-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72403528-T-G

93760596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72403519-G-A

93760596-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72403519-G-C

93760596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72403519-G-T

93760630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72403485-G-A

93760630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72403485-G-T

93760650-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72403447-T-A

93760650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72403447-T-C

93760658-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72403439-T-G

93760706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: non coding transcript exon variant
orthologous variants: 72403402-C-T

93760750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: non coding transcript exon variant
orthologous variants: 72403355-C-T

http://identifiers.org/hco/15/GRCh38#93760771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72403334-C-A

93760798-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: non coding transcript exon variant
orthologous variants: 72403310-G-C

93760798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: non coding transcript exon variant
orthologous variants: 72403310-G-T

93760832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: non coding transcript exon variant
orthologous variants: 72403278-G-T

93760853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: non coding transcript exon variant
orthologous variants: 72403242-G-T

http://identifiers.org/hco/15/GRCh38#93761128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72403008-C-A

93761363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72402779-G-A

93763265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72402350-G-T

93763561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72402090-G-A

93763567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72402084-A-G

93763660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72402004-G-A

93763677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72401987-A-G

93763786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72401893-C-T

93763998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72401627-C-T

93764015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72401610-C-T

93764016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72401609-G-A

93764537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72401096-A-G

93765123-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72397126-A-T

93765352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72396947-G-T

93765459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72396839-A-G

93765477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72396820-G-A

93765586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72396707-A-G

http://identifiers.org/hco/15/GRCh38#93765908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72396371-C-A

93765908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72396371-C-T

93766179-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72396023-C-G

93766406-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72395799-C-G

93766728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72395433-A-G

93766755-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72395406-C-G

93766882-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72395327-A-T

93766934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72395275-A-G

93766952-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72395258-C-G

93767059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72395143-G-A

93767150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72395053-C-T

93767192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72395012-T-C

93770104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72393635-G-A

93770104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72393635-G-T

93770126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72393613-C-T

93770197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72393552-G-A

93770197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72393552-G-T

93770566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72393487-G-A

93770702-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72393343-C-G

93770702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72393343-C-T

93770733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72393314-A-G

93770855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72393211-G-T

93770927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72393137-C-T

93770986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72393093-A-G

93770990-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72393089-A-T

93770992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72393087-C-T

93771062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72393022-G-A

93771116-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72392968-T-G

93771124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72392960-C-T

93771163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72392921-G-A

93771527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72392579-A-G

93771549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72392557-G-A

93771549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72392557-G-T

93771833-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72392273-T-A

93772262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72391668-A-G

93772892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72390854-C-T

93772925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72390809-G-A

93772925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72390809-G-T

93772963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72390741-G-A

http://identifiers.org/hco/15/GRCh38#93774417-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72389301-A-C

93774448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72389270-T-C

93774568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72389138-G-T

93774604-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72389106-G-C

93774783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72388371-A-G

93775283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72387872-G-A

http://identifiers.org/hco/15/GRCh38#93775368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72387789-C-A

93775368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72387789-C-T

93775408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72387746-C-T

93775422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72387732-A-G

93775479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72387674-G-A

93775584-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72387564-A-T

93775891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72386982-G-A

93776118-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72386749-T-A

93777161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72386301-A-G

93778521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72383754-T-C

93778533-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72383742-T-G

93778730-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72383543-T-A

93778730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72383543-T-C

http://identifiers.org/hco/15/GRCh38#93779021-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72383245-A-C

93779407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72383164-A-G

93779456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72383130-C-T

93779496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72383089-G-A

93779498-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72383087-T-A

93779500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72383085-T-C

93779536-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72383049-C-G

93779744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72382848-A-G

93780607-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72382465-T-G

93780618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72382454-A-G

93780879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72382174-G-A

93780889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72382166-T-C

93781428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72381574-G-A

93781443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72381559-G-T

93781570-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72381432-G-C

93781620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72381383-T-C

http://identifiers.org/hco/15/GRCh38#93782681-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72380481-A-C

93782701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72380461-C-T

93782818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72380349-T-C

93782825-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72380342-G-C

93782928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72380208-A-G

93782933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72380203-A-G

http://identifiers.org/hco/15/GRCh38#93782942-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72380194-A-C

93783072-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72380090-A-T

93783197-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72379972-C-G

93783212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72379958-G-A

93783395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72379307-T-C

93783445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72379258-G-A

93783466-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72379237-G-C

93783532-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72379154-C-G

93783635-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72379050-T-G

93783638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72379047-A-G

93783705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72378990-C-T

http://identifiers.org/hco/15/GRCh38#93783822-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72378864-A-C

93783865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72378822-T-C

93784348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72377788-C-T

93784455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72377697-A-G

93784482-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72377685-T-A

93784851-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72377346-G-C

93785166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72377038-C-T

93785183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72377021-G-A

http://identifiers.org/hco/15/GRCh38#93785430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72376778-C-A

http://identifiers.org/hco/15/GRCh38#93785494-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72376698-A-C

http://identifiers.org/hco/15/GRCh38#93785916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72376424-C-A

93786153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72376246-T-C

93786258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72376141-A-G

93786258-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72376141-A-T

93786622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72375786-G-A

93788180-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72374770-T-G

93788245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72374718-A-G

http://identifiers.org/hco/15/GRCh38#93788372-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72374603-A-C

http://identifiers.org/hco/15/GRCh38#93788401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72374574-C-A

http://identifiers.org/hco/15/GRCh38#93788552-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72368238-A-C

http://identifiers.org/hco/15/GRCh38#93788572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72368218-C-A

93788603-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72368198-G-C

http://identifiers.org/hco/15/GRCh38#93788607-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72368194-A-C

93788808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72368052-T-C

93789830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72367768-A-G

http://identifiers.org/hco/15/GRCh38#93789925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72367676-C-A

93789956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72367647-T-C

93789963-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72367640-G-C

93790012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72367591-G-A

93790174-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72367443-T-G

93790235-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72367394-T-A

http://identifiers.org/hco/15/GRCh38#93790277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72367351-C-A

93790278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72367350-A-G

93790288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72367341-G-A

93790288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72367341-G-T

93790335-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72367288-C-G

93790556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72367080-A-G

93791026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72366629-G-A

93791112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72366543-A-G

93791255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72366440-C-T

93791423-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72366256-G-C

93791454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72366229-C-T

93791622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72366067-T-C

http://identifiers.org/hco/15/GRCh38#93791630-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72366059-C-A

93791630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72366059-C-T

93791762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72365915-G-A

93791762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72365915-G-T

93791928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72365759-T-C

93792165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72365578-G-A

93798702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72365517-A-G

93798998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72365225-G-T

93799174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72365055-G-T

93799188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72365041-C-T

93799340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72364889-C-T

93799644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72364584-T-C

93799685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72364543-C-T

93802337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72364079-G-A

93802384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72364029-A-G

93802384-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72364029-A-T

http://identifiers.org/hco/15/GRCh38#93802403-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72364010-A-C

93802472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72363942-T-C

93802636-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72363788-T-G

93802749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72363676-G-A

93803571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72361493-T-C

93803628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72361437-G-A

93803628-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72361437-G-C

93803737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72361329-G-A

93803846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72361218-G-A

93803936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72361129-G-T

93804011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72361063-G-T

http://identifiers.org/hco/15/GRCh38#93804027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72361047-C-A

93804034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72361040-A-G

93804631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72360488-A-G

93804693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72360427-G-T

93804952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72360368-T-C

93804976-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72360344-C-G

93805111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72360207-A-G

93805244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72360079-T-C

93806159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72359608-C-T

93806198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72359589-G-A

93806223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72359571-A-G

93806707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72359146-A-G

93806707-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72359146-A-T

http://identifiers.org/hco/15/GRCh38#93806713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72359140-C-A

93806715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72359138-G-A

93806715-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72359138-G-C

93806728-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72359127-G-C

93807068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72358924-T-C

93807502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72358724-G-A

http://identifiers.org/hco/15/GRCh38#93807522-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72358699-A-C

93807522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72358699-A-G

93809580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72357625-C-T

http://identifiers.org/hco/15/GRCh38#93809616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72357590-C-A

93809665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72357536-T-C

93809895-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72357319-A-T

93809993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72357147-C-T

93810044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72357101-A-G

93810193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72356986-A-G

93810299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72356898-G-T

93810657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72356562-C-T

93810702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72356505-C-T

http://identifiers.org/hco/15/GRCh38#93810825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72356419-C-A

93810825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72356419-C-T

93810894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72356350-G-T

93810982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72356259-G-A

93811034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72356205-G-A

93811178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72356063-T-C

93811178-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72356063-T-G

93811258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72355990-T-C

93811319-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72355930-T-A

93811437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72355809-G-A

93811454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72355792-T-C

93811493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72355731-A-G

93811496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72355728-C-T

93811519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72355703-G-T

http://identifiers.org/hco/15/GRCh38#93811557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72355666-C-A

http://identifiers.org/hco/15/GRCh38#93811807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72355467-C-A

93812004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72355226-G-A

93812020-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72355210-G-C

http://identifiers.org/hco/15/GRCh38#93812066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72355167-C-A

93812085-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72355015-T-A

93812212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72354845-T-C

93812350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72354701-T-C

93812381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72354670-C-T

93812390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72354661-G-T

93812448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72354597-T-C

93812663-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72354349-C-G

93819348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72354273-A-G

93819398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72354232-G-A

93819609-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72354038-A-T

93819622-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72354025-G-C

93819645-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72354002-T-A

93819754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72353897-G-T

93819801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72353850-G-A

93819801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72353850-G-T

93819945-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72353697-T-G

93820025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72353617-C-T

93820075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72353573-A-G

93820227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72353432-T-C

93820392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72353275-G-A

93820423-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72353243-T-G

93820495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72353178-G-A

93820520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72353153-T-C

93820665-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72353031-G-C

93822475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72352707-A-G

93822541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72352650-C-T

93823884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72350366-G-A

93823884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72350366-G-T

http://identifiers.org/hco/15/GRCh38#93823910-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72350341-A-C

93823943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72350301-C-T

93823948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72350296-G-A

93823948-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72350296-G-C

93823948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72350296-G-T

http://identifiers.org/hco/15/GRCh38#93823964-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72350280-A-C

93823978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72350266-G-T

93824013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72350240-A-G

93824032-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72350215-A-T

93824072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72350140-G-T

93824183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72350030-A-G

93824412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72349825-T-C

93824571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72349686-A-G

93824804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72349472-G-T

93825297-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72349385-T-A

http://identifiers.org/hco/15/GRCh38#93825308-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72349374-A-C

http://identifiers.org/hco/15/GRCh38#93825309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72349373-C-A

93825309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72349373-C-T

93825622-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72347043-A-T

93826513-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72346180-T-G

93826611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72346080-A-G

93826621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72346070-G-A

93826622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72346069-T-C

93826637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72346060-C-T

93826736-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72345962-T-A

93826766-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72345923-C-G

http://identifiers.org/hco/15/GRCh38#93826784-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72345912-A-C

http://identifiers.org/hco/15/GRCh38#93826888-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72345803-A-C

93826939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72345753-A-G

93826957-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72345735-T-A

93826957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72345735-T-C

93827076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72345620-G-A

93827076-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72345620-G-C

93827101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72345594-C-T

93827255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72345444-C-T

93827330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72345361-C-T

93827333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72345358-G-A

93827457-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72345253-C-G

93827466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72345244-T-C

93832482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72344320-G-A

93832842-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72344387-C-G

93832842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72344387-C-T

93834983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72343996-G-A

93834985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72343994-G-A

93835110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72343862-A-G

93835110-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72343862-A-T

93835891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72342272-G-T

93837583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72341866-C-T

http://identifiers.org/hco/15/GRCh38#93837722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72341734-C-A

http://identifiers.org/hco/15/GRCh38#93837724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72341732-C-A

93837750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72341705-G-T

93837779-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72341678-A-T

93837827-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72341638-A-T

93837917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72341524-A-G

93838005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72341441-G-T

93838042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72341404-A-G

93838042-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72341404-A-T

93838125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72341322-T-C

93839149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72341025-T-C

93839322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72340854-A-G

http://identifiers.org/hco/15/GRCh38#93839351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72340821-C-A

93839351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72340821-C-T

93839485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 72340686-G-A

93839485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 72340686-G-T

93847644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72337595-A-G

93847689-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72337549-A-T

93848021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72337242-T-C

http://identifiers.org/hco/15/GRCh38#93848132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72337125-C-A

93848132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72337125-C-T

93848280-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72336979-G-C

93848873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72336516-T-C

93848995-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72336398-T-A

93849017-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72336376-A-T

93849056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72336337-A-G

93849204-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72336192-T-A

93849204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72336192-T-C

93849282-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72336152-G-C

93849415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72336041-A-G

http://identifiers.org/hco/15/GRCh38#93849796-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72335632-A-C

93854349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72334031-T-C

93854490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72333819-C-T

93854882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72333411-G-T

93859728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72332157-T-C

93860439-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72325401-C-G

93860533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72325312-G-A

http://identifiers.org/hco/15/GRCh38#93860946-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72324887-A-C

93860953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72324880-A-G

93860954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72324878-T-C

http://identifiers.org/hco/15/GRCh38#93861019-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72324813-A-C

93861079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72324757-T-C

93861308-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72322219-C-G

93861308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72322219-C-T

http://identifiers.org/hco/15/GRCh38#93861427-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72322100-A-C

93861436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72322088-G-T

93862083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72321549-C-T

93862131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72321501-G-A

93865555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72319889-G-A

93865555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72319889-G-T

93865606-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72319843-T-A

93865676-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72319780-A-T

http://identifiers.org/hco/15/GRCh38#93866002-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72319436-A-C

93866118-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72319320-G-C

http://identifiers.org/hco/15/GRCh38#93866119-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72319319-A-C

93866359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72319108-T-C

93866416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72319051-G-A

93866423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72319044-G-A

93866423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72319044-G-T

http://identifiers.org/hco/15/GRCh38#93866490-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72318976-A-C

93866556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72318913-T-C

93866556-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72318913-T-G

http://identifiers.org/hco/15/GRCh38#93866803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72318660-C-A

93866803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72318660-C-T

93866851-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72318612-T-A

93866893-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72318570-T-A

93866893-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72318570-T-G

93866925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72318534-G-T

93866997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72318458-T-C

93867090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72318365-A-G

93867203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72318262-C-T

http://identifiers.org/hco/15/GRCh38#93867258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72318210-C-A

93867258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72318210-C-T

93867300-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72318170-A-T

93867372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72318098-A-G

93867372-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72318098-A-T

93867402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 72318069-T-C

93867456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72318014-G-T

93867630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72317846-A-G

93867725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72317405-C-T

93867776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72317361-G-A

http://identifiers.org/hco/15/GRCh38#93867805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72317332-C-A

93867813-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72317324-G-C

93867834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72317306-C-T

93867937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72317243-T-C

93867963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72317217-G-A

93868500-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72316167-A-T

93868745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72315871-A-G

93868825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72315808-C-T

93869046-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72315488-G-C

93869553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72315213-A-G

93869741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72315081-C-T

93874922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72314803-T-C

93874923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72314802-C-T

93874945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72314779-T-C

93874984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72314740-A-G

93874999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72314718-T-C

http://identifiers.org/hco/15/GRCh38#93877466-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72287967-A-C

93877510-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72287925-G-C

93877592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72287845-A-G

93878007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72287286-G-A

93878007-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72287286-G-T

93878261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 72287032-C-T

93878778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72286460-G-A

93879027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72286331-G-A

93879744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72285951-T-C

93879744-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72285951-T-G

93879830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72285875-T-C

93879873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72285833-G-T

93880112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72285654-C-T

93880205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72285562-G-T

93880210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72285557-T-C

93880314-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72285447-C-G

http://identifiers.org/hco/15/GRCh38#93880343-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72285418-A-C

93880343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72285418-A-G

93880386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72285375-T-C

93880387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72285374-G-A

93880517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72284858-G-A

93880643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72284745-G-A

93881304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72284490-C-T

93881338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72284456-G-A

93881572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72284343-A-G

93881673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72284274-T-C

http://identifiers.org/hco/15/GRCh38#93881812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72284135-C-A

93881812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72284135-C-T

93882273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72283726-T-C

93882329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72283664-G-T

93882436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72278369-A-G

93882517-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72278305-T-A

93882549-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72278277-T-G

93882556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72278270-T-C

93882763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72278141-T-C

93883674-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72277439-T-A

93884413-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72276719-T-G

93884534-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72276597-A-T

93885673-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72267661-G-C

93885776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72267558-G-A

93885822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72267504-A-G

93885836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72267490-T-C

93885980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 72267455-A-G

93885992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72267443-G-A

93886037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72267398-T-C

93886037-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72267398-T-G

93886062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72267377-T-C

93886132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72267325-A-G

93886191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72267265-C-T

93886214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72267242-G-A

93886214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72267242-G-T

93886264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72267191-T-C

http://identifiers.org/hco/15/GRCh38#93886305-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72267150-A-C

93886492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72266567-G-A

93886492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72266567-G-T

93886533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72266526-T-C

93886572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72266487-G-A

93886688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72266383-A-G

93886710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72266364-G-A

93886853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72266240-T-C

93886853-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72266240-T-G

93886897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72266201-G-A

93886899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72266199-A-G

93886970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72266138-A-G

93887038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72266075-T-C

93887314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72265795-A-G

93887350-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72265763-A-T

93887666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72265423-A-G

93887841-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72265248-T-A

93887854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72265235-T-C

93887903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72265186-T-C

93887911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72265180-G-T

93887924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72265167-C-T

http://identifiers.org/hco/15/GRCh38#93889386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72261470-C-A

93889537-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72261339-A-T

93889639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72261227-G-T

93889640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72261226-A-G

93889643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72261223-G-A

93889661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72261206-C-T

93889772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72261096-G-A

93890367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72260523-C-T

93890642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72260292-T-C

93890728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72260200-G-A

93890728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72260200-G-T

93890772-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72260161-T-A

93891086-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72259559-G-C

93891163-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72259490-T-A

http://identifiers.org/hco/15/GRCh38#93891218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72259440-C-A

http://identifiers.org/hco/15/GRCh38#93891246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72259413-C-A

93891246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72259413-C-T

93891269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72259395-A-G

93891270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72259394-A-G

http://identifiers.org/hco/15/GRCh38#93891738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72257822-C-A

93891748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72257813-A-G

93891949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72257657-T-C

93892097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72257529-C-T

93892480-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72256611-G-C

93892781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72256318-G-A

93893045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72256080-A-G

93893346-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72255123-T-A

93893377-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72255098-T-G

93893467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72255046-G-A

93893520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72254993-G-A

93893675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72254865-C-T

93893809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72254726-A-G

93893926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72254623-A-G

93894175-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72254377-C-G

93894180-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72254372-C-G

93894335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72254209-G-A

93894456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72254100-C-T

93894511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72254047-C-T

93894638-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72253920-G-C

93894766-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72253795-T-G

93895077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72253419-C-T

93895149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72253355-G-A

93895162-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72253338-T-A

93895266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72253236-T-C

93895266-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72253236-T-G

93895341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72253166-G-A

93895917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72252574-A-G

93895949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72252539-T-C

http://identifiers.org/hco/15/GRCh38#93896079-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72252234-A-C

93896135-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72252185-A-T

93896197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72252123-T-C

93896197-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72252123-T-G

93896221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72252102-G-A

http://identifiers.org/hco/15/GRCh38#93896223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72252100-C-A

93896228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72252095-A-G

93896404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72251923-T-C

93896411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72251916-A-G

93896530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72251797-G-A

93896530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72251797-G-T

http://identifiers.org/hco/15/GRCh38#93896545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72251782-C-A

93896640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72251687-T-C

93896891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72251461-G-A

93896966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72251390-T-C

93897091-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72251267-T-G

93897161-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72251198-C-G

93897790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72250565-C-T

93897908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72250455-A-G

93898072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72250288-T-C

93898077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72250283-G-A

93904900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72249817-A-G

93904935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72249785-C-T

http://identifiers.org/hco/15/GRCh38#93904976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72249768-C-A

93904976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72249768-C-T

http://identifiers.org/hco/15/GRCh38#93905220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72249586-C-A

93905277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72249530-C-T

93905338-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72249477-T-G

93905495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72249388-G-A

93905802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72249243-C-T

93905984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72249066-A-G

93905998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72249052-G-T

93906076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72248984-G-A

93906076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72248984-G-T

93906160-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72248904-T-G

93906217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72248848-G-A

93906387-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72248688-T-G

http://identifiers.org/hco/15/GRCh38#93906969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72248289-C-A

93907192-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72247978-C-G

http://identifiers.org/hco/15/GRCh38#93910737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72243584-C-A

http://identifiers.org/hco/15/GRCh38#93911321-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72243038-A-C

93924908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72241855-A-G

93924958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72241806-A-G

93925050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72241752-C-T

93925134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72241671-T-C

93925329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72241499-G-A

93925376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72241450-T-C

93925501-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72241318-T-G

93925929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72240854-T-C

93926052-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72240729-T-G

93926053-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72240728-T-G

93926188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72240593-G-T

93926245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72240544-T-C

http://identifiers.org/hco/15/GRCh38#93926264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72240525-C-A

http://identifiers.org/hco/15/GRCh38#93926424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72240353-C-A

93926424-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72240353-C-G

93926427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72240350-G-A

93926439-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72240336-A-T

93926441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72240334-T-C

93929070-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72239687-T-A

93929070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72239687-T-C

93929090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72239667-G-A

93929175-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72239604-C-G

93929323-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72239474-C-G

93929609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72239298-C-T

93929610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72239297-G-A

93929629-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72239277-C-G

93929697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72239190-C-T

93929849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72239070-A-G

93929931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72238985-A-G

93929998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72238918-C-T

93930080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72238833-A-G

93934501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72236285-A-G

93934753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72236057-T-C

93934929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72235883-A-G

93935056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72235744-C-T

93937457-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72232078-T-A

93937995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72231570-A-G

93938144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72231425-G-A

93938144-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72231425-G-C

93942526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72229631-T-C

93942622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72229536-C-T

http://identifiers.org/hco/15/GRCh38#93942710-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72229453-A-C

93942728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72229435-A-G

93942789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72229363-A-G

93943085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72229075-A-G

93943085-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72229075-A-T

93943787-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72228326-A-T

93943867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72228255-G-A

93944044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72228104-A-G

93945905-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72228018-C-G

93945905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72228018-C-T

93945909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72228014-T-C

93946400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72227538-A-G

93946539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72227432-C-T

93946578-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72227395-G-C

93946578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72227395-G-T

93947066-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72226969-T-A

93947171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72226849-C-T

93947359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72226657-G-A

93947359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72226657-G-T

93947417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72226601-G-A

93947417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72226601-G-T

93947429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72226576-T-C

93947436-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72226569-T-A

http://identifiers.org/hco/15/GRCh38#93947439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72226566-C-A

93947439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72226566-C-T

http://identifiers.org/hco/15/GRCh38#93947538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72226472-C-A

93947538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72226472-C-T

93947548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72226462-G-T

http://identifiers.org/hco/15/GRCh38#93947550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72226460-C-A

93947674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72226331-T-C

93947737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72226292-T-C

93947898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72226113-C-T

93948756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72225302-G-A

93948777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72225273-C-T

93948835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72225205-C-T

93948868-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72225168-C-G

93948888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72225148-C-T

93948905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72225131-G-A

93949016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72225025-T-C

http://identifiers.org/hco/15/GRCh38#93949057-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72224984-A-C

93949066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 72224975-T-C

http://identifiers.org/hco/15/GRCh38#93949214-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72224819-A-C

93949247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72224786-A-G

http://identifiers.org/hco/15/GRCh38#93949263-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72224770-A-C

93949263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72224770-A-G

93949296-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72224735-C-G

93949372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72224658-T-C

93949474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72224559-G-A

93949964-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72224017-T-G

93950026-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72223815-T-G

93950205-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72223653-T-G

93950529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72223419-G-A

93950720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72223231-T-C

93951137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72222472-T-C

http://identifiers.org/hco/15/GRCh38#93951161-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72222431-A-C

93951286-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72222293-G-C

93951502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72222092-A-G

93952431-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72222036-A-T

93952633-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72221837-T-G

93952684-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72221788-A-T

93953110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72221360-G-A

93953201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72220871-A-G

http://identifiers.org/hco/15/GRCh38#93953297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72220763-C-A

93953333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72220727-G-A

93953364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72220697-T-C

93953604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72220462-A-G

93953886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72220303-C-T

93954160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72220073-G-A

93954691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72219585-C-T

93954823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72219449-C-T

93954970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72219328-G-T

93955180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72219136-T-C

http://identifiers.org/hco/15/GRCh38#93955423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72218113-C-A

93955423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72218113-C-T

93955526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72217976-A-G

93955652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72217852-G-T

93955966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72217200-G-A

93956352-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72216830-C-G

93956438-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72216740-C-G

93956668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72216546-T-C

93956686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72216528-A-G

93956796-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72216339-G-C

93956834-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72216304-T-A

93957263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72215901-A-G

93957335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72215826-T-C

93957390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72215769-G-A

93961313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72215671-A-G

93961447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72215544-C-T

http://identifiers.org/hco/15/GRCh38#93962581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72214542-C-A

93962581-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72214542-C-G

93962632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72214497-T-C

93962634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72214495-T-C

93962749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72214416-T-C

93962760-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72214405-T-A

93962760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72214405-T-C

93962760-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72214405-T-G

93962767-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72214399-G-C

93962767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72214399-G-T

http://identifiers.org/hco/15/GRCh38#93962853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72214335-C-A

93963780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72214140-G-A

93964048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72213886-G-A

93964938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72212898-G-A

93965038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72212792-G-A

93965073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72212762-C-T

93965324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72212532-T-C

93965362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72212499-C-T

93965442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72212369-G-T

93965792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72212063-G-A

93968184-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72208534-T-G

93968266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72208462-T-C

93968822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72207943-T-C

93968872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72207893-T-C

http://identifiers.org/hco/15/GRCh38#93971491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-A

93971810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-T

http://identifiers.org/hco/15/GRCh38#93972022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72204103-C-A

93972252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72203890-C-T

93972271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72203871-A-G

93972330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72203810-T-C

93972393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72203746-A-G

93972395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72203744-G-T

http://identifiers.org/hco/15/GRCh38#93972475-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72203661-A-C

93972643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72203515-G-A

93972654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72203504-C-T

93972655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72203503-A-G

93972867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72203275-A-G

http://identifiers.org/hco/15/GRCh38#93972954-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72203192-A-C

93973205-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72202954-A-T

93973438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72202699-T-C

93973472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72202656-G-T

93973563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72202568-T-C

http://identifiers.org/hco/15/GRCh38#93973567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72202564-C-A

93973567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72202564-C-T

93973590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72202540-A-G

93973760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72202379-T-C

93973835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72202320-G-A

93973835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72202320-G-T

93976384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72198585-T-C

http://identifiers.org/hco/15/GRCh38#93976533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72198457-C-A

93976533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72198457-C-T

93976586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72198404-G-A

93976852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72198172-T-C

93977104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72197568-G-A

http://identifiers.org/hco/15/GRCh38#93977566-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72197150-A-C

93977583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72197133-G-A

93977638-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72196887-T-G

93977819-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72196722-T-G

93977867-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72196677-A-T

93978194-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72196332-C-G

93978290-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72196285-A-T

93978342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72196233-A-G

93978383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72196191-G-T

http://identifiers.org/hco/15/GRCh38#93978860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72196116-C-A

93978860-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72196116-C-G

93979114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72195877-G-A

93979352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72195643-G-A

93980243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72193967-G-A

http://identifiers.org/hco/15/GRCh38#93980402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72193836-C-A

93980471-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72193772-T-G

http://identifiers.org/hco/15/GRCh38#93980626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72193646-C-A

93980964-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72193311-T-A

93980964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72193311-T-C

93981119-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72193177-C-G

93981200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72193120-G-A

93981202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72193118-G-T

93981881-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72192789-G-C

93981925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72192746-C-T

93982022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72192005-A-G

http://identifiers.org/hco/15/GRCh38#93982324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72191713-C-A

http://identifiers.org/hco/15/GRCh38#93982416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72191599-C-A

93982416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72191599-C-T

93982790-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72191222-A-T

93982857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72191177-T-C

93982862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72191172-A-G

93982965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72191087-T-C

93983101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72190958-T-C

93983101-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72190958-T-G

93983106-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72190953-T-G

93983124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72190935-T-C

93983191-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72190915-G-C

93983367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72190709-C-T

93983641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72190434-G-A

93983641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72190434-G-T

93983676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72190395-G-A

http://identifiers.org/hco/15/GRCh38#93983739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72190330-C-A

93983739-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72190330-C-G

93983764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72190302-G-A

93983764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72190302-G-T

93983771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72190295-G-A

http://identifiers.org/hco/15/GRCh38#93983813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72190254-C-A

93983837-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72190230-T-A

http://identifiers.org/hco/15/GRCh38#93983888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72190189-C-A

93983888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72190189-C-T

93983910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72190167-A-G

93983923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72190154-G-A

93983947-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72190122-C-G

93983947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72190122-C-T

http://identifiers.org/hco/15/GRCh38#93983948-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72190121-A-C

93983948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72190121-A-G

93983964-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72190105-A-T

93983972-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72190096-T-G

93983986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72190082-G-T

93984933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72189726-A-G

93985315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72189443-A-G

93985517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72189238-G-A

93985533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72189222-G-A

93985759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72189044-C-T

93986418-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72188563-G-C

93986492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72188502-C-T

93986871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72188164-C-T

93987045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72188005-G-A

93987100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72187968-T-C

93987166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72187927-C-T

93987231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72187863-G-A

93987231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72187863-G-T

93987245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72187845-C-T

93987263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72187827-A-G

93987296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72187794-G-A

http://identifiers.org/hco/15/GRCh38#93987318-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72187772-A-C

93987503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72186772-A-G

93987504-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72186771-C-G

93987537-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72186738-A-T

93987617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72186664-C-T

93988033-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72186275-C-G

93988033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72186275-C-T

93988057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72186251-G-A

93988120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72186228-A-G

93988182-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72186179-C-G

93988182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72186179-C-T

93988267-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72186135-T-A

http://identifiers.org/hco/15/GRCh38#93988318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72186077-C-A

93988380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72186011-A-G

93988444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72185937-G-A

93988621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72185789-C-T

93989111-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72185202-C-G

93989245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72185093-C-T

93989322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72185014-T-C

93989349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72184985-T-C

93989642-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72184735-T-A

http://identifiers.org/hco/15/GRCh38#93989818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72184563-C-A

93989818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72184563-C-T

93990173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72184015-G-A

93990344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72183830-T-C

93990479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72183706-T-C

http://identifiers.org/hco/15/GRCh38#93990607-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72183572-A-C

93990607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72183572-A-G

93990725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72183535-C-T

93990905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72183379-C-T

93991049-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72183233-T-A

93991051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72183231-T-C

93991089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72183197-C-T

http://identifiers.org/hco/15/GRCh38#93993837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72182984-C-A

93993837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72182984-C-T

93993868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72182956-A-G

93994006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72182819-G-A

93994028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72182797-A-G

http://identifiers.org/hco/15/GRCh38#93994085-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72182740-A-C

93994085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72182740-A-G

http://identifiers.org/hco/15/GRCh38#93994108-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72182717-C-A

http://identifiers.org/hco/15/GRCh38#93994126-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72182700-A-C

93994157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72182664-T-C

93994846-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72180906-A-T

93994922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72180830-G-A

93995086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72180693-A-G

93995137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72180639-A-G

93995140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72180636-G-T

93995234-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72180552-G-C

93995234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72180552-G-T

93995416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72180392-G-T

93995427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72180381-T-C

93995532-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72180279-C-G

93995532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72180279-C-T

93995556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72180255-T-C

93995564-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72180248-T-A

93996232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72179699-T-C

93996291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72179595-C-T

93996359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72179501-G-A

93996379-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72179481-G-C

93996379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72179481-G-T

93996486-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72179384-A-T

93996534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72179326-C-T

93996543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72179317-G-A

93996731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72179118-G-A

http://identifiers.org/hco/15/GRCh38#93996779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72179070-C-A

93997000-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72178997-T-G

93997282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72178799-T-C

93997288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72178793-A-G

93997303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72178778-T-C

93997403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72178685-G-T

93997445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72178654-A-G

93997565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72178527-G-T

93997792-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72178243-G-C

93997963-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72178105-C-G

93997963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72178105-C-T

http://identifiers.org/hco/15/GRCh38#93998004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72178064-C-A

93998004-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72178064-C-G

93998004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72178064-C-T

93998030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72178041-A-G

93998452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72170199-G-A

93998484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72170163-T-C

93998484-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72170163-T-G

93998510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72170140-A-G

94000473-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72169923-C-G

94000480-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72169913-G-C

94000484-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72169909-T-G

94001061-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72169478-C-G

94001061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72169478-C-T

94001080-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72169459-T-A

94001117-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72169422-G-C

94001155-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72169386-T-G

94001163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72169378-A-G

94001243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72169299-C-T

94001519-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72169013-A-T

94001553-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72168988-T-A

94001662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72168912-G-A

94001740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72168839-T-C

94001988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72168665-T-C

http://identifiers.org/hco/15/GRCh38#94004986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72167366-C-A

94004986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72167366-C-T

94005186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72167176-G-A

94005357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72167044-T-C

94005366-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72167035-T-G

94005379-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72167022-G-C

94005379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72167022-G-T

94005695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72166914-G-A

94005719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72166891-T-C

94005859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72166747-C-T

94007764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72165280-A-G

94007779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72165265-C-T

94007846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72165199-A-G

94008031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72165036-C-T

94008080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72165002-C-T

http://identifiers.org/hco/15/GRCh38#94008156-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72164925-A-C

94008156-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72164925-A-T

94008635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72164461-T-C

94008949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72164162-T-C

94008997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72164040-A-G

94009218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72163841-A-G

94009395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72163679-T-C

94009604-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72163493-A-T

94009722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72163377-T-C

94009951-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72163047-G-C

94010128-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72162867-C-G

94010798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72161348-C-T

94011062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72161088-C-T

94011095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72161055-C-T

94012302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72159143-A-G

94019388-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72158148-C-G

94019397-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72158139-C-G

94019397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72158139-C-T

94019412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72158127-C-T

94019522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72158017-T-C

94020445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72157649-G-A

94021071-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72156741-T-G

94021248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72156572-T-C

http://identifiers.org/hco/15/GRCh38#94021325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72156496-C-A

94021340-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72156481-A-T

http://identifiers.org/hco/15/GRCh38#94021364-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72156457-C-A

94021364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72156457-C-T

94021850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72155963-G-A

94022211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72155621-G-A

94022214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72155618-G-A

94022214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72155618-G-T

94022311-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72155522-A-T

94022833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72154975-A-G

94023274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72154674-T-C

94023929-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72154003-T-A

94023989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72153938-A-G

94024073-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72153862-A-T

94024244-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72153678-G-C

94025805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72152160-T-C

94025815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72152153-T-C

94025914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72152093-T-C

94026035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72151999-T-C

94026564-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72151479-C-G

94026566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 72151477-A-G

94027092-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72150952-G-C

94027228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72150828-G-A

94027630-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72150473-A-T

94027767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72150354-A-G

94027877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72150247-G-A

94030345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72147284-G-T

94030465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72147168-G-A

94030728-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72146922-C-G

94030728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72146922-C-T

http://identifiers.org/hco/15/GRCh38#94030856-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72146854-A-C

94031260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72146315-T-C

94031589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72145973-A-G

94031599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72145962-A-G

94031607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72145954-T-C

94031607-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72145954-T-G

94032001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72145602-A-G

94032269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72145338-T-C

94032931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72145171-T-C

94033239-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72144859-C-G

http://identifiers.org/hco/15/GRCh38#94033279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72144817-C-A

94033396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72144721-A-G

94033573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72144560-A-G

94033626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72144507-G-A

94033626-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72144507-G-C

94033626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72144507-G-T

http://identifiers.org/hco/15/GRCh38#94035226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72144042-C-A

94035313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72143959-T-C

94035459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72143860-C-T

94035732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72143597-A-G

94036210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72142799-A-G

94036401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72142614-G-A

94036403-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72142612-T-A

94036413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72142602-A-G

94036464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72142553-C-T

94043593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72140084-G-A

94043612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72140047-A-G

94043629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72140030-A-G

94043803-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72139870-T-G

94044281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72132617-A-G

http://identifiers.org/hco/15/GRCh38#94046735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72131246-C-A

http://identifiers.org/hco/15/GRCh38#94046816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72131172-C-A

94046816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72131172-C-T

94046896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72131093-A-G

94046933-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72131056-A-T

94047163-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72130824-T-A

94047256-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72130738-T-A

94047256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72130738-T-C

94047290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72130704-T-C

94047388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72130598-T-C

94048110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72130010-T-C

94048214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72129345-C-T

http://identifiers.org/hco/15/GRCh38#94048248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72129311-C-A

94048248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72129311-C-T

94048260-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72129293-C-G

94048369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72129176-G-A

94048537-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72128996-T-A

94048537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72128996-T-C

94048771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72128777-T-C

94049687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72128484-A-G

94055821-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72123078-T-G

94055945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72122956-T-C

94056175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72122714-A-G

94056789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72122067-T-C

http://identifiers.org/hco/15/GRCh38#94056932-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72121933-A-C

94056981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72121888-G-T

94057176-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72121711-G-C

http://identifiers.org/hco/15/GRCh38#94057252-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72121450-A-C

94057439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72121265-G-A

94057539-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72121156-C-G

94057565-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72121130-A-T

94057877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72120678-G-A

94058243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72120302-C-T

94058320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72120236-G-A

94058320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72120236-G-T

94058439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72120119-A-G

http://identifiers.org/hco/15/GRCh38#94058504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72120056-C-A

94058929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72119887-A-G

94058996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72119827-T-C

94059202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72119619-A-G

94059337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72119471-G-T

94059481-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72119325-G-C

94059499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72119307-A-G

94059700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72119095-T-C

94062449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72116917-T-C

94062541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72116825-C-T

94062649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72116734-T-C

94062654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72116729-A-G

http://identifiers.org/hco/15/GRCh38#94062910-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72116496-A-C

94063525-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72115759-A-T

94063614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72115676-C-T

94063691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72115600-C-T

94063835-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72115081-A-T

94063842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72115074-G-T

94064022-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72114939-T-A

94064241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72114831-A-G

94064313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72114754-A-G

94064366-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72114700-G-C

94064366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72114700-G-T

94064399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72114688-C-T

94064411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72114676-T-C

94064439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72114648-A-G

94064439-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72114648-A-T

94064464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72114626-G-T

http://identifiers.org/hco/15/GRCh38#94064473-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72114617-C-A

94064502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72114590-G-A

94064502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72114590-G-T

94070333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72113205-G-A

http://identifiers.org/hco/15/GRCh38#94070361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72113180-C-A

94070361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72113180-C-T

94070382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72113164-C-T

94070403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72113144-T-C

94070520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 72113028-T-C

94070537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 72113011-G-A

http://identifiers.org/hco/15/GRCh38#94070607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#72112941-C-A

94070607-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72112941-C-G

94070817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72112733-A-G

94070874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72112672-C-T

94070882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72112645-G-A

94070882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72112645-G-T

94070885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27519
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 72112642-G-A