http://identifiers.org/hco/2/GRCh38#191846549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#51328919-C-A

191846549-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 51328919-C-G

191846549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 51328919-C-T

191846561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 51328907-C-T

191846696-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 51328772-T-G

191846714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 51328754-G-A

http://identifiers.org/hco/2/GRCh38#191846753-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#51328715-A-C

191846873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51328595-A-G

191846934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51328534-A-G

http://identifiers.org/hco/2/GRCh38#191847043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#51328448-C-A

191847043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51328448-C-T

191847045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51328446-G-A

191847045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51328446-G-T

http://identifiers.org/hco/2/GRCh38#191847104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51328393-C-A

http://identifiers.org/hco/2/GRCh38#191847121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51328376-C-A

191847121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51328376-C-T

http://identifiers.org/hco/2/GRCh38#191847483-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51328014-A-C

191847665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51327826-T-C

191847770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51327709-G-A

191847940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51327573-A-G

191848001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51327512-T-C

191848164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51327352-G-A

191848265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51327255-G-A

191848402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51327143-A-G

191848499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51327051-G-A

191848511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51327039-T-C

191848548-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51327004-T-G

191848629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51326920-A-G

191848699-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51326849-A-T

191848744-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51326804-T-G

191848837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51326720-C-T

http://identifiers.org/hco/2/GRCh38#191848947-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51326615-A-C

191848957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51326605-C-T

191848983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51326579-C-T

191848984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51326578-G-A

191849298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51326147-T-C

191849471-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51325990-G-C

191849650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51325841-G-A

191850006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51325606-T-C

191850109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51325516-T-C

191850206-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51325412-T-A

191850247-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51325356-T-G

191850335-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51325263-A-T

191850555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51324733-C-T

191850589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51324699-T-C

191850761-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51324498-T-A

191851035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51324235-A-G

191851244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51323333-A-G

191852711-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51319475-A-T

191852880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51319346-G-T

191852882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51319344-T-C

191853013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51319214-G-T

191853093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51319141-G-A

191853154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51319084-G-A

191853187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51319060-C-T

191853237-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51319011-A-T

191853274-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51318976-T-A

http://identifiers.org/hco/2/GRCh38#191853487-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51318764-A-C

191853487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51318764-A-G

191854076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51317666-C-T

191854287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51317449-A-G

191854416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51317314-T-C

191854571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51317170-C-T

191854655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51316962-G-A

191854707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51316913-G-T

191854782-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51316863-G-C

191854811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51316834-C-T

191854832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51316813-A-G

191854832-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51316813-A-T

191854915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51316734-G-A

191854915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51316734-G-T

191854990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51316660-A-G

191855248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51316399-G-A

191855442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51316176-C-T

191855498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51316123-G-A

191855498-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51316123-G-C

191855650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51316005-A-G

191855665-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51315990-G-C

http://identifiers.org/hco/2/GRCh38#191855811-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51315842-A-C

191856030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51315194-A-G

191856080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51315144-C-T

191856120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51315112-G-T

191856209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51315025-C-T

http://identifiers.org/hco/2/GRCh38#191856551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#51314438-C-A

191856551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51314438-C-T

191856987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51314073-T-C

http://identifiers.org/hco/2/GRCh38#191857207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51313739-C-A

191857352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51313583-A-G

191857423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51313522-T-C

191857656-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51313303-T-A

191857705-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51313258-T-A

191857727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51313237-T-C

191857873-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51313086-T-G

191857938-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51313021-T-G

191858084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51312868-A-G

191858569-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51312444-T-G

191858649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51312365-T-C

191858650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51312364-T-C

191858849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51312144-C-T

191859035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51311962-G-A

191859394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51311605-T-C

191859402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51311597-T-C

191859545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51311469-T-C

191859573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51311441-A-G

191859585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51311429-G-A

191859590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51311424-A-G

191861501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51310373-C-T

http://identifiers.org/hco/2/GRCh38#191861840-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51310036-A-C

http://identifiers.org/hco/2/GRCh38#191861845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51310031-C-A

191861924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51309934-C-T

191861978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51309892-C-T

http://identifiers.org/hco/2/GRCh38#191862085-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51309799-A-C

191862552-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51309346-T-G

191862568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51309333-C-T

191862600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51309301-G-A

191862683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51309216-A-G

191862728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51309185-C-T

191862809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51309098-C-T

191862975-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51308957-G-C

191862991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51308944-A-G

191863431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51308382-G-A

191863649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51308126-G-A

191863708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51308067-C-T

191863852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51307915-A-G

http://identifiers.org/hco/2/GRCh38#191863920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51307848-C-A

191863932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51307836-A-G

191863969-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51307800-T-G

191864016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51307743-T-C

http://identifiers.org/hco/2/GRCh38#191864159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51307601-C-A

191864196-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51307564-A-T

191864241-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51307519-A-T

191864576-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51307185-T-G

191864588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51307167-G-A

http://identifiers.org/hco/2/GRCh38#191864648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51307110-C-A

191864803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51306923-T-C

191864888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51306821-T-C

191864888-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51306821-T-G

191865176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51306545-G-T

191865275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51306447-T-C

191865539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51306190-A-G

191865590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51306143-T-C

191865606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51306127-A-G

191865852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51305933-C-T

191866020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51305520-T-C

191866038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51305505-C-T

191866254-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51305338-G-C

191866540-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51305057-T-A

191866835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51304765-C-T

191867076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51304532-G-A

191867146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51304468-G-T

191869330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51303040-G-A

191869359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51303010-T-C

191869399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51302972-A-G

191869511-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51302866-C-G

191869577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51302800-G-A

191869577-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51302800-G-C

191869770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51302646-A-G

191869954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51302457-G-A

191870149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51302269-C-T

http://identifiers.org/hco/2/GRCh38#191871060-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51301793-A-C

191871429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51301271-A-G

191871595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51301126-T-C

191871667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51301037-A-G

191871875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51300871-A-G

191872089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51300680-G-A

191872683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51300409-C-T

191872791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51300088-C-T

191873039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51299825-T-C

191874028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51298444-C-T

191874031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51298441-C-T

191874046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51298426-A-G

http://identifiers.org/hco/2/GRCh38#191874120-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51298368-A-C

191874164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51298330-G-A

191874164-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51298330-G-C

191874218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51298273-A-G

191874284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51298195-T-C

191874574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51297692-C-T

191874615-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51297651-G-C

191874620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51297646-A-G

191874839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51297428-T-C

191875253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51296989-C-T

191875258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51296984-T-C

191875479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51296770-C-T

http://identifiers.org/hco/2/GRCh38#191875604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51296649-C-A

191876882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51290147-G-A

191876896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51290133-T-C

http://identifiers.org/hco/2/GRCh38#191877276-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51289791-A-C

191877324-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51289736-T-A

191877326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51289734-G-A

http://identifiers.org/hco/2/GRCh38#191877421-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51289650-A-C

191877430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51289640-C-T

191877700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51289390-G-T

191877736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51289344-G-A

191877743-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51289337-T-G

191877746-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51289334-G-C

191878236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51288881-A-G

191878247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51288870-G-A

191878331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51288787-A-G

191878884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51288266-G-A

191879130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51288031-A-G

191879547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51286599-T-C

191879574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51286565-G-T

191879642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51286497-C-T

191879692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51286447-T-C

191882338-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51286169-T-A

191882465-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51286065-A-T

191882660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51285529-A-G

191882871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51285356-T-C

191882966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51285283-T-C

191883103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51285153-G-T

http://identifiers.org/hco/2/GRCh38#191883536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51285032-C-A

191883536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51285032-C-T

191883887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51284654-A-G

http://identifiers.org/hco/2/GRCh38#191883944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51284601-C-A

191884193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51284380-G-A

191884193-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51284380-G-C

191884203-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51284371-T-A

191884235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51284349-T-C

191884281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51284307-T-C

http://identifiers.org/hco/2/GRCh38#191884331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51284253-C-A

191884331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51284253-C-T

191884537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51284057-A-G

191884568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51284027-G-A

191885055-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51283500-C-G

http://identifiers.org/hco/2/GRCh38#191885144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51283391-C-A

191885225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51283309-A-G

191885452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51283082-G-A

191885542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51283003-A-G

191885721-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51282827-G-C

191885738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51282810-G-A

191885763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51282786-G-A

191885920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51282633-G-A

http://identifiers.org/hco/2/GRCh38#191886079-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51282474-A-C

191886427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51282212-G-A

191886823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51281859-A-G

191886871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51281814-C-T

191886873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51281812-G-A

191886887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51281795-T-C

191887534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51281198-T-C

191887547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51281185-T-C

191887549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51281183-T-C

191888017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51280745-T-C

191888143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51280619-C-T

191888761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51280003-T-C

191889314-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51279474-C-G

191889452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51279103-A-G

191889557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51278998-C-T

191889923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51278643-T-C

191890546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51278405-A-G

191890590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51278360-G-A

191890638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51278320-G-A

191891100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51277893-A-G

191891120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51277873-T-C

191891212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51277731-A-G

191891297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51277655-G-A

191891297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51277655-G-T

191894420-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51276564-A-T

191894921-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51276140-T-A

191894993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51276068-C-T

191898222-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51275707-A-T

191899258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51275117-C-T

191899380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51274995-C-T

191899412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51274966-T-C

191904718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51271285-T-C

191904719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51271284-T-C

191904775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51271231-A-G

http://identifiers.org/hco/2/GRCh38#191905173-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51270834-A-C

191905173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51270834-A-G

191905200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51270811-G-A

191905308-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51270706-T-A

191905308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51270706-T-C

191905444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51270598-T-C

191906363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51268922-G-A

191906553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51268560-G-T

191906674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51268236-A-G

191907002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51267908-T-C

191907201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51267716-T-C

191909948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51267520-T-C

191910258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51267248-G-T

http://identifiers.org/hco/2/GRCh38#191910541-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51266977-A-C

191910542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51266976-T-C

http://identifiers.org/hco/2/GRCh38#191910578-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51266943-A-C

191910619-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51266909-G-C

191910634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51266894-C-T

191910860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51266632-A-G

http://identifiers.org/hco/2/GRCh38#191911054-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51266534-A-C

191911054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51266534-A-G

191911054-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51266534-A-T

191911538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51266288-C-T

191911712-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51266101-G-C

191911822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51266015-A-G

191911847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51265990-T-C

191911979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51265860-G-A

191912295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51265539-T-C

191912471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51265377-T-C

191912530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51265238-A-G

191913745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51263839-G-A

191913824-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51263760-T-G

191914422-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51263163-C-G

http://identifiers.org/hco/2/GRCh38#191914442-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51263143-A-C

191914541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51263049-T-C

191914821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51262580-A-G

191914839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51262562-A-G

191914870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51262531-C-T

191915133-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51262016-G-C

http://identifiers.org/hco/2/GRCh38#191915897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51261341-C-A

http://identifiers.org/hco/2/GRCh38#191917048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51257247-C-A

191917086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51257209-A-G

191917186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51257104-G-A

191917186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51257104-G-T

191917286-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51257004-T-A

http://identifiers.org/hco/2/GRCh38#191918083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51256063-C-A

http://identifiers.org/hco/2/GRCh38#191918315-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51255846-A-C

191918938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51255237-A-G

191918951-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51255225-T-A

191918951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51255225-T-C

http://identifiers.org/hco/2/GRCh38#191919158-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51255020-A-C

191919897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51253298-C-T

191920016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51253204-G-T

191920018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51253202-T-C

191920018-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51253202-T-G

http://identifiers.org/hco/2/GRCh38#191920125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51253080-C-A

191920137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51253068-G-A

191920162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51253044-C-T

191920262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51252954-A-G

191920459-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51252802-A-T

191920498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51252785-A-G

191920498-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51252785-A-T

191920736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51252538-C-T

191920809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51252465-T-C

191920923-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51252357-C-G

191921058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51252204-A-G

191921098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51252163-A-G

191921407-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51251878-T-G

191923003-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51251679-C-G

http://identifiers.org/hco/2/GRCh38#191923091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51251598-C-A

191923171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51251530-T-C

191923473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51251218-A-G

191923634-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51251048-T-G

191923888-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51250793-A-T

191923935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51250746-T-C

191923938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51250743-C-T

191924112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51250568-A-G

191924172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51250514-A-G

191924227-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51250459-T-A

191924556-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51250141-T-A

191924616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51250084-A-G

191924729-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51249973-T-G

191925815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51249245-G-T

191925925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51249127-C-T

http://identifiers.org/hco/2/GRCh38#191926311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51248833-C-A

191926366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51248782-A-G

191926439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51248717-A-G

191926800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51248393-A-G

191928316-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51244750-C-G

191928318-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51244748-T-G

191928810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51244383-A-G

191928936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51244254-T-C

191929120-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51244099-A-T

191929391-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51243839-T-A

191929419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51243814-G-A

191929669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51243553-C-T

191929698-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51243524-T-A

191930208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51243200-G-A

191930392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51243007-G-A

191930537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51242897-T-C

191930548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51242886-G-A

191930581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51242854-G-A

191930595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51242840-A-G

191930813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51242635-A-G

191931066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51242501-A-G

191931306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51242421-A-G

191931460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51242239-T-C

191931518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51242183-G-A

191931694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51242053-G-A

191931758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51241992-G-T

191932151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51241594-C-T

191932195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51241542-A-G

191932250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51241491-T-C

191932645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51240949-G-A

http://identifiers.org/hco/2/GRCh38#191933088-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51240527-A-C

http://identifiers.org/hco/2/GRCh38#191933157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51240459-C-A

191933157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51240459-C-T

191933216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51240391-T-C

191933254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51240356-T-C

191933745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51239954-C-T

191933790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51239911-G-T

191933807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51239894-T-C

191934729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51239561-C-T

191934753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51239538-T-C

191935171-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51239062-A-T

191935179-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51239054-C-G

191935179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51239054-C-T

http://identifiers.org/hco/2/GRCh38#191936540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51237692-C-A

191936908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51237379-G-A

191936985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51237317-C-T

http://identifiers.org/hco/2/GRCh38#191937051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51237267-C-A

http://identifiers.org/hco/2/GRCh38#191937363-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51236965-C-A

191937386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51236952-C-T

191937970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51236461-G-A

191938019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51236362-A-G

191938019-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51236362-A-T

191938306-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51235985-C-G

191938340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51235928-A-G

191938581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51235546-C-T

191938701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51235444-A-G

191939591-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51234604-T-G

191939889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51234368-T-C

191940595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51233297-A-G

191940798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51233093-A-G

191940904-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51232988-T-G

191940962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51232944-T-C

191941073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51232844-A-G

191941102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51232817-T-C

191941153-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51232762-T-A

191941428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51232492-C-T

http://identifiers.org/hco/2/GRCh38#191942044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51231859-C-A

191942113-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51231794-T-A

191942211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51231706-A-G

http://identifiers.org/hco/2/GRCh38#191942289-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#51231619-A-C

191942289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51231619-A-G

191942309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51231507-A-G

191942812-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51231005-C-G

191942920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51230898-T-C

191943110-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51230731-T-G

191943155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51230689-C-T

191943451-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51230453-T-A

191944858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51229568-G-A

191944959-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51229473-T-A

191945002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51229430-G-A

191945070-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51229382-A-T

191945422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51229080-A-G

191945500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51229003-T-C

191945745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51228768-G-A

191945979-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51228536-A-T

191946099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51228418-C-T

191946109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51228404-C-T

191946118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51228395-T-C

191946210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51228307-T-C

191946299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51228217-C-T

191946439-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51228076-T-G

191946869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51227701-G-A

191946933-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51227639-T-A

191947034-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51227562-C-G

191947034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51227562-C-T

191947095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51227504-T-C

191947648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51227267-A-G

191947688-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51227233-G-C

191947897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51227021-T-C

191947909-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51227009-C-G

191947921-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51226998-C-G

191947921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51226998-C-T

191948003-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51226910-T-A

191948003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51226910-T-C

191948003-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51226910-T-G

191948052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51226862-A-G

191948118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51226800-A-G

191948233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51226683-C-T

191948534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51226406-T-C

191948534-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51226406-T-G

191948686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51226256-G-A

191948824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51226122-G-A

191949011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51225925-G-A

191949011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51225925-G-T

191949052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51225888-G-A

191949143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51225787-T-C

191949161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51225769-A-G

191949242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51225689-G-T

191949302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51225641-A-G

191949393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51225550-T-C

191949403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51225538-G-T

191949488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51225462-G-A

http://identifiers.org/hco/2/GRCh38#191949834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#51225112-C-A

191949834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51225112-C-T

http://identifiers.org/hco/2/GRCh38#191949848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#51225098-C-A

191949848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51225098-C-T

191949916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51225030-G-T

191950576-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51224326-T-A

191950603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51224299-G-A

191950603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51224299-G-T

191950611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51224291-T-C

191950614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51224285-A-G

191950614-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51224285-A-T

191950971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51223914-T-C

191951382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51223505-G-T

191951511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51223362-G-A

191952649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51222213-G-T

191952715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51222147-T-C

191952872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51222003-G-A

191953327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51221592-A-G

191953543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51221178-A-G

191953554-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51221167-A-T

191953576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51221145-G-T

191953654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51221077-G-A

191953746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51220985-A-G

191953809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51220922-A-G

191953819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51220912-A-G

191953819-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51220912-A-T

191953832-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51220899-T-G

191954809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51220553-G-A

191955168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51220227-A-G

191955190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51220205-A-G

191956033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51219767-T-C

191956106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51219672-G-A

191956106-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51219672-G-C

191956106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51219672-G-T

191956112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51219666-G-A

191956112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51219666-G-T

191956116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51219662-G-A

191956116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51219662-G-T

http://identifiers.org/hco/2/GRCh38#191956117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51219661-C-A

191956117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51219661-C-T

191956327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51219460-G-A

191956327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51219460-G-T

191956408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51219379-C-T

191956415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51219372-T-C

191956667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51219113-C-T

191956789-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51218991-T-G

191957601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51215267-A-G

191957786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51215077-A-G

191957931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51214926-T-C

191957988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51214871-G-A

191958017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51214841-A-G

http://identifiers.org/hco/2/GRCh38#191958090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51214760-C-A

191958493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51214322-A-G

191958493-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51214322-A-T

191958605-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51214219-G-C

191958618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51214206-T-C

191958748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51214089-T-C

191958769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51214068-C-T

191959148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51213683-T-C

191959157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51213675-A-G

191959181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51213652-G-T

191959673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51213186-G-A

191959722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51213141-T-C

http://identifiers.org/hco/2/GRCh38#191960783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51212014-C-A

191960802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51211995-A-G

191961068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51211745-A-G

191961367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51211438-A-G

191961783-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51211051-G-C

191961783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51211051-G-T

191961863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51210967-T-C

191961888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51210942-T-C

191961917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51210913-G-A

191962506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51209717-A-G

191962535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51209689-A-G

191962764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51209041-T-C

191962830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51208980-C-T

191963089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51208748-C-T

http://identifiers.org/hco/2/GRCh38#191963134-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51208704-A-C

191963344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51208505-G-A

191963595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51208254-A-G

191963668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51208135-A-G

191963829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51207968-G-A

http://identifiers.org/hco/2/GRCh38#191963951-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51207855-A-C

191963963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51207843-A-G

191966657-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51206262-G-C

191966770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51206181-G-A

191966818-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51206144-A-T

191967026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51205942-G-A

191967057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51205906-A-G

191967304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51205145-T-C

191967335-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51205097-T-G

191967563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51204874-G-A

191967706-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51204761-C-G

191967706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51204761-C-T

191967843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51204640-A-G

191967908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51204575-C-T

191968080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51204452-T-C

191968206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51204317-A-G

191968802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51203760-G-A

191969006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51203571-A-G

191969189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51203495-G-A

191969497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51203181-T-C

http://identifiers.org/hco/2/GRCh38#191969713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51202967-C-A

191969713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51202967-C-T

191969738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51202942-G-A

http://identifiers.org/hco/2/GRCh38#191969854-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51202831-A-C

191970022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51202664-C-T

191970122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51202568-G-A

191970742-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51202140-T-G

191970776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51202108-A-G

191971260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51201031-A-G

191971273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51201017-C-T

191971470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51200656-G-A

191971782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51200329-C-T

191971869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51200194-T-C

191971871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51200192-C-T

191972045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51200023-G-T

191972958-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51198959-T-A

191973212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51198724-T-C

191973515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51198430-G-A

191973518-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51198427-T-G

http://identifiers.org/hco/2/GRCh38#191974072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: -C-A

191974326-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51198025-C-G

191974617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51197744-T-C

191974797-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51197550-T-A

191974797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51197550-T-C

191974911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51197447-G-A

191974981-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51197386-T-A

191975151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51196667-T-C

191975308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51196507-G-A

191975308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51196507-G-T

191975315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51196500-A-G

191975347-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51196472-G-T

191975358-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51196460-G-C

191975358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51196460-G-T

http://identifiers.org/hco/2/GRCh38#191975734-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#51196157-A-C

191975734-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51196157-A-T

http://identifiers.org/hco/2/GRCh38#191976070-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#51195838-A-C

191976074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51195834-G-T

http://identifiers.org/hco/2/GRCh38#191976130-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#51195778-A-C

191976209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51195704-A-G

191976748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51195631-G-A

191976958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51194385-G-A

http://identifiers.org/hco/2/GRCh38#191976965-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#51194378-A-C

191977191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51194184-A-G

191977237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51194137-T-C

191977373-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51194009-C-G

191977460-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51193905-T-A

191977702-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51193655-A-T

http://identifiers.org/hco/2/GRCh38#191978453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#51192918-C-A

http://identifiers.org/hco/2/GRCh38#191978750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#51192610-C-A

191978750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51192610-C-T

191978835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51192532-T-C

191979820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51191755-A-G

191979890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51191730-G-A

191980039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51191600-C-T

191980081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51191569-G-A

191980099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51191551-G-A

191980140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51191510-G-A

191980371-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51191289-C-G

http://identifiers.org/hco/2/GRCh38#191980934-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#51190748-A-C

191980963-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51190721-G-C

191980974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51190716-C-T

191981007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51190682-G-A

191981007-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51190682-G-C

191981153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51190581-T-C

191981170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51190564-G-A

191981170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51190564-G-T

191981291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51190443-T-C

191981772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51189574-C-T

191981898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51189368-G-A

191982315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51188991-T-C

191982374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51188936-T-C

191982459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51188850-T-C

191982459-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51188850-T-G

191982697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51188768-A-G

191982778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51188652-A-G

191983149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51188304-A-G

191983319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51188134-G-A

191983485-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51187968-T-G

191983661-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51187797-C-G

191984101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51187350-C-T

191984838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51186396-A-G

191985584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51185148-C-T

191985707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51185024-A-G

191986217-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51184528-G-C

191986422-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51184332-T-G

191986452-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51184301-A-T

191988412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51183301-T-C

191988953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51182847-A-G

191989025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51182742-G-T

191989375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51182463-T-C

191990006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51182036-G-T

191990051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51181991-C-T

191990258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51181788-T-C

191990517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51181396-G-A

191990548-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51181369-A-T

http://identifiers.org/hco/2/GRCh38#191990559-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51181358-A-C

191990595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51181318-T-C

191990687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51181239-C-T

191991164-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51180790-A-T

191991664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51180319-T-C

191992051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51179925-A-G

191992127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51179855-T-C

http://identifiers.org/hco/2/GRCh38#191992158-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51179824-A-C

191992280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51179706-T-C

http://identifiers.org/hco/2/GRCh38#191992636-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51179354-A-C

191992797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51178794-T-C

191993448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51178118-G-A

191993499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51178068-A-G

191993549-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51178011-T-A

191993581-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51177976-T-G

191993713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51177826-T-C

191993841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51177699-A-G

191993878-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51177663-A-T

191994022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51177519-T-C

191994166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51177378-G-A

191994379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51177174-T-C

http://identifiers.org/hco/2/GRCh38#191994460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51177091-C-A

191994514-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51177035-A-T

191994590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51176955-C-T

191994723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51176830-T-C

191995247-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51176300-T-A

191995247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51176300-T-C

191995387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51176173-G-A

191995515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51176045-C-T

191995708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51175868-G-A

191996241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51174854-T-C

191996281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51174816-G-A

191996729-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51174364-C-G

http://identifiers.org/hco/2/GRCh38#191996738-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51174357-A-C

191997120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51173615-C-T

191997443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51173306-A-G

191997510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51173239-G-T

http://identifiers.org/hco/2/GRCh38#191997661-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51172902-A-C

191997893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51172657-A-G

191998123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51172420-A-G

http://identifiers.org/hco/2/GRCh38#191998131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51172412-C-A

191998131-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51172412-C-G

191998131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51172412-C-T

191998149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51172390-G-A

191998149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51172390-G-T

191998209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51172324-G-A

191998209-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51172324-G-C

http://identifiers.org/hco/2/GRCh38#191998212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51172321-C-A

191998212-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51172321-C-G

http://identifiers.org/hco/2/GRCh38#191998337-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51172200-A-C

http://identifiers.org/hco/2/GRCh38#191998345-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51172192-A-C

191998345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51172192-A-G

191998976-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51171534-G-C

191998976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51171534-G-T

http://identifiers.org/hco/2/GRCh38#191998987-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51171523-A-C

http://identifiers.org/hco/2/GRCh38#191999200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#51171308-C-A

191999200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 51171308-C-T

http://identifiers.org/hco/2/GRCh38#191999242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51171267-C-A

191999242-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51171267-C-G

http://identifiers.org/hco/2/GRCh38#191999345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51171168-C-A

191999599-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51170981-T-A

191999659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51170921-A-G

191999671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51170909-A-G

191999710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51170870-C-T

191999714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51170866-C-T

191999842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51170740-C-T

http://identifiers.org/hco/2/GRCh38#191999885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51170697-C-A

191999885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51170697-C-T

191999899-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51170684-T-A

192000236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51170123-T-C

192000432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51169901-T-C

http://identifiers.org/hco/2/GRCh38#192000503-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51169832-A-C

192000668-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51169661-G-C

192000682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51169647-G-A

192000731-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51169607-A-T

192000743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51169597-A-G

192000824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51169517-C-T

192000900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51169449-C-T

192001017-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51169337-T-G

192001058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51169292-G-T

192001083-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51169267-T-A

192001239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51169132-A-G

192002897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51167858-A-G

192003002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51167755-C-T

192003010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51167747-C-T

http://identifiers.org/hco/2/GRCh38#192003152-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51167601-A-C

http://identifiers.org/hco/2/GRCh38#192003263-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51167502-A-C

192003440-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51167344-A-T

192003455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51167329-A-G

192003958-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51166874-T-G

192005007-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51165580-A-T

192005564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51165026-A-G

http://identifiers.org/hco/2/GRCh38#192005586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51165004-C-A

192005600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51164990-G-A

192005712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51164881-A-G

192006086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51164540-T-C

192006096-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51164530-T-A

http://identifiers.org/hco/2/GRCh38#192006614-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51163793-A-C

192006743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51163667-A-G

192006795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51163617-C-T

192006860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51163562-C-T

192006964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51163477-A-G

http://identifiers.org/hco/2/GRCh38#192007064-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51163377-A-C

192007064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51163377-A-G

192007335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51163160-G-A

192007535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51162939-G-A

192007603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51162870-A-G

192007805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51162663-G-A

192007857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51162611-A-G

192008252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51162263-C-T

192008582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51161354-C-T

192009033-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51160947-A-T

192009948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51159362-A-G

192010106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51159173-C-T

192010157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51159123-C-T

192010190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51159085-A-G

192011498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51156038-C-T

192011599-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51155320-A-T

http://identifiers.org/hco/2/GRCh38#192011650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51155276-C-A

192012841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51153641-C-T

192012869-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51153613-T-A

192012887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51153596-T-C

192013157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51153313-T-C

192013159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51153311-G-A

192013168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51153303-G-A

192013168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51153303-G-T

192013176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51153295-T-C

192013420-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51153112-A-T

192013638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51153057-C-T

192014269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51152532-G-A

192014401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51152142-A-G

192014469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51152074-C-T

192014475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51152068-A-G

192014527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51152018-A-G

http://identifiers.org/hco/2/GRCh38#192014558-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51151997-A-C

192014583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51151977-C-T

192015026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51151173-G-A

192015101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51151105-G-A

192015711-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51150516-C-G

192015711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51150516-C-T

192015775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51150455-G-A

192015837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51150394-C-T

http://identifiers.org/hco/2/GRCh38#192015873-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51150358-A-C

192016056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51150166-T-C

192016091-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51150138-A-T

http://identifiers.org/hco/2/GRCh38#192016456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51148253-C-A

192016894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51147842-T-C

192017112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51147691-G-A

192017352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51147513-A-G

192018192-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51147219-T-A

192018679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51146738-C-T

192018690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51146727-T-C

192018981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51146453-C-T

192019008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51146444-T-C

192019231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51146202-C-T

192019247-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51146186-T-A

http://identifiers.org/hco/2/GRCh38#192019299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51146136-C-A

192019299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51146136-C-T

192019536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51145889-T-C

192019928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51145495-C-T

192020157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51145288-T-C

192020158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51145287-G-A

192020216-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51145229-C-G

192020310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51145162-A-G

192020554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51144945-A-G

192020592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51144916-T-C

192021066-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51144473-A-T

192021397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51144186-T-C

192021763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51140961-G-T

192021773-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51140952-A-T

http://identifiers.org/hco/2/GRCh38#192021793-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51140935-A-C

192021818-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51140915-A-T

192021993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51140705-T-C

192022026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51140671-T-C

http://identifiers.org/hco/2/GRCh38#192022041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51140656-C-A

http://identifiers.org/hco/2/GRCh38#192022074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51140625-C-A

192022074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51140625-C-T

http://identifiers.org/hco/2/GRCh38#192022221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51140491-C-A

192022221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51140491-C-T

http://identifiers.org/hco/2/GRCh38#192022428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51140262-C-A

192022563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51140159-C-T

192022642-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51140080-T-G

192022944-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51139842-A-T

192023123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51139684-G-A

http://identifiers.org/hco/2/GRCh38#192023265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51139556-C-A

192023285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51139537-A-G

192023576-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51139298-C-G

192023639-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51139190-C-G

http://identifiers.org/hco/2/GRCh38#192023699-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51139104-A-C

192023699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51139104-A-G

192023797-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51138929-T-G

192024004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51138717-G-A

192024402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51138316-C-T

http://identifiers.org/hco/2/GRCh38#192024433-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51138282-A-C

192024460-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51138255-T-G

192024556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51138150-T-C

192024556-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51138150-T-G

192024574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51138135-C-T

192024611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51138084-T-C

192024711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51137989-T-C

192024711-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51137989-T-G

http://identifiers.org/hco/2/GRCh38#192024986-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51137741-A-C

192025212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51137520-G-A

192025675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51136752-G-A

192026028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51136389-T-C

192026441-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51135986-T-G

http://identifiers.org/hco/2/GRCh38#192027045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51135382-C-A

192027400-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51135031-A-T

http://identifiers.org/hco/2/GRCh38#192029616-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51133368-A-C

192029800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51133188-A-G

192029810-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51133178-T-A

192029921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51133063-A-G

192031342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51132415-T-C

192031500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51132262-A-G

192031501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51132261-T-C

192031514-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51132248-G-C

http://identifiers.org/hco/2/GRCh38#192031957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51131848-C-A

192031957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51131848-C-T

192032147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51131708-T-C

192032308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51131552-C-T

192032325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51131537-A-G

192032426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51131438-G-A

192032503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51131361-A-G

192032580-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51131284-G-T

192032601-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51131259-A-T

192032619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51131241-C-T

192032658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51131201-A-G

192032684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51131175-G-T

192032718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51131143-G-T

192032719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51131142-G-A

192032719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51131142-G-T

192032747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51131108-T-C

192032762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51131097-A-G

192032778-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51131085-T-A

http://identifiers.org/hco/2/GRCh38#192032781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51131079-C-A

192032797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51131063-A-G

192032857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51131007-A-G

http://identifiers.org/hco/2/GRCh38#192032865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51130999-C-A

192032898-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51130982-T-G

192032986-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51130895-C-G

192033173-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51130721-T-A

192033540-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51129792-T-A

192034210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51128895-A-G

http://identifiers.org/hco/2/GRCh38#192034591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51128463-C-A

192034691-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 51128366-T-G

192034752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 51128310-T-C

192034822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 51128240-G-A

192034822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 51128240-G-T

http://identifiers.org/hco/2/GRCh38#192034857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51128204-C-A

192034868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 51128193-T-C

http://identifiers.org/hco/2/GRCh38#192034877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51128184-C-A

192034877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 51128184-C-T

192034897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51128164-C-T

192034936-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51128124-C-G

http://identifiers.org/hco/2/GRCh38#192035133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51127953-C-A

192035159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51127927-A-G

192035272-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51127839-T-A

192035448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51127695-G-T

192035555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51127609-T-C

192035903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51127084-G-A

192035987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 51126995-G-T

http://identifiers.org/hco/2/GRCh38#192036092-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#51126894-A-C

192036488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51126649-G-A

192036488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51126649-G-T

192036581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51126582-G-T

192036596-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51126567-T-A

192036701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51126465-G-A

192036701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51126465-G-T

192036718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51126447-T-C

http://identifiers.org/hco/2/GRCh38#192036838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#51125897-C-A

192037114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51125662-A-G

192037119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51125657-A-G

192037554-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51125402-A-T

192037611-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51125345-A-T

192037855-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51124992-T-A

192038050-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 51124794-G-C

192039843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51124380-G-A

192039848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51124375-T-C

192039934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51124294-G-A

192040865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51123403-T-C

192040897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51123371-G-A

192040897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51123371-G-T

192040908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 51123360-A-G

192057589-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 51110864-A-T

192057852-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40517
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 51110547-T-A