104330554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39601633-T-C

104331235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39601918-A-G

104331262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39601943-G-A

104331402-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39602035-G-C

http://identifiers.org/hco/8/GRCh38#104331584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39602195-C-A

104331584-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39602195-C-G

104331665-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: non coding transcript exon variant
orthologous variants: 39602267-C-G

104331695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: non coding transcript exon variant
orthologous variants: 39602295-G-A

104331695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: non coding transcript exon variant
orthologous variants: 39602295-G-T

104331710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: non coding transcript exon variant
orthologous variants: 39602310-G-T

http://identifiers.org/hco/8/GRCh38#104331838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39602417-C-A

104331838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39602417-C-T

104331878-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39602444-C-G

104331878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39602444-C-T

104331883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39602449-A-G

104331953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: non coding transcript exon variant
orthologous variants: 39602513-A-G

104331986-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39602540-G-C

http://identifiers.org/hco/8/GRCh38#104331989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39602543-C-A

104332020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39602574-T-C

http://identifiers.org/hco/8/GRCh38#104332048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39602602-C-A

http://identifiers.org/hco/8/GRCh38#104332100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39602654-C-A

104332100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39602654-C-T

http://identifiers.org/hco/8/GRCh38#104332209-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39602769-A-C

http://identifiers.org/hco/8/GRCh38#104332267-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39602803-A-C

104337366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39606269-G-A

104337635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39606493-G-A

http://identifiers.org/hco/8/GRCh38#104337655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39606513-C-A

104339297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39608857-A-G

http://identifiers.org/hco/8/GRCh38#104339445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39608977-C-A

104339459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39608991-A-G

104339559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39609076-G-A

104339559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39609076-G-T

104339570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39609087-C-T

http://identifiers.org/hco/8/GRCh38#104339814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39609314-C-A

104339814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39609314-C-T

104339831-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39609332-T-G

104340032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39609544-C-T

104340161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39609691-T-C

104340214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39609747-G-A

104340214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39609747-G-T

http://identifiers.org/hco/8/GRCh38#104340217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39609750-C-A

http://identifiers.org/hco/8/GRCh38#104340236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39609769-C-A

104340236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39609769-C-T

104340252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39609785-G-T

104340290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39609819-G-A

104340290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39609819-G-T

104340347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39609875-G-A

104340510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39610054-T-C

104340816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39610346-A-G

104341786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39611172-G-A

104342071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39611459-T-C

104342135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39611507-G-A

104342202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39611554-G-A

104342285-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39611634-C-G

104342298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39611639-A-G

104344835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39612864-G-A

104344835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39612864-G-T

104345231-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39613819-G-C

104345273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39613867-G-A

104345825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39614383-A-G

104345897-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39614462-G-C

104346413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39614938-C-T

104346527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39615058-C-T

104346879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39616463-G-A

104346916-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39616502-T-A

104346936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39616522-T-C

104346946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39616532-A-G

104346946-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39616532-A-T

104346952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39616538-A-G

http://identifiers.org/hco/8/GRCh38#104347025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39616608-C-A

104347068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39616650-C-T

104348556-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39617596-G-C

104348840-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39617880-T-A

104348840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 39617880-T-C

http://identifiers.org/hco/8/GRCh38#104349089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39618129-C-A

104349089-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 39618129-C-G

104349089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 39618129-C-T

104349148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 39618188-A-G

104349153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 39618193-G-A

104349161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 39618201-C-T

104349219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 39618259-G-A

104349219-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 39618259-G-C

104349356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 39618396-G-A

104349356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 39618396-G-T

104349387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 39618427-A-G

104349392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 39618432-C-T

104349404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 39618444-G-T

104349422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 39618462-G-A

http://identifiers.org/hco/8/GRCh38#104349426-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39618466-A-C

104349427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 39618467-A-G

104349427-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 39618467-A-T

104349662-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39618698-C-G

104349666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39618702-G-A

104349666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39618702-G-T

104349685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39618718-T-C

104349891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39618898-G-A

104349918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39618954-C-T

104349919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39618955-G-A

104350019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39619028-C-T

104351022-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39619280-T-G

104351172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39619420-T-C

104351254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39619479-T-C

104352338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39619813-C-T

104352375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39619849-T-C

104352398-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39619871-G-C

104352494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39619969-C-T

104352931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39620716-G-A

104352931-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39620716-G-C

104353149-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39620931-C-G

104353342-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39621120-T-G

104353351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39621129-C-T

104353486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39621263-C-T

104353635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39621412-C-T

104353742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39621475-A-G

104353830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39621578-C-T

104354009-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39621758-C-G

104354254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39621959-G-A

104354254-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39621959-G-C

104354264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39621969-T-C

104354459-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39622154-A-T

http://identifiers.org/hco/8/GRCh38#104354641-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39622312-A-C

104354641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39622312-A-G

http://identifiers.org/hco/8/GRCh38#104354755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39622587-C-A

104354755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39622587-C-T

104354795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39622626-G-T

104354844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39622677-A-G

104354844-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39622677-A-T

http://identifiers.org/hco/8/GRCh38#104354935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39622768-C-A

104354935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 39622768-C-T

104355231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39623067-G-A

104355231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39623067-G-T

104355246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39623080-G-A

104355246-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39623080-G-C

104355249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39623083-A-G

104355803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39623471-A-G

104355890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39623556-T-C

http://identifiers.org/hco/8/GRCh38#104355976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39623634-C-A

104355976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39623634-C-T

104355977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39623635-A-G

104356136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 39623737-C-T

104356220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39623823-C-T

104356281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39623851-T-C

http://identifiers.org/hco/8/GRCh38#104356354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39623928-C-A

104356354-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39623928-C-G

http://identifiers.org/hco/8/GRCh38#104356360-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39623934-A-C

104356429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39624003-G-A

104356429-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39624003-G-C

104356429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39624003-G-T

104356472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39624404-G-A

104356472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39624404-G-T

http://identifiers.org/hco/8/GRCh38#104356493-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39624444-A-C

104356493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39624444-A-G

http://identifiers.org/hco/8/GRCh38#104356536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39624489-C-A

104356536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39624489-C-T

104356570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39624520-T-C

104356616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39624591-C-T

http://identifiers.org/hco/8/GRCh38#104356661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39624634-C-A

104356733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39624699-T-C

104356820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39624771-G-T

104357297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39628862-G-A

104357510-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39628990-T-G

http://identifiers.org/hco/8/GRCh38#104357531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39629011-C-A

104357554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39629034-C-T

http://identifiers.org/hco/8/GRCh38#104357855-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39629319-A-C

104358358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39629729-T-C

104358519-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39629883-C-G

104358519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39629883-C-T

104358522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39629886-T-C

104358555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39629915-C-T

104358789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39630456-C-T

104359071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39630736-C-T

104359532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39631160-G-A

104359538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39631166-A-G

104360125-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39631693-C-G

104360125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39631693-C-T

104360618-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39632174-T-A

104360618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39632174-T-C

104360758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39632317-A-G

104360835-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39632392-T-A

104360981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39634066-T-C

104360981-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39634066-T-G

104360999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39634075-A-G

104361085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39634160-T-C

104361086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39634161-G-A

104361158-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39634250-G-C

http://identifiers.org/hco/8/GRCh38#104361384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39634475-C-A

104361782-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39634888-T-G

104361930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39635038-A-G

104362311-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39635341-G-C

104362340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39635370-G-T

104362352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39635382-G-A

104362382-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39635410-T-A

104362383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39635411-C-T

104362750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39636527-G-A

104362792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39636568-G-T

104362862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39636598-A-G

104362910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39636640-C-T

104362944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39636666-G-T

104364327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39637739-T-C

104364327-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39637739-T-G

104364730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39638143-A-G

104364766-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39638165-A-T

104364785-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39638177-C-G

104364846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39638236-C-T

http://identifiers.org/hco/8/GRCh38#104364946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39638340-C-A

104364946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39638340-C-T

104365094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39638460-C-T

104365095-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39638461-T-A

104365095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39638461-T-C

104365155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39638886-A-G

104365327-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39639052-G-C

104365519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39639879-A-G

104365550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39639905-C-T

104365627-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39640153-G-C

104365754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39640245-C-T

104365819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39640291-C-T

104365976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39640399-T-C

104365977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39640400-C-T

http://identifiers.org/hco/8/GRCh38#104366041-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#39640444-A-C

104366041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 39640444-A-G

104366195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39640590-C-T

104366526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39640890-T-C

104366541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39640905-C-T

104366566-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39640930-C-G

104366568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39640932-G-A

104366613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39640977-A-G

104366622-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39640987-G-T

104366894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39641238-G-A

104367427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39641773-G-A

104367502-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39641837-G-C

http://identifiers.org/hco/8/GRCh38#104375026-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39642579-A-C

104375027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39642580-G-A

104375044-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39642598-A-T

104375046-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39642600-T-G

104375103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39642653-C-T

104375162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39642714-G-A

104375545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39643042-C-T

104375747-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39643501-T-A

104375766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39643520-C-T

http://identifiers.org/hco/8/GRCh38#104375927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39643615-C-A

104375927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39643615-C-T

104376246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39643909-C-T

104378392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39644671-T-C

104378478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39644761-T-C

104378596-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39644898-C-G

104378688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39645225-G-T

http://identifiers.org/hco/8/GRCh38#104378708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39645245-C-A

104378708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39645245-C-T

104378715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39645252-A-G

104378867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39645622-T-C

104378941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39645696-C-T

104378961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39645706-C-T

104378969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39645714-C-T

104379119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39645794-T-C

104379296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39645967-G-T

104379324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39645993-T-C

http://identifiers.org/hco/8/GRCh38#104379632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39646299-C-A

http://identifiers.org/hco/8/GRCh38#104379666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39646333-C-A

104379666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39646333-C-T

104379818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39646478-A-G

104379969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39646628-T-C

104379977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39646636-T-C

104380151-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39646811-T-G

104380291-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39646971-T-G

http://identifiers.org/hco/8/GRCh38#104380295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39646975-C-A

104380349-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39647167-A-T

104380354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39647172-T-C

104380622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39647424-A-G

http://identifiers.org/hco/8/GRCh38#104380702-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39647496-A-C

http://identifiers.org/hco/8/GRCh38#104380788-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39647589-A-C

104380788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39647589-A-G

104380788-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39647589-A-T

http://identifiers.org/hco/8/GRCh38#104380816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39647617-C-A

104380816-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39647617-C-G

104380816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39647617-C-T

104380859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39647666-A-G

http://identifiers.org/hco/8/GRCh38#104380869-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39647675-A-C

104380869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39647675-A-G

http://identifiers.org/hco/8/GRCh38#104380930-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39647733-A-C

104380948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39647751-G-A

104380948-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39647751-G-C

http://identifiers.org/hco/8/GRCh38#104380954-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39647757-A-C

104381030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39647829-G-T

104381145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39647923-T-C

104381185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 39647981-G-A

104381185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 39647981-G-T

104381228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 39648024-T-C

104381252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 39648048-G-A

104381308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 39648104-T-C

104381323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39648119-G-T

104381332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39648130-A-G

104381366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39648167-A-G

104382434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39648732-G-A

http://identifiers.org/hco/8/GRCh38#104382455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39648763-C-A

104382511-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39648830-A-T

104382531-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39648850-G-C

104382532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39648851-G-A

104382611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39648896-G-A

104382611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39648896-G-T

104382640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39648924-G-A

104382738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39649022-G-A

104382912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39649147-C-T

104383571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39649952-G-A

104383627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39649979-A-G

104383627-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39649979-A-T

104383632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39649984-C-T

104383966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39650076-C-T

104384114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39650236-G-A

104384141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39650260-C-T

http://identifiers.org/hco/8/GRCh38#104384233-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39650342-A-C

104384489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39650576-G-A

104384489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39650576-G-T

http://identifiers.org/hco/8/GRCh38#104384508-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39650595-A-C

104384536-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39650623-T-G

104384860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39650900-C-T

104384962-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39650995-G-C

104384982-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39651012-T-G

104385470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39651453-A-G

104387127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39651975-G-A

http://identifiers.org/hco/8/GRCh38#104387157-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39652013-A-C

104387461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39652239-C-T

104387663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39652348-T-C

http://identifiers.org/hco/8/GRCh38#104387884-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39652720-A-C

104387942-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39652775-G-C

104387943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39652776-C-T

104387983-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39652815-T-G

104387998-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39652830-C-G

104387998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39652830-C-T

104388666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39653572-T-C

104390970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39654350-T-C

104391011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39654387-T-C

104391017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39654393-C-T

104391048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39654425-C-T

104392446-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39656307-T-A

104392535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39656395-A-G

104392550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39656408-A-G

104392550-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39656408-A-T

104392641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39656491-C-T

104392698-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39656548-A-T

104392729-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39656580-T-A

104392729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39656580-T-C

104392736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39656587-G-A

104392777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 39656616-C-T

104392925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 39656764-G-A

104393050-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39656877-T-A

104393050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39656877-T-C

104393106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39656926-A-G

http://identifiers.org/hco/8/GRCh38#104393116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39656930-C-A

104393116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39656930-C-T

104393126-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39656940-T-A

104393385-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39657169-A-T

104393387-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39657171-T-G

104393411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39657194-G-A

104396430-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39659474-C-G

104396439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39659483-C-T

http://identifiers.org/hco/8/GRCh38#104396789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39659772-C-A

104396843-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39659818-T-A

104396843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39659818-T-C

104396843-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39659818-T-G

104396870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39659846-G-A

104396956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39659935-A-G

104397076-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39660052-A-T

104397247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39660314-C-T

104397258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39660325-A-G

104397287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39660411-G-A

104397362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39660525-G-A

104397604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39660749-C-T

104397685-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39660832-T-A

104397749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39660866-G-A

104397803-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39660920-G-C

104398933-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-T

http://identifiers.org/hco/8/GRCh38#104398938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-A

104400431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39662557-A-G

104400919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39662985-C-T

104401166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39663235-A-G

104401354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39663403-G-A

104401795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39663800-C-T

http://identifiers.org/hco/8/GRCh38#104402061-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39664085-A-C

104402347-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39664357-T-G

104402445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39664455-G-A

104402447-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39664457-T-G

104404490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39666221-C-T

104404657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39666597-T-C

104404661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39666601-A-G

104404685-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39666627-T-G

104404846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39666790-T-C

104404926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39666871-G-A

http://identifiers.org/hco/8/GRCh38#104405097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39667026-C-A

104405206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39667157-C-T

104405515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39667488-T-C

104405544-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39667517-C-G

104405546-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39667519-G-C

http://identifiers.org/hco/8/GRCh38#104405581-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39667552-A-C

104405586-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39667557-C-G

104405646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39667614-G-T

104405744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39667721-G-A

104405880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39667874-G-A

104406210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39668216-G-A

104406715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39669043-T-C

104406784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39669150-T-C

104406840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39669206-T-C

104406955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39669306-A-G

104406987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39669334-T-C

104407008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39669355-G-A

104407559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39669826-G-T

104407647-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39669916-A-T

104407667-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39669929-C-G

104407667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39669929-C-T

104407994-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39670302-T-A

104408029-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39670332-C-G

104408065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39670368-C-T

104408135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39670444-T-C

104408287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39670594-A-G

104408464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39670764-G-A

104408535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39670835-G-T

104408555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39670853-T-C

104408556-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39670854-T-G

http://identifiers.org/hco/8/GRCh38#104408599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39670908-C-A

104408599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39670908-C-T

http://identifiers.org/hco/8/GRCh38#104409542-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39671205-A-C

104409562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39671226-C-T

104409568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39671232-T-C

104409660-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39671317-T-A

104409704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39671348-T-C

104410152-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39671851-C-G

104410152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39671851-C-T

104410170-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39671865-T-G

104410254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39671984-C-T

104410305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39672034-T-C

104410331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39672064-C-T

104410340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39672073-C-T

104410688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39673107-A-G

104410837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39673255-C-T

104410870-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39673278-C-G

104410923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39673332-C-T

104410993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39673402-C-T

104411235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39673625-A-G

104411468-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39673809-G-C

104411535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39673852-C-T

104411584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39673899-A-G

http://identifiers.org/hco/8/GRCh38#104411634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39673937-C-A

104411634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39673937-C-T

104411649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39673951-T-C

104411696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39674002-G-A

104411696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39674002-G-T

http://identifiers.org/hco/8/GRCh38#104411712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39674018-C-A

http://identifiers.org/hco/8/GRCh38#104411934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39674202-C-A

104412408-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39674610-T-G

104412556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39674728-A-G

104412827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39675985-G-T

104412830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39675988-A-G

104412873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39676032-A-G

http://identifiers.org/hco/8/GRCh38#104412885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39676040-C-A

104414422-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39676335-G-C

104414425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39676338-T-C

104414425-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39676338-T-G

104414463-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39676372-G-C

104414518-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39676413-T-A

104414560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39676526-C-T

104414668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39676634-G-A

104414691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39676656-A-G

104414931-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39676844-T-G

104415039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39676960-C-T

104415081-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39677044-T-A

http://identifiers.org/hco/8/GRCh38#104415140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39677113-C-A

104415369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39677313-G-T

104415704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39677684-T-C

104415761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39677732-G-A

104415815-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39677780-A-T

104415840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39677809-G-A

104415890-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39677859-A-T

104415962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39677913-G-A

104416138-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39678057-T-A

104416181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39678123-G-T

104416206-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39678145-A-T

104416237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39678186-A-G

104416448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39678333-A-G

104416514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39678399-A-G

104416750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39679192-C-T

104416963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39679377-T-C

104417349-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39679780-T-A

104417391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39679822-T-C

http://identifiers.org/hco/8/GRCh38#104417408-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39679839-A-C

104417689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39680133-C-T

104417845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39680301-C-T

104417859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39680315-T-C

104418042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39680512-C-T

104418457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39680832-C-T

104418626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39680963-A-G

http://identifiers.org/hco/8/GRCh38#104418672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39680999-C-A

104418672-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39680999-C-G

104418672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39680999-C-T

104418676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39681002-A-G

http://identifiers.org/hco/8/GRCh38#104418695-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39681020-A-C

104418695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39681020-A-G

http://identifiers.org/hco/8/GRCh38#104418700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39681025-C-A

104418723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 39681045-G-A

104418723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 39681045-G-T

104418780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 39681108-T-C

104418780-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 39681108-T-G

104418833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 39681789-T-C

104418915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 39681853-A-G

104418920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 39681858-G-T

http://identifiers.org/hco/8/GRCh38#104418950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39681886-C-A

104418950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 39681886-C-T

104418963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 39681899-A-G

104419082-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39682000-T-G

104419458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39682516-A-G

http://identifiers.org/hco/8/GRCh38#104419471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39682529-C-A

104419544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 39682595-C-T

http://identifiers.org/hco/8/GRCh38#104419639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39682693-C-A

104419639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 39682693-C-T

104419640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 39682694-G-A

104419640-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 39682694-G-C

104419640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 39682694-G-T

http://identifiers.org/hco/8/GRCh38#104419641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39682695-C-A

104419648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 39682702-A-G

104419696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 39682747-G-A

104419704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 39682755-T-C

104419899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 39682951-T-C

104420043-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 39683062-T-A

104420043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 39683062-T-C

104420131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 39683137-A-G

104420151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 39683157-G-T

104420369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 39683372-G-T

104420403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 39683390-T-C

104420492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 39683478-T-C

http://identifiers.org/hco/8/GRCh38#104420500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39683486-C-A

104420500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 39683486-C-T

104420513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 39683496-T-C

104420513-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 39683496-T-G

104420569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 39683541-G-T

http://identifiers.org/hco/8/GRCh38#104420677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39683622-C-A

http://identifiers.org/hco/8/GRCh38#104420702-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39683647-A-C

http://identifiers.org/hco/8/GRCh38#104420799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39683729-C-A

104420799-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 39683729-C-G

104420801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 39683731-T-C

http://identifiers.org/hco/8/GRCh38#104421859-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39684665-A-C

104422059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39684866-G-T

104422076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39684883-G-A

104422225-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39685809-C-G

104422292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39685873-T-C

104422684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39686118-T-C

104422684-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39686118-T-G

104422693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39686123-C-T

104422908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39686313-A-G

104422939-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39686331-A-T

104423056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39686395-T-C

104423225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39686565-T-C

104423225-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39686565-T-G

104423394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39686727-C-T

http://identifiers.org/hco/8/GRCh38#104423401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39686734-C-A

104423412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39686746-C-T

104423627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39686956-G-A

104423819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39687145-G-T

104423830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39687156-G-T

104423899-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39687225-A-T

104423968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, stop_gained
orthologous variants: 39687295-G-A

104423968-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, missense_variant
orthologous variants: 39687295-G-C

104424006-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, missense_variant
orthologous variants: 39687333-G-C

http://identifiers.org/hco/8/GRCh38#104424045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39687361-C-A

104424045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, missense_variant
orthologous variants: 39687361-C-T

104424107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39687423-T-C

104424112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39687428-A-G

104424201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39687516-C-T

104424363-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: missense variant
orthologous variants: 39687678-T-A

104424427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39687749-T-C

104424446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39687768-G-A

104424446-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39687768-G-T

104424464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39687786-G-A

104424464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39687786-G-T

104424527-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39688020-G-C

104424527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39688020-G-T

104424739-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39688239-C-G

104424763-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39688262-G-C

http://identifiers.org/hco/8/GRCh38#104425697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39688410-C-A

104425697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39688410-C-T

http://identifiers.org/hco/8/GRCh38#104426367-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39689056-A-C

104426400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39689070-T-C

http://identifiers.org/hco/8/GRCh38#104426497-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39689166-A-C

104426871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39689907-C-T

104427698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39689977-C-T

104427841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39690112-G-A

104427841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39690112-G-T

104427852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39690128-C-T

104427983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: synonymous variant
orthologous variants: 39690263-G-A

104427983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: synonymous variant
orthologous variants: 39690263-G-T

104429461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 39691286-G-A

104429470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 39691294-G-A

104429511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 39691337-C-T

104429529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 39691355-T-C

104429700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 39691526-C-T

104429720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39691546-G-A

104429753-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39691578-C-G

104429753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39691578-C-T

http://identifiers.org/hco/8/GRCh38#104429789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39691611-C-A

104429789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39691611-C-T

104429808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39691629-T-C

http://identifiers.org/hco/8/GRCh38#104429818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39691639-C-A

104430138-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39692037-C-G

104430228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39692125-G-A

104430606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39693093-C-T

104430965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39693440-C-T

104431017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39693489-T-C

104431092-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 39693563-T-G

104431668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39694274-A-G

104431735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39694328-T-C

104431937-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39694525-T-A

104432036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39694624-A-G

104432036-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39694624-A-T

104432186-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39694754-C-G

104432365-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39694927-G-C

104432369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39694931-G-T

104432450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39694980-G-A

104432463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39694993-A-G

104432474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39695005-G-A

104432581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39695103-T-C

104432621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39695143-A-G

104432793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39695303-G-A

104432804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39695314-A-G

104432974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39695848-A-G

104433086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39695962-C-T

104433163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39696158-C-T

104434612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39696727-C-T

http://identifiers.org/hco/8/GRCh38#104434663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39696773-C-A

http://identifiers.org/hco/8/GRCh38#104434830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39696935-C-A

104434830-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39696935-C-G

104435402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39698218-T-C

104435625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39698357-G-A

104435625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39698357-G-T

http://identifiers.org/hco/8/GRCh38#104439275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39701522-C-A

104439275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39701522-C-T

104440064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39702164-G-T

http://identifiers.org/hco/8/GRCh38#104440347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39702399-C-A

104440409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39702457-T-C

http://identifiers.org/hco/8/GRCh38#104440416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39702469-C-A

104441048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39702799-A-G

104441094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39702857-G-T

104441131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39702892-A-G

http://identifiers.org/hco/8/GRCh38#104441160-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39702921-A-C

104441218-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39702984-T-G

104441448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39703205-T-C

104441609-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39703374-A-T

104441685-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39703446-G-C

http://identifiers.org/hco/8/GRCh38#104441960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39703762-C-A

104442077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39703879-G-A

104442129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39703928-A-G

http://identifiers.org/hco/8/GRCh38#104442167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39703975-C-A

104442263-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39704070-C-G

104442283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39704089-T-C

104442332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39704134-G-T

104442476-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39704253-C-G

104442476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39704253-C-T

104442585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39704379-C-T

104443142-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39704661-T-A

104443149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39704668-A-G

104443268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39704756-G-T

104443480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39704928-T-C

104443893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39705064-A-G

104443946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39705082-G-A

104444197-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39705271-T-A

104444215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39705288-T-C

104444215-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39705288-T-G

104444255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 39705326-C-T

104444264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 39705335-C-T

104444305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 39705376-T-C

104444305-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 39705376-T-G

104444416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: synonymous variant
orthologous variants: 39705487-G-A

104444416-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: missense variant
orthologous variants: 39705487-G-C

104444491-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39705562-A-T

104444498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39705566-T-C

104444550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39705619-G-T

104446330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39706074-A-G

104446445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39706196-T-C

104446518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39706257-T-C

104446569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39706309-T-C

104446751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39706469-T-C

104446891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39706609-G-A

http://identifiers.org/hco/8/GRCh38#104446964-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39706679-A-C

104447318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39707248-G-A

104447411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: missense variant
orthologous variants: 39707341-G-T

104447475-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: missense variant
orthologous variants: 39707405-T-A

104447600-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39707532-T-A

104447600-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39707532-T-G

http://identifiers.org/hco/8/GRCh38#104447620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39707552-C-A

104447620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39707552-C-T

http://identifiers.org/hco/8/GRCh38#104447680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39707600-C-A

104447680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39707600-C-T

104447731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39707682-G-A

104447810-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39707761-T-A

104447861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39707810-T-C

104449627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39708565-G-T

104449672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39708610-G-T

104449682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39708620-C-T

104449716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39708640-C-T

104449758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39708682-G-T

http://identifiers.org/hco/8/GRCh38#104449769-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39708695-A-C

104449897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39708790-G-T

104450002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39708839-G-A

104450203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39709011-A-G

104450253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39709071-C-T

104450341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39709157-T-C

104450404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39709219-T-C

104450409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39709224-T-C

104450527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39709341-A-G

104450577-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39709390-T-A

104450613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39709425-G-T

104450756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39709563-C-T

104450927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39709701-A-G

104450964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39709736-C-T

104451056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39709830-A-G

104451119-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39709858-T-A

104451208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39709966-G-A

104451208-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39709966-G-C

104451208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39709966-G-T

104451261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 39710020-C-T

104451424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39710183-T-C

http://identifiers.org/hco/8/GRCh38#104451467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39710228-C-A

104451467-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39710228-C-G

104451495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39710256-G-A

104451495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39710256-G-T

http://identifiers.org/hco/8/GRCh38#104451533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39710292-C-A

104451533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39710292-C-T

104451611-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39710369-G-C

104451611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39710369-G-T

104452171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39711702-A-G

104452400-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39711918-G-C

104452405-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39711923-C-G

104452405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39711923-C-T

104452458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39711972-C-T

104453151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39712395-C-T

104453217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39712462-T-C

104453334-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39712576-G-C

104453390-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39712635-G-C

104453434-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39712680-T-G

104457622-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39714684-A-T

104457626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39714688-G-A

104457637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39714699-G-A

104457705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39714767-A-G

http://identifiers.org/hco/8/GRCh38#104457924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39714980-C-A

104457961-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39715017-C-G

104458033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39715099-T-C

104458167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39715210-G-A

104458435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39715511-C-T

104461815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39716358-C-T

104461862-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39716404-A-T

http://identifiers.org/hco/8/GRCh38#104461866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39716408-C-A

104461874-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39716416-A-T

104462286-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39716780-C-G

http://identifiers.org/hco/8/GRCh38#104462492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39716936-C-A

104462515-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39716959-G-C

104462654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39717139-A-G

104462763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39717239-T-C

104463325-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39717785-T-A

104463809-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39718283-C-G

104463809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39718283-C-T

104463883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39718325-A-G

104463895-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39718337-T-A

104463970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39718409-G-T

104464515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39718898-G-T

104464829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39719184-T-C

104465080-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39719418-T-A

104465363-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39719586-A-T

104465453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39719678-T-C

http://identifiers.org/hco/8/GRCh38#104465465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39719690-C-A

104465465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron variant
orthologous variants: 39719690-C-T

104466192-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39720117-A-T

104466245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39720148-T-C

104466338-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39720248-T-A

104466415-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39720327-T-G

104466534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39720410-C-T

104466623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39720478-G-A

104466623-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39720478-G-C

104466623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 39720478-G-T

http://identifiers.org/hco/8/GRCh38#104466690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39720528-C-A

104466690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 39720528-C-T

104466744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 39720582-G-A

104466744-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 39720582-G-C

104466744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 39720582-G-T

http://identifiers.org/hco/8/GRCh38#104466750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39720588-C-A

104466750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 39720588-C-T

http://identifiers.org/hco/8/GRCh38#104466771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39720609-C-A

104466771-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 39720609-C-G

104466771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 39720609-C-T

http://identifiers.org/hco/8/GRCh38#104466777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39720615-C-A

104466777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 39720615-C-T

http://identifiers.org/hco/8/GRCh38#104466793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#39720631-C-A

104466811-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 39720649-T-A

104466811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 39720649-T-C

104466811-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 39720649-T-G

104466849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 39720687-G-A

104466849-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 39720687-G-C

104466849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 39720687-G-T

104466863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 39720701-A-G

104466870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 39720708-A-G

http://identifiers.org/hco/8/GRCh38#104466881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39720719-C-A

104466881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 39720719-C-T

http://identifiers.org/hco/8/GRCh38#104466883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39720721-C-A

104466883-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 39720721-C-G

104466883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 39720721-C-T

104466896-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 39720734-T-A

104466896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 39720734-T-C

http://identifiers.org/hco/8/GRCh38#104466897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39720735-C-A

104466897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 39720735-C-T

104466907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 39720745-G-A

104466907-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 39720745-G-C

104466907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 39720745-G-T

104466929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39720767-G-A

104466929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39720767-G-T

http://identifiers.org/hco/8/GRCh38#104466930-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39720768-C-A

104466930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39720768-C-T

http://identifiers.org/hco/8/GRCh38#104466958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39720780-C-A

104466958-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39720780-C-G

104466958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39720780-C-T

104466961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39720783-G-A

104466961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39720783-G-T

http://identifiers.org/hco/8/GRCh38#104467030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#39720823-C-A

104467030-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39720823-C-G

104467030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39720823-C-T

104467045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39720838-G-A

104467045-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39720838-G-C

104467045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39720838-G-T

104467049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3013
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 39720855-C-T