64340357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6835414-G-A

64340357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6835414-G-T

64340396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6835367-G-A

64340396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6835367-G-T

64340401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6835362-G-A

64340401-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6835362-G-C

64340401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6835362-G-T

64340408-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6835356-T-A

64340408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6835356-T-C

64340408-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6835356-T-G

http://identifiers.org/hco/11/GRCh38#64340417-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6835347-A-C

64340417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6835347-A-G

64340475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6835288-G-A

64340475-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6835288-G-C

64340475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6835288-G-T

64340477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6835286-T-C

64340627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6835137-G-T

64340667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: non_coding_transcript_exon_variant, stop_gained, undefined
orthologous variants: 6835085-G-T

http://identifiers.org/hco/11/GRCh38#64340709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6835043-C-A

64340709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6835043-C-T

http://identifiers.org/hco/11/GRCh38#64340799-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#6834973-A-C

64340799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6834973-A-G

64340839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6834947-G-A

64340851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6834936-G-A

64340851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6834936-G-T

64340879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6834906-G-A

64340879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6834906-G-T

64340932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6834836-C-T

http://identifiers.org/hco/11/GRCh38#64340946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6834822-C-A

64341130-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6834651-C-G

64341257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6834536-A-G

64341518-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6834286-T-G

64341592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 6833625-G-A

64341592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 6833625-G-T

64341698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6833519-G-A

64341698-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6833519-G-C

64341840-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6833460-T-A

64341840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6833460-T-C

64342057-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6833290-G-C

http://identifiers.org/hco/11/GRCh38#64342155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6833192-C-A

http://identifiers.org/hco/11/GRCh38#64342286-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#6833107-C-A

64342286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 6833107-C-T

64342355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6833038-A-G

http://identifiers.org/hco/11/GRCh38#64342423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6832966-C-A

64342423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6832966-C-T

64342440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6832945-T-C

64342474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6832928-C-T

64342522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: 6832880-G-A

64342522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: 6832880-G-T

http://identifiers.org/hco/11/GRCh38#64342636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#6832766-C-A

64342636-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6832766-C-G

64342636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6832766-C-T

64342722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6832670-G-A

64342722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6832670-G-T

64342728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6832664-G-A

64342728-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6832664-G-C

64342728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6832664-G-T

64342759-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6832638-G-C

http://identifiers.org/hco/11/GRCh38#64342803-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6832591-A-C

64342806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 6832588-G-A

64342806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 6832588-G-T

64342810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6832584-G-A

64342810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6832584-G-T

64342830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6832569-G-A

http://identifiers.org/hco/11/GRCh38#64342847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6832554-C-A

64342847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6832554-C-T

64342852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6832549-G-A

64342852-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6832549-G-C

64342852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6832549-G-T

64342987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6832435-G-A

64343077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6832355-A-G

64343077-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6832355-A-T

64343082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6832350-G-A

64343082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6832350-G-T

http://identifiers.org/hco/11/GRCh38#64343162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6832271-C-A

64343162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6832271-C-T

http://identifiers.org/hco/11/GRCh38#64343221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6832212-C-A

http://identifiers.org/hco/11/GRCh38#64343224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6832209-C-A

64343224-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6832209-C-G

64343245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6832188-G-T

64343398-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6832038-T-A

64343627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6831832-C-T

64343635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6831824-G-A

64343738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6831731-G-A

64343738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6831731-G-T

64343825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6831643-G-A

64343825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6831643-G-T

http://identifiers.org/hco/11/GRCh38#64343863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6831605-C-A

64343863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6831605-C-T

64343938-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6831528-T-A

64344168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6831294-G-A

64344168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6831294-G-T

http://identifiers.org/hco/11/GRCh38#64344172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: non_coding_transcript_exon_variant, stop_gained, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#6831290-C-A

64344172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6831290-C-T

64344192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6831270-C-T

64344221-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6831244-T-A

64344221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6831244-T-C

http://identifiers.org/hco/11/GRCh38#64344451-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6831017-A-C

64344451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6831017-A-G

64344482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6830986-G-A

64344532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6830933-A-G

64344580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6830885-G-A

64344580-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6830885-G-C

64344646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6830819-C-T

64344678-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6830787-G-C

64344767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6830698-G-A

64344847-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6830618-T-A

64344894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6830571-G-A

64344894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6830571-G-T

http://identifiers.org/hco/11/GRCh38#64344914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6830551-C-A

64344914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6830551-C-T

64344936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6830529-G-A

64344936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6830529-G-T

64345119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6830346-G-A

64345119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6830346-G-T

http://identifiers.org/hco/11/GRCh38#64345133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6830332-C-A

64345133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6830332-C-T

64345140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6830325-A-G

64345140-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 6830325-A-T

64345186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6830285-G-A

64345186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6830285-G-T

64345447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6830048-A-G

64348401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6829145-T-C

64348401-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6829145-T-G

64348408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6829138-G-A

64348438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6829119-C-T

http://identifiers.org/hco/11/GRCh38#64348743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#6828570-C-A

64348743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6828570-C-T

http://identifiers.org/hco/11/GRCh38#64348862-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#6828477-A-C

64348862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6828477-A-G

64348993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 6828378-G-T

64349031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 6828343-G-T

64349039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 6828335-G-A

64349039-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 6828335-G-C

64349130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6828235-A-G

64349130-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6828235-A-T

http://identifiers.org/hco/11/GRCh38#64349317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6827952-C-A

64349317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6827952-C-T

64349347-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6827922-T-A

64349347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6827922-T-C

64349594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6827696-G-A

64349702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6827595-G-A

64349702-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6827595-G-C

64349702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6827595-G-T

http://identifiers.org/hco/11/GRCh38#64349747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6827551-C-A

64349747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6827551-C-T

64349766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6827533-G-A

64349766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6827533-G-T

64349780-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6827519-T-A

64349780-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6827519-T-G

http://identifiers.org/hco/11/GRCh38#64349790-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6827510-A-C

64349800-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6827500-T-A

64349929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6827430-G-A

64349929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6827430-G-T

http://identifiers.org/hco/11/GRCh38#64351166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6827357-C-A

64351166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 6827357-C-T

64351195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6827328-G-A

64351195-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6827328-G-C

64351214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6827309-G-A

64351230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6827293-T-C

64351241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 6827282-G-T

64351427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6827226-A-G

64351476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 6827190-A-G

64351554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6827112-G-A

64351554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6827112-G-T

64351590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6827076-G-A

64351590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6827076-G-T

http://identifiers.org/hco/11/GRCh38#64351657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6827013-C-A

64351657-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6827013-C-G

64351657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6827013-C-T

http://identifiers.org/hco/11/GRCh38#64351700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6826996-C-A

64351700-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6826996-C-G

64351700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6826996-C-T

64351846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6826867-G-A

64351846-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6826867-G-C

http://identifiers.org/hco/11/GRCh38#64352009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6826703-C-A

64352009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6826703-C-T

64352011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6826701-T-C

http://identifiers.org/hco/11/GRCh38#64352013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6826699-C-A

64352042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6826676-T-C

64352042-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6826676-T-G

64352043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6826675-A-G

64352102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6826623-C-T

http://identifiers.org/hco/11/GRCh38#64352154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6826573-C-A

64352154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 6826573-C-T

http://identifiers.org/hco/11/GRCh38#64352262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6826465-C-A

64352262-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6826465-C-G

64352262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6826465-C-T

64352403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6826324-G-A

64352403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6826324-G-T

http://identifiers.org/hco/11/GRCh38#64352415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6826311-C-A

64352415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6826311-C-T

http://identifiers.org/hco/11/GRCh38#64352434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6826293-C-A

64352434-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6826293-C-G

64352434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6826293-C-T

64352488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6826250-T-C

http://identifiers.org/hco/11/GRCh38#64352634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6826150-C-A

http://identifiers.org/hco/11/GRCh38#64352968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6825801-C-A

64352968-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6825801-C-G

64352968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6825801-C-T

64353070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6825718-G-A

64353112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6825676-G-A

64353293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6825497-A-G

64353372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6825424-G-A

http://identifiers.org/hco/11/GRCh38#64353689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6825126-C-A

64353689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6825126-C-T

64353840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6824981-G-A

http://identifiers.org/hco/11/GRCh38#64353903-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6824908-A-C

64353935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6824875-T-C

64354062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6824751-G-A

64354062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6824751-G-T

http://identifiers.org/hco/11/GRCh38#64354106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6824707-C-A

64354106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 6824707-C-T

64354200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6824614-G-A

64354200-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6824614-G-C

64354200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6824614-G-T

http://identifiers.org/hco/11/GRCh38#64354218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6824603-C-A

64354218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6824603-C-T

http://identifiers.org/hco/11/GRCh38#64354226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6824595-C-A

64354226-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6824595-C-G

64354226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6824595-C-T

64354251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6824570-G-A

64354251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6824570-G-T

http://identifiers.org/hco/11/GRCh38#64354309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6824522-C-A

64354309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6824522-C-T

64354471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6824358-G-A

64354666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6824190-T-C

64354666-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6824190-T-G

http://identifiers.org/hco/11/GRCh38#64355198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#6824131-C-A

64355198-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 6824131-C-G

64355198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 6824131-C-T

64355273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 6824056-G-A

http://identifiers.org/hco/11/GRCh38#64355295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#6824034-C-A

64355295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 6824034-C-T

http://identifiers.org/hco/11/GRCh38#64355369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#6823960-C-A

64355369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 6823960-C-T

64355372-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 6823957-C-G

64355372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 6823957-C-T

64355412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 6823918-G-A

64355412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 6823918-G-T

64355438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6823895-A-G

64355441-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6823892-C-G

64355549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 6823792-G-A

64355549-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 6823792-G-C

http://identifiers.org/hco/11/GRCh38#64355608-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#6823733-A-C

64355661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6823698-T-C

http://identifiers.org/hco/11/GRCh38#64355717-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6823643-A-C

64355717-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6823643-A-T

64355779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6823578-G-A

64355779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6823578-G-T

64355871-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 6823435-T-A

64355983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6823235-G-T

http://identifiers.org/hco/11/GRCh38#64356015-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6823216-A-C

64356015-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6823216-A-T

64356070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6823146-C-T

64356079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6823129-G-A

64356125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6823089-C-T

64356696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 6822726-G-A

64356696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 6822726-G-T

http://identifiers.org/hco/11/GRCh38#64356721-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6822702-A-C

64356721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6822702-A-G

64356728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 6822695-G-A

64356728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 6822695-G-T

64356732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 6822691-G-A

64356732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 6822691-G-T

64357010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6822514-G-A

64357010-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6822514-G-C

64357039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 6822485-G-T

http://identifiers.org/hco/11/GRCh38#64357056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6822468-C-A

64357056-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6822468-C-G

64357056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6822468-C-T

http://identifiers.org/hco/11/GRCh38#64357110-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6822414-A-C

64357110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6822414-A-G

64357142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6822382-G-A

64357142-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6822382-G-C

64357170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6822354-G-A

64357170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6822354-G-T

64357299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 6822225-G-A

64357299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6822225-G-T

http://identifiers.org/hco/11/GRCh38#64357345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6822179-C-A

64357345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6822179-C-T

http://identifiers.org/hco/11/GRCh38#64357351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6822173-C-A

64357351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6822173-C-T

64357465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6822061-G-A

64357465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6822061-G-T

http://identifiers.org/hco/11/GRCh38#64357494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6822030-C-A

64357494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26757
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6822030-C-T