5748190-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37477694-C-G

5748190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37477694-C-T

5748191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37477693-T-C

5748323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37477558-C-T

5748353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37477539-A-G

5748383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37477531-A-G

5748411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37477505-T-C

5748523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37477421-T-C

5748563-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37477387-T-A

5752861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37476422-G-A

5752861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37476422-G-T

5753010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 37476273-C-T

5753066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37476216-A-G

5753067-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37476215-T-G

5753095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37476212-T-C

5753207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37476129-T-C

5753464-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37475912-A-T

5753554-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37475831-C-G

http://identifiers.org/hco/4/GRCh38#5753713-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37475725-A-C

5753713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 37475725-A-G

5753757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 37475681-C-T

5753789-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37475649-T-A

5753793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 37475645-C-T

5753884-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 37475554-G-C

5753910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 37475528-G-A

5753910-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 37475528-G-C

5753960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 37475474-A-G

5753960-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 37475474-A-T

http://identifiers.org/hco/4/GRCh38#5754048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37475407-C-A

5754048-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 37475407-C-G

5754048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 37475407-C-T

5754157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37475333-T-C

5754205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37475290-C-T

5754206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37475289-G-A

5754206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37475289-G-T

5755368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37474664-G-T

5755392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37474640-G-A

5755445-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37474578-G-C

5755462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37474564-C-T

5755463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37474563-G-A

5755529-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37474496-A-T

5755562-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37474463-G-C

5755792-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37474244-T-G

5756137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37473886-T-C

5756177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37473851-A-G

5756177-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37473851-A-T

5756189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37473838-G-A

5756189-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37473838-G-T

5756193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37473831-G-A

5756193-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37473831-G-C

5756193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37473831-G-T

http://identifiers.org/hco/4/GRCh38#5756237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37473793-C-A

5756237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37473793-C-T

http://identifiers.org/hco/4/GRCh38#5756330-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37473699-A-C

5756330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 37473699-A-G

5756823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37473089-G-A

5756823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37473089-G-T

5756873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37473041-G-T

5756897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37473017-G-A

5757203-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37472728-T-G

5757390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37472560-A-G

5783626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 37471839-G-T

5783641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 37471824-G-A

5783641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 37471824-G-T

5783653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 37471812-C-T

5783663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 37471802-C-T

http://identifiers.org/hco/4/GRCh38#5783744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37471721-C-A

5783744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 37471721-C-T

http://identifiers.org/hco/4/GRCh38#5783811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37471655-C-A

5783848-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37471624-C-G

5783861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37471611-A-G

5783861-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37471611-A-T

http://identifiers.org/hco/4/GRCh38#5793665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37470823-C-A

5793665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37470823-C-T

5793681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37470807-G-A

5793681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37470807-G-T

http://identifiers.org/hco/4/GRCh38#5793746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37470746-C-A

5793746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37470746-C-T

5793777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37470717-T-C

5793780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37470714-G-A

5793780-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37470714-G-C

5793797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37470697-G-T

5794010-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37470493-C-G

5794188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37470356-G-T

5794202-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37470339-T-G

5794215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37470326-A-G

5796595-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37469429-G-C

5796800-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37469240-G-C

http://identifiers.org/hco/4/GRCh38#5796911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37469179-C-A

5796911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37469179-C-T

5796954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37469145-G-A

5796954-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37469145-G-C

5796954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37469145-G-T

http://identifiers.org/hco/4/GRCh38#5796960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37469139-C-A

5796987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37469113-G-T

5796992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37469108-G-A

5796992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37469108-G-T

http://identifiers.org/hco/4/GRCh38#5797048-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37469058-A-C

5797048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37469058-A-G

http://identifiers.org/hco/4/GRCh38#5797256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37468849-C-A

http://identifiers.org/hco/4/GRCh38#5797276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37468829-C-A

5797276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37468829-C-T

http://identifiers.org/hco/4/GRCh38#5797278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37468827-C-A

5797278-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37468827-C-G

5797278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37468827-C-T

http://identifiers.org/hco/4/GRCh38#5797342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37468796-C-A

5797342-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37468796-C-G

5797342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37468796-C-T

http://identifiers.org/hco/4/GRCh38#5797343-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37468795-A-C

5797343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37468795-A-G

5797343-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37468795-A-T

5797388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37468743-A-G

5797397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37468736-A-G

5797397-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37468736-A-T

5797404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37468729-A-G

5797406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37468727-T-C

5797406-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37468727-T-G

5797472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37468663-C-T

5797473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37468662-T-C

5797506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37468630-A-G

5797541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37468595-C-T

5797596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37468527-C-T

http://identifiers.org/hco/4/GRCh38#5797615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37468516-C-A

5797730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37468410-G-A

5797750-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37468390-G-C

5797842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37468304-C-T

5797855-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37468289-G-C

5797872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37468272-C-T

5797886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37468260-T-C

5797959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37468194-C-T

http://identifiers.org/hco/4/GRCh38#5797969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37468184-C-A

5797969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37468184-C-T

5798344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37467844-A-G

5798353-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37467835-G-C

5798357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37467831-C-T

5798362-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37467826-T-G

http://identifiers.org/hco/4/GRCh38#5798395-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37467794-A-C

5798443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37467769-C-T

http://identifiers.org/hco/4/GRCh38#5798560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37467729-C-A

5798560-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37467729-C-G

5798560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37467729-C-T

http://identifiers.org/hco/4/GRCh38#5798561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37467728-C-A

5798561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37467728-C-T

http://identifiers.org/hco/4/GRCh38#5798578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37467717-C-A

5798578-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 37467717-C-G

5798578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 37467717-C-T

5798628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37467667-G-A

5798666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 37467629-G-A

5798673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37467622-G-T

5798727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37467568-G-T

http://identifiers.org/hco/4/GRCh38#5801707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37466756-C-A

5801707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37466756-C-T

5801710-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37466753-T-G

5801729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37466735-A-G

5801867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37466581-T-C

5801868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37466580-G-T

5801874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37466574-G-T

5801907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37466560-G-A

5801907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37466560-G-T

5801923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37466545-G-T

http://identifiers.org/hco/4/GRCh38#5802010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37466458-C-A

5802010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 37466458-C-T

http://identifiers.org/hco/4/GRCh38#5802103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37466365-C-A

5802103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37466365-C-T

http://identifiers.org/hco/4/GRCh38#5802121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37466338-C-A

5802946-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37466111-T-G

http://identifiers.org/hco/4/GRCh38#5803264-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37465793-A-C

5803308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37465749-T-C

5803308-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37465749-T-G

5803426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37465620-C-T

5803434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37465612-A-G

5803533-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37465535-G-C

http://identifiers.org/hco/4/GRCh38#5804597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37464796-C-A

5804607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37464786-G-A

5804607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37464786-G-T

5804729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 37464667-G-A

5804779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 37464617-C-T

5804780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 37464616-C-T

http://identifiers.org/hco/4/GRCh38#5804784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: http://identifiers.org/mco/5/GRCm39#37464612-C-A

5804784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 37464612-C-T

5807259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37461552-G-A

5807381-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37461429-G-C

5807389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37461421-T-C

5807479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37461351-G-A

5807498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37461330-T-C

5807590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37461240-G-T

5807625-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37461179-C-G

http://identifiers.org/hco/4/GRCh38#5807638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37461166-C-A

5807649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37461156-G-T

http://identifiers.org/hco/4/GRCh38#5808081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37460802-C-A

5808081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37460802-C-T

5808095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37460788-G-A

http://identifiers.org/hco/4/GRCh38#5808113-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37460768-A-C

5808186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37460668-C-T

5808205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 37460649-C-T

5808208-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 37460646-T-A

5808208-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 37460646-T-G

5808223-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 37460631-T-G

5808235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 37460619-T-C

http://identifiers.org/hco/4/GRCh38#5808390-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37460425-A-C

5808409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37460405-G-A

5808409-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37460405-G-C

5808483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37460334-G-A

5808538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37460291-C-T

5808620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37460221-G-T

5808771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37460079-T-C

5809369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37459119-T-C

5809373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37459111-G-T

http://identifiers.org/hco/4/GRCh38#5809402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37459085-C-A

5809402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37459085-C-T

5809406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37459082-A-G

5809420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37459068-G-A

5809420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37459068-G-T

5809434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37459048-G-T

5809531-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 37458980-A-T

5809633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37458890-T-C

5809633-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37458890-T-G

5809708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37458816-A-G

http://identifiers.org/hco/4/GRCh38#5809781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37458750-C-A

5810046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37458501-A-G

5810196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37458368-G-A

5810196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37458368-G-T

http://identifiers.org/hco/4/GRCh38#5810197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37458367-C-A

5810197-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37458367-C-G

5810365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 37458239-A-G

5810451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 37458153-G-A

5810528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37458093-G-T

http://identifiers.org/hco/4/GRCh38#5810583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37458050-C-A

5810583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37458050-C-T

http://identifiers.org/hco/4/GRCh38#5810592-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37458045-A-C

5810592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37458045-A-G

5810611-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37458026-A-T

5810668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37457953-T-C

5810670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37457951-G-A

5810880-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37457845-T-G

5810930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37457826-C-T

5811021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 37457735-G-A

5811021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 37457735-G-T

5811040-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37457716-T-A

5811040-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37457716-T-G

5811439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37457133-A-G

http://identifiers.org/hco/4/GRCh38#5811553-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37457041-A-C

5811553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37457041-A-G

5811561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37457033-G-A

5811561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37457033-G-T

http://identifiers.org/hco/4/GRCh38#5811571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37457023-C-A

5811571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37457023-C-T

http://identifiers.org/hco/4/GRCh38#5811582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37457012-C-A

5811582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37457012-C-T

5811620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37456974-A-G

5811622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37456972-C-T

5811627-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37456967-T-A

5811628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37456966-C-T

5811644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37456952-G-T

http://identifiers.org/hco/4/GRCh38#5811646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37456950-C-A

5811646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37456950-C-T

http://identifiers.org/hco/4/GRCh38#5820948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37449308-C-A

5820974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37449284-G-A

5820974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37449284-G-T

5821193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37449077-G-A

http://identifiers.org/hco/4/GRCh38#5821291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37448992-C-A

5821291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37448992-C-T

5821636-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37448664-T-A

5821740-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 37448571-G-C

5821740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 37448571-G-T

5821785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 37448525-C-T

5821809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 37448501-C-T

http://identifiers.org/hco/4/GRCh38#5821872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37448433-C-A

5821872-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37448433-C-G

5821872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37448433-C-T

http://identifiers.org/hco/4/GRCh38#5821896-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37448409-C-A

5821896-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37448409-C-G

5821896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37448409-C-T

http://identifiers.org/hco/4/GRCh38#5821906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37448397-C-A

5821906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 37448397-C-T

5821926-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37448387-C-G

5821926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37448387-C-T

http://identifiers.org/hco/4/GRCh38#5821971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37448350-C-A

5821971-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37448350-C-G

http://identifiers.org/hco/4/GRCh38#5821981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37448341-C-A

5821981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37448341-C-T

5821998-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37448324-G-C

5821998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37448324-G-T

http://identifiers.org/hco/4/GRCh38#5822055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37448271-C-A

5822097-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37448255-C-G

5822237-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37448133-C-G

5822436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37447951-T-C

5822437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37447950-G-A

http://identifiers.org/hco/4/GRCh38#5824045-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37447522-A-C

5824370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37447242-A-G

http://identifiers.org/hco/4/GRCh38#5824490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37447147-C-A

5824629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37447043-T-C

5824722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37446961-G-A

5824769-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37446904-G-C

5824816-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37446840-T-G

5824877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37446782-C-T

5824946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37446746-T-C

5824994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37446706-G-A

5825088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37446633-G-A

5825111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37446612-A-G

http://identifiers.org/hco/4/GRCh38#5825201-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37446525-A-C

5825538-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37446268-G-C

5825667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 37446138-G-A

5825717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37446096-G-A

5825771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37446026-T-C

5825774-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37446023-A-T

http://identifiers.org/hco/4/GRCh38#5825781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37446016-C-A

5825781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37446016-C-T

http://identifiers.org/hco/4/GRCh38#5826609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37445775-C-A

5826609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37445775-C-T

5826673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37445713-G-A

5826673-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37445713-G-C

5826673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37445713-G-T

5826697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37445689-G-T

5826706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37445681-A-G

http://identifiers.org/hco/4/GRCh38#5826763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37445665-C-A

5826763-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37445665-C-G

5826763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37445665-C-T

http://identifiers.org/hco/4/GRCh38#5826776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37445652-C-A

5826776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37445652-C-T

5826785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37445643-G-A

5826785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37445643-G-T

5826838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37445607-G-A

5827014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37445524-A-G

5827564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 37444669-A-G

5827565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 37444668-G-A

5827565-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 37444668-G-C

http://identifiers.org/hco/4/GRCh38#5827952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37444300-C-A

http://identifiers.org/hco/4/GRCh38#5827971-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37444281-A-C

5827979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37444273-C-T

5828053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37444203-G-A

http://identifiers.org/hco/4/GRCh38#5828124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37444162-C-A

5828124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37444162-C-T

5828168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37444124-G-A

5828215-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 37444072-T-G

5828279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37444027-G-A

5828361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37443987-A-G

5828363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37443985-A-G

5828378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37443970-T-C

5828438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37443924-C-T

5828568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37443810-A-G

5828568-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37443810-A-T

http://identifiers.org/hco/4/GRCh38#5828708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37443656-C-A

5828708-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37443656-C-G

5828719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37443653-G-A

5828719-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37443653-G-C

5828719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37443653-G-T

5828782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37443601-T-C

5829588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37442640-A-G

5829623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37442579-G-A

5829672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37442540-T-C

5835643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37441798-G-T

5835659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37441777-A-G

5835802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37441652-G-A

5835802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37441652-G-T

5835866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37441592-T-C

http://identifiers.org/hco/4/GRCh38#5835888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37441570-C-A

http://identifiers.org/hco/4/GRCh38#5835889-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37441569-A-C

5835889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37441569-A-G

5835967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37441488-A-G

http://identifiers.org/hco/4/GRCh38#5836006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37441449-C-A

5836689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37440410-G-T

5836711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37440390-C-T

5836714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37440387-A-G

5836768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37440332-C-T

http://identifiers.org/hco/4/GRCh38#5838179-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37439242-A-C

5838187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37439237-C-T

5838293-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37439111-G-C

5838293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37439111-G-T

5838306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37439098-G-A

5838306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37439098-G-T

5838310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37439094-G-A

5838353-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37439068-G-C

5838431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37438986-G-T

5838447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37438970-G-A

5838453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37438964-T-C

5838453-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37438964-T-G

5838469-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37438956-T-A

5838469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37438956-T-C

5838604-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37438826-G-C

5838699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37438730-C-T

5838797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37438626-C-T

5838888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37438563-C-T

5838942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37438538-C-T

5839051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37438425-T-C

5839151-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37438342-G-C

5839179-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37438314-C-G

5839179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37438314-C-T

5839285-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37438184-T-G

5839429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37438045-G-A

5839429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37438045-G-T

5839446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37438029-C-T

http://identifiers.org/hco/4/GRCh38#5839453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37438022-C-A

http://identifiers.org/hco/4/GRCh38#5839511-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37437976-A-C

5839522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 37437965-C-T

5839675-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37437812-G-T

5839688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37437800-G-A

5839688-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37437800-G-C

5841288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37437137-G-A

5841434-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 37436993-C-G

5841434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 37436993-C-T

5841466-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37436958-T-A

5841466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37436958-T-C

5842899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37436479-G-A

5842910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37436468-T-C

http://identifiers.org/hco/4/GRCh38#5842915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37436463-C-A

http://identifiers.org/hco/4/GRCh38#5842976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37436384-C-A

5842976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37436384-C-T

5843003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37436357-G-A

5843003-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37436357-G-T

http://identifiers.org/hco/4/GRCh38#5843151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37436215-C-A

5843151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37436215-C-T

5849252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37435653-G-A

5849252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37435653-G-T

5849340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37435553-C-T

http://identifiers.org/hco/4/GRCh38#5849345-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37435548-A-C

5849345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37435548-A-G

5849440-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37435459-C-G

5849440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37435459-C-T

5849489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37435412-A-G

5850154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37434756-A-G

5850178-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37434679-T-G

5850198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37434659-G-A

5850368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37434502-T-C

5850395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37434475-A-G

5850397-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37434473-T-A

5850444-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37434431-G-C

5850533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37434350-C-T

5850541-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37434342-T-A

5850805-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37434135-T-G

5850897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37434076-T-C

5850960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37434040-C-T

http://identifiers.org/hco/4/GRCh38#5851001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37434003-C-A

5851105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37433904-A-G

5851194-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37433819-G-C

http://identifiers.org/hco/4/GRCh38#5851374-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37433707-A-C

5851567-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37433527-C-G

http://identifiers.org/hco/4/GRCh38#5851592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37433504-C-A

5851592-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37433504-C-G

5851609-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37433487-T-A

5851609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37433487-T-C

5851616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37433479-T-C

5854931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37431944-T-C

5855117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37431760-A-G

http://identifiers.org/hco/4/GRCh38#5855152-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37431725-A-C

5855160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37431717-A-G

5855170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37431707-A-G

5855393-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37431510-T-G

5855406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37431497-G-A

5855447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37431452-C-T

5855518-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37431374-T-G

5855647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37431281-A-G

5855779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37431149-T-C

5855850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37431081-T-C

5855935-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37431004-G-C

5855999-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37430943-T-A

http://identifiers.org/hco/4/GRCh38#5856036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37430909-C-A

http://identifiers.org/hco/4/GRCh38#5856122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37430873-C-A

5856122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37430873-C-T

5856298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37430698-A-G

5856348-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37430647-G-C

5856384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37430609-C-T

5856398-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37430595-T-A

5856398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37430595-T-C

http://identifiers.org/hco/4/GRCh38#5856414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37430579-C-A

5856430-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37430565-A-T

5860891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37426343-A-G

5860891-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37426343-A-T

5860942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37426293-G-A

5860942-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37426293-G-C

5860942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37426293-G-T

5860943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37426292-A-G

http://identifiers.org/hco/4/GRCh38#5860956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37426279-C-A

5860956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37426279-C-T

5860957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37426278-T-C

5860967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37426267-G-T

5860969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37426265-T-C

5860971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37426264-A-G

5860994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37426241-A-G

5860998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37426237-C-T

5861049-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37426186-A-T

5861224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37426011-A-G

5864966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37423131-A-G

5864977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37423120-G-A

5866793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37422546-A-G

5867388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37421557-T-C

5867389-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37421556-T-G

5867411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37421534-G-A

5868227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37420995-C-T

5868237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37420985-C-T

5870587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37419578-G-A

5870587-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37419578-G-C

5870654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37419513-G-A

5870654-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37419513-G-C

5870774-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37419402-G-C

5870901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37419267-A-G

5870902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37419266-T-C

5870905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37419263-G-A

5870905-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37419263-G-C

5870943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37419247-G-A

http://identifiers.org/hco/4/GRCh38#5871139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37419052-C-A

5871141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37419050-G-A

5871166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37419026-G-A

5871895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37417945-T-C

5872112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37417755-A-G

5873872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37416383-A-G

5873875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37416380-G-A

5874072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37416254-T-C

5874152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37416199-A-G

http://identifiers.org/hco/4/GRCh38#5874260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37416110-C-A

5874273-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37416097-G-C

5874361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37416028-G-A

5874428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37415979-C-T

5874551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37415859-A-G

5874860-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37415591-C-G

http://identifiers.org/hco/4/GRCh38#5874897-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37415553-A-C

5874898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37415552-C-T

5874916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37415536-A-G

http://identifiers.org/hco/4/GRCh38#5875378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37415102-C-A

5875391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37415089-G-A

5875391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37415089-G-T

5875609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 37414891-A-G

http://identifiers.org/hco/4/GRCh38#5875683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#37414834-C-A

5875695-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 37414822-G-C

5875754-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 37414763-G-C

5876530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37414359-G-A

5876740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37414225-C-T

5876770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37414195-C-T

5876827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37414176-C-T

5877295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37413852-G-A

5877295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37413852-G-T

5877361-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37413817-G-C

5877599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37413624-C-T

5877665-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37413557-G-C

5877854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37413397-T-C

5877922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37413334-T-C

5877925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37413331-T-C

5878112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37413271-G-A

5878219-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37413234-T-A

5878219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37413234-T-C

5878352-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37413105-T-A

5878658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37412834-C-T

5878973-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37412307-C-G

5878977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37412303-T-C

5879078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37412204-G-A

5879433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37411914-A-G

5879447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37411904-C-T

5879484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37411863-T-C

5879648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37411720-A-G

5879658-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37411710-T-A

5879684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37411693-T-C

5879802-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37411623-T-G

5879851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37411574-A-G

http://identifiers.org/hco/4/GRCh38#5879855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37411570-C-A

5879872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37411555-C-T

5879873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37411554-G-A

5879873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37411554-G-T

5879877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37411550-G-A

5880186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37410813-A-G

5880340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37410686-G-A

5880398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37410559-A-G

http://identifiers.org/hco/4/GRCh38#5880695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37410255-C-A

5880728-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37410239-A-T

5880853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37410113-C-T

5881180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37409773-A-G

http://identifiers.org/hco/4/GRCh38#5881234-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37409460-A-C

5881234-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37409460-A-T

5881260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37409434-C-T

5881385-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37409316-T-G

5881582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 37409143-T-C

5881891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37408862-G-A

5881984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37408796-C-T

5882233-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37408610-T-A

5882233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37408610-T-C

5882295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37408553-T-C

5882480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37408404-A-G

5882484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37408400-G-A

5882492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37408392-C-T

5882505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37408379-A-G

5882621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37408275-T-C

5882791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37408162-G-T

5883885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37407377-G-A

http://identifiers.org/hco/4/GRCh38#5884081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37407201-C-A

http://identifiers.org/hco/4/GRCh38#5884311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37406979-C-A

5884324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37406966-C-T

5884353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37406937-C-T

http://identifiers.org/hco/4/GRCh38#5884500-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37406797-A-C

5884592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37406689-A-G

5884836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37406461-C-T

5885019-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37406278-T-A

5885043-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37406254-T-A

5885043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37406254-T-C

5885043-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37406254-T-G

5885083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37406218-G-A

5885083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37406218-G-T

http://identifiers.org/hco/4/GRCh38#5885119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37406185-C-A

5885119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37406185-C-T

5885128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37406176-A-G

5885194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37406104-C-T

5885415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37405915-A-G

5885437-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37405910-C-G

5885541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37405819-G-A

5885755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37405668-A-G

5885803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37405632-C-T

5885871-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37405613-A-T

5886069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37405473-T-C

5886161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37405392-T-C

5886364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37405204-T-C

5886787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37404767-T-C

5886930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37404680-G-A

5886932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37404678-T-C

5887031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37404612-G-A

5887193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37404423-T-C

5887228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37404385-C-T

5887359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37404282-G-A

5887359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37404282-G-T

http://identifiers.org/hco/4/GRCh38#5887380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37404261-C-A

5887425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37404212-A-G

http://identifiers.org/hco/4/GRCh38#5887519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37404125-C-A

5887519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37404125-C-T

http://identifiers.org/hco/4/GRCh38#5887572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37404072-C-A

5887572-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37404072-C-G

5887572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37404072-C-T

http://identifiers.org/hco/4/GRCh38#5887677-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37403971-A-C

5887677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37403971-A-G

5887716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37403931-T-C

5887728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37403919-C-T

http://identifiers.org/hco/4/GRCh38#5887877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37403789-C-A

5887877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37403789-C-T

http://identifiers.org/hco/4/GRCh38#5887958-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37403690-A-C

5887958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37403690-A-G

5887958-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37403690-A-T

5888078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37403574-A-G

http://identifiers.org/hco/4/GRCh38#5888149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37403507-C-A

5888149-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37403507-C-G

5888149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37403507-C-T

5888152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37403504-G-A

5888152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37403504-G-T

5888471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 37403202-G-A

5888471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 37403202-G-T

http://identifiers.org/hco/4/GRCh38#5888764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37402925-C-A

5888764-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 37402925-C-G

5888891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 37402817-G-A

5889020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 37402721-T-C

5889344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 37402493-G-A

5889344-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 37402493-G-C

5889539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron variant
orthologous variants: 37402326-G-A

http://identifiers.org/hco/4/GRCh38#5889567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37402315-C-A

http://identifiers.org/hco/4/GRCh38#5889646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37402252-C-A

5889712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 37402189-T-C

http://identifiers.org/hco/4/GRCh38#5889797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37402133-C-A

5889867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 37402082-T-C

http://identifiers.org/hco/4/GRCh38#5889873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37402076-C-A

5889899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 37402054-G-A

5889899-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 37402054-G-C

5889946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 37402003-T-C

5889983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 37401982-T-C

5889996-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 37401969-A-T

5890006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 37401959-G-A

5890006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 37401959-G-T

5890195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 37401810-G-A

5890195-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 37401810-G-C

5890550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 37401476-G-A

5890887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 37401180-G-A

5890996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 37401085-T-C

5891757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron variant
orthologous variants: 37400513-C-T

5892440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron variant
orthologous variants: 37400001-A-G

5892440-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron variant
orthologous variants: 37400001-A-T

http://identifiers.org/hco/4/GRCh38#5892454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37399987-C-A

5892454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron variant
orthologous variants: 37399987-C-T

5892466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: intron variant
orthologous variants: 37399977-T-C

http://identifiers.org/hco/4/GRCh38#5892605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37399851-C-A

5892605-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: missense variant
orthologous variants: 37399851-C-G

5892605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: missense variant
orthologous variants: 37399851-C-T

5892650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: missense variant
orthologous variants: 37399806-G-A

5892650-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: missense variant
orthologous variants: 37399806-G-C

5892650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: missense variant
orthologous variants: 37399806-G-T

5892662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: missense variant
orthologous variants: 37399794-T-C

5892788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: missense variant
orthologous variants: 37399668-G-A

5892788-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: missense variant
orthologous variants: 37399668-G-C

5892788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: missense variant
orthologous variants: 37399668-G-T

5892923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: missense variant
orthologous variants: 37399533-A-G

5892923-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: missense variant
orthologous variants: 37399533-A-T

http://identifiers.org/hco/4/GRCh38#5893066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#37399421-C-A

5893066-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 5 prime UTR variant
orthologous variants: 37399421-C-G

5893066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 5 prime UTR variant
orthologous variants: 37399421-C-T

5893079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 5 prime UTR variant
orthologous variants: 37399408-G-A

5893079-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 5 prime UTR variant
orthologous variants: 37399408-G-C

5893079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2365
most severe consequence: 5 prime UTR variant
orthologous variants: 37399408-G-T