98796239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58289223-C-T

98796327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58289153-G-T

98796446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58288930-T-C

98796509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58288896-A-G

98796694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58288730-C-T

98796744-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58288675-A-T

http://identifiers.org/hco/3/GRCh38#98796832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58288592-C-A

98796833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58288591-A-G

98797035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58288393-G-A

98797035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58288393-G-T

98797036-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58288392-T-A

98797179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58288290-T-C

http://identifiers.org/hco/3/GRCh38#98797247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58288222-C-A

98797247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58288222-C-T

98797248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58288221-A-G

98797425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58288097-T-C

98797475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58288045-A-G

98797539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58287983-A-G

98797704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58287812-A-G

98797738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58287791-G-A

98797749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58287780-A-G

98797808-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58287721-G-C

98797852-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58287678-A-T

98798060-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58287535-T-A

http://identifiers.org/hco/3/GRCh38#98798133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58287481-C-A

98798136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58287478-G-T

98798137-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58287477-T-A

98798137-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58287477-T-G

http://identifiers.org/hco/3/GRCh38#98798216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58287395-C-A

98798251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58287359-A-G

98798591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58286931-A-G

98798723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58286817-G-T

http://identifiers.org/hco/3/GRCh38#98798791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58286749-C-A

98798791-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58286749-C-G

98798791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58286749-C-T

http://identifiers.org/hco/3/GRCh38#98798801-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58286739-A-C

98798926-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58286590-G-C

http://identifiers.org/hco/3/GRCh38#98799029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58286491-C-A

98799147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58286371-A-G

98799189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58286329-T-C

http://identifiers.org/hco/3/GRCh38#98799195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58286321-C-A

98799280-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58286236-A-T

http://identifiers.org/hco/3/GRCh38#98799344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58286179-C-A

98799344-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58286179-C-G

98799344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58286179-C-T

98799502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 58286023-T-C

98799508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 58286017-T-C

98799508-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 58286017-T-G

98799553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 58285972-T-C

98799572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 58285953-G-A

98799572-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 58285953-G-C

http://identifiers.org/hco/3/GRCh38#98799723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58285802-C-A

98799723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 58285802-C-T

98799940-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58285587-T-G

98799946-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58285580-T-A

http://identifiers.org/hco/3/GRCh38#98799972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58285541-C-A

98800318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58285187-G-A

98800318-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58285187-G-C

98800540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58284725-C-T

98800616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 58284651-T-C

98800880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58284458-A-G

98800880-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58284458-A-T

98800882-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58284456-T-A

98800890-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58284448-A-T

http://identifiers.org/hco/3/GRCh38#98800902-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58284436-A-C

98800902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58284436-A-G

http://identifiers.org/hco/3/GRCh38#98801248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58284158-C-A

98801248-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58284158-C-G

98801256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58283965-G-T

http://identifiers.org/hco/3/GRCh38#98801306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58283920-C-A

http://identifiers.org/hco/3/GRCh38#98801338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58283886-C-A

98801338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58283886-C-T

98801398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58283841-T-C

http://identifiers.org/hco/3/GRCh38#98801511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58283550-C-A

98801511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58283550-C-T

98801521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58283543-A-G

98801527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58283537-T-C

http://identifiers.org/hco/3/GRCh38#98801543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#58283519-C-A

98801543-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 58283519-C-G

98801543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 58283519-C-T

http://identifiers.org/hco/3/GRCh38#98808090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58281400-C-A

98808168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58281322-G-A

98808168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58281322-G-T

http://identifiers.org/hco/3/GRCh38#98808221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58281282-C-A

98808221-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58281282-C-G

98808221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58281282-C-T

98808288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58281225-T-C

98808288-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58281225-T-G

98808300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58281213-T-C

98808300-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58281213-T-G

98808301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58281212-A-G

98808314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58281195-G-A

98808314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58281195-G-T

98808315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58281194-G-T

98808600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58279967-G-A

98808973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58279609-A-G

98808978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58279604-T-C

98808981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58279601-A-G

98809230-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58279425-T-G

98809401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58279265-G-A

98809401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58279265-G-T

98810320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58278222-A-G

98810393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58278172-C-T

98810398-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58278167-T-A

98810468-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58277446-T-A

98810479-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58277436-G-C

98810520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58277395-T-C

98810529-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58277385-G-C

98810598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58277314-T-C

http://identifiers.org/hco/3/GRCh38#98810716-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58277190-A-C

98811060-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58276882-A-T

http://identifiers.org/hco/3/GRCh38#98811061-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58276881-A-C

98811121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58276820-A-G

98811250-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58276713-T-A

98811250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58276713-T-C

98811259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58276704-T-C

http://identifiers.org/hco/3/GRCh38#98811268-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58276695-A-C

98811460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 58276526-A-G

98811460-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 58276526-A-T

98811511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 58276475-G-A

98811511-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58276475-G-C

98811511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58276475-G-T

98811565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58276427-G-A

98811565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58276427-G-T

98811619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58276369-T-C

http://identifiers.org/hco/3/GRCh38#98811777-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58276200-A-C

http://identifiers.org/hco/3/GRCh38#98811891-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58276116-A-C

98811904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58276105-T-C

http://identifiers.org/hco/3/GRCh38#98812070-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58275924-A-C

98812216-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58275822-A-T

http://identifiers.org/hco/3/GRCh38#98812258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58275748-C-A

http://identifiers.org/hco/3/GRCh38#98812274-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58275723-A-C

98812307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58275662-T-C

98812544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58275426-C-T

98812600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58275392-G-A

98812600-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58275392-G-C

98812600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58275392-G-T

http://identifiers.org/hco/3/GRCh38#98812601-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58275391-A-C

98812601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58275391-A-G

http://identifiers.org/hco/3/GRCh38#98812610-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58275383-A-C

98812610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58275383-A-G

98812610-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58275383-A-T

http://identifiers.org/hco/3/GRCh38#98812631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58275357-C-A

98812631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58275357-C-T

http://identifiers.org/hco/3/GRCh38#98812659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58275325-C-A

98812659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58275325-C-T

98812722-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58275262-T-A

98812722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58275262-T-C

98812759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58275222-A-G

98812825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58275155-T-C

98812981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58275078-T-C

98813679-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58274958-A-T

98813716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58274921-A-G

http://identifiers.org/hco/3/GRCh38#98813891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58274767-C-A

http://identifiers.org/hco/3/GRCh38#98813953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58274696-C-A

98813973-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58274676-T-A

98813973-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58274676-T-G

98814458-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58274126-T-A

98814549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58274052-T-C

98814549-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58274052-T-G

http://identifiers.org/hco/3/GRCh38#98814668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58273964-C-A

http://identifiers.org/hco/3/GRCh38#98814682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58273950-C-A

98814682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58273950-C-T

http://identifiers.org/hco/3/GRCh38#98814739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58273907-C-A

98814739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58273907-C-T

http://identifiers.org/hco/3/GRCh38#98814862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58273752-C-A

http://identifiers.org/hco/3/GRCh38#98814908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58273708-C-A

98815241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58273419-G-A

98815306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58273359-G-T

98815458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58273275-A-G

http://identifiers.org/hco/3/GRCh38#98815517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58273196-C-A

98815518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58273195-A-G

98815650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58273146-T-C

98815735-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58273074-A-T

98817052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58272777-C-T

98817093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58272750-A-G

http://identifiers.org/hco/3/GRCh38#98817531-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58272321-A-C

http://identifiers.org/hco/3/GRCh38#98817535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58272317-C-A

98817656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58272192-G-T

98817760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58272155-T-C

http://identifiers.org/hco/3/GRCh38#98818027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58271910-C-A

98818027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58271910-C-T

98818030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58271907-T-C

98819036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58271466-T-C

98819063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58271441-A-G

98819160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58271354-A-G

98819279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58271223-C-T

98819456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58271045-A-G

98819595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58270955-C-T

98819665-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58270884-C-G

98819978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58270501-A-G

http://identifiers.org/hco/3/GRCh38#98820125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58270327-C-A

98820125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58270327-C-T

98820131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58270321-A-G

98820131-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58270321-A-T

98820196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58270259-G-A

98820196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58270259-G-T

98820220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58270232-A-G

98822255-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: missense variant
orthologous variants: 58269283-G-C

98822255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: missense variant
orthologous variants: 58269283-G-T

98822267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: missense variant
orthologous variants: 58269271-T-C

98822312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 58269226-G-A

98822312-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 58269226-G-C

98822312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 58269226-G-T

98822402-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58269131-C-G

98822497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58269065-T-C

http://identifiers.org/hco/3/GRCh38#98822499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58269063-C-A

98822499-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58269063-C-G

98822499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58269063-C-T

http://identifiers.org/hco/3/GRCh38#98822529-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58269020-A-C

http://identifiers.org/hco/3/GRCh38#98822568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58268988-C-A

98822568-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58268988-C-G

98822602-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58268947-A-T

http://identifiers.org/hco/3/GRCh38#98822797-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58268757-A-C

98822797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58268757-A-G

http://identifiers.org/hco/3/GRCh38#98822809-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58268751-A-C

98822815-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58268745-T-A

98822815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58268745-T-C

98822819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58268741-A-G

98822821-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58268739-A-T

http://identifiers.org/hco/3/GRCh38#98824974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58266600-C-A

98825126-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58265940-G-C

http://identifiers.org/hco/3/GRCh38#98825208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58265874-C-A

http://identifiers.org/hco/3/GRCh38#98825227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58265855-C-A

98825258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58265815-G-A

98825258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58265815-G-T

http://identifiers.org/hco/3/GRCh38#98825271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58265802-C-A

98825271-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58265802-C-G

98825271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58265802-C-T

98825275-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58265798-T-A

98825275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58265798-T-C

http://identifiers.org/hco/3/GRCh38#98825279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58265794-C-A

98825279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58265794-C-T

98825287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58265786-A-G

98825290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58265780-A-G

98825462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58265661-A-G

http://identifiers.org/hco/3/GRCh38#98825613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58265531-C-A

98825804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58265405-C-T

98825945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58265282-C-T

98825948-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58265279-G-C

98826156-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58265132-G-C

98826156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58265132-G-T

98826299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58264969-G-A

98826299-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58264969-G-C

98826312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58264955-C-T

98826317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58264950-C-T

98826323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58264934-T-C

98826332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58264914-G-A

98826335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58264911-T-C

http://identifiers.org/hco/3/GRCh38#98826340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58264905-C-A

98826463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58264742-A-G

98826635-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58264589-G-C

http://identifiers.org/hco/3/GRCh38#98826778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58264415-C-A

98826855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58264041-A-G

98826970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58263932-G-T

98826994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58263908-A-G

http://identifiers.org/hco/3/GRCh38#98827198-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58263727-A-C

98827264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58263678-C-T

98827413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58263554-C-T

98827642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58263362-A-G

98827642-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58263362-A-T

http://identifiers.org/hco/3/GRCh38#98827818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58263187-C-A

98827851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58263140-A-G

98827871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58263120-T-C

http://identifiers.org/hco/3/GRCh38#98827882-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58263106-A-C

98827923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58263078-C-T

98828001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58262995-A-G

98828053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58262930-C-T

98828205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58262781-T-C

98839743-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58260661-G-C

98839997-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58260411-C-G

98840083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58260335-G-A

98840310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58260115-T-C

98840455-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58260001-T-A

98840455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58260001-T-C

98841022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58259748-C-T

98841042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58259728-C-T

98841054-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58259716-C-G

98841054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58259716-C-T

98841375-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58259532-A-T

98841562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58259357-C-T

98841579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58259336-G-A

98842081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58259120-A-G

98842129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58259071-T-C

98842130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58259070-A-G

98842257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58258953-A-G

98842554-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58258870-A-T

98842779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58258646-A-G

98842979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58258483-T-C

98843141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58258120-C-T

98843148-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58258113-G-C

98843220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58258038-A-G

98843221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58258037-T-C

98843354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58257913-A-G

98843381-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58257885-C-G

98843388-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58257878-A-T

98843425-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58257841-T-G

98843535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58257730-T-C

98843820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58257391-A-G

http://identifiers.org/hco/3/GRCh38#98843853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58257361-C-A

98843937-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58257288-G-C

98844124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58257120-T-C

http://identifiers.org/hco/3/GRCh38#98844135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58257109-C-A

98844298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58256679-A-G

98844321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58256666-T-C

98844649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58256431-C-T

98844742-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58256341-T-G

98844771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58256308-T-C

http://identifiers.org/hco/3/GRCh38#98844807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58256276-C-A

98844859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58256230-G-A

98844876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58256222-A-G

98844918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58256142-G-A

98845177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58255698-T-C

98845225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58255646-G-A

98845238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58255633-T-C

98845389-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58255493-C-G

98845412-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58255467-A-T

98845429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58255449-A-G

98845429-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58255449-A-T

98845469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58255412-T-C

98847825-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58254420-C-G

http://identifiers.org/hco/3/GRCh38#98849247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58254034-C-A

98849247-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58254034-C-G

98849247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58254034-C-T

98849351-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58253929-A-T

98849412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 58253872-T-C

98849446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 58253839-A-G

98849571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 58253714-A-G

98849571-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 58253714-A-T

98849611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58253674-G-T

98849677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58253618-A-G

98849711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58253584-T-C

98849729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58253569-G-T

98849859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58253427-T-C

98849927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58253367-G-A

98849961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58253338-T-C

98849967-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58253332-A-T

98878826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58248851-A-G

98878948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58248711-T-C

98879019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58248649-T-C

98879037-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58248631-C-G

98879037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58248631-C-T

98879766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58246463-T-C

http://identifiers.org/hco/3/GRCh38#98879813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58246418-C-A

98879815-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58246416-G-C

98879983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58246289-G-A

98879983-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58246289-G-C

98880117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58246168-C-T

98880135-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58246150-G-C

98880140-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58246146-T-G

98880268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58246069-G-T

98880277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58246060-T-C

98880335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58246015-T-C

98880712-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58245655-T-G

98880754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58245597-T-C

98880778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58245575-A-G

http://identifiers.org/hco/3/GRCh38#98881417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58245257-C-A

98881417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58245257-C-T

http://identifiers.org/hco/3/GRCh38#98881483-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58245205-A-C

98881545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58245144-T-C

98881746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58244943-A-G

http://identifiers.org/hco/3/GRCh38#98883246-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58244494-A-C

98883654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58244120-A-G

98883666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58244109-T-C

98883738-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58244036-T-G

98883939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58243859-G-A

98883974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58243822-T-C

http://identifiers.org/hco/3/GRCh38#98884275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58243551-C-A

98884290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58243536-T-C

98884385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58243455-T-C

98884731-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58243146-T-A

98884743-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58243134-T-A

98884743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58243134-T-C

98884817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58243080-A-G

http://identifiers.org/hco/3/GRCh38#98885489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58242221-C-A

98885518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58242153-G-A

http://identifiers.org/hco/3/GRCh38#98885823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58241750-C-A

98885845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58241746-G-A

98885845-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58241746-G-C

98886098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58241533-T-C

98886410-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58241349-A-T

98886579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58241211-C-T

98886684-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58241107-T-G

98886718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58241074-T-C

http://identifiers.org/hco/3/GRCh38#98886803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58240988-C-A

98886803-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58240988-C-G

98887262-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58240558-T-A

98887363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58240461-G-A

98887580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58240272-T-C

98892739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58235484-C-T

98894638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58234743-A-G

98894638-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58234743-A-T

98894666-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58234705-C-G

98894989-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58234445-G-C

98895091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58234351-G-A

98895172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58234268-G-T

98895184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58234235-A-G

98895203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58234216-G-A

98895203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58234216-G-T

98895208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58234204-G-T

98895214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58234198-G-T

98895252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58234160-C-T

98895279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58234133-G-A

98895279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58234133-G-T

98895419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58233991-A-G

98895441-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58233973-T-A

98895441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58233973-T-C

98895459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58233955-A-G

98895864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58233698-A-G

98895868-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58233694-A-T

98895875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58233687-C-T

98896305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58233447-A-G

98896575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58233227-T-C

http://identifiers.org/hco/3/GRCh38#98896578-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58233224-A-C

98896628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58233186-G-A

98896846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58232965-T-C

98896953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58232885-T-C

98897430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58232342-C-T

98897851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58231936-G-A

98898009-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58231771-T-G

98898367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58231413-C-T

98898393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58231393-T-C

98898604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58231196-C-T

98898757-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58231059-C-G

98898781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58231035-T-C

http://identifiers.org/hco/3/GRCh38#98899110-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58230743-A-C

98900236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58230009-C-T

98900356-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58229945-T-A

98900494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58229826-T-C

http://identifiers.org/hco/3/GRCh38#98900711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58229620-C-A

98900711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58229620-C-T

98900718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 58229613-T-C

98900770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58229570-T-C

http://identifiers.org/hco/3/GRCh38#98900884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#58229516-C-A

98900942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58229458-G-A

98900942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58229458-G-T

98900954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58229449-G-A

98900954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58229449-G-T

http://identifiers.org/hco/3/GRCh38#98900972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58229439-C-A

98900972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58229439-C-T

98900987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 58229427-A-G

98901261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: synonymous variant
orthologous variants: 58229182-G-A

98901261-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: synonymous variant
orthologous variants: 58229182-G-T

http://identifiers.org/hco/3/GRCh38#98901269-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#58229174-C-A

98901269-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: missense variant
orthologous variants: 58229174-C-G

98901269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: missense variant
orthologous variants: 58229174-C-T

http://identifiers.org/hco/3/GRCh38#98901382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#58229062-C-A

98901382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 58229062-C-T

http://identifiers.org/hco/3/GRCh38#98901398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/16/GRCm39#58229045-C-A

98901398-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 58229045-C-G

98901398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 58229045-C-T

98901410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 5 prime UTR variant
orthologous variants: 58229033-G-A

98901410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 5 prime UTR variant
orthologous variants: 58229033-G-T

98901486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 5 prime UTR variant
orthologous variants: 58228987-T-C

98901529-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 5 prime UTR variant
orthologous variants: 58228962-A-T

98901544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 5 prime UTR variant
orthologous variants: 58228947-G-A

98901544-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 5 prime UTR variant
orthologous variants: 58228947-G-C

98901544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 5 prime UTR variant
orthologous variants: 58228947-G-T

98901672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 58228880-T-C

98901672-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24627
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 58228880-T-G