241847970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: 175708136-A-G

http://identifiers.org/hco/1/GRCh38#241847979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#175708145-C-A

241847979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 175708145-C-T

http://identifiers.org/hco/1/GRCh38#241848046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#175708226-C-A

241848046-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 175708226-C-G

241848046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 175708226-C-T

241848083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 175708248-A-G

241848083-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 175708248-A-T

241848126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 175708299-G-A

241848126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 175708299-G-T

241848141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 175708315-G-T

241848147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 175708321-C-T

241848259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 175708382-G-A

241848259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 175708382-G-T

241848267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 175708390-G-T

241848312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 175708410-T-C

http://identifiers.org/hco/1/GRCh38#241848321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#175708417-C-A

241848322-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 175708418-T-A

241848322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 175708418-T-C

241848349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 175708445-G-A

241848349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 175708445-G-T

241848401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, undefined
orthologous variants: 175708504-G-A

241848401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, undefined
orthologous variants: 175708504-G-T

http://identifiers.org/hco/1/GRCh38#241848404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#175708507-C-A

241848404-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, undefined
orthologous variants: 175708507-C-G

241848404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, undefined
orthologous variants: 175708507-C-T

241848410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron variant
orthologous variants: 175708513-G-T

241848597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, undefined
orthologous variants: 175708585-G-T

241848621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, undefined
orthologous variants: 175708593-G-A

http://identifiers.org/hco/1/GRCh38#241848637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#175708609-C-A

http://identifiers.org/hco/1/GRCh38#241848673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#175708632-C-A

241848795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: 5 prime UTR variant
orthologous variants: 175708758-A-G

241848795-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: 5 prime UTR variant
orthologous variants: 175708758-A-T

241848904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: 5 prime UTR variant
orthologous variants: 175708852-T-C

241848938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: 5 prime UTR variant
orthologous variants: 175708883-G-A

http://identifiers.org/hco/1/GRCh38#241848940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#175708885-C-A

241848940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: 5 prime UTR variant
orthologous variants: 175708885-C-T

241848981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: 5 prime UTR variant
orthologous variants: 175708933-G-A

241848984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 175708955-T-C

241848990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 175708961-G-A

241849073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175709036-T-C

http://identifiers.org/hco/1/GRCh38#241849124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#175709089-C-A

241849177-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 175709144-T-G

241849200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 175709166-G-A

241849238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175709201-G-A

241849347-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175709786-T-A

241849684-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175710052-C-G

241850359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175710414-A-G

241850359-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175710414-A-T

241850382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175710436-T-C

241850478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 175710526-A-G

241850515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 175710563-T-C

241850575-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 175710623-A-T

241850627-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175710663-T-A

http://identifiers.org/hco/1/GRCh38#241850641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#175710677-C-A

241850641-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175710677-C-G

241850641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175710677-C-T

241850643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175710679-T-C

241850643-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175710679-T-G

241852253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175714212-G-A

241852253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175714212-G-T

http://identifiers.org/hco/1/GRCh38#241852270-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#175714230-A-C

241852270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175714230-A-G

241852349-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 175714313-T-G

http://identifiers.org/hco/1/GRCh38#241852385-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#175714349-A-C

241852424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175714387-T-C

241852441-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175714403-T-A

241852441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175714403-T-C

241852442-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175714404-T-A

241852442-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175714404-T-G

241852989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175714753-G-A

241853046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175714801-T-C

241853253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175715043-A-G

241853264-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175715050-G-C

241853264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175715050-G-T

http://identifiers.org/hco/1/GRCh38#241853299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#175715085-C-A

241853299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175715085-C-T

241853320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175715105-T-C

241853340-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175715119-A-T

241853342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175715121-T-C

241853343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175715122-G-A

241853343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175715122-G-T

241853406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 175715192-G-A

241853406-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 175715192-G-C

241853406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 175715192-G-T

241853523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175715328-T-C

241853529-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175715334-T-G

241856616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175715649-A-G

241856630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175715666-C-T

241856721-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175715765-G-C

241857208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175716205-A-G

241857208-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175716205-A-T

241857233-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175716231-G-T

241857291-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175716266-G-C

241857323-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175716271-T-A

241857351-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 175716296-C-G

241857351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 175716296-C-T

241857374-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 175716319-C-G

241857374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 175716319-C-T

241857383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 175716328-C-T

241857489-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 175716434-A-T

241857496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175716441-A-G

241857502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175716447-A-G

241857511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175716456-T-C

241857520-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175716465-T-A

241857520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175716465-T-C

241857536-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175716481-T-A

241857536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175716481-T-C

241858411-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175719404-G-C

241858411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175719404-G-T

241858441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175719434-G-T

241858589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 175719583-A-G

241858664-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 175719658-A-T

241858690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 175719684-G-A

241858999-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175719830-T-A

241859097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175719907-T-C

241859180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175719980-C-T

241859202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175720003-G-A

241860184-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175720182-G-C

http://identifiers.org/hco/1/GRCh38#241860424-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#175720349-A-C

241860424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175720349-A-G

241860456-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175720372-T-G

241860476-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175720399-T-A

241860481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175720404-T-C

241860702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 175720625-G-A

241860702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 175720625-G-T

241860724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron variant
orthologous variants: 175720646-A-G

241861008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron variant
orthologous variants: 175720920-G-A

241861153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron variant
orthologous variants: 175721054-C-T

241861170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron variant
orthologous variants: 175721071-G-A

241861253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron variant
orthologous variants: 175721154-C-T

241861330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron variant
orthologous variants: 175721231-A-G

241861414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: missense variant
orthologous variants: 175721315-A-G

241861455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 175721356-A-G

241861526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron variant
orthologous variants: 175721421-T-C

241861539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron variant
orthologous variants: 175721434-T-C

http://identifiers.org/hco/1/GRCh38#241861608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#175721500-C-A

241861625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron variant
orthologous variants: 175721516-T-C

241866202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron variant
orthologous variants: 175722814-C-T

http://identifiers.org/hco/1/GRCh38#241866272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#175722888-C-A

241866272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron variant
orthologous variants: 175722888-C-T

241866279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron variant
orthologous variants: 175722895-A-G

241866789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron variant
orthologous variants: 175723653-T-C

http://identifiers.org/hco/1/GRCh38#241866797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#175723661-C-A

241866868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: synonymous variant
orthologous variants: 175723732-A-G

241866887-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: missense variant
orthologous variants: 175723751-G-C

241866892-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: missense variant
orthologous variants: 175723756-C-G

241866892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: synonymous variant
orthologous variants: 175723756-C-T

241866970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: synonymous variant
orthologous variants: 175723834-A-G

241867033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: synonymous variant
orthologous variants: 175723897-C-T

241871795-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron variant
orthologous variants: 175726673-T-G

241871934-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron variant
orthologous variants: 175726817-T-A

241871934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron variant
orthologous variants: 175726817-T-C

241871934-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron variant
orthologous variants: 175726817-T-G

241871937-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron variant
orthologous variants: 175726820-T-A

241871937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron variant
orthologous variants: 175726820-T-C

241871937-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron variant
orthologous variants: 175726820-T-G

241871940-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron variant
orthologous variants: 175726823-T-A

http://identifiers.org/hco/1/GRCh38#241871963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#175726878-C-A

241871963-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron variant
orthologous variants: 175726878-C-G

241871963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron variant
orthologous variants: 175726878-C-T

241871998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron variant
orthologous variants: 175726920-A-G

241872000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron variant
orthologous variants: 175726922-A-G

241872065-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: missense variant
orthologous variants: 175726988-A-T

241877173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron variant
orthologous variants: 175727826-C-T

241877261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron variant
orthologous variants: 175727909-A-G

241877264-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron variant
orthologous variants: 175727912-G-C

241877264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron variant
orthologous variants: 175727912-G-T

241878367-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron variant
orthologous variants: 175728149-C-G

241878390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron variant
orthologous variants: 175728171-A-G

241878423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron variant
orthologous variants: 175728199-G-T

241878449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron variant
orthologous variants: 175728217-A-G

http://identifiers.org/hco/1/GRCh38#241878452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#175728220-C-A

241878452-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron variant
orthologous variants: 175728220-C-G

241878588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron variant
orthologous variants: 175728318-T-C

241878656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron variant
orthologous variants: 175728370-G-A

241878656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron variant
orthologous variants: 175728370-G-T

http://identifiers.org/hco/1/GRCh38#241878685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#175728385-C-A

241878685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron variant
orthologous variants: 175728385-C-T

241878798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: missense variant
orthologous variants: 175728498-A-G

241878840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: missense variant
orthologous variants: 175728543-A-G

241878869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: synonymous variant
orthologous variants: 175728575-A-G

241878878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: synonymous variant
orthologous variants: 175728584-G-A

241878890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: synonymous variant
orthologous variants: 175728596-C-T

241878906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: missense variant
orthologous variants: 175728612-A-G

241878910-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: stop gained
orthologous variants: 175728616-C-G

241879197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: missense variant
orthologous variants: 175728879-A-G

http://identifiers.org/hco/1/GRCh38#241879202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#175728884-C-A

241879202-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: missense variant
orthologous variants: 175728884-C-G

241879202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: synonymous variant
orthologous variants: 175728884-C-T

241879210-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: missense variant
orthologous variants: 175728892-C-G

241879310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: synonymous variant
orthologous variants: 175728986-T-C

241879336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: missense variant
orthologous variants: 175729012-A-G

241879336-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: missense variant
orthologous variants: 175729012-A-T

241879340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: synonymous variant
orthologous variants: 175729016-A-G

http://identifiers.org/hco/1/GRCh38#241879355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#175729031-C-A

241879355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron variant
orthologous variants: 175729031-C-T

241879378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron variant
orthologous variants: 175729054-T-C

241879378-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron variant
orthologous variants: 175729054-T-G

241880736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron variant
orthologous variants: 175730158-G-A

241880783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron variant
orthologous variants: 175730201-C-T

241881981-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 175731967-T-A

241881981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 175731967-T-C

241882010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, missense_variant
orthologous variants: 175731996-G-A

241882034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron variant
orthologous variants: 175732022-A-G

241882034-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron variant
orthologous variants: 175732022-A-T

241882047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron variant
orthologous variants: 175732036-T-C

http://identifiers.org/hco/1/GRCh38#241882069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#175732071-C-A

241882069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron variant
orthologous variants: 175732071-C-T

http://identifiers.org/hco/1/GRCh38#241882123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#175732127-C-A

241885341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: missense variant
orthologous variants: 175733389-G-A

241885405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 175733453-A-G

241888477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175735227-G-A

241889239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175735814-A-G

http://identifiers.org/hco/1/GRCh38#241889313-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#175735888-A-C

241889313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175735888-A-G

241889355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175735906-A-G

241889355-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175735906-A-T

241889377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175735918-A-G

241889377-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175735918-A-T

241889621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 175736141-T-C

241889631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 175736151-A-G

241889719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 175736202-A-G

241889719-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 175736202-A-T

241889723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 175736206-A-G

http://identifiers.org/hco/1/GRCh38#241889727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#175736210-C-A

241889727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 175736210-C-T

241889854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 175736327-G-A

241889854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 175736327-G-T

241889983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175736464-C-T

241889987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175736468-T-C

241890369-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175736733-A-T

241890448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175736800-G-A

http://identifiers.org/hco/1/GRCh38#241890600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#175736884-C-A

241890600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175736884-C-T

241890770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175737019-G-A

241890802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175737043-A-G

241890922-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3511
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 175737163-G-C