32927932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 5 prime UTR variant
orthologous variants: 80700979-G-A

32927932-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 5 prime UTR variant
orthologous variants: 80700979-G-C

32927932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 5 prime UTR variant
orthologous variants: 80700979-G-T

32927963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 5 prime UTR variant
orthologous variants: 80700989-G-A

http://identifiers.org/hco/17/GRCh38#32927990-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#80701016-A-C

32928004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 5 prime UTR variant
orthologous variants: 80701030-G-A

32928004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 5 prime UTR variant
orthologous variants: 80701030-G-T

http://identifiers.org/hco/17/GRCh38#32928262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#80701308-C-A

32928262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80701308-C-T

http://identifiers.org/hco/17/GRCh38#32928269-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#80701315-C-A

32928269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80701315-C-T

32928313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80701343-G-A

32928313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80701343-G-T

32929380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80701693-G-A

32929384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80701712-G-A

32929699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80701984-C-T

32929751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80702035-G-T

32929906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80702169-G-A

32930016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80702275-A-G

32930096-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80702353-C-G

32930185-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80702442-C-G

32930191-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80702448-G-C

32930294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80702540-G-A

32930629-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80702868-T-A

32930752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80702976-G-A

http://identifiers.org/hco/17/GRCh38#32931296-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#80703177-A-C

32931296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80703177-A-G

32931296-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80703177-A-T

32931327-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 80703189-G-C

32931327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 80703189-G-T

32931348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80703209-T-C

32931348-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80703209-T-G

http://identifiers.org/hco/17/GRCh38#32931381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#80703238-C-A

32931381-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80703238-C-G

32931403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 80703260-G-T

32931408-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80703265-A-T

http://identifiers.org/hco/17/GRCh38#32931409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#80703266-C-A

32931409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 80703266-C-T

http://identifiers.org/hco/17/GRCh38#32931414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#80703271-C-A

32931414-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80703271-C-G

32931414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80703271-C-T

32931415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80703272-T-C

32931421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 80703278-A-G

http://identifiers.org/hco/17/GRCh38#32931471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#80703328-C-A

32931471-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 80703328-C-G

32931471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 80703328-C-T

32931509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 80703365-G-A

32931742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80703607-A-G

32931771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80703635-T-C

32931896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80703756-C-T

32931911-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80703771-T-G

32931947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80703804-A-G

32932067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80703917-A-G

32932067-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80703917-A-T

32932073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80703923-G-T

32932531-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80704062-G-C

32932901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80704477-T-C

32932944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80704518-T-C

32933041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80704602-T-C

http://identifiers.org/hco/17/GRCh38#32933109-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#80704981-A-C

32933109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80704981-A-G

32933119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80704991-G-A

32933126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80704998-C-T

32933138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80705010-A-G

32933138-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80705010-A-T

32933156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80705027-G-A

32933156-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80705027-G-C

32933319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80705190-A-G

32933319-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80705190-A-T

32933327-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80705198-G-C

32933603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80705457-C-T

32933678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80705526-C-T

32933725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80705572-C-T

32933826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80705681-A-G

32933844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80705698-C-T

32934185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80706387-A-G

32934194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80706398-T-C

32934233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80706434-G-A

32934233-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80706434-G-C

http://identifiers.org/hco/17/GRCh38#32934331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#80706532-C-A

32934331-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 80706532-C-G

32934412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80706607-G-A

32934412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80706607-G-T

32934435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80706627-T-C

http://identifiers.org/hco/17/GRCh38#32934484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#80706678-C-A

32934484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80706678-C-T

32934485-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80706679-T-A

32934485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80706679-T-C

32934587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80706784-C-T

32934754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80706922-G-A

32934809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80706973-G-T

32934853-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80707018-T-G

32934887-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80707043-T-G

32934953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80707110-T-C

32935024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80707175-A-G

32935024-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80707175-A-T

32935144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80707274-A-G

32935364-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80707453-T-A

32935364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80707453-T-C

32935518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80707554-C-T

32935553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80707580-C-T

32935640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80707662-C-T

32935645-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80707667-C-G

32935741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80707752-A-G

32935742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80707753-G-A

32935801-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80707815-T-G

32936105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80708108-C-T

32936235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80708218-G-A

32936235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80708218-G-T

32936237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80708220-T-C

http://identifiers.org/hco/17/GRCh38#32936244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#80708227-C-A

32936244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80708227-C-T

32936267-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 80708251-T-G

32936476-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron variant
orthologous variants: 80708472-A-T

32936477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron variant
orthologous variants: 80708473-C-T

http://identifiers.org/hco/17/GRCh38#32936481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#80708477-C-A

32936481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron variant
orthologous variants: 80708477-C-T

32936482-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron variant
orthologous variants: 80708478-C-G

32936482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron variant
orthologous variants: 80708478-C-T

32936518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron variant
orthologous variants: 80708502-G-A

32936518-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron variant
orthologous variants: 80708502-G-C

32936518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron variant
orthologous variants: 80708502-G-T

http://identifiers.org/hco/17/GRCh38#32936529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#80708513-C-A

32936529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron variant
orthologous variants: 80708513-C-T

32936561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron variant
orthologous variants: 80708544-G-A

32936561-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron variant
orthologous variants: 80708544-G-C

32936561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron variant
orthologous variants: 80708544-G-T

32936572-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron variant
orthologous variants: 80708555-C-G

32936572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron variant
orthologous variants: 80708555-C-T

32936608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron variant
orthologous variants: 80708578-A-G

32936618-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron variant
orthologous variants: 80708591-C-G

32936618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron variant
orthologous variants: 80708591-C-T

32936748-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron variant
orthologous variants: 80708712-C-G

32936802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron variant
orthologous variants: 80708765-A-G

32936902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, undefined
orthologous variants: 80708892-C-T

32936957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, undefined
orthologous variants: 80708933-C-T

32937187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, undefined
orthologous variants: 80709163-G-A

32937195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, undefined
orthologous variants: 80709167-G-A

32937195-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, undefined
orthologous variants: 80709167-G-C

http://identifiers.org/hco/17/GRCh38#32937324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#80709243-C-A

32937352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, undefined
orthologous variants: 80709262-G-A

32937356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, undefined
orthologous variants: 80709266-C-T

http://identifiers.org/hco/17/GRCh38#32937383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#80709294-C-A

32937956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron variant
orthologous variants: 80709539-G-A

32937963-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron variant
orthologous variants: 80709546-C-G

32937963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron variant
orthologous variants: 80709546-C-T

32938180-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron variant
orthologous variants: 80709714-T-G

32938581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron variant
orthologous variants: 80710088-T-C

32938624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron variant
orthologous variants: 80710143-T-C

32938638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron variant
orthologous variants: 80710157-G-A

32938638-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron variant
orthologous variants: 80710157-G-C

32939059-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron variant
orthologous variants: 80710643-C-G

32939130-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron variant
orthologous variants: 80710651-G-C

32939156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron variant
orthologous variants: 80710663-C-T

32939420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron variant
orthologous variants: 80710700-A-G

32939426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron variant
orthologous variants: 80710706-G-A

32939426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron variant
orthologous variants: 80710706-G-T

32939427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron variant
orthologous variants: 80710707-A-G

32939433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron variant
orthologous variants: 80710713-A-G

32939433-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron variant
orthologous variants: 80710713-A-T

32939450-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron variant
orthologous variants: 80710735-T-A

32939450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron variant
orthologous variants: 80710735-T-C

32939450-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron variant
orthologous variants: 80710735-T-G

http://identifiers.org/hco/17/GRCh38#32939588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#80710859-C-A

32939588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron variant
orthologous variants: 80710859-C-T

32939669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron variant
orthologous variants: 80710940-T-C

32939670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron variant
orthologous variants: 80710941-G-A

32939670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron variant
orthologous variants: 80710941-G-T

32939797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron variant
orthologous variants: 80711053-C-T

32939955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron variant
orthologous variants: 80711205-G-A

32939974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron variant
orthologous variants: 80711237-C-T

32940172-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron variant
orthologous variants: 80711409-C-G

32940176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron variant
orthologous variants: 80711413-G-T

32940313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron variant
orthologous variants: 80711605-G-T

http://identifiers.org/hco/17/GRCh38#32940686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#80711934-C-A

32940686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron variant
orthologous variants: 80711934-C-T

32940714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron variant
orthologous variants: 80711963-T-C

32940807-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 80712059-T-A

32940807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 80712059-T-C

32940807-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 80712059-T-G

32940852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 80712104-G-A

32940852-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 80712104-G-C

32940852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 80712104-G-T

32940960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 80712212-T-C

http://identifiers.org/hco/17/GRCh38#32941034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#80712267-C-A

32941035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80712268-A-G

32941056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80712280-G-A

32941056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80712280-G-T

32941085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80712306-G-T

32941122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80712343-G-A

32941122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80712343-G-T

32941157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80712377-T-C

32941165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80712385-G-A

32941165-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80712385-G-T

http://identifiers.org/hco/17/GRCh38#32941170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#80712390-C-A

http://identifiers.org/hco/17/GRCh38#32941216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#80712436-C-A

32941216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80712436-C-T

32941238-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80712456-T-A

32941253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80712471-G-T

http://identifiers.org/hco/17/GRCh38#32941303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#80712521-C-A

32941303-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80712521-C-G

32941303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80712521-C-T

32941415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80712609-A-G

http://identifiers.org/hco/17/GRCh38#32941442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#80712636-C-A

32941474-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80712659-A-T

http://identifiers.org/hco/17/GRCh38#32941498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#80712684-C-A

32941506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80712692-C-T

32941565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80712775-G-A

32941588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80712798-G-A

32941680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80712890-A-G

32941707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80712924-G-T

32941714-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80712931-G-C

32941718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80712935-G-T

32941722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80712939-A-G

http://identifiers.org/hco/17/GRCh38#32941742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#80712959-C-A

32941749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80712966-T-C

http://identifiers.org/hco/17/GRCh38#32942367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#80714305-C-A

32942367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80714305-C-T

32942449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80714385-A-G

32942453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80714389-A-G

32942456-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80714392-T-G

32942524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80714452-T-C

32942837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80714713-A-G

http://identifiers.org/hco/17/GRCh38#32942857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#80714734-C-A

32942858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80714735-T-C

32942918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80714781-G-A

32943014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80714871-G-T

32943133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80714968-T-C

http://identifiers.org/hco/17/GRCh38#32943203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#80715103-C-A

32943203-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80715103-C-G

32943203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80715103-C-T

32943230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80715143-G-T

32943296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80715221-G-T

32943374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80715302-C-T

32943446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80715368-C-T

http://identifiers.org/hco/17/GRCh38#32943504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#80715426-C-A

32943517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80715439-G-T

32943518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80715440-G-T

32943534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80715452-T-C

32943555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80715473-A-G

32943567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80715485-T-C

32943747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80715673-A-G

32943814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80715740-T-C

32943829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80715755-G-A

32943829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80715755-G-T

32943844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80715770-G-T

32944029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80716304-T-C

http://identifiers.org/hco/17/GRCh38#32944040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#80716316-C-A

http://identifiers.org/hco/17/GRCh38#32944126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#80716394-C-A

32944126-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80716394-C-G

32944126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80716394-C-T

32944143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80716411-A-G

32944218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80716485-T-C

32944266-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 80716532-A-T

32944880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: splice_region_variant, undefined
orthologous variants: 80718352-A-G

32945003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24529
most severe consequence: 3 prime UTR variant
orthologous variants: 80718493-C-T