52903597-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: 3 prime UTR variant
orthologous variants: 30541417-G-C

52903597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: 3 prime UTR variant
orthologous variants: 30541417-G-T

52904242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: 3 prime UTR variant
orthologous variants: 30540657-C-T

52904315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: 3 prime UTR variant
orthologous variants: 30540593-C-T

52904547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: 3 prime UTR variant
orthologous variants: 30540366-C-T

52904704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: 3 prime UTR variant
orthologous variants: 30540214-G-A

52904704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: 3 prime UTR variant
orthologous variants: 30540214-G-T

52904847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: 3 prime UTR variant
orthologous variants: 30540071-A-G

52904847-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: 3 prime UTR variant
orthologous variants: 30540071-A-T

http://identifiers.org/hco/3/GRCh38#52904890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30540036-C-A

52904890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: 3 prime UTR variant
orthologous variants: 30540036-C-T

http://identifiers.org/hco/3/GRCh38#52904894-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30540032-A-C

52904894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: 3 prime UTR variant
orthologous variants: 30540032-A-G

52904977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: 3 prime UTR variant
orthologous variants: 30539961-T-C

52905115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: 3 prime UTR variant
orthologous variants: 30539823-A-G

http://identifiers.org/hco/3/GRCh38#52905303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30539639-C-A

52905309-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30539633-T-A

52905309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30539633-T-C

52905371-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30539590-G-C

52905554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30539452-C-T

52905877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30538989-G-A

52905980-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30538926-A-T

52906071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30538866-G-T

http://identifiers.org/hco/3/GRCh38#52906328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30538617-C-A

52906328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30538617-C-T

52906430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30538493-C-T

52906673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30538089-T-C

52906788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30537971-A-G

52907132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: synonymous variant
orthologous variants: 30537545-C-T

http://identifiers.org/hco/3/GRCh38#52907150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30537527-C-A

52907150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: synonymous variant
orthologous variants: 30537527-C-T

52907477-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30537266-G-C

52907568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: missense variant
orthologous variants: 30537194-G-A

52907568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: missense variant
orthologous variants: 30537194-G-T

52907592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: missense variant
orthologous variants: 30537170-G-A

52907780-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30536977-T-G

52910820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30533676-C-T

52910928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30533575-G-A

52910928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30533575-G-T

52910959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30533561-A-G

52911029-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: missense variant
orthologous variants: 30533493-C-G

52911029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: missense variant
orthologous variants: 30533493-C-T

52911307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30533155-G-A

52911307-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30533155-G-C

52911307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30533155-G-T

52911315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30533134-A-G

52911517-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30532731-A-T

52912628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: missense variant
orthologous variants: 30532270-T-C

52912794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30532137-T-C

52913731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30524373-G-A

52913731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30524373-G-T

52916208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: synonymous variant
orthologous variants: 30523819-T-C

52916320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30523724-G-A

52916320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30523724-G-T

52916347-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30523697-T-A

52916347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30523697-T-C

52916347-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30523697-T-G

52917823-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30522421-C-G

52918435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30521796-T-C

52918435-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30521796-T-G

52918439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30521789-T-C

52918449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30521779-A-G

52918505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: missense variant
orthologous variants: 30521717-G-A

52918505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: missense variant
orthologous variants: 30521717-G-T

http://identifiers.org/hco/3/GRCh38#52918585-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30521641-A-C

52918585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30521641-A-G

52919939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30520390-G-A

http://identifiers.org/hco/3/GRCh38#52920127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30520146-C-A

http://identifiers.org/hco/3/GRCh38#52920458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30519723-C-A

52920458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30519723-C-T

52920461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30519720-G-T

http://identifiers.org/hco/3/GRCh38#52920531-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30519650-A-C

52920572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: missense variant
orthologous variants: 30519609-T-C

52921261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30518807-C-T

52921337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30518736-T-C

52921477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30518603-G-T

52921672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30518439-C-T

http://identifiers.org/hco/3/GRCh38#52921925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30518184-C-A

52921958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30518145-T-C

52925990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30512808-C-T

52926001-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30512797-T-A

52926001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30512797-T-C

52926012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30512790-A-G

52926014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30512788-G-A

52926014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30512788-G-T

52926017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30512785-G-A

52926062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30512740-G-A

52926162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30512652-C-T

52926176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30512639-C-T

52926435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30512377-G-A

52926439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30512373-G-A

52926443-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30512369-T-G

52926535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30512274-G-A

52926549-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30512260-T-A

52926561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30512248-T-C

52927036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30511195-C-T

52927161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30511069-C-T

52927245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30510985-T-C

52927528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30510778-A-G

http://identifiers.org/hco/3/GRCh38#52928486-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30509362-A-C

52928489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30509359-A-G

52928569-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30509352-T-A

52928569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30509352-T-C

52928583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30509338-C-T

http://identifiers.org/hco/3/GRCh38#52928608-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30509310-A-C

http://identifiers.org/hco/3/GRCh38#52928610-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30509308-A-C

52928610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30509308-A-G

52928610-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30509308-A-T

52928612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30509306-A-G

52928616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30509302-A-G

52929057-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30509019-A-T

52929645-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30508547-T-A

52930127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30508071-G-T

52930131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30508063-A-G

http://identifiers.org/hco/3/GRCh38#52930264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30507941-C-A

52930264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30507941-C-T

52930336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: missense variant
orthologous variants: 30507863-A-G

52930857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30506829-G-A

52930857-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30506829-G-C

52930857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30506829-G-T

52930883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30506801-G-A

52930989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: synonymous variant
orthologous variants: 30506702-G-A

52932055-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 30506151-T-G

52932082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: missense variant
orthologous variants: 30506124-T-C

52932151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: missense variant
orthologous variants: 30506055-T-C

52932304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: missense variant
orthologous variants: 30505902-C-T

52932405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30505812-T-C

http://identifiers.org/hco/3/GRCh38#52932412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30505805-C-A

52933215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30505209-T-C

http://identifiers.org/hco/3/GRCh38#52934682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30500037-C-A

52934682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30500037-C-T

http://identifiers.org/hco/3/GRCh38#52934746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30500002-C-A

52934746-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30500002-C-G

52934746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30500002-C-T

http://identifiers.org/hco/3/GRCh38#52934902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: splice acceptor variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30499858-C-A

52943204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30496208-T-C

52943208-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30496204-T-G

52943215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30496197-T-C

http://identifiers.org/hco/3/GRCh38#52943300-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30496116-A-C

52943323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30496093-G-A

52943382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: missense variant
orthologous variants: 30496051-T-C

52943400-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: missense variant
orthologous variants: 30496033-G-C

52943400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: missense variant
orthologous variants: 30496033-G-T

52943469-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: missense variant
orthologous variants: 30495964-C-G

52943469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: missense variant
orthologous variants: 30495964-C-T

52943496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: missense variant
orthologous variants: 30495937-G-A

52943496-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: missense variant
orthologous variants: 30495937-G-C

52943526-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: missense variant
orthologous variants: 30495907-G-C

52943616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30495818-G-A

52943718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30495712-G-A

52943718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30495712-G-T

http://identifiers.org/hco/3/GRCh38#52943740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30495690-C-A

52943740-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30495690-C-G

52943740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30495690-C-T

52943768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30495659-T-C

52943768-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30495659-T-G

52943845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30495590-A-G

52943910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30495525-A-G

52943973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30495478-T-C

52944255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30495248-T-C

52944329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30495161-T-C

52944419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron variant
orthologous variants: 30495133-A-G

http://identifiers.org/hco/3/GRCh38#52954485-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30491690-A-C

52969045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30488112-G-T

52969211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30487951-G-A

52969380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30487787-T-C

52988615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30478195-T-C

52989209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30477665-G-A

52989327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30476784-T-C

52989966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30470585-T-C

52990010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30470542-A-G

52990171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30470382-A-G

http://identifiers.org/hco/3/GRCh38#53012998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30467389-C-A

53013061-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30467316-G-C

53013371-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30467016-T-A

http://identifiers.org/hco/3/GRCh38#53013596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30465399-C-A

53013596-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30465399-C-G

53014139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30465186-C-T

53014208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30465106-G-T

53030802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30458405-C-T

53031293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30457974-C-T

http://identifiers.org/hco/3/GRCh38#53032529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30456304-C-A

53032529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30456304-C-T

53032738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30456080-C-T

53032865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30455679-C-T

53038702-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30451626-T-A

53039852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30449752-G-A

53040524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30447530-C-T

53040703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30447408-A-G

53040703-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30447408-A-T

53041920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30443233-G-A

53041920-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30443233-G-C

53041920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30443233-G-T

53041975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30443178-T-C

53042335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30442847-T-C

53042482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30442694-G-A

53042629-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30442474-C-G

53042660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30442427-G-A

53042779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30442177-A-G

53043044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30441829-C-T

53043078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30441795-C-T

53043175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 30441683-G-A

53043649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30440186-A-G

http://identifiers.org/hco/3/GRCh38#53044035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30439640-C-A

53044035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30439640-C-T

http://identifiers.org/hco/3/GRCh38#53044491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30439145-C-A

53044491-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30439145-C-G

53044491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30439145-C-T

53044935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30438706-G-T

53044971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30438670-G-T

53045130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30438514-G-A

53045130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30438514-G-T

53045222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 30438405-G-T

53045225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 30438402-G-A

53045267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30438362-T-C

53045472-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30438188-G-C

53045835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 30437811-G-A

53045835-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 30437811-G-C

53045835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 30437811-G-T

http://identifiers.org/hco/3/GRCh38#53046130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30437510-C-A

53046182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30437459-G-A

53046182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30437459-G-T

53046332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 30437322-G-T

http://identifiers.org/hco/3/GRCh38#53046416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30437245-C-A

53046416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30437245-C-T

http://identifiers.org/hco/3/GRCh38#53046519-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30437147-A-C

53046519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30437147-A-G

53046519-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30437147-A-T

http://identifiers.org/hco/3/GRCh38#53046520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30437146-C-A

53046520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30437146-C-T

http://identifiers.org/hco/3/GRCh38#53046569-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#30437095-A-C

53046569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 30437095-A-G

53046571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 30437093-G-A

53046601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 30437056-C-T

53046608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 30437049-G-A

53046612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 30437045-G-A

53046612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 30437045-G-T

53046656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30437002-G-A

53046656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30437002-G-T

http://identifiers.org/hco/3/GRCh38#53046666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#30436992-C-A

53046666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20255
most severe consequence: non coding transcript exon variant
orthologous variants: 30436992-C-T