41301900-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81629691-T-A

41301900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81629691-T-C

41302127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81629925-C-T

41302517-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81630315-C-G

41302549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81630342-G-A

41302549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81630342-G-T

41302617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81630405-G-T

http://identifiers.org/hco/22/GRCh38#41302836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81630621-C-A

41302900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81630704-G-A

41303272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81631238-G-A

41305613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81633934-T-C

41305937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81634189-G-A

41305960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81634211-A-G

41307399-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81637283-C-G

41307457-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81637333-G-C

41307487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81637357-T-C

41307591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81637441-G-A

41307736-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81637537-G-C

41307765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81637566-A-G

41307993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81639190-G-A

41308119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81639310-G-A

41308138-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81639329-C-G

41308138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81639329-C-T

41308146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81639337-A-G

41308326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81639471-C-T

41308383-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81639535-C-G

41308456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81639611-A-G

41308617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81639802-C-T

41308775-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81639926-C-G

41308775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81639926-C-T

41308780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81639931-C-T

41308794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81639945-C-T

http://identifiers.org/hco/22/GRCh38#41308856-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#81639975-A-C

http://identifiers.org/hco/22/GRCh38#41308872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#81639991-C-A

41308967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81640061-G-A

41309008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81640105-C-T

41310255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81642010-G-A

41310256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81642011-C-T

http://identifiers.org/hco/22/GRCh38#41310267-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81642022-A-C

41310558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81642238-C-T

41310569-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81642249-C-G

41310572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81642252-G-A

41311163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81645645-C-T

41311400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81645894-G-A

41311587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81646531-G-T

41311635-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81646570-T-G

41311829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81646759-C-T

41320505-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81652014-G-C

41320505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81652014-G-T

41320554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81652063-G-A

41320554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81652063-G-T

41320758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81652276-G-A

41320758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81652276-G-T

41320804-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81652300-T-A

http://identifiers.org/hco/22/GRCh38#41320817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81652309-C-A

41320817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81652309-C-T

41320832-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81652317-T-A

41320832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81652317-T-C

41320857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81652342-G-A

41320857-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81652342-G-C

41320857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81652342-G-T

41320929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81652396-C-T

http://identifiers.org/hco/22/GRCh38#41320992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81652443-C-A

41320994-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81652445-C-G

41325416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81652901-G-A

41325416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81652901-G-T

http://identifiers.org/hco/22/GRCh38#41325419-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81652904-A-C

41325419-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81652904-A-T

41325423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81652913-A-G

41325448-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81652938-G-C

41325458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81652945-G-A

41325670-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81653137-C-G

http://identifiers.org/hco/22/GRCh38#41325914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81653378-C-A

41325914-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 81653378-C-G

http://identifiers.org/hco/22/GRCh38#41325979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81653435-C-A

41325979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81653435-C-T

41325980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81653436-G-A

41325980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81653436-G-T

41326003-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81653447-G-C

41326003-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81653447-G-T

41326007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81653451-G-A

41326007-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81653451-G-T

41326010-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81653454-G-C

41326010-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81653454-G-T

http://identifiers.org/hco/22/GRCh38#41326014-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81653458-A-C

41326014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81653458-A-G

http://identifiers.org/hco/22/GRCh38#41326025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81653469-C-A

41326025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81653469-C-T

http://identifiers.org/hco/22/GRCh38#41326029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81653473-C-A

41327102-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81655864-C-G

41327104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81655866-G-A

41327104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81655866-G-T

http://identifiers.org/hco/22/GRCh38#41327105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81655867-C-A

41327105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81655867-C-T

http://identifiers.org/hco/22/GRCh38#41327430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81656160-C-A

41327430-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81656160-C-G

41327430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81656160-C-T

41327480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81656211-A-G

41329973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81656569-T-C

41329973-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81656569-T-G

41330000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81656595-G-A

41330133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81656729-G-A

41330133-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81656729-G-C

41330133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81656729-G-T

41330202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81656794-G-A

41330202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81656794-G-T

41330249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81656839-G-T

41330251-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81656841-T-A

41330251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81656841-T-C

41330255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81656845-T-C

41330421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81657029-C-T

http://identifiers.org/hco/22/GRCh38#41332058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81657393-C-A

41332058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81657393-C-T

41332061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81657396-T-C

41332107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81657439-A-G

http://identifiers.org/hco/22/GRCh38#41332133-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81657449-A-C

41332133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81657449-A-G

41332133-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81657449-A-T

41332233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81657549-A-G

http://identifiers.org/hco/22/GRCh38#41332235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81657551-C-A

41332235-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 81657551-C-G

41332235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 81657551-C-T

41332264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81657605-C-T

http://identifiers.org/hco/22/GRCh38#41334429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81657653-C-A

41334429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81657653-C-T

41334434-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81657658-A-T

41334443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81657667-T-C

41334448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81657672-G-A

41334448-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81657672-G-C

41334448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81657672-G-T

http://identifiers.org/hco/22/GRCh38#41334464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81657686-C-A

41334472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81657694-G-A

http://identifiers.org/hco/22/GRCh38#41334485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81657706-C-A

http://identifiers.org/hco/22/GRCh38#41334490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81657711-C-A

41334490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81657711-C-T

41334556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81657761-T-C

41334573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81657782-G-T

41334718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81657869-G-T

41334761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81657944-A-G

http://identifiers.org/hco/22/GRCh38#41334769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81657952-C-A

41334826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81658007-T-C

41334875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81658053-A-G

41334921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81658078-A-G

41334955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81658099-A-G

41335001-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81658144-G-C

41335001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81658144-G-T

41335011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81658154-G-T

41335076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81658191-A-G

41335148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81658240-C-T

41335163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81658254-G-A

41335163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81658254-G-T

41335183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81658272-G-T

http://identifiers.org/hco/22/GRCh38#41335470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81658557-C-A

41335470-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81658557-C-G

41335485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81658572-T-C

41335621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81658666-A-G

41335629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81658674-G-A

41335633-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81658678-T-A

41335633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81658678-T-C

41335707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81658740-G-A

41335707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81658740-G-T

41335774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81658790-C-T

41335802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81658812-G-T

41335838-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81658848-T-A

http://identifiers.org/hco/22/GRCh38#41335850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81658857-C-A

41335850-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81658857-C-G

41335850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81658857-C-T

41335859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81658864-G-A

41335859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81658864-G-T

41335862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81658867-G-A

41335862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81658867-G-T

41335900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81658893-A-G

41335960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81658923-G-A

41335960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81658923-G-T

41335978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81658941-T-C

41335999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81658960-G-T

41336022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81658984-C-T

http://identifiers.org/hco/22/GRCh38#41336066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81659027-C-A

41338348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 81660042-C-T

41338493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81660102-G-A

41338622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81660163-C-T

41338913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81660407-T-C

http://identifiers.org/hco/22/GRCh38#41338954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81660433-C-A

41338954-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81660433-C-G

41338981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81660458-C-T

http://identifiers.org/hco/22/GRCh38#41339028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81660506-C-A

41339028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 81660506-C-T

41339053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 81660531-G-A

41339149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 81660630-G-A

41339149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 81660630-G-T

41339170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 81660651-G-A

41339260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81660746-G-A

41339260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81660746-G-T

41339278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81660763-T-C

http://identifiers.org/hco/22/GRCh38#41339731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81660897-C-A

41339731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81660897-C-T

http://identifiers.org/hco/22/GRCh38#41339783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81660949-C-A

41339783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81660949-C-T

41339878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 81661044-C-T

http://identifiers.org/hco/22/GRCh38#41339941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81661107-C-A

41339986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 81661152-G-T

41340123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 81661289-C-T

41340124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 81661290-T-C

41340162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81661331-A-G

41340166-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81661337-T-A

41340176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81661348-G-T

41340276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81661433-G-A

41340276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81661433-G-T

41340509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81661629-G-A

41340593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81661703-G-A

41340859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81661899-C-T

http://identifiers.org/hco/22/GRCh38#41340958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81661968-C-A

41340989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81661995-G-T

41341198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81662188-G-A

http://identifiers.org/hco/22/GRCh38#41341267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81662258-C-A

41341267-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81662258-C-G

http://identifiers.org/hco/22/GRCh38#41342201-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81662513-A-C

41342635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 81662917-T-C

http://identifiers.org/hco/22/GRCh38#41342641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81662923-C-A

41342641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81662923-C-T

http://identifiers.org/hco/22/GRCh38#41342656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81662937-C-A

41342656-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81662937-C-G

41342656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81662937-C-T

41342719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81662996-T-C

41342733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81663010-G-A

41342754-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81663031-T-A

41342754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81663031-T-C

41342754-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81663031-T-G

41343053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81663099-G-A

41343398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81663293-G-A

41343473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 81663368-C-T

41343530-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 81663425-C-G

http://identifiers.org/hco/22/GRCh38#41343557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81663452-C-A

41343560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 81663455-C-T

41343613-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81663509-G-C

http://identifiers.org/hco/22/GRCh38#41343615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81663511-C-A

41343659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81663533-G-A

41343660-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81663534-T-A

41343660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81663534-T-C

41343660-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81663534-T-G

http://identifiers.org/hco/22/GRCh38#41343669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81663543-C-A

41343669-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81663543-C-G

41343738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81663574-G-T

41343810-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81663638-T-G

41343836-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81663663-G-C

41343897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81663717-T-C

http://identifiers.org/hco/22/GRCh38#41344160-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81663904-A-C

41344160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81663904-A-G

41344215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81663951-G-A

41344297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81664031-G-A

41344297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81664031-G-T

http://identifiers.org/hco/22/GRCh38#41344418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81664087-C-A

41344418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81664087-C-T

41344425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81664094-G-A

41344425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81664094-G-T

41344641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81664272-G-A

41345986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81664588-C-T

41346061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 81664663-G-A

41346145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 81664747-C-T

41346166-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 81664768-G-C

http://identifiers.org/hco/22/GRCh38#41346196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81664798-C-A

41346196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 81664798-C-T

41346294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81664870-G-A

41346294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81664870-G-T

41346312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81664888-G-A

41346312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81664888-G-T

41346322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81664899-G-T

http://identifiers.org/hco/22/GRCh38#41346337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81664914-C-A

41347912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81666006-G-T

41347938-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81666032-T-A

http://identifiers.org/hco/22/GRCh38#41347941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81666035-C-A

41347941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81666035-C-T

http://identifiers.org/hco/22/GRCh38#41347951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81666045-C-A

41347951-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81666045-C-G

41347951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81666045-C-T

41348115-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 81666208-T-A

41348115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 81666208-T-C

41348115-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 81666208-T-G

http://identifiers.org/hco/22/GRCh38#41348116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81666209-C-A

http://identifiers.org/hco/22/GRCh38#41348254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81666343-C-A

41348254-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81666343-C-G

41348254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81666343-C-T

41348256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81666345-G-A

41348256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81666345-G-T

41348337-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81666384-C-G

41348337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81666384-C-T

41348356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81666403-A-G

41348364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81666411-A-G

41348377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81666424-G-T

41348502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81666536-G-A

41348610-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81666634-T-G

41348711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81666754-G-A

41348720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81666763-C-T

41349020-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81667094-G-C

41349020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81667094-G-T

41349042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81667145-G-T

41349098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81667208-C-T

41349399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81667466-G-T

41349415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81667482-G-A

41349415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81667482-G-T

http://identifiers.org/hco/22/GRCh38#41349423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81667490-C-A

41349423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81667490-C-T

41349441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81667509-G-T

http://identifiers.org/hco/22/GRCh38#41349448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81667516-C-A

41349448-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81667516-C-G

41349448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81667516-C-T

41349628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81667743-C-T

41349802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81667887-C-T

41349820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81667903-T-C

41349846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81667919-A-G

41350226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81668194-C-T

41350248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81668216-C-T

41350480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81669188-G-A

41350527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81669239-G-A

41350527-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81669239-G-C

41350697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81669406-C-T

41350753-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81669466-T-A

41350754-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81669467-G-C

41350876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81669587-G-A

41350900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81669610-A-G

41350950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81669645-C-T

41351095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81669762-G-A

41351369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81669901-C-T

http://identifiers.org/hco/22/GRCh38#41351386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81669910-C-A

41351546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81670072-C-T

http://identifiers.org/hco/22/GRCh38#41351640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81670162-C-A

41352951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81670863-G-T

41353046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81670969-C-T

41353049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81670972-C-T

41353139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81671033-T-C

41353222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81671111-A-G

41353710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81671519-G-T

41354774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81671908-A-G

41354952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81672045-C-T

41355015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81672105-T-C

41355284-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81675952-C-G

41355284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81675952-C-T

41355472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: missense variant
orthologous variants: 81676136-G-A

41355472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: missense variant
orthologous variants: 81676136-G-T

41355552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: synonymous variant
orthologous variants: 81676216-G-T

41355629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81676292-A-G

41355646-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81676309-C-G

41355777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: missense variant
orthologous variants: 81676451-T-C

41355777-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: missense variant
orthologous variants: 81676451-T-G

41355880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81676559-G-A

http://identifiers.org/hco/22/GRCh38#41356185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81676830-C-A

41356185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81676830-C-T

41356233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81676880-C-T

41356274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81676921-G-A

41356398-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: missense variant
orthologous variants: 81677036-G-C

41356401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: synonymous variant
orthologous variants: 81677039-T-C

41356434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: synonymous variant
orthologous variants: 81677072-G-A

41356513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81677140-G-A

41356513-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81677140-G-C

41356513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81677140-G-T

41356604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81677183-A-G

41356716-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: synonymous variant
orthologous variants: 81677292-C-G

41356716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: synonymous variant
orthologous variants: 81677292-C-T

41356746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: synonymous variant
orthologous variants: 81677322-C-T

41356756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: missense variant
orthologous variants: 81677332-G-A

41356756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: missense variant
orthologous variants: 81677332-G-T

41356851-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81677445-C-G

41356851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81677445-C-T

41356878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81677472-T-C

41356878-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81677472-T-G

41356916-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81677487-T-A

41356916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81677487-T-C

41356916-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81677487-T-G

http://identifiers.org/hco/22/GRCh38#41356939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81677510-C-A

41356939-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81677510-C-G

41356939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81677510-C-T

41356963-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81677530-A-T

41356964-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81677531-T-G

http://identifiers.org/hco/22/GRCh38#41357082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81677642-C-A

41357082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81677642-C-T

41357130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81677656-G-A

41357130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: intron variant
orthologous variants: 81677656-G-T

http://identifiers.org/hco/22/GRCh38#41357246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81677771-C-A

41357246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: synonymous variant
orthologous variants: 81677771-C-T

41357434-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: 3 prime UTR variant
orthologous variants: 81677971-A-T

http://identifiers.org/hco/22/GRCh38#41357547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81678042-C-A

http://identifiers.org/hco/22/GRCh38#41357662-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81678172-A-C

41357803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: 3 prime UTR variant
orthologous variants: 81678300-G-A

41357803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: 3 prime UTR variant
orthologous variants: 81678300-G-T

41357825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: 3 prime UTR variant
orthologous variants: 81678321-G-A

41357825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: 3 prime UTR variant
orthologous variants: 81678321-G-T

41357833-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: 3 prime UTR variant
orthologous variants: 81678329-C-G

41357833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: 3 prime UTR variant
orthologous variants: 81678329-C-T

41357954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: 3 prime UTR variant
orthologous variants: 81678447-G-T

http://identifiers.org/hco/22/GRCh38#41357972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81678468-C-A

41357972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: 3 prime UTR variant
orthologous variants: 81678468-C-T

http://identifiers.org/hco/22/GRCh38#41358054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81678549-C-A

41358054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: 3 prime UTR variant
orthologous variants: 81678549-C-T

41358128-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: 3 prime UTR variant
orthologous variants: 81678620-T-A

41358168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: 3 prime UTR variant
orthologous variants: 81678659-G-A

41358208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: 3 prime UTR variant
orthologous variants: 81678705-A-G

http://identifiers.org/hco/22/GRCh38#41358255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81678750-C-A

41358321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: 3 prime UTR variant
orthologous variants: 81678776-G-T

41358419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: 3 prime UTR variant
orthologous variants: 81678851-G-T

http://identifiers.org/hco/22/GRCh38#41358427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81678859-C-A

41358427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: 3 prime UTR variant
orthologous variants: 81678859-C-T

http://identifiers.org/hco/22/GRCh38#41358438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81678870-C-A

41358438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: 3 prime UTR variant
orthologous variants: 81678870-C-T

41358501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: 3 prime UTR variant
orthologous variants: 81678931-G-A

41358501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: 3 prime UTR variant
orthologous variants: 81678931-G-T

http://identifiers.org/hco/22/GRCh38#41358549-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81678969-A-C

41358549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: 3 prime UTR variant
orthologous variants: 81678969-A-G

http://identifiers.org/hco/22/GRCh38#41358592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81679007-C-A

41358645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: 3 prime UTR variant
orthologous variants: 81679061-A-G

http://identifiers.org/hco/22/GRCh38#41358714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81679141-C-A

41358714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: 3 prime UTR variant
orthologous variants: 81679141-C-T

http://identifiers.org/hco/22/GRCh38#41358780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81679201-C-A

41358780-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: 3 prime UTR variant
orthologous variants: 81679201-C-G

41358780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: 3 prime UTR variant
orthologous variants: 81679201-C-T

http://identifiers.org/hco/22/GRCh38#41358817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81679220-C-A

41358817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: 3 prime UTR variant
orthologous variants: 81679220-C-T

41358883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: 3 prime UTR variant
orthologous variants: 81679292-G-A

41358883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: 3 prime UTR variant
orthologous variants: 81679292-G-T

41358973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: 3 prime UTR variant
orthologous variants: 81679382-A-G

http://identifiers.org/hco/22/GRCh38#41359016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81679429-C-A

41359028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: 3 prime UTR variant
orthologous variants: 81679441-G-A

41359041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: 3 prime UTR variant
orthologous variants: 81679455-T-C

http://identifiers.org/hco/22/GRCh38#41359105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81679520-C-A

41359135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: 3 prime UTR variant
orthologous variants: 81679550-G-A

41359163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: 3 prime UTR variant
orthologous variants: 81679578-G-A

41359163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: 3 prime UTR variant
orthologous variants: 81679578-G-T

http://identifiers.org/hco/22/GRCh38#41359464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81679870-C-A

41359492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: 3 prime UTR variant
orthologous variants: 81679896-G-T

41359593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: 3 prime UTR variant
orthologous variants: 81679986-G-T

41359651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: 3 prime UTR variant
orthologous variants: 81680035-T-C

41359740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: 3 prime UTR variant
orthologous variants: 81680121-G-A

41359740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: 3 prime UTR variant
orthologous variants: 81680121-G-T

http://identifiers.org/hco/22/GRCh38#41359826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81680203-C-A

41359826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: 3 prime UTR variant
orthologous variants: 81680203-C-T

41359924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: 3 prime UTR variant
orthologous variants: 81680285-A-G

http://identifiers.org/hco/22/GRCh38#41359940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30869
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#81680301-C-A