40998181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4991524-T-C

http://identifiers.org/hco/5/GRCh38#40998248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4991457-C-A

40998248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4991457-C-T

40998408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 4983016-A-G

40998448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 4982976-T-C

40998525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4982900-G-A

40998525-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4982900-G-C

40998525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4982900-G-T

40998536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4982889-G-T

40998581-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4982846-T-A

40998581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4982846-T-C

40998590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4982838-A-G

40998594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4982834-A-G

40998599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4982832-G-A

40998599-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4982832-G-C

40998599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4982832-G-T

http://identifiers.org/hco/5/GRCh38#40998610-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4982821-A-C

40998610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 4982821-A-G

40998936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4982508-T-C

40999020-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4982427-T-A

http://identifiers.org/hco/5/GRCh38#40999021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4982426-C-A

40999021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4982426-C-T

40999109-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4982312-G-C

40999109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4982312-G-T

40999189-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4982234-G-C

40999328-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4982118-G-C

40999328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4982118-G-T

40999337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4982109-T-C

http://identifiers.org/hco/5/GRCh38#40999620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4981820-C-A

40999620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4981820-C-T

40999660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4981778-T-C

40999730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4981708-G-A

40999797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4981638-T-C

40999798-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4981637-T-A

40999798-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4981637-T-G

http://identifiers.org/hco/5/GRCh38#40999881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4981550-C-A

40999881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4981550-C-T

http://identifiers.org/hco/5/GRCh38#40999882-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4981549-A-C

40999882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4981549-A-G

40999925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4981510-G-A

40999925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4981510-G-T

40999942-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4981493-T-A

http://identifiers.org/hco/5/GRCh38#40999979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4981456-C-A

http://identifiers.org/hco/5/GRCh38#41000037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4981407-C-A

41000037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4981407-C-T

41000066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4981379-G-A

41000066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4981379-G-T

41000088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4981360-G-A

41000088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4981360-G-T

41000379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4981021-G-A

41000379-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4981021-G-C

41000442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4980967-A-G

41000450-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4980959-T-A

41000450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4980959-T-C

41000577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4980869-G-A

41000577-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4980869-G-C

41000577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4980869-G-T

41000619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4980827-T-C

41000667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4980779-A-G

41000796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4980650-A-G

41000796-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4980650-A-T

41000875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4980585-G-A

41000876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4980584-G-A

http://identifiers.org/hco/5/GRCh38#41000884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4980576-C-A

41000884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4980576-C-T

http://identifiers.org/hco/5/GRCh38#41000957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4980496-C-A

41000957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4980496-C-T

http://identifiers.org/hco/5/GRCh38#41000972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4980481-C-A

41004162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4978811-A-G

41004244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4978731-G-A

41004244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4978731-G-T

41004260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4978715-C-T

41004293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4978688-T-C

41004327-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4978654-C-G

41004327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4978654-C-T

http://identifiers.org/hco/5/GRCh38#41004371-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4978610-A-C

41004371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4978610-A-G

41004413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4978568-A-G

41004455-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4978526-A-T

http://identifiers.org/hco/5/GRCh38#41004628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4978349-C-A

41005028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4977981-T-C

41005028-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4977981-T-G

41005050-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4977959-T-A

http://identifiers.org/hco/5/GRCh38#41005256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4977772-C-A

41005256-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4977772-C-G

41005256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4977772-C-T

41005299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4977726-T-C

41005299-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4977726-T-G

http://identifiers.org/hco/5/GRCh38#41005399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4977623-C-A

41005399-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4977623-C-G

41005399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4977623-C-T

41005407-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4977615-T-A

41005407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4977615-T-C

41005407-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4977615-T-G

http://identifiers.org/hco/5/GRCh38#41005417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4977605-C-A

41005417-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4977605-C-G

41005417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4977605-C-T

http://identifiers.org/hco/5/GRCh38#41005450-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4977571-A-C

41005450-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4977571-A-T

http://identifiers.org/hco/5/GRCh38#41007332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4976765-C-A

41007332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4976765-C-T

41007368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 4976729-C-T

41007481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4976616-A-G

41007522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4976574-G-A

41007522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4976574-G-T

41007523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4976572-C-T

http://identifiers.org/hco/5/GRCh38#41007530-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4976565-A-C

41007542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4976553-G-A

41007542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4976553-G-T

http://identifiers.org/hco/5/GRCh38#41007554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4976540-C-A

41007555-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4976539-T-A

http://identifiers.org/hco/5/GRCh38#41007582-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4976512-A-C

41008082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4976080-G-T

41008479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4974739-T-C

http://identifiers.org/hco/5/GRCh38#41008484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4974734-C-A

41008484-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4974734-C-G

41008484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4974734-C-T

http://identifiers.org/hco/5/GRCh38#41008529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4974687-C-A

41008529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4974687-C-T

41008536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4974680-T-C

http://identifiers.org/hco/5/GRCh38#41008541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4974675-C-A

41008541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4974675-C-T

41008543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4974673-G-T

41008570-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4974646-A-T

http://identifiers.org/hco/5/GRCh38#41008571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4974645-C-A

41008571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4974645-C-T

41008597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4974624-G-A

41008597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4974624-G-T

http://identifiers.org/hco/5/GRCh38#41008839-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4974382-A-C

41008839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4974382-A-G

http://identifiers.org/hco/5/GRCh38#41008882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4974294-C-A

41008889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4974287-A-G

41009012-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4974153-T-A

41009081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4974084-G-A

41009131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4974035-G-A

41009131-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4974035-G-C

41009131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4974035-G-T

41009184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4973976-G-T

41009201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4973959-G-A

41009201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4973959-G-T

41009215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4973949-G-A

41009215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4973949-G-T

41009219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4973945-G-A

41009219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4973945-G-T

http://identifiers.org/hco/5/GRCh38#41009238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4973925-C-A

41009238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4973925-C-T

41009247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4973916-A-G

41009440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4973729-G-A

41009536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4973637-G-A

41009536-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4973637-G-C

41009536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4973637-G-T

http://identifiers.org/hco/5/GRCh38#41009824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4973354-C-A

41009937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4973262-G-A

http://identifiers.org/hco/5/GRCh38#41010166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4973040-C-A

41010166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4973040-C-T

http://identifiers.org/hco/5/GRCh38#41010175-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4973031-A-C

http://identifiers.org/hco/5/GRCh38#41010227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4972971-C-A

41010227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4972971-C-T

41010623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4972661-C-T

41011109-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4972571-A-T

41011507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4972105-T-C

41011571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4972043-G-A

41011694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4971941-G-T

41011710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4971925-C-T

http://identifiers.org/hco/5/GRCh38#41011977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4971769-C-A

41012068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4971679-C-T

41012069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4971678-C-T

41012407-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4971287-G-C

41012512-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4971187-G-C

41012512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4971187-G-T

41012515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4971184-A-G

41012519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4971180-G-A

41012519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4971180-G-T

41012599-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4971101-G-C

41012611-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 4971089-T-A

http://identifiers.org/hco/5/GRCh38#41012662-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4971038-A-C

41012789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4970921-G-T

41012810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4970901-T-C

41012907-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4970805-C-G

41012907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4970805-C-T

41013020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4970692-A-G

41013144-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4970620-A-T

41013296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4970513-A-G

41013350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4970465-G-A

41013365-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4970450-A-T

http://identifiers.org/hco/5/GRCh38#41013392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4970424-C-A

41013392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4970424-C-T

41013573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4970243-T-C

41013836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4970108-C-T

41013876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4970081-A-G

41013946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4970012-T-C

41015196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4968141-A-G

41015305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4968010-G-T

41015406-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4967905-A-T

http://identifiers.org/hco/5/GRCh38#41015469-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4967842-A-C

41015921-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4967403-T-A

41015952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4967374-G-A

http://identifiers.org/hco/5/GRCh38#41017192-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4965959-A-C

41017598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4965349-G-A

http://identifiers.org/hco/5/GRCh38#41017611-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4965334-A-C

41017705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4965218-G-A

41017705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4965218-G-T

41017774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4965135-G-A

41017774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4965135-G-T

http://identifiers.org/hco/5/GRCh38#41017879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4964847-C-A

41017879-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4964847-C-G

41017879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4964847-C-T

41018028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4964699-G-A

41018028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4964699-G-T

41018070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4964672-G-A

41018070-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4964672-G-C

41018070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4964672-G-T

41018076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4964666-T-C

41018129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4964615-C-T

41018215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4964563-G-T

41018266-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4964513-T-G

41018270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4964509-G-T

41018383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 4964415-T-C

41018396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 4964402-C-T

http://identifiers.org/hco/5/GRCh38#41018520-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4964268-A-C

41018520-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4964268-A-T

41018911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4963944-T-C

41019032-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4963823-C-G

41019032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4963823-C-T

http://identifiers.org/hco/5/GRCh38#41019059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4963799-C-A

41019059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4963799-C-T

http://identifiers.org/hco/5/GRCh38#41019086-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4963787-C-A

41019086-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4963787-C-G

41019113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4963768-G-A

41019113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4963768-G-T

41019145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4963732-G-A

41019145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4963732-G-T

41019763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4963232-G-A

41019763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4963232-G-T

41019805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4963194-G-T

41019849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4963155-T-C

41019971-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4963028-T-A

41019995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4963004-C-T

41020006-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4962981-C-G

41020006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4962981-C-T

41020201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4962806-A-G

41020237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4962760-A-G

41032718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4960891-T-C

41032808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4960800-T-C

41032846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4960750-A-G

41032846-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4960750-A-T

41032856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4960740-A-G

41032857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4960739-A-G

41032912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4960721-T-C

41032932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4960701-G-T

41033108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4960548-G-A

41033651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4960023-A-G

41033707-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4959969-T-G

41033714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4959962-T-C

41033718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4959958-G-A

41033748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4959929-G-T

41033751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4959926-C-T

41033764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4959913-C-T

41033888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4959689-T-C

41033916-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4959661-T-A

41033916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4959661-T-C

41033994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4959625-G-T

http://identifiers.org/hco/5/GRCh38#41034070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4959612-C-A

41034079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4959603-A-G

41034079-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4959603-A-T

41034080-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4959602-A-T

http://identifiers.org/hco/5/GRCh38#41034083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4959599-C-A

41034091-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4959592-A-T

41034319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4959417-T-C

41034434-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4959319-C-G

41034517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4959247-G-T

41034539-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4959225-T-A

41034539-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4959225-T-G

41037723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4956037-G-A

41037793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4955966-G-A

41038006-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4955744-G-C

41038057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4955693-A-G

41038220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4955547-G-A

http://identifiers.org/hco/5/GRCh38#41038437-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4955362-A-C

41038669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4955275-G-T

41038884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4955060-A-G

41038918-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4955026-A-T

41039311-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4954703-T-A

41039311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4954703-T-C

http://identifiers.org/hco/5/GRCh38#41039342-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4954693-A-C

41039408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4954626-C-T

41039426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4954606-T-C

41039458-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4954575-T-G

41039575-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4954460-G-C

41039575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4954460-G-T

41039576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4954459-A-G

41039633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4954403-T-C

http://identifiers.org/hco/5/GRCh38#41039681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4954361-C-A

41039681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4954361-C-T

41039828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4954254-A-G

41039898-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4954186-C-G

41041840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4953484-G-A

41041949-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4953358-A-T

http://identifiers.org/hco/5/GRCh38#41042001-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4953281-A-C

41042008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4953274-T-C

41042080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4953218-A-G

http://identifiers.org/hco/5/GRCh38#41042107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4953191-C-A

41042107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 4953191-C-T

http://identifiers.org/hco/5/GRCh38#41042221-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4953077-A-C

41042221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4953077-A-G

41044821-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4951613-A-T

41045023-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4951439-T-A

41045043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4951420-A-G

41045146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4951338-T-C

41045456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4951184-T-C

41045591-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4951059-T-G

41045678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4950981-A-G

41045678-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4950981-A-T

41045978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4950701-A-G

41045986-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4950693-T-A

41045986-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4950693-T-G

41046228-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4950450-T-A

41046256-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4950381-T-A

41046256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4950381-T-C

41046310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4950332-G-A

41046412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4950229-C-T

41046444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4950197-T-C

41046780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4949852-A-G

http://identifiers.org/hco/5/GRCh38#41047325-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4949199-A-C

41047557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4949000-G-A

41047660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4948899-G-A

41047660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4948899-G-T

41047689-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4948872-T-A

41047689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4948872-T-C

http://identifiers.org/hco/5/GRCh38#41047701-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4948823-A-C

41047701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4948823-A-G

41047701-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4948823-A-T

http://identifiers.org/hco/5/GRCh38#41047704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4948820-C-A

41047704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4948820-C-T

41048030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4948499-A-G

http://identifiers.org/hco/5/GRCh38#41048089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4948077-C-A

41048089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4948077-C-T

41048162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4948026-A-G

http://identifiers.org/hco/5/GRCh38#41048174-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4948014-A-C

41048174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4948014-A-G

41048174-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4948014-A-T

41048309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4947871-C-T

41048452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4947728-G-A

41048471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 4947709-G-A

41048485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4947698-G-A

41048485-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4947698-G-C

41048508-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4947675-T-G

41048566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4947626-A-G

41048566-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4947626-A-T

41048601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4947591-T-C

41048661-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4947383-T-A

41048671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4947373-G-A

41048710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4947328-T-C

http://identifiers.org/hco/5/GRCh38#41048723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4947315-C-A

41048962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4947021-T-C

41048962-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4947021-T-G

41049010-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4946979-A-T

41049011-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4946978-T-A

41049011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4946978-T-C

41049154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4946830-A-G

41049175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4946809-A-G

41049175-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4946809-A-T

41049234-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4946735-A-T

41049568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4946405-G-T

41049585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4946395-A-G

41049598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4946387-G-A

41049779-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4946208-A-T

41049790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4946197-C-T

41050606-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4945372-C-G

41050606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4945372-C-T

41050801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4945207-A-G

41050838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4945168-G-A

41050852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4945154-C-T

41050957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4945049-G-A

41050957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4945049-G-T

41051188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4944548-G-T

41051214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4944523-G-T

41051542-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4944221-T-G

41051572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4944191-G-A

41051572-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4944191-G-C

41051572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4944191-G-T

41051590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4944173-G-A

41051590-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4944173-G-C

41051590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4944173-G-T

41051609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4944154-G-A

41051609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4944154-G-T

41051697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4944080-G-T

41051865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4944018-A-G

http://identifiers.org/hco/5/GRCh38#41052177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4943862-C-A

41052177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4943862-C-T

41052183-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4943856-T-A

41052201-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4943838-T-A

41052201-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4943838-T-G

41052357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4943726-T-C

http://identifiers.org/hco/5/GRCh38#41052441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4943705-C-A

41052441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4943705-C-T

41052480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 4943666-C-T

41052481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4943665-G-A

41052481-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4943665-G-C

41052481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4943665-G-T

41052544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4943602-T-C

http://identifiers.org/hco/5/GRCh38#41052611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4943535-C-A

41052611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4943535-C-T

41052625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4943524-G-A

41052625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4943524-G-T

41052628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4943521-T-C

41054571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4942517-G-A

41054890-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4942211-T-A

http://identifiers.org/hco/5/GRCh38#41054913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4942188-C-A

41054913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4942188-C-T

41054933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4942173-A-G

http://identifiers.org/hco/5/GRCh38#41054988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4942152-C-A

41055091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4942052-A-G

41055610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4941605-A-G

41055638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4941579-T-C

41055638-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4941579-T-G

41055800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 4941430-A-G

http://identifiers.org/hco/5/GRCh38#41055936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4941228-C-A

41055936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4941228-C-T

http://identifiers.org/hco/5/GRCh38#41055962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4941202-C-A

41055987-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4941177-T-A

41055987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4941177-T-C

41056019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4941141-A-G

41056320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4940851-A-G

41056744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4939069-T-C

http://identifiers.org/hco/5/GRCh38#41056765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4939042-C-A

41056878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4938945-G-A

41057091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4938742-T-C

41057188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4938644-G-T

http://identifiers.org/hco/5/GRCh38#41057205-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4938615-A-C

http://identifiers.org/hco/5/GRCh38#41057255-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4938560-A-C

http://identifiers.org/hco/5/GRCh38#41057288-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4938527-A-C

http://identifiers.org/hco/5/GRCh38#41057375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4938440-C-A

http://identifiers.org/hco/5/GRCh38#41057924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4938229-C-A

41057924-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4938229-C-G

41057924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4938229-C-T

http://identifiers.org/hco/5/GRCh38#41057937-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4938211-A-C

41057967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4938194-G-A

41057967-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4938194-G-C

41057967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4938194-G-T

41058282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4937903-G-A

41058282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4937903-G-T

41058544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4937601-G-A

41061189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4935707-C-T

41061209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4935687-C-T

41061225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4935671-T-C

41061607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4935130-A-G

41061667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4935070-G-A

41061786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4934944-T-C

41061797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4934933-G-A

41061797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4934933-G-T

http://identifiers.org/hco/5/GRCh38#41061845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4934893-C-A

41061845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4934893-C-T

41061883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4934841-C-T

41061931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4934774-A-G

41064437-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4934611-T-A

41064437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4934611-T-C

41064487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4934561-C-T

41064614-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4934435-C-G

41064614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4934435-C-T

41064631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4934418-G-T

41064673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4934373-G-A

41064673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4934373-G-T

41064885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4934227-T-C

41065171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4933954-C-T

http://identifiers.org/hco/5/GRCh38#41065194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4933936-C-A

41065194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4933936-C-T

http://identifiers.org/hco/5/GRCh38#41065223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4933907-C-A

41065223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4933907-C-T

41065615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4933582-G-A

41065615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4933582-G-T

41065622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4933575-G-A

41065622-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4933575-G-T

41065627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4933570-G-A

41065627-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4933570-G-C

41065627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4933570-G-T

41066154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4933161-G-T

http://identifiers.org/hco/5/GRCh38#41066852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4932652-C-A

41067085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4932585-T-C

41067094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4932576-T-C

41067094-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4932576-T-G

41067153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 4932517-G-A

41067153-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 4932517-G-C

41067153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 4932517-G-T

http://identifiers.org/hco/5/GRCh38#41067232-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4932438-A-C

41067232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4932438-A-G

41067293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4932379-A-G

41067774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4932230-T-C

41067794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4932211-G-A

41067794-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4932211-G-C

41067845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4932160-G-A

41067913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4932129-A-G

41067941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4932102-G-T

41067943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4932100-T-C

http://identifiers.org/hco/5/GRCh38#41067956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4932087-C-A

41068086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4931951-G-A

41068645-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4931046-T-G

41069476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4930287-C-T

41069514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4930252-C-T

http://identifiers.org/hco/5/GRCh38#41069600-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4930076-A-C

41069603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4930073-G-T

http://identifiers.org/hco/5/GRCh38#41069625-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4930051-A-C

41069625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4930051-A-G

41069625-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4930051-A-T

41069637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4930039-T-C

41069639-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4930037-T-A

http://identifiers.org/hco/5/GRCh38#41069642-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4930034-C-A

41069695-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4929987-T-A

41069695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4929987-T-C

41069695-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4929987-T-G

http://identifiers.org/hco/5/GRCh38#41069725-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4929957-A-C

41069725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 4929957-A-G

http://identifiers.org/hco/5/GRCh38#41069727-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4929955-A-C

41069727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 4929955-A-G

41069846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4929836-T-C

41069944-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4929716-G-C

41070351-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4929127-T-A

41070617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4928888-C-T

41070701-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4928812-A-T

41070773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4928742-G-A

41070773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4928742-G-T

41070785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4928727-A-G

http://identifiers.org/hco/5/GRCh38#41070936-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4928573-A-C

41071050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 4928468-G-T

41071128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 4928391-C-T

http://identifiers.org/hco/5/GRCh38#41071155-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26857
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4928361-A-C