98121822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: 3 prime UTR variant
orthologous variants: 46537864-G-A

98121822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: 3 prime UTR variant
orthologous variants: 46537864-G-T

98121849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: 3 prime UTR variant
orthologous variants: 46537894-C-T

98121904-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: 3 prime UTR variant
orthologous variants: 46537928-T-A

http://identifiers.org/hco/9/GRCh38#98121941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#46537966-C-A

98121941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: 3 prime UTR variant
orthologous variants: 46537966-C-T

98122275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: 3 prime UTR variant
orthologous variants: 46538167-T-C

http://identifiers.org/hco/9/GRCh38#98122382-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#46538255-A-C

98122411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: 3 prime UTR variant
orthologous variants: 46538282-G-A

98122411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: 3 prime UTR variant
orthologous variants: 46538282-G-T

http://identifiers.org/hco/9/GRCh38#98122429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#46538299-C-A

98122463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: 3 prime UTR variant
orthologous variants: 46538328-G-T

98122479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: 3 prime UTR variant
orthologous variants: 46538377-C-T

98122679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: 3 prime UTR variant
orthologous variants: 46538572-C-T

98122697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: 3 prime UTR variant
orthologous variants: 46538590-G-T

98122722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: 3 prime UTR variant
orthologous variants: 46538609-G-T

98122773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: 3 prime UTR variant
orthologous variants: 46538658-G-T

98122948-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: 3 prime UTR variant
orthologous variants: 46538792-T-A

http://identifiers.org/hco/9/GRCh38#98124524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#46538834-C-A

98124524-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: 3 prime UTR variant
orthologous variants: 46538834-C-G

98124524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: 3 prime UTR variant
orthologous variants: 46538834-C-T

98124597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: 3 prime UTR variant
orthologous variants: 46538909-G-A

98124597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: 3 prime UTR variant
orthologous variants: 46538909-G-T

98124663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: 3 prime UTR variant
orthologous variants: 46538975-G-A

98124663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: 3 prime UTR variant
orthologous variants: 46538975-G-T

98124721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: 3 prime UTR variant
orthologous variants: 46539031-T-C

http://identifiers.org/hco/9/GRCh38#98124723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#46539033-C-A

98124727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: 3 prime UTR variant
orthologous variants: 46539089-T-C

98124796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: missense variant
orthologous variants: 46539158-C-T

98124974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46539339-T-C

98125115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46539456-T-C

98125200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46539544-T-C

98126503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46540393-A-G

98126612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: synonymous variant
orthologous variants: 46540478-C-T

98126664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: missense variant
orthologous variants: 46540530-A-G

98126785-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: missense variant
orthologous variants: 46540651-G-C

98126957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46540780-G-A

http://identifiers.org/hco/9/GRCh38#98126962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#46540785-C-A

http://identifiers.org/hco/9/GRCh38#98126993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#46540821-C-A

98127066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46540887-A-G

98127066-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46540887-A-T

98127780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46541473-T-C

98127934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46541627-C-T

http://identifiers.org/hco/9/GRCh38#98128025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#46541725-C-A

98128025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46541725-C-T

98128040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46541771-G-A

98128040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46541771-G-T

98128192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: synonymous variant
orthologous variants: 46541915-C-T

98128202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: missense variant
orthologous variants: 46541925-G-A

98128202-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: missense variant
orthologous variants: 46541925-G-C

http://identifiers.org/hco/9/GRCh38#98128231-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#46541954-A-C

98128327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46542014-G-A

http://identifiers.org/hco/9/GRCh38#98128402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#46542059-C-A

98128402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46542059-C-T

98128472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46542120-A-G

98128480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46542128-T-C

98128480-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46542128-T-G

98128481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46542129-G-A

98128481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46542129-G-T

98128486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46542134-A-G

98128755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46542386-T-C

http://identifiers.org/hco/9/GRCh38#98128804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#46542439-C-A

98128859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46542515-G-T

98128909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46542571-C-T

98128955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46542693-C-T

http://identifiers.org/hco/9/GRCh38#98129668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#46543266-C-A

http://identifiers.org/hco/9/GRCh38#98129689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#46543287-C-A

98129689-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46543287-C-G

98129689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46543287-C-T

98129995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46543542-G-A

98129995-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46543542-G-C

98129995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46543542-G-T

98130822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46543928-G-A

98130822-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46543928-G-C

98130822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46543928-G-T

98130886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46543961-G-A

98130886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46543961-G-T

98130919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46544027-G-T

98130949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46544057-G-A

http://identifiers.org/hco/9/GRCh38#98131000-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#46544108-A-C

98131077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46544184-G-A

98131077-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46544184-G-C

98131077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46544184-G-T

http://identifiers.org/hco/9/GRCh38#98131204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#46544305-C-A

98131204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46544305-C-T

98131977-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46545464-C-G

98131977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46545464-C-T

98132002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46545488-C-T

98132085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46545526-G-T

http://identifiers.org/hco/9/GRCh38#98132126-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#46545556-A-C

98132143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46545573-T-C

98132164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46545592-G-A

98132169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46545597-G-T

98132367-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46545803-G-C

98132367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46545803-G-T

http://identifiers.org/hco/9/GRCh38#98132368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#46545804-C-A

98132368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46545804-C-T

98132638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46546297-G-A

98132735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46546362-C-T

http://identifiers.org/hco/9/GRCh38#98132881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#46546525-C-A

98132921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46546568-G-A

98132972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46546597-C-T

98133047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: synonymous variant
orthologous variants: 46546658-G-A

98133047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: synonymous variant
orthologous variants: 46546658-G-T

98133188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: synonymous variant
orthologous variants: 46546799-C-T

98133296-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46546908-A-T

http://identifiers.org/hco/9/GRCh38#98133306-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#46546918-A-C

98133306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46546918-A-G

98133306-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46546918-A-T

http://identifiers.org/hco/9/GRCh38#98133442-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#46547035-A-C

98134400-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46548440-C-G

98134400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46548440-C-T

98134672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46548654-G-T

98134677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46548659-G-T

98134685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46548667-T-C

98134685-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46548667-T-G

http://identifiers.org/hco/9/GRCh38#98134696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#46548676-C-A

98134740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46548716-T-C

98134756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46548732-T-C

98134878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: synonymous variant
orthologous variants: 46548840-C-T

98134929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: synonymous variant
orthologous variants: 46548891-C-T

98135002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46548961-G-A

98135002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46548961-G-T

http://identifiers.org/hco/9/GRCh38#98135005-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#46548964-A-C

98135047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46549006-A-G

98135055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46549014-A-G

98135058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46549017-G-T

98135116-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46549051-G-C

98135163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46549079-C-T

98136198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46549812-A-G

98136286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46549891-A-G

98136459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46550100-C-T

98136671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46550308-C-T

98136732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46550366-T-C

98137062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46550737-A-G

98137076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46550751-G-A

98137293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46551058-G-A

98137539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46551311-G-A

98137559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46551320-G-T

98137713-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46551484-T-G

http://identifiers.org/hco/9/GRCh38#98137739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#46551520-C-A

98137795-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46551604-A-T

98137800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46551609-T-C

98141868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46552894-T-C

98141908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46552926-A-G

98142189-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46553761-C-G

98142229-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46553801-C-G

98142291-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron_variant, undefined
orthologous variants: 46553840-G-C

98143178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46554542-A-G

98143470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46554789-A-G

98146128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46555783-G-A

98146384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron_variant, undefined
orthologous variants: 46556026-T-C

98146384-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron_variant, undefined
orthologous variants: 46556026-T-G

98146393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron_variant, undefined
orthologous variants: 46556030-G-A

98146440-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron_variant, undefined
orthologous variants: 46556077-T-G

98146492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron_variant, undefined
orthologous variants: 46556107-C-T

98146933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46556544-C-T

98147017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46556600-A-G

98147084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46556657-T-C

http://identifiers.org/hco/9/GRCh38#98147092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#46556665-C-A

98150536-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46559901-C-G

98150543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46559908-A-G

98150780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46560205-T-C

98150802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46560223-G-A

98151020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46560450-G-A

98156794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46562254-A-G

98156819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46562286-G-A

98156844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46562311-C-T

98156938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46562409-T-C

http://identifiers.org/hco/9/GRCh38#98157280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#46562730-C-A

98157330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46562769-A-G

98157330-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46562769-A-T

98157369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46562791-G-T

98157496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: synonymous variant
orthologous variants: 46562931-A-G

http://identifiers.org/hco/9/GRCh38#98157701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#46563135-C-A

98157701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46563135-C-T

98157721-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46563172-G-C

http://identifiers.org/hco/9/GRCh38#98157763-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#46563340-A-C

98157771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46563348-G-A

98157771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46563348-G-T

98157806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46563383-A-G

98158087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46563624-G-T

98162444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46563782-C-T

98162703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46563972-C-T

98163745-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46564480-A-T

98163747-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46564482-A-T

98163749-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46564484-A-T

98163751-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46564486-A-T

98164176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46564887-C-T

98164609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46565788-G-A

98164639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46565817-T-C

98164662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46565840-G-A

98164662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46565840-G-T

98164885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46566043-T-C

98165387-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46566508-G-C

98165529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46566630-C-T

98165536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46566637-T-C

http://identifiers.org/hco/9/GRCh38#98165842-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#46567116-A-C

98165887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46567165-G-A

98165887-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46567165-G-C

98165974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46567260-T-C

98166013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46567307-T-C

98166073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46567345-T-C

98166169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46567442-A-G

98166326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46567586-T-C

98168736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46569395-T-C

98168739-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46569407-G-C

98168839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46569489-T-C

98169457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46570018-G-A

98169614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46570150-G-A

98171267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46573524-G-A

98171519-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46573736-T-A

98171602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46573905-C-T

98171615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46573921-C-T

98171699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46573995-C-T

http://identifiers.org/hco/9/GRCh38#98171716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#46574028-C-A

98171716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46574028-C-T

98171982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46574257-G-A

98171986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46574261-G-A

98172027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46574301-G-A

98176095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46585631-C-T

98176389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46585947-T-C

98176446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46585987-G-A

98176627-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46586134-G-C

98177165-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46586626-C-G

98178470-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46589024-T-G

98178624-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46589156-T-G

98178643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46589175-T-C

98178973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46589485-A-G

98179135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46589642-A-G

98179435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46589851-T-C

98179939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46590209-G-A

98179989-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46590234-T-A

98179989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46590234-T-C

98180133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46590315-G-A

98180297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46590381-C-T

98180503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46590590-C-T

98184579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46593646-T-C

98184755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46593905-C-T

98184775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46593925-G-A

http://identifiers.org/hco/9/GRCh38#98184776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#46593926-C-A

98184776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46593926-C-T

http://identifiers.org/hco/9/GRCh38#98185432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#46596059-C-A

98185442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 46596069-A-G

98185469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 46596095-C-T

98185531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 46596154-A-G

98185635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 46596232-A-G

98185652-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 46596248-A-T

98185656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 46596252-C-T

98185703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46596288-G-A

http://identifiers.org/hco/9/GRCh38#98185949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#46596489-C-A

98185952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46596492-G-A

98186003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46596555-G-A

98186040-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46596588-C-G

http://identifiers.org/hco/9/GRCh38#98186428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#46596879-C-A

98189134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46598675-G-A

98189209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46598742-G-T

98189259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46598778-A-G

98189259-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46598778-A-T

98189310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46598829-T-C

98189652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46599233-G-A

98189733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46599293-T-C

98189747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46599307-G-A

98189870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46599427-T-C

98189902-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46599483-T-G

98190066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46599648-G-A

98190066-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46599648-G-C

98190127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46599729-C-T

98190131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46599733-C-T

98190561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46600130-G-A

98190812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46600381-T-C

98190944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46600501-C-T

98191018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46600567-A-G

98191045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46600610-G-A

98191045-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46600610-G-C

98191045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46600610-G-T

http://identifiers.org/hco/9/GRCh38#98191222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#46600739-C-A

98191222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46600739-C-T

98191603-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46600976-T-G

98191737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46601094-G-A

98192006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46601324-G-A

98192028-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46601346-G-C

98192367-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46601662-G-C

98192457-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46601751-T-A

98192491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46601787-C-T

98192492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46601788-A-G

http://identifiers.org/hco/9/GRCh38#98192493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#46601789-C-A

98192493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46601789-C-T

http://identifiers.org/hco/9/GRCh38#98192498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#46601794-C-A

98192498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: 46601794-C-T

http://identifiers.org/hco/9/GRCh38#98192555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2255
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#46601813-C-A