148865341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 20296300-A-G

148865369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 20296272-T-C

148865412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20296228-A-G

148865424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20296216-G-A

148865424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20296216-G-T

148865522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 20296103-A-G

148865572-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20296052-A-T

148865596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20296028-G-T

148865616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20296009-T-C

http://identifiers.org/hco/3/GRCh38#148865619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20296006-C-A

148865619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20296006-C-T

148865628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20295997-T-C

148865630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20295995-G-A

148865630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20295995-G-T

http://identifiers.org/hco/3/GRCh38#148865651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20295975-C-A

148865651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20295975-C-T

148865658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20295968-G-A

148865658-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20295968-G-C

148865669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20295950-G-A

148865669-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20295950-G-C

148865669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20295950-G-T

148865693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20295926-G-A

148865693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20295926-G-T

148865699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20295920-A-G

148866073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20295580-T-C

148866117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20295539-G-A

148867355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20295277-G-A

148867383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20295249-G-A

148867399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20295233-A-G

148867585-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20295057-C-G

148867691-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20294963-T-A

148867720-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20294930-A-T

148868314-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20294622-G-C

148868364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20294573-T-C

148868540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20294399-C-T

148868800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20294175-T-C

148868832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20294141-G-A

148868832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20294141-G-T

148869008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 20293747-T-C

http://identifiers.org/hco/3/GRCh38#148869130-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20291465-A-C

148869130-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20291465-A-T

148869134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20291460-G-A

148869134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20291460-G-T

148869162-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20291431-T-A

148869162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20291431-T-C

148869338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20291295-G-A

148869666-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20291023-T-G

148869770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20290912-G-A

148869770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20290912-G-T

148869889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20290855-T-C

148869891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20290853-G-A

148869891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20290853-G-T

148871455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20289696-T-C

148871487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20289669-A-G

148871487-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20289669-A-T

148871582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20289582-A-G

148871848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20289337-A-G

148872206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20289001-A-G

148872290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20288917-C-T

148872845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20288328-G-A

148872933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20288284-G-A

148872959-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20288258-A-T

148873161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20288031-G-A

148873161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20288031-G-T

148873219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20287977-T-C

148873366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20287782-C-T

148873544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20287603-G-A

148874028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20287140-T-C

148874264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20286939-G-A

148874264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20286939-G-T

148874296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20286908-T-C

148874381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20286824-T-C

148874444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20286761-G-A

148874632-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20286581-T-G

148874818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20286393-G-T

148875044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20286137-C-T

148876171-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20285181-T-G

148876173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20285179-T-C

148876204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20285138-A-G

148876322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20285040-C-T

148876353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20285007-C-T

148876811-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20284704-G-C

http://identifiers.org/hco/3/GRCh38#148876845-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20284671-A-C

148876872-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20284646-T-A

http://identifiers.org/hco/3/GRCh38#148878401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20283333-C-A

148878401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20283333-C-T

148878501-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 20283218-C-G

http://identifiers.org/hco/3/GRCh38#148878511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20283208-C-A

148878511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 20283208-C-T

148878526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 20283193-T-C

148878626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20283092-A-G

148878680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 20283038-T-C

148878680-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 20283038-T-G

148878740-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 20282978-G-C

http://identifiers.org/hco/3/GRCh38#148878883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20282840-C-A

148878883-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20282840-C-G

http://identifiers.org/hco/3/GRCh38#148879044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20282698-C-A

148879277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20282511-C-T

148879369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20282429-C-T

148879574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20281603-T-C

148879574-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20281603-T-G

148879590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20281588-T-C

148879782-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 20281434-A-T

148879927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20281294-G-A

148879927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20281294-G-T

http://identifiers.org/hco/3/GRCh38#148879934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20281287-C-A

148879964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20281255-T-C

http://identifiers.org/hco/3/GRCh38#148879974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20281245-C-A

148879974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20281245-C-T

148880138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20281110-A-G

http://identifiers.org/hco/3/GRCh38#148881150-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20279695-A-C

http://identifiers.org/hco/3/GRCh38#148881199-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20279646-A-C

148881232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20279615-A-G

http://identifiers.org/hco/3/GRCh38#148881448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20279425-C-A

148881448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20279425-C-T

148881720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20279154-A-G

148882485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 20277503-T-C

http://identifiers.org/hco/3/GRCh38#148882618-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20277371-A-C

148882618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20277371-A-G

148882618-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20277371-A-T

148882648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20277347-C-T

148882702-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20277296-A-T

http://identifiers.org/hco/3/GRCh38#148882725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20277273-C-A

148882725-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20277273-C-G

148882725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20277273-C-T

148882781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20277214-A-G

148882876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20277146-C-T

148882968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20277040-A-G

148882976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20277032-A-G

148883066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20276948-C-T

148883083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20276932-C-T

148883549-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20276513-G-C

148883558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20276504-G-A

148883565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20276497-T-C

148883630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20276434-G-T

148883693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20276371-A-G

148883693-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20276371-A-T

148883813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 20276251-T-C

148883872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20276154-G-A

148883872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20276154-G-T

148883899-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20275963-A-T

http://identifiers.org/hco/3/GRCh38#148884189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20275585-C-A

http://identifiers.org/hco/3/GRCh38#148884292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20275482-C-A

148884518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20275282-T-C

148884620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20275184-G-A

148884858-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20274980-T-A

148884864-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20274974-T-A

148884864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20274974-T-C

148884874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20274964-A-G

http://identifiers.org/hco/3/GRCh38#148884881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20274960-C-A

148884881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20274960-C-T

148885076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20274762-A-G

148885600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20274308-C-T

148885631-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20274277-C-G

148885631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20274277-C-T

148886073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20274017-T-C

148886118-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 20273976-A-T

148886306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20273819-G-T

148886321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20273804-T-C

148886348-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20273777-C-G

148886508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20273608-A-G

148886807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20273494-T-C

148886965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20273390-T-C

148887095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20273273-T-C

148887205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20273179-T-C

http://identifiers.org/hco/3/GRCh38#148887364-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20273038-A-C

148887372-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20273030-T-A

148887492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20272912-C-T

148887833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20272066-G-A

148887886-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 20272027-T-A

http://identifiers.org/hco/3/GRCh38#148896525-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20270149-A-C

148896531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 20270143-G-A

148896531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 20270143-G-T

148896559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 20270115-T-C

148896612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 20270062-T-C

148896669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 20270005-A-G

148896701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 20269973-T-C

148896727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20269947-A-G

148896744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20269930-T-C

148896757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20269916-T-C

148896771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20269902-A-G

148896771-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20269902-A-T

http://identifiers.org/hco/3/GRCh38#148896798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20269897-C-A

148896798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20269897-C-T

148896809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20269886-G-A

148896809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20269886-G-T

148896820-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20269871-T-A

148896820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20269871-T-C

148896820-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20269871-T-G

148896854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20269837-T-C

148896854-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20269837-T-G

148896857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20269834-T-C

148896900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20269781-A-G

148896900-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20269781-A-T

148896929-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20269752-T-A

148896929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20269752-T-C

148896995-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20269679-T-A

148896995-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20269679-T-G

148896996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20269678-G-A

148896996-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20269678-G-C

148896996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20269678-G-T

148897001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20269673-C-T

148897020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20269654-T-C

148897020-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20269654-T-G

148897024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20269650-A-G

148897024-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20269650-A-T

http://identifiers.org/hco/3/GRCh38#148897033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20269641-C-A

http://identifiers.org/hco/3/GRCh38#148897039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#20269635-C-A

148897108-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20269572-T-A

148897129-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20269550-T-A

148897129-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20269550-T-G

148897174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2298
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 20269508-A-G