26581255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30642974-G-A

26581255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30642974-G-T

26581257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30642976-G-A

26581257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30642976-G-T

26581263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30642981-A-G

26581263-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30642981-A-T

26581343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 30643061-G-T

26581432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30643192-G-A

26581432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30643192-G-T

26581679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30643674-G-A

26581735-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30643730-G-C

26581837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30643816-G-A

26582057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30644022-G-A

26582063-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30644028-A-T

26582200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30644215-G-A

http://identifiers.org/hco/2/GRCh38#26582390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30644426-C-A

http://identifiers.org/hco/2/GRCh38#26582715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30644682-C-A

http://identifiers.org/hco/2/GRCh38#26582720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30644687-C-A

26582720-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30644687-C-G

26582720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30644687-C-T

http://identifiers.org/hco/2/GRCh38#26582744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30644711-C-A

26582744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30644711-C-T

http://identifiers.org/hco/2/GRCh38#26582784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30644749-C-A

26582784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30644749-C-T

http://identifiers.org/hco/2/GRCh38#26582947-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30644905-A-C

26582947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30644905-A-G

26582972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30644928-G-A

26582972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30644928-G-T

26583021-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30644981-T-A

26583021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30644981-T-C

26583038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30644993-G-A

26583038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30644993-G-T

26583203-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30645172-T-A

26583410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30645331-G-T

26583480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30645362-A-G

26583801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30645841-G-A

26583801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30645841-G-T

26583809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30645849-G-A

26583822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 30645862-C-T

26583828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30645868-A-G

http://identifiers.org/hco/2/GRCh38#26583885-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30645925-A-C

26583950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30645994-A-G

26583951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30645995-A-G

26583975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30646013-A-G

26583977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30646016-A-G

26584032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30646049-G-A

26584032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30646049-G-T

26584078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30646094-C-T

26584190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30646209-C-T

26584198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30646217-A-G

26584412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30646430-C-T

26586563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30646609-T-C

26586701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30646733-G-A

26586702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30646734-G-A

26586712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30646744-G-T

26586981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30646926-C-T

26586995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30646941-G-A

26587796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30647218-A-G

26587966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30647359-G-T

26588463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30647862-T-C

http://identifiers.org/hco/2/GRCh38#26588506-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30647901-A-C

http://identifiers.org/hco/2/GRCh38#26588671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30648026-C-A

26588719-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30648075-A-T

26588824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30648094-C-T

http://identifiers.org/hco/2/GRCh38#26589621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30648219-C-A

http://identifiers.org/hco/2/GRCh38#26589793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30648365-C-A

26589793-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30648365-C-G

26589975-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30648581-C-G

26589986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30648592-G-A

26590143-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30648732-G-C

26590143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30648732-G-T

26590229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30648814-G-A

http://identifiers.org/hco/2/GRCh38#26590357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30648925-C-A

26590357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30648925-C-T

26590475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30649014-G-A

26590493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30649031-G-T

26590583-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30649116-T-A

26590761-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30649309-C-G

26590883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30649434-T-C

26591067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30649604-T-C

26591116-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30649704-G-C

26591116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30649704-G-T

26591136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30649740-G-A

26591273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30649959-G-T

26591280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30649986-G-A

26591384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30650092-A-G

26591453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30650136-G-A

26591516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30650176-G-A

26591521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30650181-G-A

26591526-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30650186-A-T

26591527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30650187-C-T

26591621-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30650398-T-A

26594539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30654378-C-T

26594541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30654380-G-T

26594587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30654424-A-G

26594876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30654682-A-G

26594880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30654686-G-A

26595002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30655202-T-C

26595026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30655225-A-G

26595026-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30655225-A-T

http://identifiers.org/hco/2/GRCh38#26595063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30655262-C-A

26595118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30655309-A-G

26595118-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30655309-A-T

26595124-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30655315-T-A

26595124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30655315-T-C

26595124-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30655315-T-G

http://identifiers.org/hco/2/GRCh38#26595132-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30655323-A-C

26595132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30655323-A-G

http://identifiers.org/hco/2/GRCh38#26595147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30655347-C-A

26595147-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30655347-C-G

http://identifiers.org/hco/2/GRCh38#26595285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30655485-C-A

26595285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 30655485-C-T

26595331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30655527-G-A

26595348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30655544-T-C

26595383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30655579-T-C

26595394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30655590-A-G

26595446-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30655639-T-A

26598647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30666716-C-T

26598683-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30666760-T-A

26599344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30667394-T-C

26599571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30667667-T-C

26599600-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30667696-T-G

26599777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30668986-T-C

26600572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30669591-C-T

26600593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30669612-C-T

http://identifiers.org/hco/2/GRCh38#26600617-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30669634-A-C

26600669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30669676-G-A

26600702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30669707-T-C

http://identifiers.org/hco/2/GRCh38#26603935-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30672347-A-C

http://identifiers.org/hco/2/GRCh38#26603944-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30672356-A-C

26604140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30672533-G-A

26604209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30672572-G-T

26604273-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30672634-G-C

26604391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30672785-T-C

26604660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30673040-C-T

26604718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30673103-G-A

26604739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30673124-G-A

26604862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30673215-C-T

http://identifiers.org/hco/2/GRCh38#26604943-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30673285-A-C

26605241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30673560-A-G

26605374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30673673-G-A

26605438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30673742-G-T

26605447-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30673751-T-A

26605479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30673783-G-A

26605509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30673811-C-T

26605511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 30673813-G-T

http://identifiers.org/hco/2/GRCh38#26605521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30673824-C-A

26605521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 30673824-C-T

http://identifiers.org/hco/2/GRCh38#26605672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#30673970-C-A

26605672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30673970-C-T

http://identifiers.org/hco/2/GRCh38#26605928-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30674162-A-C

26606067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30674284-G-A

26606173-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30674378-C-G

http://identifiers.org/hco/2/GRCh38#26606181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30674386-C-A

26606200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30674405-G-T

26606385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30675120-G-A

26606385-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 30675120-G-C

26608593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30676444-G-A

26608609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30676457-G-A

26608661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30676510-G-A

26608693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30676539-G-A

26608818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30676622-G-A

26608818-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30676622-G-C

26608856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30676638-C-T

26608857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30676639-G-A

26608857-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30676639-G-C

26609337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30677067-C-T

26610017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30677671-G-A

26610036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 30677687-C-T

26610141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30677736-G-A

26610141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30677736-G-T

26610655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30678921-G-A

26610712-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30678975-T-G

26610775-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30679027-A-T

26610874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30679071-T-C

http://identifiers.org/hco/2/GRCh38#26610916-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30679085-A-C

26611209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30679321-C-T

26611455-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30679558-G-C

26611512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30679613-C-T

26611543-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30679644-A-T

26611793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30679903-G-A

26612193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30680203-C-T

26612281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30680272-A-G

26612538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30680478-T-C

26612699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30680618-G-A

26612768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30680673-C-T

26613130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30681030-T-C

26613148-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30681048-G-C

26613227-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30681108-A-T

26613297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30681149-G-A

26613365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30681206-C-T

26613680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30681457-T-C

26613680-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30681457-T-G

26613816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30681570-C-T

26613937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30681639-G-A

26614008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30681709-G-A

26614049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30681739-G-A

26614111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30681801-C-T

26614237-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30681926-C-G

26614327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30682012-G-A

http://identifiers.org/hco/2/GRCh38#26614867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30682711-C-A

26614910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30682753-T-C

26615293-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30682985-C-G

26615366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30683052-G-A

26615373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30683059-G-A

26615634-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30683197-A-T

26615652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30683215-T-C

26615652-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30683215-T-G

26615660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30683223-T-C

26615679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30683242-A-G

26615735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30683295-G-A

26615736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30683296-G-A

26615747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30683307-G-A

26615811-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30683367-T-A

26616063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30683618-C-T

http://identifiers.org/hco/2/GRCh38#26616381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30683944-C-A

26616381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30683944-C-T

26616523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30684079-G-A

26617432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30684387-C-T

26617439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30684394-C-T

26617461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30684416-C-T

26617578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30684516-G-A

26617628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30684592-C-T

26617982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30684869-C-T

26618100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30684943-G-A

26618523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30685134-C-T

26618800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30685306-G-A

26618800-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30685306-G-C

26618800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30685306-G-T

http://identifiers.org/hco/2/GRCh38#26618818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30685330-C-A

26618894-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30685414-G-C

26619127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30685623-G-A

26619249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30685769-C-T

26619253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30685773-G-T

26619306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30685820-A-G

26619399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30685911-G-A

26619562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30686032-C-T

http://identifiers.org/hco/2/GRCh38#26619661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30686121-C-A

http://identifiers.org/hco/2/GRCh38#26619718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30686176-C-A

26619749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 30686207-A-G

26623705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30688373-A-G

26623725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30688393-A-G

26628124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30690167-G-A

26628231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30690274-G-A

26628541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30690664-G-A

http://identifiers.org/hco/2/GRCh38#26628806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30691023-C-A

26628806-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30691023-C-G

26629052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30691254-G-A

26629106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30691304-C-T

26629297-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30691443-T-A

26629297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30691443-T-C

http://identifiers.org/hco/2/GRCh38#26629349-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30691507-A-C

26629349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30691507-A-G

26629349-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30691507-A-T

http://identifiers.org/hco/2/GRCh38#26629351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30691509-C-A

26629351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30691509-C-T

26629473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: synonymous variant
orthologous variants: 30691597-A-G

http://identifiers.org/hco/2/GRCh38#26629550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30691679-C-A

26629550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30691679-C-T

http://identifiers.org/hco/2/GRCh38#26629582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30691692-C-A

26629588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30691698-T-C

26629655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30691752-A-G

26629781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30691819-C-T

26629935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30691959-C-T

26629958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30691983-G-A

26630096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30692117-T-C

http://identifiers.org/hco/2/GRCh38#26630184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30692190-C-A

26630184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30692190-C-T

26630418-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30692383-G-T

26630429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30692394-G-A

26630529-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30692489-T-G

26630871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30692614-T-C

26630921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30692663-G-A

26631083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, undefined
orthologous variants: 30693221-T-C

26631924-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30693760-C-G

26632238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30694034-G-A

26632279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30694077-G-A

26632353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30694149-C-T

26633057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30694527-C-T

26633379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30694815-G-A

26633379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30694815-G-T

26633417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30694854-G-A

http://identifiers.org/hco/2/GRCh38#26633420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30694857-C-A

26633420-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30694857-C-G

26633448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30694884-G-A

26633521-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30694958-C-G

26633521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30694958-C-T

26633662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30695099-C-T

26633817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30695217-C-T

26633871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30695264-G-A

26634063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30695451-T-C

http://identifiers.org/hco/2/GRCh38#26634177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30695557-C-A

26634434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30695784-A-G

http://identifiers.org/hco/2/GRCh38#26634735-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30696067-A-C

26634735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30696067-A-G

26635105-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30696352-T-A

http://identifiers.org/hco/2/GRCh38#26635413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30696559-C-A

26635447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30696584-A-G

26635707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30696791-A-G

26635909-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30696990-T-G

26635959-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30697027-T-A

26636833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30697754-T-C

26636875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30697797-C-T

http://identifiers.org/hco/2/GRCh38#26636968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30697871-C-A

26637135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30698005-G-T

26637208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30698066-C-T

26637352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30698213-T-C

26637399-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30698254-T-G

http://identifiers.org/hco/2/GRCh38#26637507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30698361-C-A

26637507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30698361-C-T

26637609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30698467-G-A

26637785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 30698617-C-T

26637807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 30698639-G-T

26637808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 30698640-G-A

26637888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 30698710-G-A

26637888-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 30698710-G-C

26637963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 30698794-C-T

26638360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 30700405-G-A

26638394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 30700439-T-C

26638503-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 30700554-C-G

26638503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 30700554-C-T

26639537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30701016-G-A

26639537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30701016-G-T

26639574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30701059-T-C

26639645-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30701196-C-G

26640016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30701572-G-A

http://identifiers.org/hco/2/GRCh38#26640076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30701608-C-A

26640078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30701610-C-T

26640127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30701655-G-A

26640127-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30701655-G-C

26640312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30701828-C-T

http://identifiers.org/hco/2/GRCh38#26640383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30701885-C-A

26640383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30701885-C-T

26640422-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30701913-G-C

26640422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30701913-G-T

26640447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30701938-G-A

26640447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30701938-G-T

http://identifiers.org/hco/2/GRCh38#26640639-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#30702121-A-C

26640639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, undefined
orthologous variants: 30702121-A-G

26640643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, undefined
orthologous variants: 30702125-A-G

26640714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30702198-A-G

26640722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron_variant, undefined
orthologous variants: 30702206-G-A

http://identifiers.org/hco/2/GRCh38#26641230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#30703018-C-A

26641230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33703
most severe consequence: intron variant
orthologous variants: 30703018-C-T