http://identifiers.org/hco/15/GRCh38#42067284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120095986-C-A

http://identifiers.org/hco/15/GRCh38#42067397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120096069-C-A

42067399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120096071-A-G

42067399-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120096071-A-T

42067405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120096077-G-A

42067405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120096077-G-T

42067536-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120096198-T-A

42067536-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120096198-T-G

42067580-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120096215-G-T

42067743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120096351-T-C

http://identifiers.org/hco/15/GRCh38#42067803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120096424-C-A

42067911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120096528-G-A

42067914-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120096531-C-G

42067916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120096533-T-C

42068068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120096698-G-T

42068271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120096845-A-G

42068287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120096861-G-T

42068351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120096885-G-A

42068351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120096885-G-T

http://identifiers.org/hco/15/GRCh38#42068365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120096893-C-A

42068626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 120097010-A-G

42068751-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120097156-C-G

42068751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120097156-C-T

42068974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120097378-G-A

42068974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120097378-G-T

42069084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120097482-G-A

42069084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120097482-G-T

42069258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120097630-G-A

42069301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120097667-G-A

42069301-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120097667-G-C

42069809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120099203-T-C

42069809-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120099203-T-G

42069849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120099214-G-A

42069849-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120099214-G-C

42069849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120099214-G-T

42069875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120099222-A-G

http://identifiers.org/hco/15/GRCh38#42069943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120099284-C-A

42069943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120099284-C-T

42070058-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120099399-C-G

42070058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120099399-C-T

http://identifiers.org/hco/15/GRCh38#42070131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120099474-C-A

42070131-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120099474-C-G

42070131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120099474-C-T

42070300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120099600-G-A

42070300-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120099600-G-C

42070300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120099600-G-T

42070347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120099639-T-C

42070347-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120099639-T-G

42070350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120099642-G-A

42070350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120099642-G-T

http://identifiers.org/hco/15/GRCh38#42070352-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120099644-A-C

42070352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120099644-A-G

42070352-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120099644-A-T

42070353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120099645-T-C

42070353-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120099645-T-G

http://identifiers.org/hco/15/GRCh38#42070385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120099677-C-A

42070385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120099677-C-T

42070451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120099776-G-A

42070451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120099776-G-T

42070455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120099780-T-C

42070469-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120099794-T-A

42070469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120099794-T-C

http://identifiers.org/hco/15/GRCh38#42070549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120099856-C-A

42070549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120099856-C-T

42070664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120099950-T-C

42070667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120099953-G-A

http://identifiers.org/hco/15/GRCh38#42070671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120099957-C-A

42070671-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120099957-C-G

42070671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120099957-C-T

42070680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120099966-G-A

42070680-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120099966-G-T

42070684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120099970-G-A

http://identifiers.org/hco/15/GRCh38#42070915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120100201-C-A

42070915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120100201-C-T

http://identifiers.org/hco/15/GRCh38#42071012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120100315-C-A

42071042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120100348-C-T

42071081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120100387-G-A

42071160-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120100471-C-G

42071286-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120100597-G-C

42071302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120100613-G-A

42071309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120100620-G-A

42071309-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120100620-G-C

42071309-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120100620-G-T

42071323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 120100634-G-A

42071323-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 120100634-G-C

42071323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 120100634-G-T

42071393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120100703-T-C

42071557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 120100863-G-A

42071557-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 120100863-G-C

42071557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 120100863-G-T

42071584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120100896-C-T

http://identifiers.org/hco/15/GRCh38#42071585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120100897-C-A

42071585-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120100897-C-G

http://identifiers.org/hco/15/GRCh38#42071647-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120100984-A-C

42071678-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120101015-T-A

42071678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120101015-T-C

42071678-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120101015-T-G

42071689-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120101026-T-A

42071689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120101026-T-C

42071689-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120101026-T-G

42071717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120101055-G-A

42071717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120101055-G-T

42071877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120101179-G-A

42071877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120101179-G-T

42071935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120101237-A-G

42072001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120101299-G-A

42072001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120101299-G-T

42072005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120101303-G-A

42072005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120101303-G-T

http://identifiers.org/hco/15/GRCh38#42072012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120101313-C-A

42072012-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120101313-C-G

42072012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120101313-C-T

42072015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120101316-T-C

http://identifiers.org/hco/15/GRCh38#42072127-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120101419-A-C

42072127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120101419-A-G

42072127-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120101419-A-T

http://identifiers.org/hco/15/GRCh38#42072151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120101433-C-A

http://identifiers.org/hco/15/GRCh38#42072213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120101470-C-A

42072213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120101470-C-T

42072397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 120101639-G-A

42072397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 120101639-G-T

42072433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120101658-T-C

42072443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120101668-G-A

42072443-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120101668-G-C

42072443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120101668-G-T

42072521-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120101751-G-C

42072521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120101751-G-T

42072816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120102433-G-T

42075476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120103002-T-C

42075476-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120103002-T-G

42075480-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120103006-A-T

42079528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, undefined
orthologous variants: 120105706-G-A

42079528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, undefined
orthologous variants: 120105706-G-T

http://identifiers.org/hco/15/GRCh38#42079529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#120105707-C-A

42079529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 120105707-C-T

http://identifiers.org/hco/15/GRCh38#42079531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#120105709-C-A

42079531-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, undefined
orthologous variants: 120105709-C-G

42079531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, undefined
orthologous variants: 120105709-C-T

42079628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: missense variant
orthologous variants: 120105806-C-T

42079740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: missense variant
orthologous variants: 120105918-C-T

42080415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120106777-G-A

42080990-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 120107534-T-G

http://identifiers.org/hco/15/GRCh38#42081207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120107733-C-A

42081207-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120107733-C-G

42081217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120107743-G-A

42081224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120107750-G-T

42081226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120107752-G-T

http://identifiers.org/hco/15/GRCh38#42081440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120107884-C-A

42081624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120108069-T-C

42081704-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120108141-C-G

42081784-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120108219-G-C

42081789-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 120108224-T-A

42081789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 120108224-T-C

42081881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120108313-G-A

42082265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120108382-T-C

42082299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120108416-T-C

42082446-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120108547-G-C

42082709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120108937-G-A

42082907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120109137-C-T

42082924-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120109153-A-T

http://identifiers.org/hco/15/GRCh38#42082928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120109160-C-A

42083178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120109329-G-T

42083312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 120109463-C-T

42083356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120109508-T-C

42083356-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120109508-T-G

42083388-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120109540-C-G

42083388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120109540-C-T

42083434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120109586-G-A

42083434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120109586-G-T

42083451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120109603-C-T

42083564-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120109669-G-C

42083564-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 120109669-G-T

http://identifiers.org/hco/15/GRCh38#42083737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120109768-C-A

42083737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 120109768-C-T

42083825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120109856-G-A

42083825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120109856-G-T

42083973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120109994-G-A

http://identifiers.org/hco/15/GRCh38#42084028-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120110041-A-C

42084028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120110041-A-G

42084028-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120110041-A-T

http://identifiers.org/hco/15/GRCh38#42084036-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120110049-A-C

42084036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 120110049-A-G

42084061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120110074-A-G

42084061-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120110074-A-T

42084082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120110095-T-C

42084083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120110096-G-T

42084929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120110950-C-T

http://identifiers.org/hco/15/GRCh38#42084955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120110971-C-A

42084971-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120110982-G-C

42084971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120110982-G-T

42085185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120111208-T-C

42085369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120111365-T-C

42085454-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120111443-T-A

42085455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120111444-C-T

http://identifiers.org/hco/15/GRCh38#42085560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120111533-C-A

42085560-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120111533-C-G

42085561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120111534-A-G

42085590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120111551-C-T

http://identifiers.org/hco/15/GRCh38#42085625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120111586-C-A

42085625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120111586-C-T

42085880-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120111808-T-G

42085931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120111859-G-A

42085972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120111924-T-C

42086023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120111968-G-A

42086088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120112026-G-A

42086088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120112026-G-T

42086105-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120112040-A-T

42086242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: missense variant
orthologous variants: 120112145-G-A

42086242-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: missense variant
orthologous variants: 120112145-G-C

42086242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: missense variant
orthologous variants: 120112145-G-T

42086330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: synonymous variant
orthologous variants: 120112233-A-G

42086985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120113965-C-T

http://identifiers.org/hco/15/GRCh38#42087084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120114066-C-A

http://identifiers.org/hco/15/GRCh38#42087155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120114120-C-A

42087155-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120114120-C-G

42087155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120114120-C-T

42087191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120114156-G-A

42087191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120114156-G-T

42087256-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120114222-C-G

42087423-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: missense variant
orthologous variants: 120114396-G-C

42087423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: missense variant
orthologous variants: 120114396-G-T

42087534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120114513-G-A

http://identifiers.org/hco/15/GRCh38#42087644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120114601-C-A

42087718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120114669-C-T

42087749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120114701-T-C

42087749-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120114701-T-G

http://identifiers.org/hco/15/GRCh38#42087800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120114758-C-A

42087800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120114758-C-T

42088263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120115370-G-A

42088306-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120115410-T-A

42088394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120115472-G-T

42088576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120115643-G-A

http://identifiers.org/hco/15/GRCh38#42088626-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120115685-A-C

42088626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120115685-A-G

42088628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120115687-C-T

42088668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120115711-C-T

42089016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120116027-C-T

42089068-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120116062-C-G

42089381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120116335-G-T

42090037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120117169-G-A

42090086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120117215-C-T

42090238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120117363-G-A

42092546-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron_variant, undefined
orthologous variants: 120117877-C-G

42092699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120118019-G-A

42093482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120118571-G-A

42093605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120118683-G-T

42093623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120118701-C-T

42093713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120118780-G-T

42093981-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120119020-C-G

http://identifiers.org/hco/15/GRCh38#42094298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120119330-C-A

42094298-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120119330-C-G

42094298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120119330-C-T

42094386-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120119412-G-C

42094396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: intron variant
orthologous variants: 120119422-G-T

42094431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: missense variant
orthologous variants: 120119457-G-T

http://identifiers.org/hco/15/GRCh38#42094442-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#120119468-A-C

42094507-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30038
most severe consequence: 5 prime UTR variant
orthologous variants: 120119531-G-C