http://identifiers.org/hco/3/GRCh38#3799460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#107506759-C-A

3799460-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107506759-C-G

3799460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107506759-C-T

3799471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107506770-C-T

3799511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107506809-G-A

http://identifiers.org/hco/3/GRCh38#3799516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#107506814-C-A

3799530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107506828-G-A

3799573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107506885-G-A

3799573-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107506885-G-C

3799573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107506885-G-T

3799585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107506897-T-C

http://identifiers.org/hco/3/GRCh38#3799599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#107506910-C-A

http://identifiers.org/hco/3/GRCh38#3799601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#107506912-C-A

3799601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107506912-C-T

3799633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107506944-A-G

3799647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107506958-T-C

http://identifiers.org/hco/3/GRCh38#3799668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#107506979-C-A

3799668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107506979-C-T

http://identifiers.org/hco/3/GRCh38#3799724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#107507036-C-A

3799734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107507046-G-A

3799734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107507046-G-T

3799754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107507066-G-A

3799754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107507066-G-T

3799807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107507118-T-C

3799934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107507220-G-A

3799934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107507220-G-T

3800000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107507306-A-G

3800073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107507379-A-G

3800073-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107507379-A-T

3800300-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107507573-A-T

3800426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107507688-T-C

3800434-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107507696-G-C

3800437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107507699-G-A

3800443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107507708-G-A

3800443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107507708-G-T

3800489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107507754-T-C

3800824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107507890-C-T

http://identifiers.org/hco/3/GRCh38#3800892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#107507938-C-A

3800941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107507991-G-A

http://identifiers.org/hco/3/GRCh38#3800961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#107508024-C-A

3800961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 107508024-C-T

http://identifiers.org/hco/3/GRCh38#3800962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#107508025-C-A

3800963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107508026-A-G

3800984-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 107508075-C-G

3800984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 107508075-C-T

3800993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 107508084-G-A

3801024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 107508140-G-A

3801116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 107508232-C-T

3801140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 107508256-G-A

3801140-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 107508256-G-C

3801140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 107508256-G-T

3801162-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 107508270-G-C

3801162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 107508270-G-T

3801247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107508345-G-A

3801247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107508345-G-T

3801270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107508368-T-C

http://identifiers.org/hco/3/GRCh38#3801324-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#107508422-A-C

3801788-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107508895-G-C

3801948-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107509044-C-G

3802201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107509293-G-A

3802255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107509342-G-T

3802387-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107509471-C-G

3802403-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107509487-C-G

3802411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107509495-C-T

3802553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107509611-A-G

http://identifiers.org/hco/3/GRCh38#3802614-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#107509686-A-C

3802642-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107509714-T-G

3802663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107509739-G-T

3802765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107509841-A-G

3802963-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107510087-C-G

3802963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107510087-C-T

3803266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107510399-T-C

3803282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107510413-G-A

3804174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107511091-G-A

http://identifiers.org/hco/3/GRCh38#3804333-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#107511238-A-C

3804333-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107511238-A-T

3804394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107511300-T-C

3804566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107511470-G-A

3804588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107511492-T-C

3804973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107511881-G-A

3805080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107511989-C-T

3805121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107512031-C-T

http://identifiers.org/hco/3/GRCh38#3805156-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#107512066-A-C

3805156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107512066-A-G

3805569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107512469-T-C

http://identifiers.org/hco/3/GRCh38#3805596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#107512496-C-A

3805642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107512556-C-T

3805654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107512567-G-A

3805927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107513116-G-A

3806026-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107513217-T-A

3806131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107513303-G-A

3806351-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107513512-T-A

3806416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107513577-G-A

3806437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107513593-T-C

3806583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107513724-A-G

3806656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107513789-G-A

3806711-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107513849-C-G

3806740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107513876-C-T

3806930-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107514068-G-C

3806930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107514068-G-T

3807129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107514236-C-T

3807194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107514304-C-T

3807241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107514352-G-A

3807599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107515031-T-C

3808061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107515518-C-T

3808255-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107515707-T-A

http://identifiers.org/hco/3/GRCh38#3808419-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#107515888-A-C

3808426-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107515897-G-C

3808474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107515945-G-A

3808629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107516130-G-T

http://identifiers.org/hco/3/GRCh38#3808646-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#107516147-C-A

3808646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107516147-C-T

3808720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107516220-T-C

http://identifiers.org/hco/3/GRCh38#3808742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#107516243-C-A

3808768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107516274-A-G

3808894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107516389-A-G

3808895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107516390-C-T

3808959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107516454-C-T

3808967-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107516462-C-G

3809619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107517136-G-A

3809684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107517192-C-T

3809791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107517282-G-A

3810043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107517520-T-C

3811093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107518126-A-G

3811661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107518682-G-A

3811787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107518804-A-G

3811956-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107518976-T-A

3811991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107519016-A-G

3812267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107519275-G-A

http://identifiers.org/hco/3/GRCh38#3812374-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#107519370-A-C

3812461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107519459-A-G

3812470-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107519468-G-C

3812697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107519983-A-G

3812745-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107520040-A-T

http://identifiers.org/hco/3/GRCh38#3812781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#107520077-C-A

3812781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107520077-C-T

3812800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107520096-G-A

3812800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107520096-G-T

3812982-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107520243-T-A

3812986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107520247-A-G

3813269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107520355-T-C

3813278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107520364-C-T

3813366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107520458-T-C

3813557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107520817-G-A

3813683-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107521116-T-A

3813952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107521342-A-G

3814192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107521594-G-A

http://identifiers.org/hco/3/GRCh38#3815322-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#107521936-A-C

3815366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107521982-C-T

http://identifiers.org/hco/3/GRCh38#3815472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#107522053-C-A

3815533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107522106-G-A

3815901-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107523061-C-G

http://identifiers.org/hco/3/GRCh38#3816040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#107523205-C-A

3816275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107523447-A-G

http://identifiers.org/hco/3/GRCh38#3816511-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#107523715-A-C

3816620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107523801-T-C

3816977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107524170-A-G

3817182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107524363-C-T

3817416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107524570-C-T

http://identifiers.org/hco/3/GRCh38#3817443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#107524689-C-A

3817707-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107525101-A-T

3817773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107525154-A-G

3817813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107525196-A-G

3817966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107525364-C-T

3818099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107525491-C-T

3818184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107525579-A-G

3818473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107525861-G-A

3818483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107525871-A-G

3818923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107526249-G-A

3820778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107529532-A-G

3821203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107529939-A-G

3821373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107530129-T-C

3821403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107530164-C-T

3821470-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107530220-G-T

3821514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107530280-A-G

3821627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107530396-G-A

http://identifiers.org/hco/3/GRCh38#3822514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#107530749-C-A

3822745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107530999-A-G

3822757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107531011-A-G

3822823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107531384-G-T

3822856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107531417-C-T

3823020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107531555-G-A

3823020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107531555-G-T

3823194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107531701-C-T

3823269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107531782-C-T

3823324-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107531823-A-T

3823386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107531860-G-A

3823634-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107532112-G-C

3823991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107532458-C-T

3824065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107532626-C-T

3824315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107533135-T-C

3824703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107533533-G-A

3824703-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107533533-G-C

3824785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107533614-A-G

3825094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107534077-T-C

http://identifiers.org/hco/3/GRCh38#3825159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#107534166-C-A

3825159-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107534166-C-G

3825219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107534227-C-T

http://identifiers.org/hco/3/GRCh38#3825308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#107534317-C-A

3825315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107534324-C-T

3825374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107534383-G-A

3825374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107534383-G-T

3825390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107534399-G-A

3825390-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107534399-G-C

3825694-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107534684-C-G

3825775-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107534767-A-T

3825776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107534768-A-G

3826003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107534987-T-C

3826589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107535534-C-T

3826609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107535553-G-A

3826694-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107535634-G-C

3826698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107535638-A-G

3826762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107535697-G-T

3826841-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107535768-C-G

3826919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107535847-C-T

3827088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107536006-C-T

3827100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107536018-G-A

3827100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107536018-G-T

3827542-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107536446-A-T

3835862-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107538149-T-A

3835894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107538177-G-A

3840641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107540591-G-A

3840661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107540611-G-A

3840845-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107540729-A-T

3841875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107541353-A-G

3842564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107541657-C-T

3842587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107541682-A-G

3842764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107542653-T-C

3842835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107542728-A-G

3843444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107543271-G-A

3843480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107543309-A-G

3843930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107543616-T-C

3843990-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107543674-G-C

3843990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107543674-G-T

http://identifiers.org/hco/3/GRCh38#3844340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#107543928-C-A

3844340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107543928-C-T

http://identifiers.org/hco/3/GRCh38#3844437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#107544024-C-A

3844518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 107544096-G-A

3844518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 107544096-G-T

http://identifiers.org/hco/3/GRCh38#3844567-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#107544144-A-C

3844567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 107544144-A-G

3844572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 107544149-T-C

3845124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 107544686-T-C

http://identifiers.org/hco/3/GRCh38#3845271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#107544833-C-A

3845271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 107544833-C-T

3845463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 107545025-C-T

3845508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 107545070-A-G

3845649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 107545211-C-T

3845727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 107545289-T-C

http://identifiers.org/hco/3/GRCh38#3845850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#107545412-C-A

3845850-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 107545412-C-G

3845850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 107545412-C-T

http://identifiers.org/hco/3/GRCh38#3845925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#107545487-C-A

3845925-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 107545487-C-G

3845925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 107545487-C-T

3845958-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 107545520-C-G

3845958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 107545520-C-T

3846078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 107545640-T-C

3846213-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 107545775-C-G

3846213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 107545775-C-T

3846267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 107545829-C-T

http://identifiers.org/hco/3/GRCh38#3846432-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#107545994-A-C

3846477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 107546039-C-T

3846498-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 107546060-C-G

3846498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 107546060-C-T

3846534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 107546096-C-T

3846738-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 107546300-T-A

3846878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 107546442-G-A

3846878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 107546442-G-T

http://identifiers.org/hco/3/GRCh38#3846976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#107546540-C-A

3846976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 107546540-C-T

3847007-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 107546571-T-G

3847038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 107546602-T-C

http://identifiers.org/hco/3/GRCh38#3847039-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#107546603-A-C

3847039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 107546603-A-G

3847039-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 107546603-A-T

3847480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 107547036-T-C

http://identifiers.org/hco/3/GRCh38#3847676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#107547216-C-A

3847676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 107547216-C-T

3847718-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 107547254-T-A

3847847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 107547398-G-T

3847896-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 107547444-C-G

3847896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 107547444-C-T

3847936-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 107547483-T-G

3848216-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 107547843-C-G

3848259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 107547884-A-G

3848334-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 107547965-G-C

3848336-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 107547967-T-G

3848419-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 107548074-C-G

3848419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 107548074-C-T

http://identifiers.org/hco/3/GRCh38#3848427-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#107548082-A-C

3848427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 107548082-A-G

3848563-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 107548266-T-G

3848778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 107548462-A-G

3849081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 107548714-T-C

3849272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 107548866-C-T

3849394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 107548979-G-A

3849425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 107549010-T-C

3849425-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 107549010-T-G

3849581-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 107549166-T-A

3849634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 107549200-A-G

3849808-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20980
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 107549367-C-G