http://identifiers.org/hco/2/GRCh38#98346282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37257239-C-A

98346322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37257286-G-T

98346393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37257357-A-G

98346405-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37257370-A-T

98346456-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37257431-G-C

98346456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37257431-G-T

98346479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37257469-G-A

http://identifiers.org/hco/2/GRCh38#98346504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37257495-C-A

98346504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37257495-C-T

98346529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37257517-G-A

98346529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 37257517-G-T

98346675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37257644-G-A

98346675-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37257644-G-T

http://identifiers.org/hco/2/GRCh38#98346773-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37257699-A-C

98346883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37257803-G-A

98346883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37257803-G-T

98346886-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37257806-G-C

98346886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37257806-G-T

http://identifiers.org/hco/2/GRCh38#98346963-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37257867-A-C

http://identifiers.org/hco/2/GRCh38#98346977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37257879-C-A

98346977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37257879-C-T

98347093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37258013-G-T

98347107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37258027-G-A

98347107-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37258027-G-C

98347107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37258027-G-T

http://identifiers.org/hco/2/GRCh38#98347113-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37258035-A-C

98347113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37258035-A-G

98347113-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37258035-A-T

http://identifiers.org/hco/2/GRCh38#98347122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37258044-C-A

98347122-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37258044-C-G

98347122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37258044-C-T

http://identifiers.org/hco/2/GRCh38#98347137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37258066-C-A

98347137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37258066-C-T

98347206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37258135-A-G

http://identifiers.org/hco/2/GRCh38#98347207-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37258136-A-C

98347207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37258136-A-G

98347257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37258171-G-T

98347263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37258177-C-T

http://identifiers.org/hco/2/GRCh38#98347285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37258205-C-A

98347285-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37258205-C-G

98347285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37258205-C-T

98347432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37258349-C-T

98347450-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37258368-C-G

98347460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37258452-G-T

98347716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37258726-C-T

98347906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37258907-G-T

http://identifiers.org/hco/2/GRCh38#98348274-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37259254-A-C

http://identifiers.org/hco/2/GRCh38#98348558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37259548-C-A

98348558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37259548-C-T

98348866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37259835-G-A

98348886-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37259855-A-T

98348910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37259877-G-A

98349197-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37259997-G-C

98349458-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37260136-C-G

98349809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37260363-T-C

98349894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37260457-G-T

98349920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37260483-C-T

98350060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37260624-T-C

98350174-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37260739-C-G

98350178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37260743-G-A

98350259-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37260803-T-A

98350260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37260804-T-C

98350266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37260810-G-T

98350289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37260841-A-G

http://identifiers.org/hco/2/GRCh38#98350396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37260954-C-A

98350396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37260954-C-T

98350592-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37261197-C-G

98350592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37261197-C-T

98350612-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37261217-T-A

98350652-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37261257-T-A

98350664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37261269-A-G

98350673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37261278-C-T

98350683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37261289-G-T

98350708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37261314-T-C

http://identifiers.org/hco/2/GRCh38#98350720-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37261326-A-C

98350737-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37261355-T-A

98350818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37261432-G-A

http://identifiers.org/hco/2/GRCh38#98351016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37261599-C-A

98351721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37263040-T-C

98351761-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37263080-C-G

http://identifiers.org/hco/2/GRCh38#98351883-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37263238-A-C

98352034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37263376-T-C

98352060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37263399-G-A

98352203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37263548-C-T

98352209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37263554-C-T

98356146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37263887-T-C

98356149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37263890-G-A

98356149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37263890-G-T

98356941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37264008-G-A

98357068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37264145-T-C

98357095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37264172-A-G

98357110-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37264187-G-C

http://identifiers.org/hco/2/GRCh38#98357269-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37264329-C-A

98357269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37264329-C-T

98357275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37264335-A-G

98357275-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37264335-A-T

98357386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37264411-A-G

98357812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37264874-C-T

98357971-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37265037-T-G

98358020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37265084-G-A

98358517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37265636-G-A

98358531-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37265645-A-T

98358537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37265651-T-C

98358557-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37265675-T-A

98358986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37266024-A-G

98359248-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37266282-A-T

98359259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37266300-T-C

98359431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37266458-G-T

98359473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37266500-C-T

98359537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37266571-G-A

98359546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37266580-C-T

98367591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37268578-A-G

http://identifiers.org/hco/2/GRCh38#98367597-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37268584-A-C

98367623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37268611-G-A

98367642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37268630-C-T

98367700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37268687-G-A

98367807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37268821-T-C

98367842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37268855-A-G

98367942-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37268954-G-C

98368199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37269505-C-T

98368250-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37269548-G-C

98368504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37269822-G-A

98368505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37269823-G-A

98368535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37269858-A-G

98369945-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: 5 prime UTR variant
orthologous variants: 37271296-T-A

98369945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: 5 prime UTR variant
orthologous variants: 37271296-T-C

98370056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: synonymous variant
orthologous variants: 37271406-C-T

98370132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37271460-A-G

98370133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37271461-G-A

http://identifiers.org/hco/2/GRCh38#98370139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37271463-C-A

98370139-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37271463-C-G

98370139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37271463-C-T

98370197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37271523-A-G

http://identifiers.org/hco/2/GRCh38#98370221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37271544-C-A

98370390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37273227-C-T

98370523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37273339-A-G

98370523-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37273339-A-T

98370572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37273386-C-T

98370789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37273566-A-G

98370910-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37273624-G-C

98371035-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37273708-T-A

98371166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37273784-G-A

98371193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37273818-T-C

98371365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37273977-A-G

98371637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37274528-C-T

98371668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37274569-T-C

98371707-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37274608-A-T

98373513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37275940-C-T

98373750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37276299-T-C

98373787-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37276336-G-C

98374071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37276620-G-A

98374128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37276671-G-A

98374184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37276719-G-T

98374209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37276743-A-G

98374243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37276779-G-A

98374269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37276805-T-C

98376067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37277990-C-T

98376254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37278133-T-C

98376292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37278197-T-C

98376471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37278363-G-T

98376550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37278441-C-T

98376774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37278654-T-C

98376774-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37278654-T-G

98377022-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37280130-G-T

http://identifiers.org/hco/2/GRCh38#98377219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37280293-C-A

98377224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: 37280298-G-A

http://identifiers.org/hco/2/GRCh38#98377275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37280334-C-A

98377306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 37280365-G-A

http://identifiers.org/hco/2/GRCh38#98377309-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37280368-A-C

http://identifiers.org/hco/2/GRCh38#98377378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37280418-C-A

98377378-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 37280418-C-G

98377378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 37280418-C-T

http://identifiers.org/hco/2/GRCh38#98377383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37280423-C-A

98377383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 37280423-C-T

98377412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37280450-A-G

http://identifiers.org/hco/2/GRCh38#98377419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37280457-C-A

98377419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37280457-C-T

98377427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37280465-G-A

98377427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37280465-G-T

http://identifiers.org/hco/2/GRCh38#98377428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37280466-C-A

98377428-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37280466-C-G

98377428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37280466-C-T

http://identifiers.org/hco/2/GRCh38#98377441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37280479-C-A

98377441-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37280479-C-G

98377441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37280479-C-T

98377455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37280493-A-G

98377468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37280506-C-T

98377602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37280826-A-G

98377617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37280841-A-G

98377630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37280852-T-C

98377634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37280856-G-T

98377638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37280860-G-A

98377641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37280863-G-A

98377643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37280865-T-C

98377736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37280957-G-A

98377736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37280957-G-T

http://identifiers.org/hco/2/GRCh38#98377765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37280986-C-A

98377765-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37280986-C-G

98377765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37280986-C-T

98377784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37281005-G-A

98377784-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37281005-G-C

98377797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37281018-C-T

http://identifiers.org/hco/2/GRCh38#98377814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37281035-C-A

http://identifiers.org/hco/2/GRCh38#98377821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37281042-C-A

http://identifiers.org/hco/2/GRCh38#98377842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37281061-C-A

98377842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37281061-C-T

98377885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37281103-G-A

98377899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37281111-T-C

98377925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37281135-G-A

98377925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37281135-G-T

98377959-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37281165-T-A

98378028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37281239-A-G

98378038-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37281249-A-T

98378040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37281251-A-G

98378081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37281286-G-A

98378261-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37281453-T-A

98378261-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37281453-T-G

http://identifiers.org/hco/2/GRCh38#98378309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37281495-C-A

98378488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37281626-A-G

98378511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37281647-A-G

http://identifiers.org/hco/2/GRCh38#98378568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37281728-C-A

98379111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37283216-G-A

98379111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37283216-G-T

98379119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37283224-T-C

98379782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37283560-A-G

98379783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37283561-T-C

98379783-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37283561-T-G

98379785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37283563-G-A

98379785-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37283563-G-C

98379785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37283563-G-T

98379789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37283567-T-C

98379798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37283579-T-C

98379848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37283646-C-T

98379859-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37283657-T-G

http://identifiers.org/hco/2/GRCh38#98379874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37283672-C-A

98379875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37283673-T-C

98379924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37283717-C-T

98379949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37283743-A-G

http://identifiers.org/hco/2/GRCh38#98379953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37283747-C-A

98379953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37283747-C-T

98379956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37283750-G-A

98379956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37283750-G-T

98379970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37283764-G-T

98380015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37283805-G-A

98380016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37283806-G-A

98380050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37283835-G-T

98380067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37283851-T-C

98380067-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37283851-T-G

98380203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37283942-A-G

98380402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37284126-G-A

98380402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37284126-G-T

98380447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37284162-G-T

98380460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37284175-G-A

98380460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37284175-G-T

http://identifiers.org/hco/2/GRCh38#98380465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37284180-C-A

98380465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37284180-C-T

98380505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37284220-G-A

98380505-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37284220-G-C

98380505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37284220-G-T

98380709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37284393-T-C

98380727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37284411-C-T

98380930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37284606-A-G

98381495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37285233-T-C

98381528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37285260-C-T

98382059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37286290-G-A

98382083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37286316-G-A

http://identifiers.org/hco/2/GRCh38#98382124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37286353-C-A

98382124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37286353-C-T

98382283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37286473-C-T

98382287-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37286477-G-C

98382302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37286492-G-A

98382302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37286492-G-T

98382307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37286497-C-T

98382559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37286884-T-C

98382561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37286886-G-A

98382561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37286886-G-T

98382753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37287067-C-T

98382915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37287277-C-T

98383087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37287418-G-A

98383260-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37287617-T-A

98383260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37287617-T-C

98383303-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37287653-T-A

98383303-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37287653-T-G

98383373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37287727-T-C

98383382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 37287736-C-T

http://identifiers.org/hco/2/GRCh38#98383388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37287742-C-A

98383388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 37287742-C-T

http://identifiers.org/hco/2/GRCh38#98383467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37287880-C-A

98383488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37287906-T-C

98383894-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37288307-T-G

98384393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37288894-G-A

http://identifiers.org/hco/2/GRCh38#98384683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37289405-C-A

98384810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37289518-C-T

98384843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37289538-G-A

98384857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37289552-T-C

98385161-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 37289860-G-C

98385256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 37289946-G-A

98387885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37292350-C-T

98387982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37292433-G-A

98388006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37292456-G-T

98388046-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37292493-T-G

98388049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37292496-A-G

98388056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37292503-G-T

98388077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37292523-A-G

98389159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37292578-G-A

http://identifiers.org/hco/2/GRCh38#98389186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37292603-C-A

98389186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37292603-C-T

98389201-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37292618-A-T

98389299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37292705-G-A

98389453-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37292858-G-C

http://identifiers.org/hco/2/GRCh38#98389507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37292893-C-A

98389507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37292893-C-T

http://identifiers.org/hco/2/GRCh38#98389555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37292940-C-A

http://identifiers.org/hco/2/GRCh38#98389569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37292954-C-A

98389569-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37292954-C-G

98389569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37292954-C-T

98389612-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37293003-C-G

98389612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37293003-C-T

98389620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37293011-G-A

98389620-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37293011-G-C

98389620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37293011-G-T

98389643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37293023-T-C

98389643-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37293023-T-G

98389644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37293024-G-A

98389648-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37293028-G-C

http://identifiers.org/hco/2/GRCh38#98389736-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37293107-C-A

98389736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37293107-C-T

98389789-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37293159-T-G

98389800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37293170-G-A

98389811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37293181-G-A

98389909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37293411-G-A

98389909-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37293411-G-C

98389909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37293411-G-T

98390096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37293582-C-T

98390177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37293654-C-T

98390190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37293667-C-T

98390199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37293676-G-A

98390199-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37293676-G-C

98390613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37294058-C-T

98390790-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37294195-C-G

98390850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37294250-C-T

98391194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37294887-G-A

98391222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37294919-C-T

http://identifiers.org/hco/2/GRCh38#98391841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37297051-C-A

98391841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37297051-C-T

98391847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37297057-C-T

98391861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 37297071-T-C

98391943-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37297153-T-G

http://identifiers.org/hco/2/GRCh38#98391987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37297208-C-A

98392025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37297252-G-A

http://identifiers.org/hco/2/GRCh38#98392033-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37297260-A-C

http://identifiers.org/hco/2/GRCh38#98392085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37297312-C-A

98392085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37297312-C-T

98392280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37297483-C-T

98392691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37297803-C-T

98392759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37297847-G-T

98392805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37297893-G-A

http://identifiers.org/hco/2/GRCh38#98392970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37298052-C-A

http://identifiers.org/hco/2/GRCh38#98393124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37298182-C-A

98393133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37298191-G-A

98393134-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37298192-T-G

98393514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37298434-G-A

98393594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37298489-C-T

98393704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37298596-A-G

98393733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37298625-A-G

98395682-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37299653-G-C

98395756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37299723-T-C

98396019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37299953-G-A

98396079-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37300013-T-A

98396079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37300013-T-C

98396079-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37300013-T-G

98396094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37300028-G-A

98396103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37300037-C-T

98396427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37300361-C-T

98396520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37300454-G-A

98396520-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37300454-G-C

98396559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37300493-G-A

http://identifiers.org/hco/2/GRCh38#98396611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37300545-C-A

98396611-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37300545-C-G

98396611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37300545-C-T

98396739-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37300673-C-G

98396739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37300673-C-T

98396799-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37300733-T-A

98396799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37300733-T-C

98396820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37300754-C-T

98396934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37300868-C-T

98397081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37301015-G-A

98397081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37301015-G-T

98397085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37301019-A-G

98397226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37301160-G-A

98397298-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37301235-G-C

98397298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37301235-G-T

98397301-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37301238-G-T

98397392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37301323-G-A

98397392-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37301323-G-C

98397392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37301323-G-T

98397420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37301353-G-T

http://identifiers.org/hco/2/GRCh38#98397431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#37301365-C-A

98397484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37301401-A-G

98397494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37301411-G-A

98397494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37301411-G-T

98397505-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37301422-T-G

98398015-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: 3 prime UTR variant
orthologous variants: 37302967-C-G

98398019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: 3 prime UTR variant
orthologous variants: 37302971-A-G

98398019-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: 3 prime UTR variant
orthologous variants: 37302971-A-T

98398067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: 3 prime UTR variant
orthologous variants: 37303123-A-G

98398105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: 3 prime UTR variant
orthologous variants: 37303161-A-G

98398127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: 3 prime UTR variant
orthologous variants: 37303414-C-T

98398457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2150
most severe consequence: 3 prime UTR variant
orthologous variants: 37303703-C-T